GB231809A - Manufacture of new cellulose derivatives - Google Patents
Manufacture of new cellulose derivativesInfo
- Publication number
- GB231809A GB231809A GB13357/24A GB1335724A GB231809A GB 231809 A GB231809 A GB 231809A GB 13357/24 A GB13357/24 A GB 13357/24A GB 1335724 A GB1335724 A GB 1335724A GB 231809 A GB231809 A GB 231809A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali
- acid
- lye
- molecular
- fatty acid
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/02—Alkyl or cycloalkyl ethers
- C08B11/04—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals
- C08B11/10—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals substituted with acid radicals
- C08B11/12—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals substituted with acid radicals substituted with carboxylic radicals, e.g. carboxymethylcellulose [CMC]
Abstract
Cellulose derivatives soluble in aqueous alkalies, and which are precipitated as products insoluble in water by the addition of alcohol to the solutions in aqueous alkalies, are prepared by carrying out the treatment of cellulose or a cellulose conversion product insoluble in alkali, with a monohalogen fatty acid, or a salt or ester of such acid, and alkali, in the absence of alcohol or in the presence of not more than 20 parts of alcohol for each 100 parts of water present; the process is conducted so that the maximum quantity of halogen fatty acid &c. is inversely proportional to the strength of the alkali solution. Other conditions are:-the halogen fatty acid should not be used in more than 18/a molecular proportions to each molecular proportion of caustic alkali, where a represents the percentage strength of the alkali lye; for each molecular proportion of caustic alkali, if this is used as a solution of not more than 25 per cent strength, there should be used not more than 180 (n + 1)/a molecular proportions of halogen fatty acid (a being the percentage strength of the alkali lye, and n the number of parts of alkali lye used to each part of cellulose), or, if the alkali lye is of more than 25 per cent strength, not more than 60/a (n + 1) molecular equivalents of halogen fatty acid, or generally, with lye up to 25 per cent strength, not more than 0.75-1 molecular proportions of halogen fatty acid, and with stronger lye, not more than 0.5-0.6 molecular equivalents, although smaller amounts than these are usually sufficient; and there should be used not more than one molecular equivalent of halogen fatty acid to one molecular proportion of cellulose. The cellulose &c. to be treated may be soaked in an excess of alkali lye, the surplus being subsequently removed, or it may be mixed or kneaded with the required quantity of lye, or with solid caustic alkali, or with a mixture of solid caustic alkali and saturated lye; the reaction is carried out at room temperature or below, or with the application of heat; and contact substances such as copper, iron, silver, and benzoyl superoxide may be added. Suitable halogen fatty acids &c. are:-monochloracetic acid, methyl or ethyl chloracetate, a-bromopropionic acid, bromosuccinic acid, a-bromo-isobutyric acid and their salts and esters. The products are isolated from the reaction mixtures by the addition of an acid, an acid salt, &c., or by treating with alcohol. When precipitated in the form of threads and films from their solutions, they give solid, flexible, and transparent products. The cellulose derivatives may be employed in the manufacture of artificial fibres, films, plastic compositions, coatings, dressings for fabrics, sizes, thickening-agents for textile printing, agents for fixing pigments, &c. Specifications 138,116, 177,810, 203,346, and 203,347 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT231809X | 1924-04-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB231809A true GB231809A (en) | 1925-09-30 |
Family
ID=3669955
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB13357/24A Expired GB231809A (en) | 1924-04-04 | 1924-05-30 | Manufacture of new cellulose derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB231809A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003010206A1 (en) * | 2001-07-20 | 2003-02-06 | Unilever Plc | Polymers and their synthesis |
-
1924
- 1924-05-30 GB GB13357/24A patent/GB231809A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003010206A1 (en) * | 2001-07-20 | 2003-02-06 | Unilever Plc | Polymers and their synthesis |
US7041730B2 (en) | 2001-07-20 | 2006-05-09 | Unilever Home & Personal Care Usa Division Of Conopco, Inc. | Polymers and their synthesis |
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