Process for preparing branched Si-H functional polysiloxanes and use thereof for preparing liquid SiC- or SiOC-linked, branched modified organomodified polysiloxanes
View Patent ↗The invention provides a process for preparing liquid, branched SiH-functional siloxanes by reacting a mixture of one or more low molecular weight SiH-functional siloxanes, one or more low molecular weight SiH-free siloxanes, one or more tetraalkoxysilanes, and optionally one or more trialkoxysilanes with addition of water and in the presence of a Brønsted-acidic ion exchanger, which is characterized in that the reaction is performed in one process step.
1. A process for preparing a branched SiH-functional siloxane liquid at a temperature of 25° C. and a pressure of 101 325 Pa, said process comprising reacting in a single step a mixture that comprises
a) one or more SiH-functional siloxanes,
b) one or more SiH function-free siloxanes,
c) one or more tetraalkoxysilanes, and optionally
d) one or more trialkoxysilanes,
in the presence of added water and at least one solid, Brønsted-acidic catalyst selected from an acidic ion exchanger, wherein 0.5 to 30 mol of water per mole of alkoxysilane is used.
2. The process according to claim 1 , wherein said mixture includes said one or more trialkoxysilanes.
3. The process according to claim 1 , wherein said mixture excludes said one or more trialkoxysilanes.
4. The process according to claim 1 , wherein the reacting is performed at a temperature of 0° C. to 100° C.
5. The process according to claim 1 , wherein the acidic ion exchanger is a sulphonic acid ion exchange resin.
6. The process according to claim 1 , wherein at least one non-solid, Brønsted-acidic catalyst is used in conjugation with said acidic ion exchanger.
7. The process according to claim 1 , wherein the catalyst is a mixture of trifluoromethanesulphonic acid and a sulphonic acid ion exchange resin.
8. The process according to claim 1 , wherein the sum total of the acidic catalysts used is from 0.01 to 20% by weight based on the sum total of the mass of starting materials used.
9. The process according to claim 1 , wherein the branched SiH-functional siloxane includes SiH functions that are purely in terminal positions, purely in pendant positions or in a mixture of terminal and pendant positions in the siloxane.
10. The process according to claim 1 , wherein said added water is introduced in one step.
11. The process according to claim 1 , wherein said added water is metered in over a period of time.
12. The process according to claim 1 , wherein said added water is present in an amount sufficient to prevent phase separation.
13. A method for preparing a branched organomodified polysiloxane, the method comprising reacting in a single step a mixture that comprises:
a) one or more SiH-functional siloxanes,
b) one or more SiH function-free siloxanes,
c) one or more tetraalkoxysilanes, and optionally
d) one or more trialkoxysilanes,
in the presence of water and at least one solid Brønsted-acidic catalyst selected from an acidic ion exchanger to afford a branched Si—H functional polysiloxane; and subsequently reacting said branched Si—H functional polysiloxane with one or more compounds having one double bond per molecule by platinum-catalyzed hydrosilylation.
14. The method according to claim 13 , wherein said one or more compounds having one double bond per molecule are selected from vinylpolyoxyalkylene, allylpolyoxyalkylene, and a mixture thereof.
15. A method for preparing a branched organomodified polysiloxane, the method comprising reacting in a single step a mixture that comprises:
a) one or more SiH-functional siloxanes,
b) one or more SiH function-free siloxanes,
c) one or more tetraalkoxysilanes, and optionally
d) one or more trialkoxysilanes,
in the presence of water and at least one solid Brønsted-acidic catalyst selected from an acidic ion exchanger to afford a branched Si—H functional polysiloxane; and subsequently reacting said branched Si—H functional polysiloxane with one or more compounds having one hydroxyl group per molecule by Lewis acid-catalyzed dehydrogenative bond formation.