Aromatic sulfide/sulfone polymer production

Claim 2

In a process for the production of an aromatic sulfide/sulfone polymer comprising contacting a dihaloaromatic sulfone, an alkali metal sulfide, and an organic amide under polymerization conditions sufficient to cause the reactants to react and form said polymer, the improvement for increasing melt flow stability of the polymer produced by said contacting which comprises end-capping the polymer by introducing a small, but effective, amount sufficient to impart increased melt flow stability of additional dihaloaromatic sulfone into the crude reaction mixture at or near completion of the polymerization reaction.

Claim 3

A process according to claim 1 wherein said additional dihaloaromatic sulfone used as end-capping agent is the same as the dihaloaromatic sulfone used for initial contacting.

Claim 4

A process according to claim 1 wherein the amount of additional dihaloaromatic sulfone employed as end-capping agent ranges from about 0.01:1 to about 0.2:1 moles per mole of alkali metal sulfide and said end-capping agent is added between 1.5 and 6 hours after the desired polymerization temperature is reached.

Claim 5

A process according to claim 1 wherein said additional dihaloaromatic sulfone is introduced into the crude reaction mixture in a solvent.

Claim 6

A process according to claim 1 wherein an alkali metal carboxylate is present during contacting of said dihaloaromatic sulfone, said alkali metal sulfide, and said organic amide to increase the molecular weight of the produced polymer.

Claim 7

A process according to claim 1 wherein the temperature during the introduction of end-capping agent is in the range of about 170°-240° C. and the reaction conditions are maintained from about 1 minute to about 5 hours after addition of the end-capping agent.

Claim 8

A process according to claim 1 wherein said additional dihaloaromatic sulfone end-capping agent is the same as the dihaloaromatic sulfone used in the initial contacting and is introduced into the crude reaction mixture in an organic amide corresponding to the organic amide used in the initial contacting.

Claim 9

A process according to claim 5 wherein the initial reactants are bis(4-chlorophenyl)sulfone, sodium sulfide, N-methyl-2-pyrrolidone and lithium acetate and the end-capping agent is bis(4-chlorophenyl)sulfone which is introduced into the crude reaction mixture dissolved in N-methyl-2-pyrrolidone.

Claim 10

A process for the production of a high molecular weight aromatic sulfide/sulfone polymer exhibiting improved physical properties which comprises: (a) initially contacting (1) at least one dihaloaromatic sulfone, (2) at least one alkali metal sulfide, and (3) at least one organic amide under polymerization conditions of temperature ranging from about 170°-240° C. for a period of time sufficient to form said polymer, (b) adding a small but effective amount sufficient to impart increased melt flow stability of an end-capping agent comprising a dihaloaromatic sulfone to the crude reaction mixture thus formed in step (a) about 21/2 to about 5 hours after reactants (1), (2), (3) and (4) have been subjected to said polymerization conditions, and (c) subjecting the reaction mixture containing said end-capping agent obtained in step (b) to said polymerization conditions for a period of time sufficient to form said high molecular weight aromatic sulfide/sulfone polymer having improved melt flow stability.

Claim 11

A process for the production of a high molecular weight aromatic sulfide/sulfone polymer exhibiting improved physical properties which comprises: (a) initially contacting (1) at least one dihaloaromatic sulfone, (2) at least one alkali metal sulfide, and (3) at least one organic amide under polymerization conditions of temperature ranging from about 170°-240° C. for a period of time sufficient to form said polymer, (b) adding a small but effective amount sufficient to impart increased melt flow stability of an end-capping agent comprising a dihaloaromatic sulfone to the crude reaction mixture thus formed in step (a) about 21/2 to about 5 hours after reactants (1), (2), (3) and (4) have been subjected to said polymerization conditions, and (c) subjecting the reaction mixture containing said end-capping agent obtained in step (b) to said polymerization conditions for a period of time sufficient to form said high molecular weight aromatic sulfide/sulfone polymer having improved melt flow stability.

Claim 12

A process according to claim 9 wherein (1) and said end-capping agent in step (c) are the same dihaloaromatic sulfone.

Claim 13

A process according to claim 9 wherein said end-capping agent is introduced in step (b) in a solvent comprising an organic amide corresponding to (3).

Claim 14

A process according to claim 9 wherein an alkali metal carboxylate is present during contacting of (1), (2), and (3) in step (a) to increase the molecular weight of the produced polymer.

Claim 15

A process according to claim 9 wherein step (c) is carried out for about 1 minute to about 5 hours after the end-capping agent is added in step (b).

Claim 16

A process according to claim 12 wherein (1) is bis(4-chlorophenyl)sulfone, (2) is sodium sulfide, (3) is N-methyl-2-pyrrolidone, (4) is lithium acetate, and said end-capping agent in step (b) is bis(4-chlorophenyl)sulfone.

Claim 17

A process according to claim 14 wherein said end-capping agent is introduced into the crude reaction mixture dissolved in N-methyl-2-pyrrolidone.