POLYAMIDE-IMIDE POLYMER AND PROCESS FOR ITS MANUFACTURE
A process for preparing a polyamide-imide (PAI) polymer is provided. The process comprises the melt polymerization of a reaction mixture comprising at least one cycloaliphatic acid component comprising three carboxyl moieties, the carboxyl moieties selected from the group consisting of carboxylic acid, acid anhydride and ester functional groups, and at least one diamine component. The process comprises maintaining the reaction mixture in a liquid state and at a temperature of at least 200° C. during polymerization.
1 - 16 . (canceled)
17 . A process for preparing a polyamide-imide (PAI) polymer by melt polymerization of a reaction mixture comprising:
a) at least one cycloaliphatic acid component comprising three carboxyl moieties, the carboxyl moieties selected from the group consisting of carboxylic acid, acid anhydride and ester functional groups; and
b) at least one diamine component,
said process comprising maintaining the reaction mixture in a liquid state and at a temperature of at least 200° C. during polymerization.
18 . The process of claim 17 , wherein said at least one cycloaliphatic acid component is according to formulae (I) and/or (II):
Z is a cycloaliphatic moiety selected from the group consisting of substituted or unsubstituted, monocyclic or polycyclic groups having 5 to 50 carbon atoms, preferably 6 to 18 carbon atoms;
Y is OR a , with R a being H or an alkyl, preferably an alkyl having 1 to 5 carbon atoms; and
In formula II, at least two Y(C═O) moieties are in ortho position with respect to one another.
19 . The process of claim 18 , wherein Z is a cycloaliphatic moiety comprising from one to four aliphatic rings, said aliphatic rings being condensed or bridged together either directly or by the following bridges: —O—, —CH 2 —, —C(CH 3 ) 2 —, —C(CF 3 ) 2 —, or —(CF 2 ) q —, wherein q is an integer from 1 to 5.
20 . The process of claim 18 , wherein Z is a trivalent cycloaliphatic moiety selected from the group consisting of moieties having formulae (III-A), (III-B), (III-C) and (III-D):
Wherein:
X is —O—, —CH 2 —, —C(CH 3 ) 2 —, —C(CF 3 ) 2 —, or —(CF 2 ) q —, and
q is an integer from 1 to 5.
21 . The process of claim 17 , wherein said at least one cycloaliphatic acid component is according to formulae (Ia) and/or (IIa):
22 . The process of claim 17 , wherein the diamine component is aliphatic, cycloaliphatic or aromatic, and comprises at least two amine moieties and optionally at least one heteroatom selected from the group consisting of N, S and O.
23 . The process of claim 22 , wherein said diamine component is selected from the group consisting of putrescine, cadaverine, hexamethylenediamine, 2,2,4-trimethyhexamethylenediamine, 2,4,4-trimethyhexamethylenediamine, 1,9-diaminononane, 2-methyl-1,8-diaminooctane, dodecamethylenediamine, 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane, isophorone diamine, 1,4-diaminocyclohexane, 1,3-diaminocyclohexane, 4,4′-methylenebis(cyclohexylamine), 4,4′-methylenebis(2-methylcyclohexylamine), p-xylylenediamine, m-xylylenediamine, and mixtures thereof.
24 . The process of claim 17 , wherein the reaction mixture further comprises at least one aliphatic, cycloaliphatic or aromatic diacid component or derivative thereof, which optionally comprises at least one heteroatom selected from the group consisting of N, S and 0.
25 . The process of claim 24 , wherein said diacid component is selected from the group consisting of adipic acid, azelaic acid, sebacic acid, dodecanedioic acid, isophthalic acid, terephthalic acid, 2,6-naphthalene dicarboxylic acid, 4,4′-bibenzoic acid, 5-hydroxyisophthalic acid, 5-sulfophthalic acid, 1,3-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, and mixtures thereof.
26 . The process of claim 17 , wherein the process is carried out in the absence of an organic solvent and in the presence of an amount of added water less than 50 wt. % based on the total weight of the reaction mixture.
27 . The process of claim 17 , wherein either the cycloaliphatic acid component or the diamine component is added sequentially, progressively or continuously to the reaction mixture.
28 . The process of claim 17 , wherein the water generated during the polymerisation is evaporated by fractional distillation at a pressure between 1 mbar and 30 bar.
29 . A polyamide-imide (PAI) polymer obtained by melt polymerization of a reaction mixture comprising:
a) at least one cycloaliphatic acid component comprising three carboxyl moieties, the carboxyl moieties selected from the group consisting of carboxylic acid, acid anhydride and ester functional groups; and
b) at least one diamine component,
wherein the reaction mixture is maintained in a liquid state and at a temperature of at least 200° C. during polymerization.
30 . The PAI polymer of claim 29 , having a glass transition temperature of at least 100° C., and/or at most 250° C. as determined by DSC according to ASTM D3418.
31 . The PAI polymer of claim 29 , having a number average molecular weight (Mn) of at least 5,000 g/mol and/or at most 50,000 g/mol as determined by gel permeation chromatography using a fluorinated solvent, 2 HFIP gel columns and UV-vis/refractive index detectors.
32 . The PAI polymer of claim 29 , being soluble in hexafluoro-2-propanol, o-cresol, sulfuric acid 98%, and/or dimethylformamide.
33 . A polymer composition comprising a polyamide-imide (PAI) polymer obtained by melt polymerization of a reaction mixture comprising:
a) at least one cycloaliphatic acid component comprising three carboxyl moieties, the carboxyl moieties selected from the group consisting of carboxylic acid, acid anhydride and ester functional groups; and
b) at least one diamine component,
wherein the reaction mixture is maintained in a liquid state and at a temperature of at least 200° C. during polymerization.
34 . An article comprising the PAI polymer of claim 29 .
35 . An article comprising the polymer composition of claim 33 .