GB965588A - Improvements in or relating to epoxy resin compositions - Google Patents

Improvements in or relating to epoxy resin compositions

Info

Publication number
GB965588A
GB965588A GB1187362A GB1187362A GB965588A GB 965588 A GB965588 A GB 965588A GB 1187362 A GB1187362 A GB 1187362A GB 1187362 A GB1187362 A GB 1187362A GB 965588 A GB965588 A GB 965588A
Authority
GB
United Kingdom
Prior art keywords
guanamine
phenol
carbon atoms
formula
finely divided
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
GB1187362A
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 GB965588A publication Critical patent/GB965588A/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)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A heat curable composition comprises an epoxidized novolac resin and a guanamine of the formula (A)#cB where A is <FORM:0965588/C3/1> #c is 1 or 2 where possible and B represents an aliphatic hydrocarbon radical containing up to 21 carbon atoms, R2NHCH2.CH2-, -CH2CH2.N(R2)CH2.CH2- (where R2 is an aliphatic hydrocarbon radical having from 4 to 21 carbon atoms) or a hydrocarbon radical derived from a dimerised unsaturated fatty acid. Specified epoxides are the epichlorohydrin derivatives of novolacs derived from formaldehyde, acetaldehyde, chloraldehyde, butyraldehyde or furfuraldehyde and cresol, butyl phenol, t-butyl phenol, t-amyl phenol, hexyl phenol, 2-ethyl hexyl phenol, nonyl phenol, decylphenol or dodecyl phenol. Fillers e.g. aluminium oxide may be included in the compositions. The compositions may be partially cured to the storable, curable "B"-stage resins. The examples disclose compositions comprising an epoxidised novolac resin and:-(1) a guanamine of the formula A: <FORM:0965588/C3/2> where R1 has 11 carbon atoms; (2) cocoguanamine; (3) the guanamine of (1) and aluminium oxide; (4) a glycidyl ether of tetraphenol ethane, a guanamine of formula A where R1 is the aliphatic group from hydrogenated tallow oil acids and kaolin; (5) the guanamine of (1) and finely divided mica; (6) the guanamine of (1), flake glass, finely divided walnut shell flour and nylon flock; (7) the guanamine of (1) and shortfibred asbestos; (8) the guanamine of (1) and surface activated kaolin and (9) and (10) the guanamine of (1) and finely divided mica.
GB1187362A 1961-04-12 1962-03-28 Improvements in or relating to epoxy resin compositions Expired GB965588A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10239161A 1961-04-12 1961-04-12

Publications (1)

Publication Number Publication Date
GB965588A true GB965588A (en) 1964-07-29

Family

ID=22289592

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1187362A Expired GB965588A (en) 1961-04-12 1962-03-28 Improvements in or relating to epoxy resin compositions

Country Status (3)

Country Link
BE (1) BE633539A (en)
GB (1) GB965588A (en)
NL (1) NL276890A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0194895A2 (en) * 1985-03-14 1986-09-17 Shikoku Chemicals Corporation 2-substituted-4, 6-diamino-s-triazine/isocyanuric acid adduct, process for synthesis of said adduct and process for curing polyepoxy resin with said adduct

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0194895A2 (en) * 1985-03-14 1986-09-17 Shikoku Chemicals Corporation 2-substituted-4, 6-diamino-s-triazine/isocyanuric acid adduct, process for synthesis of said adduct and process for curing polyepoxy resin with said adduct
EP0194895A3 (en) * 1985-03-14 1987-09-02 Shikoku Chemicals Corporation 2-substituted-4, 6-diamino-s-triazine/isocyanuric acid adduct, process for synthesis of said adduct and process for curing polyepoxy resin with said adduct

Also Published As

Publication number Publication date
BE633539A (en)
NL276890A (en)

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