GB548137A - Improvements in polyester resins - Google Patents

Improvements in polyester resins

Info

Publication number
GB548137A
GB548137A GB13350/40A GB1335040A GB548137A GB 548137 A GB548137 A GB 548137A GB 13350/40 A GB13350/40 A GB 13350/40A GB 1335040 A GB1335040 A GB 1335040A GB 548137 A GB548137 A GB 548137A
Authority
GB
United Kingdom
Prior art keywords
oil
acid
acids
alcohols
alcohol
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
GB13350/40A
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
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 American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB548137A publication Critical patent/GB548137A/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
    • C08G63/52Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Laminated Bodies (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

548,137. Polyhydric alcohol-poly carbonylic acid condensation products. AMERICAN CYNAMID CO. Aug. 22, 1940, No. 13350. Convention date, Dec. 13, 1939. [Class 2 (iii)] Polyester resins which may be converted by heat or oxidation into infusible and insoluble compositions are obtained by esterifying dicarboxylic acids or their anhydrides simultaneously with one or more polyhydric alcohols and with allyl alcohol or derivatives thereof. Esterification is effected by heating under azeotropic condition in presence of a solvent. Esterification catalysts may be employed and hardening of the ester is obtained by heating up to 165‹C. and with or without the aid of ultra violet or infra red radiations in presence of catalysts and/or inhibitors. The products obtained may be modified by monobasic acids and monohydric alcohols and mixed with fillers, dyes, or other synthetic or natural resins. The resins obtained are suitable for the production of coating compositions food containers, laminated paper, cloth material, electrical insulation, gear wheels, abrasive discs, brake linings, tobacco pouches, gaskets, &c. There are specified : (1) dibasic acids-maleic, fumaric, itaconic, mesaconic, and halogenated acids, e.g. chloromaleic acid, phthalic, sebacic, adipic, azelaic, terephthalic, pimelic, and brassylic acids. (2) mono-basic acids-acrylic, betabenzoylic acrylic, methacrylic - cyclohexene carboxylic, cinnamic, crotonic, undecylenic acids. (3) polyhydric alcohols-ethylene and polyethylene glycols, polymethylene glycols, octadecandiol, 2.2-dimethyl propane diol-1.3 ; 1.3 butane diol ; 1.2-propane diol ; 2-ethyl 2 butyl butanediol-1.3 ; glycerol or glycerol monoethers ; trimethylolpropane ; nitroglycols. (4) unsatucrated alcohols-allyl, and methylallyl alcohols, methyl vinyl carbinol, allyl carbinol, beta allyl ethyl alcohol, crotyl alcohol, halogenated allyl alcohols e.g. 2-chlor-allyl alcohol; monoallyl and monomethallyl ethers of ethylene glycol. (5) modifiers-monohydric saturated alcohols; drying oils or their fatty acids and esters, e.g. linseed oil, perilla oil, oiticica oil, sunflower seed oil, tung oil, olein, oleic acid stearin, stearic acid, castor oil, soya bean oil, olive oil. (6) solvents benzene, toluene, xylene, chloroform, carbon tetrachloride, ethylene or butylene di- or tri-chlorides, cresols, cyclo and methylcylo hexanone ; excess of the unsaturated alcohol itself may be used as solvent. (7) esterification catalysts-p-toluene sulphonic acid, thymol sulphonic, acid d-camphor sulphonic acid, stannic chloride, stannic chloride dioxanate. (8) polymerization catalysts acidic peroxides e.g. benzoyl, phthalic, succinic, benzoyl acetic peroxides ; fatty oil acid peroxides, e.g. lauryl, cocoanut oil and oleic peroxides ; alcohol peroxides, e.g. tertiary butyl peroxide and terpene oxides ; ascaridole. soluble cobalt salts, p-toluene sulphonic acid ; aluminium chloride, stannic chloride, boron trifluoride. (9) polymerization inhibitors polyhydric phenols, e.g. hydroquinone, resorcinol, tannin ; aromatic amines, e.g. alpha, beta-naphthylparaphenylene diamine ; phenolic resins ; sulphur compounds, benzaldehyde, 1-ascorbutic acid. (10) fillers-wood flour, paper dust, clay, zein, glass wool mica dust, asbestos, casein, silk or cotton flock, steel wool, carborundum, paper, cloth, sand, pigments ; dyes ; natural resins, e.g. shellac cellulose esters and ethers, synthetic resins, urea-aldehyde, triazine-aldehyde, phenolaldehyde, alkyds ; ester gum, rubber, and synthetic rubber products.
GB13350/40A 1939-12-13 1940-08-22 Improvements in polyester resins Expired GB548137A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US548137XA 1939-12-13 1939-12-13

Publications (1)

Publication Number Publication Date
GB548137A true GB548137A (en) 1942-09-28

Family

ID=21993690

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13350/40A Expired GB548137A (en) 1939-12-13 1940-08-22 Improvements in polyester resins

Country Status (1)

Country Link
GB (1) GB548137A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2524921A (en) * 1946-08-30 1950-10-10 Westinghouse Electric Corp Unsaturated esters and synthetic resinous products produced therewith
US2570385A (en) * 1946-01-28 1951-10-09 Montclair Res Corp Addition products of esters comprising a polyhydric alcohol esterified with drying oil acids and an alkenol-dicarboxylic acid monoester and process of making same
DE1049091B (en) * 1952-07-05 1959-01-22 Dow Chemical Co Process for the production of laminated bodies, coatings and molded bodies
DE1166467B (en) * 1959-04-15 1964-03-26 Beck & Co G M B H Dr Polyester molding compounds
US3316193A (en) * 1962-01-04 1967-04-25 Vantorex Ltd Polyester resins prepared from trimethylol propane diallyl ether
US9791012B1 (en) 2016-04-20 2017-10-17 King Abdulaziz University Thermo-set resin composition for brake pads, method of preparation, and brake pad assembly
CN113874105A (en) * 2019-05-31 2021-12-31 沙特基础工业全球技术公司 Process for preparing high purity 1-butene

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2570385A (en) * 1946-01-28 1951-10-09 Montclair Res Corp Addition products of esters comprising a polyhydric alcohol esterified with drying oil acids and an alkenol-dicarboxylic acid monoester and process of making same
US2524921A (en) * 1946-08-30 1950-10-10 Westinghouse Electric Corp Unsaturated esters and synthetic resinous products produced therewith
DE1049091B (en) * 1952-07-05 1959-01-22 Dow Chemical Co Process for the production of laminated bodies, coatings and molded bodies
DE1166467B (en) * 1959-04-15 1964-03-26 Beck & Co G M B H Dr Polyester molding compounds
US3316193A (en) * 1962-01-04 1967-04-25 Vantorex Ltd Polyester resins prepared from trimethylol propane diallyl ether
US9791012B1 (en) 2016-04-20 2017-10-17 King Abdulaziz University Thermo-set resin composition for brake pads, method of preparation, and brake pad assembly
CN113874105A (en) * 2019-05-31 2021-12-31 沙特基础工业全球技术公司 Process for preparing high purity 1-butene

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