GB377265A - Improved method for the manufacture of plastic materials - Google Patents

Improved method for the manufacture of plastic materials

Info

Publication number
GB377265A
GB377265A GB11388/31A GB1138831A GB377265A GB 377265 A GB377265 A GB 377265A GB 11388/31 A GB11388/31 A GB 11388/31A GB 1138831 A GB1138831 A GB 1138831A GB 377265 A GB377265 A GB 377265A
Authority
GB
United Kingdom
Prior art keywords
oxidized
condensation
glycerine
permanganate
saponification
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
GB11388/31A
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.)
Auergesellschaft GmbH
Original Assignee
Auergesellschaft GmbH
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 Auergesellschaft GmbH filed Critical Auergesellschaft GmbH
Publication of GB377265A publication Critical patent/GB377265A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/46Polyesters chemically modified by esterification

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)
  • Polyethers (AREA)

Abstract

Plastic material is prepared by the condensation of polyhydric alcohols, e.g. glycerine, glycol, polyglycerine, polyglycol, pentaerythrite, with the product obtained on oxidizing oils containing the glycerides of unsaturated acids. The process of oxidation may also cause saponification of the oil, in which case the glycerine set free may be removed or may be utilized as part of the polyhydric alcohol required for the condensation, but it is preferred to oxidize in such a way that the ester linkage is not destroyed, so that the dicarboxylic acids produced are already partly esterified. In either case, monocarboxylic acids may be removed from the oxidation product before the final condensation. Other mono- or polybasic acids and also other artificial and natural resins may be added prior to or during the condensation. In examples, (1) olive oil, dissolved in acetone or emulsified in potash solution, is oxidized with permanganate and the saponification completed by boiling. The manganese compound is filtered off, and the filtrate extracted with ether, or neutralized and extracted with alcohol. The solvent is removed, glycerine added to the residue, and the whole heated to 170 DEG C. to yield a resin. (2) Olive oil in acetone is oxidized with permanganate, and the whole treated with dilute sulphuric acid in the cold, whereby saponification is avoided. The monocarboxylic acids are removed by distillation in vacuo and the residue condensed as before. By using much less permanganate, some of the oleic acid is not oxidized, and very soft products are obtained. (3) Nitric acid is the oxidizing agent. (4) Linseed oil in chloroform is oxidized by means of ozone. In the Specification as open to inspection under Sect. 91 (3) (a) it is stated that the oils may first be saponified and then oxidized. This subject-matter does not appear in the Specification as accepted.
GB11388/31A 1930-04-17 1931-04-17 Improved method for the manufacture of plastic materials Expired GB377265A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE377265X 1930-04-17

Publications (1)

Publication Number Publication Date
GB377265A true GB377265A (en) 1932-07-18

Family

ID=6344386

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11388/31A Expired GB377265A (en) 1930-04-17 1931-04-17 Improved method for the manufacture of plastic materials

Country Status (2)

Country Link
FR (1) FR715584A (en)
GB (1) GB377265A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2437657A (en) * 1945-01-04 1948-03-09 American Cyanamid Co Heat-stable plasticized resin compositions
US2560319A (en) * 1945-01-04 1951-07-10 American Cyanamid Co Heat-stable plasticized aminotriazine resin compositions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2437657A (en) * 1945-01-04 1948-03-09 American Cyanamid Co Heat-stable plasticized resin compositions
US2560319A (en) * 1945-01-04 1951-07-10 American Cyanamid Co Heat-stable plasticized aminotriazine resin compositions

Also Published As

Publication number Publication date
FR715584A (en)

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