GB1055444A - Resinous polyesters - Google Patents

Resinous polyesters

Info

Publication number
GB1055444A
GB1055444A GB33764/63A GB3376463A GB1055444A GB 1055444 A GB1055444 A GB 1055444A GB 33764/63 A GB33764/63 A GB 33764/63A GB 3376463 A GB3376463 A GB 3376463A GB 1055444 A GB1055444 A GB 1055444A
Authority
GB
United Kingdom
Prior art keywords
glycol
polyester
mol
dicyclopentadiene
xylol
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
GB33764/63A
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.)
DESOTO CHEMICAL COATINGS Inc
Original Assignee
DESOTO CHEMICAL COATINGS Inc
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 DESOTO CHEMICAL COATINGS Inc filed Critical DESOTO CHEMICAL COATINGS Inc
Publication of GB1055444A publication Critical patent/GB1055444A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/06Unsaturated polyesters
    • 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
    • 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
    • C08G63/676Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C09D167/025Polyesters derived from dicarboxylic acids and dihydroxy compounds containing polyether sequences

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)

Abstract

A resinous polyester comprises the heat reaction product of (a) a dicarboxylic acid component consisting wholly or mainly of ethylenically unsaturated dicarboxylic acid comprising at least a major proportion of fumaric acid and no, or at most 25 mol. per cent based on total acids, saturated dicarboxylic acid, (b) a glycol component, and (c) a diene component comprising a major molar proportion of dicyclopentadiene in an amount providing from 0.6 to 0.9 mol. of dicyclopentadiene per mol. of ethylenically unsaturated dicarboxylic acid. The glycol may be: ethylene glycol, propylene glycol, butylene glycol, 1:5-pentanediol, dimethylol propane, neopentyl glycol or a polyoxyalkylene glycol of M.W. up to 1200 and bisphenol based diols. Up to 20 mol. per cent of polyhydric alcohols, e.g. glycerine and pentaerythritol or polyepoxides may be present. Up to 50 mol. per cent of the diene component may be cyclopentadiene, 1:4-butadiene, tricyclopentadiene and tetracyclopentadiene. The polyester resin may be dissolved in an organic solvent, e.g. benzene, toluene, xylene, butanol diethylene glycol or methyl ethyl ketone. Up to 35% by weight of an amino plast resin may be incorporated into the polyester, e.g. reaction products of HCHO with urea and substituted molamines and benzoguanamine, which may be partially etherified with a C3-C8 alcohol. In Example (1) an epoxy resin of M.W. 1000 consisting of the diglycidyl ether of 221 bis-(p-hydroxyphenyl propane), diethylene glycol, azelaic acid and xylol were heated to 400 DEG F., cooled, dicyclopentadiene added and reheated to 400 DEG F. In Example (4) diethylene glycol, neopentyl glycol, fumaric acid and xylol were heated to 400 DEG F., cooled, dicyclopentadiene added and reheated. The polyester thus produced was mixed in Example (5) with a resinous chlorinated polyphenyl and xylol and applied as an enamel to tin cans. Reference has been directed by the Comptroller to Specification 937,980.ALSO:A coating composition comprising an organic solvent having dissolved therein an unsaturated polyester (derived from a reaction mixture containing fumaric acid, dicyclopentadiene and a glycol) and optionally a heat hardenable aminoplast resin is used to coat metal articles e.g. coils, cans or sheets. The metal may be aluminium. In example (3) an unsaturated polyester solution was mixed with finely divided silica, toluene, aluminium pigment and petrolatum solution and sprayed onto a metallic base to give a coating of 2.8 mils which was cured at 385 DEG F. In example (4) an unsaturated polyester was mixed with a resinous chlorinated polyphenyl and xylol and used as an enamel for the post solder side seam of tin cans. Reference has been directed by the Comptroller to Specification 937,980.
GB33764/63A 1962-10-03 1963-08-26 Resinous polyesters Expired GB1055444A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US22801962A 1962-10-03 1962-10-03
FR948312A FR1369808A (en) 1962-10-03 1963-09-23 New resinous polyesters

Publications (1)

Publication Number Publication Date
GB1055444A true GB1055444A (en) 1967-01-18

Family

ID=26203514

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33764/63A Expired GB1055444A (en) 1962-10-03 1963-08-26 Resinous polyesters

Country Status (2)

Country Link
FR (1) FR1369808A (en)
GB (1) GB1055444A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4003959A (en) 1973-12-20 1977-01-18 Nippon Zeon Co., Ltd. Epoxy resin compositions containing cyclopentadiene copolymer
DE10205065A1 (en) * 2002-02-07 2003-08-21 Ashland Suedchemie Kernfest Compositions containing cyclopentadiene adducts and their use for chemical resistant coatings

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5645951B2 (en) * 1973-05-21 1981-10-29

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4003959A (en) 1973-12-20 1977-01-18 Nippon Zeon Co., Ltd. Epoxy resin compositions containing cyclopentadiene copolymer
DE10205065A1 (en) * 2002-02-07 2003-08-21 Ashland Suedchemie Kernfest Compositions containing cyclopentadiene adducts and their use for chemical resistant coatings
AU2003210211B2 (en) * 2002-02-07 2007-11-01 Ashland-Suedchemie-Kernfest Gmbh Compositions containing cyclopentadiene adducts and the use thereof for chemically stable coatings

Also Published As

Publication number Publication date
FR1369808A (en) 1964-08-14

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