WO2004020092A1 - Preparation de catalyseurs renfermant un zeolite de type pentasile - Google Patents

Preparation de catalyseurs renfermant un zeolite de type pentasile Download PDF

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Publication number
WO2004020092A1
WO2004020092A1 PCT/EP2003/009181 EP0309181W WO2004020092A1 WO 2004020092 A1 WO2004020092 A1 WO 2004020092A1 EP 0309181 W EP0309181 W EP 0309181W WO 2004020092 A1 WO2004020092 A1 WO 2004020092A1
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WO
WIPO (PCT)
Prior art keywords
source
aluminium
pentasil
process according
type zeolite
Prior art date
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PCT/EP2003/009181
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English (en)
Inventor
Paul O'connor
Dennis Stamires
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Albemarle Netherlands B.V.
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Publication date
Application filed by Albemarle Netherlands B.V. filed Critical Albemarle Netherlands B.V.
Priority to AU2003273799A priority Critical patent/AU2003273799A1/en
Priority to CA002496899A priority patent/CA2496899A1/fr
Priority to EP03757760A priority patent/EP1531932A1/fr
Priority to JP2004532093A priority patent/JP2005536342A/ja
Priority to BR0313746-5A priority patent/BR0313746A/pt
Publication of WO2004020092A1 publication Critical patent/WO2004020092A1/fr

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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/12—Silica and alumina
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34—Chemical or biological purification of waste gases
    • B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/86—Catalytic processes
    • B01D53/8603—Removing sulfur compounds
    • B01D53/8609—Sulfur oxides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34—Chemical or biological purification of waste gases
    • B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/86—Catalytic processes
    • B01D53/8621—Removing nitrogen compounds
    • B01D53/8625—Nitrogen oxides
    • B01D53/8628—Processes characterised by a specific catalyst
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
    • B01J21/04—Alumina
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/16—Clays or other mineral silicates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/007—Mixed salts
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
    • B01J37/0027—Powdering
    • B01J37/0045—Drying a slurry, e.g. spray drying
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/08—Heat treatment
    • B01J37/10—Heat treatment in the presence of water, e.g. steam
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
    • B01J2229/30—After treatment, characterised by the means used
    • B01J2229/42—Addition of matrix or binder particles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
    • B01J29/7007—Zeolite Beta

Definitions

  • the present invention relates to a process for the preparation of catalyst compositions comprising a pentasil-type zeolite and at least one other catalyst component.
  • EP 0 156 595 discloses a process for the preparation of catalyst compositions comprising 60 wt% or less of a pentasil-type zeolite in a porous matrix by (i) mixing zeolite seeds, an aluminium source, and a silicon source in water to form a slurry, (ii) shaping the slurry to form discrete particles, (iii) mixing the particles with a source of alkali cations in an aqueous reaction mixture, and (iv) hydrothermally treating the particles to form the zeolite in the particles.
  • a slurry is formed, the slurry is shaped, the shaped particles are slurried again and hydrothermally treated.
  • the process according to the present invention provides a more convenient process for the preparation of catalyst compositions comprising a pentasil-type zeolite.
  • the process according to the present invention comprises the steps of: a) hydrothermally treating an aqueous slurry comprising an aluminium source, a silicon source, a seeding material, and optionally a divalent metal source, thereby forming a pentasil-type zeolite and at least one other compound, and b) shaping the product of step a).
  • the process according to the invention does not involve re-slurrying of shaped particles.
  • the zeolite in the process according to the invention is not formed in situ, i.e. inside the shaped particles, but ex situ, i.e. before the formation of particles.
  • this process offers a convenient way to make compositions of, for instance, ZSM-5 and boehmite, ZSM-5 and hydrotalcite, ZSM-5 and kaolin.
  • Aluminium sources which can suitably be used in the process according to the present invention include aluminium oxides and hydroxides such as transition alumina, aluminium trihydrate (BOC, gibbsite, bayerite) and its thermally treated forms (including flash-calcined aluminium trihydrate), alumina sol, alumina gel, amorphous alumina, and (pseudo)boehmite, aluminium chlorohydrol, aluminium nitrohydrol, alumina salts such as aluminium nitrate, aluminium chloride, aluminium chlorohydrate, sodium aluminate, aluminium phosphate, aluminium bearing clays including their calcined forms, and mixtures thereof.
  • Preferred aluminium sources are the aluminium oxides and hydroxides mentioned above, as these materials are relatively inexpensive. Moreover, these materials do not leave anions in the catalyst composition which either have to be washed out or will be emitted as environmentally harmful gases upon heating.
  • 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.
  • a silica sol is used that does not introduce sodium into the catalyst composition, such as an ammonium silica sol.
  • a divalent metal source is added in step (a).
  • Suitable divalent metal sources include magnesium, zinc, nickel, copper, iron, cobalt, manganese, calcium, barium, and combinations thereof.
  • a preferred divalent metal is magnesium.
  • Suitable zinc, nickel, copper, iron, cobalt, manganese, calcium, and barium sources are the respective oxides, hydroxides, carbonates, nitrates, chlorides, phosphates, titanates, and zirconates.
  • Suitable magnesium sources include magnesium oxides or hydroxides such as MgO, Mg(OH) 2 , hydromagnesite, magnesium salts such as magnesium acetate, magnesium formate, magnesium hydroxy acetate, magnesium carbonate, magnesium hydroxy carbonate, magnesium bicarbonate, magnesium nitrate, and magnesium chloride, magnesium-containing clays such as dolomite, saponite, hectorite, laponite, sepiolite, and mixtures thereof.
  • Suitable seeding materials include seeds and templates, such as faujasite-type seeds (zeolite X or Y), pentasil-type seeds (e.g. ZSM-5 seeds), amorphous seeds (e.g. amorphous Si-Al cogel), clays (e.g. bentonite, kaolin), milled zeolites with crystallites too small to be detected by X-ray diffraction techniques, and sols or gels containing an organic directing template like tetrapropyl ammonium hydroxide (TPAOH) or tetrapropyl ammonium bromide (TPABr).
  • TPAOH tetrapropyl ammonium hydroxide
  • TPABr tetrapropyl ammonium bromide
  • An example of such a template-containing sol is a Si-Al sol containing 0.1-10 wt% of tetrapropyl ammonium bromide.
  • additives may be present during step (a). These additives can be added to the mixture separately. On the other hand, it is also possible to use an aluminium source, a silicon source, a seeding material and/or a divalent metal source that is doped with such additives.
  • doped means that the desired additive (also called dopant) has been incorporated into the silicon source, aluminium source, divalent metal source, or seeding material, before the above process is performed, e.g. by preparing these metal sources or the seeding material in the presence of the desired dopant.
  • Suitable dopants are compounds comprising an element selected from the group of rare earth metals (for example La and Ce), Si, P, B, Group VI metals, Group VIII noble metals, alkaline earth metals (for instance Ca and Ba) and/or transition metals (for example Mn, Fe, Nb, Zn, Cr, Ti, Zr, Cu, Ni, Zn, Mo, W, V, Sn).
  • Suitable compounds are the oxides, hydroxides, carbonates, hydroxy- carbonates, chlorides, nitrates, sulfates, and phosphates of the above elements.
  • acids and bases can be added to adjust the pH.
  • the desired pH depends, e.g., on the type of other compound that is desired to be formed. For instance, if an anionic clay is the desired other compound, the slurry preferably has a pH above 6. If, on the other hand, boehmite is the desired other compound, the pH preferably is between about 4 and 8.
  • catalyst components can be added to the slurry before or during the hydrothermal treatment of step a). This will result in shaped bodies comprising an intimate mixture of these catalytic compounds with the pentasil- type zeolite and the other compound. It is preferred not to add such catalyst components after completion of step a) - i.e. after completion of the hydrothermal treatment - and before shaping step b).
  • Suitable catalyst components are metal traps, combustion promoters, zeolites other than pentasil-type zeolites, alumina-titania, titania, zirconia, clays, metal salts, and alkaline earth metal (hydr)oxides.
  • the slurry is treated hydrothermally.
  • Hydrothermal means under aqueous conditions at a temperature above 100°C and a pressure above atmospheric. Suitable temperatures for the process according to the present invention range from 100° to 300°C, preferably 100°-200°C. Most conveniently, autogeneous pressure is applied. If desired, more than one hydrothermal treatment is used.
  • the aluminium source, the silicon source, and the optional divalent metal source react in the presence of a suitable seeding material to form a pentasil- type zeolite and at least one other compound. If, apart form the seeding material, only a silicon and an aluminium source are used, an excess of aluminium source such as (thermally treated) aluminium trihydrate (e.g. flash-calcined aluminium trihydrate) will result in the formation of (pseudo)boehmite as the other compound.
  • a suitable seeding material to form a pentasil- type zeolite and at least one other compound.
  • aluminium source such as (thermally treated) aluminium trihydrate (e.g. flash-calcined aluminium trihydrate) will result in the formation of (pseudo)boehmite as the other compound.
  • the other compound will be an anionic clay and optionally - depending on the amount of aluminium source, the divalent metal source, and the reaction conditions - an aluminium (hydr)oxide and/or a divalent metal (hydr)oxide.
  • anionic clays can be formed, depending on the nature of the divalent metal. Typical examples are Mg-AI anionic clays, Zn-AI anionic clays, and Fe-AI anionic clays. It is noted that the term "anionic clay” is equivalent to the terms "hydrotalcite-like material" and "layered double hydroxide” frequently used in the prior art.
  • compositions comprising cationic clay can be formed.
  • cationic clays are smectites (Al-Mg-Si clays) such as saponite and montmorillonite.
  • compositions comprising zeolite and Si-Al cogel can be obtained by using a silicon source, an aluminium source, and a suitable seeding material, thereby controlling the Si-Al ratio, the amount of seeding material, and the reaction time to prevent complete conversion of the silicon and aluminium sources to zeolite.
  • the hydrothermal treatment can be conducted in one or more stages. If performed in one stage, the aluminium source, the silicon source, the seeding material, and the optional divalent metal source, additive, and other catalyst components are all added to the reactor before starting the hydrothermal treatment. If performed in two stages, one or more of the components are added during the hydrothermal treatment or in between two hydrothermal treatments.
  • a slurry comprising the aluminium source, the silicon source, and the seeding material are hydrothermally treated for a certain period of time in the first stage, thereby reacting at least partly to a pentasil-type zeolite.
  • a divalent metal source is added and the hydrothermal treatment is continued for an additional period of time, thereby forming an anionic clay and - if not already completed - completing the reaction to the pentasil-type zeolite.
  • the hydrothermal treatment can be conducted in one or a series of at least two reaction vessels. Preferably, this is done in a continuous process. If more than one reaction vessel is used, the aluminium source, the silicon source, the seeding material, and the optional divalent metal source, additive, and other catalyst components can all be added to the first vessel, but the addition of these sources can also be divided over the available reaction vessels.
  • the aluminium source and the silicon source can be mixed in the first reaction vessel to form a Si-AI cogel, the cogel and the zeolite seeds are introduced into a second reaction vessel and reacted at least partly to a pentasil-type zeolite, and the zeolite-containing slurry and a divalent metal source are finally introduced into a third reaction vessel wherein any excess of aluminium source is reacted with the divalent metal source to obtain an anionic clay.
  • aluminium source e.g. aluminium trihydrate or flash-calcined aluminium trihydrate
  • additional aluminium source e.g. aluminium trihydrate or flash-calcined aluminium trihydrate
  • the product formed during hydrothermal treatment is shaped.
  • 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 suspension used for shaping should be adapted to the specific shaping step to be conducted. It may be advisable to partially remove the liquid used in the suspension and/or add an additional or another liquid, and/or to change the pH of the precursor mixture to make the suspension 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 pentasil-type zeolite obtained during the present process preferably is a ZSM-type material, more preferably ZSM-5, ZSM-11 , ZSM-12, ZSM-22, ZSM- 23, ZSM-35, zeolite beta, or zeolite boron beta, which are described in U.S. Patent Nos.
  • compositions that can be obtained with the process according to the invention are: a composition comprising ZSM-5 and a Si-AI cogel, zeolite beta and Si-AI cogel, ZSM-5 and a Mg-AI anionic clay, zeolite beta and Mg-AI anionic clay, ZSM-5 and (pseudo)boehmite, zeolite beta and (pseudo)boehmite, ZSM-5, Mg-AI anionic clay and (pseudo)boehmite, zeolite beta, Mg-AI anionic clay and (pseudo)boehmite, ZSM-5 and smectite, zeolite beta and smectite, etc.
  • compositions may contain one or more additives, such as a phosphorus compound, or metal compounds.
  • Preferred metals include Ce, La, Mn, Fe, Nb, Zn, Cr, Ti, Zr, Cu, Ni, Zn, Mo, W, V, Sn, Pt, and Pd.
  • the composition preferably contains 5-95 wt% of pentasil-type zeolite, more preferably 20-80 wt% of pentasil-type zeolite, even more preferably 40-80 wt% of pentasil-type zeolite.
  • the catalyst compositions resulting from the process according to the invention may optionally be hydrothermally treated (e.g. in order to stabilise the zeolite), calcined and/or ion-exchanged with, for instance, rare-earth metals.
  • the catalyst compositions resulting from the process according to the invention can be calcined at temperatures between 200 and 1 ,000°C, preferably 300- 500°C.
  • an anionic clay is present in the catalyst composition, calcination will transform the anionic clay into a solid solution and optionally a spinel phase.
  • the solid solution can be transformed into an anionic clay again by rehydrating the calcined composition in an aqueous slurry.
  • this aqueous slurry may contain dissolved additives, e.g. salts of metals such as Ce, La, Mn, Fe, Nb, Zn, Cr, Ti, Zr, Cu, Ni, Zn, Mo, W, V, Sn, Pt, and Pd.
  • the resulting catalyst compositions can suitably be used as catalyst or additive in FCC processes.
  • the compositions according to the invention are suitable for the removal of SO x and/or NO x from flue gasses, reduction of the amount of sulfur and nitrogen in fuels such as gasoline and diesel, metal trapping, increasing the olefin content and reducing of the aromatics content of gasoline and light cycle oil, etc.
  • compositions comprising pentasil-type zeolite (e.g. ZSM-5, ZSM-11 , zeolite beta) and anionic clay (e.g. Mg-AI anionic clay) can lead to a product having a reduced yield of aromatics and an increased olefinicity.
  • pentasil-type zeolite e.g. ZSM-5, ZSM-11 , zeolite beta
  • anionic clay e.g. Mg-AI anionic clay
  • a seeding slurry (300 g, 14.1 w% solids) 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 ⁇ m. This seeding slurry was slowly added to the aluminium sulfate/water glass mixture under vehement stirring for 10 minutes. The resulting slurry was hydrothermally treated at 170°C for 4 hours.
  • the PXRD pattern of the spray-dried product showed the presence of ZSM-5 and hydrotalcite.
  • a seeding slurry (300 g, 14.1 w% solids) 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 ⁇ m. This seeding slurry was slowly added to the aluminium sulfate/water glass mixture under vehement stirring for 10 minutes. The resulting slurry was hydrothermally treated at 170°C for 4 hours. Then,500 g of an aqueous slurry (12 wt% solids) of flash-calcined aluminium gibbsite (Alcoa CP-3®) were pumped into the autoclave in 10 minutes. The resulting mixture was heated at 170°C for an additional hour and finally spray- dried.
  • Alcoa CP-3® flash-calcined aluminium gibbsite
  • the PXRD pattern of the spray-dried product showed the presence of ZSM-5 and boehmite.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Environmental & Geological Engineering (AREA)
  • Analytical Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Thermal Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Catalysts (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)

Abstract

Cette invention concerne la préparation d'une composition comprenant un zéolite de type pentasile, qui consiste à : a) traiter hydrothermiquement une suspension aqueuse épaisse comprenant une source d'aluminium, une source de silicium, un matériau d'ensemencement et éventuellement une source de métal divalent, pour former un zéolite de type pentasile et au moins un autre composé, et b) façonner le produit obtenu à l'opération a). Exemples d'au moins un autre composé susmentionné : argile anionique, argile cationique, cogel Si-Al, et (pseudo)boehmite.
PCT/EP2003/009181 2002-08-28 2003-08-19 Preparation de catalyseurs renfermant un zeolite de type pentasile WO2004020092A1 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
AU2003273799A AU2003273799A1 (en) 2002-08-28 2003-08-19 Process for the preparation of catalysts comprising a pentasil-type zeolite
CA002496899A CA2496899A1 (fr) 2002-08-28 2003-08-19 Preparation de catalyseurs renfermant un zeolite de type pentasile
EP03757760A EP1531932A1 (fr) 2002-08-28 2003-08-19 Preparation de catalyseurs renfermant un zeolite de type pentasile
JP2004532093A JP2005536342A (ja) 2002-08-28 2003-08-19 ペンタシル型ゼオライトを含む触媒の製造方法
BR0313746-5A BR0313746A (pt) 2002-08-28 2003-08-19 Processo para a preparação de catalisadores compreendendo um zeólito do tipo pentasila

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US40644502P 2002-08-28 2002-08-28
US60/406,445 2002-08-28
EP02079412.9 2002-10-24
EP02079412 2002-10-24

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WO2004020092A1 true WO2004020092A1 (fr) 2004-03-11

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JP (1) JP2005536342A (fr)
CN (1) CN1320960C (fr)
AU (1) AU2003273799A1 (fr)
BR (1) BR0313746A (fr)
CA (1) CA2496899A1 (fr)
WO (1) WO2004020092A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101119802B (zh) * 2004-12-21 2010-11-10 雅宝荷兰有限责任公司 Fcc催化剂及其制备和应用

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4376104A (en) * 1979-01-05 1983-03-08 The British Petroleum Company Limited Method for preparing crystalline aluminosilicates
US4430314A (en) * 1980-06-06 1984-02-07 Mobil Oil Corporation Method of preparing crystalline zeolite
WO2000044672A1 (fr) * 1999-01-29 2000-08-03 Akzo Nobel N.V. Procede de production hydrothermique d'argile anionique a l'aide de boehmite peptisee avec un acide inorganique
WO2002064504A1 (fr) * 2001-02-09 2002-08-22 Akzo Nobel N.V. Argiles anioniques dopees
WO2002064499A2 (fr) * 2001-02-09 2002-08-22 Akzo Nobel N.V. Procede de preparation de compositions renfermant de l'argile anionique et de la boehmite

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4376104A (en) * 1979-01-05 1983-03-08 The British Petroleum Company Limited Method for preparing crystalline aluminosilicates
US4430314A (en) * 1980-06-06 1984-02-07 Mobil Oil Corporation Method of preparing crystalline zeolite
WO2000044672A1 (fr) * 1999-01-29 2000-08-03 Akzo Nobel N.V. Procede de production hydrothermique d'argile anionique a l'aide de boehmite peptisee avec un acide inorganique
WO2002064504A1 (fr) * 2001-02-09 2002-08-22 Akzo Nobel N.V. Argiles anioniques dopees
WO2002064499A2 (fr) * 2001-02-09 2002-08-22 Akzo Nobel N.V. Procede de preparation de compositions renfermant de l'argile anionique et de la boehmite

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101119802B (zh) * 2004-12-21 2010-11-10 雅宝荷兰有限责任公司 Fcc催化剂及其制备和应用

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AU2003273799A1 (en) 2004-03-19
JP2005536342A (ja) 2005-12-02
EP1531932A1 (fr) 2005-05-25
CN1320960C (zh) 2007-06-13
BR0313746A (pt) 2005-07-19
CA2496899A1 (fr) 2004-03-11
CN1678393A (zh) 2005-10-05

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