GB567575A - Improvements in and relating to the production of hydroxy carboxylic acids - Google Patents
Improvements in and relating to the production of hydroxy carboxylic acidsInfo
- Publication number
- GB567575A GB567575A GB477843A GB477843A GB567575A GB 567575 A GB567575 A GB 567575A GB 477843 A GB477843 A GB 477843A GB 477843 A GB477843 A GB 477843A GB 567575 A GB567575 A GB 567575A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- water
- less
- hydroxyacetic acid
- evaporation
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/01—Saturated compounds having only one carboxyl group and containing hydroxy or O-metal groups
- C07C59/06—Glycolic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A process for the production of mixtures consisting of hydroxyacetic acid and a high proportion of polyhydroxyacetic acid comprises evaporating within a period of two minutes and, preferably, in less than 0.6 min., substantially the whole of the water from an aqueous solution of hydroxyacetic acid, the said aqueous solution containing less than 40 per cent by weight of water. The aqueous acid solution may be obtained by the hydrolysis of a water-miscible alkyl ester of hydroxyacetic acid, for example, the methyl, ethyl, propyl, or butyl esters, in the absence of added hydrolysis catalyst other than hydroxyacetic acid and removing the alcohol produced thereby before the rapid evaporation step. Evaporation of the water from the aqueous acid solution takes place preferably at temperatures between 78-110 DEG C. and in the presence of a stream of dry inert gas such as carbon dioxide or nitrogen. The evaporation process may be carried out by "flash" evaporation and a suitable process is described which is identical as regards apparatus and conditions, with the process described in Specification 567,237. The molten dehydrated acid thus obtained may be cooled rapidly; when the polyacid content is less than 10 per cent it should be cooled in less than 45 seconds, preferably in less than 30 seconds, yielding micro-flake crystals. If desired, the molten or the solid product may be further dehydrated by heating and the application of reduced pressure to remove combined water and so give a product which may contain up to 131 per cent hydroxyacetic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB477843A GB567575A (en) | 1943-03-24 | 1943-03-24 | Improvements in and relating to the production of hydroxy carboxylic acids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB477843A GB567575A (en) | 1943-03-24 | 1943-03-24 | Improvements in and relating to the production of hydroxy carboxylic acids |
Publications (1)
Publication Number | Publication Date |
---|---|
GB567575A true GB567575A (en) | 1945-02-21 |
Family
ID=9783632
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB477843A Expired GB567575A (en) | 1943-03-24 | 1943-03-24 | Improvements in and relating to the production of hydroxy carboxylic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB567575A (en) |
-
1943
- 1943-03-24 GB GB477843A patent/GB567575A/en not_active Expired
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