IP Library Granted Patent US 8,008,407
Granted Patent B2
US 8,008,407 · App. 12/294,654 · Granted Aug 30, 2011

Process for preparing silicone polyethers

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Quick Facts
Patent No.
US 8,008,407
App. No.
12/294,654
Granted
Aug 30, 2011
Kind
B2
Abstract

A process is disclosed for the preparing silicone polyethers by reacting; (A) a polyether having at least one terminally unsaturated aliphatic hydrocarbon group and an alkali metal content of less than 50 ppm, (B) an organohydrogensiloxane having an acid number of less than 0.005, via a hydrosilylation reaction. The process is particularly useful to prepare silicone polyethers of improved quality via a continuous process.

Claims (36)

1. A process for preparing a silicone polyether comprising reacting;

(A) a polyether having at least one terminally unsaturated aliphatic hydrocarbon group and an alkali metal content of less than 50 ppm,

(B) an organohydrogensiloxane having an acid number of less than 0.005, via a hydrosilylation reaction.

2. The process of claim 1 wherein the silicone polyether has a —SiOC— content of less than 1 mole percent.

3. The process of claim 1 wherein the polyether (A) has the average formula

R 1 O(C n H 2n O) m R 2 ,

where n is from 2 to 4 inclusive,

m is greater than 2,

R 1 is an unsaturated aliphatic hydrocarbon,

R 2 is R 1 , hydrogen, an acetyl group, or a monovalent hydrocarbon containing 1 to 8 carbons.

4. The process of claim 3 where

n =2, R 1 is an allyl group, and R 2 is hydrogen.

5. The process of claim 1 wherein the organohydrogensiloxane is selected from an organopolysiloxane comprising the average formula;

(R 2 HSiO 0.5 )(SiO 2 ) w (R 2 HSiO 0.5 )

(R 2 HSiO 0.5 )(SiO 2 ) w (R 2 SiO) x (R 2 HSiO 0.5 )

(R 2 HSiO 0.5 )(R 2 SiO) x (R 2 HSiO 0.5 )

(R 3 SiO 0.5 )(R 2 SiO) x (RHSiO) y (R 3 SiO 0.5 )

(R 3 SiO 0.5 )(R 2 SiO) x (HRSiO) y (RSiO 1.5 ) z (R 3 SiO 0.5 )

(R 3 SiO 0.5 )(R 2 SiO) x (RHSiO) y (SiO 2 ) w (R 3 SiO 0.5 )

where R is an organic group,

w≧0, x≧0, y≧1, and z is ≧0.

6. The process of claim 5 wherein the organohydrogensiloxane is a dimethyl, methyl-hydrogen polysiloxane having the formula;

(CH 3 ) 3 SiO[(CH 3 ) 2 SiO] x [(CH 3 )HSiO] y Si(CH 3 ) 3 or

(CH 3 ) 2 HSiO[(CH 3 ) 2 SiO] x SiH(CH 3 ) 2

where x≧0 and y≧2.

7. The process of claim 1 wherein the hydrosilylation reaction is catalyzed by a platinum compound.

8. The process of claim 1 where the molar ratio of the unsaturated groups of the polyether A) to the SiH content of the organohydrogensiloxane B) is greater than one.

9. The process of claim 8 wherein the polyether A) has the formula

H 2 C═CHCH 2 O(C 2 H 4 O) a H

where a is greater than 2,

and organohydrosiloxane B) has the average formula

(CH 3 ) 3 SiO[(CH 3 ) 2 SiO] x [(CH 3 )HSiO] y Si(CH 3 ) 3

where x≧0 and y≧1.

10. The process according to claims 1 wherein greater than 99.5 mole % of the SiH of the organohydrosiloxane reacts in the hydrosilylation reaction.

11. The process according to claims 1 wherein the hydrosilylation reaction occurs in a continuous process.

12. The process according to claim 11 wherein the continuous process occurs in a plug flow reactor.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2019
From: DOW CORNING TORAY CO., LTD.
To: DOW TORAY CO., LTD.
Reel/Frame 051322/0925 →
CHANGE OF NAME Recorded Mar 7, 2018
From: DOW CORNING CORPORATION
To: DOW SILICONES CORPORATION
Reel/Frame 045515/0548 →