Process for preparing static dissipative linear segmented polyurethanes

• US 4,939,204 A
• Filed: 11/02/1988
• Issued: 07/03/1990
• Est. Priority Date: 12/05/1986
• Status: Expired due to Fees

• Current Assignee: The Dow Chemical Company (Dow, Inc.)
• Original Assignee: The Dow Chemical Company (Dow, Inc.)
• Inventors: Efford, Elizabeth A.
• Primary Examiner(s): Jacobs, Lewis T.
• Application Number:
  US07/266,178
• Time in Patent Office: 608 Days
• Field of Search: 524/701, 524/912, 524/184, 524/746, 528/66
• US Class Current: 524/701
• CPC Class Codes: C08G 18/225 of alkali or alkaline earth metals
• CPC Class Codes: C08K 5/55 Boron-containing compounds C08K5/0091 takes precedence
• CPC Class Codes: C08L 75/08 from polyethers
• CPC Class Codes: Y10S 524/912 Contains metal, boron, phosphorus, or silicon

Abstract

This invention is an improvement in a process for preparing an static dissipative phase-segregated polyurethane polymer wherein a polyfunctional polyether and a chain extender are reacted with an organic polyisocyanate in the presence of about 500 to 10,000 parts per million metal tetraorganoboron salt or fluorinated alkylsulfonate salt, based on the weight of the polyurethane. The improvement comprises dissolving said salt in all or a portion of said chain extender prior to contacting said chain extender with said polyfunctional polyether and said polyisocyanate.

This process provides a phase-segregated polyurethane having excellent static dissipative properties.

Claims

1. In a process for preparing an static dissipative phase-segregated polyurethane polymer wherein a polyfunctional polyether containing repeating oxyethylene units and a chain extender are reacted with an organic polyisocyanate in the presence of about 500 to 10,000 parts per million metal tetraorganoboron or fluorinated alkyl sulfonate salt, based on the weight of the polyurethane, the improvement comprising dissolving said tetraorganoboron or fluorinated alkyl sulfonate salt in all or a portion of said chain extender prior to contacting said chain extender with said polyfunctional polyether and said polyisocyanate.

2. The process of claim 1 wherein said chain extender is an α

,ω

-alkylene glycol or glycol ether.

3. The process of claim 2 wherein said polyether has a functionality of about 2 to about 4 and an equivalent weight of about 800 to about 2500.

4. The process of claim 3 wherein said organic polyisocyanate comprises an aliphatic polyisocyanate having an average functionality of about 2.

5. The process of claim 4 wherein the tetraorganoboron or fluorinated alkyl sulfonate salt is a tetraphenylboron salt.

6. The process of claim 2 wherein said polyether and polyisocyanate are reacted in a first step to form an isocyanate-terminated prepolymer or quasi-prepolymer, and said prepolymer or quasi-prepolymer is subsequently reacted with said chain extender to form the polyurethane polymer.

7. The process of claim 2 wherein said tetraorganoboron or fluorinated alkyl sulfonate salt comprises an alkali metal tetraphenylboron salt.

8. The process of claim 7 wherein said polyether, chain extender and polyisocyanate are substantially difunctional.

9. The process of claim 8 wherein said polyisocyanate comprises an aliphatic polyisocyanate.

10. The process of claim 9 wherein said chain extender comprises ethylene glycol or 1,4-butanediol.

11. The process of claim 10 wherein the reaction of the polyether and the polyisocyanate is conducted at an elevated temperature in the presence of an organotin and/or tertiary amine catalyst.

12. The process of claim 11 wherein the reaction of the prepolymer or quasi-prepolymer is reacted with the chain extender at an elevated temperature in the presence of an organotin and/or tertiary amine catalyst.

13. The process of claim 12 wherein the polyether has an average equivalent weight of about 800-2500.

14. The process of claim 13 wherein the polyether is an ethylene oxide-capped poly(propylene oxide).

15. The process of claim 2 wherein the tetraorganoboron or fluorinated alkyl sulfonate salt is a sodium or potassium salt of a perfluorinated C₁ -C₄ perfluorinated alkyl sulfonic acid.

16. The process of claim 4 wherein the tetraorganoboron or fluorinated alkyl sulfonate salt is a sodium or potassium salt of a perfluorinated C₁ -C₄ perfluorinated alkyl sulfonic acid.