Title of Invention

PROCESS FOR THE PREPARATION OF DOPED PENTASIL-TYPE ZEOLITE

Abstract The present invention relates to a process for the preparation of doped pentasil-type zeolite, which process comprises the steps of: a) preparing an aqueous precursor mixture from a silicon s source, an aluminium source, and doped non-zeolitic seeds, and b) thermally treating the precursor mixture to form a doped pentasil-type zeolite.
Full Text PROCESS FOR THE PREPARATION OF DOPED PENTASIL-TYPE ZEOLITE USING DOPED SEEDS
The present invention relates to the preparation of doped pentasil-type zeolites using doped seeds.
US 5,232,675 discloses a process for the preparation of rare earth metal (RE)-doped pentasil-type zeolites using RE-doped faujasite seeds. This process leads to the crystallisation of pentasil-type zeolite on thejfaujasite-type seeds. Hence, the product consists of two types of zeolites one within the other: a core of RE-doped faujasite and a shell of pentasil-type zeolite. So, the RE-ions are located in the core and not (or at least not significantly) in the pentasil-type shell. This will hinder the RE-ions from improving the activity, selectivity, and stability of the pentasil-type zeolite.
Furthermore, upon thermal treatment (e.g. during calcination, steaming, or use in an FCC unit), the RE-ions move to the very small sodalite cages of the faujasite zeolite, thereby further decreasing their influence on the activity, selectivity, and stability of the pentasil-type zeolite.
The present invention offers a process for the preparation of doped pentasil-type zeolites in which the dopant is not only located in the core. This process involves the steps of:
a) preparing an aqueous precursor mixture from a silicon source, an aluminium source, and doped non-zeolitic seeds, and
b) thermally treating the precursor mixture to form a doped pentasil-type zeolite.
The process requires the use of doped non-zeolitic seeds. The term "non-zeolitic seeds" includes seeds made from materials selected from the group consisting of
(a) X-ray amorphous materials - i.e. materials which are either amorphous, or containing crystallites too small to be detected by X-ray diffraction - such as

an amorphous aluminosilicate nucleating gel according to, e.g., US 4,606,900, US 4,166,099, and Kasahara et al. in "Studies of Surface Science and Catalysis," Proceedings of the 7th International Conference on Zeolites 1986, pp. 185-192,
(b) milled crystalline materials, such as milled zeolites, that have a relative crystallinity of not more than 75%, and
(c) crystalline materials other than zeolites, such as clays (e.g. bentonite, sepiolites, smectites, kaolins, etc.) and (low) crystalline aluminas.
The relative crystallinity of the milled crystalline materials according to group b) preferably is not more than 60%, more preferably not more than 55%, and most preferably not more than 50%.
The relative crystallinity of the materials is detennined by Powder X-ray diffraction using copper K-alpha radiation, thereby comparing the total net integrated intensity of one or more strong reflections of the seeding material with that of the same material but having 100% crystallinity (i.e. having no amorphous phases).
For instance, the relative crystallinity of milled sodium Y-zeolite Is measured by determining the total net integrated intensity of the reflections covering the interplanar spacing range of 0.62 to 0.25 nm and comparing it with the intensity of a standard sodium Y-zeolite with a crystallinity of 100%.
The term "doped non-zeolitic seeds" refers to non-zeolitic seeds containing an additive (also called dopant). Suitable additives include compounds comprising rare earth metals such as Ce or La, alkaline earth metals such as Mg, Ca, and Ba, transition metals such as Mn, Fe, Ti, Zr, Cu, Ni, Zn, Mo, W, V, and Sn, actinides, noble metals such as Pt and Pd, gallium, boron, and/or phosphorus. Suitable compounds are the oxides, hydroxides, carbonates, hydroxy-carbonates, chlorides, nitrates, sulfates, and phosphates of the above elements.

The dopant is present in the doped non-zeolitic seed in amounts of 1-30 \Art%,
preferably 2-10 wt%, and more preferably 3-7 wt%, calculated as oxide and
based on the dry weight of the doped non-zeolitic seeds.
Seeds can be doped by, e.g., ion-exchange, preparation of the seed in the
presence of an additive, impregnation, or solid state exchange. For example,
clay or amorphous Si-Al cogel can be ion-exchanged, resulting in a doped clay
or cogel, which can serve as doped non-zeolitic seed in the process according
to the invention.
A doped non-zeolitic seed according to the above definition can also be
prepared by milling a doped seed (e.g. RE-Y) until its relative crystallinity is 60%
or less.
Without wishing to be bound by theory, it is assumed that during the process of the invention the non-zeolitic seeds will (re-)crystallise, thereby breaking down their original structure and releasing the dopant. This in contrast to the highly ordered doped faujasite seeds according to US 5,232,675, which retain their original structure containing the dopant.
The pentasil-type zeolite resulting from the process according to the invention preferably has a SiOa/A^Oa ratio of 25-90. Typical examples of pentasil-type zeolites are ZSM-type zeolites, such as ZSM-5, ZSM-5, ZSM-11, ZSM-12, ZSM-22, ZSM-23, ZSM-35, zeolite beta, or zeolite boron beta. The doped pentasil-type zeolite preferably contains 0.1-10 yNi% of dopant, more preferably 0.1-3 wt%, and most preferably 0.5-2.5 wt%, calculated as oxide and based on the dry weight of the doped pentasil-type zeolite.
The first step of the process according to the invention involves the preparation of an aqueous precursor mixture comprising a silicon source, an aluminium source, and the doped non-zeolitic seeds. Preferably, the precursor mixture comprises 1-10 v\rt% of doped non-zeolitic seeds, based on the total solids

content. More than one type of doped non-zeolitic seeds can be used in the process according to the invention.
The amount of aluminium and silicon source present in the precursor mixture depends on the desired SAR of the resulting doped pentasil-type zeolite.
It is possible for the precursor mixture to also contain an organic directing template. However, such templates are expensive and - as a result of their decomposition - environmentally harmful compounds are released upon heating of the so-prepared zeolites. Hence, it is preferred not to use a template in the process according to the invention.
Suitable aluminium sources include aluminium salts, such as Al2(S04)3, AICI3, AIPO4, Al2(HP04)3, and AI(H2P04)3, and water-insoluble aluminium compounds, e.g. aluminium trihydrate (AI(0H)3) such as gibbsite and bauxite ore concentrate (BOC), themrially treated aluminium trihydrate such as flash-1 calcined aluminium trihydrate, (pseudo)boehmite, aluminium chlorohydrol, ^ aluminium nitrohydrol. Also mixtures of one or more of these aluminium sources can be used.
Alternatively, doped aluminium sources can be used. Examples of such doped aluminium sources are doped (pseudo)boehmite, doped aluminium trihydrate, and doped flash-calcined aluminium trihydrate.
Doped aluminium sources can be prepared by preparation of the aluminium source in the presence of the dopant, impregnation of the aluminium source with the dopant, or ion-exchanging the aluminium source with the dopant. Doped (pseudo)boehmite, for instance, can be prepared by hydrolysis of aluminium alkoxide in the presence of a dopant, hydrolysis and precipitation of aluminium salts in the presence of a dopant, or by aging a slurry of (thermally treated) aluminium trihydrate, amorphous gel alumina, or less crystalline (pseudo)boehmite in the presence of a dopant. For more information concerning the preparation of doped (pseudo)boehmite reference is made to

International Patent Application Nos. WO 01/12551, WO 01/12552, and WO 01/12554.
Suitable silicon^sources include sodium silicate, sodium meta-silicate, stabilised
silica sols, silica gels, polysilicic acid, tetra ethylortho silicate, fumed silicas,
precipitated silicas, and mixtures thereof.
Also doped silicon sources can be used. Doped silicon sources can be obtained
by preparing the silicon source in the presence of the dopant, impregnating the
silicon source with the dopant, or ion-exchanging the silicon source with the
dopant.
Doped silica sol, for instance, can be obtained by preparing a silica sol from
water glass and acid (e.g. sulfuric acid), and exchanging the sodium ions with
the desired dopant. Alternatively, water glass, acid (e.g. sulfuric acid), and
dopant are coprecipitated to form a doped silica sol.
Suitable dopants for the aluminium and/or the silicon source include compounds comprising rare earth metals such as Ce or La, alkaline earth metals such as Mg, Ca, and Ba, transition metals such as Zr, Mn, Fe, Ti, Zr, Cu, Ni, Zn, Mo, W, V, and Sn, actinides, noble metals such as Pt and Pd, gallium, boron and/or phosphorus. The optional dopant(s) present in the silicon and/or aluminium source and the dopant in the doped non-zeolitic seeds can be the same or different.
If so desired, several other compounds may be added to the precursor mixture, such as templates or non-doped seeds (e.g. ZSM-5 seeds, zeolite beta seeds), metal (hydr)oxides, sols, gels, pore regulating agents (sugars, surfactants), clays, metal salts, acids, bases, etc. Furthermore, it is possible to mill the precursor mixture.
If so desired, the precursor mixture may be shaped to form shaped bodies. Suitable shaping methods include spray-drying, pelletising, extrusion (optionally

combined with kneading), beading, or any other conventional shaping method used in the catalyst and absorbent fields or combinations thereof. The amount of liquid present in the precursor mixture should be adapted to the specific shaping step to be conducted. It might be advisable to partially remove the liquid used in the precursor mixture and/or add an additional or another liquid, and/or to change the pH of the precursor mixture to make the mixture gellable and thus suitable for shaping. Additives commonly used in the different shaping methods, e.g. extrusion additives, may be added to the precursor mixture used for shaping.
The second step of the process involves thermal treatment of the precursor mixture at temperatures preferably ranging from 130 to 200""C, more preferably 150-180°C, for_3-60 hrs. During this step, the doped pentasil-type zeolite is formed by crystallisation.
The thermal treatment can be conducted in one or a series of at least two reaction vessels. If more than one such vessel is used, the process is preferably conducted in a continuous mode. Using more than one reaction vessel further allows the aqueous precursor mixture to be prepared either by adding all ingredients to the first vessel, or by spreading the addition of (part of the total amount of) the ingredients over the reaction vessels.
If so desired, the resulting doped pentasil-zeolite may be calcined and optionally ion-exchanged.
The so-formed doped pentasil-type zeolite can be used in or as a catalyst composition or catalyst additive composition for, e.g. hydrogenation, dehydrogenation, catalytic cracking (FCC), and alkylation reactions.

EXAMPLES
Example 1
A 29.8 wt% aluminium sulfate solution (484 g) and a 30.3 wt% H2SO4 solution (597 g) were added to a stirred 30-litre vessel containing 3,026 g water. To this solution, 3,084 g of water glass were slowly added in 15 minutes. A gel was formed during the addition.
A first seeding slurry was prepared by milling an aqueous slurry (Loss on Ignition at 1,000°C = 27.7 wt%) of Na- and RE-exchanged zeolite Y using a KD-03 mill (bead size 1 mm). The relative crystallinity of the resulting seeds was 49%.
This relative crystallinity was determined by X-ray-diffraction using Cu K-alpha radiation. The peak areas for the sample"s faujasite peaks within the scan range 14-36° 2-theta were determined using the Bruker profile fitting program Topasp. The pattern of a curved background was fitted according to the multiple background method and then substracted from the measured faujasite pattern. The so-obtained total net integrated intensity of the sample"s reflections covering the interplanar spacing range of 0.62 to 0.25 nm, relative to that of a standard sodium Y-zeolite with a crystallinity of 100%, was the relative crystallinity.
A second seeding slurry (Loss on ignition at I.OOO^C = 14.1 wt%) was prepared by mixing a commercial ZSM-5 and water. The slurry was milled until the ZSM-5 had an average particle size of 0.89 |am.
104 g of the first seeding slurry were mixed with 205 g of the second seeding slurry. The resulting seeding slurry was slowly added to the aluminium sulfate/water glass mixture under vehement stirring for 10 minutes. The slurry was autoclaved for 5 hours at 170°C and dried overnight in a stove at 120°C.

The PXRD pattern of the sample showed the formation of ZSM-5. No separate LaaOa, La(0H)3, or CeaOa phases were detected, meaning that the rare earth metal dopant was not precipitated as a separate phase. XPS and SEIVI/EDAX showed that the rare earth metal was present in the entire zeolite structure; not only in its core.
Example 2
A 29.8 wt% aluminium sulfate solution (530 g) and a 30.3 wt% H2SO4 solution
(616 g) were added to a stirred 30-litre vessel containing 2,879 g water. To this
solution, 3,084 g of water glass were slowly added in 15 minutes. A gel was
formed during the addition.
La-doped amorphous seeds were prepared by adding La(N03)3-6H20 to an
amorphous aluminosilicate nucleating gel. The gel was milled while diluting with
water. The resulting first seeding slurry had a Loss on Ignition (LOI) at 1,000°C
of 22.1 wt%; the La-concentration was 20 wt% (calculated as LaaOa and based
on the dry weight of the doped seeds after heating at 1,000°C).
A second seeding slurry (LOI at 1,000""C = 14.1 wt%) was prepared by mixing a
commercial ZSM-5 and water. The slurry was milled until the ZSM-5 had an
average particle size of 0.89 |j.m.
152 g of the first seeding slurry were mixed with 240 g of the second seeding
slurry. The resulting seeding slurry was slowly added to the aluminium
sulfate/water glass mixture under vehement stirring for 10 minutes. The slurry
was autoclaved for 5 hours at ITO"C and dried overnight in a stove at 120°C.
The PXRD pattern of the sample showed the fomnation of ZSM-5. No separate LaaOs or La(0H)3 phases were detected, meaning that the La-dopant was not precipitated as a separate phase.
XPS and SEM/EDAX showed that the rare earth metal was present in the entire zeolite structure; not only in its core.


WE CLAIM:
1. A process for the preparation of doped pentasil-type zeolite, which process
comprises the steps of:
a) preparing an aqueous precursor mixture from a silicon source, an aluminium source, and doped non-zeolitic seeds, and
b) thermally treating the precursor mixture to form a doped pentasil-type zeolite.

2. The process as claimed in claim 1, wherein the doped pentasil-type zeolite is doped ZSM-5.
3. The process as claimed in claim 1, wherein the non zeolitic seeds are X-ray amorphous.
4. The process as claimed in claim 1, wherein the non zeolitic seeds are milled crystalline materials that have a relative crystallinity of not more than 75%.
5. The process as claimed in claim 4, wherein the milled crystalline materials have a relative crystallinity of not more than 60%.
6. The process as claimed in claim 5, wherein the milled crystalline materials have a relative crystallinity of not more than 50%.
7. The process as claimed in claim 1, wherein the non-zeolitic seeds are
crystalline materials other than zeolites.

8. The process as claimed in claim 1, wherein the non-zeolitic seeds are doped
with a dopant selected from the group consisting of Ce, La, Zr, Mn, Fe, Ti, Cu, Ni, Zn,
Mo, W, V, Sn, Pt, Pd, Ga, B, and P.
9. The process as claimed in claim 1, wherein the silicon source is selected from
the group consisting of sodium (meta)silicate, stabilised silica sols, silica gels, polysilicic
acid, tetra ethylortho silicate, fumed silicas, precipitated silicas, and mixtures thereof.
10. The process as claimed in claim 1, wherein the aluminium source is selected
from the group consisting of Al2(S04)3,AlCl3,AlP04,Al2(HP04)3, Al(H2PO)3, aluminium
trihydrate (A1(0H)3), thermally treated aluminium trihydrate, (pseudo) boehmite,
aluminium chlorohydrol, aluminium nitrohydrol, and mixtures thereof.
11. The process as claimed in claim 1, wherein a shaping step is performed
between steps a) and b).

Documents:

0291-chenp-2005 abstract-duplicate.pdf

0291-chenp-2005 abstract.pdf

0291-chenp-2005 assignment.pdf

0291-chenp-2005 claims-duplicate.pdf

0291-chenp-2005 claims.pdf

0291-chenp-2005 correspondence-others.pdf

0291-chenp-2005 correspondence-po.pdf

0291-chenp-2005 description (complete)-duplicate.pdf

0291-chenp-2005 description (complete).pdf

0291-chenp-2005 form-1.pdf

0291-chenp-2005 form-18.pdf

0291-chenp-2005 form-26.pdf

0291-chenp-2005 form-3.pdf

0291-chenp-2005 form-4.pdf

0291-chenp-2005 form-5.pdf

0291-chenp-2005 others document.pdf

0291-chenp-2005 others.pdf

0291-chenp-2005 pct.pdf


Patent Number 215369
Indian Patent Application Number 291/CHENP/2005
PG Journal Number 13/2008
Publication Date 31-Mar-2008
Grant Date 26-Feb-2008
Date of Filing 28-Feb-2005
Name of Patentee ALBEMARLE NETHERLANDS B.V
Applicant Address STATIONSPLEIN 4, NL-3818 LE AMERSFOORT,
Inventors:
# Inventor's Name Inventor's Address
1 BRADY, MIKE 4248 RHODES AVENUE, STUDIO CITY, CALIFORNIA 91604,
2 LAHEIJ, MIKE GRAAF AELBRECHTLAAN 14, 1181 SW AMSTELVEEN,
3 O CONNOR ,PAUL HOGEBRINKERWEG 9, NL-3871 KM HOEVELAKEN,
4 STAMIRES, DENNIS 3401 COLONY PLAZA, NEWPORT BEACH, CA 92660,
PCT International Classification Number C01B 39/36
PCT International Application Number PCT/EP03/09187
PCT International Filing date 2003-08-19
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 60/406,442 2002-02-28 EUROPEAN UNION
2 02079434.3 2002-10-24 EUROPEAN UNION