BR0300752A - Processo produtivo para aldeìdo insaturado - Google Patents

Processo produtivo para aldeìdo insaturado

Info

Publication number
BR0300752A
BR0300752A BR0300752-9A BR0300752A BR0300752A BR 0300752 A BR0300752 A BR 0300752A BR 0300752 A BR0300752 A BR 0300752A BR 0300752 A BR0300752 A BR 0300752A
Authority
BR
Brazil
Prior art keywords
catalyst
reaction
density
unsaturated
catalysts
Prior art date
Application number
BR0300752-9A
Other languages
English (en)
Other versions
BR0300752B1 (pt
Inventor
Hiromi Yunoki
Original Assignee
Nippon Catalytic Chem Ind
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 Nippon Catalytic Chem Ind filed Critical Nippon Catalytic Chem Ind
Publication of BR0300752A publication Critical patent/BR0300752A/pt
Publication of BR0300752B1 publication Critical patent/BR0300752B1/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/37Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/002Mixed oxides other than spinels, e.g. perovskite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/85Chromium, molybdenum or tungsten
    • B01J23/88Molybdenum
    • B01J23/887Molybdenum containing in addition other metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/8876Arsenic, antimony or bismuth
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00Catalysts, in general, characterised by their form or physical properties
    • B01J35/30Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
    • B01J35/31Density
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/33Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
    • C07C45/34Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
    • C07C45/35Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds in propene or isobutene
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/25Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
    • C07C51/252Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2523/00Constitutive chemical elements of heterogeneous catalysts
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/0009Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02Impregnation, coating or precipitation
    • B01J37/0236Drying, e.g. preparing a suspension, adding a soluble salt and drying

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

"PROCESSO PRODUTIVO PARA ALDEìDO INSATURADO". A presente invenção proporciona um processo no qual, quando um aldeído insaturado e/ou um ácido carboxílico insaturado é (são) produzido (s) , por condução de uma reação de oxidação em fase gasosa catalítica por uso de um reator multitubular de leito fixo, que é recheado com um catalisador contendo molibdênio, a deterioração do catalisador localizado em uma parte de ponto quente pode ser eliminada, de modo que a reação pode ser continuada por um longo tempo, enquanto um alto rendimento é mantido, independentemente de onde ocorre a parte de ponto quente e também mesmo se a concentração de um gás bruto seja alta. Um óxido e/ou um óxido complexo, incluindo molibdênio, bismuto e ferro como os componentes essenciais, é(são) usado(s) como os catalisadores, e a parte interna de cada tubo de reação do reator multitubular de leito fixo é dividida em uma direção axial tubular, para, desse modo, dispor pelo menos duas zonas reacionais, e depois essas zonas reacionais são recheadas com os catalisadores, de uma maneira tal que a relação R da densidade aparente do catalisador para a densidade real do catalisador (densidade aparente do catalisador / densidade real do catalisador) em cada zona reacional difira daquela na outra zona reacional.
BRPI0300752-9A 2002-03-29 2003-03-25 processo produtivo para aldeìdo insaturado. BR0300752B1 (pt)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002096886 2002-03-29

Publications (2)

Publication Number Publication Date
BR0300752A true BR0300752A (pt) 2004-09-14
BR0300752B1 BR0300752B1 (pt) 2012-12-11

Family

ID=28035874

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0300752-9A BR0300752B1 (pt) 2002-03-29 2003-03-25 processo produtivo para aldeìdo insaturado.

Country Status (8)

Country Link
US (1) US6960684B2 (pt)
EP (1) EP1350784B1 (pt)
KR (1) KR100660988B1 (pt)
CN (1) CN1233609C (pt)
BR (1) BR0300752B1 (pt)
DE (1) DE60323424D1 (pt)
MY (1) MY127777A (pt)
SG (1) SG115529A1 (pt)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4295521B2 (ja) * 2003-02-13 2009-07-15 株式会社日本触媒 アクリル酸製造用触媒およびアクリル酸の製造方法
WO2005053844A1 (ja) * 2003-12-04 2005-06-16 Mitsubishi Chemical Corporation 不飽和アルデヒド及び不飽和カルボン酸の製造用触媒の製造方法
EP1621247A1 (de) * 2004-07-30 2006-02-01 MAN DWE GmbH Durchführung von exothermen Gasphasenreaktionen
KR100714606B1 (ko) * 2005-02-25 2007-05-07 주식회사 엘지화학 불포화 알데히드 및/또는 불포화 산의 제조방법
DE102005019911A1 (de) 2005-04-27 2006-11-02 Basf Ag Verfahren der rektifikativen Auftrennung einer Acrylsäure und/oder Methacrylsäure enthaltenden Flüssigkeit
US9724680B2 (en) * 2012-12-07 2017-08-08 Exxonmobil Research And Engineering Company Fiber reinforced zeolite extrudates with enhanced physical properties
MY182262A (en) 2013-07-18 2021-01-18 Nippon Kayaku Kk Method for producing unsaturated aldehyde and/or unsaturated carboxylic acid
TWI592209B (zh) 2016-03-31 2017-07-21 國立清華大學 反應器及其溫度的控制方法
KR102084768B1 (ko) 2016-11-01 2020-03-04 주식회사 엘지화학 불포화 알데하이드 및 불포화 카르복실산의 제조 방법
KR20180055154A (ko) 2016-11-16 2018-05-25 주식회사 엘지화학 촉매의 제조 방법
US11254634B2 (en) 2018-04-10 2022-02-22 Nippon Kayaku Kabushiki Kaisha Method for producing at least one of unsaturated aldehyde and unsaturated carboxylic acid and catalyst for producing at least one of unsaturated aldehyde and unsaturated carboxylic acid
SG11202109109YA (en) 2019-03-29 2021-11-29 Nippon Kayaku Kk Method for producing unsaturated aldehyde
KR102795505B1 (ko) * 2020-10-16 2025-04-11 주식회사 엘지화학 몰리브덴-비스무트계 복합 금속 산화물의 제조방법
CN115569650A (zh) * 2021-07-06 2023-01-06 惠生工程(中国)有限公司 一种用于合成不饱和醛的催化剂及其制备方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2056614C3 (de) 1970-11-18 1981-04-16 Basf Ag, 6700 Ludwigshafen Verfahren zur Herstellung von Acrylsäure aus Propylen
JPS55113730A (en) * 1979-02-26 1980-09-02 Mitsubishi Petrochem Co Ltd Preparation of acrolein and acrylic acid
EP0456837B1 (en) 1989-12-06 1996-10-09 Nippon Shokubai Co., Ltd. Process for producing methacrolein and methacrylic acid
JP2659839B2 (ja) 1990-01-26 1997-09-30 株式会社日本触媒 メタクロレインおよびメタクリル酸の製造方法
JPH0784400B2 (ja) 1990-04-03 1995-09-13 株式会社日本触媒 不飽和アルデヒドおよび不飽和酸の製造方法
JP2809476B2 (ja) 1990-04-11 1998-10-08 株式会社日本触媒 アクロレインおよびアクリル酸の製造方法
DE4307509A1 (de) 1993-03-10 1994-09-15 Basf Ag Verfahren zur Herstellung von 3 bis 5 C-Atome aufweisenden alpha,beta-monoethylenisch ungesättigten Aldehyden, Carbonsäuren oder Nitrilen
JP3139285B2 (ja) 1994-06-20 2001-02-26 住友化学工業株式会社 アクロレインおよびアクリル酸の製造方法
JP3775872B2 (ja) 1996-12-03 2006-05-17 日本化薬株式会社 アクロレイン及びアクリル酸の製造方法
JP3943291B2 (ja) * 1999-08-04 2007-07-11 株式会社日本触媒 アクロレインおよびアクリル酸の製造方法

Also Published As

Publication number Publication date
MY127777A (en) 2006-12-29
CN1448380A (zh) 2003-10-15
CN1233609C (zh) 2005-12-28
KR100660988B1 (ko) 2006-12-22
EP1350784B1 (en) 2008-09-10
US6960684B2 (en) 2005-11-01
BR0300752B1 (pt) 2012-12-11
US20030191344A1 (en) 2003-10-09
SG115529A1 (en) 2005-10-28
EP1350784A1 (en) 2003-10-08
DE60323424D1 (de) 2008-10-23
KR20030078689A (ko) 2003-10-08

Similar Documents

Publication Publication Date Title
BR0300752A (pt) Processo produtivo para aldeìdo insaturado
BR0002417A (pt) Catalisador e processo para a produção de aldeìdo insaturado e de acìdo carboxìlico insaturado
CN101400639B (zh) 丙烯酸的制备方法
BR0300753A (pt) Processo de oxidação catalìtica em fase gasosa
Corey et al. Homoconjugate addition of organocopper reagents to cyclopropanes and its application to the synthesis of prostanoids
Sayer et al. Novel bay-region diol epoxides from benzo [c] phenanthrene
BR0008825A (pt) Processo para a oxidação catalìtica em fase gasosa de acroleìna para ácido acrìlico
US5077434A (en) Process for production of acrylic acid
MY121141A (en) Method for the catalytic gas-phase oxidation of propene into acrolein
BRPI0408539B8 (pt) processo para a oxidação parcial de acroleína para ácido acrílico em fase gasosa
ES2194505T3 (es) Proceso de dos fases para la produccion de 1,3-propanodiol por hidrogenacion catalitica de 3-hidroxipropanal.
Zhu et al. A mild and efficient catalyst for the Beckmann rearrangement, BOP-Cl
BRPI0417591A (pt) método para produção de ácido (met)acrìlico ou (met)acroleìna
Kim et al. Reaction pathway and kinetics for uncatalyzed partial oxidation of p-xylene in sub-and supercritical water
TW546283B (en) Method for production of acrolein and acrylic acid
CN103012063B (zh) 一种制备丙二醇的方法
ES2146840T3 (es) Procedimiento para la produccion de acido acetico por carbonilacion de dimetileter.
BRPI0416633A (pt) processo para preparar acroleìna por oxidação parcial em fase gasosa heterogeneamente catalisada, e, catalisador anular não suportado
Ahn et al. Solvent‐Free Chelation‐Assisted Catalytic C C Bond Cleavage of Unstrained Ketone by Rhodium (I) Complexes under Microwave Irradiation
US2649477A (en) Process for the manufacture of maleic acid
CN103012366B (zh) 一种噻吩类硫化物氧化的方法
BRPI0418699A (pt) processo para a produção de ácido (met) acrìlico ou (met) acroleìna
CN103338859B (zh) 使脂肪酸、它们的酯及其混合物环氧化的改进方法
KR100841604B1 (ko) 테트라히드로푸란을 제조하는 방법
Wang et al. Reaction kinetics for the heterogeneously resin-catalyzed and homogeneously self-catalyzed esterification of thioglycolic acid with 2-ethyl-1-hexanol

Legal Events

Date Code Title Description
B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B16A Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]

Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 25/03/2003, OBSERVADAS AS DEMAIS CONDICOES LEGAIS.