GB416885A - Improvements in the manufacture and production of artificial compositions - Google Patents
Improvements in the manufacture and production of artificial compositionsInfo
- Publication number
- GB416885A GB416885A GB33909/33A GB3390933A GB416885A GB 416885 A GB416885 A GB 416885A GB 33909/33 A GB33909/33 A GB 33909/33A GB 3390933 A GB3390933 A GB 3390933A GB 416885 A GB416885 A GB 416885A
- Authority
- GB
- United Kingdom
- Prior art keywords
- esters
- products
- saponification
- solution
- aqueous
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/12—Hydrolysis
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Artificial compositions are manufactured by treating with strong acids the saponification products of the mixed polymerization products obtainable by interpolymerizing acrylic acid esters and such vinyl esters as yield saponifiable polymerization products. When the saponification products are in the form of ammonium salts they may alternatively be subjected to a simple heat treatment, e.g. at 100--150 DEG C. in the absence of solvents. Suitable vinyl esters are the acetate, chloracetate, propionate, butyrate and stearate. Suitable acrylic acid esters are the alkyl esters, e.g. the methyl, ethyl and butyl esters, the cycloalkyl esters, e.g. the cyclohexyl ester, and the aralkyl esters, e.g. the benzyl ester. The esters are preferably used in equimolecular proportions, but either may be in excess. The saponification may be carried out in organic solvents, e.g. ethyl alcohol or, advantageously, in aqueous dispersion, and is effected by treating the polymerization products with aqueous acids and alkalies consecutively or with alkalies alone, at temperatures between room temperature and boiling point. Suitable strong acids for the subsequent treatment are sulphuric, hydrochloric, nitric, phosphoric, perchloric and trichloracetic acids. The products are suitable for the preparation of films, threads, coatings and dressings and may be worked up in a similar manner to celluloid, e.g. by hot pressing. In photographic films they may be employed as an intermediate layer between the nitrocellulose film and the layer of gelatine for increasing the electrical conductivity and preventing discharges. They may be worked up together with other substances of high molecular weight, e.g. with tragacanth, British gum, polyvinyl alcohol or starch to yield waterproof dressings or sizes, or with cellulose derivatives such as ammoniacal cupric oxide cellulose solution or cellulose xanthate to yield films or threads. In the latter case the alkaline solution of the saponification product may be added to an alkaline cellulose xanthate solution before its precipitation with acid. In examples: (1) an aqueous dispersion obtained by polymerization of an aqueous emulsion of vinyl acetate and acrylic acid methyl ester in the presence of emulsifying agents, e.g. a -hydroxyoctodecanesulphonic acid, and hydrogen peroxide, is saponified with caustic soda solution and then treated with dilute sulphuric acid ; the product may be pressed at 100--150 DEG C.; the aqueous alkaline solution of the saponification product may be mixed with a cellulose xanthate solution and the mixture coagulated in acid baths to produce films or threads; (2) the dispersion employed in (1) is saponified with aqueous ammonia and a highly viscous solution of the saponification product is inspissated and heated at 140 DEG C.ALSO:As sizes may be employed mixtures of tragacanth, British gum, polyvinyl alcohol or starch with the products obtained by the action of strong acids on the saponification products of the mixed polymerization products obtainable by interpolymerizing acrylic acid esters and such vinyl esters as yield saponifiable polymerization products, or by simple heat treatment when the saponification products are in the form of ammonium salts.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE416885X | 1932-12-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB416885A true GB416885A (en) | 1934-09-24 |
Family
ID=6448636
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB33909/33A Expired GB416885A (en) | 1932-12-10 | 1933-12-02 | Improvements in the manufacture and production of artificial compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB416885A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE747740C (en) * | 1936-09-27 | 1944-10-11 | Petrol-soluble paints |
-
1933
- 1933-12-02 GB GB33909/33A patent/GB416885A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE747740C (en) * | 1936-09-27 | 1944-10-11 | Petrol-soluble paints |
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