GB1012047A - Improvements in or relating to polyglycidyl ethers - Google Patents

Improvements in or relating to polyglycidyl ethers

Info

Publication number
GB1012047A
GB1012047A GB1926262A GB1926262A GB1012047A GB 1012047 A GB1012047 A GB 1012047A GB 1926262 A GB1926262 A GB 1926262A GB 1926262 A GB1926262 A GB 1926262A GB 1012047 A GB1012047 A GB 1012047A
Authority
GB
United Kingdom
Prior art keywords
compositions
esterification
substituted
resins
products
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
GB1926262A
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.)
Tenneco Chemicals Inc
Original Assignee
Tenneco Chemicals 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 Tenneco Chemicals Inc filed Critical Tenneco Chemicals Inc
Publication of GB1012047A publication Critical patent/GB1012047A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08G59/02—Polycondensates containing more than one epoxy group per molecule
    • C08G59/12—Polycondensates containing more than one epoxy group per molecule of polycarboxylic acids with epihalohydrins or precursors thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02—Compounds containing oxirane rings
    • C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
    • C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
    • C07D303/24—Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy compounds
    • 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
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/22—Di-epoxy compounds
    • C08G59/24—Di-epoxy compounds carbocyclic
    • C08G59/245—Di-epoxy compounds carbocyclic aromatic
    • 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
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • C08G59/4292—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with monocarboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Laminated Bodies (AREA)

Abstract

Resinous products are obtained by reacting the polyglycidyl ethers of terpene-phenol condensation products of Specification 1,012,046 with one or more dicarboxylic acids R(COOH)2, R being a C2- 42 substituted or unsubstituted hydrocarbon group, or anhydrides thereof, and optionally also with up to 0.9 esterification equivalents of a monocarboxylic acid per esterification equivalent of the polyglycidyl ether. R may be saturated or unsaturated and may be substituted by halogen, hydroxyl, alkoxy, amino or nitro. Many dicarboxylic and monocarboxylic acids are specified. The products of the invention are used in surface-coating compositions as solutions in inert solvents, such as toluene, xylene, benzene, mineral spirits, methyl isobutyl ketone, butanol and "Cellosolve" (Trade Mark). The compositions may also include fillers, pigments, dyes, plasticizers, driers, alkyd resins, urea-aldehyde resins, phenolic resins or polyamides. Examples produce air-dried and baked films from such compositions.ALSO:The invention comprises the resinous products obtainable by reacting the polyglycidyl ethers of terpene-phenol condensation products with one or more dicarboxylic acids R(COOH)2, R being a C2- 42 substituted or unsubstituted hydrocarbon group, or anhydrides thereof, and optionally also with up to 0.9 esterification equivalents of a monocarboxylic acid per esterification equivalent of the polyglycidyl ether. R may be saturated or unsaturated, and may be substituted by halogen, hydroxyl, alkoxy, amino or nitro. Many dicarboxylic and monocarboxylic acids are specified. Specification 1,012,046 is referred to.ALSO:Surfaces are coated with compositions which are solutions in inert solvents, such as toluene, xylene, benzene, mineral spirits, methyl isobutyl ketone, butanol and "Cellosolve" (Registered Trade Mark), of the reaction product of the polyglycidyl ethers of terpene-phenol condensation products of Specification 1,012,046, with one or more substituted or unsubstituted dicarboxylic acids containing 2-42 carbon atoms, or anhydrides thereof, and optionally also with up to 0,9 esterification equivalents per esterification equivalent of the polyglycidyl ether. The compositions may also include fillers, pigments, dyes, plasticizers, driers, alkyd resins, urea-aldehyde resins, phenolic resins or polyamides. In an example, glass plates are coated with such compositions and the films air-dried or baked.
GB1926262A 1961-05-18 1962-05-18 Improvements in or relating to polyglycidyl ethers Expired GB1012047A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11087661A 1961-05-18 1961-05-18

Publications (1)

Publication Number Publication Date
GB1012047A true GB1012047A (en) 1965-12-08

Family

ID=22335395

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1926262A Expired GB1012047A (en) 1961-05-18 1962-05-18 Improvements in or relating to polyglycidyl ethers

Country Status (2)

Country Link
GB (1) GB1012047A (en)
NL (1) NL278593A (en)

Also Published As

Publication number Publication date
NL278593A (en)

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