GB909313A - Improvements in or relating to the production of polyamine/epoxide reaction products - Google Patents

Improvements in or relating to the production of polyamine/epoxide reaction products

Info

Publication number
GB909313A
GB909313A GB1476760A GB1476760A GB909313A GB 909313 A GB909313 A GB 909313A GB 1476760 A GB1476760 A GB 1476760A GB 1476760 A GB1476760 A GB 1476760A GB 909313 A GB909313 A GB 909313A
Authority
GB
United Kingdom
Prior art keywords
glycidyl
hydrogen atoms
reaction products
aminomethyl
poly
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
GB1476760A
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.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
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 Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Publication of GB909313A publication Critical patent/GB909313A/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
    • C08G59/182Macromolecules 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 using pre-adducts of epoxy compounds with curing agents
    • C08G59/184Macromolecules 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 using pre-adducts of epoxy compounds with curing agents with amines

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)

Abstract

Reaction products are prepared from poly-(aminomethyl)-benzenes containing at least three amino-hydrogen atoms and glycidyl compounds, in such proportions that at least 4 such hydrogen atoms are available per epoxy group. The reaction products are used as secondary curing agents for polyepoxides. The glycidyl compounds specified are glycidyl esters of carboxylic acids, polyglycidyl polyethers and glycidyl ethers. When a polyglycidyl compound is used the poly-(aminomethyl)-benzene should have at least four amino-hydrogen atoms. Any remaining nitrogen valencies are satisfied by alkyl and preferably methyl groups. The glycidyl compound is added to an excess of the polyamine (there are preferably 4-25 amino hydrogen atoms available per epoxy group) and they are reacted at temperatures between 20 DEG and 150 DEG C. Optional additives include accelerators, e.g. phenol, and triphenyl phosphite; fluxing agents, e.g. urea-formaldehyde resins, and solvents, e.g. butanol and toluene. The reaction products are used to cure polyepoxides such as polyglycidyl polyethers. Optional additives include fillers, e.g. glass fibres and coal tar; pigments, e.g. titanium dioxide, and solvents, e.g. dioctyl phthalate. In a typical example, meta-xylylene diamine, a glycidyl polyether of bisphenol A, butyl glycidyl ether, triphenyl phosphite, a urea-formaldehyde resin, butanol and toluene are reacted by heating at 60 DEG C. for one hour with stirring. The reaction product is mixed with a glycidyl polyether of bisphenol A containing butyl glycidyl ether to give a lacquer which is cured at room temperature. In comparative examples the reaction product used in the lacquer is replaced meta-phenylene diamine, a cyclo-aliphatic polyamine, the reaction products of these amines with epoxides and metaxylylene diamine.ALSO:Reaction products are prepared from poly-(aminomethyl)-benzenes containing at least three amino-hydrogen atoms and glycidyl compounds, in such proportions that at least 4 such hydrogen atoms are available per epoxy group. The glycidyl compounds specified are polyglycidyl polyethers, e.g. diphenylol propane diglycidyl ether and glycerol polyglycidyl ethers; butyl glycidyl ether; phenyl glycidyl ether and glycidyl esters of carboxylic acids. Meta-xylylene diamine is specified as a poly-(aminomethyl)-benzene. The products are used as curing agents for epoxy resins.
GB1476760A 1959-04-29 1960-04-27 Improvements in or relating to the production of polyamine/epoxide reaction products Expired GB909313A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL238708 1959-04-29

Publications (1)

Publication Number Publication Date
GB909313A true GB909313A (en) 1962-10-31

Family

ID=19751698

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1476760A Expired GB909313A (en) 1959-04-29 1960-04-27 Improvements in or relating to the production of polyamine/epoxide reaction products

Country Status (3)

Country Link
DE (1) DE1117871B (en)
GB (1) GB909313A (en)
NL (1) NL238708A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3317468A (en) * 1964-08-13 1967-05-02 James R Griffith Epoxyamine resin
WO2018210861A1 (en) * 2017-05-16 2018-11-22 Jotun A/S Compositions

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL97242C (en) * 1954-12-11
NL206722A (en) * 1955-04-28

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3317468A (en) * 1964-08-13 1967-05-02 James R Griffith Epoxyamine resin
WO2018210861A1 (en) * 2017-05-16 2018-11-22 Jotun A/S Compositions

Also Published As

Publication number Publication date
DE1117871B (en) 1961-11-23
NL238708A (en)

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