IP Library Granted Patent US 7,671,161
Granted Patent B2
US 7,671,161 · App. 11/549,137 · Granted Mar 2, 2010

Process for producing controlled viscosity fluorosilicone polymers

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Quick Facts
Patent No.
US 7,671,161
App. No.
11/549,137
Granted
Mar 2, 2010
Kind
B2
Abstract

A process for making a fluorosilicone MD a D F b M′ where M=R 1 R 2 R 3 SiO 1/2 ; M′=(OH)R 6 R 7 SiO 1/2 or (OH)R 4 R 5 SiO 1/2 ; D=R 4 R 5 SiO 2/2 ; and D F =R 6 R 7 SiO 2/2 ; where the subscript a is zero or positive, the subscript b is positive and the subscripts a and b satisfy the following relationship: b>0.4(a+b) and R 1 is selected from the group of 1 to 20 carbon atom monovalent alkyl, aryl, or alkaryl hydrocarbon radicals and terminally unsaturated alkenyl groups of from 2 to 10 carbon atoms; R 2 , R 3 are each independently any monovalent hydrocarbon radical: alkyl, aryl, or alkaryl of from 1 to 20 carbon atoms or R 1 and each R 4 and R 5 are any monovalent hydrocarbon radical: alkyl, aryl, alkenyl, or alkaryl of from 1 to 20 carbon atoms, and R 6 is a fluorine substituted 3 to 20 carbon atom monovalent hydrocarbon radical having no fluorine substitution on the alpha or beta carbon atoms of the radical and R 7 is any monovalent hydrocarbon radical: alkyl, aryl, or alkaryl of from 1 to 20 carbon atoms or R 6 by reacting 1) b moles of (R 6 R 7 SiO) 3 , with 2) a moles of (R 4 R 5 SiO) 3 , 3) R 1 R 2 R 3 SiOH and 4) an oxygenated promoter. Compositions made by the process and articles of manufacture made from the compositions.

Claims (58)

1. A process for making a fluorositicone having the formula:

MD a D F b M′ or MD a D F b M

where

M=R 1 R 2 R 3 SiO 1/2 ;

M′=(OH)R 6 R 7 SiO 1/2 or (OH)R 4 R 5 SiO 1/2 ;

D=R 4 R 5 SiO 2/2 ; and

D F =R 6 R 7 SiO 2/2 ;

where both the subscript and stoichiometric coefficient a are zero or positive, the subscript and stoichiometric coefficient b is positive and the subscripts a and b satisfy the following relationship: b>0.4(a+b) and R 1 is selected from the group of 1 to 20 carbon atom monovalent alkyl, aryl, or alkaryl hydrocarbon radicals and terminally unsaturated alkenyl groups of from 2 to 10 carbon atoms; R 2 , R 3 are each independently any monovalent hydrocarbon radical: alkyl, aryl, or alkaryl of from 1 to 20 carbon atoms or R 1 and each R 4 and R 5 are any monovalent hydrocarbon radical: alkyl, aryl, alkenyl, or alkaryl of from 1 to 20 carbon atoms, and R 6 is a fluorine substituted 3 to 20 carbon atom monovalent hydrocarbon radical having no fluorine substitution on the alpha or beta carbon atoms of the radical and R 7 is any monovalent hydrocarbon radical: alkyl, aryl, or alkaryl of from 1 to 20 carbon atoms or R 6 by reacting

1) b moles of (R 6 R 7 SiO) 3

with

2) a moles of (R 4 R 5 SiO) 3 ,

3) a silanol having the formula R 1 R 2 R 3 SiOH;

4) an oxygenated promoter and

5) a basic catalyst.

2. The process of claim 1 wherein R 1 is methyl.

3. The process of claim 1 where R 1 is vinyl.

4. The process of claim 1 where R 6 is trifluoropropyl.

5. The process of claim 1 where the oxygenated promoter is selected from the group consisting of acetone, methylethyl ketone, tetrahydrofuran, dioxane, dimethoxyethane, di(ethyleneglycol)dimethylether, tetra(ethyleneglycol)dimethylether, dimethylsulfoxide, tetramethylurea, dibutylether, methyisopropylketone and mixtures thereof.

6. The process of claim 5 where R 6 is trifluoropropyl.

7. The process of claim 6 wherein R 1 is methyl.

8. The process of claim 6 wherein R 1 is vinyl.

9. A process for making a fluorosilicone rubber comprising:

a) the process of claim 1 ; and

b) the addition of a filler

wherein said process is conducted in a single vessel.

10. The process of claim 9 wherein the filler is fumed silica.

11. The process of claim 1 further comprising the condensation of MD a D F b M′ with itself using a condensation catalyst.

12. The process of claim 11 wherein the condensation catalyst is sodium hydroxide.

13. The process of claim 12 wherein the condensation catalyst is a phosphonitrilic halide.

14. A process for making a fluorosilicone having the formula:

MD a D F b M′ or MD a D F b M

where

M=R 1 R 2 R 3 SiO 1/2 ;

M′=(OH)R 6 R 7 SiO 1/2 or (OH)R 4 R 5 SiO 1/2 ;

D=R 4 R 5 SiO 2/2 ; and

D F =R 6 R 7 SiO 2/2 ;

where both the subscript and stoichiometric coefficient a are zero or positive, the subscript and stoichiometric coefficient b is positive and the subscripts a and b satisfy the following relationship: b>0.4(a+b) and R 1 is selected from the group of 1 to 20 carbon atom monovalent alkyl, aryl, or alkaryl hydrocarbon radicals and terminally unsaturated alkenyl groups of from 2 to 10 carbon atoms; R 2 , R 3 are each independently any monovalent hydrocarbon radical: alkyl, aryl, or alkaryl of from 1 to 20 carbon atoms or R 1 and each R 4 and R 5 are any monovalent hydrocarbon radical: alkyl, aryl, alkenyl, or alkaryl of from 1 to 20 carbon atoms, and R 6 is a fluorine substituted 3 to 20 carbon atom monovalent hydrocarbon radical having no fluorine substitution on the alpha or beta carbon atoms of the radical and R 7 is any monovalent hydrocarbon radical: alkyl, aryl, or alkaryl of from 1 to 20 carbon atoms or R 6 by reacting at a temperature ranging from about 20° C. to about 90° C.:

1) b moles of (R 6 R 7 SiO) 3

with

2) a moles of (R 4 R 5 SiO) 3 ,

3) a silanol having the formula R 1 R 2 R 3 SiOH;

4) an oxygenated promoter and

5) a basic catalyst;

wherein said fluorosilicone has a viscosity ranging from about 300 centipoise to about 200,000 centipoise at 25° C.

15. A process for making a fluorosilicone having the formula:

MD a D F b M′ or MD a D F b M

where

M=R 1 R 2 R 3 SiO 1/2 ;

M′=(OH)R 6 R 7 SiO 1/2 or (OH)R 4 R 5 SiO 1/2 ;

D=R 4 R 5 SiO 2/2 ; and

D F =R 6 R 7 SiO 2/2 ;

where both the subscript and stoichiometric coefficient a are zero or positive, the subscript and stoichiometric coefficient b is positive and the subscripts a and b satisfy the following relationship: b>0.4(a+b) and R 1 is selected from the group of 1 to 20 carbon atom monovalent alkyl, aryl, or alkaryl hydrocarbon radicals and terminally unsaturated alkenyl groups of from 2 to 10 carbon atoms; R 2 , R 3 are each independently any monovalent hydrocarbon radical: alkyl, aryl, or alkaryl of from 1 to 20 carbon atoms or R 1 and each R 4 and R 5 are any monovalent hydrocarbon radical: alkyl, aryl, alkenyl, or alkaryl of from 1 to 20 carbon atoms, and R 6 is a fluorine substituted 3 to 20 carbon atom monovalent hydrocarbon radical having no fluorine substitution on the alpha or beta carbon atoms of the radical and R 7 is any monovalent hydrocarbon radical: alkyl, aryl, or alkaryl of from 1 to 20 carbon atoms or R 6 by reacting

1) b moles of (R 6 R 7 SiO) 3

with

2) a moles of (R 4 R 5 SiO) 3 ,

3) a silanol having the formula R 1 R 2 R 3 SiOH;

4) an oxygenated promoter and

5) a basic catalyst to produce a fluorosilicone; and further reacting the fluorosilicone with a silazane selected from the group consisting of 1,1,3,3-tetramethyl-1,3-diphenyldisilazane, 1,1,3,3-tetramethyldisilazene, and hexamethyldisilazane.

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