ES2063920T3 - Procedimiento de preparacion de catalizadores de oxidacion a base de oxidos metalicos que contienen hierro, antimonio y fosforo. - Google Patents

Procedimiento de preparacion de catalizadores de oxidacion a base de oxidos metalicos que contienen hierro, antimonio y fosforo.

Info

Publication number
ES2063920T3
ES2063920T3 ES90306700T ES90306700T ES2063920T3 ES 2063920 T3 ES2063920 T3 ES 2063920T3 ES 90306700 T ES90306700 T ES 90306700T ES 90306700 T ES90306700 T ES 90306700T ES 2063920 T3 ES2063920 T3 ES 2063920T3
Authority
ES
Spain
Prior art keywords
containing iron
antimony
phosphorus
procedure
preparation
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.)
Expired - Lifetime
Application number
ES90306700T
Other languages
English (en)
Inventor
Yutaka C O Nitto Chem I Sasaki
Masato C O Nitto Chem In Otani
Hiroshi C O Nitto Chem Utsumi
Kazuo C O Nitto Chem Morishita
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nitto Chemical Industry Co Ltd
Original Assignee
Nitto Chemical Industry Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nitto Chemical Industry Co Ltd filed Critical Nitto Chemical Industry Co Ltd
Application granted granted Critical
Publication of ES2063920T3 publication Critical patent/ES2063920T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
    • C01C3/00—Cyanogen; Compounds thereof
    • C01C3/02—Preparation, separation or purification of hydrogen cyanide
    • C01C3/0208—Preparation in gaseous phase
    • C01C3/0212—Preparation in gaseous phase from hydrocarbons and ammonia in the presence of oxygen, e.g. the Andrussow-process
    • C01C3/0216—Preparation in gaseous phase from hydrocarbons and ammonia in the presence of oxygen, e.g. the Andrussow-process characterised by the catalyst used
    • 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
    • B01J23/002—Mixed oxides other than spinels, e.g. perovskite
    • 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
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14—Phosphorus; Compounds thereof
    • B01J27/185—Phosphorus; Compounds thereof with iron group metals or platinum group metals
    • B01J27/1853—Phosphorus; Compounds thereof with iron group metals or platinum group metals with iron, cobalt or nickel
    • 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
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14—Phosphorus; Compounds thereof
    • B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J27/188—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
    • 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
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14—Phosphorus; Compounds thereof
    • B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J27/195—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with vanadium, niobium or tantalum
    • B01J27/198—Vanadium
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
    • C01C3/00—Cyanogen; Compounds thereof
    • C01C3/02—Preparation, separation or purification of hydrogen cyanide
    • C01C3/0208—Preparation in gaseous phase
    • C01C3/0241—Preparation in gaseous phase from alcohols or aldehydes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00—Preparation of carboxylic acid nitriles
    • C07C253/24—Preparation of carboxylic acid nitriles by ammoxidation of hydrocarbons or substituted hydrocarbons
    • C07C253/26—Preparation of carboxylic acid nitriles by ammoxidation of hydrocarbons or substituted hydrocarbons containing carbon-to-carbon multiple bonds, e.g. unsaturated aldehydes
    • 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
    • B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Inorganic Chemistry (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

UN CATALIZADOR DE OXIDO METALICO CONTENIENDO HIERRO-ANTIMONIOFOSFORO PARA LA OXIDACION CATALITICA, COMPRENDIENDO UN ANTIMONATO DE HIERRO CRISTALINO, ESTANDO REPRESENTADO EL CATALIZADOR POR LA SIGUIENTE FORMULA EMPIRICA: EN LA QUE X REPRESENTA POR LO MENOS UN ELEMENTO SELECCIONADO DE UN GRUPO FORMADO POR V, MO Y W; Q REPRESENTA POR LO MENOS UN ELEMENTO SELECCIONADO DE UN GRUPO FORMADO POR LI, NA, K, RB, CS, BE, MG, CA, SR, BA, SC, Y, LA, CE, PR, ND, SM, TH, U, TI, ZR, HF, NB, TA, CR, MN, RE, CO, NI, RU, RH, PD, OS, IR, PT, CU, AG, AU, ZN, CD, HG, AL, GA, IN, TL, GE, SN Y PB; R REPRESENTA AL MENOS UN ELEMENTO SELECCIONADO DE UN GRUPO FORMADO POR B, AS, BI, SE Y TE; A, B, C, D, E, F, G Y H, CADA UNO ES UNA PROPORCION ATOMICA EN LA FORMA SIGUIENTE: A = DE 5 A 15 B = DE 5 A 100 C = DE 1 A 30 D = DE 0 A 10 E = DE 0 A 15 F = DE 0 A 10 H = DE 0 A 300 G ES UN NUMERO DE ATOMOS DE OXIGENO CONFORME A LO DETERMINADO CORRESPONDIENTE A LOS OXIDOS FORMADOS POR LA COMBINACION DE COMPONENTES ANTERIORMENTE MENCIONADOS; LA PROPORCION ATOMICA DE P/FE ES AL MENOS 0''3; LA PROPORCION ATOMICA DE P/SB ES AL MENOS 0''1; Y LA PROPORCION ATOMICA DE P/X ES AL MENOS 1 CUANDO D > 0.
ES90306700T 1989-06-23 1990-06-20 Procedimiento de preparacion de catalizadores de oxidacion a base de oxidos metalicos que contienen hierro, antimonio y fosforo. Expired - Lifetime ES2063920T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1159457A JP2950851B2 (ja) 1989-06-23 1989-06-23 鉄・アンチモン・リン含有金属酸化物触媒組成物およびその製法

Publications (1)

Publication Number Publication Date
ES2063920T3 true ES2063920T3 (es) 1995-01-16

Family

ID=15694183

Family Applications (1)

Application Number Title Priority Date Filing Date
ES90306700T Expired - Lifetime ES2063920T3 (es) 1989-06-23 1990-06-20 Procedimiento de preparacion de catalizadores de oxidacion a base de oxidos metalicos que contienen hierro, antimonio y fosforo.

Country Status (5)

Country Link
US (1) US5094990A (es)
EP (1) EP0404529B1 (es)
JP (1) JP2950851B2 (es)
DE (1) DE69012450T2 (es)
ES (1) ES2063920T3 (es)

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US5134105A (en) * 1990-03-19 1992-07-28 The Standard Oil Company Catalyst for propylene ammoxidation to acrylonitrile
JP3371112B2 (ja) * 1990-09-18 2003-01-27 ダイヤニトリックス株式会社 鉄・アンチモン含有金属酸化物触媒組成物およびその製法
TR27951A (tr) * 1992-06-23 1995-11-08 Standard Oil Co Ohio Akrilonitrile propilen amoksidasyonu icin gelistirilmis bir islem ve katalizör.
JP4310389B2 (ja) * 1997-03-07 2009-08-05 サントリーホールディングス株式会社 新規泡蛋白質及びその利用
JP3506872B2 (ja) * 1997-03-13 2004-03-15 三菱レイヨン株式会社 青酸の製造方法
US5840648A (en) * 1997-09-02 1998-11-24 The Standard Oil Company Catalyst for the manufacture of acrylonitrile and hydrogen cyanide
DE19743621C1 (de) * 1997-10-02 1999-03-25 Rwe Dea Ag Verfahren zur Herstellung von Aldehyden und Carbonsäuren durch Oxidation primärer Alkohole
JP3875023B2 (ja) * 1998-02-13 2007-01-31 コリア リサーチ インスティチュート オブ ケミカル テクノロジイ コアー殻触媒相の固形触媒とその製造方法
DE19815279A1 (de) * 1998-04-06 1999-10-07 Basf Ag Multimetalloxidmassen
US6479691B1 (en) * 1998-04-23 2002-11-12 Mitsubishi Rayon Co., Ltd. Catalyst for producing unsaturated nitrile
CA2363035C (en) * 1999-02-22 2007-09-04 Symyx Technologies, Inc. Compositions comprising nickel and their use as catalyst in oxidative dehydrogenation of alkanes
US6436871B1 (en) * 1999-02-22 2002-08-20 Symyx Technologies, Inc. Catalysts for oxidative dehydrogenation
US6355854B1 (en) 1999-02-22 2002-03-12 Symyx Technologies, Inc. Processes for oxidative dehydrogenation
JP2001029788A (ja) * 1999-07-21 2001-02-06 Mitsubishi Rayon Co Ltd モリブデン−ビスマス−鉄含有金属酸化物流動層触媒の製法
JP3262324B2 (ja) * 1999-09-22 2002-03-04 科学技術振興事業団 低級アルコール部分酸化物の製造方法
JP3819192B2 (ja) * 1999-10-18 2006-09-06 ダイヤニトリックス株式会社 アクリロニトリルの製造法
US6723869B1 (en) 1999-10-18 2004-04-20 Mitsubishi Rayon Co., Ltd. Method for producing acrylonitrile, catalyst for use therein and method for preparing the same
US6407280B1 (en) 2000-09-28 2002-06-18 Rohm And Haas Company Promoted multi-metal oxide catalyst
US6677497B2 (en) 2001-03-22 2004-01-13 Symyx Technologies, Inc. Ni catalysts and methods for alkane dehydrogenation
JP4159759B2 (ja) * 2001-04-13 2008-10-01 ダイヤニトリックス株式会社 モリブデン−ビスマス−鉄含有複合酸化物流動層触媒の製法
JP4030740B2 (ja) * 2001-10-11 2008-01-09 ダイヤニトリックス株式会社 アンモ酸化用触媒の製造方法
US6916763B2 (en) * 2002-11-27 2005-07-12 Solutia Inc. Process for preparing a catalyst for the oxidation and ammoxidation of olefins
JP4242197B2 (ja) * 2003-04-18 2009-03-18 ダイヤニトリックス株式会社 アクリロニトリル合成用触媒
US7649112B2 (en) 2005-07-25 2010-01-19 Saudi Basic Industries Corporation Integrated plant for producing 2-ethyl-hexanol and methacrylic acid and a method based thereon
US7851397B2 (en) * 2005-07-25 2010-12-14 Saudi Basic Industries Corporation Catalyst for methacrolein oxidation and method for making and using same
US7732367B2 (en) * 2005-07-25 2010-06-08 Saudi Basic Industries Corporation Catalyst for methacrolein oxidation and method for making and using same
US7649111B2 (en) * 2005-07-25 2010-01-19 Saudi Basic Industries Corporation Catalyst for the oxidation of a mixed aldehyde feedstock to methacrylic acid and methods for making and using same
US7799946B2 (en) * 2007-02-14 2010-09-21 Saudi Basic Industries Corporation Process for separating methacrolein from methacrylic acid in a gas phase product from the partial oxidation of isobutene
JP5011176B2 (ja) * 2008-03-14 2012-08-29 ダイヤニトリックス株式会社 アクリロニトリル合成用触媒およびアクリロニトリルの製造方法
FR2931477B1 (fr) * 2008-05-21 2012-08-17 Arkema France Acide cyanhydrique derive de matiere premiere renouvable
FR2938838B1 (fr) 2008-11-27 2012-06-08 Arkema France Procede de fabrication d'un methacrylate de methyle derive de la biomasse
JP5560642B2 (ja) 2009-10-09 2014-07-30 三菱レイヨン株式会社 複合酸化物触媒の製造方法
JP5609254B2 (ja) * 2010-05-14 2014-10-22 三菱レイヨン株式会社 複合酸化物触媒の製造方法
US8921257B2 (en) 2011-12-02 2014-12-30 Saudi Basic Industries Corporation Dual function partial oxidation catalyst for propane to acrylic acid conversion
US8722940B2 (en) 2012-03-01 2014-05-13 Saudi Basic Industries Corporation High molybdenum mixed metal oxide catalysts for the production of unsaturated aldehydes from olefins
JP6357047B2 (ja) * 2014-08-05 2018-07-11 広栄化学工業株式会社 ニトリル化合物の製造方法
TWI781916B (zh) 2016-01-09 2022-11-01 美商阿散德性能材料營運公司 用於在丙烯腈反應器饋入流中氰化氫之直接製備的催化劑組合物及方法
CN107684927B (zh) * 2016-08-03 2020-07-28 万华化学集团股份有限公司 一种用于氯化氢氧化制备氯气的催化剂及其制备方法和用途
CN114100652B (zh) * 2021-12-10 2023-10-13 北京道思克矿山装备技术有限公司 一种甲醇气相催化氨氧化生产氰化氢的催化剂及其制备方法和应用

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JPH0764555B2 (ja) * 1988-04-05 1995-07-12 日東化学工業株式会社 青酸製法

Also Published As

Publication number Publication date
EP0404529A1 (en) 1990-12-27
US5094990A (en) 1992-03-10
DE69012450T2 (de) 1995-03-02
EP0404529B1 (en) 1994-09-14
JP2950851B2 (ja) 1999-09-20
JPH0326342A (ja) 1991-02-04
DE69012450D1 (de) 1994-10-20

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