Indian Patents
Title of Invention

"A PROCESS TO POLYMERISE AN OLEFIN"
Abstract The invention provides for polymerization catalyst compositions, .and for methods for introducing the catalyst compositions into a polymerization reactor. More particularly, the method combines a catalyst component containing slurry and a catalyst component containing solution to form the completed catalyst composition for introduction into the polymerization reactor. The invention is also directed to methods of preparing the catalyst component slurry, the catalyst component solution and the catalyst compositions, to methods of controlling the properties of polymer products utilizing the catalyst compositions, and to polymers produced therefrom.
Full Text POLYMERIZATION PROCESS
FIELD OF THE INVENTION
The invention relates to a process for polymerizing olefin(s). Generally, the invention relates to polymerization catalyst compositions, and to methods for introducing the catalyst compositions into a polymerization reactor. More particularly, the method combines a catalyst component slurry with a catalyst component solution to form the completed catalyst composition for introduction into the polymerization reactor. The invention also relates to methods of preparing the catalyst component slurries, the catalyst component solutions, and the catalyst compositions, to methods of controlling the properties of polymer products utilizing the catalyst compositions, and to polymers produced therefrom.
BACKGROUND OF THE INVENTION
Advances in polymerization and catalysis have resulted in the capability to produce many new polymers having improved physical and chemical properties useful in a wide variety of superior products and applications. With the development of new catalysts the choice of polymerization (solution, slurry, high pressure or gas phase) for producing a particular polymer has been greatly expanded. Also, advances in polymerization technology have provided more efficient, highly productive and economically enhanced processes. Especially illustrative of these advances is the development of technology utilizing bulky ligand metallocene catalyst systems and other advanced metallocene-type catalyst systems.
To utilize these systems in industrial slurry or gas phases processes, it is useful that the catalyst compound be immobilized on a earner or support such as, for example silica or alumina. The use of supported or heterogeneous catalysts increases process efficiencies by assuring that the forming polymeric particles achieve a shape and density that improves reactor operability and ease of handling. However, bulky ligand metallocene and metallocene-type catalysts typically exhibit lower activity when supported than when

utilized in unsupported or homogeneous form. This "support effect" makes commercialization of these promising catalyst systems more difficult.
U.S. Patent Nos. 5,3 17,036 and 5,693,727 and European publication EP-A-0 593 083 and PCT publication WO 97/46599 all describe various processes and techniques for introducing liquid unsupported catalysts to a polymerization reactor.
U.S. Patent No. 6,069,213 discloses combining a supported and an unsupported metallocene catalysts in the polymerization of olefms, European publication EP 0 965 601 A disclose a combination of a solid Ziegler-Natta catalyst with a liquid catalyst in toluene or Kaydol activated with methyl alumoxane or modified methyl alumoxane, and Chinese Published Patent Application No. 971 16451.7 discloses combining an unsupported metallocene with a supported methylalumoxane. None of these references, however, discloses a catalyst composition prepared by continuously combining a catalyst component slurry with a catalyst component solution, then introducing the combination into an operating polymerization reactor.
While all these methods have been described in the art, there exists a need to reduce the support effect for bulky ligand metallocene and metallocene-type polymerization catalyst compositions, for an improved method for introducing catalyst compositions, and especially for introducing mixed catalyst compositions, into a polymerization reactors, and for methods to control the properties of polymer products utilizing such catalyst compositions.
The invention generally provides polymerization catalyst compositions and methods for introducing the catalyst compositions into a polymerization reactor. More particularly, the method combines a catalyst component containing slurry and a catalyst component containing solution to form the completed catalyst composition for introduction into the polymerization reactor. The invention is also directed to methods of preparing the catalyst component shiny, the catalyst component solution, and the catalyst compositions, to methods of controlling the properties of polymer products utilizing the catalyst compositions, arid to polymers produced therefrom.

In one aspect, (he invention provides a process to polymerize olefin(s) which includes the steps of continuously combining a catalyst component slurry with a catalyst component solution to form a catalyst composition and introducing the catalyst composition and one or more olefin(s) into an operating polymerization reactor.
In another aspect, the invention provides a process to control polymer properties which includes the steps of continuously combining a catalyst component slurry with a catalyst component solution to form a catalyst composition, introducing the catalyst composition into a polymerization reactor with one or more olefm(s) to form a polymer product, measuring a sample of the polymer product to obtain an initial product property and changing a process parameter to obtain a second product property.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 illustrates an embodiment of one equipment configuration to utilize the invention.
Figure 2 illustrates the catalyst feed configuration used for Example 2. Figure 3 illustrates the catalyst feed configuration used for Example 3. Figure 4 illustrates the catalyst feed configuration used for Example 4. Figure 5 is a typical SEC curve of a polymer of the invention. Figure 6 illustrates the catalyst feed configuration used for Examples 11-14. Figure 7 is a plot showing the plenum flow effects on particle size over time.
DETAILED DESCRIPTION OF THE INVENTION L. Introduction
The components of the catalyst composition of the invention include catalyst compounds, activator compounds and support materials. The catalyst components are utilized in a slurry and/or in a solution where the slurry and solution are combined then introduced into a polymerization reactor. ti-jCabijyst Coinjjouiids
The catalyst compounds which may be utilized in the catalyst compositions of the invention include: Group 15 containing metal compounds; bulky ligand rnetallocene

compounds; phenoxide catalyst compounds; additionally discovered catalyst compounds; and conventional-type transition metal catalysis.
A: Group 15 Coiitaiiihig Metal Catalyst Compound
The catalyst composition of the invention may include one or more Group 15 containing metal catalyst compounds. The Group 15 containing compound generally includes a Group 3 to 14 metal atom, preferably a Group 3 to 7, more preferably a Group 4 to 6, and even more preferably a Group 4 metal atom, bound to at least one leaving group and also bound to at least two Group 15 atoms, at least one of which is also bound to a Group 15 or 16 atom through another group.
In one embodiment, at least one of the Group 15 atoms is also bound to a Group 15 or 16 atom through another group which may be a C, to C20 hydrocarbon group, a heteroatom containing group, silicon, germanium, tin, lead, or phosphorus, wherein the Group 15 or 16 atom may also be bound to nothing or a hydrogen, a Group 14 atom containing group, a halogen, or a heteroatom containing group, and wherein each of the two Group 15 atoms are also bound to a cyclic group and may optionally be bound to hydrogen, a. halogen, a heteroatom or a hydrocarbyl group, or a heteroatom containing group.
In another embodiment, the Group 15 containing metal compound of the present invention may be represented by the formulae: (Formula Remove)
wherein
M is a Group 3 to 12 transition metal or a Group 13 or 14 main group metal, preferably a
Group 4, 5, or 6 metal, and more preferably a Group 4 metal, and most preferably
zirconium, titanium or hafnium,
each X is independently a leaving group, preferably, an anionic leaving group, and more
preferably hydrogen, a hydrocarbyl group, a heteroatom or a halogen, and most preferably
an alkyl.
y is 0 or 1 (when y is 0 group L' is absent),
n is the oxidation state of M, preferably +3, +4, or +5, and more preferably +4,
m is the formal charge of the YZL or the YZL' ligand, preferably 0, -1, -2 or-3, and more
preferably -2,
L is a Group 15 or 16 element, preferably nitrogen,
L' is a Group 15 or 16 element or Group 14 containing group, preferably carbon, silicon or
germanium,
Y is a Group 15 element, preferably nitrogen or phosphorus, and more preferably nitrogen,
Z is a Group 15 element, preferably nitrogen or phosphorus, and more preferably nitrogen,
R' and R2 are independently a C, to C20 hydrocarbon group, a heteroatom containing group
having up to twenty carbon atoms, silicon, germanium, tin, lead, or phosphorus, preferably
a C, to C20 alkyl, aryl or aralkyi group, more preferably a linear, branched or cyclic C2 to
G,n alkyl group, most preferably a C2 to C6 hydrocarbon group. R1 and R2 may also be
interconnected to each other.
RJ is absent or a hydrocarbon group, hydrogen, a halogen, a heteroatom containing group,
preferably a linear, cyclic or branched alkyl group having 1 to 20 carbon atoms, more
preferably R3 is absent, hydrogen or an alkyl group, and most preferably hydrogen
R4 and R5 are independently an alkyl group, an aryl group, substituted aryl group, a cyclic
alkyl group, a substituted cyclic alkyl group, a cyclic aralkyi group, a substituted cyclic
aralkyi group or multiple ring system, preferably having up to 20 carbon atoms, more
preferably between 3 and 10 carbon atoms, and even more preferably a C, to C20
hydrocarbon group, a C, to C2n aryl group or a C, to C20 aralkyi group, or a heteroatom
containing group, for example PR3 where R is an alkyl group,
R1 and R2 may be interconnected to each other, and/or R4 and R5 may be interconnected to
each other,
Rfl and R7 are independently absent, hydrogen, an alkyl group, halogen, heteroatom, or a
hydrocarbyl group, preferably a linear, cyclic or branched alkyl group having 1 to 20
carbon atoms, and more preferably absent, and
R* is absent, or is hydrogen, a Group 14 atom containing group, a halogen, or a heleroatom
containing group.
By "formal charge of the YZL or YZL1 iigand", it is meant the charge of the entire ligand absent the metal and the leaving groups X.
By "R1 and R2 may also be interconnected" it is meant that R1 and R2 may be directly bound to each other or may be bound to each other through other groups. By "R4 and R5 may also be interconnected" it is meant that R4 and R3 may be directly bound to each other or may be bound to each other tlirough oilier groups.
An alkyl group may be linear, branched alkyl radicals, alkenyl radicals, alkynyl radicals, cycloalkyl radicals, aryl radicals, acyl radicals, aroyl radicals, alkoxy radicals, aryloxy radicals, alkylthio radicals, dialkylamino radicals, alkoxycarbonyl radicals, aryloxycarbonyl radicals, carbomoyl radicals, alkyl- or dialkyl- carbamoyl radicals, acyloxy radicals, acylamino radicals, aroylamino radicals, straight, branched or cyclic,
alkylene radicals, or combination thereof. An aralkyl group is defined to be a substituted aiyl group.
In a preferred embodiment R" and R5 are independently a group represented by the following formula:
(Figure Remove)
Bond to Z or Y
"orrnula 1
wherein
R8 to R12 are each independently hydrogen, a C, to CAO alkyl group, a halide, a heteroatom,
a heteroatom containing group containing up to 40 carbon atoms, preferably a C, to C20 linear or branched alkyl group, preferably a methyl, ethyl, propyl or butyl group, any two R groups may form a cyclic group and/or a heterocyclic group. The cyclic groups may be aromatic. In a preferred embodiment R9, R10 and R12 are independently a methyl, ethyl, propyl or butyl group (including all isomers), in a preferred embodiment R9, R10 and R12 are methyl groups, and R8 and R1' are hydrogen.
In a particularly preferred embodiment R4 and R5 are both a group represented by the following formula:
(Figure Remove)
In this embodiment, M is a Group 4 metal, preferably zirconium, titanium or hafnium, and even more preferably zirconium; each of L, Y, and Z is nitrogen; each of R1 and R2 is -CH2-CH2-; R3 is hydrogen; and R6 and R7 are absent.
In a particularly preferred embodiment the Group 15 containing metal compound is represented by Compound 1 below:
(Figure Remove)

In compound I, Ph equals phenyl.
The, Group 15 containing metal compounds utilized in the catalyst composition of the-invention are prepared by methods known in the art, such as those disclosed in EP 0
893 454 Al, U.S. Patent No. 5,889,128 and the references cited in U.S. Patent No. 5,889,128 which are all herein incorporated by reference. U.S. Application Serial Number 09/312,878, filed May 17, 1999, discloses a gas or slurry phase polymerization process using a supported bisamide catalyst, which is also incorporated herein by reference.
A preferred direct synthesis of these compounds comprises reacting the neutral ligand, (see for example YZL or YZL' of formula I or II) with M"Xn (M is a Group 3 to 14 metal, n is the oxidation state of M, each X is an anionic group, such as halide, in a non-coordinating or weakly coordinating solvent, such as ether, toluene, xylene, benzene, methylene chloride, and/or hexane or other solvent having a boiling point above 60 °C, at about 20 to about 150 °C (preferably 20 to 100 °C), preferably for 24 hours or more, then treating the mixture with an excess (such as four or more equivalents) of an alkylating agent, such as methyl magnesium bromide in ether. The magnesium salts are removed by filtration, and the metal complex isolated by standard techniques.
In one embodiment the Group 15 containing metal compound is prepared by a method comprising reacting a neutral ligand, (see for example YZL or YZL' of fonnula I or II) with a compound represented by the fonnula IVTX,, (where M is a Group 3 to 14 metal, n is the oxidation stale of M, each X is an anionic leaving group) in a non-coordinating or weakly coordinating solvent, at about 20 °C or above, preferably at about 20 to about 100 °C, then treating the mixture with an excess of an alkylating agent, then recovering the metal complex. In a preferred embodiment the solvent has a boiling point above 60 °C, such as toluene, xylene, benzene, and/or hexane. In another embodiment the solvent comprises ether and/or methylene chloride, either being preferable.
For additional information of Group 15 containing metal compounds, please see Mitsui Chemicals, Inc. in HP 0 893 454 Al which discloses transition metal amides combined with activators to polymerize olefins.
In one embodiment the Group 15 containing metal compound is allowed to age prior to use as a polymerization. It has been noted on at least one occasion that one such catalyst compound (aged at least 48 hours) performed better than a newly prepared catalyst compound.
Metallocene Compounds
The catalyst composition of the invention may include one or more bulky ligand melallocene compounds (also referred to herein as metallocenes).
Generally, bulky ligand metallocene compounds include half and full sandwich compounds having one or more bulky ligands bonded to at least one metal atom. Typical bulky ligaud metallocene compounds are generally described as containing one or more bulky ligand(s) and one or more leaving group(s) bonded to at least one metal atom.
The bulky ligands are generally represented by one or more open, acyclic, or fused ring(s) or ring system(s) or a combination thereof. These bulky ligands, preferably the ring(s) or ring system(s) are typically composed of atoms selected from Groups 13 to 16 atoms of the Periodic Table of Elements, preferably the atoms are selected from the group consisting of carbon, nitrogen, oxygen, silicon, sulfur, phosphorous, germanium, boron and aluminum or a combination thereof. Most preferably, the ring(s) or ring system(s) are composed of carbon atoms such as but not limited to those cyclopentadienyl ligands or cyclopentadienyl-type ligand structures or other similar functioning ligand structure such as a pentadiene, a cyclooclatetraendiyl or an imide ligand. The metal atom is preferably selected from Groups 3 through 15 and the lanthanide or actinide series of the Periodic Table of Elements. Preferably the metal is a transition metal from Groups 4 through 12, more preferably Groups 4, 5 and 6, and most preferably the transition metal is from Group 4.
In one embodiment, the catalyst composition of the invention includes one or more bulky ligand metallocene catalyst compounds represented by the formula:
LALHMQ,, (III)
where M is a metal atom from the Periodic Table of the Elements and may be a Group 3 to 12 metal or from the lanthanide or actinide series of the Periodic Table of Elements, preferably M is a Group 4, 5 or 6 transition metal, more preferably M is a Group 4 transition metal, even more preferably M is zirconium, hafnium or titanium. The bulky ligands, LA and LB, are open, acyclic or fused ring(s) or ring system(s) and are any
ancillary' ligand system, including unsubstituted or substituted, cyclopentadienyl ligands or cyclopentadienyl-type ligands, heteroatom substituted and/or heteroatom containing cyclopentadienyl-lype ligands. Non-limiting examples of bulky ligands include cyclopentadienyl ligands, cyclopentaphenanthreneyl ligands, indenyl ligands, benzindenyl ligands, fluorenyl ligands, octahydrofluorenyl ligands, cyclooctatetraendiyl ligands, cyclopentacyclododecene ligands, azenyl ligands, azulene ligands, pentalene ligands, pliosplioyl ligands, phosphinimine (WO 99/40125), pyrrolyl ligands, pyrozolyl ligands, carbazolyl ligands, borabenzene ligands and the like, including hydrogenated versions thereof, for example letrahydroindenyl ligands. In one embodiment, LA and LR may be any other ligand structure capable of TT-bonding to M. In yet another embodiment, the atomic molecular weight (MW) of LA or L" exceeds 60 a.m.u., preferably greater tlian 65 a.m.u. In another embodiment, LA and LB may comprise one or more heteroatoms, for example, nitrogen, silicon, boron, gemianium, sulfur and phosphorous, in combination with carbon atoms to form an open, acyclic, or preferably a fused, ring or ring system, for example, a hetero-cyclopentadienyl ancillary ligand. Other LA and LB bulky ligands include but are not limited to bulky amides, phosphides, alkoxides, aryloxides, imides, catbolides, borolhdes, porphyrins, phthalocyanines, corrins and other polyazomacrocycles. Independently, each LA and LB may be the same or different type of bulky ligand that is bonded to M. In one embodiment of Formula 111 only one of either LA or LB is present.
Independently, each LA and Ln may be unsubstituted or substituted with a combination of subsliluent groups R. Non-limiting examples of substituent groups R include one or more from the group selected from hydrogen, or linear, branched alkyi radicals, or alkenyl radicals, alkynyl radicals, cycloalkyl radicals or aryl radicals, acyl radicals, aroyl radicals, alkoxy radicals, aryloxy radicals, alkylthio radicals, dialkylamino radicals, alkoxycarbonyl radicals, aryloxycarbonyl radicals, carbomoyl radicals, alkyi- or dialkyl- carbamoyl radicals, acyloxy radicals, acylamino radicals, aroylamino radicals, straight, branched or cyclic, alkylene radicals, or combination thereof. In a preferred embodiment, substituent groups R have up to 50 non-hydrogen atoms, preferably from 1 to 30 carbon, (hat can also be substituted with halogens or heteroatoms or the like. Non-limiting examples of alkyi substituents R include methyl, ethyl, propyl, butyl, pentyl,
hexyl, cyclopentyl, cyclohexyl, benzyl or phenyl groups and the like, including all their isomers, for example tertiary butyl, isopropyl, and the like. Other hydrocarbyl radicals include fluoromethyl, fluoroethyl, difluoroethyl, iodopropyl, bromohexyl, chlorobenzyl and hydrocarbyl substituted organometalloid radicals including trimethylsilyl, triniethylgennyl, methyldiethylsilyl and the like; and halocarbyl-substituted organometalloid radicals including tris(trifluorornethyi)-silyl, methyl-bis(difluoromethyl)silyl, brornomelhyldiinethylgermyl and the like; and disubstitiuted boron radicals including dijnethylboron for example; and disubstituted pnictogen radicals including dimethylamine, dimethyiphosphine, diphenylamine, methylphenylphosphine, chalcogen radicals including methoxy, ethoxy, propoxy, phenoxy, methylsulfide and ethylsulfide. Non-hydrogen substituents R include the atoms carbon, silicon, boron, aluminum, nitrogen, phosphorous, oxygen, tin, sulfur, germanium and the like, including olefins such as but not limited to olefmically unsaturated substituents including vinyl-terminated ligands, for example but-3-enyl, prop-2-enyl, hex-5-enyl and the like. Also, at least two .R groups, preferably two adjacent R groups, are joined to form a ring structure having from 3 to 30 atoms selected from carbon, nitrogen, oxygen, phosphorous, silicon, germanium, aluminum, boron or a combination thereof. Also, a substituent group R group such as 1-bulanyl may form a carbon sigma bond to the metal M.
Other ligands may be bonded to the metal M, such as at least one leaving group Q. In one embodiment, Q is a monoanionic labile ligand having a sigma-bond to M. Depending on the oxidation state of the metal, the value for n is 0, 1 or 2 such that Formula III above represents a neutral bulky ligand metallocene catalyst compound.
Non-limiting examples of Q ligands include weak bases such as amines, phosphlnes, ethers, carboxylates, dienes, hydrocarbyl radicals having from 1 to 20 carbon atoms, hydrides or halogens and the like or a combination thereof. In another embodiment, two or more Q's form a part of a fused ring or ring system. Other examples of Q ligands include those substituents for R as described above and including cyclobutyl, cyclohexyl, heptyl, tolyl, trifluromethyl, tetramethylene, pentamethylehe, methylidene, metliyoxy, elhyoxy, propoxy, phenoxy, bis(N-methylanilide), dimethylamide, dimethylphosphide radicals and the like.
In another embodiment, the catalyst composition of the invention may include one or more bulky ligand metallocene catalyst compounds where LA and LB of Formula III are bridged to each other by at least one bridging group, A, as represented by Formula IV,
LAALBMQn (IV)
The compounds of Formula IV are known as bridged, bulky ligand metallocene catalyst compounds. LA, LB, M, Q and n are as defined above. Non-limiting examples of bridging group A include bridging groups containing at least one Group 13 to 16 atom, often referred to as a divalent moiety such as but not limited to at least one of a carbon, oxygen, nitrogen, silicon, aluminum, boron, germanium and tin atom or a combination thereof. Preferably bridging group A contains a carbon, silicon or germanium atom, most preferably A contains at least one silicon atom or at least one carbon atom. The bridging group A may also contain substituent groups R as defined above including halogens and iron. Non-limiting examples of bridging group A may be represented by R'2C, R'2Si, R'2Si R'2Si, R'2Ge, R'P, where R' is independently, a radical group which is hydride, hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, hydrocarbyl-substituted organometalloid, halocarbyl-substituted organometalloid, disubstituled boron, disubstituted puictogen, substituted chalcogen, or halogen or two or more R' may be joined to form a ring or ring system. In one embodiment, the bridged, bulky ligand metallocene catalyst compounds of Formula IV have two or more bridging groups A (EP 664 301 Bl).
In another embodiment, the bulky ligand metallocene catalyst compounds are those where the R substituents on the bulky ligands LA and LB of Formulas III and IV are substituted with the same or different number of substituents on each of the bulky ligands. In another embodiment, the bulky ligands LA and LD of Formulas III and IV are different from each other.
Other bulky ligand metallocene catalyst compounds and catalyst systems useful in (he invention may include those described in U.S. Patent Nos. 5,064,802, 5,145,819, 5,149,819, 5,243,001, 5,239,022, 5,276,208, 5,296,434, 5,321,106, 5,329,031, 5,304,614,
5,677,401, 5,723,398, 5,753,578, 5,854,363, 5,856,547 5,858,903, 5,859,158, 5,900,517 and 5,939,503 and PCT publications WO 93/08221, WO 93/08199, WO 95/07140, WO 98/11144, WO 98/41530, WO 98/41529, WO 98/46650, WO 99/02540 and WO 99/14221 and European publications EP-A-0 578 838, EP-A-0 638 595, EP-B-0 513 380, EP-A1-0 816 372, EP-A2-0 839 834, EP-Bl-0 632 819, EP-Bl-0 748 821 andEP-Bl-0 757 996, all of which are herein fully incorporated by reference.
In another embodiment, the catalyst compositions of the invention may include bridged heteroatom, mono-bulky ligand metallocene compounds. These types of catalysts and catalyst systems are described in, for example, PCT publication WO 92/00333, WO 94/07928, WO 91/ 04257, WO 94/03506, WO96/00244, WO 97/15602 and WO 99/20637 and U.S. Patent Nos. 5,057,475, 5,096,867, 5,055,438, 5,198,401, 5,227,440 and 5,264,405 and European publication EP-A-0 420 436, all of which are herein fully incorporated by reference.
In another embodiment, the catalyst composition of the invention includes one or more bulky ligand metallocene catalyst compounds represented by Formula V:
LCAJMQ,, (V)
where M is a Group 3 to 16 metal atom or a metal selected from the Group of actinides and lantham'des of the Periodic Table of Elements, preferably M is a Group 4 to 12 transition metal, and more preferably M is a Group 4, 5 or 6 transition metal, and most preferably M is a Group 4 transition metal in any oxidation state, especially titanium; Lc is a substituted or unsubstituted bulky ligand bonded to M; J is bonded to M; A is bonded to J and L(; J is a heteroatom ancillary Hgand; and A is a bridging group; Q is a univalent anionic ligand; and n is (he integer 0,1 or 2. In Formula V above, Lc, A and J form a fused ring system. In an embodiment, Lc of Formula V is as defined above for LA. A, M and Q of Formula V are as defined above in Formula III.
In Formula V J is a heteroatom containing ligand in which J is an element with a coordinalion number of three from Group 15 or an element with a coordination number of

two from Group 16 of the Periodic Table of Elements. Preferably J contains a nitrogen, phosphorus, oxygen or sulfur atom with nitrogen being most preferred.
In an embodiment of the invention, the bulky ligand metallocene catalyst compounds are heterocyclic ligand complexes where the bulky ligands, the ring(s) or ring system(s), include one or more heteroatoms or a combination thereof. Non-limiting examples of heteroatoms include a Group 13 to 16 element, preferably nitrogen, boron, sulfur, oxygen, aluminum, silicon, phosphorous and tin. Examples of these bulky ligand metallocene catalyst compounds are described in WO 96/33202, WO 96/34021, WO 97/17379 and WO 98/22486 and EP-A1-0 874 005 and U.S. Patent No. 5,637,660, 5,539,124, 5,554,775, 5,756,611, 5,233,049, 5,744,417, and 5,856,258 all of which are herein incorporated by reference.
In one embodiment, the bulky ligand metallocene catalyst compounds are those complexes known as transition metal catalysts based on bidentate ligands containing pyridine or quinoline moieties, such as those described in U.S. Application Serial No. 09/103,620 filed June 23, 1998, which is herein incorporated by reference. In another embodiment, the bulky ligand metallocene catalyst compounds are those described in PCT publications WO 99/01481 and WO 98/42664, which are fully incorporated herein by reference.
In another embodiment, the bulky ligand metallocene catalyst compound is a complex of a metal, preferably a transition metal, a bulky ligand, preferably a substituted or unsubstiluted pi-bonded ligand, and one or more heteroallyl moieties, such as those described in U.S. Patent Nos. 5,527,752 and 5,747,406 and EP-Bl-0 735 057, all of which are herein fully incorporated by reference.
In another embodiment, the catalyst composition of the invention includes one or more bulky ligand metallocene catalyst compounds is represented by Formula VI:
LDMQ2(YZ)X,, (VI)
where M is a Group 3 to i6 metal, preferably a Group 4 to 12 transition metal, and most preferably a Group 4, 5 or 6 transition metal; LD is a bulky ligand that is bonded (o M; each Q is independently bonded to M and Q2(YZ) forms a ligand,

preferably a unicharged polydentate ligand; or Q is a univalent aiiionic ligand also bonded to M; X is a univalent anionic group when n is 2 or X is a divalent anionic group when nisi; n is 1 or 2.
In Formula VI, L and M are as defined above for Formula III. Q is as defined above for Formula III, preferably Q is selected from the group consisting of-O-, -NR-, -CR-2- and -S-; Y is either C or S; Z is selected from the group consisting of-OR, -NR2, -CR3, -SR, ~SiR3, -PRz, -H, and substituted or imsubstituted aryl groups, with the proviso that when Q is -NR- then Z is selected from one of the group consisting of-OR, -NR2> -SR, -SiR3, -PR2 and -H; R is selected from a group containing carbon, silicon, nitrogen, oxygen, and/or phosphorus, preferably where R is a hydrocarbon group containing from 1 to 20 carbon atoms, most preferably an alkyl, cycloalkyl, or an aryl group; n is an integer from 1 to 4, preferably 1 or 2; X is a univalent anionic group when n is 2 or X is a divalent anionic group when n is 1; preferably X is a carbarn ate, carboxylale, or other heteroallyl moiety described by the Q, Y and Z combination.
In another embodiment, the bulky ligand metallocene catalyst compounds are (hose described in PCT publications WO 99/01481 and WO 98/42664, which are fully incorporated herein by reference.
Useful Group 6 bulky ligand metallocene catalyst systems are described in U.S. Patent No. 5,942,462, which is incorporated herein by reference.
Still other useful catalysts include those multinuclear metallocene catalysts as described in WO 99/20665 and 6,010,794, and transition metal metaaracyle structures described in EP 0 969 101 A2, which are herein incorporated herein by reference. Other metallocene catalysts include those described in EP 0 950 667 Al, double cross-linked metallocene catalysts (EP 0 970 074 Al), tethered metallocenes (EP 970 963 A2) and those sulfonyl catalysts described in U.S. Patent No. 6,008,394, which are incorporated herein by reference.
It is also contemplated that in one embodiment the bulky ligand metallocene catalysts, described above, include their structural or optical or enantiomeric isomers

(meso and racemic isomers, for example see U.S. Patent No. 5,852,143, incorporated herein by reference) and mixtures thereof.
It is further contemplated that any one of the bulky ligand metallocene catalyst compounds, described above, have at least one fluoride or fluorine containing leaving group as described in U.S. Application Serial No. 09/191,916 filed November 13, 1998.
Illustrative but non-limiting examples of bulky ligand metallocene catalyst compounds include: bis(cyclopentadienyl)titanium dimethyl, bis(cyclopentadienyl) titanium diphenyl, bis(cyclopentadienyl)zirconium dimethyl, bis(cyclopentadienyl) zirconium diphenyl, bis(cyclopentadienyl)haffium dimethyl or diphenyl, bis(cyclopentadienyl)titanium di-neopentyl, bis(cyclopentadienyl)zirconium di-neopentyl, bis(cyclopentaclienyl)titanium dibenzyl, bis(cyclopentadienyl)zirconium dibenzyl, bis(cyclopentadienyl)vanadium dimethyl, bis(cyclopentadienyl)titanium metliyJ chloride, bis(cyclopentadienyl)titanium ethyl chloride, bis(cyclopentadienyl) titanJum phenyl cliloride, bis(cyclopentadienyl)zirconium methyl chloride, bis(cyclopentadienyl)zirconium ethyl chloride, bis(cyclopentadienyl)zirconium phenyl chloride, bis(cyclopentadienyl)titanium methyl bromide, cyclopentadienyl titanium trimethyl, cyclopentadienyl zirconium triphenyl, cyclopentadienyl zirconium trineopentyl, cyclopentadienyl zirconium trimethyl, cyclopentadienyl hafnium triphenyl, cyclopentadienyl hafnium trineopentyl, cyclopentadienyl hafilium trimethyl, pentamelhylcyclopentadienyl titanium trichloride, pentaethylcyclopentadienyl titanium trichloride, bis(indenyl)titanium diphenyl or dichloride, bis(methylcyclopentadienyl) titanium diphenyl or dihalide, bis(l,2-dimethylcyclopentadienyl)titanium diphenyl or dichloride, bis(l,2-diethylcyclopentadienyl)titanium diphenyl or dichloride, bis(pentamethyl cyclopentadienyl) titanium diphenyl or dichloride; dimethyl silyldicyclopentadienyl titanium diphenyl or dichloride, methyl phosphine dicyclopentadienyl titanium diphenyl or dichloride, methylenedicyclopentadienyl titanium diphenyl or dichloride, isopropyl(cyclopentadienyl)(fluorenyl)zirconium dichloride, isopropyl(cyclopentadienyl)(octahydronuorenyl)zirconium dichloride,

diisopropylmelhylene(cyclopentadienyl)(fluorenyl)zirconium dichloride, diisobutylmethyjene(cyclopentadienyl)(fluoreny[) zirconium dichloride, ditertbut>Tmethylene(cyclopentadienyl)(fluorenyl)zirconium dichloride, cyclohexylidene(cyclopentadienyl)(fluorenyl)zirconium dichloride, diisopropybiiethylene(2,5-dimethylcyclopentadienyl)(fluorenyl)zirconium dicllloride, isopropyl(cyclopentadienyl)(fluorenyl)hafniium dichloride, diphenylmethylene (cyclopentadieiiyl)(iTuorenyl)hafTiium dichloride, diisopropylniethylene (cyclopentadienyl)(fluorenyl)hafium dichloride, diisobutylmethylene(cyclopentadienyl) (fluorenyl)hafhium dichloride, dilertbutylmelhylene(cyclopentadienyl)(fluorenyl) hafnium dichloride, cyclohexylidene(cydopentadienyl)(fluorenyl)hamium dicllloride, diisopropylmethylene(2,5-dimethylcyclopentadienyi) (fluorenyl)-hafmuni dichloride, isopropyl(cyclopenladienyl)(fluorenyl)titanium dichloride, diphenylmelhylene (cyclopentadienyl)(fluorenyl)titanium dichloride, diisopropylmethylene (cyclopentadiejiyl)(fluorenyl)titanium dichloride, diisobutylmethylene (cyclopeiUadienyl)(fluoreny])iitam'urn dichloride, ditertbutylmethylene (cyclopentadienyl)(fluorenyl)titanium dichloride, cyclohexylidene(cyclopentadienyl) (fluorenyl)titan;ium dichloride, diisopropylmethylene(2,5 dimethylcyclopentadienyl fluorenyl)tilanium dichloride, racemic-ethylene bis(l-indenyl)zirconiurn (W) dichloride, racemic-ethylene bis (4,5,6,7-teuahydro-l -indenyl) zirconium (IV) dichloride, racemic-dimethylsilyl bis (1-indenyl) zirconium (IV) dichloride, racemic-dimethylsilyl bis (4,5,6,7-tetrahydro-1-indenyl) zirconium (TV) dichloride, racemic-l,l,2,2-tetramethylsilanylene bis (1-indenyl) zirconium (IV) dichloride, racemic-l,l,2,2-tetramethylsilanylene bis (4,5,6,7-tetrahydro-l-indenyl) zirconium (IV) dichloride, ethylidene (1-indenyl telramelhylcyclopentadienyl) zirconium (IV) dichloride, racemic-dimethylsilyl bis (2-meU]yl-4-t-butyi-l-cyclopentadienyl) zirconium (TV) dichloride, ra'cemic-ethylene bis (1-indenyl) hafnimn (IV) dicllloride, racemic-ethylene bis (4,5,6,7-tetrahydro-l-indenyl) hafiium (IV) dichloride, racemic-dimethylsilyl bis (1-indenyl) hafaium (IV) dichloride, racemic-dimelhylsilyl bis (4,5,6,7-tetrahydro-l-indenyl) hafnium (IV)

dichlonde, racemic-1,1,2,2-tetrametliylsilanylene bis (1-indenyl) hafnium (IV) dichloride, racemic-1,1,2,2-tetramethylsilanylene bis (4,5,6,7-tetrahydro-1-indenyl) hafnium (IV), dichloride, ethylidene (l-indenyl-2,3,4,5-tetramethyl-l-cyclopenladienyl) hafnium (IV) dichloride, racemic-ethylene bis (1-indenyl) titanium (IV) dichloride, racemic-etbylene bis (4,5,6,7-tetrahydro-1-indenyl) titanium (IV) dichloride, racemic-dimethylsilyl bis (1-indenyl) titanium (IV) dichloride, racemic-dimethylsilyl bis (4,5,6,7-tetrahydro-1-indenyl) titanium (IV) dichloride, racemic-1,1,2,2-tetramethylsilanylene bis (1-indenyl) titanium (IV) dichloride racemic-l,l,2,2-tetramethylsilanylene bis (4,5,6,7-tetrahydro-1-indenyl) titanium (IV) dichloride, and ethylidene (l-indenyl-2,3,4,5-tetramethyl-1-cyclopentadienyl) titanium (IV) dichloride.
Preferred bidky ligaiid metallocene catalyst compounds are diphenylmethylene (cyclopentadienyl)(fluorenyl)zirconium dichloride, racemic-dimelhylsilyl bis (2-methyl-l-indenyl) zirconium (IV) dichloride, racemic-dimethylsilyl bis (2-methyl-4-(l-naphthyl-l-indenyl) zirconium (IV) dichloride, and racemic-dimethylsilyl bis (2-methyl-4-phenyl-l-indenyl) zirconium (IV) dichloride. Other preferred bulky ligand metallocene catalyst compounds include, indenyl zirconium tris(dielhylcarbamate), indenyl zirconium Iris(pivalate), indenyl zirconium tris(p-toluate), indenyl zirconium tris(benzoate), (1-methylindenyl) zirconium tris(pivalate), (2-methylindenyl) zirconium tris(diethylcarbamate), (methylcyclopentadienyl) zirconium tris(pivalate), cyclopentadienyl tris(pivalate), and (pentamethylcyclopentadienyl) zirconium tris(benzoate).
C. Phenoxide Catalyst Compound
The catalyst composition of the invention may include one or more phenoxide catalyst compounds represented by the following formulae:
(Figure Remove)
Formula (\TII)
wherein R' is hydrogen or a C4 lo C,00 group, preferably a tertiary alkyl group, preferably a C4 to C20 alkyl group, preferably a C4 to C30 tertiary alkyl group, preferably a neutral Q. to Cloo group and may or may not also be bound to M, and at least one of R2 to R5 is a group

I 00
containing a heteroatoin, the rest of R2 to R5 are independently hydrogen or a C, to C
group, preferably a C4 to C20 alkyl group (preferably butyl, isobutyl, pentyl hexyl, heptyl, isohexyl, octyl, isooctyl, decyl, nonyl, dodecyl) and any of R2 to R5 also may or may not be bound to M,
O is oxygen, M is a group 3 to group 10 transition metal or lanlhanide metal, preferably a group 4 metal, preferably Ti, Zr or Hf, n is the valence state of the metal M, preferably 2, 3, 4, or 5, Q is an alkyl, halogen, benzyl, amide, carboxylate, carbamate, thiolate, hydride or alkoxide group, or a bond to an R group containing a heteroatom which may be any of R1 to Rs A heteroatoin containing group may be any heteroatom or a heteroatoin bound to
carbon silica or another heleroalom. Preferred heleroatoms include boron, aluminum, silicon, nitrogen, phosphorus, arsenic, tin, lead, antimony, oxygen, selenium, tellurium. Particularly prefen-ed heteroatoms include nitrogen, oxygen, phosphorus, and sulfur. Even more particularly preferred heteroatoms include oxygen and nitrogen. The heleroatom itself may be directly bound to the phenoxide ring or it may be bound to another atom or atoms tliat are bound to the phenoxide ring. The heteroatom containing group may contain one or more of the same or different heteroatoms. Preferred heteroatom groups include imines, amines, oxides, phosphines, ethers, kelenes, oxoazolines heterocyclics, oxazolines, Ihioelhers, and the like. Particularly preferred heteroatom groups include imines. Any two adjacent R groups may form a ring structure, preferably a 5 or 6 membered ring. Likewise the R groups may form multi-ring structures. In one embodiment any two or more R groups do not form a 5 membered ring.
In a preferred embodiment, Q is a bond to any of R2 to R5 and the R group that Q is
bound to is a heteroatom containing group.
This invention may also be practiced with the catalysts disclosed in EP 0 874 005
A1, which in incorporated by reference herein.
hi a preferred embodiment the phenoxide catalyst compound comprises one or
more of:
bis(//-methyI-3,5-di-/-butylsalicylimino)zirconium(IV) dibenzyl;
bis(Af-ethyl-3,5-di-/-butylsalicylimino)zirconium(rV) dibenzyl;
bis(yV-;'.vo-propyl-3,5-di-^-butylsalicylimino)zircoiiium(rV) dibenzyl;
bis(A/-/-butyI-3,5-di-/-butylsalicylimin.o)zirconium(IV) dibenzyl;
bis(Ar-benzyl-3,5-di-r-butylsalicylimino)zirconiuni(IV) dibenzyl;
bis(//-hexyI-3,5-di-?-butylsalicylimino)zirconium(IV) dibenzyl;
bis(A'-pheiiyl-3,5-di-/-butylsalicylimino)zirconium(TV) dibenzyl;
bis(Ar-methyl-3,5-di~;-butylsalicyliniino)zirconium(IV) dibenzyl;
bis(ALbenzyl-3,5-di-f-butylsa]icylimino)zirconium(IV) dichloride;
bis(//-benzyI-3,5-di-f-butylsalicylimino)zirconium(IV) dipivalate;
bis(Ar-ben7yl-3,5-di-;-butylsalicylimino)tilaniuni(lV) dipivalate;
bis(jV-benzyl-3,5-di-f-bulyIsalicylimino)zirconium(IV) di(bis(dimethylamide));
bis(jY-/.yo-propyl-3,5-di-C-amylsalicylimino)zirconium(IV) dibenzyl; bis(//-wo-propyl-3,5-di-?-octylsalicylimino)zirconium(IV) dibenzyl; bis(//-w0-propyl-3,5-di-(l ',1 '-dimethylbenzyl)salicylimino)zirconium(IV) dibenzyl; bis(A/-wo-propyl-3,5-di-(l ',1 '-dimethylbenzyl)salicylimino)titanium(IV) dibenzyl; bis(7Vr-wo-propyl-3,5-di-( 1', 1 '-dimethylbenzyl)salicylimino)hafiiium(IV) dibenzyl; bis(Ar-wo-butyl-3,5-di-(l ',1 '-dimethylbenzyl)salicylimino)zirconium(IV) dibenzyl; bis(A'-wo-butyl-3,5-di-(l ',1 '-dimethylbenzyl)salicylimino)zirconium(IV) dichloride; bis(yV-hexyl-3,5-di-(l',I '-dimethylbenzyl)salicyliraino)zirconium(IV) dibenzyl; bis(7V-phenyl-3,5-di-(l', 1 '-dimethylbenzyl)salicylimino)zirconium(IV) dibenzyl; bis(A'-wo-propyl-3,5-di-(r-methylcyclohexyl)lsalicylimiiio)zirconium(IV) dibenzyl; bis(7V-benzyl-3-;-butylsalicylimino)zirconium(IV) dibenzyl; bis(7V-benzyl-3-triphenylmethylsalicylimino)zirconium(IV) dibenzyl; bis(7V-wo-propyl-3,5-di-(riiTielhylsilylsalicylimino)zirconium(rV) dibenzyl; bis(//-wo-propyl-3-(i)heny])salicylimmo)zirconiura(IV) dibenzyl; bis(//-benzyl-3-(2',6'-di-/5o-propylphenyl)salicylimino)zirconium(IV) dibenzyl; bis(A^-benzyl-3-(2',6'-di-phenylphenyl)salicylimino)zirconium(lV) dibenzyl; bis(7vr-benzyl-3-/-butyl-5-methoxysalicylimino)zirconium(IV) dibenzyl; bis(2-(21I-bejizotriazol-2-yl)-4,6-di-r-amylphenoxide)zirconium(IV) dibenzyl; bis(2-(2H-benzotriazol-2-yl)-4,6-di-f-amylphenoxide)zirconium(IV) dichloride; bis(2-(2H-benzotriazol-2-yl)-4,6-di-^-amylphenoxide)zirconium(IV) di(bis(dimethylamide)); bis(2-(2H-benzotriazol-2-yl)-4,6-di-(l',!'-dimethylbenzyl)phenoxide)zirconiura(IV) dibenzyl;
bis(2-(2H-benzotriazol-2-yl)-4,6-di-/-amylphenoxide)titanium(IV) dibenzyl; bis(2-(2H-benzotriazol-2-yl)-4,6-di-(l', 1 '-dimeth3'lbenzyl)phenoxide)titanium(lV) dibenzyl;
bis(2-(2H-benzotriazol-2-yl)-4,6-di-(r,r-dimethylbenzyl)phenoxide)titanium(IV) dichloride;
bis(2-(2H-benzotriazol-2-yl)-4,6-di-(l',] '-diraethylbenzyl)phenoxide)hafhium(IV) dibenzyl; (A'-phenyl-3,5-di-(l', 1 '-dimethylbenzyl)salicylimino)zirconium(IV) tribenzyl;
(jV-(2',6'-di-Mc;-propylphenyl)-3,5-di-(r,r-dimethy]benzyl)salicylimino)zkcomum(IV)
tribenzyl; (A/-(2\6'-di-/jo-propylphenyl)-3,5-di-(r,l'-dimethylbeiizyl)salicylimmo)titaiu'un](IV)
tribenzyl; and (7V-(2',6'-di-iJo-propylphenyl)-3,5-di-(l ',1 '-dimethylbenzyl)salicylimino) zircotiium(rV) trichloride.
P. Additional .Catalyst Compounds
The catalyst compositions of the invention may include one or more complexes known as transition metal catalysts based on bidentate ligands containing pyridine or quinoline moieties, such as those described in U.S. Application Serial No. 09/103,620 filed June 23, 1998, which is herein incorporated by reference. In one embodiment, these catalyst compounds are represented by the formula:
((Z)XAi(YJ))qMQn (IX)
where M is a metal selected from Group 3 to 13 or lanthanide and actinide series of the Periodic Table of Elements; Q is bonded to M and each Q is a monovalent, bivalent, or trivalent anion; X and V are bonded to M; one or more of X and Y are heteroatoms, preferably both X and Y are heteroatoms; Y is contained in a heterocyclic ring J, where J comprises from 2 to 50 non-hydrogen atoms, preferably 2 to 30 carbon atoms; Z is bonded to X, where Z comprises 1 to 50 non-hydrogen atoms, preferably 1 to 50 carbon atoms, preferably Z is a cyclic group containing 3 to 50 atoms, preferably 3 to 30 carbon atoms; t is 0 or 1; when I is 1, A is a bridging group joined to at least one of X,Y or J, preferably X and J; q is 1 or 2; n is an integer from 1 to 4 depending on the oxidation state of M. In one embodiment, where X is oxygen or sulfur then Z is optional. In another embodiment, where X is nitrogen or phosphorous then Z is present. In an embodiment, Z is preferably an aryl group, more preferably a substituted aiyl group.
It is within the scope of this invention, in one embodiment, the catalyst compounds include complexes of Ni2+ and Pd2+ described in the articles Johnson, et
al., "New Pci(ll)- and Ni(ll)- Based Catalysts for Polymerization of Ethylene and a-Olefms", J. Am. Chem. Soc. 1995, 117, 6414-6415 and Johnson, et al., "Copolymerization of Ethylene and Propylene with Functionalized Vinyl Monomers by Palladium(II) Catalysts", J. Am. Chem. Soc., 1996, 118, 267-268, and WO 96/23010 published August 1, 1996, WO 99/02472, U.S. Patent Nos. 5,852,145, 5,866,663 and 5,880,241, which are all herein fully incorporated by reference. These complexes can be either dialkyl ether adducts, or alkylated reaction products of the described dihalide complexes that can be activated to a cationic state by the activators of lliis invention described below.
Other catalyst compounds include those nickel complexes described in WO 99/50313, which is incorporated herein by reference.
Also included are those diimine based ligands of Group 8 to 10 metal catalyst compounds disclosed in PCT publications WO 96/23010 and WO 97/48735 and Gibson, et al., Chem. Comm., pp. 849-850 (1998), all of which are herein incorporated by reference.
Other useful catalyst compounds are those Group 5 and 6 metal imido complexes described in EP-A2-0 816 384 and U.S. Patent No. 5,851,945, which is incorporated herein by reference. In addition, metallocene catalysts include bridged bis(arylamido) Group 4 compounds described by D.H. McConville, et al., in Organometallics 1195, 14, 5478-5480, which is herein incorporated by reference. In addition, bridged bis(amido) catalyst compounds are described in WO 96/27439, which is herein incorporated by reference. Other useful catalysts are described as bis(hydroxy aromatic nitrogen ligands) in U.S. Patent No. 5,852,146, which is incorporated herein by reference. Other useful catalysts containing one or more Group 15 atoms include those described in WO 98/46651, which is herein incorporated herein by reference.
E. CouvciitioDal Transition Metal Catalysts
In another embodiment, conventional-type transition metal catalysts may be used in the practice of this invention. Conventional-type transition metal catalysts are those

traditional Ziegler-Natta, vanadium and Phillips-type catalysts well known in the art. Such as, for example Ziegler-Natta catalysts as described in Ziegler-Natta Catalysts and
Boor, Academic Press, New York, 1979. Examples of
conventional-type transition metal catalysts are also discussed in U.S. Patent Nos. 4,1 15,639, 4,077,904, 4,482,687, 4,564,605, 4,721,763, 4,879,359 and 4,960,741, all of which are herein fully incorporated by reference. The conventional-type transition metal catalyst compounds that may be used in the present invention include transition metal compounds from Groups 3 to 17, preferably 4 to 12, more preferably 4 to 6 of the Periodic Table of Elements.
Preferred conventional-type transition metal catalysts may be represented by the formula: MRX, where M is a metal from Groups 3 to 17, preferably Group 4 to 6, more preferably Group 4, most preferably titanium; R is a halogen or a hydrocarbyloxy group; and x is the oxidation stale of the metal M. Non-limiting examples of R include alkoxy, phenoxy, bromide, chloride and fluoride. Non-limiting examples of conventional-type transition metal catalysts where M is titanium include TiCl4, TiBr4, Ti(OC2H5)3Cl, Ti(OC2H5)Cl3, Ti(OC+H9)3CI, Ti(OC,H7)2Cl2, Ti(OC2H5)2Br2, TiCl3«l/3AlCl3and Ti(OC12H2J)Cl.v
Conventional-type transition metal catalyst compounds based on magnesium/titanium electron-donor complexes that are useful in the invention are described in, for example, U.S. Patent Nos. 4,302,565 and 4,302,566, which are herein fully incorporate by reference. The MgTiCl6 (ethyl acetate),, derivative is particularly preferred.
British Patent Application 2,105,355 and U.S. Patent No. 5,317,036, herein incorporated by reference, describes various conventional-type vanadium catalyst compounds. Non-limiting examples of conventional-type vanadium catalyst compounds include vanadyl trihalide, alkoxy halides and alkoxides such as VOC13, VOCl2(OBu) where Bu =butyl and VO(OC2H5)j; vanadium tetra-halide and vanadium alkoxy halides such as VC14 and VCl3(OBu); vanadium and vanadyl acetyl acetonates and chloroacetyl acetonates such as V(AcAc)3 and VOCl2(AcAc) where (AcAc) is an acetyl acetonate. The preferred conventional-type vanadium catalyst compounds are VOC13, VC14 and VOC12-

OR where R is a hydrocarbon radical, preferably a C, to C,0 aliphatic or aromatic hydrocarbon radical such as ethyl, phenyl, isopropyl, butyl, propyl, n-butyl, iso-butyl, tertiary-butyl, hexyl, cyclohexyl, naphthyl, etc., and vanadium acetyl acetonates.
Conventional-type chromium catalyst compounds, often referred to as Phillips-type catalysts, suitable for use in the present invention include CrO3, chromocene, silyl chromate, chromyl chloride (CrO2Cl2), chromium-2-ethyl-hexanoate, chromium acetylacetonate (Cr(AcAc)3), and the like. Non-limiting examples are disclosed in U.S. Patent Nos. 3,709,853, 3,709,954, 3,231,550, 3,242,099 and 4,077,904, which are herein fully incorporated by reference.
Still other conventional-type transition metal catalyst compounds and catalyst systems suitable for use in the present invention are disclosed in U.S. Patent Nos. 4,124,532, 4,302,565, 4,302,566, 4,376,062, 4,379,758, 5,066,737, 5,763,723, 5,849,655, 5,852,144, 5,854,164 and 5,869,585 and published EP-A2 0 416 815 A2 and EP-A1 0 420 436, which are all herein incorporated by reference.
Other catalysts may include cationic catalysts such as A1C13, and other cobalt, iron, nickel and palladium catalysts well known in the art. See for example U.S. Patent Nos. 3,487,112, 4,472,559, 4,182,814 and 4,689,437, all of which are incorporated herein by reference.
It is also contemplated that other catalysts can be combined with the catalyst compounds in the catalyst composition of the invention. For example, see U.S. Patent Nos. 4,937,299, 4,935,474, 5,281,679, 5,359,015, 5,470,811, and 5,719,241 all of which are herein fully incorporated herein reference.
It is further contemplated that one or more of the catalyst compounds described above or catalyst systems may be used in combination with one or more conventional catalyst compounds or catalyst systems. Non-limiting examples of mixed catalysts and catalyst systems are described in U.S. Patent Nos. 4,159,965, 4,325,837, 4,701,432, 5,124,418, 5,077,255, 5,183,867, 5,391,660, 5,395,810, 5,691,264, 5,723,399 and 5,767,031 and PCT Publication WO 96/23010 published August 1, 1996, all of which are herein fully incorporated by reference.

!!L_ Activators and Activation Methods for Catalyst Compounds
* The polymerization catalyst compounds, described above, are typically activated in various ways to yield compounds having a vacant coordination site that will coordinate, insert, and polymerize olefin(s). For the purposes of this patent specification and appended claims, the term "activator" is defined to be any compound which can activate any one of the catalyst compounds described above by converting the neutral catalyst compound to a catalytically active catalyst compound cation. Non-limiting activators, for example, include alumoxanes, aluminum alkyls, ionizing activators, which may be neutral or ionic, and conventional-type cocatalysts.
A. Aluminoxaue and Aluminum Alkyl Activators
In one embodiment, alumoxanes activators are utilized as an activator in the catalyst composition of the invention. Alumoxanes are generally oligomeric compounds containing -A1(R)-O- subunits, where R is an alkyl group. Examples of alumoxanes include methylalumoxane (MAO), modified methylalumoxane (MMAO), ethylalumoxane and isobutylalumoxarie. Alumoxanes may be produced by the hydrolysis of the respective trialkylaliuninum compound. MMAO may be produced by the hydrolysis of trimethylaluminum and
Aluminum Alkyl or organoaluminum compounds which may be utilized as activators include Irimethylaluminum, triethylaluminum, triisobutylaluminum, tri-n-hexylaluminum, Iri-n-octylaJuminuin and the like.
13. Ionizing Activators
It is within the scope of this invention to use an ionizing or stoichiometric activator, neutral or ionic, such as tri (n-butyl) ammonium tetrakis (pentafluorophenyl) boron, a trisperfluorophenyl boron metalloid precursor or a trisperfluoronaphtyl boron metalloid precursor, polyhalogenated heteroborane anions (WO 98/43983), boric acid (U.S. Patent No. 5,942,459) or combination thereof. It is also within the scope of this invention to use neutral or ionic activators alone or in combination with alumoxane or modified alumoxane activators.
Examples of neutral stoichiometric activators include tri-substituted boron, tellurium, aluminum, gallium and indium or mixtures thereof. The three substituent groups are each independently selected from alkyls, alkenyls, halogen, substituted alkyls, aryls, arylhalides, alkoxy and halides. Preferably, the three groups are independently selected from halogen, mono or multicyclic (including halosubstituted) aryls, alkyls, and alkenyl compounds and mixtures thereof, preferred are alkenyl groups having 1 to 20 carbon atoms, alky] groups having 1 to 20 carbon atoms, alkoxy groups having 1 to 20 carbon atoms and aryl groups having 3 to 20 carbon atoms (including substituted aryls). More preferably, the three groups are alkyls having 1 to 4 carbon groups, phenyl, napthyl or mixtures thereof. Even more preferably, the three groups are halogenated, preferably fluorinated, aryl groups. Most preferably, the neutral stoichiometric activator is trisperfluorophenyl boron or trisperfluoronapthyl boron.
Ionic stoichiometric activator compounds may contain an active proton, or some other cation associated with, but not coordinated to, or only loosely coordinated to, the remaining ion of the ionizing compound. Such compounds and the like are described in European publications EP-A-0 570 982, EP-A-0 520 732, EP-A-0 495 375, EP-B1-0 500 944, EP-A-0 277 003 and EP-A-0 277 004, and U.S. Patent Nos. 5,153,157, 5,198,401, 5,066,741, 5,206,197, 5,241,025, 5,384,299 and 5,502,124 and U.S. Patent Application

Serial No. 08/285,380, filed August 3, 1994, all of which are herein fully incorporated by reference.
In a preferred embodiment, the stoichiometric activators include a cation and an anion component, and may be represented by the following formula:
(L-H)/ (Ad-) (X)
wherein L is an neutral Lewis base;
H is hydrogen;
(L-H)f is a Bronsted acid
Ad is a non-coordinating anion having the charge d-
d is an integer from 1 to 3.
The cation component, (L-H)/ may include Bronsted acids such as protons or protonated Lewis bases or reducible Lewis acids capable of protonating or abstracting a moiety, such as an akyl or aryl, from the bulky ligand metallocene or Group 15 containing transition metal catalyst precursor, resulting in a cationic transition metal species.
The activating cation (L-H)/ may be a Bronsted acid, capable of donating a proton to the transition metal catalytic precursor resulting in a transition metal cation, including ammoniums, oxoniums, phosphoniums, silyliums and mixtures thereof, preferably ammoniums of melhylamine, aniline, dimethylamine, diethylamine, N-methylaniline, diphenylamine, trimethylamine, triethylamine, N.N-dimethylaniline, methyldiphenylamine, pyridine, p-bromo N,N-dimethylaniline, p-nitro-N,N-dimethylaniline, phosphoniums from triethylphosphine, triphenylphosphine, and diphenylphosphine, oxomiuns from ethers such as dimethyl ether diethyl ether, tetrahydrofuran and clioxane, sulfoniums from thioethers, such as diethyl thioethers and letrahydrothiophene and mixtures thereof. The activating cation (L-H)/ may also be an abstracting moiety such as silver, carboniums, tropylium, carbeniums, ferroceniums and mixtures, preferably carboniums and ferroceniums. Most preferably (L-H)/ is triphenyl carbonium.

The anion component Ad~ include those having the formula [Mk+QJd~ wherein k is an integer from 1 to 3; n is an integer from 2-6; n - k = d; M is an element selected from Group 13 of the Periodic Table of the Elements, preferably boron or aluminum, and Q is independently a hydride, bridged or unbridged dialkylamido, halide, alkoxide, aryloxide, hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, and lialosubstiluted-hydrocarbyl radicals, said Q having up to 20 carbon atoms with the proviso that in not more than 1 occurrence is Q a halide. Preferably, each Q is a fluorinated hydrocarbyl group having 1 to 20 carbon atoms, more preferably each Q is a Huorinated aryl group, and most preferably each Q is a pentafluoryl aryl group. Examples of suitable Ad also include diboron compounds as disclosed in U.S. Pat. No. 5,447,895, which is fully incoiporaled herein by reference.
Illustrative, but not limiting examples of boron compounds which may be used as
an activating cocatalyst in the preparation of the improved catalysts of this invention are
tri-substituted ammonium salts such as:
Iriinelhylaminonium tetraphenylborate,
triethylammonium tetraphenylborate,
tripropylammonium tetraphenylborate,
lri(n-butyl)aminonium tetraphenylborate,
tri(t-bulyl)ainmonium tetraphenylborate,
N.N-dimeUiylaiiilinium tetraphenylborate,
N,N-diethyianilim"um tetraphenylborate,
N,N-dimethyl-(2,4,6-trimelhylanilinium) tetraphenylborate,
Irimethylammonium tetrakis(pentafluorophenyl)borate,
triethylammonium tetrakis(pentafluorophenyl)borate,
(ripropylammoniuni tetrakis(pentafluorophenyl)borate,
tri(n-butyl)ammonium tetrakis(pentafluorophenyl)borate,
tri(sec-butyl)ammonium telrakis(pentafluorophenyl) borate,
N,N-dimethylanilinium tetiakis(pentafluorophenyl) borate,
N,N-diethylaniIiniuni tetrakis(pentafluorophenyl) borate,

N,N-dimethyl-(2,4,6-trimethylanilinium) tetrakis(pentafluorophenyl) borate, trimethylammonium letrakis-(2,3,4,6-tetrafluorophenylborate, Irietliylainmonium tetrakis-(2,3,4,6-tetrafluorophenyl) borate, tripropylammoniuni tetrakts-(2,3,4,6-tetrafluorophenyl) borate, tri(n-bulyl)ammoniuin tetrakis-(2,3,4,6-letrafluoro-phenyl) borate, (limethyl(l-butyl)ammonium tetrakis-(2,3,4,6-tetrafiuorophenyl) borate, N,N-dimethylanilinium tetrakis-(2,3,4,6-tetrafluorophenyl) borate, N,N-diethylanilinium tetrakis-(2,3,4,6-tetrafluoro-phenyl) borate, and N,N-dimethyl-(2, 4, 64rimethylanilinium)tetrakis-(2,3,4,6-tetrafluorophenyl) borate; dialkyl ammonium salts such as: di-(i-propyl)animonium tetrakis(pentafluorophenyl) borate, and dicycloJiexylamrnonium tetrakis(pentafluorophenyl) borate; and tri-substituted phosphonium sails such as: triphenylphosphoniuni tetrakis(pentafluorophenyl) borate, (i i(o~tolyl)phosphonium tetrakis(pentafJuorophenyl) borate, and tri(2,6-(limethylphenyl)phosphonium tetrakis(pentafluorophenyl) borate.
Most preferably, the ionic stoichiometric activator (L-H)/ (Ad~) is N,N-dimethylaniliniuin tetra(perfluorophenyl)borate or triphenylcarbenium telra(perfluorophenyl)borate.
In one embodiment, an activation method using ionizing ionic compounds not
containing an active proton but capable of producing a bulky ligand metallocene catalyst
cation and (heir non-coordinating anion are also contemplated, and are described in EP-A-
0 426 637, EP-A- 0 573 403 and U.S. Patent No. 5,387,568, which are all herein
incorporated by reference. ;
Typically, conventional transition metal catalyst compounds excluding some conventional-type chromium catalyst compounds are activated with one or more of the conventional cocalalysts which may be represented by the formula M3M4vXzcR3b^c , wherein M1 is a metal from Group 1 to 3 and 12 to 13 of the Periodic Table of Elements-M"1 is a metal of Group 1 of the Periodic Table of Elements; v is a number from 0 to 1; each X2 is any halogen; c is a number from 0 to 3; each R3 is a monovalent hydrocarbon

radical or hydrogen; b is a number from 1 to 4; and wherein b minus c is at least 1. Other conventional-type organometallic cocatalyst compounds for the above conventional-type transition metal catalysts have the formula M3R\, where M3 is a Group IA, IIA, IIB or IIIA metal, such as lithium, sodium, beryllium, barium, boron, aluminum, zinc, cadmium, and gallium; k equals 1, 2 or 3 depending upon the valency of M3 which valency in turn normally depends upon the particular Group to which M3 belongs; and each R3 may be any monovalent hydrocarbon radical.
Non-limiting examples of conventional-type organometallic cocatalyst compounds useful with the conventional-type catalyst compounds described above include methyllithium, butyllithium, dihexylmercury, bulylmagnesium, diethylcadmium, benzylpotassium, diethylzinc, (ri-n-butylalummum, diisobutyl ethylboron, diethylcadmium, di-n-butylzinc and tri-n-ainylboron, and, in particular, the aluminum alkyls, such as Iri-hexyl-aluminum, triethylaluminum, trimethylaluminum, and tri-isobutylaluminum. Other conventional-type cocatalyst compounds include mono-organohalides and hydrides of Group 2 metals, and mono- or di-organohalides and hydrides of Group 3 and 13 metals. Non-limiting examples of such conventional-type cocatalyst compounds include di-isobutylaluminum bromide, isobutylboron dichloride, methyl magnesium chloride, ethylberyllium chloride, ethylcalcium bromide, di-isobutylaluminum hydride, methylcadmium hydride, diethylboron hydride, hexylberyllium hydride, dipropylboron hydride, octylmagnesium hydride, butylzinc hydride, dichloroboron hydride, di-bromo-aluminum hydride and bromocadmium hydride. Conventional-type organometallic cocatalyst compounds are known to those in the art and a more complete discussion of these compounds may be found in U.S. Patent Nos. 3,221,002 and 5,093,415, which are herein fully incorporated by reference.
D. Additional Activators
Other activators include those described in PCT publication WO 98/07515 such as tris (2, 2', 2"- nonafluorobiphenyl) fluoroaluminate, which publication is fully incorporated herein by reference. Combinations of activators are also contemplated by the invention, for example, alumoxanes and ionizing activators in combinations, see for

example, EP-B1 0 573 120, PCT publications WO 94/07928 and WO 95/14044 and U.S. Patent Nos. 5,153,157 and 5,453,410 all of which are herein fully incorporated by reference.
Other suitable activators are disclosed in WO 98/09996, incorporated herein by reference, which describes activating bulky ligand metallocene catalyst compounds with perchlorates, periodates and iodates including their hydrates. WO 98/30602 and WO 98/30603, incorporated by reference, describe the use of lithium (2,2'-bisphenyl-ditrimethylsilicate)«4THF as an activator for a bulky ligand metallocene catalyst compound. WO 99/18135, incorporated herein by reference, describes the use of organoboron-aluminum acitivators. EP-B1-0 781 299 describes using a silylium salt in combination with a non-coordinating compatible anion. Also, methods of activation such as using radiation (see EP-B1-0 615 981 herein incorporated by reference), electrochemical oxidation, and the like are also contemplated as activating methods for the purposes of rendering the neutral bulky ligand metallocene catalyst compound or precursor to a bulky ligand metallocene cation capable of polymerizing olefins. Other activators or methods for activating a bulky ligand metallocene catalyst compound are described in for example, U.S. Patent Nos. 5,849,852, 5,859,653 and 5,869,723 and WO 98/32775, WO 99/42467 (dioctadecylmethylarnmonium-bis(tris(pentafluorophenyl)borane) benzimidazolide), which are herein incorporated by reference.
Another suitable ion forming, activating cocatalyst comprises a salt of a cationic oxidizing agent and a noncoordinating, compatible anion represented by the formula: (OXct)d (A'1),, wherein: OXe4 is a cationic oxidizing agent having a charge of e+; e is an integer from 1 to 3; and A , and d are as previously defined. Examples of cationic oxidizing agents include: ferrocenium, hydrocarbyl-substituted ferrocenium, Ag+, or Pb+2. Preferred embodiments of Ad~ are those am'ons previously defined with respect to the Bronsted acid containing activators, especially telrakis(pentafluorophenyl)borate.
It within the scope of this invention that catalyst compounds can be combined one or more activators or activation methods described above. For example, a combination of activators have been described in U.S. Patent Nos. 5,153,157 and 5,453,410, European publication EP-I31 0 573 120, and PCT publications WO 94/07928 and WO 95/14044.

These documents all discuss the use of an alumoxane and an ionizing activator with a bulky ligand metallocene catalyst compound.
IV. Supports, Carriers and General Supportmg Techniques
The catalyst composition of the invention includes a support material or carrier, and preferably includes a supported activator. For example, the catalyst composition component, preferably the activator compound and/or the catalyst compound, is deposited on, contacted with, vaporized with, bonded to, or incorporated within, adsorbed or absorbed in, or on, a support or carrier.
The support material is any of the conventional support materials. Preferably the supported material is a porous support material, for example, talc, inorganic oxides and inorganic chlorides. Other support materials include resinous support materials such as polystyrene, functionalized or crosslinked organic supports, such as polystyrene divinyl benzene polyolefms or polymeric compounds, zeolites, clays, or any other organic or inorganic support material and the like, or mixtures thereof.
The preferred support materials are inorganic oxides that include those Group 2, 3, 4, 5, 13 or 14 metal oxides. The preferred supports include silica, which may or may not: be dehydrated, fumed silica, alumina (WO 99/60033), silica-alumina and mixtures thereof. Other useful supports include magnesia, titania, zirconia, magnesium chloride (U.S. Patent No. 5,965,477), montmorillonite (European Patent EP-B1 0511 665), phyllosilicate, zeolites, talc, clays (U.S. Patent No. 6,034,187) and the like. Also, combinations of these support materials may be used, for example, silica-chromium, silica-alumina, silica-titania and the like. Additional support materials may include those porous acrylic polymers described in EP 0 767 1 84 13 1 , which is incorporated herein by reference. Other support materials include nanocomposites as described in PCT WO 99/47598, aerogels as described in WO 99/48605, spherulites as described in U.S. Patent No. 5,972,510 and polymeric beads as described in WO 99/5031 1, which are all herein incorporated by reference.

It is preferred that the support material, most preferably an inorganic oxide, has a surface area in the range of from about 10 to about 700 m^/g, pore volume in the range of from about 0.1 to about 4.0 cc/g and average particle size in the range of from about 5 to about 500 u.m. More preferably, the surface area of the support material is in the range of from about 50 to about 500 m2/g, pore volume of from about 0.5 to about 3.5 cc/g and average particle size of from about 10 to about 200 um. Most preferably the surface area of the support material is in the range is from about 100 to about 400 m2/g, pore volume from about 0.8 to about 3.0 cc/g and average particle size is from about 5 to about 100 um. The average pore size of (he carrier of the invention typically has pore size in the range of from 10 to lOOOA, preferably 50 to about 500A, and most preferably 75 to about 350A.
The support materials may be treated chemically, for example with a fluoride compound as described in WO 00/12565, which is herein incorporated by reference. Other supported activators are described in for example WO 00/13792 that refers to supported boron containing solid acid complex.
In a preferred embodiment, fumed silica available under the trade name Cabosil™ TS-610, available from Cabot Corporation is utilized as a nucleating agent or as a viscosity builder in the catalyst component slurry discussed below. Fumed silica is typically a silica with particles 7 to 30 nanometers in size that has been treated with dimelhylsilyldichloricle such that a majority of the surface hydroxyl groups are capped. In another embodiment the fumed silica utilized has a particle size of less than 40microns, preferably less than 20 microns or preferably less than 10 microns.
In a preferred method of forming a supported catalyst composition component, the amount of liquid in which the activator is present is in an amount that is less than four times the pore volume of the support material, more preferably less than three times, even more preferably less than two limes; preferred ranges being from 1.1 times to 3.5 times range and most preferably in the 1.2 to 3 times range. In an alternative embodiment, the amount of liquid in which the activator is present is from one to less than one times the pore volume of the support material utilized in forming the supported activator.
Procedures for measuring the total pore volume of a porous support are well known in the art. Details of one of these procedures is discussed in Volume 1, Experimental

Methods in Catalytic Research (Academic Press, 1968) (specifically see pages 67-96). This preferred procedure involves the use of a classical BET apparatus for nitrogen absorption. Another method well known in the art is described in Innes, Total Porosity and Particle Density of Fluid Catalysts By Liquid Titration, Vol. 28, No. 3, Analytical Chemistry 332-334 (March, 1956).
B. Supported Activators
In one embodiment, the catalyst composition includes a supported activator. Many supported activators are described in various patents and publications which include: U.S. Patent No. 5,728,855 directed to the forming a supported oligomeric alkylaluminoxane formed by treating a trialkylaluminum with carbon dioxide prior to hydrolysis; U.S. Patent No. 5,831,109 and 5,777,143 discusses a supported methylalumoxane made using a non-hydrolytic process; U.S. Patent No. 5,731,451 relates to a process for making a supported alumoxane by oxygenation with a trialkylsiloxy moiety; U.S. Patent No. 5,856,255 discusses forming a supported auxiliary catalyst (alumoxane or organoboron compound) at elevated temperatures and pressures; U.S. Patent No. 5,739,368 discusses a process of heat treating alumoxane and placing it on a support; EP-A-0 545 152 relates to adding a metallocene to a supported alumoxane and adding more methylalumoxane; U.S. Patent Nos. 5,756,416 and 6,028,151 discuss a catalyst composition of a alumoxane impregnated support and a metallocene and a bulky aluminum alkyl and methylalumoxane; EP-B1-0 662 979 discusses the use of a metallocene with a catalyst support of silica reacted with alumoxane; PCT WO 96/16092 relates to a heated support treated with alumoxane and washing to remove unfixed alumoxane; U.S. Patent Nos. 4,912,075, 4,937,301, 5,008,228, 5,086,025,5,147,949, 4,871,705, 5,229,478, 4,935,397, 4,937,217 and 5,057,475, and PCT WO 94/26793 all directed to adding a metallocene to a supported activator; U.S. Patent No. 5,902,766 relates to a supported activator having a specified distribution of alumoxane on the silica particles; U.S. Patent No. 5,468,702 relates to aging a supported activator and adding a metallocene; U.S. Patent No. 5,968,864 discusses treating a solid with alumoxane and introducing a metallocene; EP 0 747 430 Al relates to a process using a metallocene on a supported methylalumoxane and trimethylaluminum; EP 0 969 019 Al discusses the

use of a metallocene and a supported activator; EP-B2-0 170 059 relates to a polymerization process using a metallocene and a organo-aluminuim compound, which is formed by reacting aluminum trialkyl with a water containing support; U.S. Patent No. 5,212,232 discusses the use of a supported alumoxane and a metallocene for producing styrene based polymers; U.S. Patent No. 5,026,797 discusses a polymerization process using a solid component of a zirconium compound and a water-insoluble porous inorganic oxide preliminarily treated with alumoxane; U.S. Patent No. 5,910,463 relates to a process for preparing a catalyst support by combining a dehydrated support material, an alumoxane and a polyfunctional organic crosslinker; U.S.Patent Nos. 5,332,706, 5,473,028, 5,602,067 and 5,420,220 discusses a process for making a supported activator where the volume of alumoxane solution is less than the pore volume of the support material; WO 98/02246 discusses silica treated with a solution containing a source of aluminum and a metallocene; WO 99/03580 relates to the use of a supported alumoxane and a metallocene; EP-A1-0 953 581 discloses a heterogeneous catalytic system of a supported alumoxane and a metallocene; U.S. Patent No. 5,015,749 discusses a process for preparing a polyhydrocarbyl-alumoxane using a porous organic or inorganic imbiber material; U.S. Patent Nos. 5,446,001 and 5,534,474 relates to a process for preparing one or more alkylaluminoxanes immobilized on a solid, particulate inert support; and EP-A1-0 819 706 relates to a process for preparing a solid silica treated with alumoxane. Also, me following articles, also fully incorporated herein by reference for purposes of disclosing useful supported activators and methods for their preparation, include: W. Kaminsky, et al., "Polymerization of Styrene with Supported Half-Sandwich Complexes", Journal of Polymer Science Vol. 37, 2959-2968 (1999) describes a process of adsorbing a inethylalumoxane to a support followed by the adsorption of a metallocene; Junting Xu, et al. "Characterization of isotactic polypropylene prepared with dimethylsilyl bis(l-indenyl)zirconium dichloride supported on methylaluminoxane pretreated silica", European Polymer Journal 35 (1999) 1289-1294, discusses the use of silica treated with nielliylalumoxane and a metallocene; Stephen O'Brien, et al., "EXAFS analysis of a chiral alkene polymerization catalyst incoiporated in the mesoporous silicate MCM-41" Chem. Commun. 1905-1906 (1997) discloses an immobilized alumoxane on a modified

mesoporous silica; and F.Bonini, et al, "Propylene Polymerization through Supported Metallocene/MAO Catalysts: Kinetic Analysis and Modeling" Journal of Polymer Science, Vol. 33 2393-2402 (1995) discusses using a methylalumoxane supported silica with a metallocene. Any of the methods discussed in these references are useful for producing the supported activator component utilized in the catalyst composition of the invention and all are incorporated herein by reference.
In another embodiment, the supported activator, such as supported alumoxane, is aged for a period of time prior to use herein. For reference please refer to U.S. Patent Nos. 5,468,702 and 5,602,217, incorporated herein by reference.
In an embodiment, the supported activator is in a dried state or a solid. In another embodiment, the supported activator is in a substantially dry state or a slurry, preferably in a mineral oil slurry.
In another embodiment, two or more separately supported activators are used, or alternatively, two or more different activators on a single suppoit are used.
In another embodiment, the support material, preferably partially or totally dehydrated support material, preferably 200°C to 600°C dehydrated silica, is then contacted with an organoaluminum or alumoxane compound. Preferably in an embodiment where an organoaluminum compound is used, the activator is formed in situ on and in the support material as a result of the reaction of, for example, trimethylaluminurn and water.
In another embodiment, Lewis base-containing supports are reacted with a Lewis acidic activator to form a support bonded Lewis acid compound. The Lewis base hydroxyl groups of silica are exemplary of metal/metalloid oxides where this method of bonding to a support occurs. This embodiment is described in U.S. Patent Application No. 09/191,922, filed November 13, 1998, which is herein incorporated by reference.
Other embodiments of supporting an activator are described in U.S. Patent No. 5,427,991, where supported non-coordinating anions derived from trisperfluorophenyl boron are described; U.S. Patent No. 5,643,847 discusses the reaction of Group 13 Lewis acid compounds with metal oxides such as silica and illustrates the reaction of trisperfluorophenyl boron with silanol groups (the hydroxyl groups of silicon) resulting in

bound anions capable of protonating transition metal organometallic catalyst compounds to form catalytically active cations counter-balanced by the bound anions; immobilized Group II1A Lewis acid catalysts suitable for carbocationic polymerizations are described in U.S. Patent No. 5,288,677; and James C.W. Chien, Jour. Poly. Sci.: Pt A: Poly. Chern, Vol. 29, 1603 - 1607 (1991), describes the olefin polymerization utility of methylalumoxane (MAO) reacted with silica (SiO2) and metallocenes and describes a covalent bonding of the aluminum atom to the silica through an oxygen atom in the surface hydroxyl groups of the silica.
In a preferred embodiment, a supported activator is formed by preparing in an agitated, and temperature and pressure controlled vessel a solution of the activator and a suitable solvent, then adding the support material at temperatures from 0°C to 100°C, contacting the support with the activator solution for up to 24 hours, then using a combination of heat and pressure to remove the solvent to produce a free flowing powder. Temperatures can range from 40 to 120°C and pressures from 5 psia to 20 psia (34.5 to 138kPa). An inert gas sweep can also be used in assist in removing solvent. Alternate orders of addition, such as slurrying the support material in an appropriate solvent then adding the activator, can be used.
C. Spray Dried Catalyst Composition Components
In another embodiment a support is combined with one or more activators and is spray dried to form a supported activator. In a preferred embodiment, fumed silica is combined with methyl alumoxane and then spray dried to from supported methyl alumoxane. Preferably a support is combined with alumoxane, spray dried and then placed in mineral oil to form a slurry useful in the instant invention. •
In another embodiment, the catalyst compounds described above have been combined with optional support material(s) and or optional activator(s) and spray dried prior to being combined with the slurry diluent.
In another embodiment, the catalyst compounds and/or the activators are preferably combined with a support material such as a particulate filler material and then spray dried, preferably to form a free flowing powder. Spray drying may be by any means known in

the art. Please see EP A 0 668 295 Bl, U.S. Patent No. 5,674,795 and U.S. Patent No. 5,672,669 and U.S. Patent Application Serial No. 09/464,114 filed December 16, 1999, which particularly describe spray diying of supported catalysts. In general one may spray diy the catalysts by placing the catalyst compound and the optional activator in solution (allowing the catalyst compound and activator to react, if desired), adding a filler material such as silica or fumed silica, such as Gasil™ or Cabosil ™, then forcing the solution at high pressures through a nozzle. The solution may be sprayed onto a surface or sprayed such that the droplets diy in midair. The method generally employed is to disperse the silica in toluene, stir in the activator solution, and then stir in the catalyst compound solution. Typical slurry concentrations are about 5 to 8 wt%. This formulation may sit as a slurry for as long as 30 minutes with mild stirring or manual shaking to keep it as a suspension before spray-diying. In one preferred embodiment, the makeup of the dried material is about 40-50 wt% activator (preferably alumoxane), 50-60 SiO2 and about~2 wt% catalyst compound.
In another embodiment, fumed silica such as such as Gasil™ or Cabosil ™ may be added to a solution containing a catalyst compound such that when that solution is added to the catalyst component slurry or injected into a polymerization reactor, the fumed silica acts as a template for "in situ spray" drying.
For simple catalyst compound mixtures, the two or more catalyst compounds can be added together in the desired ratio in the last step. In another embodiment, more complex procedures are possible, such as addition of a first catalyst compound to the activator/filler mixture for a specified reaction time t, followed by the addition of the second catalyst compound solution, mixed for another specified time x, after which the mixture is cosprayecl. Lastly, another additive, such as 1-hexene in about 10 vol% can be present in the activator/filler mixture prior to the addition of the first metal catalyst compound.
In another embodiment binders are added to the mix. These can be added as a means of improving the particle morphology, i.e. narrowing the particle size distribution, lower porosity of the particles and allowing for a reduced quantity of alumoxane, which is acting as the 'binder'.

In another embodiment a solution of a bulky ligand metallocene compound and optional activator can be combined with a different slurried spray dried catalyst compound and then introduced into a reactor.
The spray dried particles are generally fed into the polymerization reactor as a mineral oil slurry. Solids concentrations in oil are about 10 to 30 weight %, preferably 15 to 25 weight %. In some embodiments, the spray dried particles can be from less than about 10 micrometers in size up to about 100 micrometers, compared to conventional supported catalysts which are about 50 micrometers. In a preferred embodiment the support has an average particle size of 1 to 50 microns, preferably 10 to 40 microns.
V. Catalyst Compositions of tlie Invention
To prepare the catalyst composition of the invention, the catalyst components described above are utilized in a catalyst component slurry and/or in a catalyst component solution. For the purposes of this invention, a slurry is defined to be a suspension of a solid, where the solid may or may not be porous, in a liquid. The catalyst component slurry and the catalyst component solution are combined to form the catalyst composition which is then introduced into a polymerization reactor.
A. Catalyst Component Slurry
In one embodiment, the catalyst component slurry includes an activator and a support, or a supported activator. In another embodiment, the catalyst component slurry includes a fumed silica. In another embodiment, the slurry also includes a catalyst compound in addition to the activator and the support and/or the supported activator. In one embodiment, the catalyst compound in the slurry is supported.
In another embodiment, the slurry includes one or more activator(s) and support(s) and/or supported activator(s) and/or one more catalyst compound(s). For example, the slurry may include two or more activators (such as a supported alumoxane and a modified alumoxane) and a catalyst compound, or the slurry may include a supported activator and more than one catalyst compounds. Preferably, the slurry comprises a supported activator and two catalyst compounds.

In another embodiment the slurry comprises supported activator and two different catalyst compounds, which may be added to the slurry separately or in combination.
In another embodiment the slurry, containing a supported alumoxane, is contacted with a catalyst compound, allowed to react, and (hereafter the slurry is contacted with another catalyst compound. In another embodiment the slurry containing a supported alumoxane is contacted with two catalyst compounds at the same time, and allowed to react.
In another embodiment the molar ratio of metal in the activator to metal in the catalyst compound in the slurry is 1000:1 to 0.5:1, preferably 300:1 to 1:1, more preferably 150:1 to 1:1.
In another embodiment the slurry contains a support material which may be any inert particulale carrier material known in the art, including, but not limited to, silica, fumed silica, alumina, clay, talc or other support materials such as disclosed above. In a preferred embodiment, the slurry contains a supported activator, such as those disclosed above, preferably methyl alumoxane and/or modified methyl alumoxane on a support of silica.
The catalyst component slurry used in the process of this invention is typically prepared by suspending the catalyst components, preferably the support, the activator and optional catalyst compounds in a liquid diluent. The liquid diluent is typically an alkane having from 3 to 60 carbon atoms, preferably having from 5 to 20 carbon atoms, preferably a branched alkane, or an organic composition such as mineral oil or silicone oil. The diluent employed is preferably liquid under the conditions of polymerization and relatively inert. The concentration of the components in the slurry is controlled such that a desired ratio of catalyst compound(s) to activator, and/or catalyst compound to catalyst compound is fed into the reactor.
Typically, the catalyst compound and the support and activator, or supported activator, and the slurry diluent are allowed to contact each other for a time sufficient for at least 50% of the catalyst compounds to be deposited into or on the support, preferably at least 70%, preferably at least 75%, preferably at least 80%, more preferably at least 90%, preferably at least 95%, preferably at least 99%. In an embodiment, the catalyst

component slurry is prepared prior to its use in the catalyst feed system of the invention. Times allowed for mixing are up to 10 hours, typically up to 6 hours, more typically 4 to 6 hours. In one embodiment of this invention a catalyst compound will be considered to be in or on the support if the concentration of the catalyst compound in the liquid portion of (he slurry is reduced over time after adding the catalyst compound to the slurry. Concentration of the catalyst compound in the liquid diluent may be measured for example, by inductively coupled plasma spectroscopy (ICPS), or by ultraviolet (UV) speclroscopy, after standardization with a calibration curve prepared at the appropriate concentration range, as is known in the art. Thus for example, 70 % of a catalyst compound will be considered to have deposited in or on a support if the concentration of the catalyst compound in the liquid (not including the support) is reduced by 70% from its initial concentration.
In one embodiment, the catalyst compounds can be added to the slurry as a solution, shiny, or powder. The catalyst component slurry is prepared prior to its use in the polymerization process of the invention or the catalyst component slurry may be prepared in-line.
In one embodiment, the slurry is prepared by combining the catalyst components, such as for example the catalyst or supported catalyst and the support and activator or supported activator, all at once. In another embodiment, the slurry is prepared by first adding a support material, then adding the combination of a catalyst and an activator component.
In another embodiment the slurry comprises a supported activator and at least one catalyst compound where the catalyst compound is combined with the slurry as a solution. A preferred solvent is mineral oil.
In a another embodiment, alumoxane, preferably methyl alumoxane or modified methyl alumoxane, is combined with a support such, as calcined silica or fumed silica to form a supported activator, the supported activator is then dispersed in a liquid, such as degassed mineral oil, and then one or more catalyst compounds are added to the dispersion and mixed to form the catalyst component slurry. The catalyst compounds are preferably added to the dispersion as a solid, powder, solution or a slurry, preferably a slurry of

mineral oil. If more than one catalyst compound is added to the dispersion, the catalyst Compounds can be added sequentially, or at the same time.
In another embodiment the catalyst compound is added to the slurry in solid or powder form. In a preferred embodiment, a Group 15 containing catalyst compound is added to the slurry in powder or solid form. In another preferred embodiment, [(2,4,6-Me3C6H2)NCH2CH2]2NHZrBz2 and or [(2,4,6-Me3C6H2)NCH2CHJ2NHHfBz2 is added to the slurry as a powder.
In a preferred embodiment the catalyst component slurry comprises mineral oil and has a viscosity of about 130 to about 2000 cP at 20°C, more preferably about 180 to about 1500 cP at 20°C and even more preferably about 200 to about 800 cP at 20°C as measured with a Brookfield model LVDV-UI Rheometer housed in a nitrogen purged drybox (in such a manner that the atmosphere is substantially free of moisture and oxygen, i.e. less than several ppmv of each). The catalyst component slurries are made in a nitrogen purged drybox, and rolled in their closed glass containers until immediately before the viscosity measurements are made, in order to ensure that they are fully suspended at the start of the trial. Temperature of the viscometer is controlled via an external temperature bath circulating heat transfer fluid into the viscometer. The rheometer was fitted with the appropriate spindle for the test material as specified in the unit's application guide. Typically, a SC4-34 or SC4-25 spindle was used. Data analysis was performed using Rheocalc Vl.l software, copyright 1995, Brookfield Engineering Laboratories, preferably purchased and used with the unit.
In one embodiment, the catalyst component slurry comprises a supported activator and one or more or a combination of the catalyst compound(s) described in Formula I to IX above.
In another embodiment, the catalyst component slurry comprises a supported activator and one or more or a combination of the Group 15 catalyst compound(s) represented by Formula I or II described above.
In another embodiment, the catalyst component slurry comprises a supported activator and one or more or combination of the bulky ligand catalyst compound(s) represented by Formula III to VI described above.

Ill another embodiment, the slurry comprises supported activator, a Group 15 catalyst compound(s) represented by Formula I or II described above, and a the bulky ligand catalyst compound(s) represented by Formula III to VI.
In another embodiment, the slurry comprises supported alumoxane and [(2,4,6-Me3C6H2)NCH2CH2]2NH MBz2 where M is a Group 4 metal, each Bz is a independently a benzyl group and Me is methyl.
In another embodiment, the slurry comprises a supported alumoxane, a Group 15 catalysts compound and one of the following: bis(n-propyl cyclopentadienyl)-MX2, (pentamethylcyclopentadienyl)(n-propylcyclopentadienyl)MX2, bis(indenyl)-MX2, or (tetramethylcyclopentadienyl) (n-propyl cyclopentadienyl) MX2, where M is zirconium., hafnium or titanium and X is chlorine, bromine, or fluorine.
In the polymerization process of the invention, described below, any of the above described catalyst component containing slurries may be combined with any of the catalyst component containing solutions described below. In addition, more than one catalyst component containing slurry may be utilized.
B. Catalyst Component Solution
In one embodiment, the catalyst component solution includes a catalyst compound. In another embodiment, the solution also includes an activator in addition to the catalyst compound.
The solution used in the process of this invention is typically prepared by dissolving the catalyst compound and optional activators in a liquid solvent. The liquid solvent is typically an alkane, such as a C5 to C30 alkane, preferably a C5 to C,0 alkane. Cyclic alkanes such as cyclohexane and aromatic compounds such as toluene may also be used. In addition, mineral oil may be used as a solvent. The solution employed should be liquid under the conditions of polymerization and relatively inert. In one embodiment, the liquid utilized in the catalyst compound solution is different from the diluent used in the catalyst component slurry. In another embodiment, the liquid utilized in the catalyst compound solution is the same as the diluent used in the catalyst component solution.

In a preferred embodiment the ratio of metal in the activator to metal in the catalyst compound in the solution is 1000:1 to 0.5 :1, preferably 300:1 to 1:1, more preferably 150:1 to 1:1.
In a preferred embodiment, the activator and catalyst compound is present in the solution at up to about 90 wt %, preferably at up to about 50 wt %, preferably at up t6 about 20 wt %, preferably at up to about 10 wt%, more preferably at up to about 5 wt%, more preferably at less than 1 wt%, more preferably between 100 ppm and 1 wt % based upon (he weight of the solvent and the activator or catalyst compound.
In one embodiment, the catalyst component solution comprises any one of the catalyst compounds described in Formula I to IX above.
In another embodiment, the catalyst component solution comprises a Group 15 catalyst compound represented by Formula I or II described above.
In another embodiment, the catalyst component solution comprises a bulky ligand catalyst compound represented by Formula III to VI described above.
In a preferred embodiment the solution comprises bis(n-propyl cyclopentadienyl)-MX2, (pentamelhylcyclopenladienyl)(n-propylcyclopentadienyl)MX2, bis(indenyl)-MX2, (tetramethylcyclopentadienyl) (n-propylcyclopentadienyl) MX2, where M is a Group 4 metal, preferably zirconium, hafnium or titanium and X is chlorine, bromine, or fluorine.
In the polymerization process of the invention, described below, any of the above described catalyst component containing solution(s) may be combined with any of the catalyst component containing slurry/slurries described above. In addition, more than one catalyst component containing solution may be utilized.
C. Catalyst Compositions
The catalyst composition of the invention is formed by combining any one of the catalyst component slurries with any one of the catalyst component solutions described above. Generally, the catalyst component slurry and the catalyst component solution are mixed in the process of the invention to form the final catalyst composition, which is then introduced into a polymerization reactor and combined with and one or more olefins.

Preferably the catalyst component slurry and the catalyst component solution are continuously mixed and introduced into the polymerization reactor.
In one embodiment, the slurry contains at least one support and at least one activator, preferably a supported activator, and the solution contains at least one catalyst compound.
hi another embodiment, the catalyst component slurry contains a support, and an activator and/or a supported activator, and the catalyst component solution contains at least one catalyst compound and at least one activator.
In one embodiment, the slurry contains at least one support and at least one activator, preferably a supported activator, and the solution contains one or more catalyst compound(s) and/or one or more activator compound(s).
In another embodiment, the catalyst component slurry contains more than one support(s), activator(s) and/or supported activator(s), and the catalyst component solution contains at least one catalyst compound.
In another embodiment, the catalyst component slurry contains more than one support(s), activator(s) and/or supported activator(s), and the catalyst component solution contains at least one catalyst compound and at least one activator.
In another embodiment, the catalyst component slurry contains more than one support(s), activator(s) and/or supported activator(s), and the catalyst component solution contains one or more catalyst compound(s) and/or one or more activator compouhd(s).
In another embodiment, the catalyst component slurry contains a support, an activator and/or a supported activator, and also contains a catalyst compound and/or a supported catalyst compound, and the catalyst component solution contains at least one catalyst compound.
In another embodiment, the catalyst-component slurry contains a support, an activator and/or a supported activator, and also contains a catalyst compound and/or a supported catalyst compound, and the catalyst component solution contains at least one catalyst compound and at least one activator.
In another embodiment, the catalyst component slurry contains a support, an activator and/or a supported activator, and also contains a catalyst compound and/or a

supported catalyst compound, and the catalyst component solution contains one or more catalyst compound(s) and/or one or more activator compound(s).
In another embodiment, the catalyst component slurry contains a support, an activator and/or a supported activator and more than one catalyst compound(s) and/or supported catalyst compounds, and the catalyst component solution contains at least one catalyst compound.
In another embodiment, the catalyst component slurry contains a support, an activator and/or a supported activator and more than one catalyst compound(s) and/or supported catalyst compounds, and the catalyst component solution contains at least one catalyst compound and at least one activator.
In another embodiment, the catalyst component slurry contains a support, an activator and/or a supported activator and more than one catalyst compound(s) and/or supported catalyst compounds, and the catalyst component solution contains one or more catalyst compound(s) and/or one or more activator compound(s).
In another embodiment, the catalyst component slurry contains more than one support(s), activator(s) and/or supported activators and more than one catalyst compound(s) and/or supported catalyst compound(s), and the catalyst component solution contains at least one catalyst compound.
In another embodiment, the catalyst component slurry contains more than one support(s), activator(s) and/or supported activators and more than one catalyst compound(s) and/or supported catalyst compound(s), and the catalyst component solution contains at least one catalyst compound and at least one activator.
In another embodiment, the catalyst component slurry contains more than one support(s), activator(s) and/or supported activators and more than one catalyst compound(s) and/or supported catalyst compound(s), and the catalyst component solution contains one or more catalyst compound(s) and/or one or more activator compound(s). In one embodiment the catalyst composition, formed by combining the catalyst component slurry and the catalyst component solution, has a viscosity of about 130 to about 2000 cP at 20°C, more preferably about 180 to about 1500 cP at 20°C even more preferably about 200 to about 800 cP at 20°C.

In another embodiment, the catalyst component solution comprises, up to 80 weight %, preferably up to 50 weight %, preferably up to 20 weight %, preferably up to 15 weight %, more preferably between 1 to 10 weight %, more preferably 3 to 8 weight % of the combination of the catalyst component solution and the catalyst component slurry, based upon the weight of the solution and the slurry, hi another preferred embodiment, the catalyst component solution comprises mineral oil and comprises up to 90 weight %, preferably up to 80 weight %, more preferably between 1 to 50 weight %, and more preferably 1 to 20 weight % of the combination of the catalyst component solution and the catalyst component slurry, based upon the weight of the solution and the slurry.
In one embodiment, the catalyst component slurry is fed to the polymerization reactor utilizing a slurry feeder. In another embodiment the catalyst composition, which includes the catalyst component slurry and the catalyst component solution, is fed to the polymerization reactor utilizing a slurry feeder. A slurry feeder, for example, is described U.S. Patent 5,674,795, incorporated herein by reference.
In one embodiment, the catalyst component solution, comprising a catalyst compound, is contacted with the catalyst component slurry so that at least 50% of the catalyst compound originally in the catalyst component solution is deposited in or on the support, preferably at least 70%, preferably at least 75%, preferably at least 80%, more preferably at least 90%, preferably at least 95%, preferably at least 99%.
In another embodiment, the catalyst component solution comprising a metallocene catalyst compound, is contacted with a catalyst component slurry comprising a support and an activator, preferably a supported activator, to form an immobilized catalyst composition. After contacting, all or substantially all, preferably at least 50% preferably at least 70%, preferably at least 75%, preferably at least 80%, more preferably at least 90%, preferably at least 95%, preferably at least 99% of the catalyst compound from the catalyst component solution is deposited in or on the support initially contained in the catalyst component shiny. In one embodiment, a catalyst compound will be considered to be in or on the support if the concentration of the catalyst compound in the liquid portion of the combination is reduced over time after adding the catalyst compound from the solution. The catalyst concentration may be measured as described above.

In another embodiment, the supported activator is in a mineral oil that is then contacted with a metallocene catalyst solution prior to introducing the catalyst composition to the reactor, preferably where the contacting takes place in-line.
In another embodiment, the immobilized catalyst composition system or components thereof may be contacted with a carboxylate metal salt as described in PCT publication WO 00/02930 and WO 00/02931, which are herein incorporated by reference.
In another embodiment the solution comprises a catalyst compound and the slurry comprises a supported activator, such as supported alumoxane, and two or more catalyst compounds, that may be the same or different from the catalyst compound in the solution. The two catalyst compounds may be added to the slurry before or after the supported activator. In a preferred embodiment the supported activator is added to the liquid diluent first to form a slurry, then a catalyst compound is added to the slurry, and thereafter another catalyst compound is added to the slurry. The second catalyst is preferably added after the first catalyst compound and the supported activator have been contacted for at least 1 minute, preferably at least 15 minutes, more preferably at least 30 minutes, more preferably at least 60 minutes, more preferably at least 120 minutes, more preferably at least 360 minutes.
In another embodiment the two catalyst compounds are added to the slurry at the same time, in the same or different solutions. In another embodiment, a catalyst compound is contacted with an unsupported activator prior to being placed in the slurry. In a preferred embodiment, the unsupported activator is a modified or unmodified alumoxane, such as methyl alumoxane.
In another embodiment, the catalyst compound may be added to the solution or slurry in its constituent parts of metal compound and ligands. For example, cyclopentadienyl groups such as substituted or unsubstituted cyclopentadiene, indene, fluorene groups and metal compounds such as zirconium tetrahalide may be added to the slurry or solution or both and allowed to react therein. Likewise, one may also add metal compounds and or ligands to the solution and or slurry that already contains catalyst compounds. The metal compounds and ligands may be the same or different from the

components of the catalyst compound in the solution or slurry. In another embodiment ligands and/or metal compounds may be added to both the solution and the slurry.
In another embodiment the catalyst composition comprises a "bisamide" catalyst compound (i.e., a bridged bis(arylamido) Group 4 compounds described by D.H, McConville, et al., in Organometallics 1195, 14, 5478-5480, or a bridged bis(amido) catalyst compounds described in WO 96/27439) combined with an activator, spray dried to a powder state, then combined with mineral oil to form a slurry. This combination may then be combined with various catalyst component solutions to form a particularly effective multiple catalyst systems. Preferred catalyst compounds include those described above as bulky ligand metallocene catalysts. In another preferred embodiment the slurry comprises a supported activator and the solution comprises a catalyst compound. The catalyst compounds may be selected from various catalyst compounds described above including bulky ligand metallocenes.
In another embodiment, the slurry comprises [(2,4,6-Me3C6H2) NCH2CH2]2NHZrBz2 or [(2,4,6-Me3C6H2)NCH2CH2]2NHHfBz2, where each Bz is independently a benzyl group, Me is methyl, and the solution comprises bis(n-propyl cyc!opentadienyl)-MX2, (pentamethylcyclopentadienyl)(n-propylcyclopentadienyl)MX2, bis(indenyi)-MX2, or (tetramethylcyclopentadienyl) (n-propylcyclopeiitadienyl) MX2 where M is zirconium, hafnium or titanium and X is chlorine, bromine, or fluorine.
In another embodiment, the solution comprises [(2,4,6Me3C6H2) NCH2CH2]2NIIZrBz2 or [(2,4,6-Me3C6H2)NCH2CH2]2NHHffiz2, where each Bz is independently a benzyl group, Me is methyl, and the slurry comprises: 1) supported alumoxane, and 2) bis(n-propyl cyclopentadienyl)-MX2, pentamethylcyclopentadienyl)(n-propylcyclopentadienyl)MX2, bis(indenyl)-MX2, or (tetramethylcyclopentadienyl) (n-propylcyclopentadienyl) MX2 where M is zirconium, hafnium or titanium and X is chlorine, bromine, or fluorine.
In another embodiment, the slurry comprises: 1) a supported alumoxane, 2) bis(n-propyl cyclopentadienyl)-MX2, (pentamethylcyclopentadienyl)(n-propyl-cyclopentadienyl)MX2, bis(indenyl)-MX2, (tetramethylcyclopentadienyl) (n-propylcyclopenladienyl) MX2, where M is zirconium, hafnium or titanium and X is

chlorine, bromine, or fluorine, and 3) [(2,4,6-Me3C6H2)NCH2CH2]2NHZrBz2 or [(2,4,6-Me3C6H2)NCH2CH2]2NHHfBz2, and the solution comprises a bulky ligand metallocene compound.
In another embodiment, the slurry comprises mineral oil and a spray dried catalyst compound. In another embodiment, the spray dried catalyst compoufid is a Group 15 containing metal compound. In a preferred embodiment, the spray dried catalyst compound comprises [(2,4,6-Me3C6H2)NCH2CH2]2NHZrBz2or its hafnium analog.
In another embodiment, the catalyst compound and the supported activator may be combined before being combined with the slurry diluent or after.
In another embodiment the solution comprises a catalyst compound of bis-indenyl zirconium dichloride, bis(n-propyl cyclopentadienyl) zirconium dichloride, (pentamethylcyclopentadienyl)(n-propylcyclopentadienyl)zirconium dichloride, (tetramethylcyclopentadienyl)(n-propylcyclopentadienyl)zirconium dichloride, or a mixture thereof.
In another embodiment, a first catalyst compound is combined with a supported activator in the slurry, and a second catalyst compound and an activator are combined in the solution and thereafter the two are mixed in line. In another embodiment, the one activator is an alumoxane and the other activator is a boron based activator.
In another embodiment the slurry comprises mineral oil, spray dried [(2,4,6-Me3C6H2)NCH2CH2]2NHZrBz2, and the solution comprises bis(n-propyl cyclopentadienyl) zirconium dichloride.
In a one embodiment of this invention the slurry comprises supported activator and a catalyst compound and the solution comprises a catalyst compound different in some way from the catalyst compound in the slurry. For example, the slurry catalyst compound could lie a compound represented by the Fonnula I or II described above, while the solution catalyst compound could be a catalyst compound described by Fonnula III, IV, V, VI, or VII, or vice versa.
In another embodiment, if a bimodal polymer product were desired, one could mix a first catalyst compound with an activator in the slurry, then on-line add a solution of a different catalyst compound (hat is capable of being activated by the same activator. Since

the two catalyst compounds are introduced into the feed line independently, it will be easier to control the amount of the two species in the final bimodal product, assuming that each catalyst produces at least one species of polymer.
In another embodiment, a Group 15 metal containing compound and a bulky ligand metallocene catalyst compound are combined with supported alumoxane in the process of this invention. Typically the two catalyst compounds are combined in the slurry with the supported alumoxane and the solution will comprise a trim solution of one or the other of the two catalyst compounds.
In another embodiment, [(2,4,6-Me3C6H2)NCH2CH2]2NHHfBz2, and bis(n-propyl cyclopentadienyl) zirconium dichloride are combined with supported methyl alumoxane in the process of this invention. Typically the two catalyst compounds are combined in the slurry with the supported alumoxane and the solution will comprise one or the other of the two catalyst compounds. The solution is preferably used as a trim solution to regulate the product formed in the reactor by varying the amount of solution combined with the slurry on-liae, i.e. to trim the mix. In one embodiment this catalyst combination is then used to polymerize olefm(s), preferably ethylene, at a polymerization temperature of 80 to 110°C and in the presence of little or no comonomer(s) for example hexene.
In another embodiment the slurry concentration is maintained at greater than 0 to 90 wt % solids, more preferably 1 to 50 wt %, more preferably 5 to 40 wt %, even more preferably 10 to 30 wt %, based upon the weight of the slurry. In another preferred embodiment the activator is present on the support at between about 0.5 to about 7 mmol/g, preferably about 2 to about 6 mmol/g, more preferably between about 4 to about 5 mmol/g. In another preferred embodiment the total amount of catalyst compound present on the support, preferably a supported activator, is about 1 to about 40 fimol/g, preferably about 10 to about 38 umol/g, more preferably 30 to 36 fimol/g.
In one embodiment the final mole ratio (i.e. after combination of the solution and the slurry) of the metal of the catalyst compounds and the metal of the activator is in the range of from about 1000:1 to about 0.5:1 preferably from about 300:1 to about 1:1 more preferably from about 150:1 to about 1:1; for boranes, borates, aluminates, etc., the ratio is preferably about 1:1 to about 10:1 and for alkyl aluminum compounds (such as

dielhylaluminum chloride combined with water) the ratio is preferably about 0.5:1 to about 10:1.
In one embodiment, the catalyst compound used in the slurry is not soluble in the solvent used in the solution. By "not soluble" is meant that the not more than 5 weight % of the material dissolves into the solvent at 20 °C and less than 3 minutes of stirring, preferably not more than 1 weight %, preferably not more than 0.1 weight %, preferably not more than 0.01 weight%. In a preferred embodiment, the catalyst compound used in the slurry at least only sparingly soluble in an aromatic hydrocarbon. In a particularly preferred embodiment the catalyst compound used in the slurry is not soluble in mineral oil, aromatic solvent or aliphatic hydrocarbon (pentane, heptane, etc.).
D. Delivery of the Catalyst Composition
In the process of the invention, the catalyst component slurry is combined with and/or reacted with the catalyst component solution to form a catalyst composition in-line. The catalyst composition so formed is then is introduced into the polymerization reactor. Generally the catalyst composition is introduced to the reactor utilizing a catalyst feed system which includes a catalyst component slurry holding vessel, a catalyst component solution holding vessel, and a slurry feeder.
Referring to Figure 1, in one embodiment, the catalyst component slurry, preferably a mineral oil slurry including at least one support and at least one activator, preferably at least one supported activator, and optional catalyst compound(s) is placed in a vessel (A). In a preferred embodiment (A) is an agitated holding tank designed to keep the solids concentration homogenous. The catalyst component solution, prepared by mixing a solvent and at least one catalyst compound and/or activator, is placed in a vessel (C). The catalyst component slurry is then combined in-line with the catalyst component solution to form a final catalyst composition. A nucleating agent, such as silica, alumina, fumed silica or any other particulate matter (B) may be added to the slurry and/or the solution in-line or in the vessels (A) or (C). Similarly, additional activators or catalyst compounds may be added in-line. The catalyst component slurry and solution are preferably mixed in-line at some point (E) for a period of time. For example, the solution

and slurry may be mixed by utilizing a static mixer or an agitating vessel. The mixing of the catalyst component slurry and the catalyst component solution should be long enough to allow the catalyst compound in the catalyst component solution to disperse in the catalyst component shiny such that the catalyst component, originally in the solution, migrates to the supported activator originally present in the slurry. The combination thereby becomes a uniform dispersion of catalyst compounds on the supported activator forming the catalyst composition of the invention. The length of time that the slurry and the solution are contacted is typically up to about 120 minutes, preferably about 1 to about 60 minutes, more preferably about 5 to about 40 minutes, even more preferably about 10 to about 30 minutes.
In another embodiment, an aluminum alkyl, an ethoxylated aluminum alkyl, an alumoxane, an anti-static agent or a borate activator, such as a C, to C,5 alkyl aluminum (for example tri-isobutyl aluminum, trimethyl aluminum or the like), a C, to C,5 elhoxylated alkyl aluminum or methyl alumoxane, ethyl alumoxane, isoburylalumoxane, modified alumoxane or the like are added to the mixture of the slurry and the solution in line. The alkyls, antistatic agents, borate activators and/or alumoxanes may be added (F), directly to the combination of the solution and the slurry, or may be added via an additional alkane (such as isopentane, hexane, heptane, and or octane) carrier stream (G). Preferably, the additional alkyls, antistatic agents, borate activators and/or alumoxanes are present at up to about 500 ppm, more preferably at about 1 to about 300 ppm, more preferably at 10 to about 300 ppm, more preferably at about 10 to about 100 ppm. Preferred carrier streams include isopentane and or hexane. The alkane may be added (G) to the mixture of the slurry and the solution, typically at a rate of about 0.5 to about 60 Ibs/hr (27 kg/hr). Likewise carrier gas, such as nitrogen, argon, ethane, propane and the like may be added in-line (H) to the mixture of the slurry and the solution. Typically the carrier gas may be added at the rate of about 1 to about 100 Ib/hr (0.4 to 45 kg/hr), preferably about 1 to about 50 Ib/hr (5 to 23 kg/hr), more preferably about 1 to about 25 Ib/hr (0.4 to 11 kg/hr).
In another embodiment, a liquid earner stream is introduced into the combination of the solution and slurry (hat is moving in a downward direction. The mixture of the

solution, the slurry and the liquid earner stream may pass through an optional mixer or length of tube for mixing before being contacted with a gaseous carrier stream.
Similarly, hexene (or other alpha-olefm or diolefm) may be added in-line (J) to the mixture of the slurry and the solution. The shiny/solution mixture is then preferably passed tlirough an injection tube (O) to the reactor (Q). In some embodiments, the injection tube may aerosolize the slurry/solution mixture. In a preferred embodiment the injection tube has a diameter of about 1/16 inch to about 1/2 inch (0.16 cm to 1.27 cm), preferably about 3/16 inch to about 3/8 inch (0.5 cm to 0.9 cm), more preferably 1/4 inch to about 3/8ths inch (0.6 cm to 0.9 cm).
In one embodiment cycle gas (also called re-cycle gas) is introduced into the support lube (S), in another embodiment monomer gas, such as ethylene gas, is introduced into the support tube. Nucleating agents (K), such as fumed silica, can be added directly in to the reactor.
In another embodiment a plenum may be used in this invention. A plenum is a device used to create a particle lean zone in a fluidized bed gas-phase reactor, as described in detail in U.S. Patent No. 5,693,727 which is incorporated herein by reference. A plenum may have one, two, or more injection nozzles.
In another embodiment when a metallocene catalyst or other similar catalyst is used in the gas phase reactor, oxygen and or fluorobenzene can be added to the reactor directly or to the recycle gas to affect the polymerization rate. Thus, when a metallocene catalyst (which is sensitive to oxygen or fluorobenzene) is used in combination with another catalyst (that is not sensitive to oxygen) in a gas phase reactor; oxygen can be used to modify the metallocene polymerization rate relative to the polymerization rate of the other catalyst. An example of such a catalyst combination is bis(n-propyl cyclopentadienyl) zirconium dichloride and [(2,4,6-Me3C6H2)NCH2CH2]2NHZrBz2, where Me is methyl or bis(indenyl) zirconium dichloride and [(2,4,6-Me,C6H2)NCH2CH2]2NHHfBz2, where Me is methyl. For example if the oxygen concentration in the nitrogen feed is altered from 0.1 ppm to 0.5 ppm, significantly less polymer from the bisindenyl ZrCl2 will be produced and the relative amount of polymer

produced from the [(2,4,6-Me3C6H2)NCH2CH2]2NHHfBz2 is increased. WO/09328 discloses the addition of water and or carbon dioxide to gas phase polymerization reactors.
In another embodiment, referring still to Figure 1, the slurry .comprising mineral oil, at least one catalyst compound, a support and an activator is mixed in and/or introduced from (A). The catalyst component solution comprising a solvent, such as toluene, hexane, mineral oil or tetrahydrofuran, and a catalyst compound and/or an activator is mixed in and/or introduced from (C). Nucleating agent (B) and (K), such as fumed silica, may be added on line at one or more positions and may be wet or dry. The slurry and the solution are combined and typically mixed at (E). Optional light alkyls (F), such as triisobutyl aluminum, an alumoxane, modified methylalumoxane and/or trimethyl aluminum, may be added in line directly to the combination or via an alkane, such as isopenlane, feed (G). Nitrogen (H) and/or olefin, such as hexene, (J) may also be added in line. The combination may then be injected through an injection tube (O) (such as a 1/8 inch (0.3cm) tube) into a gas phase reactor (Q). The injection tube (O) may be supported inside a larger support tube (S), such as a 1 inch (2.54 cm) tube. Oxygen can be added directly to the reactor (Q) or to the recycle gas (P) to alter the activity of one or more catalysts. (R) is How (monomer, recycle gas, alkane) to the support tube (S).
In another embodiment, catalyst ball formation and or general nozzle fouling were reduced by first feeding isopentane carrier from the feed line (G) into the combination of the solution and the slurry, thereafter the combination of the solution slurry and isopentane preferably moves in a vertical orientation with a downward flow into the reactor using a nitrogen sweep (H) to disperse the isopentane/slurry mixture into the reactor.
The catalyst injection tube passes into the reactor through a compressed chevron packing and extends into the fluid bed a distance of about 0.1 inch to 10 feet (0.25 cm to 3.1 in), preferably about 1 inch to 6 ft (2.5 cm to 1.8 m), and more preferably about 2 inches to 5 feet (5 cm to 1.5 m). Typically, the depth of insertion depends on the diameter of the reactor and typically extends in about 1/20 to 1/2 of the reactor diameter, preferably about l/10th to 1/2 and more preferably about l/5th to l/3rd of the reactor diameter. The end of the tube may be cut perpendicular to the axis to create a nozzle cone or point with an angle ranging from 0 to 90 degrees, preferably ranging from about 10 to 80 degrees.

The lip of the hole can be taken to a new knife-edge. The tube can be positioned to reduce resin adhesion or coated with an antifouling or antistatic compound. The tube can also be cut diagonally at an angle simply from about 0 to 80 degrees off the axial line of the tube, preferably about 0 to 60 degrees. The opening of the tube can be the same as the bore of the tube or expanded or diminished to create a nozzle, with sufficient pressure drop and geometry to provide a dispersed spray of a solution slurry and or powder into the reactor, preferably into the fluid bed.
The injection tube can optionally be supported inside a structure within the fluid bed to provide structural integrity. This support tube is typically a heavy walled pipe with an internal diameter of from about 1/4 inch to about 5 inches (0.64 cm to 12.7 cm), preferably about 1/2 inch to about 3 inches (1.3 cm to 7.6 cm), and more preferably about 3/4 inch to about 2 inches (1.9 cm to 5 cm). The support tube preferably extends through (he reactor wall to approximately the length of the injection tube, allowing the injection tube to end just inside the end of the support lube or to extend past it up to about 10 inches (25.4 cm). Preferably, the injection tube extends about 0.5 to 5 inches (1.8 cm to 12.7 cm) beyond the end of the support tube and more preferably about 1 to 3 inches (2.5 cm to 7.6 cm). The end of the support tube in the reactor may be cut flat and perpendicular to the axis of the tube or preferably, may be tapered at an angle ranging from about 10 to 80 degrees. The end of the support tube may be polished or coated with an anti-static or antifouling material.
A purge flow of fluid (R) (typically fresh monomer, ethylene, hexane, isopentane, recycle gas, and the like) is preferably introduced from outside the reactor down the support tube to aid in dispersion of the catalyst composition allowing the production of resin granular particles of good morphology with decreased agglomeration and an APS (average particle size) in the range of about 0.005 to 0.10 inches (.01 cm to 0.3 cm). The purge flow of fluid helps minimize fouling of the end of the catalyst injection tube and support tubes. The fluid introduced to the support tube may comprise hydrogen; olefins or dioleflns, including but not limited to C2 to C40 alpha olefins and C2 to C40 diolefins, ethylene, propylene, butene, hexene, octene, norbomene, pentene, hexadiene, pentadiene, isobutylene, octadiene, cyclopentadiene, comonomer being used in the polymerization

reaction, hydrogen; alkanes, such C, to C40 alkanes, including but not limited to isopetane, hexane, ethane, propane, butane, and the like; mineral oil, cycle gas with or without condensed liquids; or any combination thereof. Preferably the support tube flow is fresh ethylene or propylene that may be heated. In addition, an alkane, such as for instance' isopenlane or hexane, can be included in the flow at the level ranging from about 0.001 wt %. to about 50% of the flow. The alkane can be dispersed in the flow and may exist as dispersed liquid droplets or be vaporized at the exit of the support tube. The presence of liquid may reduce fouling at the exit.
The flow rate of fluid in the support tube ranges from about 5 to 10,000 pph and is somewhat dependent upon the reactor size. The linear velocity of the fluid in the support lube ranges from about 10 to 500 ft/sec (11 to 549 km/hr), preferably about 20 to 300 ft/sec (22 to 329 km/hr) and more preferably about 30 to 200 ft/sec (33 to 219 km/hr).
Alternatively, the exit of the support tube may be fashioned as a nozzle at the end to form a jet or dispersion of gas to aid in the distribution of the catalyst composition. In one embodiment, the internal diameter of the support tube is reduced gradually by about 3 to 80% at the end, preferably about 5 to 50% in a taper to create a nozzle to accelerate to and or disperse the fluid flow. The insertion of the injection tube is not impacted by the internal taper of the support tube.
In another embodiment of the invention the contact time of the slurry and the solution can be varied to adjust or control formation of the active catalyst complex. The contact time of the slurry and the solution is preferably in the range of from 1 minute to 120 minutes, preferably in the range of from 2 minutes to 60 minutes, preferably 5 minutes to 45 minutes, more preferably from about 10 minutes to about 30 minutes.
In another embodiment, the contact temperature of the slurry and the solution is in the range of from 0°C to about 80°C, preferably from about 0°C to about 60°C, more preferably from about 10°C to about 50°C and most preferably from about 20°C to about 40°C.
In another embodiment, the invention provides introducing the immobilized catalyst system in the presence of a mineral oil or a surface modifier or a combination thereof as described in PCT publication WO 96/11960 and USSN 09/113,261 filed July

10, 1998, which are herein fully incorporated by reference. In another embodiment a slurry or surface modifier, such as an aluminum stearate in mineral oil) is introduced (T) into the reactor with the combination of the shiny and the solution. In another embodiment the surface modifier, such as aluminum stearate, was added into the slurry vessel (A).
In another embodiment the one or all of the catalysts are combined with up to 6 weight % of a metal stearate, (preferably a aluminum stearate, more preferably aluminum distearate) or an anti-static agent based upon the weight of the catalyst, any support and the stearate or anti-static agent, preferably 2 to 3 weight %. In one embodiment, a solution or slurry of the metal stearate or anti-static agent is fed into the reactor. The stearate or anti-static agent may be combined with the slurry (A) or the solution (C) or may be co-fed (R) with the combination of the slurry and the solution. In a preferred embodiment the catalyst compounds and or activators are combined with about 0.5 to about 4 weight % of an antistat, such as a methoxylated amine, such as Witco's Kemamine AS-990 from ICI Specialties in Bloomington Delaware.
In another embodiment the catalyst system or the components thereof are combined with benzil, xylitol, Irganox™ 565, sorbitol or the like and then fed into the reactor. These agents may be combined with the catalyst compounds and/or activators or may be fed into the reactor in a solution with or without the catalyst system or its components. Similarly these agents may be combined with the slurry (A) or the solution (C) or may be co-fed (R) with the combination of the slurry and the solution.
In another embodiment the process of this invention may further comprise additional solutions and slurries. For example, in a preferred embodiment a slurry can be combined with two or more solutions having the same or different catalyst compounds and or activators. Likewise, the solution may be combined with two or more slurries each having the same or different supports, and the same or different catalyst compounds and or activators. Similarly the process of this invention may comprise two or more slurries • combined with two or more solutions, preferably in-line, where the slurries each comprise the same or different supports and may comprise the same or different catalyst compounds and or activators and the solutions comprise the same or different catalyst compounds and

or activators. For example, the slurry may contain a supported activator and two different catalyst compounds, and two solutions, each containing one of the catalysts in the slurry, are each independently combined, in-line, with the slurry.
E. Use of Catalyst Composition to Control Product Properties
The timing, temperature, concentrations, and sequence of the mixing of the solution, the slurry and any optional added materials (nucleating agents, catalyst compounds, activators, etc) described above can be used to alter product properties. The melt index, relative amount of polymer produced by each catalyst, and other properties of the polymer produced may also be changed by manipulating process parameters which include manipulating hydrogen concentration in the polymerization system or by:
1) changing the amount of the first catalyst in the polymerization system, and/or
2) changing the amount of the second catalyst in the polymerization system, and/or
3) changing the hydrogen concentration in the polymerization process; and/or
4) changing the relative ratio of the catalyst in the polymerization process (and
optionally adjusting their individual feed rates to maintain a steady or constant resin
production rate); and/or
5) changing the amount of liquid and/or gas that is withdrawn and/or purged from the
process; and/or
6) changing the amount and/or composition of a recovered liquid and/or recovered
gas returned to the polymerization process, said recovered liquid or recovered gas being
recovered from polymer discharged from the polymerization process; and/or
7) using a hydrogenation catalyst in the polymerization process; and/or
8) changing the polymerization temperature; and/or
9) changing the ethylene partial pressure in the polymerization process; and/or
10) changing the ethylene to comonomer ratio in the polymerization process; and/or
11) changing the activator to transition metal ratio in the activation sequence; and/or
12) changing the relative feed rates of the slurry and/or solution; and/or
13) changing the mixing time, the temperature and or degree of mixing of the slurry
and the solution in-line; and/or

14) adding different types of activator compounds to the polymerization process;
and/or
15) adding oxygen or fluorobenzene or other catalyst poison to the polymerization
process.
For example to alter the flow index and or melt index of a polymer produced according to the invention using a slurry of supported methylalumoxane and [(2,4,6-Me3C6H2)NCH2CH2]2NH} ZrBz2 and a solution of bis(n-propyl cyclopentadienyl) zirconium dichloride one can alter the temperature of the reaction in the polymerization reactor, one can alter the concentration of hydrogen in the reactor, or one can alter the concentration of the bis(n-propyl cyclopentadienyl) zirconium dichloride in the solution prior to contacting the solution with the slurry, or one can alter the relative feed rate of the catalyst component solution and/or the catalyst component slurry.
In a preferred embodiment, the flow index (I2I-measured according to ASTM D-1238, Condition E, at 190°C) of the polymer product is measured at regular intervals and one of the above factors, preferably temperature, catalyst compound feed rate, the ratio of the two or more catalysts to each other, monomer partial pressure, oxygen concentration, and or hydrogen concentration, is altered to bring the flow index to the desired level, if necessary. Preferably the samples for flow index measurements are melt- homogenized by extruding in an extruder that is equipped with either a single screw, preferably with a mixing head, or a twin screw, to make either tape or strand(s). The tape and or strands are typically cut into small pieces for flow property measurements.
In an embodiment, a polymer product property is measured in-line and in response the ratio of the catalysts being combined is altered. In one embodiment, the molar ratio of the catalyst compound in the catalyst component slurry to the catalyst compound in the • catalyst component solution, after the slurry and solution have been mixed to form the final catalyst composition, is 500:1 to 1:500, preferably 100:1 to 1:100, more preferably 50:1 to 1:50 and most preferably 40:1 to 1:10. In another embodiment; the molar ratio of a Group 15 catalyst compound in the slurry to a bulky ligand metallocene catalyst compound in the solution, after the slurry and solution have been mixed to form the catalyst composition, is 500:1, preferably 100:1, more preferably 50:1, more preferably

10:1 and even more preferably 5:1. Preferably, the product property measured is the polymer product's flow index, melt index, density, MWD, comonomer content and combinations thereof. In another embodiment, when the ratio of the catalyst compounds is altered, the introduction rate of the catalyst composition to the reactor, or other process parameters, is altered to maintain a desired production rate.
Likewise, the support architecture, the number of functional groups on the support (such as-OH groups on silica) the activator loading and the pre-impregnated catalyst loading can also affect the product formed.
Similarly, altering the ethylene partial pressure can alter product properties. For example in a system where the solution comprised bis(n-propyl cyclopentadienyl) zirconium dichloride and the slurry comprised [(2,4,6-Me3C6H2)NCH2CH2]2NHZrBz2 and supported methyl alumoxane, increasing the ethylene partial pressure in the gas phase reactor from 220 to 240 psi (1.5-1.7 MPa) increased the Flow Index from 100 to over 700 dg/rnin.
While not wishing to be bound by or limited to any theory, the inventors believe, that the processes described herein immobilize the solution catalyst compound in and on a support, preferably a supported activator. The in-line immobilization techniques described herein preferably result in a supported catalyst system that when introduced to the reactor provides for better particle morphology, bulk density, and/or higher catalyst activities and without the need for additional equipment in order to introduce catalyst compound solution into a reactor, particularly a gas phase or slurry phase reactor. It is known in the art that typical support techniques for supporting, metallocene catalyst compounds results in lower overall productivity of the formed supported catalysts. In some instances the supporting process in fact renders certain of these catalyst compounds useless in commercial polymerization processes that especially prefer the utilization of supported catalysts. This is particularly true when comparing introducing an unsupported catalyst system into a gas phase process versus a conventional supported catalyst system. By conventional supported catalysts system it is meant those supported catalyst systems that are formed by contacting a support material, an activator and a catalyst compound in various ways under a variety of conditions outside of a catalyst feeder apparatus.

Examples of conventional methods of supporting rnetallocene catalyst systems are described in U.S. Patent Nos. 4,701,432, 4,808,561, 4,912,075, 4,925,821, 4,937,217, 5,008,228, 5,238,892, 5,240,894, 5,332,706, 5,346,925, 5,422,325, 5,466,649, 5,466,766, 5,468,702, 5,529,965, 5,554,704, 5,629,253, 5,639,835, 5,625,015, 5,643,847, 5,665,665, 5,698,487, 5,714,424, 5,723,400, 5,723,402, 5,731,261, 5,759,940, 5,767,032, 5,770,664, 5,846,895 and 5,939,348 and U.S. Application Serial Nos. 271,598 filed July 7, 1994 and 788,736 filed January 23, 1997 and PCT publications WO 95/32995, WO 95/14044, WO 96/06187 and WO 97/02297, and EP-B1-0 685 494. It was also surprisingly discovered that catalyst systems not commercially supportable in a gas phase process in particular were found to be useful when immobilized using the process of the invention.
VI. Polymerization Process
The catalyst systems prepared and the method of catalyst system addition described above are suitable for use in any prepolyinerization and/or polymerization process over a wide range of temperatures and pressures. The temperatures may be in the range of from -60 "C to about 280°C, preferably from 50°C to about 200°C, and the pressures employed may be in the range from 1 atmosphere to about 500 atmospheres or higher.
Polymerization processes include solution, gas phase, slurry phase and a high pressure process or a combination thereof. Particularly preferred is a gas phase or slurry phase polymerization of one or more olefins at least one of which is ethylene or propylene and more preferably ethylene.
In one embodiment, the process of this invention is directed toward a solution, high pressure, slurry or gas phase polymerization process of one or more olefin monomers having from 2 to 30 carbon atoms, preferably 2 to 12 carbon atoms, and more preferably 2 to 8 carbon atoms. The invention is particularly well suited to the polymerization of two or more olefin monomers of ethylene, propylene, butene-1, pentene-1, 4-melhyl-pentene-l, hexene-1, octene-1 and decene-1.
Other monomers useful in the process of the invention include ethylenically unsaturated monomers, diolefins having 4 to 18 carbon atoms, conjugated or nonconjugated dienes, polyenes, vinyl monomers and cyclic olefins. Non-limiting

monomers useful in the invention may include norbornene, norboniadiene, isobutylene,
isoprene, vinylbenzocyclobutane, styrenes, alkyl substituted styrene, ethylidene
norbornene, dicyclopentadiene and cyclopentene.
In the most preferred embodiment of the process of the invention, a copolymer of
ethylene is produced, where with ethylene, a comonomer having at least one alpha-olefm
having from 3 to 15 carbon atoms, preferably from 4 to 12 carbon atoms, and most
preferably from 4 to 8 carbon atoms, is polymerized in a gas phase process.
In another embodiment of the process of the invention, elhylene or propylene is
polymerized with at least two different comonomers, optionally one of which may be a
diene, to form a terpolymer.
In an embodiment, the mole ratio of comonomer to ethylene, CX/C2, where Cx is the
amount of comonomer and C2 is the amount of ethylene is between about 0.001 to 0.200
and more preferably between about 0.002 to 0.008.
In one embodiment, the invention is directed to a polymerization process, particularly a gas phase or shiny phase process, for polymerizing propylene alone or with one or more other monomers including ethylene, and/or other olefins having from 4 to 12 carbon atoms. Polypropylene polymers may be produced using the particularly bridged bulky ligand metallocene catalysts as described in U.S. Patent Nos. 5,296,434 and 5,278,264, both of which are herein incorporated by reference.
Typically in a gas phase polymerization process a continuous cycle is employed where in one part of the cycle of a reactor system, a cycling gas stream, otherwise known as a recycle stream or fluidizing medium, is heated in the reactor by the heat of polymerization. This heat is removed from the recycle composition in another part of the cycle by a cooling system external to the reactor. Generally, in a gas fluidized bed process for producing polymers, a gaseous stream containing one or more monomers is continuously cycled through a fluidized bed in the presence of a catalyst under reactive conditions. The gaseous stream is withdrawn from the fluidized bed and recycled back into the reactor. Simultaneously, polymer product is withdrawn from the reactor and fresh monomer is added to replace the polymerized monomer. (See for example U.S. Patent Nos. 4,543,399, 4,588,790, 5,028,670, 5,317,036, 5,352,749, 5,405,922, 5,436,304,

5,453,471, 5,462,999, 5,616,661 and 5,668,228, all of which are fully incorporated herein hy reference.)
The reactor pressure in a gas phase process may vary from about 100 psig (690 kPa) to about 600 psig (4138 kPa), preferably in the range of from about 200 psig (1379 kPa) to about 400 psig (2759 kPa), more preferably in the range of from about 250 psig (1724 kPa) to about 350 psig (2414 kPa).
The reactor temperature in a gas phase process may vary from about 30°C to about 120°C, preferably from about 60°C to about 115°C, more preferably in the range of from about 70°C to 110°C, and most preferably in the range of from about 70°C to about 95°C.
Other gas phase processes contemplated by the process of the invention include series or multistage polymerization processes. Also gas phase processes contemplated by the invention include those described in U.S. Patent Nos. 5,627,242, 5,665,818 and 5,677,375, and European publications EP-A- 0 794 200 EP-B1-Q 649 992, EP-A- 0 802 202 and EP-B- 634 421 all of which are herein fully incorporated by reference.
In a preferred embodiment, the reactor utilized in the present invention is capable of and the process of the invention is producing greater than 500 Ibs of polymer per hour (227 Kg/hr) to about 200,000 Ibs/hr (90,900 Kg/hr) or higher of polymer, preferably greater than 1000 Ibs/hr (455 Kg/hr), more preferably greater than 10,000 Ibs/hr (4540 ' Kg/hr), even more preferably greater than 25,000 Ibs/hr (11,300 Kg/hr), still more preferably greater than 35,000 Ibs/hr (15,900 Kg/hr), still even more preferably greater than 50,000 Ibs/hr- (22,700 Kg/hr) and most preferably greater than 65,000 Ibs/hr (29,000 Kg/hr) to greater than 100,000 Ibs/hr (45,500 Kg/hr).
A slurry polymerization process generally uses pressures in the range of from about 1 to about 50 atmospheres and even greater and temperatures in the range of 0°C to about 120°C. In a slimy polymerization, a suspension of solid, particulate polymer is formed in a liquid polymerization diluent medium to which ethylene and comonomers and often hydrogen along with catalyst are added. The suspension including diluent is intermittently or continuously removed from the reactor where the volatile components are separated from the polymer and recycled, optionally after a distillation, to the reactor. The liquid diluent employed in the polymerization medium is typically an alkane having from

3 to 7 carbon atoms, preferably a branched alkane. The medium employed should be liquid under the conditions of polymerization and relatively inert. When a propane medium is used the process must be operated above the reaction diluent critical temperature and pressure. Preferably, a hexane or an isobutane medium is employed.
A preferred polymerization technique of the invention is referred to as a particle form polymerization, or a slimy process where the temperature is kept below the temperature at which the polymer goes into solution. Such technique is well known in the art, and described in for instance U.S. Patent No. 3,248,179 which is fully incorporated herein by reference. Other slurry processes include those employing a loop reactor and those utilizing a plurality of stirred reactors in series, parallel, or combinations thereof. Non-limiting examples of slurry processes include continuous loop or stirred tank processes. Also, other examples of slurry processes are described in U.S. Patent No. 4,613,484 and 5,986,021, which are herein fully incorporated by reference.
In an embodiment the reactor used in the slurry process of the invention is capable of and the process of the invention is producing greater than 2000 Ibs of polymer per hour (907 Kg/hr), more preferably greater than 5000 Ibs/hr (2268 Kg/lrr), and most preferably greater than 10,000 Ibs/hr (4540 Kg/hr). In another embodiment the slurry reactor used in the process of the invention is producing greater than 15,000 Ibs of polymer per hour (6804 Kg/hr), preferably greater than 25,000 Ibs/hr (11,340 Kg/hr) to about 100,000 Ibs/hr (45,500 Kg/hr).
Examples of solution processes are described in U.S. Patent Nos. 4,271,060, 5,001,205, 5,236,998, 5,589,555 and 5,977,251 and PCT WO 99/32525 and PCT WO 99/40130, which are full}' incorporated herein by reference.
A preferred process of the invention is where the process, preferably a slurry or gas phase process is operated in the presence of a bulky ligand metallocene catalyst system of the invention and in the absence of or essentially free of any scavengers, such as triethylaluminum, trimethylaluminum, tri-isobutylaluminum and tri-n-hexylaluminum and diethyl aluminum chloride, dibutyl zinc and the like. This preferred process is described in PCT publication WO 96/08520 and U.S. Patent No. 5,712,352 and 5,763,543, which are herein fully incorporated by reference.

In one embodiment of the invention, olefm(s), preferably €2 to C3Q olefin(s) or alpha-olefin(s), preferably ethylene or propylene or combinations thereof are prepolymerized in the presence of the metallocene catalyst systems of the invention described above prior to the main polymerization. The prepolymerization can be carried out batchwise or continuously in gas, solution or slurry phase including at elevated pressures. The prepolymerization can take place with any olefin monomer or combination and/or in the presence of any molecular weight controlling agent such as hydrogen. For examples of prepolymerization procedures, see U.S. Patent Nos. 4,748,221, 4,789,359, 4,923,833, 4,921,825, 5,283,278 and 5,705,578 and European publication EP-B-0279 863 and PCT Publication WO 97/44371 all of which are herein fully incorporated by reference.
In one embodiment, toluene is not used in the preparation or polymerization process of this invention.
VjJL. Polymer Products
The polymers produced by the process of the invention can be used in a wide variety of products and end-use applications. The polymers produced by the process of the invention include linear low density polyethylene, elastomers, plaslomers, high density polyethylenes, medium density polyethylenes, low density polyethylenes, multimodal or bimodal high molecular weight polyethylenes, polypropylene and polypropylene copolymers.
The polymers, typically ethylene based polymers, have a density in the range of from 0.86g/cc to 0.97 g/cc, depending on the desired use. For some applications a density in the range of from 0.88 g/cc to 0.920 g/cc is preferred while in other applications, such as pipe, film and blow molding, a density in the range of from 0.930 g/cc to 0.965 g/cc is preferred. For low density polymers, such as for film applications, a density of 0.910 g/cc to 0.940 g/cc is preferred. Density is measured in accordance with standard ASTM methods.
The polymers produced by the process of the invention may have a molecular weight distribution, a ratio of weight average molecular weight to number average molecular weight (MyMJ, of greater than 1.5 to about 70. In some embodiments the

polymer produced has a narrow M^M,, of about 1.5 to 15, while in other embodiments the polymer produced has an MJMn of about 30 to 50. Also, the polymers of the invention may have a nairow or broad composition distribution as measured by Composition Distribution Breadth Index (CDBI). Further details of determining the CDBI of a copolyraer are known to those skilled in the art. See, for example, PCT Patent Application WO 93/03093, published February 18, 1993, which is fully incorporated herein by reference. In some embodiments the polymer produced may have a CDBI of 80% or more or may have a CDBI of 50% or less.
The polymers of the invention in one embodiment have CDBI's generally in the range of greater than 50% to 100%, preferably 99%, preferably in the range of 55% to 85%, and more preferably 60% to 80%, even more preferably greater than 60%, still even more preferably greater than 65%.
In another embodiment, polymers produced using this invention have a CDBI less than 50%, more preferably less than 40%, and most preferably less than 30%.
The polymers of the present invention in one embodiment have a melt index (MI) or (I2) as measured by ASTM-D-1238-E in the range from 0.01 dg/min to 1000 dg/min, more preferably from about 0.01 dg/min to about 100 dg/min, even more preferably from about 0.01 dg/min to about 50 dg/min, and most preferably from about 0.1 dg/min to about 10 dg/min.
The polymers of the invention in an embodiment have a melt index ratio (I2i/I2) (I2i is measured by ASTM-D-1238-F) of from 10 to less than 25, more preferably from about 15 to less than 25.
The polymers of the invention in a preferred embodiment have a melt index ratio ('21^2) ('21 is measured by ASTM-D-1238-F) of from preferably greater than 25, more preferably greater than 30, even more preferably greater that 40, still even more preferably greater than 50 and most preferably greater than 65. In an embodiment, the polymer of the invention may have a narrow molecular weight distribution and a broad composition distribution.or vice-versa, and may be those polymers described in U.S. Patent No. 5,798,427 incorporated herein by reference.

In one embodiment the polymers produced by this invention have a mullimodal molecular weight distribution (Mw/Mn) or, a typically, bimodal molecular weight distribution. In a preferred embodiment, the polymer produced has a density of 0.93 to 0.96 g/cc, an MI (I2) of 0.03 - O.lOg/lOmin, an FI (12I) of 4-12 g/ lOmin, an MFR (I21/I2) of 80-180, an overall Mw of 200,000 to 400,000, an overall Mn of 5,000-10,000 and an Mw/Mn of 20-50. Preferably the low molecular weight fraction (-500 —50,000) has a density of 0.935-0.975 g/cc and the high molecular weight fraction (-50,000 - ~ 8,000,000) has a density of 0.910 - 0.950 g/cc. These polymers are particularly useful for film and pipe, especially, for PE-100 pipe applications. More preferably, this embodiment of the polymer has the following molecular weight distribution (MWD) characteristics. The MWDs, as obtained from size exclusion chromatography (SEC), can be deconvolved using the bimodal fitting program. The preferred split of the polymer, the ratio of Wt% of HMW fraction and the Wt% of LMW fraction, is 20-80 to 80-20, more preferably 30-70 to 70-30, and even more preferably 40-60 to 60-40. Higher Wt% of HMW than LMW Wt% is preferred. The SEC curve can be further analyzed to give percent of Wt% > 1MM, which is the weight percent of the total MWD that has a molecular weight greater than 1 million, and Wt% > 100K, which is the weight perecent of the total MWD that is greater than 100,000 in molecular weight. The weight percent ratio is simply Wt% > 1 MM divided by Wt% > 1OOK. 100,000 was used as an approximate means of dividing the total MWD into a HMW (high molecular weight) and LMW (low molecular weight) region. This ratio gives a simple but sensitive indication of the relative amount of the very high molecular weight species in the HMW region of the MWD. The prefered embodiment of the polymer has the preferred range of weight percent ration (WPR), higher than 10 but less than 30, preferably higher than 15 but less than 25. The stability of blown bubble during film extrusion is found to depend on this WPR as shown in the table below. A preferred catalyst system to produce these polymers according to this invention comprises [(2,4,6-Me3C6H2)NCH2CH2]2NH}Hfflz2 or [(2,4,6-Me3C6H2)NCH2CH2J2NH}ZrBz2 combined with bis(indenyl)zirconium dichloride, (pentamethylcyclopentadienyl)(n-propylcyclopentadienyl)zirconium dichloride or

(tetramethylcyclopentadienyl)(n-propylcyclopentadienyl)zirconium dichloride, and supported methylalumoxane.
(Table Remove)
A typical SEC curve of the embodiment of the polymer is shown in the Figure 5. Two distinctive peaks of HMW and LMW fractions can be seen with the deconvoluted curves. (Figure Remove)
This mullimodal or bimodal polymer is found to exhibit excellent bubble stability and good film extrusion characteristics. The polymer demonstrated excellent draw-down characteristics and as thin as 0.35 mil film was obtained. The film appearance rate was excellent with no speck of gels. The film dart impact strength was excellent suitable which is suitable for grocery sacks applications.
In another embodiment the polymer produced by this invention has a bimodal molecular weight distribution (Mw/Mn). In a preferred embodiment, the polymer produced has a density of 0.93 to 0.97 g/cc, an MI (I2) of 0.02 - 0.5 g/lOrain, an FI (I21) of 10-40 g/ lOmin, an MFR (I2I/I2) of 50-300, an Mw of 100,000 to 500,000, an Mn of 8,000-20,000 and an Mw/Mn of 10-40. These polymers are particularly useful for blow molding applications. These bimodal polymers exhibited extraordinary Bent Strip ESCR (environmental stress crack resistance) performance, which far exceeds the performance of unimodal HDPE. Also, the blow molded bottles trimmed easier and had opaque finish, which is preferred over translucent finish of unimodal HDPE.
In yet another embodiment, propylene based polymers are produced in the process of the invention. These polymers include atactic polypropylene, isotactic polypropylene, hemi-isotactic and syndiotactic polypropylene or mixtures thereof produced by using two or more different catalysts in the practice of this invention. Other propylene polymers include propylene block or impact copolymers. Propylene polymers of these types are well known in the art, see for example U.S. Patent Nos. 4,794,096, 3,248,455, 4,376,851, 5,036,034 and 5,459,117, all of which are herein incorporated by reference.
The polymers of (he invention may be blended and/or coextruded with any other polymer. Non-limiting examples of other polymers include linear low density polyethylenes produced via conventional Ziegler-Natta and/or bulky ligand metallocene catalysis, elastomers, plastomers, high pressure low density polyethylene, high density polyethylenes, polypropylenes and the like.
Polymers produced by the process of the invention and blends thereof are useful in such forming operations as film, sheet, and fiber extrusion and co-extrusion as well as blow molding, injection molding and rotary molding. Films include blown or cast films formed by coexlrusion or by lamination useful as shrink film, cling film, stretch film, sealing .films, oriented films, snack packaging, heavy duty bags, grocery sacks, baked and frozen food packaging, medical packaging, industrial liners, membranes, etc. in food-contact and non-food contact applications. Fibers include melt spinning, solution spinning and melt blown fiber operations for use in woven or non-woven form to make filters, diaper fabrics, medical garments, geotextiles, etc. Extruded articles include medical tubing, wire and cable coatings, pipe, geomembranes, and pond liners. Molded articles include single and multi-layered constructions in the form of bottles, tanks, large hollow articles, rigid food containers and toys, etc.
In another embodiment, the polymer of the invention is made into a pipe by methods known in the art. For pipe applications, the polymers of the invention have a I21 of from about 2 to about 10 dg/min and preferably from about 2 to about 8 dg/min. In another embodiment, the pipe of the invention satisfies ISO qualifications. In another embodiment, the present invention is used to make polyethylene pipe having a predicted
S-4 Tc for 110mm pipe of less than -5°C, preferably of less than -15°C and more preferably less than -40°C (ISO DIS 13477/ASTM F1589).
In another embodiment, the polymer has an extrusion rate of greater than about 17 Ibs/hour/inch of die circumference and preferably greater than about 20 Ibs/hour/inch of die circumference and more preferably greater than about 22 Ibs/hour/inch of die circumference.
The polyolefms of the invention can be made into films, molded articles (including pipes), sheets, wire and cable coating and the like. The films may be formed by any of the conventional techniques known in the art including extrusion, co-extrusion, lamination, blowing and casting. The film may be obtained by the flat film or tubular process which may be followed by orientation in a uniaxial direction or in two mutually perpendicular directions in the plane of the film to the same or different extents. Orientation may be to (he same extent in both directions or may be to different extents. Particularly preferred methods to form the polymers into films include extrusion or coextrusion on a blown or cast film line.
In another embodiment, the polymer of the invention is made into a film by methods known in the art. For film application, the polymers of the invention have a I21 of from about 2 to about 50 dg/min, preferably from about 2 to about 30 dg/min, even more preferably from about 2 to about 20 dg/min, still more preferably about 5 to about 15 dg/min and yet more preferably from about 5 to about 10 dg/min.
The objects produced (such as films, pipes, etc) may further contain additives such as slip, anliblock, antioxidants, pigments, fillers, antifog, UV stabilizers, antistats, polymer processing aids, neutralizers, lubricants, surfactants, pigments, dyes and nucleating agents. Preferred additives include silicon dioxide, synthetic silica, titanium dioxide, polydimethylsiloxane, calcium carbonate, metal stearates, calcium stearate, zinc stearate, talc, BaS04, diatomaceous earth, wax, carbon black, flame retarding additives, low molecular weight resins, hydrocarbon resins, glass beads and the like. The additives may be present in (he typically effective amounts well known in the art, such as 0.001 weight % to 10 weight %.
In another embodiment, the polymer of the invention is made into a molded article by methods known in the art, for example, by blow molding and injection-stretch molding. For molded applications, the polymers of the invention have a I2I of from about 20 dg/min to about 50 dg/min and preferably from about 35 dg/min to about 45 •dg/min.
Further, while not wishing to be bound by any theory, it is believed that the polymers produced by this invention have the unique advantage of the two polymer products being so intimately blended that there is an even distribution of the two polymers across the polymer particles as they exit the reactor. The unprocessed, untreated granular polymer is referred to as neat polymer. The neat polymer is then separated into fractions by standard sieve sizes according to ASTM D 1921 particle size (sieve analysis) of Plastic Materials, Method A or PEG Method 507. (Table Remove)
The individual fractions (Fraction 2, 3, 4, 5) are then tested for physical properties. Melt index is measured according to ASTM 1238, condition E, 190°C.
A unique attribute of the polymer produced herein is that the melt indices of the different fractions do not vary significantly. In a preferred embodiment the melt indices of Fractions 3, 4 and 5 do not vary by more than 40% relative, preferably by not more than 30% relative, preferably by not more than 10% relative, preferably by not more than 8% relative, preferably by not more that 6% relative, preferably by not more than 4% relative. Relative means relative to the mean of the values for Fractions 3. 4 and 5.
In another embodiment, fractions 2; 3, 4 and 5 comprise more than 90% of the total weight of the resin sample, preferably fractions 2, 3 and 4 comprise more than 90% of the total weight of the resin sample.
Another desirable attribute of the polymer produced herein is that the Mw/Mn ef the different fractions do not vary significantly. In a preferred embodiment the Mw/Mn of Fractions 1, 4, 5 and 6 do not vaiy by more than 20% relative, preferably by not more than 10% relative, preferably by not more than 8% relative, preferably by not more than 6% relative, preferably by not more that 4% relative, preferably by not more than 2% relative. In a preferred embodiment the Mw/Mn of Fractions 1, 4 arid 6 do not vary by more than 20% relative, preferably by not more than 10% relative, preferably by not more than 8% relative, preferably by not more than 6% relative, preferably by not more that 4% relative, preferably by not more than 2% relative. Relative means relative to the mean of the values for Fractions 1, 4 and 6. In another preferred embodiment the Mw/Mn of Fractions 2, 3, 4 and 5 do not vary by more than 20% relative, preferably by not more than 10% relative, preferably by not more than 8% relative, preferably by not more than 6% relative, preferably by not more that 4% relative, preferably by not more than 2% relative. Relative means relative to the mean of the values for Fractions 2, 3, 4 and 5. In another preferred embodiment the Mw/Mn of Fractions 3, 4 and 5 do not vary by more than 20% relative, preferably by not more than 10% relative, preferably by not more than 8% relative, preferably by not more than 6% relative, preferably by not more that 4% relative, preferably by not more than 2% relative. Relative means relative to the mean of the values for Fractions 3, 4 and 5. Mn and Mw are measured by gel permeation chromatography on a waters 150 °C GPC instrument equipped with differential refraction index detectors. The GPC columns are calibrated by running a series of narrow polystyrene standards and the molecular weights are calculated using broad polyethylene standards National Bureau of Standards 1496 for the polymer in question.
In another preferred embodiment the polymer produced according to this invention comprises 10-90 weigh(% of low molecular weight polymer (low is 50,000 or less preferably 40,000 or less), preferably 20 to 80 weight%, more preferably 40-60 weight%, based upon the weight of the polymer.
In one embodiment the fractions have the following characteristics.

(Table Remove)
In another embodiment the polyolefin produced is found to have at least two species of molecular weights present at greater than 20 weight% based upon the weight of the polymer.
In another embodiment of this invention the polymer produced is bi- or multi-modal (on the SEC graph). By bi- or multi-modal is meant that the SEC graph of the polymer has two or more positive slopes, two or more negative slopes, and three or more inflection points (an inflection point is that point where the second derivative of the curve becomes negative) OR the graph has at least has one positive slope, one negative slope, one inflection point and a change in the positive and or negative slope greater than 20% of the slope before the change. In another embodiment the SEC graph has one positive slope, one negative slope, one inflection point and an Mw/Mn of 10 or more, preferably 15 or more, more preferably 20 or more. The SEC graph is generated by gel permeation chromatography on a waters 150 °C GPC instrument equipped with differential refraction index detectors. The columns are calibrated by running a series of narrow polystyrene standards and the molecular weights were calculated using Mark Houwink coefficients for the polymer in question.
The films produced using the polymers of this invention have extremely good appearance properties. The films have a low gel content and/or have good haze and gloss. In a preferred embodiment the 1 mil film (1.0 mil =0.25|.im) has a 45° gloss of 7 or more, preferably 8 or more as measured by ASTM D 2475. In a preferred embodiment the 1 mil

film (1.0 mil = 25f.imJ has a haze of 75 of less, preferably 70 or less as measured by ASTM D 1003, condition A.
In order to provide a better understanding of the present invention including representative advantages thereof, the following examples are offered.
EXAMPLES
Mn and Mw were measured by gel permeation chromatography on a waters 150°C GPC
instrument equipped with differential refraction index detectors. The GPC columns were
calibrated by running a series of molecular weight standards and the molecular weights
were calculated using Mark Houwink coefficients for the polymer in question.
Density was measured according to ASTM D 1505.
Melt Index (MI) and Flow Index (FI) I2 and I21 were measured according to ASTM D-
1238, Condition E, at 190°C.
Melt Index Ratio (MLR) is the ratio of I2I over I2 as determined by ASTM D-1238.
Weight % coinonomer was measured by proton NMR.
MWD = MJMn
Dart Impact was measured according to ASTM D 1709.
MD and TD Elmencloi f Tear were measured according to ASTM D 1922.
MD and TD 1% Secant modulus were measured according to ASTM D 882.
MD and TD tensile strength and ultimate tensile strength were measured according to
ASTM D 882.
MD and TD elongation and ultimate elongation were measured according to ASTM D
412.
MD and TD Modulus were measured according to ASTM 882-91
Haze was measured according to ASTM 1003-95, Condition A.
45° gloss was measured according to ASTM D 2457.
BUR is blow up ratio.
"PPH" is pounds per hour. "mPPH" is millipounds per hour, "ppmw" is parts per million
by weight.
ExanijjleJ.
Preparation of SMAO Supported Activator
For a IKg batch, 1158.43 grams of 30 wt % MAO in toluene (7.3 wt% Al) available from Albemarle Corporation, Baton Rouge, LA, and 2400 grams of extra toluene are charged into an 8 liter mix tank equipped with ribbon helical agitator. 984 grams of Davison 955-600 silica is added to MAO in toluene solution at ambient temperature. A 10°C exolhenn occurs
from reaction of the MAO with the hydroxyl groups. The slurry mixes for 30 minutes at ambient temperature. Drying then occurs by heating the mix tank jacket to about 70°C and reducing pressure to 0.00 mm/hg. As the slurry thickens the agitator rpm is reduced to minimum rotation, about 40 - 60 RPM. Then the rotation is slowly increased (to about 600 RPM) and the temperature is raised to 95 ° C as the slurry turns to a diy powder. A nitrogen sweep (about 0.5 cc/min per gram of silica charged) can be used during the end of the drying step to help remove toluene from the silica pores. The material is typically held at 95°C until toluene removal stops, and material temperature lines out near jacket temperature. The material temperature does not change for at least 30 minutes before the supported melhylalumoxane (SMAO) is considered diy. Residual toluene is reduced to less than 2 wt% on the solids.
Example!
Solution catalyst compound activated with slurry comprising supported activator in
fluidized gas-phase reactor with shorter contact time
Polymerization performance of in-line supported bis(n-propyl cyclopentadienyl) zirconium dichloride (P-MCN) was evaluated in a 8 inch (20.3 cm) fluidized bed pilot plant reactor. The catalyst feed configuration is shown schematically in Figure 2. P-MCN ( 1.7 umol/ml in hexane) was introduced in line at 0.65 g/hr. 0.5 weight % of TiBA in isopentane (200-250 cc/hr of isopentane carrier and 75-90 cc/hr of 0.5 wt% TiBA) was introduced in line. Thereafter a slurry comprising Kaydol mineral oil and 16 weight % of SMAO produced in Example 1 (4.5 rnmol/g solids) was introduced in line and allowed to mix with the solution of P-MCN and TiBA for 25-35 minutes. Following the mixer, the catalyst was injected using a standard 1/8 inch (0.32 cm) injection tube with 1.05 pph of N2 blowback.
The catalyst was evaluated at LLDPE conditions, 75 C, 350 psig (2.4 MPa) total pressure, 120 psi (0.8 MPa) ethylene, 0.017 hexene-1 comonomer to ethylene ratio. No hydrogen was fed to the reactor since this catalyst makes sufficient hydrogen to produce 2-5 dg/min melt index polymer under the conditions employed. The superficial gas velocity (SGV) was maintained at 1.54 ft/s (0.47m/s) and the steady state bed weight at 27 Ibs (12.3 kg). The reactor was operated continuously, i.e. for approximately 13 hours per day, generally holding bed weight constant to yield a bed level near the top of the straight section. Where possible, the reactor was left closed overnight with the bed being fluidized

in a nitrogen atmosphere. TiBA (triisobutyl aluminum) in isopentane was fed as a scavenger at approximately 75 ppm in the bed to give catalyst productivity that is commercially relevant.
The product had a 6.1 dg/min (12), 1 7.6 MFR and 0.93 g/cc density. The resin average particle size was 0.022 inches (0.056 cm) with 2.4 wt% fines ( Solution catalyst compoimd activated with slurry comprising supported activator in fluidized gas-phase reactor with longer contact time
Polymerization performance of in-line supported bis(n-propyl cyclopentadienyl) zirconium dichloride (P-MCN) was evaluated in a 8 inch (20.3 cm) fluidized bed pilot plant reactor. The catalyst feed configuration is shown schematically in Figure 3. P-MCN, fed at 0.56 g/hr with 65-100 cc/hr of 0.5 wt% TIBA in isopentane upstream, was contacted with 16 wt% SMAO (as produced in Example 1) in Kaydol mineral oil upstream of the 150 ml mixer. The solution and the slurry were allowed to mix for 90 to 1 30 minutes. 200-250 cc/hr of isopentane carrier was used to sweep the catalyst exiting the mixer to the reactor. Following the mixer, catalyst was injected using a standard 1/8 inch (0.32 cm) injection tube with 1.1 pph Nj blowback.
Catalyst was evaluated at LLDPE conditions, 75°C, 350 psig (2.4 MPa) total pressure, 120 psi (0.8 MPa) ethylene, 0.017 hexene-1 comonomer to ethylene ratio. No hydrogen was fed to the reactor since this catalyst makes sufficient hydrogen to produce 2-5 dg/min melt index polymer under the conditions employed. The superficial gas velocity (SGV) was maintained at 1 .38 ft/s (0.42 m/s) and the steady state bed weight at 30.5 Ibs (13.6 kg). The reactor was operated continuously for -13 hours per day, generally holding bed weight constant to yield a bed level near the top of the straight section. Where possible, the reactor was left closed overnight with the bed being fluidized in a nitrogen atmosphere. TIBA(triisobutyl alumium) in isopentane was fed as a scavenger at ~75 ppm in the bed to give catalyst productivity that is commercially relevant.

The product had a 5.3 dg/niin (12), 18.9 MFR and 0.928 g/cc density. The resin average particle size was 0.021 inches (0.053 cm) with 2.8 wt% fines ( The data for Examples 2 and 3 are summarized in Table 1.
TABLE 1. 8 INCH (20.3 CM) FLUIDIZED BED DATA SUMMARY
(Table Remove)


15 wt % SMAO in Kaydol mineral oil upstream of the 100 ml agitated mixer. Following the mixer, catalyst was injected using a standard 1/8 inch (0.32 cm) injection tube with 1.5 pph isopentane carrier and 4.0 pph N2 blowback.
The catalyst system was evaluated at LLDPE conditions, 85° C, 350 psig (2.4 MPa) total pressure, 200 psi (1.4 MPa) ethylene, 0.016 hexene-1 comonomer to ethylene ratio (C6/C2). A concentration of 195 ppm hydrogen was maintained in the reactor. The superficial gas velocity (SGV) was maintained at 2.0 ft/s (0.6 m/s) and the bed weight at 110 Ibs (50 kg). The reactor production rate was 38 pph.
The product had a 8.4 dg/min (I2), 16.5 MFR and 0.9273 g/cc density. The resin average particle size was 0.0357 inches (0.091 cm) with 0.44 wt% fines ( ExampJeJ[.
Solution P-MCN catalyst compound activated with slurry comprising SMAO and
second catalyst compound in fluidized gas-phase reactor
Polymerization performance of a solution comprising bis(n-
propylcyclopentadienyl) zirconium dichloride catalyst compound and a slurry comprising SMAO and [(2,4,6-Me3Cf,H2)NCH2CIi2]2NHZrBz2 was evaluated in a 14 inch (35.6 cm) fluidized bed pilot plant reactor. The catalyst feed configuration used for in-line activation of the solution used the bis(n-propylcyclopentadienyl) zirconium dichloride at 0.5 weight %, and a slurry comprising 17.3 weight % SMAO (from Example 1) in Kaydol. (The SMAO contained 4.5mmol Al per gram of solid). The [(2,4,6-
Me3CJi2)NCH2CII2]2NHZrBz2 was added to the slurry off-line to make a 150:1 molar ratio of Al:Zr. The remaining portion of the slurry was Kaydol mineral oil. Catalyst, fed at 4 cc/lir, was contacted with 75 cc/hr of the SMAO/[(2,4,6-
Me1C6H2)NCH2CH2]2NHZrBz2 mixture iti Kaydol mineral oil upstream of the series of two ten inch (25.4 cm) long 1/4 inch (0.64 cm) diameter Kinecs static mixers (by Chemineer). The contact lime between the solution and the slurry was approximately 5 minutes. Following the mixer, catalyst was injected using a standard 1/8 inch (0.32 cm) injection tube with 3 pph isopenlane carrier and 5 pph N2 carrier.
The catalyst system was evaluated at the following conditions, 105° C, 350 psig (2.4 MPa) total pressure, 220 psi (1.5 MPa) ethylene, and 0.0035 hexene-1 to ethylene molar ratio. A concentration of 1800 ppm hydrogen was maintained in the reactor. The superficial gas velocity (SGV) was maintained at 2.0 ft/s (0.6 m/s) and the bed weight at 75 Ibs (34 kg). The reactor production rate was 21 pph.
The product had a 0.051 dg/min (I2), 7.74 dg/rain flow index, 151 MFR and 0.9502 g/cc density. The resin average particle size was 0.016 inches (0.04 cm) with 1.25 wt% fines ( The data of examples 4, 5 and 6 are summarized in Table 2.
TABLE 2. 14 INCH (35.6 CM) FLUIDIZED BED DATA SUMMARY
(Table Remove)

Several product samples made from polymerization with a slurry comprising SMAO and [(2,4,6-Me3C(,H2)NCH2CH2]2NHZrBz2, and solution bis(n-propyl cyclopentadienyl) zirconium dichloride (P-MCN) catalyst were evaluated for film applications. This bimodal HMW HDPE granular polymer was compounded on a 2.5 inch, 24:1L/D single screw, equipped with double mixing head, at 210°C, after tumble mixed with a stabilizer package comprising 1,000 ppm of Irganox 1076, 1,500 ppm of Irgafos 168, and 1,500 ppm of Calcium Slearate. Two pelleted samples showed 8.4 and 9.9 FI, respectively, and 155 and 140 MFR. The density was 0.9524 and 0.9490, respectively. The pelleted polymer was film extruded on an Alpine film line equipped with a 50min, 18:1 L/D single screw, a lOOmni die with 1mm die gap. The die temperature was set at 210"C. The output was maintained at about lOOlb/hr, the blow-up ratio of the bubble was set at 4.0, and the frost line height was 36 inches. As shown in Table 3 below, the bimodal polymer exhibited excellent bubble stability and film extrusion characteristics. The film dart impact strength was over 200g and over 300g, respectively for 1.0 mil and 0.5 mil gauge. The film samples also exhibited excellent tensile strength and modulus. (Table Remove)
* ESCORENE HD7755 is a polyethylene polymer available from ExxonMobil Chemical Company in Mt. Belvue, Texas, having an I21 of 7.5, and MIR of 125, an Mw of 180,000, a density of 0.95 g/cc, produced using a dual reactor system.
Example 8.
K2.4,6-Me?C«H,)NCH;CHilzNHZrBz, Spraydried catalyst with
pentametliyIcyclopentadieuyl(ii-propylcyclopeutadienyl)ZrCI? trimmed on-line
An ethylene hexene copolymer was produced in a 14-inch pilot plant scale gas phase fluidized bed reactor operating at 100°C and 350 psig total reactor pressure having a water cooled heat exchanger. Ethylene was fed to the reactor at a rate :of about 50 pounds per hour, hexene was fed to the reactor at a rate of about 0.5 pounds per hour and hydrogen was fed to the reactor at a rate of 20 mPPH. Ethylene was fed to maintain 200 psi elhylene partial pressure in the reactor. Hexene was continuously fed to maintain a 0.01 C6/C2 molar ratio. Hydrogen feed rate was controlled to maintain a 0.0035 H2/C2 molar gas ratio in the cycle gas. The production rale was about 28PPH. The reactor was equipped with a plenum having about 12001b/hr of recycle gas flow. (The plenum is a device used to create a particle lean zone in a fluidized bed gas-phase reactor. See US Patent 5,693,727.) A tapered catalyst injection nozzle having a 0.055" hole size was positioned in the plenum gas flow.
[(2,4,6-Me3C6H2)NCH2CH2]2NIIZrBz2 (HN3-Zr) spraydried, slurried catalyst (20 wl% solids) was prepared. The targeted composition for the catalyst were to be: 34.2% Cabosil, 12.8% Gasil, 50.7% MAO, 2.3% HN3-Zr, 8.7 mmole Al/g, 0.037 mmole Zr/g, and 234 Al/Zr. The resulting powder was added into mineral oil to make a 25 wt% slurry.

The catalyst was further diluted with hexane to make a 20 wt% slurry and mixed for 24 hours before feeding to the reactor.
The slurried catalyst was continuously fed through a 1/8" line at a rate of 35 cc/hr. An additional flow rate of 1 Ib/hr isopentane helped carry the catalyst to a mixing "T". 3 cc/hr of a 0.5 wt% pentamethylcyclopentadienyl(n-ropylcyclopentadienyl) ZrCl2 ((Cp*)(n-propCp)Zrd2) catalyst solution in purified Kaydol mineral oil was added in the mixing "T" and the catalysts were contacted in 2 1A" Chemineer Kinecs static mixers in series. The contact time between the 2 catalysts was less than 5 minutes. The catalysts were finally injected through the tapered injection nozzle along with an additional 1 Ib/hr isopentane and 4 Ib/hr purified nitrogen. The molar ratio of HN3/(Cp*)(n-propCp)ZrCl2 catalyst was approximately 7.
The resulting polymer was analyzed after processing the granulars through a brabender extruder. The flow index measure 6.5 and the melt index measured 0.049, resulting in a 133 MFR. The density was 0.9528 g/cc.
Example 9.
HN3-Zr Spraydried catalyst with (Cp*)(n-propCp)ZrCI1 dipped off-liae
An ethylene hexene copolymer was produced in a 14-inch pilot plant scale gas phase fluidized bed reactor operating at 85°C and 350 psig total reactor pressure having a water cooled heat exchanger. Ethylene was fed to the reactor at a rate of about 36 pounds per hour, hexene was fed to the reactor at a rate of about 0.7 pounds per hour and hydrogen was fed to the reactor at a rate of 18 mPPH. Ethylene was fed to maintain 200 psi ethylene partial pressure in the reactor. Hexene was continuously fed to maintain a 0.015 C6/C2 molar ratio. Hydrogen feed rate was controlled to maintain a 0.0035 H2/C2 molar gas ratio in the cycle gas. The production rate was about 19 PPH. The reactor was equipped with a plenum having about 12001b/hr of recycle gas flow. (The plenum is a device used to create a particle lean zone in a fluidized bed gas-phase reactor. See US Patent 5,693,727.) A tapered catalyst injection nozzle having a 0.055" hole size was positioned in the plenum gas flow.
HN3-Zr spraydried,slurried catalyst with (Cp*)(n-propCp)ZrCl2 (17 wt% solids, 8 HN3/(Cp*)(n-propCp)ZrCl2 molar ratio) was produced offline. The targeted composition for the catalyst were to be: 34.2% Cabosil, 12.8% Gasil, 50.7% MAO, 2.3% HN3-Zr, 8.7

nimole Al/g, 0.037 mniole Zr/g, and 234 Al/Zr. The resulting powder was added into mineral oil to make a 20 wt% slurry. (Cp*)(n-propCp)ZrCl2 was added to the mixture to make a 8:1 PIN3-(Cp*)(n-propCp)ZrCl2 molar ratio of catalyst. The catalyst was further diluted with hex an e to result in a 17 wt% solid slurry. It was continuously fed tlirough a 1/8" line at a rate of 30 cc/hr. An additional flow rate of 1 Ib/hr isopentane helped carry the catalyst to the reactor. The catalyst was finally injected through the tapered injection nozzle along with an additional 1 Ib/hr isopentane and 2.5 Ib/hr purified nitrogen.
The resulting polymer was analyzed after processing the granulars through a brabender extruder. The flow index measured 9.7 and the melt index measured 0.041, resulting in a 237 MFR. The density was 0.9501 g/cc.
Catalyst preparatioa (HN3-Zr/MMAO/Cabosil slurry) for Examples 11-14
A catalyst slurry containing HN3-Zr, modified methyl aluminoxane (MMAO) and
fumed silica (TS-610 Cabosil) in hexane and heptane was prepared. 468 grams of MMAO from Albemarle as a 7 wt% Al in heptane was diluted with 1 liter of purified hexane. 30.1 grains of cabosil were added to for a 3 wt% solids concentration. The mixture was stirred for 30 minutes. 3.6 grams of HN3-Zr powder was added, stirred and charged to a clean 2-liler stainless steel vessel. The molar Al/Zr ratio was 150 and the HN3-Zr was 0.35 wt%. (Cp*)(n-propCp)ZrCl2 was dissolved in purified hexane at a concentration of 0. 1 5 wt%.
Example 11.
An ethylene hexene copolymer was produced in a 14-inch pilot plant scale gas phase fluidized bed reactor operating at 85°C and 350 psig total reactor pressure having a water cooled heal exchanger. Ethylene was fed to the reactor at a rate of about 60 pounds per hour, hexene was fed to the reactor at a rate of about .95 pounds per hour and hydrogen was fed to the reactor at a rate of 20 mPPII. Ethylene was fed to maintain 220 psi ethylene partial pressure in the reactor. Hexene was continuously fed to maintain a 0.005 C6/C2 molar ratio. Hydrogen feed rate was controlled to maintain a 0.003 H2/C2 in the cycle gas. The production rate was about 30 PPH.
The reactor was equipped with a plenum, feeding 1600 Ib/hr of recycle gas flow. (The plenum is a device used to create a particle lean zone in a fluidized bed gas-phase reactor. See US Patent 5,693,727.) The catalyst system was injected into a tapered catalyst

injection nozzle having a 0.055" hole size made from 1/8" stainless steel tubing was positioned in the center of an addition shroud tube measuring Vi". The shroud tube contained nitrogen that was fed at 10 Ib/hr.
The catalyst slurry (HN3-Zr/MMAO/Cabosil, prepared in Example 10) was placed in a continuously stirred agitated vessel was earned through 1/8" tubing using 120 cc/hr of isopenlane. The catalyst slurry flow rate was 16 cc/hr. It was contacted with 0.15 wt% solution of (Cp*)(n-propCp)ZrCl2 in hexane (24 cc/hr) and additional 0.2 Ib/hr hexene and mixed in-line with two '/T kinecs static mixers in series. Isopentane was optionally fed between the two kinecs mixers at a rate of 0-1 Ib/hr. The molar ratio of HN3-Zr/(Cp*)(n-propCp)ZrCl2 catalyst was 1.4. The contact time of the (Cp*)(n-propCp)ZrCl2 solution and the HN3-Zr/MMAO/Cabosil slurry before entering the reactor was about 5-10 minutes, depending on isopentane flow rate. In addition to the catalysts and isopentane, nitrogen was added to the injection tube to atomize the slurry at a rate of 3 Ib/hr. All materials were combined and were passed through the 1/8" tubing and injection nozzle and into the fluidized bed. A diagram describing the entire feed delivery system is shown in Figure 6.
The polyethylene produced was 1.6 FI, 0.022 MI and 0.9487 density. The particle size was 0.0139 inch and contained 5 wt% fines. The resin contained 0.2% material that was larger than a 10 mesh screen. The catalyst activity was excellent, containing 18 ppm Al and 1.29 ppm Zr by X-ray. Exampjc_12.
An ethylene hexene copolymer was produced in a 14-inch pilot plant scale gas phase fluidized bed reactor operating at 90°C and 350 psig total reactdr pressure having a water cooled heat exchanger. Ethylene was fed to the reactor at a rate of about 50 pounds per hour, hexene was fed to the reactor at a rate of about 1 pounds per hour and hydrogen was fed to the reactor at a rate of 14 mPPH. Ethylene was fed to maintain 220 psi ethylene partial pressure in the reactor. Hexene was continuously fed to maintain a 0.007 C6/C2 molar ratio. Hydrogen feed rate was controlled to maintain a 0.0035 H2/C2 in the cycle gas. The production rate was about 25 PPH.

The reactor was equipped with a plenum, feeding 1050 Ib/hr of recycle gas flow. (The plenum is a device used to create a particle lean zone in a fluidized bed gas-phase reactor. See US Patent 5,693,727.) The catalyst system was injected into a tapered catalyst injection nozzle having a 0.055" hole size made from 1/8" stainless steel tubing was positioned in the center of an addition shroud tube measuring 1A". The shroud tube contained nitrogen that was fed at 10 Ib/hr.
The catalyst slurry (HN3/MMAO/Cabosil, prepared in Example 10) above) was placed in a continuously stirred agitated vessel was carried through 1/8" tubing using 300 cc/hr of isopentane. The catalyst shiny flow rate was 16 cc/hr. It was contacted with 0.15 wl% solution of X-catalyst in hexane (31 cc/hr) and additional 0.2 Ib/hr hexene and mixed in-line with two %" kinecs static mixers in series. Isopentane was fed between the two kinecs mixers at a rale of 3 Ib/hr. The molar ratio of HN3/X catalyst was 1.06. The contact time of the X-catalysl solution and the HN3/MMAO/Cabosil slurry before entering the reactor was about 1.5 minutes. Ln addition to the catalysts and isopentane, nitrogen was added to the injection tube to atomize the slurry at a rate of 5 Ib/hr. All materials were combined and were passed through the 1/8" tubing and injection nozzle and into the fluidized bed. A diagram describing the entire feed delivery system is shown in Figure 6.
The polyethylene produced was 2.2 FI, .028 MI and 0.9439 density. The particle size was 0.0662 inch and contained 0.2 fines. The resin contained 43.5% material which larger than the 10 mesh screen. The catalyst activity was excellent, containing 24 ppm Al and 1.07 ppm Zr by X-ray. Example 13.
An ethylene hexene copolymer was produced in a 14-inch pilot plant scale gas phase fluidized bed reactor operating at 90°C and 350 psig total reactor pressure having a water cooled heat exchanger. Ethylene was fed to the reactor at a rate of about 50 pounds per hour, hexene was fed to the reactor at a rate of about 1 pounds per hour and hydrogen was fed to the reactor at a rate of 14 mPPH: Ethylene was fed to maintain 220 psi ethylene partial pressure in the reactor. Hexene was continuously fed to maintain a 0.0068 C6/C2 molar ratio. Hydrogen feed rate was controlled to maintain a 0.0035 H2/C2 in the cycle gas. The production rale was about 35 PPH.

The reactor was equipped with a plenum having up to 1200 Ib/hr of recycle gas flow. (The plenum is a device used to create a particle lean zone in a .fluidized bed gas-phase reactor. See US Patent 5,693,727.) The catalyst system was injected into a tapered catalyst injection nozzle having a 0.055" hole size made from 1/8" stainless steel tubing was positioned in the center of an addition shroud tube measuring 'XT'. The shroud tube contained nitrogen that was fed at 10 Ib/hr.
The catalyst shiny (ITN3/MMAO/Cabosil, prepared in Example 10) was placed in a continuously stirred agitated vessel was earned through 1/8" tubing using 120 cc/hr of isopentane. The catalyst slurry flow rate was 12 cc/hr. It was contacted with 0.15 wt% solution of X-catalyst in hexane (22 cc/hr) and additional 0.2 Ib/hr hexene and mixed inline with two 1A" kinecs static mixers in series. Isopentane was fed between the two kinecs mixers at a rate of 0.5 Ib/hr. The molar ratio of HN3/X catalyst was 1.12. The contact time of the X-catalyst solution and the HN3/MMAO/Cabosil slurry before entering the reactor was about 6 minutes. In addition to the catalysts and isopentane, nitrogen was added to the injection tube to atomize the slurry at a rate of 3 Ib/hr. All materials were combined and were passed through (he 1/8" tubing and injection nozzle and into the fluidized bed. A diagram describing the entire feed delivery system is shown in Figure 6.
The polyethylene produced was 7.1 FI, 0.046 MI and 0.951 density. The particle size was 0.0125 inch and contained 9.4% fines. The resin contained no material which was larger than the 10 mesh screen. The catalyst activity was excellent.
Exara£leJL4_.
An ethylene hexene copolymer was produced in a 14-inch pilot plant scale gas phase fluidized bed reactor operating at 90°C and 350 psig total reactor pressure having a water cooled heat exchanger. Ethylene was fed to the reactor at a rate of about 45 pounds per hour, hexene was fed to the reactor at a rate of about 0.8 pounds per hour and hydrogen was fed to the reactor at a rate of 12 mPPH. Ethylene was fed to maintain 220 psi elhylene partial pressure in the reactor. Hexene was continuously fed to maintain a 0.0068 C6/C2 molar ratio. Hydrogen feed rate was controlled to maintain a 0.0035 H2/C2 in the cycle , gas. The production rate was about 23 PPH.

The reactor was equipped with a plenum feeding 640 Ib/hr of recycle gas flow. (The plenum is a device used to create a particle lean zone in a fluidized bed gas-phase reactor. See US Patent 5,693,727.) The catalyst system was injected into a tapered catalyst injection nozzle having a 0.055" hole size made from 1/8" stainless steel tubing was positioned in the center of an addition shroud tube measuring V". The shroud tube contained nitrogen that was fed at 10 Ib/hr.
The catalyst slurry (HN3/MMAO/Cabosil, prepared in Example 10) was placed in a continuously stirred agitated vessel was carried through 1/8" tubing using 120 cc/hr of isopentane. The catalyst slurry flow rate was 16 cc/hr. It was contacted with 0.15 wt% solution of X-catalyst in hexane (25 cc/hr) and additional 0.2 Ib/hr hexene and mixed inline with two '/T kinecs static mixers in series. Isopentane was fed between the two kinecs mixers at a rate of 0.5 Ib/hr. The molar ratio of ITN3/X catalyst was 1.32. The contact time of the X-catalyst solution and the HN3/MMAO/Cabosil slurry before entering the reactor was about 6 minutes. In addition to the catalysts and isopentane, nitrogen was added to the injection tube to atomize the slurry at a rate of 3 Ib/lir. All materials were combined and were passed through the 1/8" tubing and injection nozzle and into the fluidized bed. A diagram describing the entire feed delivery system is shown in Figure 6.
The polyethylene produced was 4.7 FI, 0.045 MI and 0.9493 density. The particle size was 0.0231 inch and contained 2 % fines. The resin contained 0.1 wt% material which was larger than the 10 mesh screen. The catalyst activity was excellent, with Al residuals at 19 ppm and Zr residuals at 1.31 ppm by X-ray fluoresce.
Table 4 below summarizes the data from Examples 11-14. Examples 12 and 13 demonstrate that the different flow rates of the isopentane and nitrogen effect the particle size generated. Examples 13 and 14 show that the plenum flow may be used to control particle size. In addition, Figure 7 is a graph illustrating the change in fines and particle size, with the change in plenum cycle gas flow rate.
(Table Remove)
While the present invention has been described and illustrated by reference to particular embodiments, those of ordinary skill in the art will appreciate that the invention lends itself to variations not necessarily illustrated herein. For this reason, then, reference should be made solely to the appended claims for purposes of determining the true scope of the present invention. It is also contemplated that the combination of the slurry and the solution immobilization technique of the invention can be used to essentially form, for example, a metallocene catalyst compound that is combined with an activator and fed to a polymerization reactor.
All documents described herein are incorporated by reference herein, including any priority documents and/or testing procedures. As is apparent form the foregoing general description and the specific embodiments, while forms of the invention have been illustrated and described, various modifications can be made without departing from the spirit and scope of the invention. Accordingly it is not intended that the invention be limited thereby.





WE CLAIM:
1. A process to polymerize olefin(s) comprising:
(a) continuously combining a catalyst component slurry of with a catalyst component solution to form a catalyst composition, wherein the catalyst component solution comprises a C5 to C30 alkane diluent and at least one catalyst compound;
(b) introducing the catalyst composition and one or more olefin(s) into an operating polymerization reactor; and
(c) isolating a polymer;
characterized in that
the catalyst component slurry comprises mineral oil or silicon oil, a support of the kind such as herein described, an activator of the kind such as herein described, and a Group 15 element containing catalyst compound of the kind such as described herein comprising at least one metal M which is selected from Group 4, 5, or 6 metal atoms of the kind such as described herein.
2. The process as claimed in Claim 1, wherein the activator of the catalyst component slurry is a supported activator comprising the support.
3. The process as claimed in Claim 1, wherein at least 50% of the catalyst compound is deposited on or in the support material; and wherein the catalyst component solution comprises a catalyst compound which is the same as at least one of the catalyst compounds in the catalyst component slurry.
4. The process as claimed in Claim 1, wherein the Group 15 element containing catalyst compound is spray dried onto the support.

5. The process as claimed in Claim 1, wherein the catalyst compound in the catalyst component solution is a metallocene catalyst compound.
6. The process as claimed in Claim 1, wherein the Group 15 element containing catalyst compound is represented by:
(Formula Removed)

wherein
M is a Group 4, 5, or 6 metal;
each X is independently an anionic leaving group;
y is 0 or 1;
n is the oxidation state of M;
m is the formal charge of the ligand represented by YZL or YZL';
L is a Group 15 or 16 element;
L' is a Group 15 or 16 element or Group 14 element containing group;
Y is a Group 15 element;
Z is a Group 15 element;
R1 and R2 are independently a C1 to C20 hydrocarbon group, a heteroatom containing group
having up to twenty carbon atoms, silicon, germanium, tin, lead, or phosphorus;
R1 and R2 may also be interconnected to each other;
R3 is absent, a hydrocarbon group, hydrogen, a halogen, or a heteroatom containing group;
R4 and R5 are independently an alkyl group, an aryl group, a substituted aryl group, a
cyclic alkyl group, a substituted cyclic alkyl group, a cyclic aralkyl group, a substituted
cyclic aralkyl group or a multiple ring system;
R4 and R5 may be interconnected to each other;

R6 and R7 are independently absent, hydrogen, an alkyl group, halogen, heteroatom, or a hydrocarbyl group; and
R* is absent, hydrogen, a Group 14 atom containing group, a halogen, or a heteroatom containing group.
7. The process as claimed in Claim 1, wherein the polymerization reactor is a gas phase reactor.
8. The process as claimed in Claim 1, wherein the polymerization reactor is a slurry phase reactor.

Documents:

00860-delnp-2003-abstract.pdf

00860-delnp-2003-claims.pdf

00860-delnp-2003-correspondence-others.pdf

00860-delnp-2003-description (complete).pdf

00860-delnp-2003-drawings.pdf

00860-delnp-2003-form-1.pdf

00860-delnp-2003-form-18.pdf

00860-delnp-2003-form-2.pdf

00860-delnp-2003-form-3.pdf

00860-delnp-2003-form-5.pdf

00860-delnp-2003-gpa.pdf

00860-delnp-2003-pct-105.pdf

00860-delnp-2003-pct-301.pdf

00860-delnp-2003-pct-304.pdf

00860-delnp-2003-pct-409.pdf

00860-delnp-2003-pct-416.pdf

00860-delnp-2003-pct-request form.pdf

860-DELNP-2003-Abstract (31-12-2007).pdf

860-DELNP-2003-Claims (31-12-2007).pdf

860-DELNP-2003-Claims-(05-09-2008).pdf

860-DELNP-2003-Claims-(08-09-2008).pdf

860-DELNP-2003-Correspondence-Others (31-12-2007).pdf

860-DELNP-2003-Correspondence-Others-(05-09-2008).pdf

860-DELNP-2003-Correspondence-Others-(08-09-2008).pdf

860-DELNP-2003-Correspondence-Others-(10-09-2008).pdf

860-DELNP-2003-Description (Complete) (31-12-2007).pdf

860-DELNP-2003-Drawings (31-12-2007).pdf

860-DELNP-2003-Form-1 (31-12-2007).pdf

860-DELNP-2003-Form-2 (31-12-2007).pdf

860-DELNP-2003-Form-2-(05-09-2008).pdf

860-DELNP-2003-Form-3 (31-12-2007).pdf

860-DELNP-2003-GPA (31-12-2007).pdf

860-DELNP-2003-Petition-137-(05-09-2008).pdf


« Previous Patent
Next Patent »
Patent Number 256176
Indian Patent Application Number 00860/DELNP/2003
PG Journal Number 20/2013
Publication Date 17-May-2013
Grant Date 11-May-2013
Date of Filing 03-Jun-2003
Name of Patentee UNIVATION TECHNOLOGIES LLC
Applicant Address 5555 SAN FELIPE, SUITE 1950, HOUSTON, TEXAS 77056, UNITED STATES OF AMERICA
Inventors:
# Inventor's Name Inventor's Address
1 TIMOTHY T. WENZEL 888 POPLAR ROAD, CHARLESTON, WV 25302 ,USA
2 MARK G. GOODE 17 MEADOWBROOK CIRCLE, HURRICANE, WEST VIRGINIA 25526-8906, USA
3 JOHN HENRY OSKAM 14 FAWN DRIVE, FLEMINGTON, NJ 08822,USA
4 ROBERT J. JORGENSEN 38 BUNKER DRIVE, BELLE MEAD, NJ 08502, USA
5 SIMON MAWSON 8839 HERITAGE BAY CIRCLE, ORLANDO, FL 32836 USA
6 SUN-CHUEH KAO 7 DURHAM COURT, HILLSBORO, NEW JERSEY 08844, USA
7 TAE HOON KWALK 241 BERKLEY AVENUE, BELLE MEAD, NEW JERSEY 08502, USA
8 TIMOTHY ROGER LYNN 575 ROCKPORT ROAD, HACKETTSTOWN, NJ 07840 USA
9 DAVID H. MCCONVILLE 4015 CINNAMON FERN COURT, HOUSTON, TEXAS 77059M USA
10 MATTHEW GARY MCKEE 702 MCBRYDE DRIVE, BLACKBURGM VA 24060, USA
11 JOHN F. SZUL 5 LAKE LANE, NITRO, WEST VIRGINIA 25143, USA
12 KERSTEN ANNE TERRY 825-A GLENDALE AVENUE, SOUTH CHARLESTON, WV 25302,USA
13 ROBERT HAROLD VOGEL 6115 PINEWOOD DRIVE, MIDLANDM, MICHIGAN 48640,USA
PCT International Classification Number C08F 10/00
PCT International Application Number PCT/US2001/44436
PCT International Filing date 2001-11-27
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 09/729,550 2000-12-04 U.S.A.