GB1442511A - Preparation of isocyanate resins - Google Patents

Preparation of isocyanate resins

Info

Publication number
GB1442511A
GB1442511A GB1800174A GB1800174A GB1442511A GB 1442511 A GB1442511 A GB 1442511A GB 1800174 A GB1800174 A GB 1800174A GB 1800174 A GB1800174 A GB 1800174A GB 1442511 A GB1442511 A GB 1442511A
Authority
GB
United Kingdom
Prior art keywords
resins
methacrylate
acrylate
resin
acrylic acid
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
GB1800174A
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.)
Allnex Austria GmbH
Original Assignee
Vianova Resins AG
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 Vianova Resins AG filed Critical Vianova Resins AG
Publication of GB1442511A publication Critical patent/GB1442511A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
    • C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
    • C08F299/06—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67—Unsaturated compounds having active hydrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/81—Unsaturated isocyanates or isothiocyanates
    • C08G18/8141—Unsaturated isocyanates or isothiocyanates masked
    • C08G18/815—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen
    • C08G18/8158—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/14—Polycondensates modified by chemical after-treatment
    • C08G59/1494—Polycondensates modified by chemical after-treatment followed by a further chemical treatment thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

1442511 Radiation curable resins VIANOVA KUNSTHARZ AG 24 April 1974 [24 April 1973] 18001/74 Headings C3B C3P and C3R A process for preparing a radiation curable resin comprises reacting a resin containing free hydroxy and/or carboxyl groups with 10 to 100 mol. per cent, based on the glycidyl reactive hydrogen atoms in the resin, of glycidyl acrylate or methacrylate and reacting the product so obtained with a compound containing one free isocyanate group obtained by reacting diisocyanate with a polymerizable monomer containing the group and at least one hydrogen atom reactive to an isocyanate group. The resins used in the examples are (i) an epoxy resin based on bisphenol A and reacted with acrylic acid, (ii) an unsaturated polyester derived from fumaric acid, phthalic anhydride, propylene glycol and diethylene glycol, dissolved in styrene, (iii) a dehydrated castor oil fatty acids alkyd resin dissolved in methyl methacrylate and (iv) an addition polymer obtained from acrylic acid, styrene, ethyl acrylate and methyl methacrylate; these resins, after reaction with glycidyl acrylate or methacrylate, are reacted with a solution in methyl methacrylate of the reaction product of tolylene diisocyanate with (a) hydroxyethyl methacrylate, (b) hydroxyethyl acrylate, (c) hydroxypropyl acrylate, (d) acrylic acid or (e) monobutyl maleate. The resins may be coated on aluminium panels and exposed to an electron beam.
GB1800174A 1973-04-24 1974-04-24 Preparation of isocyanate resins Expired GB1442511A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
AT363573A AT323298B (en) 1973-04-24 1973-04-24 PROCESS FOR THE PRODUCTION OF COATING COMPOUNDS CURBED BY MEANS OF IONIZING RADIATION

Publications (1)

Publication Number Publication Date
GB1442511A true GB1442511A (en) 1976-07-14

Family

ID=3553244

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1800174A Expired GB1442511A (en) 1973-04-24 1974-04-24 Preparation of isocyanate resins

Country Status (3)

Country Link
AT (1) AT323298B (en)
DE (1) DE2411506A1 (en)
GB (1) GB1442511A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4591518A (en) * 1984-08-13 1986-05-27 Ppg Industries, Inc. Acrylic functional urethane alkyd resin coating compositions
US4748211A (en) * 1986-07-21 1988-05-31 Ppg Industries, Inc. Hydroxyl functional graft copolymers
CN101173033B (en) * 2007-10-12 2010-04-21 广东天银化工实业有限公司 Method for producing expediting setting type aquosity ultraviolet light solidifying composition
CN101805514A (en) * 2010-03-17 2010-08-18 上海大学 Castor oil type polyurethane/acrylic resin double-component damping material and preparation method thereof
CN109957086A (en) * 2017-12-14 2019-07-02 惠州市长润发涂料有限公司 A kind of synthetic method of the polyurethane acrylate resin of high-performance and low-cost

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2915011A1 (en) * 1979-04-12 1980-10-30 Herberts Gmbh MODIFIED POLYESTERIMIDES CURRENT BY ENERGY RADIATION, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR THE INSULATION OF ELECTRIC WIRE
EP0231666B1 (en) * 1986-01-06 1990-10-31 E.I. Du Pont De Nemours And Company Polyester graft copolymers and flexible coating compositions comprising same

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4591518A (en) * 1984-08-13 1986-05-27 Ppg Industries, Inc. Acrylic functional urethane alkyd resin coating compositions
US4748211A (en) * 1986-07-21 1988-05-31 Ppg Industries, Inc. Hydroxyl functional graft copolymers
CN101173033B (en) * 2007-10-12 2010-04-21 广东天银化工实业有限公司 Method for producing expediting setting type aquosity ultraviolet light solidifying composition
CN101805514A (en) * 2010-03-17 2010-08-18 上海大学 Castor oil type polyurethane/acrylic resin double-component damping material and preparation method thereof
CN101805514B (en) * 2010-03-17 2012-01-04 上海大学 Castor oil type polyurethane/acrylic resin double-component damping material and preparation method thereof
CN109957086A (en) * 2017-12-14 2019-07-02 惠州市长润发涂料有限公司 A kind of synthetic method of the polyurethane acrylate resin of high-performance and low-cost

Also Published As

Publication number Publication date
DE2411506A1 (en) 1974-11-14
AT323298B (en) 1975-07-10

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee