GB636295A - Improvements in and relating to the production of water-soluble mixed cellulose ethers - Google Patents
Improvements in and relating to the production of water-soluble mixed cellulose ethersInfo
- Publication number
- GB636295A GB636295A GB472748A GB472748A GB636295A GB 636295 A GB636295 A GB 636295A GB 472748 A GB472748 A GB 472748A GB 472748 A GB472748 A GB 472748A GB 636295 A GB636295 A GB 636295A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ether
- cellulose
- water
- solution
- mixed
- 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
- C08B11/14—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with nitrogen-containing groups
- C08B11/155—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with nitrogen-containing groups with cyano groups, e.g. cyanoalkyl ethers
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Artificial Filaments (AREA)
Abstract
A water-soluble mixed ether of cellulose containing the cyano-ethyl group is obtained by dissolving a water-insoluble alkali-soluble cellulose ether, the degree of substitution of which does not exceed one ether group per anhydroglucose unit of the cellulose, in a dilute aqueous alkali hydroxide solution containing not more than 6 per cent by weight of caustic alkali, and reacting on the solution obtained with from 0.1 to 2.5 mols. of acrylonitrile per anhydroglucose unit originally present in the cellulose. The water-insoluble cellulose ether may be a lowly substituted methyl or hydroxyethyl cellulose ether. The acrylonitrile may be added in drops to the solution of cellulose ether while stirring or shaking, the temperature of the reaction being maintained at 20 DEG C. The water-soluble mixed ethers may be obtained from the reaction mixture by stirring the mixture into a weak aqueous solution of hydrochloric acid to obtain a clear, slightly acid, solution which can then be purified by dialysis in a regenerated cellulose casing. If the mixed ether is required as a paste, the dialyzed solution may be concentrated by evaporation under reduced pressure. If the solid ether is required, the dialyzed liquid may be concentrated by vacuum distillation and the ether is precipitated by adding alcohol or acetone. The mixed ether may be obtained by directly precipitating from the neutralized reaction mixture by the addition of alcohol or acetone. The mixed ethers are readily soluble in acidic, neutral, or alkaline aqueous solutions as well as in hot or cold water. They may be used as sizes for textile yarns, particularly for viscose rayon warp yarns. They may be used as emulsifying agents, thickeners for printing pastes, and adhesives for wall-papers. They are resistant to attack by micro-organisms. In an example, a mixed ether containing 0.36 cyano-ethyl groups per anhydroglucose unit is obtained by the action of acrylonitrile on a solution in 4 per cent caustic soda of a water-insoluble hydroxyethyl cellulose. In another example, a mixed ether containing 0.4 cyanoethyl groups per anhydroglucose unit is obtained by the action of acrylonitrile on a solution in 5 per cent caustic soda of a water-insoluble methyl cellulose. Specifications 344,488, 374,964, 588,751 and 592,352, are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB472748A GB636295A (en) | 1948-02-18 | 1948-02-18 | Improvements in and relating to the production of water-soluble mixed cellulose ethers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB472748A GB636295A (en) | 1948-02-18 | 1948-02-18 | Improvements in and relating to the production of water-soluble mixed cellulose ethers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB636295A true GB636295A (en) | 1950-04-26 |
Family
ID=9782644
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB472748A Expired GB636295A (en) | 1948-02-18 | 1948-02-18 | Improvements in and relating to the production of water-soluble mixed cellulose ethers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB636295A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3093629A (en) * | 1961-08-11 | 1963-06-11 | American Cyanamid Co | Water insoluble cyanoethylated hydroxyethyl cellulose of high nitrogen content |
US3096289A (en) * | 1961-08-11 | 1963-07-02 | American Cyanamid Co | Dielectric plastic |
US3315329A (en) * | 1963-10-21 | 1967-04-25 | Kurashiki Rayon Co | Process for the manufacture of chemical lace |
-
1948
- 1948-02-18 GB GB472748A patent/GB636295A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3093629A (en) * | 1961-08-11 | 1963-06-11 | American Cyanamid Co | Water insoluble cyanoethylated hydroxyethyl cellulose of high nitrogen content |
US3096289A (en) * | 1961-08-11 | 1963-07-02 | American Cyanamid Co | Dielectric plastic |
US3315329A (en) * | 1963-10-21 | 1967-04-25 | Kurashiki Rayon Co | Process for the manufacture of chemical lace |
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