GB839404A - New polyesters - Google Patents

New polyesters

Info

Publication number
GB839404A
GB839404A GB3256157A GB3256157A GB839404A GB 839404 A GB839404 A GB 839404A GB 3256157 A GB3256157 A GB 3256157A GB 3256157 A GB3256157 A GB 3256157A GB 839404 A GB839404 A GB 839404A
Authority
GB
United Kingdom
Prior art keywords
heating
polyesters
ester
propane
diphenyl ether
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
GB3256157A
Inventor
George Isaac Maurice Bloom
Brian Edmund Jennings
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB3256157A priority Critical patent/GB839404A/en
Publication of GB839404A publication Critical patent/GB839404A/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
    • C08G63/66Polyesters containing oxygen in the form of ether groups
    • C08G63/668Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/672Dicarboxylic acids and dihydroxy compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)

Abstract

New polyesters, suitable for the manufacture of mouldings, films, lacquers and protective coatings have repeated units of the formula: <FORM:0839404/IV (a)/1> The polyesters may be made (1) by reacting an aqueous solution of a di-alkali metal salt of 2,2 - (4,41 - dihydroxy diphenyl) propane with a solution of the acid chloride or bromide of 4,41-dicarboxy diphenyl ether in a non-solvent for the polyester (e.g. benzene or toluene) or in a solvent for the polyester (e.g. methylene chloride, 1,2 - dichloroethane, 1,1,2 - trichloroethane or tetrachloroethane); catalysts for the reaction being trimethyl (or triethyl) benzyl ammonium hydroxide or chloride; (2) by heating equimolecular proportions of 2,2-(4,41-dihydroxy diphenyl) propane and the acid chloride or bromide of 4,41-dicarboxy diphenyl ether; (3) by heating at about 200 DEG C. 1 mol. of 2,2-(4,41-dihydroxy diphenyl) propane with slightly more than 1 mol. of the dimethyl, diethyl, dipropyl or dibutyl ester of 4,41-di-carboxy diphenyl ether and 1.5 mols. of a polymethylene glycol containing 2-10 carbon atoms in the presence of an ester-interchange catalyst whereby alkyl alcohol is distilled off and then heating at about 300 DEG C. to distil off most of thepoly methylene glycol; specified ester-interchange catalysts being lead oxide; alcoholates or glycolates of the alkali metals, the alkaline earth metals or magnesium; borates or carbonates of the alkali metals; magnesium oxide; and esters of ortho-titanic acid; (4) by effecting ester-interchange between the diacetate of 2,2-(4,41-dihydroxy diphenyl) propane and 4,41-dicarboxy diphenyl ether or its dimethyl ester. The molecular weight of the polyesters may be increased by heating them above their melting point in vacuo or by heating them in powder form at just below their sintering temperature. Before use the polyesters are preferably dried by heating them at 110-120 DEG C. in vacuo. The polyesters may be used in the manufacture of housings, gears, bearings, bushings and electrical components. The polyester films may be used in the manufacture of container liners, electrical insulating tapes and sound recording tapes. Plasticizers, stabilizers, fillers, dyes or pigments may be added.
GB3256157A 1957-10-18 1957-10-18 New polyesters Expired GB839404A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3256157A GB839404A (en) 1957-10-18 1957-10-18 New polyesters

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3256157A GB839404A (en) 1957-10-18 1957-10-18 New polyesters

Publications (1)

Publication Number Publication Date
GB839404A true GB839404A (en) 1960-06-29

Family

ID=10340563

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3256157A Expired GB839404A (en) 1957-10-18 1957-10-18 New polyesters

Country Status (1)

Country Link
GB (1) GB839404A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0146361A2 (en) * 1983-12-16 1985-06-26 E.I. Du Pont De Nemours And Company Melt-Spinnable copolyesters

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0146361A2 (en) * 1983-12-16 1985-06-26 E.I. Du Pont De Nemours And Company Melt-Spinnable copolyesters
EP0146361A3 (en) * 1983-12-16 1985-07-24 E.I. Du Pont De Nemours And Company Melt-spinnable copolyesters

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