ES2178179T3 - Procedimiento para preparar acido 2,6-naftalenodicarboxilico. - Google Patents

Procedimiento para preparar acido 2,6-naftalenodicarboxilico.

Info

Publication number
ES2178179T3
ES2178179T3 ES98911730T ES98911730T ES2178179T3 ES 2178179 T3 ES2178179 T3 ES 2178179T3 ES 98911730 T ES98911730 T ES 98911730T ES 98911730 T ES98911730 T ES 98911730T ES 2178179 T3 ES2178179 T3 ES 2178179T3
Authority
ES
Spain
Prior art keywords
reaction zone
solvent
cobalt
manganese
reaction
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
ES98911730T
Other languages
English (en)
Inventor
Rosemary F Mcmahon
James D Greene Jr
David A Peterson
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
Application granted granted Critical
Publication of ES2178179T3 publication Critical patent/ES2178179T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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)
  • Catalysts (AREA)

Abstract

Se describe un procedimiento de producción de ácido 2,6- naftalendicarboxílico mediane oxidación exotérmica en fase líquida de 2,6-dimetilnataleno que comprende la adición en una zona de reacción los componenetes de la reacción de oxidación que comprenden el 2,6- dimetilnaftaleno, una fuente de oxígeno molecular, un disolvente que comprende un ácido monocarboxílico alifático y un catalizador que comprende componentes de cobalto, manganeso y bromo en el que la relación atómica de cobalto a manganeso es de al menos aproximadamente 1:1 y el cobalto y manganeso totales, calculado como cobalto elemental y manganeso elemental añadido a la zona de reacción, es menor de aproximadamente 0,40% en peso basado en el peso del disolvente añadido a la zona de reacción; se mantiene el contenido de la zona de reacción a una temperatura y a una presión suficiente para causar la oxidación del 2,6-dimetilnaftaleno a ácido 2,6-naftalendicarboxílico y la vaporización de al menos una parte del disolvente de la reacción mientras se mantiene una mezcla de reacción en fase líquida; se condensa el disolvente vaporizado y se devuelve una cantidad del disolvente condensado a la zona de reacción para mantener la cantidad de agua en la zona de reacción y no más del 15% en peso basado en el peso del disolvente en la zona de reacción; y se extrae de la zona de reacción una mezcla que comprende ácido 2,6-naftalendicarboxílico.
ES98911730T 1997-03-25 1998-03-17 Procedimiento para preparar acido 2,6-naftalenodicarboxilico. Expired - Lifetime ES2178179T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/827,039 US6114575A (en) 1997-03-25 1997-03-25 Process for preparing 2,6-naphthalenedicarboxylic acid

Publications (1)

Publication Number Publication Date
ES2178179T3 true ES2178179T3 (es) 2002-12-16

Family

ID=25248172

Family Applications (1)

Application Number Title Priority Date Filing Date
ES98911730T Expired - Lifetime ES2178179T3 (es) 1997-03-25 1998-03-17 Procedimiento para preparar acido 2,6-naftalenodicarboxilico.

Country Status (12)

Country Link
US (1) US6114575A (es)
EP (1) EP0971872B1 (es)
JP (1) JP2002510287A (es)
KR (1) KR100660308B1 (es)
AT (1) ATE218529T1 (es)
AU (1) AU6561798A (es)
CA (1) CA2284721C (es)
DE (1) DE69805786T2 (es)
ES (1) ES2178179T3 (es)
ID (1) ID23802A (es)
TW (1) TW500717B (es)
WO (1) WO1998042649A1 (es)

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WO2003022791A1 (en) * 2001-09-07 2003-03-20 Lonza Spa Process for the preparation of 2,6-naphthalenedicarboxylic acid
KR20030069370A (ko) * 2002-02-20 2003-08-27 주식회사 효성 나프탈렌디카르복실산의 제조 방법
KR20030072789A (ko) * 2002-03-06 2003-09-19 주식회사 효성 2,6-나프탈렌디카복실산의 제조방법
US6657068B2 (en) 2002-03-22 2003-12-02 General Electric Company Liquid phase oxidation of halogenated ortho-xylenes
US6657067B2 (en) 2002-03-22 2003-12-02 General Electric Company Method for the manufacture of chlorophthalic anhydride
KR100717650B1 (ko) * 2002-08-08 2007-05-11 에스케이케미칼주식회사 나프탈렌 디카르복실산의 제조 방법
US7541489B2 (en) 2004-06-30 2009-06-02 Sabic Innovative Plastics Ip B.V. Method of making halophthalic acids and halophthalic anhydrides
KR100770516B1 (ko) * 2004-12-30 2007-10-25 주식회사 효성 벤즈알데히드 디하이드로게나제를 발현하는 형질전환체의제조방법 및 이를 이용한 2,6-나프탈렌 디카르복실산의정제방법
US7955674B2 (en) * 2005-03-02 2011-06-07 Eastman Chemical Company Transparent polymer blends containing polyesters comprising a cyclobutanediol and articles prepared therefrom
US20060199871A1 (en) * 2005-03-02 2006-09-07 Hale Wesley R Multilayered, transparent articles and a process for their preparation
US20100184940A1 (en) * 2005-03-02 2010-07-22 Eastman Chemical Company Polyester Compositions Which Comprise Cyclobutanediol and Certain Thermal Stabilizers, and/or Reaction Products Thereof
US7959836B2 (en) * 2005-03-02 2011-06-14 Eastman Chemical Company Process for the preparation of transparent, shaped articles containing polyesters comprising a cyclobutanediol
US7510768B2 (en) 2005-06-17 2009-03-31 Eastman Chemical Company Thermoplastic articles comprising cyclobutanediol having a decorative material embedded therein
US7959998B2 (en) * 2005-03-02 2011-06-14 Eastman Chemical Company Transparent, oxygen-scavenging compositions containing polyesters comprising a cyclobutanediol and articles prepared therefrom
US7704605B2 (en) 2006-03-28 2010-04-27 Eastman Chemical Company Thermoplastic articles comprising cyclobutanediol having a decorative material embedded therein
US8193302B2 (en) 2005-10-28 2012-06-05 Eastman Chemical Company Polyester compositions which comprise cyclobutanediol and certain phosphate thermal stabilizers, and/or reaction products thereof
US8586701B2 (en) * 2005-10-28 2013-11-19 Eastman Chemical Company Process for the preparation of copolyesters based on 2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1,4-cyclohexanedimethanol
MY146045A (en) * 2005-10-28 2012-06-15 Eastman Chem Co Polyester compositions containing cyclobutanediol having a certain combination of inherent viscosity and moderate glass transition temperature and articles made therefrom
US20070106054A1 (en) * 2005-10-28 2007-05-10 Crawford Emmett D Polyester compositions containing cyclobutanediol having a certain combination of inherent viscosity and high glass transition temperature and articles made therefrom
US9598533B2 (en) 2005-11-22 2017-03-21 Eastman Chemical Company Polyester compositions containing cyclobutanediol having a certain combination of inherent viscosity and moderate glass transition temperature and articles made therefrom
US7737246B2 (en) 2005-12-15 2010-06-15 Eastman Chemical Company Polyester compositions which comprise cyclobutanediol, cyclohexanedimethanol, and ethylene glycol and manufacturing processes therefor
US9169388B2 (en) 2006-03-28 2015-10-27 Eastman Chemical Company Polyester compositions which comprise cyclobutanediol and certain thermal stabilizers, and/or reaction products thereof
KR100790206B1 (ko) 2006-12-28 2008-01-02 주식회사 효성 2,6-나프탈렌디카르복실산의 제조방법
US8501287B2 (en) 2007-11-21 2013-08-06 Eastman Chemical Company Plastic baby bottles, other blow molded articles, and processes for their manufacture
JP5635411B2 (ja) 2007-11-21 2014-12-03 イーストマン ケミカル カンパニー プラスチック製哺乳瓶、他のブロー成形物品及びそれらの製造方法
US8198371B2 (en) 2008-06-27 2012-06-12 Eastman Chemical Company Blends of polyesters and ABS copolymers
US20100099828A1 (en) * 2008-10-21 2010-04-22 Eastman Chemical Company Clear Binary Blends of Aliphatic Polyesters and Aliphatic-Aromatic Polyesters
US8895654B2 (en) * 2008-12-18 2014-11-25 Eastman Chemical Company Polyester compositions which comprise spiro-glycol, cyclohexanedimethanol, and terephthalic acid
US8394997B2 (en) 2010-12-09 2013-03-12 Eastman Chemical Company Process for the isomerization of 2,2,4,4-tetraalkylcyclobutane-1,3-diols
US8420868B2 (en) 2010-12-09 2013-04-16 Eastman Chemical Company Process for the preparation of 2,2,4,4-tetraalkylcyclobutane-1,3-diols
US8420869B2 (en) 2010-12-09 2013-04-16 Eastman Chemical Company Process for the preparation of 2,2,4,4-tetraalkylcyclobutane-1,3-diols
US20130217830A1 (en) 2012-02-16 2013-08-22 Eastman Chemical Company Clear Semi-Crystalline Articles with Improved Heat Resistance
CN112479861A (zh) * 2020-12-10 2021-03-12 成家钢 液相常压催化氧气氧化安全方法及氧气氧化安全反应设备
CN113845414B (zh) * 2021-11-25 2022-03-04 中化学科学技术研究有限公司 一种合成2,6-萘二甲酸的方法

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US3856855A (en) * 1970-02-17 1974-12-24 Teijin Ltd Process for preparation of naphthalene monocarboxylic acid or naphthalene dicarboxylic acid
US3870754A (en) * 1972-08-28 1975-03-11 Teijin Ltd Process for the preparation of 2,6-naphthalenedicarboxylic acid
JPS5621017A (en) * 1979-07-31 1981-02-27 Toukiyouto Electronic liquid meter
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JPS62212340A (ja) * 1986-03-14 1987-09-18 Kureha Chem Ind Co Ltd 2,6−ナフタレンジカルボン酸とトリメリツト酸の併産方法
CA1303059C (en) * 1986-03-14 1992-06-09 Toshiharu Matsuda Process for producing 2,6-naphthalenedicarboxylic acid by oxidizing 2,6-diisopropylnaphthalene
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
CA1328115C (en) * 1988-09-28 1994-03-29 David Allen Young Method for making 2,6-naphthalenedicarboxylic acid
US5055612A (en) * 1988-12-19 1991-10-08 Nkk Corporation Process for the preparation of naphthalene carboxylic acids
US4933491A (en) * 1989-10-02 1990-06-12 Amoco Corporation Method for purifying a crude naphthalene dicarboxylic acid
US5183933A (en) * 1991-10-15 1993-02-02 Amoco Corporation Process for preparing 2,6-naphthalene-dicarboxylic acid
JPH06157403A (ja) * 1992-11-30 1994-06-03 Mitsubishi Petrochem Co Ltd 2,6−ナフタレンジカルボン酸の製造方法
US5510521A (en) * 1995-03-27 1996-04-23 Eastman Chemical Company Process for the production of aromatic carboxylic acids

Also Published As

Publication number Publication date
AU6561798A (en) 1998-10-20
DE69805786D1 (de) 2002-07-11
TW500717B (en) 2002-09-01
EP0971872A1 (en) 2000-01-19
US6114575A (en) 2000-09-05
CA2284721A1 (en) 1998-10-01
KR20010005647A (ko) 2001-01-15
DE69805786T2 (de) 2003-02-20
WO1998042649A1 (en) 1998-10-01
KR100660308B1 (ko) 2006-12-22
JP2002510287A (ja) 2002-04-02
EP0971872B1 (en) 2002-06-05
ID23802A (id) 2000-05-11
ATE218529T1 (de) 2002-06-15
CA2284721C (en) 2007-06-12

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