|Title of Invention||
"A CRYSTALLINE MATERIAL AND METHOD OF SYNTHESIZING THE SAME"
|Abstract||A crystalline material having, in its as-synthesized form, an X-ray diffraction pattern including the lines listed in Table 4 and represented, in its as-synthesized form and on an anhydrous basis, by the empirical formula: mR:Fa:(MxAlyPz)O2, wherein R represents at least one directing agent at least one of which is 4-dimethylaminopyridine; wherein m is from 0 to 1, being the number of moles of R per mole of (MxAlyPz)O2; wherein a is the number of moles of fluoride ion (F) per mole of (MxAlyPz)O2 and a/y is less than 0.25; wherein x, y, and z represent the mole fraction of M, Al and P, as tetrahedral oxides, x being from 0 to 0.25, y being from 0.3 to 0.7 and z being from 0.25 to 0.7; and wherein M is a metal selected from one of Groups 1 to 14 and Lanthanoids of the Periodic Table of Elements.|
 This invention relates to a large pore aluminophosphate molecular
sieve, or a substituted derivative thereof, to a method of its synthesis in a low fluoride or fluoride-free medium and to its use in organic conversion reactions.
 Crystalline molecular sieves have a 3-dimensional, four-connected
framework structure of corner-sharing [TO4] tetrahedra, where T is any tetrahedrally coordinated cation. Among the known forms of molecular sieve are aluminosilicates, which contain a three-dimensional microporous crystal framework structure of [SiO4] and [AlO4] corner sharing tetrahedral units, aluminophosphates (ALPOs), in which the framework structure is composed of [AlO4] and [PO4] corner sharing tetrahedral units and silicoaluminophosphates (SAPOs), in which the framework structure is composed of [SiO4], [AlO4] and [PO4] corner sharing tetrahedral units.
 Molecular sieves have been classified by the Structure Commission
of the International Zeolite Association according to the rules of the IUPAC Commission on Zeolite Nomenclature. According to this classification, framework-type zeolite and zeolite-type molecular sieves, for which a structure has been established, are assigned a three letter code and are described in the Atlas of Zeolite Framework Types, 5th edition, Elsevier, London, England (2001), which is herein fully incorporated by reference.
 Molecular sieves are typically described in terms of the size of the
ring that defines a pore, where the size is based on the number of T atoms in the ring. Other framework-type characteristics include the arrangement of rings that form a cage, and when present, the dimension of channels, and the spaces between the cages. See van Bekkum, et al., Introduction to Zeolite Science and Practice,
Second Completely Revised and Expanded Edition, Volume 137, pages 1-67, Elsevier Science, B.V., Amsterdam, Netherlands (2001).
 In general, molecular sieves can be divided into small, medium and
large pore materials. Thus small pore molecular sieves typically have pores defined by a ring of no more than 8 T atoms and have an average pore size less than about 0.5 nm (5A). Medium pore molecular sieves typically have pores defined by a ring of 10 T atoms and have an average pore size about 0.5 to 0.6 nm (5 to 6A), whereas large pore materials have pores defined by rings of 12 or more T atoms and a pore size greater than 0.6 nm (6A).
 Crystalline molecular sieves, as exemplified by zeolites and
(metallo)aluminophosphates, are commercially important materials for petroleum
processing and petrochemical applications. Because each unique structure type
offers new potential for applications in catalysis and separations, there has been
sustained research effort, both in industry and academia, for their discovery.
 Many molecular sieves are synthesized in the presence of an
organic directing agent, such as an organic nitrogen compound. For example, it is known from, for example, U.S. Patent No. 6,680,278 that a crystalline silicoaluminophosphate molecular sieve of the CHA framework type (a small pore material), can be synthesized in the presence of an organic directing agent mixture comprising tetraethylammonium cations and one or more dimethylamino moieties selected from one or more of N,N-dimethylethanolamine, N,N-dimethylpropanolamine, N,N-dimethylbutanolamine, N,N-dimethylheptanolamine, N,N-dimethylhexanolamine, N,N-dimethylethylenediamine, N,N-dimethylbutylenediamine, N,N-dimethylheptylenediamine, N,N-dimethylhexylenediamine 1 -dimethylamino-2-propanol, N,N-dimethylethylamine, N,N-dimethylpropylamine, N,N-dimethylpentylamine, N,N-dimethylhexylamine and N,N-dimethylheptylamine. Other organic directing agents that have been used in the synthesis of CHA framework type materials include isopropylamine or di-n-propylamine triethylamine, cyclohexylamine, 1-methylamidazole, morpholine, pyridine, piperidine, diethylethanolamine, and N,N,N',N'-tetraethylethylene diamine.
 It is also known to use fluoride-containing compounds, such as
hydrogen fluoride, as mineralizing agents in molecular sieve synthesis. For
example, EP-A-337,479 discloses the use of hydrogen fluoride in water at low pH
to mineralize silica in glass for the synthesis of ZSM-5. In addition, U.S. Patent
Application Publication No. 2003/0231999 published December 18, 2003 and
incorporated herein by reference, discloses that aluminophosphate or
silicoaluminophosphate molecular sieves having the CHA framework type can be
synthesized in the presence of fluoride ions using the dimethylamino compounds
disclosed in U.S. Patent No. 6,680,278 as directing agents. However, fluoride-
based syntheses pose environmental problems in that they use hydrogen fluoride
in the synthesis medium and/or produce hydrogen fluoride on calcination to
remove the organic directing agent from the molecular sieve product.
 Currently, an entirely rational approach that leads to the synthesis
of unique framework materials is not available, due to the fact that all crystalline microporous materials are metastable phases and they are kinetic products. Their discovery is therefore often serendipitous.
 Our research has led to' two findings: that 4-DMAPy can direct the
synthesis of low-silica SAPO-CHA in a low fluoride or fluoride-free medium and in the presence of colloidal SAPO-34 seeds; and, from parallel experiments, that without SAPO-34 seeds, use of the same directing agent under no- or low-fluoride conditions unexpectedly led to the production of the present large pore aluminophosphate designated EMM-8.
 According to an article in the Chemical Journal of Chinese
Universities, Vol. 22, No. 10, pages 192-195, dated October 2001, DMAPy has been used as a template in the synthesis of NK-101, an aluminophosphate. However, Figure 1 provides a comparison of the X-ray diffraction pattern of NK-101 with that of EMM-8 and it is apparent from this comparison that the material of the invention is different from NK-101. In particular, in the X-ray diffraction pattern of NK-101, the most prominent diffraction peaks are at 2-theta values of approximately 17° and 19°, whereas these peaks are not present in the X-ray diffraction pattern of EMM-8.
 In an article entitled "SSZ-51 - A New Aluminophosphate
Zeotype: Synthesis, Crystal Structure, NMR, and Dehydration Properties", published on the Web by the American Chemical Society on June 23, 2004, Morris et al. report that they have synthesized and solved the structure of a new aluminophosphate zeotype framework structure, SSZ-51, having the empirical formula AUCPOF.CyHi i'0.5H2O. The synthesis employs 4-dimethylaminopyridine as a structure directing agent and requires the presence of fluoride ion as a mineralizing agent. The structure of SSZ-51 is said to be closely related to that of SAPO-40, an APR framework type material, and to contain intersecting channels defined by 8- and 12-membered ring windows. It appears that SSZ-51 is isostructural with EMM-8.
 U.S. Patent Application Publication No. 2003/0232718 published
December 18, 2003 discloses the synthesis of silicoaluminophosphate molecular sieves using templates that contain at least one dimethylamino moeity. The use of such templates is said to result in good quality SAPO molecular sieves of CHA framework type.
 EP-A-0 324 082 discloses the synthesis of non-zeolite molecular
sieves by contacting alumina or silica-alumina bodies with a liquid reaction mixture containing a reactive source of phosphorus and an organic templating agent.
 In one aspect, the invention resides in a crystalline molecular sieve
having a framework comprising tetrahedrally coordinated atoms (T) connected by bridging atoms and having the coordination sequence and vertex symbols listed in Table 3 below.
 In another aspect, the invention resides in a crystalline molecular
sieve having, in its as-synthesized form, an X-ray diffraction pattern including the lines listed in Table 4 below. In its calcined form, the crystalline molecular sieve of the invention has an X-ray diffraction pattern including the lines listed in Table 5 below. The phrase "including the lines" as used herein means that peaks are
expected to be present at or close to the lines indicated in the Tables, but not necessarily in the relative intensities specified, which can vary depending on a number of factors as discussed later.
 In yet another aspect, the invention resides in a crystalline material
having, in its as-synthesized form, an X-ray diffraction pattern including the lines listed in Table 4 below and represented, in its as-synthesized form and on an anhydrous basis, by the empirical formula:
wherein R represents at least one directing agent, preferably 4-
dimethylaminopyridine; m is the number of moles of R per mole of (MxAlyPz)O2
and m has a value from 0 to 1, such as from 0.1 to about 0.5, for example from 0.1
to about 0.3; wherein a is the number of moles of fluoride ion (F) per mole of
(MxAlyPz)O2 and a/y is less than 0.25 and preferably is 0; wherein x, y, and z
represent the mole fraction of M, Al and P, as tetrahedral oxides; and wherein M
is a metal selected from one of Groups 1 to 14 and Lanthanoids of the Periodic
Table of Elements, and preferably M is selected from B, Co, Cr, Cu, Fe, Ga, Ge,
Mg, Mn, Ni, Si, Sn, Ti, Zn and Zr. Most preferably, M is silicon. In one
embodiment, x is from 0 to about 0.25, y is from about 0.3 to about 0.7 and z is
from about 0.25 to about 0.7. In another embodiment, x is from 0 to about 0.15, y
is from about 0.4 to about 0.6 and z is from about 0.3 to about 0.6. In yet another
embodiment, x is from about 0 to about 0.12, y is from about 0.45 to about 0.55
and z is from about 0.35 to about 0.55. For ALPO molecular sieves, x is zero.
 In still another aspect, the invention resides in a method of
synthesizing the crystalline material of the invention, the process comprising: (a) forming a reaction mixture comprising water, a source of aluminum, a source of phosphorus, at least one structure directing agent comprising 4-dimethylaminopyridine, optionally a source of metal M and optionally a source of fluoride ion, wherein F: AOs molar ratio of said reaction mixture is preferably
less than 0.5 and most preferably is 0; (b) inducing crystallization of said crystalline material from the reaction mixture; and (c) recovering said crystalline material from the reaction mixture.
 In a further aspect, the invention resides in a method of
synthesizing a crystalline material having the CHA framework type, the process comprising: (a) forming a reaction mixture comprising a source of aluminum, a source of phosphorus, optionally a source of metal M, at least one directing agent comprising 4-dimethylaminopyridine and seeds of a CHA framework type material, such as SAPO-34; (b) inducing crystallization of said crystalline material from the reaction mixture; and (c) recovering said crystalline material from the reaction mixture.
 In still a further aspect, the invention resides in the use of the
crystalline material of said one aspect of the invention as a sorbent and as a catalyst in organic conversion reactions.
DESCRIPTION OF THE DRAWINGS
 Figure 1 is a comparison of the X-ray diffraction pattern of NK-101
with the X-ray diffraction pattern of Sample A in Example 1 after calcination as in Example 4. The ordinates for the two patterns are to the same scale and reflect intensity counts.
 Figure 2 gives the X-ray diffraction patterns of the as-synthesized
products of Example 1 after crystallization for 2 days and 4 days.
 Figure 3 compares the X-ray diffraction pattern of Sample A of
Example 1 with that of Sample B of Example 2.
 Figure 4 gives scanning electron micrographs of Sample A of
Example 1 and Sample B of Example 2.
 Figure 5 is a comparison of the X-ray diffraction patterns of
Sample A of Example 1 and Samples C and D of Example 3.
 Figure 6 is a comparison of the X-ray diffraction pattern of Sample
A, as-synthesized, with the X-ray diffraction patterns of Samples A, C and D after
calcination as in Example 4.
 Figure 7 gives the X-ray diffraction patterns of Sample C as-
synthesized and after undergoing a series of calcination, hydration and dehydration treatments as described in Example 5.
 Figure 8 gives the X-ray diffraction patterns of the as-synthesized
products of Example 8 after crystallization for 2 days and 4 days.
 Figure 9 is an illustration of the framework structure of EMM-8
showing only the tetrahedral atoms.
DETAILED DESCRIPTION OF THE EMBODIMENTS
 In one embodiment, the present invention relates to a porous
crystalline material, EMM-8, and its synthesis in a low fluoride or fluoride-free medium with the organic directing agent, 4-dimethylaminopyridine. The crystalline structure remains intact after calcination to remove the directing agent and adsorption data indicate that the resultant material has large pores. In particular, the calcined material adsorbs a significant amount of mesitylene, as well as 2,2-dimethylbutane, n-hexane, and methanol. The invention also resides in the use of EMM-8 as a sorbent and as a catalyst in organic conversion reactions and to synthesis of CFIA framework materials with the organic directing agent, 4-dimethylaminopyridine.
 The EMM-8 of the invention is a porous crystalline material having
a framework of tetrahedral atoms connected by bridging atoms, the tetrahedral atom framework being defined by the interconnections between the tetrahedrally coordinated atoms in its framework. As with any porous crystalline material, the structure of EMM-8 can be defined by the interconnections between the tetrahedrally coordinated atoms in its framework. In particular, EMM-8 has a framework of tetrahedral (T) atoms connected by bridging atoms, wherein the tetrahedral atom framework is defined by connecting the nearest tetrahedral (T) atoms in the manner shown in Table 1 below.
 In addition to describing the structure of EMM-8 by the
interconnections of the tetrahedral atoms as in Table 1 above, it may be defined by is the srqallestierjeating unit containing all the structural -
elements of the material. The pore structure of EMM-8 is illustrated in Figure 9 (which shows only the tetrahedral atoms) down the direction of the 12-member ring channel. There are four unit cell units in Figure 9, whose limits are defined
by four boxes. Table 2 lists the typical positions of each tetrahedral atom in the
unit cell in units of Angstroms. Each tetrahedral atom is bonded to bridging
atoms, which are also bonded to adjacent tetrahedral atoms. Tetrahedral atoms are
those capable of having tetrahedral coordination, including one or more of, but not
limiting, lithium, beryllium, boron, magnesium, aluminum, silicon, phosphorus,
titanium, chromium, manganese, iron, cobalt, nickel, copper, zinc, zirconium,
gallium, germanium, arsenic, indium, tin, and antimony. Bridging atoms are those
capable of connecting two tetrahedral atoms, examples of which include, but are
not limited to oxygen, nitrogen, fluorine, sulfur, selenium, and carbon atoms.
 In the case of oxygen, it is also possible that the bridging oxygen is
also connected to a hydrogen atom to form a hydroxyl group (-OH-). In the case of carbon it is also possible that the carbon is also connected to two hydrogen atoms to form a methylene group (-CHb-). For example, bridging methylene groups have been seen in the zirconium diphosphonate, MEL-57. See: C. Serre, G. Ferey, J. Mater. Chem. 12, p. 2367 (2002). Bridging sulfur and selenium atoms have been seen in the UCR-20-23 family of microporous materials. See: N. Zheng, X. Bu, B. Wang, P. Feng, Science 298, p. 2366 (2002). Bridging fluorine atoms have been seen in lithium hydrazinium fluoroberyllate, which has the ABW structure type. See: M.R. Anderson, I.D. Brown, S. Vilminot, Acta Cryst. B29, p. 2626 (1973). Since tetrahedral atoms may move about due to other crystal forces (presence of inorganic or organic species, for example), or by the choice of tetrahedral and bridging atoms, a range of ± 0.1 nm (±1 Angstrom) is implied for the x and y coordinate positions and a range of ± 0.05 nm (±0.5 Angstrom) for the z coordinate positions in Table 2.
 The complete structure of EMM-8 is built by connecting multiple
unit cells as defined above in a fully-connected three-dimensional framework. The tetrahedral atoms in one unit cell are connected to certain tetrahedral atoms in all of its adjacent unit cells. While Table 1 lists the connections of all the tetrahedral atoms for a given unit cell of EMM-8, the connections may not be to
the particular atom in the same unit cell but to an adjacent unit cell. All of the
connections listed in Table 1 are such that they are to the closest tetrahedral (T)
atoms, regardless of whether they are in the same unit cell or in adjacent unit cells.
 Although the Cartesian coordinates given in Table 2 above may
accurately reflect the positions of tetrahedral atoms in an idealized structure, the
true structure can be more accurately described by the connectivity between the
framework atoms as shown in Table 1 above. Another way to describe this
connectivity is by the use of coordination sequences as applied to microporous
frameworks by W,M. Meier and H. J. Moeck, in the Journal of Solid State
Chemistry 27, p. 349 (1979). In a microporous framework, each tetrahedral atom,
No, (T-atom) is connected to NI = 4 neighboring T-atoms through bridging atoms
(typically oxygen). These neighboring T-atoms are then connected to N2 T-atoms
in the next shell. The N2 atoms in the second shell are connected to N3 T-atoms in
the third shell, and so on. Each T-atom is only counted once, such that, for
example, if a T-atom is in a 4-membered ring, at the fourth shell the N0 atom is
not counted a second time, and so on. Using this methodology, a coordination
sequence can be determined for each unique T-atom of a 4-connected net of T-
atoms. The following line lists the maximum number of T-atoms for each shell.
 For a given T-atom in a 3-dimensional framework, there are sixangles associated with the connections to its 4 neighboring T-atoms. A way of indicating the size of the smallest ring associated with each of these six angles, called the vertex symbol, was developed by M.O'Keeffe and S.T. Hyde in Zeolites 19, p. 370 (1997). The order is such that opposite pairs of angles are grouped together. The vertex symbol 188.8.131.52.62.8, for example, indicates that the first pair of opposite angles contains 4-rings, the second pair contains 6-rings, and the third pair contains two 6-rings and an 8-ring. The Structure Commission of the International Zeolite Association recognize that the combination of coordination sequence and vertex symbol together appear unique for a particular framework topology such that they can be used to unambiguously distinguish microporous frameworks of different types (see "Atlas of Zeolite Framework Types", Ch.
Baerlocher. W.M. Meier, D,H. Olson, Elsevier, Amsterdam (2001). One way to determine the coordination sequence and vertex symbol for a given structure is from the atomic coordinates of the framework atoms using the computer program zeoTsites (see G, Sastre, J.D. Gale, Microporous and mesoporous Materials 43, p, 27(2001).
 The coordination sequence and vertex symbols for the EMM-8
structure are given in Table 3. The T-atom connectivity as listed in Table 3 is for T-atoms only. Bridging atoms, such as oxygen usually connect the T-atoms. Although most of the T-atoms are connected to other T-atoms through bridging atoms, it is recognized that in a particular crystal of a material having a framework structure, it is possible that a number of T-atoms may not be connected to one another. Reasons for non-connectivity include, but are not limited by, T-atoms located at the edges of the crystals and by defect sites caused by, for example, vacancies in the crystal. The framework listed in Table 3 is not limited in any way by its composition, unit cell dimensions or space group symmetry.
 While the idealized structure contains only 4-coordinate T-atoms, it
is possible under certain conditions that some of the framework atoms may be 5-or 6-coordinate. This may occur, for example, under conditions of hydration when material contains mainly phosphorus and aluminum T-
atoms. When this occurs it is found that T-atoms may be also coordinated to one or two oxygen atoms of water molecules (-OH2), or of hydroxyl groups (-OH). For example, the molecular sieve AlPO4-34 is known to reversibly change the
coordination of some aluminum T-atoms from 4-coordinate to 5- and 6-coordinate upon hydration as described by A. Tuel et al. in J. Phys. Chem. B 104, p. 5697 (2000). It is also possible that some framework T-atoms can be coordinated to fluoride atoms (-F) when materials are prepared in the presence of fluorine to make materials with 5-coordinate T-atoms as described by H. Koller in J. Am. ChemSoc. 121, p. 3368 (1999).
 It may happen in some particular compositions that, because of a
specific ordering of T-atoms, the actual unit cell may double in size to allow the specific ordering to occur. This is the case in the aluminophosphate and metalloalumino-phosphate compositions of EMM-8 where there are alternating aluminum and phosphorus T-atoms. For example, the unit cell of the A1PO form of EMM-8 is actually twice the length along the z-axis as indicated in Table 2, such that there are 64 T-atoms in the unit cell.
 In its as-calcined anhydrous form, EMM-8 is porous and has an X-
ray diffraction pattern including the lines listed in Table 5 below:
 These, and all other X-ray diffraction data referred to herein, were
collected with a Siemens D500 diffractometer with a voltage of 40 kV and a current of 30 mA using a copper target (A, = 0.154nm) and a curved graphite monochrometer. The diffraction data were recorded by step-scanning at 0.02 degrees of two-theta, where theta is the Bragg angle, and a counting time of 1 second for each step. The interplanar spacings, d's, were calculated in nanometres (nm), and the relative intensities of the lines, I/ lo, where lo is one-hundredth of the intensity of the strongest line, above background, were derived with the use of a profile fitting routine (or second derivative algorithm). The intensities are uncorrected for Lorentz and polarization effects. The relative intensities are given in terms of the symbols vs=very strong (75-100), s=strong (50-74), m=medium (25-49) and w=weak (0-24). It should be understood that diffraction data listed for this sample as single lines may consist of multiple overlapping lines which under certain conditions, such as differences in crystallite sizes or very high experimental resolution or crystallographic change, may appear as resolved or partially resolved lines. Typically, crystallographic changes can include minor changes in unit cell parameters and/or a change in crystal symmetry, without a change in topology of the structure. These minor effects, including changes in relative intensities, can also occur as a result of differences in cation content,- framework composition, nature and degree of pore filling, and thermal and/or hydrothermal history. In practice, therefore, at least some of the lines in the X-ray
patterns of the crystalline material of the invention may exhibit significant
variations in relative intensity from the values indicated in Tables 4 and 5.
 To generate the as-calcined X-ray data listed in Table 5, about 0.5
grams of the dried, as-synthesized crystalline material are heated in an oven from
room temperature under a flow of nitrogen at a rate of 10°C/minute to 400°C and,
while retaining the nitrogen flow, the sample is held at 400°C for 30 minutes. The
nitrogen flow is then ceased and air is passed over the sample while the
temperature of the oven is raised at a rate of 10°C/minute to 600°C. The sample is
then retained at 600°C for 2 hours under air, whereafter the oven is cooled to room
temperature to allow the XRD pattern to be recorded.
 The XRD patterns of Tables 4 and 5 can be indexed to a
monoclinic unit cell, in the space group C2/c (#15), having the following unit cell dimensions in nm:
wherein R represents at least one directing agent, preferably an organic directing agent and most preferably 4-dimethylaminopyridine; m is the number of moles of R per mole of (MxAlyP2)O2 and m has a value from 0 to 1, such as from 0.1 to about 0.5, preferably from 0.1 to about 0.3; wherein F represents fluoride ion which may be present in the synthesis mixture, a is the number of moles of F per mole of (MxAlyPz)O2 and a/y is less than 0.25 and preferably is 0; wherein x, y, and z represent the mole fraction of M, Al and P as tetrahedral oxides; and wherein M is a metal selected from one of Groups 1 to 14 and Lanthanoids of the Periodic Table of Elements. Preferably M is selected from B, Co, Cr, Cu, Fe, Ga, lie, Mg, Mn, Mi, Si, Sri, Ti, Zn and ZrTTVlost prelefably, ;M is
 In one embodiment, x is from 0 to about 0.25, y is from about 0.3
to about 0.7 and z is from about 0.25 to about 0.7. In another embodiment x is
from about 0 to about 0.15, y is from about 0.4 to about 0.6 and z is from about 0.3 to about 0.6. In yet another embodiment x is from about 0 to about 0.12, y is from about 0.45 to about 0.55 and z is from about 0.35 to about 0.55. For ALPO molecular sieves, x is zero.
 In its calcined form, the large pore (metallo) aluminophosphate of
the present invention typically has an alpha value of at least 0.1, and more preferably at least 0.5, indicating that the material is useful as an acid catalyst in organic, and in particular hydrocarbon, conversion reactions. The alpha value test is a measure of the cracking activity of a catalyst and is described in U.S. Patent No. 3,354,078 and in the Journal of Catalysis, Vol. 4, p. 527 (1965); Vol. 6, p. 278 (1966); and Vol. 61, p. 395 (1980), each incorporated herein by reference as to that description. The experimental conditions of the test used herein include a constant temperature of 538°C and a variable flow rate as described in detail in the Journal of Catalysis, Vol. 61, p. 395.
 The crystalline (metallo)aluminophosphate material of the present
invention can be produced from a synthesis mixture containing water, a source of phosphorus, a source of aluminum, optionally a source of metal M, such as silicon, optionally a source of fluoride ions and 4-dimethylaminopyridine (R). The synthesis mixture typically has a composition, expressed in terms of mole ratios of oxides, as follows:
 A suitable source of phosphorus in the above mixture is phosphoric
acid. Examples of suitable aluminum sources include hydrated aluminum oxides
such as boehmite and pseudoboehmite. Suitable sources of silicon include silicates, e.g., fumed silica, such as Aerosil and Cabosil, tetraalkyl orthosilicates, and aqueous colloidal suspensions of silica, for example that sold by E.I. du Pont de Nemours under the tradename Ludox.
 If present, the source of fluoride ions may be any compound
capable of releasing fluoride ions in the synthesis mixture. Non-limiting examples of such sources of fluoride ions include salts containing one or several fluoride ions, such as metal fluorides, preferably, sodium fluoride, potassium fluoride, calcium fluoride, magnesium fluoride, strontium fluoride, barium fluoride, ammonium fluoride, tetraalkylammonium fluorides, such as tetramethylammonium fluoride, tetraethylammonium fluoride, hydrogen fluoride, and mixtures thereof. The preferred source of fluoride is hydrogen fluoride but, more preferably, the synthesis is conducted in the absence of added fluoride, that is with the F: A12O3 molar ratio being zero.
 Crystallization is carried out under either stirred or static
conditions, preferably stirred conditions, at a temperature between about 100°C
and about 250°C, typically between about 150°C and about 200°C, preferably
between about 155°C and about 180°C. Preferably, crystallization is conducted
for about 2 to about 150 hours, preferably about 20 to about 100 hours, whereafter
the resultant crystalline material is separated from the mother liquor and
recovered, such as by centriftigation or filtration. The separated product can also
be washed, recovered by centrifugation or filtration and dried. The crystalline
product is typically in the form of platelets having a d5o (50 % by volume of
crystals is smaller than the d50 value) particle size less than 1 urn.
 Synthesis of the large pore (metallo)aluminophosphate material of
the invention may be facilitated by the presence of at least 0.1 ppm, such as at least 10 ppm, for example at least 100 ppm, conveniently at least 500 ppm of seed crystals from a previous synthesis based on total weight of the reaction mixture. It is, however, found that where seed crystals of a CHA framework-type molecular sieve, such as SAPO-34, are added to the synthesis mixture, the resultant productis a CHA framework-type molecular sieve rather than the large pore (metallo)aluminophosphate material of the invention.
 As a result of the crystallization process, the recovered crystalline
product contains within its pores at least a portion of the organic directing agent used in the synthesis. In a preferred embodiment, activation is performed in such a manner that the organic directing agent is removed from the molecular sieve, leaving active catalytic sites within the microporous channels of the molecular sieve open for contact with a feedstock. The activation process is typically accomplished by calcining, or essentially heating the molecular sieve comprising the template at a temperature of from about 200°C to about 800°C, typically in the presence of an oxygen-containing gas. This type of process can be used for partial or complete removal of the organic directing agent from the intracrystalline pore system.
 Once the crystalline material of the invention has been synthesized,
it can be formulated into a catalyst composition by combination with other materials, such as binders and/or matrix materials, that provide additional hardness or catalytic activity to the finished catalyst.
 Materials which can be blended with the crystalline material of the
invention can be various inert or catalytically active materials. These materials include compositions such as kaolin and other clays, various forms of rare earth metals, other non-zeolite catalyst components, zeolite catalyst components, alumina or alumina sol, titania, zirconia, quartz, silica or silica sol, and mixtures thereof. These components are also effective in reducing overall catalyst cost, acting as a thermal sink to assist in heat shielding the catalyst during regeneration, densifying the catalyst and increasing catalyst strength. When blended with such components, the amount of crystalline material contained in the final catalyst product ranges from 10 to 90 weight percent of the total catalyst, preferably 20 to 80 weight percent of the total catalyst.
 The large pore crystalline material described herein can be used to
dry gases and liquids; for selective molecular separation based on size and polar properties; as an ion-exchanger; as a catalyst in organic conversion reactions, suchas cracking, hydrocracking, disproportionate, alkylation, isomerization,
oxidation and synthesis of monoalkylamines and dialkylamines; as a chemical
carrier; in gas chromatography; and in the petroleum industry to remove normal
paraffins from distillates. Where the synthesis method of the invention produces a
CHA framework-type molecular sieve, such a product would have similar uses
and in particular would be useful as a catalyst in the conversion of oxygenates,
such as methanol, to olefins, such as ethylene and propylene.
 In order to more fully illustrate the nature of the invention and the
manner of practising same, the following examples are presented.
 The following ingredients were mixed, in sequence, and blended
into a uniform gel using a microhomogenizer (Tissue Tearor Model 98730, available from Biospec Products, Inc, USA): 85 wt% H3PO4 (obtained from Aldrich Chemical Company), deionized H2O, Catapal™ A (73.9 wt% A12O3, available from CONDEA Vista Company, Texas, USA), and then 4-dimethylaminopyridine (4-DMAPy) (obtained from Aldrich Chemical Company, USA). The molar ratio of the ingredients was as follows:
2.0 DMAPy:1.0 A12O3:1.0 P2O5:40 H2O
 The gel was then placed into a Parr bomb with Teflon liner, and
was heated to 170°C for 2 to 4 days while the bomb was tumbled at 40 rpm. The
solid product was centrifuged and washed five times with deionized water, and
was then dried in a 60°C vacuum oven overnight. X-ray powder patterns of the
product showed, in Figure 2, that a crystalline product was obtained after two days
of crystallization (Sample A). After four days of crystallization, additional
diffraction peaks corresponding to an unidentified impurity appeared.
 Solid product yield of Sample A was 13.2%, based on the total
weight of the starting gel. Elemental analysis gave the following results: Al, 16.0%;P, 17.9%. These results correspond toXli.oPo.975 in composition and 71.2% for calculated total oxides. The residual weight was separately determined with TGA (Thermal Gravimetric Analysis) to be 72.6%. Sample A gave the
scanning electron micrograph shown in Figure 4 and had an XRD pattern with the peaks listed Table 6 below.
 The procedure was identical to Example 1, except that hydrofluoric
acid was added as the last ingredient and the ingredient ratio was the following:
0.5HF:2.0DMAPy: 1 .OA12O3:1 .OP2O5:40H2O
 The crystallization was carried out for three days at 180 °C
statically. The product yield was 12.9 wt%. The XRD pattern of the product (Sample B) is shown in Figure 3 along with that of Sample A. The former is nearly identical to that of Sample A, although the peak width and relative intensity are somewhat different. The relative peak intensity difference is expected with the presence of F in Sample B. The broader peaks of Sample B are possibly due to the small platelet (  The fact that the same crystalline product was obtained with
different starting synthesis compositions (Examples 1 and 2), and that the XRD patterns of the products can be indexed establish that a pure phase material has been synthesized. The as-synthesized material has a unique XRD pattern.
 The procedure of Example 1 was repeated to produce two
additional samples, Samples C and D, except that Cabosil™ silica was added to each synthesis mixture after the Catapal™ alumina and before 4-dimethylaminopyridine. The ingredient molar ratios were as follows: 2.0DMAPy:1.0Al203:(0.1 & 0.3)SiO2:1.0P2O5:40H2O
 To the synthesis gel 0.15wt% Sample B was added as seeds. The
crystallization was carried out for two days at 170°C with tumbling at 40 rpm.
The product yield was 18.9 and 19.6 wt%, for 0.1 SiO2 and 0.3 SiO2, respectively.
The XRD patterns of the products (Samples C and D for 0.1 and 0.3 SiO2,
respectively) are shownjn Figure 5 along with thatof Sample A. This Figure
along with the elemental analysis results below, shows that silicon atoms can be
incorporated into the framework of Sample A.
 Elemental analysis results were as follows:
Sample C: Al=16.1%; P=16.9%; Si=2.38%. This corresponds to Ali.oSio.o5sPo.9H
in composition and 71.2% for calculated total oxides.
Sample D: Al=14.8%; P=15.7%; Si= 2.38%. This corresponds to Ali.0Si0.i54Po.924
in composition and 69.1% for calculated total oxides.
 The powder pattern of Sample C was indexed successfully in the
same monoclinic unit cell as Sample A, in the Space Group C2/c(#15). The unit
cell dimensions in nm are: a=2.169, b=1.386, c=0.705, (3=98.9°. The unit cell
volume is 2.0983 nm3. These unit cell parameters are similar to those of Sample
 Calcination of the samples A, C and D (10 °C/min to 400°C in
nitrogen, then dwell for 30 minutes in nitrogen before ramping to 600°C at 10 °C/min in air, and finally dwell at 600°C for 2 hours in air) resulted in white crystalline products with the organic directing agent removed. The XRD patterns of the calcined samples, taken in ambient air so there may be some degree of rehydration, are shown in Figure 6, along with that of the as-synthesized Sample A.
 All three samples gave different XRD patterns from their as-
synthesized counterparts. The calcined Sample A, being an A1PO4, shows a
different pattern from those of the calcined Samples C and D. The latter two, both
being SAPOs, have similar XRD patterns. A similar phenomenon has been found
in A1PO4 and SAPOs having the CHA framework type. AlPO4-34, for example,
adopts a triclinic unit cell when exposed to moisture, whereas SAPO-34s having
sufficiently high Si levels retain their rhombohedral symmetry after rehydration.
 The XRD pattern of calcined Sample C was indexed in a
monoclinic unit cell similar to that for the as-synthesized sample. The unit cell constants in nm are a = 2.233, b = 1.336, c = 0.716, .(3-99.88°. The unit cell volume is 2.1050 nm3. These unit cell parameters are very similar to those of as-synthesized Sample C, with only about 0.3% increase in unit cell volume upon calcination.
 Calcination of Sample C was conducted and XRDs were taken on a
platinum sample stage that was enclosed in a chamber equipped with different sources of inert and reactive gases. The platinum sample stage also served as an XRD sample holder so that XRD patterns could be taken at different temperatures as well as under different atmospheres. First a pattern was taken on the as-synthesized Sample C. Then, after a ramp in temperature at 10°C/min to 600°C and dwelling at the temperature for two hours under a flow of dry air (15 ppm moisture), and cooling to 200°C, a second XRD pattern was taken. The flowing gas was switched to N2 and the sample was cooled to room temperature before a third XRD pattern was taken in N2. Afterwards the chamber was opened to the ambient air, which had a relative humidity of 82% (22°C), for 16 hours, to ensure that the sample was fully hydrated. A fourth XRD pattern was then taken. Finally, the chamber was closed again, and the temperature was raised to 200°C under N2 to dehydrate the sample. A final fifth XRD pattern was taken at 200°C
 The results are shown in Figure 7 and indicate that calcination
results in some change in the XRD pattern as well as an increase in the overall diffraction intensity. Exposure to moisture reduces the diffraction intensity to the pre-calcination level, and the XRD pattern is again slightly changed. Then dehydration of the hydrated sample leads to an XRD pattern identical to that of the post-calcination sample, indicating the hydration process is at least partially reversible.
 Calcined (600°C for two hours) and degassed (at 500°C) Sample A
was exposed to different adsorbate molecules under specified conditions as listed in Table 7 below in a Thermal Gravimetric Analysis (TGA) unit. In all cases complete adsorption was attained. The diffusivity number D/r2 given in Table 7
was obtained by analyzing the initial portion of the adsorption uptake curve. In all cases adsorption was found to be too fast for accurate determination of diffusivity. Therefore the numbers reported are the best estimates. Table 7 also provides, for comparison purposes, some adsorption data for the 10x10x9 ring material ITQ-13.
 The significant amount of mesitylene adsorption indicates that the
new material has pore openings larger or equal to 0.7 nm (7A )(12-ring), and the large adsorption capacity suggests that the framework is very open.
 Samples C and D, having Si/Al ratio of 0.058 and 0.154,
respectively, were calcined at 600°C for 2 hours before n-hexane cracking test was conducted. The standard a-test conditions (538°C) were used. The a-numbers for these two samples were determined to be 9.1 and 23.3, respectively. These values show that the new material has potential for hydrocarbon conversion applications.
 The synthesis procedure was identical to Example 1, except that
Cabosil™ was added after Catapal™ and before 4-dimethylaminopyridine, and 100 ppm colloidal SAPO-34 seeds were added as the last ingredient. The ingredient ratio was as follows:
days of crystallization were 17.85% and 21.07%, respectively.
 The XRD patterns are shown in Figure 8, which shows that SAPO-
34 has been made, although impurities were present. The product of two-day crystallization had trace amount of API (A1PO4-5) and what appeared to be AWO (A1PO4-21), while that of four-day crystallization had no API but an increased amount of AWO.
 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.
1. A crystalline material having, in its as-synthesized form, an X-ray diffraction pattern
including the lines listed as follows:
2-Theta d, nm Relative Intensity
7.58±0.05 1.164±0.008 25-49
8.26±0.05 1.069±0.007 25-49
12.66±0.05 0.698±0.003 50-74
13.94±0.05 0.634±0.002 50-74
14.18±0.05 0.623±0.002 75-100
18.94±0.05 0.468±0.001 50-74
19.18±0.05 0.462±0.001 25-49
19.60±0.05 0.452±0.001 50-74
25.48±0.05 0.349±0.001 25-29
25.62±0.05 0.347+0.001 75-100
25.94±0.05 0.343±0.001 75-100
26.12±0.05 0.341±0.001 25-49
28.08±0.05 0.317±0.001 25-49
and represented, in its as-synthesized form and on an anhydrous basis, by the empirical formula:
mR:Fa:(MxAlyPz)O2 wherein R represents at least one directing agent at least one of which is 4-dimethylaminopyridine; wherein m is from 0 to 1, being the number of moles of R per mole of (MxAlyPz)O2; wherein a is the number of moles of fluoride ion (F) per mole of (MxAlyPz)O2 and a/y is less than 0.25; wherein x, y, and z represent the mole fraction of M, Al and P, as tetrahedral oxides, x being from 0 to 0.25, y being from 0.3 to 0.7 and z being from 0.25 to 0.7; and wherein M is a metal selected from one of Groups 1 to 14 and Lanthanoids of the Periodic Table of Elements.
2. The crystalline material as claimed in claim 1, wherein m has a value from 0.1 to 0.5.
3. The crystalline material as claimed in claim 1 or 2 wherein a/y is 0.
4. The crystalline material as claimed in any preceding claim wherein M is selected from one of the group consisting of B, Co, Cr, Cu, Fe, Ga, Ge, Mg, Mn, Ni, Si, Sn, Ti, Zn and Zr.
5. The crystalline material as claimed in any preceding claim wherein M is silicon.
6. The crystalline material as claimed in any preceding claim wherein x is from 0 to 0.15, y is from 0.4 to 0.6 and z is from 0.3 to 0.6.
7. A porous, crystalline material produced by calcining the crystalline material as claimed in any preceding claim and having an X-ray diffraction pattern including the lines listed as follows:
2-Theta d, nm Relative Intensity
7.54±0.05 1.171±0.008 75-100
7.94±0.05 1.112+0.007 25-49
12.68±0.05 0.697±0.003 0-24
13.54±0.05 0.653±0.003 0-24
14.24±0.05 0.621+0.002 25-49
18.82±0.05 0.471±0.001 0-24
19.80±0.05 0.448±0.001 0-24
20.10±0.05 0.441 ±0.001 0-24
25.46±0.05 0.349+0.001 0-24
25.90±0.05 0.344±0.001 0-24
26.46±0.05 0.336±0.001 0-24
8. A method of synthesizing the crystalline material as claimed in claim 1, the process
comprising: (a) forming a reaction mixture comprising water; a source of aluminum, a
source of phosphorus, optionally a source comprising water; a source of aluminum, a
source of phosphorus, optionally a source of metal other than aluminum, optionally a
source of fluoride ions, and at least one directing agent comprising 4-
dimethylaminopyridine (R); (b) inducing crystallization of said crystalline material from
the reaction mixture; and (c) recovering said crystalline material from the reaction
9. The method as claimed in claim 8, wherein the reaction mixture has a composition, in
terms of mole ratios, within the following ranges:
P2O5:A12O3 = 0.7 to 1.3
SiO2:Al2O3 = 0 to 0.9
H2O:A12O3 = 10 to 100
R: A12O3 = 0.5 to 0.5
F: A12O3 = 0 to 10. The method as claimed in claim 9 wherein the reaction mixture has a composition, in
terms of mole ratios, within the following ranges:
P2O5:A12O3 = 0.9 to 1.1
SiO2: A12O3 = 0.05 to 0.5
H2O : A12O3 = 20 to 50
R:A12O3 = 1.0 to 4.0
F: A12O3 = 0 to 0.5 or zero
11. The method as claimed in claim 8, 9 or 10 wherein the reaction mixture comprises no added source of fluoride ions.
12. The method as claimed in any one of claims 8 to 11, wherein crystallization of said crystalline material is conducted at a temperature of 100°C to 250°C.
13. The method as claimed in claim 12, wherein crystallization of said crystalline material is conducted at a temperature of 130°C to 200°C.
|Indian Patent Application Number||2275/DELNP/2007|
|PG Journal Number||09/2012|
|Date of Filing||23-Mar-2007|
|Name of Patentee||EXXONMOBIL CHEMICAL PATENTS INC.|
|Applicant Address||5200 BAYWAY DRIVE,BAYTOWN, TEXAS 77520-5200, USA|
|PCT International Classification Number||C01B 39/00|
|PCT International Application Number||PCT/EP2005/009878|
|PCT International Filing date||2005-09-12|