Process for preparing wholly aromatic polyamides by mixing solid particulate reactants and polymerizing

Claim 2

A process for the preparation of a wholly aromatic polyamide from an aromatic diamine and an aromatic diacid halide comprising: a. mixing solid particulate diamine and solid particulate aromatic diacid halide in the substantial absence of oxygen and in the absence of a solvent or diluent therefor to obtain a uniform stoichiometrically balanced solids mixture; and b. thereafter polymerizing the resulting uniform solids mixture in an amide solvent to obtain said wholly aromatic polyamide having an inherent viscosity of at least above about 0.7 to about 6.0, said inherent viscosity being measured on a solution of 0.4 grams of polyamide per 100 cc. of cencentrated H 2 SO 4 at 25° C.

Claim 3

The process of claim 1, wherein the aromatic diamine corresponds to the formula H 2 N--Ar--NH 2 , wherein Ar is a divalent aromatic radical which is meta or para oriented and which is selected from the group consisting of ##STR6## where R is alkyl or alkoxy of 1 to 6 carbons, chlorine, bromine or phenyl; n is an integer of 0 to 4; and X is -O--, --S--, ##STR7## alkenylene of 2 to 6 carbons, cycloalkylidene of up to 8 carbons, azo, azoxy, or ##STR8## wherein Y 1 and Y 2 are independently hydrogen, alkyl of 1 to 6 carbons, phenyl or substituted phenyl.

Claim 4

The process of claim 2, wherein the aromatic diacid halide is of the formula: ##STR9## wherein Hal is chlorine or bromine and wherein Ar is as defined in claim 2.

Claim 5

The process of claim 3, wherein the amide solvent is selected from the group consisting of compounds of the formula ##STR10## wherein R 1 is hydrogen or alkyl of 1 to 4 carbons and R 2 and R 3 are independently alkyl of 1 to 4 carbons; tetramethylurea; N-methylpyrrolidone and hexamethylphosphoramide.

Claim 6

The process of claim 4 wherein the polymerization step (b) is carried out in a batch process and wherein the uniform solids mixture of (a) is added to the amide solvent with agitation.

Claim 7

The process of claim 4 wherein the solution polymerization step (b) is carried out in a continuous process and wherein the uniform solids mixture of (a) is metered to a reaction zone simultaneously with the amide solvent.

Claim 8

The process of claim 5 wherein the polymerization step (b) is carried out for a time sufficient to form an aromatic polyamide product having an inherent viscosity of from about 1.0 to about 6.0.

Claim 9

The process of claim 5 wherein the wholly aromatic polyamide product is polyparaphenylene terephthalamide.

Claim 10

The process of claim 5 wherein the aromatic diamine and aromatic diacid halide have a particle size of less than about 24 mesh.

Claim 11

A process for the preparation of a wholly aromatic polyamide which comprises: a. mixing, in about an equimolar ratio, a solid aromatic diamine of the formula H 2 N--Ar--NH 2 and a solid aromatic diacid halide of the formula ##STR11## wherein Ar is a divalent aromatic radical which is meta or para oriented and which is selected from the group consisting of ##STR12## wherein R is alkyl or alkoxy of 1 to 6 carbons, chlorine, bromine or phenyl; n is an integer of 0 to 4; and X is --O--, --S--, ##STR13## --C--, alkenylene of 2 to 6 carbons, cycyloalkylidene of up to 8 carbons, azo, azoxy, or ##STR14## wherein Y 1 and Y 2 are independently hydrogen, alkyl of 1 to 6 carbons, phenyl or substituted phenyl; and Hal is chlorine or bromine, to obtain a uniform stoichiometrically balanced solids mixture, and b. thereafter polymerizing the resulting uniform solids mixture in an amine solvent selected from the group consisting of compounds of the formula ##STR15## wherein R 1 is hydrogen or alkyl of 1 to 4 carbons and R 2 and R 3 are alkyl of 1 to 4 carbons; tetramethylurea; N-methyl pyrrolidone and hexamethylphosphoramide, for a time sufficient to obtain a wholly aromatic polyamide having an inherent viscosity of from about 1.0 to about 6.0, said inherent viscosity being measured on a solution of 0.4 grams of polyamide per 100 cc. of concentrated H 2 SO 4 at 25° C.

Claim 12

A process for the preparation of a wholly aromatic polyamide which comprises: a. mixing, in about an equimolar ratio, a solid aromatic diamine of the formula H 2 N--Ar--NH 2 and a solid aromatic diacid halide of the formula ##STR11## wherein Ar is a divalent aromatic radical which is meta or para oriented and which is selected from the group consisting of ##STR12## wherein R is alkyl or alkoxy of 1 to 6 carbons, chlorine, bromine or phenyl; n is an integer of 0 to 4; and X is --O--, --S--, ##STR13## --C--, alkenylene of 2 to 6 carbons, cycyloalkylidene of up to 8 carbons, azo, azoxy, or ##STR14## wherein Y 1 and Y 2 are independently hydrogen, alkyl of 1 to 6 carbons, phenyl or substituted phenyl; and Hal is chlorine or bromine, to obtain a uniform stoichiometrically balanced solids mixture, and b. thereafter polymerizing the resulting uniform solids mixture in an amine solvent selected from the group consisting of compounds of the formula ##STR15## wherein R 1 is hydrogen or alkyl of 1 to 4 carbons and R 2 and R 3 are alkyl of 1 to 4 carbons; tetramethylurea; N-methyl pyrrolidone and hexamethylphosphoramide, for a time sufficient to obtain a wholly aromatic polyamide having an inherent viscosity of from about 1.0 to about 6.0, said inherent viscosity being measured on a solution of 0.4 grams of polyamide per 100 cc. of concentrated H 2 SO 4 at 25° C.

Claim 13

The process of claim 10 wherein the aromatic diamine is paraphenylene diamine and the aromatic diacidhalide is terephthaloyl chloride.