BE847474A - Oxydation secondaire d'un effluent fluide de l'oxydation primaire du m-xylene ou du p-xylene, - Google Patents

Oxydation secondaire d'un effluent fluide de l'oxydation primaire du m-xylene ou du p-xylene,

Info

Publication number
BE847474A
BE847474A BE171665A BE171665A BE847474A BE 847474 A BE847474 A BE 847474A BE 171665 A BE171665 A BE 171665A BE 171665 A BE171665 A BE 171665A BE 847474 A BE847474 A BE 847474A
Authority
BE
Belgium
Prior art keywords
xylene
oxidation
fluid effluent
primary
secondary oxidation
Prior art date
Application number
BE171665A
Other languages
English (en)
French (fr)
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 filed Critical
Publication of BE847474A publication Critical patent/BE847474A/xx

Links

Classifications

    • 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)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
BE171665A 1975-10-24 1976-10-20 Oxydation secondaire d'un effluent fluide de l'oxydation primaire du m-xylene ou du p-xylene, BE847474A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US62567575A 1975-10-24 1975-10-24

Publications (1)

Publication Number Publication Date
BE847474A true BE847474A (fr) 1977-04-20

Family

ID=24507104

Family Applications (1)

Application Number Title Priority Date Filing Date
BE171665A BE847474A (fr) 1975-10-24 1976-10-20 Oxydation secondaire d'un effluent fluide de l'oxydation primaire du m-xylene ou du p-xylene,

Country Status (11)

Country Link
JP (1) JPS6048497B2 (enrdf_load_stackoverflow)
BE (1) BE847474A (enrdf_load_stackoverflow)
CA (1) CA1062279A (enrdf_load_stackoverflow)
DE (1) DE2647698A1 (enrdf_load_stackoverflow)
DK (1) DK159259C (enrdf_load_stackoverflow)
FR (1) FR2328688A1 (enrdf_load_stackoverflow)
GB (1) GB1555246A (enrdf_load_stackoverflow)
IT (1) IT1073924B (enrdf_load_stackoverflow)
LU (1) LU76048A1 (enrdf_load_stackoverflow)
NL (1) NL188637C (enrdf_load_stackoverflow)
YU (1) YU42274B (enrdf_load_stackoverflow)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2714985C2 (de) * 1977-04-04 1982-05-06 Chemische Werke Hüls AG, 4370 Marl Verfahren zur Reinigung von Terephthalsäure
JPS5470235A (en) * 1977-11-14 1979-06-05 Mitsubishi Chem Ind Ltd Preparation of terephthalic acid
US4334086A (en) * 1981-03-16 1982-06-08 Labofina S.A. Production of terephthalic acid
DE3128147C2 (de) * 1981-07-16 1986-03-06 Dynamit Nobel Ag, 5210 Troisdorf Verfahren zur Gewinnung von aromatischen Monocarbonsäuren
JP2893860B2 (ja) * 1990-05-17 1999-05-24 三菱瓦斯化学株式会社 高純度イソフタル酸の製造法
US5132450A (en) * 1990-06-25 1992-07-21 Mitsubishi Gas Chemical Company, Inc. Process for producing high purity isophthalic acid
US5183933A (en) * 1991-10-15 1993-02-02 Amoco Corporation Process for preparing 2,6-naphthalene-dicarboxylic acid
US7589231B2 (en) 2004-09-02 2009-09-15 Eastman Chemical Company Optimized liquid-phase oxidation
US7563926B2 (en) 2004-09-02 2009-07-21 Eastman Chemical Company Optimized liquid-phase oxidation
US7741515B2 (en) 2004-09-02 2010-06-22 Eastman Chemical Company Optimized liquid-phase oxidation
US7495125B2 (en) 2004-09-02 2009-02-24 Eastman Chemical Company Optimized liquid-phase oxidation
US7399882B2 (en) 2004-09-02 2008-07-15 Eastman Chemical Company Optimized liquid-phase oxidation
US7361784B2 (en) 2004-09-02 2008-04-22 Eastman Chemical Company Optimized liquid-phase oxidation
US7572932B2 (en) * 2004-09-02 2009-08-11 Eastman Chemical Company Optimized liquid-phase oxidation
US7371894B2 (en) 2004-09-02 2008-05-13 Eastman Chemical Company Optimized liquid-phase oxidation
US7692036B2 (en) * 2004-11-29 2010-04-06 Eastman Chemical Company Optimized liquid-phase oxidation
US7683210B2 (en) 2004-09-02 2010-03-23 Eastman Chemical Company Optimized liquid-phase oxidation
US7582793B2 (en) 2004-09-02 2009-09-01 Eastman Chemical Company Optimized liquid-phase oxidation
US7390921B2 (en) 2004-09-02 2008-06-24 Eastman Chemical Company Optimized liquid-phase oxidation
US7504535B2 (en) 2004-09-02 2009-03-17 Eastman Chemical Company Optimized liquid-phase oxidation
US7586000B2 (en) 2004-09-02 2009-09-08 Eastman Chemical Company Optimized liquid-phase oxidation
US7608733B2 (en) 2004-09-02 2009-10-27 Eastman Chemical Company Optimized liquid-phase oxidation
US7507857B2 (en) 2004-09-02 2009-03-24 Eastman Chemical Company Optimized liquid-phase oxidation
US7692037B2 (en) 2004-09-02 2010-04-06 Eastman Chemical Company Optimized liquid-phase oxidation
US7381836B2 (en) 2004-09-02 2008-06-03 Eastman Chemical Company Optimized liquid-phase oxidation
US7482482B2 (en) 2004-09-02 2009-01-27 Eastman Chemical Company Optimized liquid-phase oxidation
US7608732B2 (en) 2005-03-08 2009-10-27 Eastman Chemical Company Optimized liquid-phase oxidation
US7572936B2 (en) 2004-09-02 2009-08-11 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
CN110944972A (zh) * 2017-06-29 2020-03-31 Bp北美公司 制造芳族羧酸的方法
CN112110813A (zh) * 2020-09-18 2020-12-22 中国石化扬子石油化工有限公司 一种促进偏苯三甲酸结晶的方法

Also Published As

Publication number Publication date
DK159259C (da) 1991-04-08
CA1062279A (en) 1979-09-11
NL188637C (nl) 1992-08-17
DK477776A (da) 1977-04-25
YU42274B (en) 1988-08-31
FR2328688B1 (enrdf_load_stackoverflow) 1978-12-15
JPS6048497B2 (ja) 1985-10-28
IT1073924B (it) 1985-04-17
DE2647698C2 (enrdf_load_stackoverflow) 1989-06-15
FR2328688A1 (fr) 1977-05-20
YU260576A (en) 1982-05-31
GB1555246A (en) 1979-11-07
DE2647698A1 (de) 1977-04-28
DK159259B (da) 1990-09-24
JPS5285136A (en) 1977-07-15
LU76048A1 (enrdf_load_stackoverflow) 1977-05-31
NL7611720A (nl) 1977-04-26

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Legal Events

Date Code Title Description
RE20 Patent expired

Owner name: AMOCO CORP.

Effective date: 19961020