GB366022A - Manufacture of acetic acid - Google Patents

Manufacture of acetic acid

Info

Publication number
GB366022A
GB366022A GB3216930A GB3216930A GB366022A GB 366022 A GB366022 A GB 366022A GB 3216930 A GB3216930 A GB 3216930A GB 3216930 A GB3216930 A GB 3216930A GB 366022 A GB366022 A GB 366022A
Authority
GB
United Kingdom
Prior art keywords
acetic acid
scrubbing
liquid
reaction
oxidation
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
GB3216930A
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.)
Acordis UK Ltd
Original Assignee
British Celanese Ltd
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 British Celanese Ltd filed Critical British Celanese Ltd
Priority to GB3216930A priority Critical patent/GB366022A/en
Publication of GB366022A publication Critical patent/GB366022A/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
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/23Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups
    • C07C51/235Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups of —CHO groups or primary alcohol groups

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

In the oxidation of liquid acetaldehyde to acetic acid the gases or vapours leaving the reaction vessel are scrubbed with a liquid, and the scrubbings passed to the reaction liquor. Preferably the scrubbing is effected continuously during the oxidation, e.g. by means of a condenser, scrubbing tower, or the like through which the scrubbing liquor flows and arranged so that the scrubbing liquor flows therefrom into the vapour space above the liquid in the reaction vessel. Several such scrubbing vessels may be employed, arranged for instance in series, in which case the scrubbing liquid may be passed successively through the vessels of the series. Any liquid which does not deleteriously affect the oxidation may be used for the scrubbing, but it is preferred to use acetic acid, particularly glacial acetic acid or a reaction liquor containing acetic acid, particularly a liquor containing 40-50 per cent of acetic acid. The acetaldehyde to be oxidized need not be pure, e.g. mixtures of acetaldehyde and acetic acid may be treated, but the aldehyde should be as free as possible from water. The oxygen may be pure or admixed with inert gases, as in air, and is preferably introduced into the reaction liquid in the form of fine bubbles, this finely divided state being further promoted by agitation of the liquid. The reaction liquor may contain any catalyst capable of promoting the oxidation of aldehyde to acetic acid, e.g. manganese compounds such as manganous acetate, uranium dioxide, ferric oxide, ferric acetate, chromium sesquioxide, or vanadium pentoxide, or the catalysts described in Specifications 154,304 and 154,680, [both in Class 2 (iii), Dyes &c.], i.e. china clay or kaolin, or the residue which remains after igniting animal charcoal, or mixtures thereof with sodium acetate. The oxidation may be performed under ordinary or raised pressures, for example 20-40 pounds per square inch, or more, the use of raised pressure being especially useful in cases where air or other gaseous mixture containing oxygen is employed. The temperature may be between 0 DEG and 50 DEG C., low temperatures up to 20 DEG C. being useful when oxygen is employed, while with air or like mixtures temperatures between 20 DEG and 50 DEG C. are employed. During the initial stages, and intermittently throughout the reaction, the vapour space or the reaction space or both may be cooled to low temperatures, e.g. 0-5 DEG C., and the scrubbing vessels are preferably provided with water or brine cooling. Any aldehyde escaping condensation may be covered e.g. by subjecting the gases to scrubbing with acetic acid, water, or the like. In the example, the oxidation is effected in an aluminium vessel, and the vapours are scrubbed with glacial acetic acid, which passes to the reaction vessel.
GB3216930A 1930-10-27 1930-10-27 Manufacture of acetic acid Expired GB366022A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3216930A GB366022A (en) 1930-10-27 1930-10-27 Manufacture of acetic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3216930A GB366022A (en) 1930-10-27 1930-10-27 Manufacture of acetic acid

Publications (1)

Publication Number Publication Date
GB366022A true GB366022A (en) 1932-01-27

Family

ID=10334368

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3216930A Expired GB366022A (en) 1930-10-27 1930-10-27 Manufacture of acetic acid

Country Status (1)

Country Link
GB (1) GB366022A (en)

Similar Documents

Publication Publication Date Title
US2461740A (en) Process of making organic acids from carbonaceous material
GB948687A (en) Process for producing acrylic acid and acrylic acid methyl ester
GB434302A (en) Improvements in or relating to the absorption of nitrogen oxides
GB366022A (en) Manufacture of acetic acid
GB410394A (en) Improvements in or relating to a process for making diketene
GB455734A (en) Process for the absorption, in highly-concentrated nitric acid, of nitrous gases formed by the combustion of ammonia
GB456518A (en) Improvements in or relating to the production of highly concentrated nitric acid
US2830080A (en) Preparation of peracetic acid
GB368348A (en) Improvements in or relating to the manufacture of acetic acid
GB478318A (en) Improvements in the conversion of carbon monoxide with hydrogen into hydrocarbons or their oxygen-containing derivatives
GB593571A (en) Improvements in or relating to the manufacture of crotonic acid
US1937528A (en) Process for the production of acetic acid
US1487020A (en) Oxidation process
GB786747A (en) Improvements in and relating to the production of aromatic di-carboxylic acids
GB907926A (en) Improvements in or relating to the production of trimellitic acid and trimellitic anhydride
SU13005A1 (en) Acetone Production Method
SU555084A1 (en) The method of obtaining 2-or 4-methylcyclohexanone
US2027420A (en) Process for removing water from vaporous mixtures containing aliphatic anhydrides
GB698165A (en) Improvements in the production of gases containing sulphur trioxide
GB797213A (en) Manufacture of terephthalic acid
GB350874A (en) Process for the production of acetic acid
GB308937A (en) Improvements in the production of acetic acid
GB811870A (en) Preparation of para-nitrobenzoic acid
GB405173A (en) Manufacture of substituted malonic acids
GB302759A (en) Improved process for the production of aliphatic ketones