GB868892A - Improvements in or relating to hardenable epoxide resinous compositions - Google Patents

Improvements in or relating to hardenable epoxide resinous compositions

Info

Publication number
GB868892A
GB868892A GB3461358A GB3461358A GB868892A GB 868892 A GB868892 A GB 868892A GB 3461358 A GB3461358 A GB 3461358A GB 3461358 A GB3461358 A GB 3461358A GB 868892 A GB868892 A GB 868892A
Authority
GB
United Kingdom
Prior art keywords
phenol
mixture
aldehyde
hardening agent
hardening
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
GB3461358A
Inventor
Eric John Bloxham
Reginald Norman Lewis
Eric George Kemp Pritchett
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.)
Bakelite Ltd
Original Assignee
Bakelite Ltd
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 Bakelite Ltd filed Critical Bakelite Ltd
Priority to GB3461358A priority Critical patent/GB868892A/en
Publication of GB868892A publication Critical patent/GB868892A/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
    • C08G59/62Alcohols or phenols
    • C08G59/621Phenols
    • C08G59/623Aminophenols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins

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 hardenable resinous composition comprises a glycidyl ether containing more than one 1, 2-epoxy group per average molecule and as hardening agent the product obtained by reacting a phenol, an aldehyde and a polyamine containing at least four hydrogen atoms bonded to nitrogen atoms, either by the addition of the aldehyde to the phenol/polyamine mixture or by the addition of the phenol to an aldehyde/polyamine mixture, in such proportions that the reaction product contains at least "three active hydrogen atoms" (which denotes hydrogen atoms which will react with the epoxy groups in the glycidyl ether). Preferred glycidyl ethers are those obtained by reacting polyphenols such as diphenylol propane with epichlorhydrin or chemically related compounds such as dichlorhydrin or 1, 2-dichloro-3-hydroxy-propane. In the preparation of the hardening agents there may be used phenol, xylenol or diphenylol propane or a mixture of phenols; formaldehyde, acetaldehyde, paraldehyde and furfuraldehyde; diethylene triamine, triethylene tetramine, tetraethylene pentamine and 1, 6-hexamethylene diamine. Preferably the phenol and aldehyde are used in equimolecular amounts. In examples hardening agents are prepared by (a) slowly adding two molecular equivalents of formalin to a mixture of two equivalents of phenol and one equivalent of tetraethylene pentamine at 45 DEG C.; (b) similarly reacting equimolecular proportions of xylenol, 1, 6-hexamethylene diamine and formaldehyde. The hardening agents can be modified by reaction with ethylene oxide or acrylonitrile. In examples a liquid epoxide resin of epoxide equivalent 190, prepared from diphenylol propane and epichlorhydrin, is hardened with (1) hardening agent A; (2) cyanoethylated hardening agent A; (3) a mixture of hardening agent A and tetraethylene pentamine. The compositions can be used as coating compositions and in glass fibre laminates, brush setting cements, adhesives, foundry patterns, flexible sealing compounds and cable jointing. Specification 789,475 is referred to.
GB3461358A 1958-10-29 1958-10-29 Improvements in or relating to hardenable epoxide resinous compositions Expired GB868892A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3461358A GB868892A (en) 1958-10-29 1958-10-29 Improvements in or relating to hardenable epoxide resinous compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3461358A GB868892A (en) 1958-10-29 1958-10-29 Improvements in or relating to hardenable epoxide resinous compositions

Publications (1)

Publication Number Publication Date
GB868892A true GB868892A (en) 1961-05-25

Family

ID=10367837

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3461358A Expired GB868892A (en) 1958-10-29 1958-10-29 Improvements in or relating to hardenable epoxide resinous compositions

Country Status (1)

Country Link
GB (1) GB868892A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3950451A (en) * 1971-02-27 1976-04-13 Asahi Denka Kogyo K.K. Hardenable epoxy resin composition
EP0066447A1 (en) * 1981-05-25 1982-12-08 Mitsubishi Gas Chemical Company, Inc. Reaction of a phenol, aldehyde and amine to produce hardening agent for epoxy resins
WO2009126393A3 (en) * 2008-04-07 2010-05-20 Dow Global Technologies Inc. Epoxy resin compositions having improved low temperature cure properties and processes and intermediates for making the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3950451A (en) * 1971-02-27 1976-04-13 Asahi Denka Kogyo K.K. Hardenable epoxy resin composition
EP0066447A1 (en) * 1981-05-25 1982-12-08 Mitsubishi Gas Chemical Company, Inc. Reaction of a phenol, aldehyde and amine to produce hardening agent for epoxy resins
WO2009126393A3 (en) * 2008-04-07 2010-05-20 Dow Global Technologies Inc. Epoxy resin compositions having improved low temperature cure properties and processes and intermediates for making the same
US8759457B2 (en) 2008-04-07 2014-06-24 Dow Global Technologies, Llc Epoxy resin compositions having improved low temperature cure properties and processes and intermediates for making the same

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