GB573468A - Improvements in or relating to the manufacture of acetic anhydride - Google Patents
Improvements in or relating to the manufacture of acetic anhydrideInfo
- Publication number
- GB573468A GB573468A GB935841A GB935841A GB573468A GB 573468 A GB573468 A GB 573468A GB 935841 A GB935841 A GB 935841A GB 935841 A GB935841 A GB 935841A GB 573468 A GB573468 A GB 573468A
- Authority
- GB
- United Kingdom
- Prior art keywords
- paraldehyde
- acid
- vanadic
- acetaldehyde
- acetate
- 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
Links
Landscapes
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Acetic anhydride is produced by oxidation with molecular oxygen of a mixture of acetaldehyde and paraldehyde at below 60 DEG C. followed by distillation in which the water is entrained by the paraldehyde. The initial mixture may be obtained by partial polymerization of acetaldehyde or partial depolymerization of paraldehyde. Suitable depolymerizing agents are sulphuric, phosphoric and sulphonic acids and acidic salts such as zinc, aluminium and ferric chlorides and vanadic acid. The oxidation catalyst should be of such nature and quantity as not to neutralize the depolymerization agent; for instance, manganese or cobalt acetate should be used in small quantity; vanadic acid, especially when activated with acetic acid, may be used with or without cobalt or manganese acetates. An active vanadic catalyst may be made by adding hydrogen peroxide or another peroxidic compound to vanadium pentoxide in acetic acid, whereby the pentoxide is dissolved. Suitable apparatus is described. Examples describe the oxidation with oxygen of (1) paraldehyde, acetaldehyde, and vanadic acid; (2) paraldehyde, sulphuric acid and vanadic acid; (3) paraldehyde, acetic acid, sulphuric acid, cobalt acetate and copper acetate. In each case the water is removed with paraldehyde by azeotropic distillation. The concentration of percompounds in the reaction product can be reduced by diluting with paraldehyde or by adding manganese acetate, preferably after neutralizing any acid depolymerizing agent present. Specification 461,808 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB935841A GB573468A (en) | 1941-07-23 | 1941-07-23 | Improvements in or relating to the manufacture of acetic anhydride |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB935841A GB573468A (en) | 1941-07-23 | 1941-07-23 | Improvements in or relating to the manufacture of acetic anhydride |
Publications (1)
Publication Number | Publication Date |
---|---|
GB573468A true GB573468A (en) | 1945-11-22 |
Family
ID=9870399
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB935841A Expired GB573468A (en) | 1941-07-23 | 1941-07-23 | Improvements in or relating to the manufacture of acetic anhydride |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB573468A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111116348A (en) * | 2019-12-27 | 2020-05-08 | 浙江工业大学 | Preparation method for synthesizing carboxylic acid by oxidizing aldehyde with bimetallic catalyst |
-
1941
- 1941-07-23 GB GB935841A patent/GB573468A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111116348A (en) * | 2019-12-27 | 2020-05-08 | 浙江工业大学 | Preparation method for synthesizing carboxylic acid by oxidizing aldehyde with bimetallic catalyst |
CN111116348B (en) * | 2019-12-27 | 2023-02-03 | 浙江工业大学 | Preparation method for synthesizing carboxylic acid by oxidizing aldehyde with bimetallic catalyst |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB633354A (en) | Process for the production of dibasic carboxylic acids | |
US4032569A (en) | Process for converting cyclohexane to adipic acid | |
US2373942A (en) | Catalytic hydroxylation of olefinic double bonds | |
US4158739A (en) | Process for converting cyclopentane to glutaric acid | |
IE35149L (en) | Vicinal glycol esters | |
GB573468A (en) | Improvements in or relating to the manufacture of acetic anhydride | |
GB872355A (en) | Improvements in or relating to the production of a tetrabasic acid and esters thereof | |
US2259895A (en) | Process for manufacture of aliphatic carboxylic acid anhydrides | |
GB1056125A (en) | Palladium salts of condensed phosphoric acid | |
GB173004A (en) | Improvements in and relating to the production of butyric aldehyde and butyric acid therefrom | |
US2397891A (en) | Oxidation of acrolein to acrylic acid | |
GB782430A (en) | Improvements in the oxidation of organic aldehydes | |
GB482736A (en) | Process for the manufacture of methacrylic acid and esters thereof | |
GB577992A (en) | Production of allyl alcohol and esters thereof | |
GB595170A (en) | Production of crotonic acid | |
GB830671A (en) | Process for oxidizing glutaraldehydes | |
Ipatieff et al. | The Dehydration of the Lower Aliphatic Alcohols in the Presence of Dilute Aqueous Solutions of Acids and Salts | |
DE1643158B2 (en) | ||
GB824116A (en) | Process for the oxidation of organic compounds | |
GB573467A (en) | Improvements in or relating to the manufacture of acetic acid | |
GB837321A (en) | Improvements in and relating to an oxidation process for the production of aromatic carboxylic acids | |
GB405173A (en) | Manufacture of substituted malonic acids | |
GB573531A (en) | Improvements in or relating to the reduction of the peracid content of oxidation reaction products | |
GB767416A (en) | Process for oxidizing glutaraldehyde | |
GB745594A (en) | Recovery and preparation of lower percarboxylic acids |