GB1252698A - - Google Patents

Info

Publication number
GB1252698A
GB1252698A GB1252698DA GB1252698A GB 1252698 A GB1252698 A GB 1252698A GB 1252698D A GB1252698D A GB 1252698DA GB 1252698 A GB1252698 A GB 1252698A
Authority
GB
United Kingdom
Prior art keywords
aliphatic
catalyst
acid
weight
water
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
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
Priority claimed from ZA712199A external-priority patent/ZA712199B/en
Priority claimed from FR7114809A external-priority patent/FR2135729A5/en
Publication of GB1252698A publication Critical patent/GB1252698A/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
    • C07C51/10Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
    • C07C51/14Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on a carbon-to-carbon unsaturated bond in organic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/43Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • C07C51/44Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation
    • 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
    • Y02P20/584Recycling of catalysts

Landscapes

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

Abstract

1,252,698. Preparation of aliphatic acids. AMERICAN CYANAMID CO. 24 Dec., 1969 [18 Feb., 1969 (2)], No. 62843/69. Heading C2C. C 4-9 aliphatic carboxylic acids are prepared and recovered by (a) reacting CO with a C 3-8 aliphatic olefin in the presence of concentrated H 2 SO 4 as catalyst, (b) adding water to the product mixture from step (a), (c) distilling aliphatic acid and water from the product mixture of step (b) at a pressure less than 300 mm. Hg and temperature less than 200‹ C. until substantially all the aliphatic acid product is distilled over and water constitutes less than 20 % by weight of the distillation residue, and (d) repeating the steps (a), (b) and (c) using the distillation residue from step (c) as catalyst in step (a). The distillation step may be performed in the presence of steam, added for heating and stripping. In a modification of the process the catalyst of step (a) preferably comprises 15- 90% by weight of a mixture of hydroxyalkanesulphonic acid and its sulphuric acid ester, 0- 75% by weight H 2 SO 4 and less than 20% by weight of water, which catalyst is the distillation residue from step (c) of an earlier aliphatic carboxylic acid synthesis. In the examples propylene is converted to isobutyric acid.
GB1252698D 1969-02-18 1969-12-24 Expired GB1252698A (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US80025069A 1969-02-18 1969-02-18
US80028969A 1969-02-18 1969-02-18
ZA712199A ZA712199B (en) 1970-04-09 1971-04-07 New propionic acid and processes for its manufacture
FR7114809A FR2135729A5 (en) 1969-02-18 1971-04-26 Lower aliphatic acids - prepd and separated by a process allowing recycling of catalyst
BE766340A BE766340A (en) 1969-02-18 1971-04-27 PERFECTED PROCESS FOR THE SYNTHESIS AND ISOLATION OF LOWER ALIPHATIC ACIDS.
NL7105799A NL7105799A (en) 1969-02-18 1971-04-28

Publications (1)

Publication Number Publication Date
GB1252698A true GB1252698A (en) 1971-11-10

Family

ID=27543129

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1252698D Expired GB1252698A (en) 1969-02-18 1969-12-24

Country Status (1)

Country Link
GB (1) GB1252698A (en)

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PLNP Patent lapsed through nonpayment of renewal fees