GB969256A - Improvements in or relating to epoxy resin compositions - Google Patents

Improvements in or relating to epoxy resin compositions

Info

Publication number
GB969256A
GB969256A GB415662A GB415662A GB969256A GB 969256 A GB969256 A GB 969256A GB 415662 A GB415662 A GB 415662A GB 415662 A GB415662 A GB 415662A GB 969256 A GB969256 A GB 969256A
Authority
GB
United Kingdom
Prior art keywords
guanamine
formula
phenol
derived
bis
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
GB415662A
Inventor
Richard Warren Fulmer
Dwight Ellsworth Peerman
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.)
General Mills Inc
Original Assignee
General Mills 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 General Mills Inc filed Critical General Mills Inc
Publication of GB969256A publication Critical patent/GB969256A/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
    • C08G59/00Polycondensates 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
    • C08G59/18Macromolecules 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
    • C08G59/40Macromolecules 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
    • C08G59/50Amines
    • C08G59/5046Amines heterocyclic
    • C08G59/5053Amines heterocyclic containing only nitrogen as a heteroatom
    • C08G59/508Amines heterocyclic containing only nitrogen as a heteroatom having three nitrogen atoms in the ring
    • C08G59/5086Triazines; Melamines; Guanamines

Landscapes

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

Abstract

A heat-curable composition comprises a mixture of a polyglycidyl ether of a polyhydric phenol and a guanamine of the formula <FORM:0969256/C3/1> <FORM:0969256/C3/2> <FORM:0969256/C3/3> or <FORM:0969256/C3/4> where R is a fatty aliphatic hydrocarbon radical containing from 4 to 21 carbon atoms and R1 is the divalent hydrocarbon radical of a dimerised unsaturated fatty acid. Specified polyhydric phenols are resorcinol and bis-phenol-A. The compositions may be partially reacted to a stable curable B-stage resin. The examples disclose compositions of epoxy resins derived from bis-phenol-A and epichlorohydrin and: (1) and (3) soya guanamine; (2) soya guanamine and aluminium oxide; (4) a guanamine derived from hydrogenated tallow fatty acids and alumina; (5) a guanamine derived from the mixed C6-C10 acids of coconut oil; (6) hydrogenated tallow guanamine and kaolin; (7) lauroguanamine, kaolin and glass fibres; (8) and (12) a guanamine of formula D in which R is the hydrocarbon residue of dimerised linoleic acids; (9) and (13) a guanamine of formula C where R is C12H25; (10) a guanamine of formula B where R is C18H37; (11) and (14) cocoguanamine and (15), (16) and (17), a guanamine of formula A where R is a C11 alkyl group.ALSO:In Example 17, steel bars are coated with a partially cured mixture of a guanamine of the formula <FORM:0969256/B1-B2/1> where R is a C11 alkyl group and an epoxy resin derived from bis-phenol-A and epichlorohydrin, the coating being cured by heating.
GB415662A 1963-12-20 1962-02-02 Improvements in or relating to epoxy resin compositions Expired GB969256A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEG0042859 1963-12-20

Publications (1)

Publication Number Publication Date
GB969256A true GB969256A (en) 1964-09-09

Family

ID=7127029

Family Applications (1)

Application Number Title Priority Date Filing Date
GB415662A Expired GB969256A (en) 1963-12-20 1962-02-02 Improvements in or relating to epoxy resin compositions

Country Status (4)

Country Link
BE (1) BE630605A (en)
DE (1) DE1570649A1 (en)
GB (1) GB969256A (en)
NL (1) NL275418A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4515934A (en) * 1984-03-19 1985-05-07 The Dow Chemical Company Vinyl ester resins containing triazine or both triazine and oxazoline groups

Also Published As

Publication number Publication date
NL275418A (en)
BE630605A (en)
DE1570649A1 (en) 1969-09-18

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