GB776758A - Improvements in or relating to the oxidation of aliphatic carboxylic acids to peracids - Google Patents

Improvements in or relating to the oxidation of aliphatic carboxylic acids to peracids

Info

Publication number
GB776758A
GB776758A GB1751556A GB1751556A GB776758A GB 776758 A GB776758 A GB 776758A GB 1751556 A GB1751556 A GB 1751556A GB 1751556 A GB1751556 A GB 1751556A GB 776758 A GB776758 A GB 776758A
Authority
GB
United Kingdom
Prior art keywords
acid
per cent
hydrogen peroxide
aryl compounds
sulphonated
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
GB1751556A
Inventor
Alfred Theodore Hawkinson
William Rudolph Schmitz
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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
Priority to US471882A priority Critical patent/US2910504A/en
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to GB1751556A priority patent/GB776758A/en
Publication of GB776758A publication Critical patent/GB776758A/en
Expired legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/06—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
    • B01J31/08—Ion-exchange resins
    • B01J31/10—Ion-exchange resins sulfonated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C407/00—Preparation of peroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C407/00—Preparation of peroxy compounds
    • C07C407/003—Separation; Purification; Stabilisation; Use of additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

A method of preparing an aliphatic peracid comprises oxidizing with hydrogen peroxide an aliphatic carboxylic acid in the presence of a nuclear sulphonated aromatic hydrocarbon cation-exchange resin in its hydrogen form. Suitable resins are sulphonated polymers of polyvinyl aryl compounds, such as divinyl benzene and the sulphonated copolymers of such polyvinyl aryl compounds with monovinyl aryl compounds such as styrene described in Specification 571,029, [Group IV]. Preferred are aliphatic acids of 1 to 4 carbon atoms. When a liquid, the acid is usually employed in excess as the reaction medium. Reaction temperatures of 15 DEG to 70 DEG C., preferably 25 DEG to 50 DEG C. are suitable. The hydrogen peroxide is of at least 25 per cent and is preferably of 35 per cent strength. In Examples (1) and (2), glacial acetic acid is oxidized to peracetic acid by treatment with 50 per cent aqueous hydrogen peroxide at 40-45 DEG C. in the presence of a cation exchange resin (in the hydrogen form) obtained by sulphonating a copolymer of styrene and about 8 per cent divinyl benzene, the resin containing about one -SO3H group per benzene ring; (3) perpropionic acid is similarly prepared from propionic acid.
GB1751556A 1954-11-29 1954-12-02 Improvements in or relating to the oxidation of aliphatic carboxylic acids to peracids Expired GB776758A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US471882A US2910504A (en) 1954-11-29 1954-11-29 Preparation of aliphatic peracids
GB1751556A GB776758A (en) 1954-12-02 1954-12-02 Improvements in or relating to the oxidation of aliphatic carboxylic acids to peracids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1751556A GB776758A (en) 1954-12-02 1954-12-02 Improvements in or relating to the oxidation of aliphatic carboxylic acids to peracids

Publications (1)

Publication Number Publication Date
GB776758A true GB776758A (en) 1957-06-12

Family

ID=10096547

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1751556A Expired GB776758A (en) 1954-11-29 1954-12-02 Improvements in or relating to the oxidation of aliphatic carboxylic acids to peracids

Country Status (1)

Country Link
GB (1) GB776758A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5122538A (en) * 1990-07-23 1992-06-16 Ecolab Inc. Peroxy acid generator

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5122538A (en) * 1990-07-23 1992-06-16 Ecolab Inc. Peroxy acid generator

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