GB416885A - Improvements in the manufacture and production of artificial compositions - Google Patents

Improvements in the manufacture and production of artificial compositions

Info

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
Application number
GB33909/33A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB416885A publication Critical patent/GB416885A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/12Hydrolysis

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.
GB33909/33A 1932-12-10 1933-12-02 Improvements in the manufacture and production of artificial compositions Expired GB416885A (en)

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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE747740C (en) * 1936-09-27 1944-10-11 Petrol-soluble paints

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE747740C (en) * 1936-09-27 1944-10-11 Petrol-soluble paints

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