MX172140B - ,DILUYENTES ANHIDROS PARA LA REACCION DE OXIDACION DE ISOBUTILENO EN METACROLEINA Y LA OXIDACION DE METACROLEINA Y LA OXIDACION DE METACROLEINA EN ACIDO METACRILICO C); y utilizar uno o más gases diluyentes esencia - Google Patents

,DILUYENTES ANHIDROS PARA LA REACCION DE OXIDACION DE ISOBUTILENO EN METACROLEINA Y LA OXIDACION DE METACROLEINA Y LA OXIDACION DE METACROLEINA EN ACIDO METACRILICO C); y utilizar uno o más gases diluyentes esencia

Info

Publication number
MX172140B
MX172140B MX017677A MX1767789A MX172140B MX 172140 B MX172140 B MX 172140B MX 017677 A MX017677 A MX 017677A MX 1767789 A MX1767789 A MX 1767789A MX 172140 B MX172140 B MX 172140B
Authority
MX
Mexico
Prior art keywords
oxidation
metacrolein
anhydrous
essentially
isobutylene
Prior art date
Application number
MX017677A
Other languages
English (en)
Inventor
William George Etzkorn
Gordon Gene Haerkreader
Original Assignee
Union Carbide Chem Plastic
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 Union Carbide Chem Plastic filed Critical Union Carbide Chem Plastic
Publication of MX172140B publication Critical patent/MX172140B/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • C07C57/03—Monocarboxylic acids
    • C07C57/04—Acrylic acid; Methacrylic acid
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/33—Preparation 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
    • C07C45/34—Preparation 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
    • C07C45/35—Preparation 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/25—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
    • C07C51/252—Preparation 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

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)

Abstract

La presente invención se refiere a un procedimiento para producir metacroleina por oxidación catalítica de isobutileno y un procedimiento para producir metacroleina y ácido metacrílico mediante una oxidación catalítica de dos etapas de isobutileno, en donde la primera etapa produce principalmente metacroleina y la segunda etapa produce principalmente ácido metacrílico mediante oxidación de la metacroleina, el procedimiento utiliza una o más corrientes de recirculación hacia cualesquiera o ambas etapas, ambas etapas funcionan en corrientes de alimentación que contienen oxígeno y un gas diluyente inerte; la mejora consiste de utilizar uno o más gases diluyentes esencialmente anhídridos y esencialmente inertes como la alimentación de gas diluyente esencialmente inerte adicionada en la priemra etapa, teniendo la alimentación de gas diluyente esencialmente anhidra y esencialmente inerte adicionada una capacidad termica compuesta de por lo menos aproximadamente 6.5 calorías/gramo-mol (gradoslmente anhidros y esencialmente inertes como el gas diluyente alimentado a la segunda etapa, teniendo el diluyente esencialmente anhidro y esencialmente inerte adicionado, una capacidad termica compuesta de por lo menos aproximadamente 6.5 calorías/gramo-mol (oC).
MX017677A 1988-09-26 1989-09-25 ,DILUYENTES ANHIDROS PARA LA REACCION DE OXIDACION DE ISOBUTILENO EN METACROLEINA Y LA OXIDACION DE METACROLEINA Y LA OXIDACION DE METACROLEINA EN ACIDO METACRILICO C); y utilizar uno o más gases diluyentes esencia MX172140B (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US24977288A 1988-09-26 1988-09-26

Publications (1)

Publication Number Publication Date
MX172140B true MX172140B (es) 1993-12-06

Family

ID=22944929

Family Applications (1)

Application Number Title Priority Date Filing Date
MX017677A MX172140B (es) 1988-09-26 1989-09-25 ,DILUYENTES ANHIDROS PARA LA REACCION DE OXIDACION DE ISOBUTILENO EN METACROLEINA Y LA OXIDACION DE METACROLEINA Y LA OXIDACION DE METACROLEINA EN ACIDO METACRILICO C); y utilizar uno o más gases diluyentes esencia

Country Status (6)

Country Link
EP (1) EP0361372A1 (es)
JP (1) JPH02191236A (es)
KR (1) KR920010573B1 (es)
CN (1) CN1025731C (es)
CA (1) CA1327814C (es)
MX (1) MX172140B (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2135120T3 (es) * 1995-03-10 1999-10-16 Basf Ag Procedimiento de oxidacion en fase gaseosa de propileno a acroleina, acido acrilico, o su mezcla, realizada continuamente, catalizada por via heterogenea.
US6215027B1 (en) 1998-10-20 2001-04-10 Praxair Technology, Inc. Ballast gas use in liquid phase oxidation
DE10122027A1 (de) * 2001-05-07 2002-05-23 Basf Ag Verfahren zur Herstellung von Acrylsäure durch heterogen katalysierte Partialoxidation von Propan
US10358395B2 (en) 2014-09-16 2019-07-23 Sekisui Chemical Co., Ltd. Method for producing butadiene and device for producing butadiene
CN106410277A (zh) * 2016-11-21 2017-02-15 电子科技大学中山学院 一种改善电池高温性能的电解液及锂离子电池
CN114225848B (zh) * 2022-02-24 2022-05-13 北京弗莱明科技有限公司 一种高收率连续氧化制备丁烯-2-酸的装置和方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1467865A (en) * 1973-07-27 1977-03-23 Basf Ag Catalytic oxidation or ammoxidation of a-olefins to alpha,beta- olefinically unsaturated aldehydes acids or nitriles
DE2436818C3 (de) * 1974-07-31 1985-05-09 Basf Ag, 6700 Ludwigshafen Verfahren zur Herstellung von Acrylsäure durch Oxidation von Propylen mit Sauerstoff enthaltenden Gasen in zwei getrennten Oxidationsstufen
JPS52108917A (en) * 1976-03-11 1977-09-12 Nippon Shokubai Kagaku Kogyo Co Ltd Preparation of acrylic acid by vapor-phase catalytic oxidation of prop ylene
JPS584694B2 (ja) * 1978-12-27 1983-01-27 宇部興産株式会社 アクロレインまたはメタクロレインの製造方法
CA1299193C (en) * 1986-07-17 1992-04-21 Gordon Gene Harkreader Anhydrous diluents for the propylene oxidation reaction to acrolein and acrolein oxidation to acrylic acid
JPH0813777B2 (ja) * 1986-12-11 1996-02-14 三菱化学株式会社 アクリル酸の製造法

Also Published As

Publication number Publication date
CN1043123A (zh) 1990-06-20
EP0361372A1 (en) 1990-04-04
KR900004669A (ko) 1990-04-12
KR920010573B1 (ko) 1992-12-07
JPH02191236A (ja) 1990-07-27
CN1025731C (zh) 1994-08-24
CA1327814C (en) 1994-03-15

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