Process for making polyarylethers and use in membrane preparation

Patent metadata

Field	Value
Publication number	US-9353220-B2
Application number	US-201313965453-A
Country	US
Kind code	B2
Filing date	Aug 13, 2013
Priority date	Aug 13, 2013
Publication date	May 31, 2016
Grant date	May 31, 2016

Abstract

A process for making polyarylethers provides a reaction mixture that includes a dipolar aprotic solvent for polyarylether and polyarylether forming reactants, and reacts the polyarylether-forming reactants, with removing of water with nitrogen in the absence of azeotrope forming cosolvent and optionally replacing removed amounts with dipolar aprotic solvent. The process can further include directly wet spinning the reactor solution without recovery of the polymer from the dipolar aprotic solvent through a spinneret to form hollow fibers or flat sheets suitable for membranes.

First claim

What is claimed is:

1. A process for preparation of at least one polyarylether comprising reacting polyarylether forming reactants in a reactor solution, said reaction solution comprising at least one polar aprotic solvent and the polyarylether forming reactants with removing of water in the absence of azeotrope forming cosolvent and adding fresh polar aprotic solvent to the reactor solution in substantially equal amount to any polar aprotic solvent removed from the reactor solution during the reacting, wherein the polar aprotic solvent is dimethylacetamide, N-methylpyrrolidone, dimethylsulfoxide, diphenylsulfone, or any combinations thereof.

2. The process of claim 1 , wherein the adding of fresh polar aprotic solvent occurs during the reacting to replace a polar aprotic solvent removed so as to maintain solvent concentration of the solvent in the reactor solution to within ±10% of a starting concentration thereof throughout the reacting.

3. The process of claim 1 , wherein the polar aprotic solvent is dimethylacetamide.

4. The process of claim 1 , wherein the polar aprotic solvent is N-methylpyrrolidone.

5. The process of claim 1 , wherein the at least one polyarylether is polysulfone.

6. The process of claim 1 , wherein the at least one polyarylether is polyethersulfone.

7. The process of claim 1 , wherein the at least one polyarylether is polyphenylsulfone.

8. The process of claim 1 , wherein the polyarylether forming reactants comprise a dihydroxyaromatic compound, a dihaloaromatic compound, a weak base, and a polar aprotic solvent.

9. The process of claim 1 , wherein the polyarylether forming reactants comprise (i) substantially equimolar amounts of bisphenol and dihalobenzenoid, and (ii) alkali metal carbonate.

10. The process of claim 1 , wherein the reacting is conducted for about 5 hours to about 70 hours.

11. The process of claim 1 , wherein the reacting is conducted for about 15 to about 30 hours.

12. The process of claim 1 , wherein polyarylether produced by the reacting has a weight average molecular weight of from about 40,000 to about 120,000.

13. The process of claim 1 , wherein polyarylether produced by the reacting has a weight average molecular weight of from about 60,000 to about 85,000.

14. The process of claim 1 , further comprising making a membrane with the polyarylether product.

15. The process of claim 1 , further comprising making a flat sheet or hollow fiber with polyarylether product of the reacting.

16. The process of claim 1 , further comprising directly spinning the reactor solution after the reacting through a spinneret to form hollow fibers without previously isolating polyarylether product of the reacting from the polar aprotic solvent.

17. The process of claim 1 , further comprising directly spinning the reactor solution after the reacting through a spinneret to form hollow fibers without previously isolating polyarylether product of the reacting from the polar aprotic solvent, wherein the polyarylether product is polysulfone, polyethersulfone, polyphenylsulfone, or any combinations thereof.

18. The process of claim 1 , further comprising directly making a coating with the reactor solution after the reacting without previously isolating polyarylether product of the reacting from the polar aprotic solvent.

19. A process for preparation of at least one polyarylether comprising reacting polyarylether forming reactants in a reactor solution, said reaction solution comprising at least one polar aprotic solvent and the polyarylether forming reactants with removing of water in the absence of azeotrope forming cosolvent and adding fresh polar aprotic solvent to the reactor solution in substantially equal amount to any polar aprotic solvent removed from the reactor solution during the reacting, wherein the polar aprotic solvent is dimethylacetamide, N-methylpyrrolidone, dimethylsulfoxide, diphenylsulfone, or any combinations thereof, said process is conducted with a stoichiometric excess of one of the two polyarylether forming reactants such that the final product contains substantially less of the stoichiometrically deficient reactant and the reaction is self-terminating.

Assignees

• Fresenius Med Care Hldg Inc

Inventors

• Savariar Selvaraj
• Hudson Kevin
• Russell Geoffrey Andrew
• White James Leslie
• Barton Brett Allen
• Ford Cheryl
• Teo Jiunn

Classifications

• C08G75/04

  from mercapto compounds or metallic derivatives thereof (C08G75/0204 takes precedence) · CPC title

• C08G65/40

  from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group · CPC title

• C08G8/02

  of ketones · CPC title

• C08G65/4093

  characterised by the process or apparatus used · CPC title

• C08G65/38 Primary

  derived from phenols · CPC title