Chain-extended poly(aryl ether ketones)

DETAILED DESCRIPTION What is claimed is: 1.
A process for preparing a poly(aryl ether ketone) polymer comprising the following steps: (a) reacting (n) moles of HAr H with (n+1) moles of YCOAr.
sub.
1 COY under Friedel-Crafts polymerization conditions to yield YCOAr.
sub.
1 CO--ArCOAr.
sub.
1 CO).
sub.
n Y (b) reacting the product obtained in step (a) with 2XAr.
sub.
2 H under Friedel-Crafts polymerization conditions to yield XAr.
sub.
2 COAr.
sub.
1 --COArCOAr.
sub.
1 CO).
sub.
n Ar.
sub.
2 X (c) reacting the product obtained in step (b) with HOAr.
sub.
3 OH in the presence of a base and an aprotic solvent to yield --Ar.
sub.
2 COAr.
sub.
1 CO--ArCOAr.
sub.
1 CO].
sub.
n Ar.
sub.
2 OAr.
sub.
3 O).
sub.
x wherein Ar and Ar.
sub.
1 are divalent aromatic groups, Ar.
sub.
2 is a divalent aromatic group wherein the substituents X and CO are in para or ortho position relative to each other, Ar.
sub.
3 is a residue of a dihydric phenol, X and Y are halogen, n is an integer of 1 to 50 and X is one or greater.
2.
A process as defined in claim 1 wherein the ingredients in steps (a) and (b) are simultaneously added to a reactor.
3.
A process as defined in claim 1 in which steps (a) and (b) are carried out in the presence of a Friedel-Crafts catalyst.
4.
A process as defined in claim 3 wherein the Friedel-Crafts catalyst is selected from aluminum chloride, antimony pentachloride, or ferric chloride.




Description:
FIELD OF THE INVENTION This invention is directed to novel crystalline chain extended polymers containing segments of crystalline poly(aryl ether ketones).
The novel materials are easy to prepare and display excellent toughness, fabricability and very good high temperature and solvent resistance.
BACKGROUND OF THE INVENTION Over the years, there has been developed a substantial body of patent and other literature directed to the formation and properties of poly(aryl ethers) (hereinafter called "PAE").
Some of the earliest work such as by Bonner, U.
S.
Pat.
No.
3,065,205, involves the electrophilic aromatic substitution (e