Polyamine compositions useful as hardening agents for epoxy resins

Claim 2

A composition consisting essentially of at least one aromatic polyamine of the general formula: ##EQU8## in which Ar is an aromatic divalent radical, said radical being unsubstituted benzene or benzene substituted by halogen or alkyl, or two fused benzene rings, or two benzene rings bonded by a single bond or by: --O--; --S--; --SO--; --SO 2 --; --CO--; ##EQU9## in which R 2 and R 3 are hydrogen atoms or monovalent hydrocarbon radicals; and in which Ar' is an aromatic divalent radical having two valences on separate carbon atoms and being a single benzene ring, or pyridine, or two fused benzene rings, or two benzene rings joined by a single bond or by --O--; --CO--; or ##EQU10## in which R 2 and R 3 are hydrogen atoms or monovalent hydrocarbon radicals; each radical R 1 is selected from the divalent saturated aliphatic, saturated alicyclic, aliphatic alicyclic and arylaliphatic hydrocarbon radicals having from 2 to 24 carbon atoms and from the divalent radicals of the formula: --(--R.sub.4 --O --)--.sub.m R.sub.4, in which R 4 is a divalent saturated aliphatic radical having from 2 to 10 carbon atoms, m is an integer from 1 to 100 and n is an integer from 1 to 10.

Claim 3

A composition according to claim 1, in which the value of n is from 1 to 6.

Claim 4

A composition according to claim 1, further comprising at least one polyamine with a branched oligoester chain.

Claim 5

A process for manufacturing a composition according to claim 1, comprising: a first step of reacting under usual esterification or transesterification conditions, at least one aromatic dicarboxylic compound of the general formula R'CO--Ar'--COR', in which Ar' is defined as in claim 1 and R' is selected from a hydroxy group, chlorine and bromine and lower alkoxy radicals, with an excess of at least one diol of the general formula HO--R 1 --OH, in which R 1 is defined as in claim 1, thereby forming a composition consisting essentially of an oligoester of the general formula: ##EQU11## in which n is defined as in claim 1, a second step of reacting said oligoester with at least one monocarboxylic aliphatic acid anhydride in order to form the corresponding carboxylate composition, a third step of reacting, under usual esterification or transesterification conditions, the composition obtained at the end of the second step with a molar amount, corresponding substantially to the number of reactive carboxylate equivalents of said composition, of at least one aromatic nitro-carboxylic compound of the general formula: NO.sub.2 --Ar -- COR" in which Ar is defined as in claim 1 and R" is selected from the hydroxy group and lower alkyl radicals, thereby forming a composition consisting essentially of at least one nitrated oligoester of the general formula: ##EQU12## and a fourth step in which the nitrated oligoester composition obtained at the end of the third step is hydrogenated to a composition accordng to claim 1.

Claim 6

A process for manufacturing a composition according to claim 1, comprising a first step of reacting, under usual esterification or transesterification conditions, at least one aromatic dicarboxylic compound of the general formula R'CO-- Ar'-- COR', in which Ar' is defined as in claim 1 and R' is selected among hydroxy group, chlorine and bromine atoms and lower alkoxy radicals with an excess of at least one diol of the general formula HO -- R 1 -- OH, in which R 1 is defined as in claim 1, thereby forming a composition consisting essentially of at least one oligoester of the general formula: ##EQU13## in which n is defined as in claim 1, and a second step of reacting, under usual esterification or transesterification conditions, the composition obtained at the end of the first step with a molar amount, substantially corresponding to the number of free hydroxy equivalents of said composition, of at least one aromatic aminocarboxy compound of the general formula NH 2 -- Ar -- COR"', in which Ar is defined as in claim 1 and R"' is selected from hydroxy group and lower alkoxy radicals, so as to form a polyamine composition according to claim 1.

Claim 7

A process according claim 4, in which the aromatic dicarboxylic compound is selected from the isophthalic and terephthalic acids, 4,4'-dicarboxylic biphenyle, 4,4'-dicarboxy diphenylether and their lower alkyl esters.

Claim 8

A process according to claim 4, in whch the diol is selected from neopentylglycol, ethyleneglycol, di-, tri- and tetraethyleneglycols and 1,4-dimethylol benzene.

Claim 9

A process according to claim 5, in which the aromatic amino-carboxylic compound is selected from p.aminobenzoic acid and its lower alkyl esters.

Claim 10

A process according to claim 4, in the first step of which the diol is used in an amount of 1.1 to 10 moles per mole of dicarboxylic compound.

Claim 11

A process accordng to claim 4, in the first step of which a small proportion of the reactants, dicarboxylic compounds, diols and mixtures thereof, is replaced by reactants, polycarboxylic compounds, diols and mixtures thereof of a functionality higher than 2, so as to form a composition according to claim 3.

Claim 12

A composition according to claim 1 wherein Ar' is 1,3-phenylene, 1,4-phenylene, a divalent biphenyl radical, or a divalent radical of diphenyl ether.

Claim 13

A composition according to claim 1 wherein R 1 is a divalent radical derived from neopentylglycol, ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, or 1,4-dimethylol benzene.

Claim 14

A composition according to claim 1 wherein Ar is 1,3-phenylene, 1,4-phenylene or a divalent radical of diphenyl ether.