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WO2011104170A1 - Catalyseurs chargés de métal précieux thermiquement et mécaniquement stables - Google Patents

Catalyseurs chargés de métal précieux thermiquement et mécaniquement stables Download PDF

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Publication number
WO2011104170A1
WO2011104170A1 PCT/EP2011/052396 EP2011052396W WO2011104170A1 WO 2011104170 A1 WO2011104170 A1 WO 2011104170A1 EP 2011052396 W EP2011052396 W EP 2011052396W WO 2011104170 A1 WO2011104170 A1 WO 2011104170A1
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WIPO (PCT)
Prior art keywords
compounds
supported catalyst
catalyst according
catalyst
support
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2011/052396
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English (en)
Inventor
Shingo Watanabe
Jason Carson
Jimmy Lile Thorn
Venugopal Arunajatesan
Michael GRÜN
Baoshu Chen
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Evonik Operations GmbH
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Evonik Degussa GmbH
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Publication of WO2011104170A1 publication Critical patent/WO2011104170A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/58—Platinum group metals with alkali- or alkaline earth metals
    • 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
    • B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/08—Silica
    • 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
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/60—Platinum group metals with zinc, cadmium or mercury
    • 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
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/63—Platinum group metals with rare earths or actinides
    • 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
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/64—Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/652—Chromium, molybdenum or tungsten
    • B01J23/6525—Molybdenum
    • 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
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/66—Silver or gold
    • 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
    • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
    • B01J23/8933—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/8946—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with alkali or alkaline earth metals
    • 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
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/03—Precipitation; Co-precipitation
    • B01J37/031—Precipitation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/04—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds
    • C07C67/05—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds with oxidation
    • C07C67/055—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds with oxidation in the presence of platinum group metals or their compounds

Definitions

  • Catalyst comprising palladium, gold and alkali metal acetate as catalytically active components on an abrasion-resistant support, which is mechanically and thermally stable, shaped bodies that are produced from synthetically pure and mixed metal oxides which may be also modified by means of aluminum, calcium, cerium, iron, lanthanum, magnesium, molybdenum, titanium, yttrium and/or zirconium or oxides thereof. It can be used for preparing vinyl acetate monomer.
  • the invention relates to a catalyst, a process for producing a catalyst which covers a catalyst form with an outer shell containing metal(s).
  • Such catalysts are useful for example, for vinyl acetate monomers (VAM) production.
  • Processes for preparing vinyl acetate monomer are known from DE 16 68 088, EP-A 0 464 633, EP-A-0 519 435, EP-A 0 634 208, EP-A 0 723 810, EP-A 0 634 209, EP-A 0 632 214, EP-A 0 654 301 , EP-A 0 723 810, U.S. Pat. No. 4,048,096, U.S. Pat. No. 5,185,308 and U.S. Pat. No. 5,371 ,277. These documents also describe processes for producing supported catalysts. Depending on the embodiment, supported catalysts having a homogeneous distribution of noble metal over the cross section of the support and catalyst having a more or less pronounced shell profile are produced.
  • These catalysts are usually obtained by impregnating the support with a basic solution and a solution containing gold and palladium salts, with the impregnations occurring simultaneously or in succession, with or without intermediate drying.
  • the support is subsequently washed to remove any chloride present. Before or after washing, the insoluble noble metal compounds precipitated on the support are reduced.
  • the catalyst precursor obtained in this way is dried and impregnated with alkal i metal acetates or alkali metal compounds which are converted completely or partly into alkali metal acetates under the reaction conditions in the production of vinyl acetate monomer in order to activate the catalyst.
  • Preferred alkali metal compounds are potassium compounds, in particular potassium acetate.
  • the reduction of the catalyst can be carried out in the aqueous phase or in the gas phase.
  • suitable reducing agents are, for example, formaldehyde or hydrazine.
  • the reduction in the gas phase can be effected using hydrogen or a hydrogen/nitrogen mixture (95% by volume of N 2 +5% by weight of H 2 ) or ethylene.
  • the reduction is carried out using hydrogen at temperatures in the range from 40 to 260 °C, preferably from 70 to 200 °C.
  • the catalyst is frequently reduced by means of ethylene directly in the production reactor only after ac t i v a t i o n b y m e a n s o f a l k a l i m e t a l a c e t a t e .
  • the catalyst is firstly supplied only slowly with the reactants. During this start-up phase, the activity of the catalyst increases and usually reaches its final level only after days or weeks.
  • the document EP 0 431 478 describes a process for preparing vinyl acetate in the gas phase from ethylene, acetic acid and oxygen over a catalyst containing palladium and gold on a support.
  • the support comprises a Si0 2 /Al 2 0 3 mixture, with the support particles being pressed with the aid of Li, Mg, Al, Zn or Mn salts of a C-2-C-2o-carboxylic acid as binder.
  • the document EP 0 723 81 0 A1 describes a supported catalyst for the production of vinyl acetate monomer, which contains palladium, gold, and alkali metal acetate as catalytically active components on a support composed of silicon dioxide, silicon dioxide gel, aluminosilicate or aluminium oxide, with the support additionally containing at least one element of groups I A, II A, III A and IV B of the Periodic Table.
  • Supported catalysts containing gold, palladium and alkali metal compounds are used for the production of vinyl acetate.
  • ethylene, acetic acid and molecular oxygen or air are reacted in the gas phase, with or without addition of inert gases, at temperatures in the range from 100 to 250 °C and under ambient or super atmospheric pressure in the presence of the supported catalyst.
  • WO 2008145389 US 2003187293, US 6072078 and WO 9962634 disclose the use of shaped bodies based on natural silicon dioxide-based support for catalysts preparation.
  • pyrogenic SiO 2 -based support shows crush strength 10 - 250 Newton and abrasion ⁇ 5 wt%.
  • crush strength is 20 - 40 Newton.
  • Catalyst prepared using a support based on synthetic material, especially spherical shape, gives rise to less abrasion problems when loading catalyst into a tubular reactor. Mechanical strength and thermal stability of a catalyst prepared on a synthetic-based material still remained a problem for prolonged operation stability using the existing technology.
  • the objective of this invention is to provide a catalyst that can maintain its performance after exposure to high abrasion or impact forces similar to those experienced when loading catalyst in a tubular reactor, said catalyst should also exhibit high thermal stability.
  • the catalysts according to the invention are particularly useful for vinyl acetate monomer production.
  • the catalyst according to the invention is a supported catalyst comprising a support molding and a catalytically active component,
  • the catalytically active component comprises at least one member selected from the group consisting of palladium and palladium compounds, at least one alkali metal compounds and at least one member selected from the group consisting of gold, gold compounds, aluminum, alumina compounds, cadmium, barium, barium compounds, cadmium compounds, calcium, calcium compounds, cerium, cerium compounds, copper, copper compounds, iron, iron compounds, lanthanum, lanthanum compounds, magnesium, magnesium compounds, molybdenum, molybdenum compounds, titanium, titanium
  • the support molding comprises a synthetically produced precipitated pure or mixed oxide.
  • Precipitated pure or mixed oxide are oxides chosen from the group consisting of Aluminium, Zirconium, Titanium or Cerium or mixtures thereof.
  • the catalyst of the invention has the advantage to avoid the problem of catalyst abrasion and thermal stability while maintaining its maximum catalytic activity.
  • catalysts having a homogeneous noble metal distribution over the cross section of the support and catalysts having a more or less pronounced shell profile are obtained.
  • the supported catalyst according to the invention is a shell type catalyst.
  • a shell type catalyst is a catalyst comprising a support and a catalytcally active component that is deposited onto the support in the form of an outer shell which partially or completely encases the support.
  • the invention preferably provides a shell-type catalyst comprising e.g. palladium, gold and al kal i metal acetate as catalytical ly active com ponents on a mechanically and thermally stable synthetic support, such as precipitated S1O2, S1O2 gel, Zr0 2 , other metal oxides, SiC and metal oxide mixture, for example aluminosilicate.
  • a shell-type catalyst comprising e.g. palladium, gold and al kal i metal acetate as catalytical ly active com ponents on a mechanically and thermally stable synthetic support, such as precipitated S1O2, S1O2 gel, Zr0 2 , other metal oxides, SiC and metal oxide mixture, for example aluminosilicate.
  • the supported catalyst preferably comprises precipitated pure or mixed oxide which is selected from one or more of the group consisting of S1O2, Si02 gel, AI2O3, ⁇ 2 and Zr0 2 in any desired combination but with the exception of S1O2/AI2O3 mixed oxides, in which at least 75wt.% of S1O2 is present.
  • At least 90 wt.% of the precipitated pure or mixed oxide is S1O2. Even more preferably at least 95 wt.% of the precipitated pure or mixed oxide is S1O2 and most preferably at least 98 wt.% of the precipitated pure or mixed oxide is Si0 2 .
  • Precipitated oxides are known in the art.
  • the synthesis process for e.g.
  • Precipitated silica is prepared by pH swing precipitation of Na silicate.
  • the catalyst when charged into the tubular reactor causes catalyst abrasion due to the length of the reactor (generally 6-8 m long). Attrition and abrasion of mechanically unstable catalyst result in reduction of activity due to loss of outer layer which consists of metals especially for the shell-type catalyst. Mechanically stable catalysts can avoid losing active sites during catalyst loading. Similarly a catalyst with low crushing strength can break during loading causing high pressure drop across the catalyst bed.
  • the supported catalyst according to the invention thus preferably exhibits abrasion of less than 1 wt%. Abrasion is measured according to ASTM D 4058- 96.
  • the crushing strength of a single bead of the supported catalyst according to the invention is preferably at least 100 N, more preferably at least 251 N and most preferably at least 260 N.
  • the crushing strength is measured according to ASTM D 4179.
  • the bulk crush strength of the supported catalyst according to the invention is preferably less than 5 wt% at 950 N.
  • the bulk crush strength of the supported catalyst is measured according to ASTM D 7084.
  • the supported catalyst exhibits less than 10% reduction of the BET surface area at temperatures higher than 500 °C for at least 30 min. More preferably the supported catalyst exhibits less than 10% reduction of the BET surface area at temperatures higher than 500 °C for at least 120min.
  • the average pore diameter of at least 50% of the pore volume of the supported catalyst is larger than 3 nm.
  • At least 50% of the pore volume of the supported catalyst according to the invention is contained in major mode of the pore size distribution.
  • BET surface area, pore volume and average pore diameter are determined by nitrogen adsorption-desorption method.
  • the invention further provides a process for producing the catalyst.
  • Said process is characterized in that the support molding is impregnated with or without a salt of at least one doping component, calcined and subsequently impregnated with the catalytically active component or the support material is mixed with an oxide of the doping component, shaped and subsequently impregnated with the catalytically active components.
  • Calcination is a thermal treatment carried out at temperatures between 200°C and 1000°C, e.g. 450°C for 20min to 4h, e.g. 1 h.
  • This precipitated silica support enables to achieve the aforementioned supported catalyst due to its excellent mechanical strength. Pyrogenic or natural S1O2 have insufficient mechanical strength.
  • the precipitated pure or mixed oxide leads t o a thermally stable and mechanically strong support that is used for the catalyst preparation with the catalytically active component.
  • the catalyst stability is maintained under exposure to high temperatures in the range from 100°C to 1000°C, preferably 300°C to 900°C during the catalyst preparation and of course when the catalyst is used in a reaction.
  • the present invention also encompasses a process for producing vinyl acetate monomer in the presence of the supported catalyst as described above.
  • ethylene, acetic acid and molecular oxygen or air are reacted in the gas phase, with or without addition of inert gases, at temperatures in the range from 100°C to 250 °C and under ambient or super atmospheric pressure in the presence of the supported catalyst according to the present invention.
  • the support material of example catalyst A comprises high purity precipitated silicon dioxide support with a particle diameter of about 5 mm.
  • the high purity S1O 2 is made by Fuji silysia.
  • Catalytically active components are palladium, gold and potassium acetate.
  • Comparative catalyst B also comprises the active components palladium, gold and potassium acetate applied to a spherical natural silica support with diameters of about 5 mm (Sud Chemie KA-160).
  • the active components palladium, gold and potassium acetate were applied to a support material comprising 1 00% of pyrogenic silicon dioxide (Degussa Aerolyst 3045).
  • test results of physical properties of catalyst support example A, B and C are disclosed in Table 1 and Table 2.
  • BET surface area, pore volume and average pore diameter were determined by nitrogen adsorption-desorption method.
  • the resistance of the support and the supported catalyst to abrasion was quantified by weighing the material before and after a period of abrasion in an apparatus, which complies to ASTM D 4058-96.
  • Crushing strength of the individual catalyst support and supported catalyst particle was implemented by following ASTM D 4179.
  • the bulk crush strength of the supported catalyst was measured by complying ASTM D 7084.
  • Example A is mechanically stronger than others. Fine powder was found at the end of the abrasion test for Example B and C. It is often reported that similar fine powder has been typically observed when loading catalyst in a tubular reactor. Fine powder was not observed after the abrasion test of Example A for 60 hours.
  • Table 2 reports the space time yield of vinyl acetate monomer as measure of the activity of the catalysts in gram of vinyl acetate monomer per hour at 150 °C, a pressure of 5 bar and a GHSV of 5000 h ⁇ 1 :
  • the results of the catalyst evaluation are shown in Table 2.
  • the results show that space time yield (STY) of a catalyst comprising precipitated S1O2 support is superior to catalysts comprising natural S1O2 and pyrogenic S1O2.
  • the catalyst evaluation after the attrition test show a distinct lessening of the STY to the catalyst comprising spherical natural S1O2 when compared to the catalyst prepared using spherical precipitated Si0 2 .
  • Example A 13 13.3 0.75 20.3 > 275 ⁇ 0.0

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

L'invention porte sur un catalyseur comprenant du palladium, de l'or et un acétate de métal alcalin en tant que composants catalytiquement actifs sur un support résistant à l'abrasion, qui est constitué de corps façonnés mécaniquement et thermiquement stables qui sont produits à partir d'oxydes métalliques purs et mélangés synthétiques qui peuvent également être modifiés par de l'aluminium, du calcium, du cérium, du fer, du lanthane, du magnésium, du molybdène, du titane, de l'yttrium et/ou du zirconium ou des oxydes de ceux-ci. Il peut être utilisé pour la préparation de monomère acétate de vinyle.
PCT/EP2011/052396 2010-02-24 2011-02-18 Catalyseurs chargés de métal précieux thermiquement et mécaniquement stables Ceased WO2011104170A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US30782610P 2010-02-24 2010-02-24
US61/307,826 2010-02-24

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WO2011104170A1 true WO2011104170A1 (fr) 2011-09-01

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106582872A (zh) * 2015-10-19 2017-04-26 中国石油化工股份有限公司 合成乙烯法醋酸乙烯所用的催化剂
CN107282105A (zh) * 2016-04-12 2017-10-24 中国石油化工股份有限公司 不饱和醋酸酯催化剂及其制备方法

Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1668088A1 (de) 1968-02-01 1971-07-29 Bayer Ag Verfahren zur Herstellung von Vinylacetat
US4048096A (en) 1976-04-12 1977-09-13 E. I. Du Pont De Nemours And Company Surface impregnated catalyst
DE2100778B2 (de) 1971-01-08 1977-11-17 Hoechst Ag, 6000 Frankfurt Verfahren zur herstellung der ester ungesaettigter alkohole
US4902823A (en) 1988-02-09 1990-02-20 Hoechst Aktiengesellschaft Process for the preparation of vinyl acetate
EP0431478A2 (fr) 1989-12-05 1991-06-12 Hoechst Aktiengesellschaft Procédé de préparation de l'acétate de vinyle
EP0464633A1 (fr) 1990-07-03 1992-01-08 Kuraray Co., Ltd. Catalyseur et procédé de production des esters insaturés
EP0519435A1 (fr) 1991-06-21 1992-12-23 Hoechst Aktiengesellschaft Catalyseur supporté, son procédé de préparation ainsi que son utilisation pour la préparation d'acétate de vinyle
US5185308A (en) 1991-05-06 1993-02-09 Bp Chemicals Limited Catalysts and processes for the manufacture of vinyl acetate
US5225388A (en) * 1989-12-05 1993-07-06 Hoechst Aktiengesellschaft Method for making a catalyst
EP0632214A1 (fr) 1993-06-29 1995-01-04 Fuji Photo Film Co., Ltd. Mécanisme de transmission à courroie
EP0634208A1 (fr) 1993-07-16 1995-01-18 Hoechst Aktiengesellschaft Catalyseur sur support, procédé pour le préparer ainsi que son utilisation pour la préparation de l'acétate de vinyle
EP0634209A1 (fr) 1993-07-16 1995-01-18 Hoechst Aktiengesellschaft Catalyseur, procédé pour le préparer ainsi que son utilisation pour la préparation de l'acétate de vinyle
EP0654301A1 (fr) 1993-11-19 1995-05-24 BP Chemicals Limited Procédé de préparation de catalyseurs utilisable pour la production de l'acétate de vinyle
JPH07196309A (ja) 1993-12-28 1995-08-01 Fuji Silysia Chem Ltd シリカゾル、シリカ被膜及びシリカ粉体並びにそれらの製造方法
EP0723810A1 (fr) 1995-01-23 1996-07-31 Degussa Aktiengesellschaft Catalyseur, procédé pour sa préparation et son utilisation pour la production du monomère d'acétate de vinyle
JPH08333112A (ja) 1995-06-02 1996-12-17 Fuji Silysia Chem Ltd シリカゾル又はシリカゲルの製造方法
EP0807615A1 (fr) 1996-05-17 1997-11-19 Degussa Aktiengesellschaft Comprimé à base de SiO2 preparé par pyrogénation
EP0916402A1 (fr) 1997-11-13 1999-05-19 Degussa Ag Comprimé à base de dioxyde de silicium préparé par pyrogénation
WO1999062634A1 (fr) 1998-06-02 1999-12-09 Celanese International Corporation Catalyseur pour acetate de vinyle a base de palladium, du cuivre et de l'or a l'etat metallique, et preparation de ce catalyseur
EP0987058A1 (fr) 1998-06-26 2000-03-22 Degussa-Hüls Aktiengesellschaft Corps moulés à base de dioxyde de silicium
EP0997192A1 (fr) 1998-09-24 2000-05-03 Degussa-Hüls Aktiengesellschaft Catalyseur supporté pour la production du monomère d'acétate de vinyle
US6072078A (en) 1997-12-12 2000-06-06 Celanese International Corporation Vinyl acetate production using a catalyst comprising palladium, gold, copper and any of certain fourth metals
JP2000169134A (ja) 1998-12-09 2000-06-20 Fuji Silysia Chemical Ltd 球状シリカの製造方法
US6207610B1 (en) 1996-05-17 2001-03-27 Degussa-Huls Ag Compacts based on pyrogenically produced silicon dioxide
EP1205246A1 (fr) * 2000-11-09 2002-05-15 Dairen Chemical Corporation Procédé de préparation de catalyseurs et leurs utilisations pour la production d'acétates d'alkènyle
EP1323469A2 (fr) 2001-12-21 2003-07-02 Degussa AG Catalyseur supporté
US20030187293A1 (en) 2002-03-27 2003-10-02 Peter Birke Process for preparing a catalyst, the catalyst and a use of the catalyst
US20080146721A1 (en) * 2006-12-19 2008-06-19 Kaminsky Mark P Inorganic oxide extrudates
WO2008145389A2 (fr) 2007-05-31 2008-12-04 Süd-Chemie AG Catalyseur sous enveloppe servant à la production de vam, procédé de production et d'utilisation dudit catalyseur

Patent Citations (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1668088A1 (de) 1968-02-01 1971-07-29 Bayer Ag Verfahren zur Herstellung von Vinylacetat
DE2100778B2 (de) 1971-01-08 1977-11-17 Hoechst Ag, 6000 Frankfurt Verfahren zur herstellung der ester ungesaettigter alkohole
US4048096A (en) 1976-04-12 1977-09-13 E. I. Du Pont De Nemours And Company Surface impregnated catalyst
US4902823A (en) 1988-02-09 1990-02-20 Hoechst Aktiengesellschaft Process for the preparation of vinyl acetate
US5225388A (en) * 1989-12-05 1993-07-06 Hoechst Aktiengesellschaft Method for making a catalyst
EP0431478A2 (fr) 1989-12-05 1991-06-12 Hoechst Aktiengesellschaft Procédé de préparation de l'acétate de vinyle
EP0464633A1 (fr) 1990-07-03 1992-01-08 Kuraray Co., Ltd. Catalyseur et procédé de production des esters insaturés
US5371277A (en) 1990-07-03 1994-12-06 Kuraray Co., Ltd. Carrier, catalyst and process for producing unsaturated ester
US5185308A (en) 1991-05-06 1993-02-09 Bp Chemicals Limited Catalysts and processes for the manufacture of vinyl acetate
EP0519435A1 (fr) 1991-06-21 1992-12-23 Hoechst Aktiengesellschaft Catalyseur supporté, son procédé de préparation ainsi que son utilisation pour la préparation d'acétate de vinyle
US5250487A (en) 1991-06-21 1993-10-05 Hoechst Aktiengesellschaft Carrier catalyst, process for its preparation, and its use for the preparation of vinyl acetate
US5292931A (en) 1991-06-21 1994-03-08 Hoechst Aktiengesellschaft Carrier catalyst, process for its preparation, and its use for the preparation of vinyl acetate
EP0632214A1 (fr) 1993-06-29 1995-01-04 Fuji Photo Film Co., Ltd. Mécanisme de transmission à courroie
EP0634208A1 (fr) 1993-07-16 1995-01-18 Hoechst Aktiengesellschaft Catalyseur sur support, procédé pour le préparer ainsi que son utilisation pour la préparation de l'acétate de vinyle
EP0634209A1 (fr) 1993-07-16 1995-01-18 Hoechst Aktiengesellschaft Catalyseur, procédé pour le préparer ainsi que son utilisation pour la préparation de l'acétate de vinyle
EP0654301A1 (fr) 1993-11-19 1995-05-24 BP Chemicals Limited Procédé de préparation de catalyseurs utilisable pour la production de l'acétate de vinyle
JPH07196309A (ja) 1993-12-28 1995-08-01 Fuji Silysia Chem Ltd シリカゾル、シリカ被膜及びシリカ粉体並びにそれらの製造方法
JP3658416B2 (ja) 1993-12-28 2005-06-08 富士シリシア化学株式会社 シリカゾル、シリカ被膜及びシリカ粉体並びにそれらの製造方法
EP0723810A1 (fr) 1995-01-23 1996-07-31 Degussa Aktiengesellschaft Catalyseur, procédé pour sa préparation et son utilisation pour la production du monomère d'acétate de vinyle
US5808136A (en) 1995-01-23 1998-09-15 Degussa Aktiengesellschaft Catalyst, method of its production and its use for the production of vinyl acetate monomer
JPH08333112A (ja) 1995-06-02 1996-12-17 Fuji Silysia Chem Ltd シリカゾル又はシリカゲルの製造方法
EP0807615A1 (fr) 1996-05-17 1997-11-19 Degussa Aktiengesellschaft Comprimé à base de SiO2 preparé par pyrogénation
US6207610B1 (en) 1996-05-17 2001-03-27 Degussa-Huls Ag Compacts based on pyrogenically produced silicon dioxide
EP0916402A1 (fr) 1997-11-13 1999-05-19 Degussa Ag Comprimé à base de dioxyde de silicium préparé par pyrogénation
US6072078A (en) 1997-12-12 2000-06-06 Celanese International Corporation Vinyl acetate production using a catalyst comprising palladium, gold, copper and any of certain fourth metals
WO1999062634A1 (fr) 1998-06-02 1999-12-09 Celanese International Corporation Catalyseur pour acetate de vinyle a base de palladium, du cuivre et de l'or a l'etat metallique, et preparation de ce catalyseur
EP0987058A1 (fr) 1998-06-26 2000-03-22 Degussa-Hüls Aktiengesellschaft Corps moulés à base de dioxyde de silicium
EP0997192A1 (fr) 1998-09-24 2000-05-03 Degussa-Hüls Aktiengesellschaft Catalyseur supporté pour la production du monomère d'acétate de vinyle
JP2000169134A (ja) 1998-12-09 2000-06-20 Fuji Silysia Chemical Ltd 球状シリカの製造方法
EP1205246A1 (fr) * 2000-11-09 2002-05-15 Dairen Chemical Corporation Procédé de préparation de catalyseurs et leurs utilisations pour la production d'acétates d'alkènyle
EP1323469A2 (fr) 2001-12-21 2003-07-02 Degussa AG Catalyseur supporté
US20030187293A1 (en) 2002-03-27 2003-10-02 Peter Birke Process for preparing a catalyst, the catalyst and a use of the catalyst
US20080146721A1 (en) * 2006-12-19 2008-06-19 Kaminsky Mark P Inorganic oxide extrudates
WO2008145389A2 (fr) 2007-05-31 2008-12-04 Süd-Chemie AG Catalyseur sous enveloppe servant à la production de vam, procédé de production et d'utilisation dudit catalyseur

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106582872A (zh) * 2015-10-19 2017-04-26 中国石油化工股份有限公司 合成乙烯法醋酸乙烯所用的催化剂
CN107282105A (zh) * 2016-04-12 2017-10-24 中国石油化工股份有限公司 不饱和醋酸酯催化剂及其制备方法
CN107282105B (zh) * 2016-04-12 2020-04-17 中国石油化工股份有限公司 不饱和醋酸酯催化剂及其制备方法

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