GB782291A - Process for the production of terephthalic acid - Google Patents

Process for the production of terephthalic acid

Info

Publication number
GB782291A
GB782291A GB7673/55A GB767355A GB782291A GB 782291 A GB782291 A GB 782291A GB 7673/55 A GB7673/55 A GB 7673/55A GB 767355 A GB767355 A GB 767355A GB 782291 A GB782291 A GB 782291A
Authority
GB
United Kingdom
Prior art keywords
oxide
potassium
lead
phthalate
diphenyl
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
GB7673/55A
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.)
Rhone Poulenc SA
Original Assignee
Rhone Poulenc SA
Societe des Usines Chimiques Rhone Poulenc SA
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 Rhone Poulenc SA, Societe des Usines Chimiques Rhone Poulenc SA filed Critical Rhone Poulenc SA
Publication of GB782291A publication Critical patent/GB782291A/en
Expired 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
    • C07C51/41Preparation of salts of carboxylic acids
    • C07C51/416Henkel reaction and related reactions, i.e. rearrangement of carboxylate salt groups linked to six-membered aromatic rings, in the absence or in the presence of CO or CO2, (e.g. preparation of terepholates from benzoates); no additional classification for the subsequent hydrolysis of the salt groups has to be given
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

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

Terephthalic acid is made by heating in the presence of an organic diluent which is liquid at the reaction temperature either potassium isoor ortho-phthalate, or a mixture thereof, at 350-480 DEG , preferably 420-480 DEG , especially 440 DEG C., under pressure in a carbon dioxide atmosphere. Pressures of 70-150 atmos. are quoted. The starting material may be obtained by converting into neutral salts the oxidation products of commercial xylenes, any potassium carbonate present being preferably converted to the sulphate. Advantageously the phthalates are anhydrous. Sufficient diluent should be present to form a mobile paste. Specified diluents are diphenyl, phenyl cresyl oxide, dicresyl oxide and diphenyl oxide, the latter being preferred. The use of a catalyst such as an oxide of zinc, iron, thallium or lead, or of an organic salt of lead such as the oxalate, leads to an increased yield, litharge being preferred. 1 to 6 per cent by weight of catalyst based on phthalate may be used. In examples terephthalic acid is obtained in the presence of diphenyl oxide and lead oxalate from (1) potassium ortho-phthalate; (2) potassium isophthalate; and (3) a mixture of potassium salts from acids obtained by oxidizing commercial xylene and in (4) from potassium isophthalate in the presence of diphenyl oxide and lead oxide. Reference has been directed by the Comptroller to Specifications 747,204 and 762,644.
GB7673/55A 1954-05-28 1955-03-16 Process for the production of terephthalic acid Expired GB782291A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR1006413X 1954-05-28

Publications (1)

Publication Number Publication Date
GB782291A true GB782291A (en) 1957-09-04

Family

ID=9565737

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7673/55A Expired GB782291A (en) 1954-05-28 1955-03-16 Process for the production of terephthalic acid

Country Status (4)

Country Link
BE (1) BE538382A (en)
DE (1) DE1006413B (en)
FR (2) FR1105556A (en)
GB (1) GB782291A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE936036C (en) * 1952-11-21 1955-12-01 Henkel & Cie Gmbh Process for the preparation of terephthalic acid

Also Published As

Publication number Publication date
BE538382A (en)
DE1006413B (en) 1957-04-18
FR67380E (en) 1958-03-06
FR1105556A (en) 1955-12-05

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