GB838854A - Improvements in the production of acrylic acid and its salts - Google Patents

Improvements in the production of acrylic acid and its salts

Info

Publication number
GB838854A
GB838854A GB5187/57A GB518757A GB838854A GB 838854 A GB838854 A GB 838854A GB 5187/57 A GB5187/57 A GB 5187/57A GB 518757 A GB518757 A GB 518757A GB 838854 A GB838854 A GB 838854A
Authority
GB
United Kingdom
Prior art keywords
acetylene
carbon monoxide
acrylic acid
nickel
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
Application number
GB5187/57A
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB838854A publication Critical patent/GB838854A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/02Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • C07C57/03Monocarboxylic acids
    • C07C57/04Acrylic acid; Methacrylic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/15Preparation of carboxylic acids or their salts, halides or anhydrides by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis

Landscapes

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

Abstract

Acrylic acid or salts thereof are prepared by the reaction of acetylene, carbon monoxide and water in the presence of a carbonylation catalyst at a temperature above 180 DEG C. and at a minimum pressure of 75 atmospheres absolute using an acetylene-carbon monoxide containing gas mixture having not more than 23% by volume of acetylene based on the carbon monoxide-acetylene content, and if desired, converting the acrylic acid formed into a salt. The reaction may be effected in the presence of an alkaline agent such as an alkali carbonate, in an amount such that all or part of the acrylic acid formed is neutralized during the reaction. Reaction temperatures of 220-300 DEG C. are preferred. The carbon monoxide may contain inert gases. The catalyst may be a nickel salt such as those of acetic, propionic, acrylic, succinic, citric, tartaric, adipic, or phthalic acid; complex alkali nickel cyanides, which may be formed in situ from a nickel salt and an alkali cyanide, may also be used; activators such as cuprous salts may be present. Generally, the reaction is effected in the absence of organic solvents. The process may be effected continuously and unused carbon monoxide may be recycled. In typical examples: (1) an aqueous solution of nickel sulphate, potassium cyanide and sodium carbonate and a gaseous CO/C2H2 mixture containing 17% by volume of acetylene are passed upwardly through a stainless steel tube under a pressure of 200 atms. absolute at 245-250 DEG C., yielding a mixture of sodium, potassium and nickel acrylates from which acrylic acid is obtained on acidification; (4) an aqueous solution of nickel acrylate and a CO/C2H2 mixture containing 20% of acetylene are passed through a similar reactor at 280-290 DEG C. and 200 atms. yielding acrylic acid. A graph is given showing the relationship between the decomposition limiting pressure of a mixture of acetylene and carbon monoxide and the acetylene content of the mixture.
GB5187/57A 1956-02-24 1957-02-15 Improvements in the production of acrylic acid and its salts Expired GB838854A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE838854X 1956-02-24

Publications (1)

Publication Number Publication Date
GB838854A true GB838854A (en) 1960-06-22

Family

ID=6761763

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5187/57A Expired GB838854A (en) 1956-02-24 1957-02-15 Improvements in the production of acrylic acid and its salts

Country Status (1)

Country Link
GB (1) GB838854A (en)

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