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ES8609191A1 - Procedimiento para la produccion continua de un acido carbo-xilico aromatico - Google Patents

Procedimiento para la produccion continua de un acido carbo-xilico aromatico

Info

Publication number
ES8609191A1
ES8609191A1 ES548283A ES548283A ES8609191A1 ES 8609191 A1 ES8609191 A1 ES 8609191A1 ES 548283 A ES548283 A ES 548283A ES 548283 A ES548283 A ES 548283A ES 8609191 A1 ES8609191 A1 ES 8609191A1
Authority
ES
Spain
Prior art keywords
alkyl aromatic
recycle
liquid phase
vaporized solvent
phase oxidation
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
Application number
ES548283A
Other languages
English (en)
Other versions
ES548283A0 (es
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.)
BP Corp North America Inc
Original Assignee
BP Corp North America Inc
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 BP Corp North America Inc filed Critical BP Corp North America Inc
Publication of ES548283A0 publication Critical patent/ES548283A0/es
Publication of ES8609191A1 publication Critical patent/ES8609191A1/es
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C63/00Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
    • C07C63/04Monocyclic monocarboxylic acids
    • 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
    • C07C51/255Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting
    • C07C51/265Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting having alkyl side chains which are oxidised to carboxyl groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PROCEDIMIENTO PARA LA PRODUCCION CONTINUA DE UN ACIDO CARBOXILICO AROMATICO. CONSISTE EN REALIZAR UNA REACCION DE OXIDACION EXOTERMICA EN FASE LIQUIDA, CON UN GAS QUE CONTIENE OXIGENO MOLECULAR, EN UN REACTOR DE OXIDACION; EN EL QUE SE INTRODUCE COMO CORRIENTE DE ALIMENTACION: EL PRODUCTO DE PARTIDA (P-XILENO); EL CATALIZADOR DE OXIDACION, QUE INCLUYE UNA MEZCLA DE COBALTO, MANGANESO Y BROMO; Y EL DISOLVENTE CONSTITUIDO POR UNA MEZCLA DE ACIDO ACETICO Y AGUA CON UNA RIQUEZA DEL 0,5 AL 20% EN PESO DE AGUA. ESTOS COMPONENTES PUEDEN SER INTRODUCIDOS AL REACTOR BIEN POR SEPARADO O COMO MEZCLA, EN UNA PROPORCION DE DISOLVENTE A PRODUCTO DE PARTIDA DE 1:1. LAS CONDICIONES DE OXIDACION MANTENIDAS SON: UNA TEMPERATURA DE 120J A 230JC Y UNA PRESION ABSOLUTA EN EL REACTOR DE 0 A 35 KG/CM. EL CALOR GENERADO EN EL REACTOR ES UTILIZADO PARA VAPORIZAR PARTE DEL DISOLVENTE, QUE SERA EXTRAIDO POR LA PARTE SUPERIOR DEL REACTOR; CONDENSANDOLO POSTERIORMENTE EN UN SISTEMA CONDENSADOR DE CABEZA, Y RECICLADO ALREACTOR POR UNA LINEA EXTERIOR. OBTENIENDO ACIDO TEREFTALICO COMO PRODUCTO FINAL.
ES548283A 1984-10-29 1985-10-28 Procedimiento para la produccion continua de un acido carbo-xilico aromatico Expired ES8609191A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/665,751 US4777287A (en) 1984-10-29 1984-10-29 Recycle of vaporized solvent in liquid phase oxidation of an alkyl aromatic

Publications (2)

Publication Number Publication Date
ES548283A0 ES548283A0 (es) 1986-09-01
ES8609191A1 true ES8609191A1 (es) 1986-09-01

Family

ID=24671431

Family Applications (1)

Application Number Title Priority Date Filing Date
ES548283A Expired ES8609191A1 (es) 1984-10-29 1985-10-28 Procedimiento para la produccion continua de un acido carbo-xilico aromatico

Country Status (7)

Country Link
US (1) US4777287A (es)
JP (1) JPS61112044A (es)
KR (1) KR920002252B1 (es)
BE (1) BE903542A (es)
BR (1) BR8505367A (es)
ES (1) ES8609191A1 (es)
MX (1) MX162387A (es)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH078821B2 (ja) * 1986-09-26 1995-02-01 三井石油化学工業株式会社 芳香族カルボン酸の製造方法
JP2504545B2 (ja) * 1988-11-15 1996-06-05 三菱化学株式会社 テレフタル酸の製造法
US5087741A (en) * 1990-11-29 1992-02-11 Eastman Kodak Company Continuous production of aromatic carboxylic acids
US5118838A (en) * 1991-06-27 1992-06-02 Amoco Corporation By-product recovery when oxidizing polymethylbenzenes to polycarboxylic acids
US5171279A (en) * 1992-03-17 1992-12-15 Danek Medical Method for subcutaneous suprafascial pedicular internal fixation
US5510521A (en) * 1995-03-27 1996-04-23 Eastman Chemical Company Process for the production of aromatic carboxylic acids
ES2104512B1 (es) * 1995-09-21 1998-07-01 Interquisa Procedimiento industrial para la fabricacion de acidos carboxilicos aromaticos.
US5763649A (en) * 1996-07-12 1998-06-09 Mitsui Petrochemical Industries, Ltd. Process for producing aromatic carboxylic acids
US6657068B2 (en) 2002-03-22 2003-12-02 General Electric Company Liquid phase oxidation of halogenated ortho-xylenes
US6649773B2 (en) 2002-03-22 2003-11-18 General Electric Company Method for the manufacture of halophthalic acids and anhydrides
US6657067B2 (en) 2002-03-22 2003-12-02 General Electric Company Method for the manufacture of chlorophthalic anhydride
US7541489B2 (en) 2004-06-30 2009-06-02 Sabic Innovative Plastics Ip B.V. Method of making halophthalic acids and halophthalic anhydrides
US7399882B2 (en) 2004-09-02 2008-07-15 Eastman Chemical Company Optimized liquid-phase oxidation
US7608732B2 (en) 2005-03-08 2009-10-27 Eastman Chemical Company Optimized liquid-phase oxidation
US7589231B2 (en) 2004-09-02 2009-09-15 Eastman Chemical Company Optimized liquid-phase oxidation
US7390921B2 (en) 2004-09-02 2008-06-24 Eastman Chemical Company Optimized liquid-phase oxidation
US7381836B2 (en) 2004-09-02 2008-06-03 Eastman Chemical Company Optimized liquid-phase oxidation
US7507857B2 (en) 2004-09-02 2009-03-24 Eastman Chemical Company Optimized liquid-phase oxidation
US7361784B2 (en) 2004-09-02 2008-04-22 Eastman Chemical Company Optimized liquid-phase oxidation
US7692037B2 (en) 2004-09-02 2010-04-06 Eastman Chemical Company Optimized liquid-phase oxidation
US7572936B2 (en) 2004-09-02 2009-08-11 Eastman Chemical Company Optimized liquid-phase oxidation
US7910769B2 (en) 2004-09-02 2011-03-22 Eastman Chemical Company Optimized liquid-phase oxidation
US7692036B2 (en) 2004-11-29 2010-04-06 Eastman Chemical Company Optimized liquid-phase oxidation
US7741515B2 (en) 2004-09-02 2010-06-22 Eastman Chemical Company Optimized liquid-phase oxidation
US7482482B2 (en) 2004-09-02 2009-01-27 Eastman Chemical Company Optimized liquid-phase oxidation
US7582793B2 (en) 2004-09-02 2009-09-01 Eastman Chemical Company Optimized liquid-phase oxidation
US7683210B2 (en) 2004-09-02 2010-03-23 Eastman Chemical Company Optimized liquid-phase oxidation
US7371894B2 (en) 2004-09-02 2008-05-13 Eastman Chemical Company Optimized liquid-phase oxidation
US7495125B2 (en) 2004-09-02 2009-02-24 Eastman Chemical Company Optimized liquid-phase oxidation
US7504535B2 (en) 2004-09-02 2009-03-17 Eastman Chemical Company Optimized liquid-phase oxidation
US7572932B2 (en) 2004-09-02 2009-08-11 Eastman Chemical Company Optimized liquid-phase oxidation
US7586000B2 (en) 2004-09-02 2009-09-08 Eastman Chemical Company Optimized liquid-phase oxidation
US7563926B2 (en) * 2004-09-02 2009-07-21 Eastman Chemical Company Optimized liquid-phase oxidation
US7608733B2 (en) 2004-09-02 2009-10-27 Eastman Chemical Company Optimized liquid-phase oxidation
US7568361B2 (en) 2004-09-02 2009-08-04 Eastman Chemical Company Optimized liquid-phase oxidation
US7884232B2 (en) 2005-06-16 2011-02-08 Eastman Chemical Company Optimized liquid-phase oxidation
US7358389B2 (en) 2006-01-04 2008-04-15 Eastman Chemical Company Oxidation system employing internal structure for enhanced hydrodynamics
US7355068B2 (en) 2006-01-04 2008-04-08 Eastman Chemical Company Oxidation system with internal secondary reactor
CN101516490B (zh) * 2006-09-22 2012-07-04 陶氏环球技术公司 液-气相反应器系统
WO2020013022A1 (ja) * 2018-07-12 2020-01-16 株式会社神戸製鋼所 反応器及びこれを備えた反応器システム

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3092658A (en) * 1957-08-12 1963-06-04 Standard Oil Co Continuous system for oxidizing substituted aromatic hydrocarbons and producing carboxylic acids
US3187038A (en) * 1961-01-09 1965-06-01 Standard Oil Co Continuous oxidation process for production of benzoic acid
JPS5384934A (en) * 1976-12-30 1978-07-26 Mitsubishi Chem Ind Ltd Preparation of terephthalic acid

Also Published As

Publication number Publication date
ES548283A0 (es) 1986-09-01
KR920002252B1 (ko) 1992-03-20
BR8505367A (pt) 1986-08-05
US4777287A (en) 1988-10-11
KR860003197A (ko) 1986-05-21
BE903542A (fr) 1986-02-17
JPS61112044A (ja) 1986-05-30
MX162387A (es) 1991-05-06

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 19970519