GB710513A - Polyester terpolymers - Google Patents

Polyester terpolymers

Info

Publication number
GB710513A
GB710513A GB23747/51A GB2374751A GB710513A GB 710513 A GB710513 A GB 710513A GB 23747/51 A GB23747/51 A GB 23747/51A GB 2374751 A GB2374751 A GB 2374751A GB 710513 A GB710513 A GB 710513A
Authority
GB
United Kingdom
Prior art keywords
anhydride
methyl
carbic
diethyl
acids
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
GB23747/51A
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.)
Union Carbide Corp
Original Assignee
Union Carbide and Carbon Corp
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 Union Carbide and Carbon Corp filed Critical Union Carbide and Carbon Corp
Publication of GB710513A publication Critical patent/GB710513A/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
    • C08G63/54Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation the acids or hydroxy compounds containing carbocyclic rings
    • C08G63/553Acids or hydroxy compounds containing cycloaliphatic rings, e.g. Diels-Alder adducts
    • 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
    • C08F283/00Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/01Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Terpolymers of (1) an organic solvent soluble polyhydric alcohol polyester of cis-3, 6-endomethylene delta-4-tetrahydrophthalic anhydride containing not more than three diacyl residues of the dibasic adduct per average polyester molecule, (2) styrene or its derivatives, and (3) a mono-olefinic compound having in conjunction with the double bond either a carboxyl or cyano group, are prepared by heating in solution in the presence of a catalyst. Styrene derivatives mentioned are, p-chlorostyrene, 2, 5-dichlorostyrene, p-methyl, p-ethyl and p-isopropyl styrenes, p-dimethyl-amino vinyl benzene and p-benzyl styrene. The monoolefinic compounds (2) may be acrylonitrile, methacrylonitrile, methacrylamide, N, N1-dimethylacrylamide, acrylic or methacrylic acid or their methyl, ethyl, propyl, methoxy or propoxy esters, mono- and diesters of unsaturated dicarboxylic acids, such as monobutyl maleate, and ethyl and diethyl crotonates (a long list of suitable mono- and di-carboxylic acids and their esters is given), vinyl ketones such as methyl and phenyl vinyl ketones and monohydric half esters of D 1, 4-dihydro phthalic acid, or of "Carbic" (R.T.M.) acid or anhydride. Dicarboxylic acids, e.g. phthalic, succinic and adipic acids, and monocarboxylic acids, e.g. those derived from linseed and soya oils may partially replace the anhydride (1). Solvents used may be benzene, toluene, xylene, butyl acetate, or propionate, diethyl phthalate, diethylene glycol monobutyl ether acetate, methyl isobutyl and diisobutyl ketones, and n-butyl ether, together with diluents such as mineral spirits or petroleum naphtha. The catalysts, e.g. benzoyl, p-chlorobenzoyl, and methyl amyl ketone peroxides, t-butyl per benzoate and t-butyl and cumene hydroperoxides may be added portionwise. Examples describe the preparation of polyesters from "Carbic" anhydride modified with castor oil, alone or with glycerol or ethylene glycol or a mixture of these, lauric acid, coconut and soya bean oils or their fatty acids, with glycerol; "Carbic" anhydride mixed with phthalic anhydride and castor oil or 2-ethylhexandiol 1, 3; "Carbic" anhydride with castor oil, glycerol and hydrogenated rosin; or mixed "Carbic" anhydride-phthalic anhydride with castor oil, glycerol and hydrogenated rosin acids or hydroabietyl alcohol. The polyesters are then polymerised with styrene and ethyl acrylate, 3-ethoxy propyl acrylate, methyl methacrylate, dimethyl, diethyl or dioctyl maleate, dimethyl dichloromaleate, diethylmonochloromaleate, diethyl dihydrophthalate, diethyl itaconate or citraconate, methylacrylonitrile, methacrylamide and the diethyl ester of "Carbic" anhydride. Terpolymers including acrylonitrile require solvents such as methoxyacetamide, N-formyl morpholine and N-formyl hexamethylene imine in their preparation. The terpolymers may be used in coating compositions with nitrocellulose dissolved in butyl acetate, or a blend of phenyl methyl carbinol with acetophenone, with partially hydrolysed vinyl chloride-acetate copolymer dissolved in methyl isobutyl ketone, with cellulose acetate or ethyl cellulose. Plasticizers such as dibutyl or dioctyl phthalate or ester gum may be added, and the addition of driers yields air-drying compositions. The terpolymers may also be used as plasticisers for alkylated urea-or melamine-formaldehyde resins.
GB23747/51A 1950-10-19 1951-10-11 Polyester terpolymers Expired GB710513A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US710513XA 1950-10-19 1950-10-19

Publications (1)

Publication Number Publication Date
GB710513A true GB710513A (en) 1954-06-16

Family

ID=22098937

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23747/51A Expired GB710513A (en) 1950-10-19 1951-10-11 Polyester terpolymers

Country Status (1)

Country Link
GB (1) GB710513A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3225117A (en) * 1962-06-15 1965-12-21 Cincinnati Milling Machine Co Weather-resistant plastics
DE1237245B (en) * 1964-02-13 1967-03-23 Basf Ag Lacquers
DE1238141B (en) * 1964-02-12 1967-04-06 Basf Ag Lacquers
US3347806A (en) * 1951-01-28 1967-10-17 Albert Ag Chem Werke New dicyclopentadiene modified unsaturated polyesters and process for preparing them
EP0008216A1 (en) * 1978-08-08 1980-02-20 Scott Bader Company Limited Improvements in unsaturated polyester resins and methods of making them
WO2010108941A1 (en) * 2009-03-25 2010-09-30 Dsm Ip Assets B.V. Resin composition

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3347806A (en) * 1951-01-28 1967-10-17 Albert Ag Chem Werke New dicyclopentadiene modified unsaturated polyesters and process for preparing them
US3225117A (en) * 1962-06-15 1965-12-21 Cincinnati Milling Machine Co Weather-resistant plastics
DE1238141B (en) * 1964-02-12 1967-04-06 Basf Ag Lacquers
DE1237245B (en) * 1964-02-13 1967-03-23 Basf Ag Lacquers
EP0008216A1 (en) * 1978-08-08 1980-02-20 Scott Bader Company Limited Improvements in unsaturated polyester resins and methods of making them
WO2010108941A1 (en) * 2009-03-25 2010-09-30 Dsm Ip Assets B.V. Resin composition
US9221973B2 (en) 2009-03-25 2015-12-29 Dsm Ip Assets B.V. Resin composition

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