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filingDate 1973-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1976-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1423270-A
titleOfInvention Epoxy resin composition
abstract 1423270 Curing epoxy resins PERMACHEM ASIA CO Ltd and MITSUBISHI PETROCHEMICAL CO Ltd 20 Nov 1973 [20 Nov 1972] 53737/73 Heading C3B Curable compositions comprise an epoxy resin and as latent hardener an aminimide R 1 is alkyl, benzyl or -CH 2 CH(OH)R<SP>5</SP>; R<SP>2</SP> and R<SP>3</SP> are alkyl; when R<SP>1</SP> is alkyl or R<SP>4</SP> is C 6 H 5 NH-, R<SP>6</SP>OCO- or R<SP>6</SP>OCOR<SP>7</SP>- and when R<SP>1</SP> is benzyl, R<SP>4</SP> may additionally be alkyl, aryl, aralkyl, cycloalkyl, alkoxy, aryloxy or alkenyl; R<SP>5</SP> is H, alkyl, aryl, alkoxyalkyl, aryloxyalkyl, allyloxyalkyl, hydroxyalkyl, methacryoxymethyl or acryloxymethyl; R<SP>6</SP> is alkyl, aryl or aralkyl; R<SP>7</SP> is a divalent hydrocarbon radical. Typical examples are 1,1-dimethyl- 1 - benzylamine methacrylamide; 1,1 - dimethyl - 1 - (2<SP>1</SP>- hydroxypropyl - 31 - phenylethyl)amine ethoxyoxalimide and similar malonimide, succinimide, adipimide, phthalimide and iso- and tere-phthalimides; bis - 1,1 - dimethyl - 1 - (2<SP>1</SP> - hydroxy - 31- phenoxypropyl)amine oxalimide and bistrimethylamine oxalimide. The aminimide may be the sole curing agent and may be used at 0À1-15 parts by weight per 100 parts by wt. of epoxy resin. Alternatively, it may be used as an accelerator at 0À1-5 parts by wt. per 100 parts of epoxy resin with 0À6-1À2 equivalent of a polycarboxylic acid anhydride per epoxide equivalent.
priorityDate 1972-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 27.