GB965828A - Improvements in or relating to epoxy resin compositions - Google Patents

Improvements in or relating to epoxy resin compositions

Info

Publication number
GB965828A
GB965828A GB415562A GB415562A GB965828A GB 965828 A GB965828 A GB 965828A GB 415562 A GB415562 A GB 415562A GB 415562 A GB415562 A GB 415562A GB 965828 A GB965828 A GB 965828A
Authority
GB
United Kingdom
Prior art keywords
epichlorohydrin
guanamine
phenol
bis
epoxy resin
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
GB415562A
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 GB965828A publication Critical patent/GB965828A/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)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

A heat-curable composition comprises a guanamine containing the grouping <FORM:0965828/C3/1> and a glycidyl ester of a polymeric fat acid. Specified guanamines are those of the formulae: <FORM:0965828/C3/2> <FORM:0965828/C3/3> <FORM:0965828/C3/4> <FORM:0965828/C3/5> wherein R1 is hydrogen, a phenyl group or an alkyl radical containing up to 21 carbon atoms; R2 is an aliphatic hydrocarbon radical containing from 6 to 22 carbon atoms and R3 is a dimeric hydrocarbon radical derived from a dimerized unsaturated acid. Many conventional polymeric fat acids are specified as being suitable for use in the preparation of the glycidyl esters. The compositions may also contain conventional epoxy resins e.g. the reaction products of epichlorohydrin with bis-phenol-A or resorcinol. The compositions may be partially cured to storable, curable "B-stage" resins. Example 5 describes the preparation of a glycidyl ester from epichlorohydrin and dimerized unsaturated vegetable oil acids and the admixture of this ester with an epoxy resin derived from bis-phenol-A and epichlorohydrin and cocoguanamine. In examples (1), (2), (4), (6), (7) and (8) a glycidyl ester of dimerized tall oil acids is mixed with:-(1) a guanamine of the formula A where R1 is a hydrocarbon radical of the C12 fraction of coconut oil fatty acids; (2) cocoguanamine and black iron oxide; (4) an epoxy resin derived from epichlorohydrin and bis-phenol-A and cocoguanamine; (6) an epoxy resin derived from epichlorohydrin and bis-phenol-A and a diguanamine of formula D where R3 is the hydrocarbon group of dimerized tall oil fatty acids; (7) the guanamine as in (6); (8) an epoxy resin derived from epichlorohydrin and bis-phenol-A and a guanamine of formula C where R2 is a dodecyl group and (9) the guanamine as in (8).ALSO:In Example 3 a layer of an adhesive composition comprising a glycidyl ester of dimerized tall oil acids mixed with cocoguanamine and finely divided black iron oxide is poured on to a steel can lid and cured by the application of heat.
GB415562A 1961-02-23 1962-02-02 Improvements in or relating to epoxy resin compositions Expired GB965828A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US9094761A 1961-02-23 1961-02-23

Publications (1)

Publication Number Publication Date
GB965828A true GB965828A (en) 1964-08-06

Family

ID=22225071

Family Applications (1)

Application Number Title Priority Date Filing Date
GB415562A Expired GB965828A (en) 1961-02-23 1962-02-02 Improvements in or relating to epoxy resin compositions

Country Status (3)

Country Link
BE (1) BE630100A (en)
GB (1) GB965828A (en)
NL (1) NL275157A (en)

Also Published As

Publication number Publication date
NL275157A (en)
BE630100A (en)

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