Process for producing diorganopolysiloxane oils

Claim 2

A process for producing a diorganopolysiloxane oil having a viscosity from 50 to 100,000 centipoise at 25°C. where at least one of the organo groups is an aliphatic or haloaliphatic radical of at least 3 carbon atoms or more comprising (a) reacting cyclic polysiloxanes of the formula, (R R' SiO).sub.4 and mixtures thereof, at a temperature in the range of 0° to 90°C. in the presence of 5 to 300 parts per million of a catalyst selected from the class consisting of CsOH, silanolates thereof, and compounds of the formula, ##EQU2## where R 2 is selected from the class consisting of alkyl radicals of 1 to 8 carbon atoms, cycloalkyl radicals of 4 to 8 carbon atoms and phenyl, B is selected from the class consisting of nitrogen and phosphorous, R 3 is selected from the class consisting of alkyl radicals of 1 to 8 carbon atoms, cycloalkyl radicals of 4 to 8 carbon atoms, phenyl, siloxane chains of the unit formula, R a 4 SiO 4 -a/2 and mixtures thereof where R 4 is selected from the class consisting of monovalent hydrocarbon radicals and halogenated monovalent hydrocarbon radicals, and a is from 1.5 to 2.5, and (b) neutralizing the catalyst in the reaction mixture after equilibration has been reached, where R is selected from the class consisting of methyl, ethyl, vinyl and phenyl, and R' is selected from the class consisting of alkyl radicals, halogenated alkyl radicals and cycloalkyl radicals of 3 to 8 carbon atoms.

Claim 3

A process as defined in claim 1 wherein the catalyst is neutralized with an ingredient selected from the class consisting of phosphoric acid and a compound of the formula, R b 6 SiX 4 -b , where R 6 is selected from the class consisting of alkyl radicals, cycloalkyl radicals, vinyl radicals and phenyl radicals, X is selected from the class consisting of bromine and chlorine, and b is from 0 to 3.

Claim 4

A process as defined in claim 1 including after step (b) the step further comprising heating the reaction mixture to 150° to 200°C. at a vacuum of 1 to 100 mm of Hg to strip off all volatiles so as to result in the desired product.

Claim 5

A process as defined in claim 1 wherein the cyclic polysiloxane is reacted with the catalyst for a period of time varying from 1/4 hour to 10 hours.

Claim 6

A process as defined in claim 1 wherein the cyclic polysiloxanes and mixtures thereof contain less than 20 parts per million of trifunctional siloxanes, less than 200 parts per million of monofunctional siloxanes, and 0 to 50% by weight of other cyclic polysiloxanes and less than 10 parts per million of water.

Claim 7

A process as defined in claim 1 wherein R' is R 5 CH 2 CH 2 -- and R 5 is a perfluoroalkyl radical of 1 to 6 carbon atoms.

Claim 8

A process for producing a diorganopolysiloxane oil having a viscosity from 50 to 100,000 centipoise at 25°C. where at least one of the organo groups is an aliphatic or haloaliphatic radical of 3 carbon atoms or more comprising (a) hydrolyzing in a water and a water-immiscible organic solvent mixture, a silane of the formula, R R' SiX.sub.2 and mixtures of said silane, where R is selected from the class consisting of methyl, ethyl, vinyl and phenyl and R' is selected from the class consisting of alkyl radicals, halogenated alkyl radicals and cycloalkyl radicals of 3 to 8 carbon atoms, and X is halogen; (b) separating the water and water-immiscible organic solvent from the hydrolyzate; (c) adding 0.5 to 2% by weight of a catalyst selected from the class consisting of KOH, and CsOH to the hydrolyzate and heating the hydrolyzate to 150°C. to 200°C; (d) removing overhead a mixture of cyclic polysiloxanes and transferring such cyclic polysiloxanes into a distillation column; (e) separating by distillation at a temperature of 80°-100°C. and 1 to 50 mm of Hg vacuum essentially pure tetracyclic polysiloxanes of the formula, (R R' SiO).sub.4 and mixtures thereof, where R and R' are as previously defined; (f) heating the tetracyclic polysiloxanes above 100°C. with a nitrogen purge to reduce the water content to less than 10 parts per million; (g) reacting the cyclic tetrapolysiloxanes at a temperature in the range of 0° to 90°C. in the presence of 5 to 300 parts per million of a catalyst selected from the class consisting of CsOH, silanolates thereof, and compounds of the formula, ##STR3## where R 2 is selected from the class consisting of alkyl radicals of 1 to 8 carbon atoms, cycloalkyl radicals of 4 to 8 carbon atoms and phenyl, B is selected from the class consisting of nitrogen and phosphorous, R 3 is selected from the class consisting of alkyl radicals of 1 to 8 carbon atoms, cycloalkyl radicals of 4 to 8 carbon atoms, phenyl, siloxane chains of the unit formula, R a 4 SiO 4 -a/2 and mixtures thereof, where R 4 is selected from the class consisting of monovalent hydrocarbon radicals and halogenated monovalent hydrocarbon radicals, and a is from 1.5 to 2.5; and (h) neutralizing the catalyst in the reaction mixture after equilibrium has been reached.

Claim 9

A process for producing a diorganopolysiloxane oil having a viscosity from 50 to 100,000 centipoise at 25°C. where at least one of the organo groups is an aliphatic or haloaliphatic radical of 3 carbon atoms or more comprising (a) hydrolyzing in a water and a water-immiscible organic solvent mixture, a silane of the formula, R R' SiX.sub.2 and mixtures of said silane, where R is selected from the class consisting of methyl, ethyl, vinyl and phenyl and R' is selected from the class consisting of alkyl radicals, halogenated alkyl radicals and cycloalkyl radicals of 3 to 8 carbon atoms, and X is halogen; (b) separating the water and water-immiscible organic solvent from the hydrolyzate; (c) adding 0.5 to 2% by weight of a catalyst selected from the class consisting of KOH, and CsOH to the hydrolyzate and heating the hydrolyzate to 150°C. to 200°C; (d) removing overhead a mixture of cyclic polysiloxanes and transferring such cyclic polysiloxanes into a distillation column; (e) separating by distillation at a temperature of 80°-100°C. and 1 to 50 mm of Hg vacuum essentially pure tetracyclic polysiloxanes of the formula, (R R' SiO).sub.4 and mixtures thereof, where R and R' are as previously defined; (f) heating the tetracyclic polysiloxanes above 100°C. with a nitrogen purge to reduce the water content to less than 10 parts per million; (g) reacting the cyclic tetrapolysiloxanes at a temperature in the range of 0° to 90°C. in the presence of 5 to 300 parts per million of a catalyst selected from the class consisting of CsOH, silanolates thereof, and compounds of the formula, ##STR3## where R 2 is selected from the class consisting of alkyl radicals of 1 to 8 carbon atoms, cycloalkyl radicals of 4 to 8 carbon atoms and phenyl, B is selected from the class consisting of nitrogen and phosphorous, R 3 is selected from the class consisting of alkyl radicals of 1 to 8 carbon atoms, cycloalkyl radicals of 4 to 8 carbon atoms, phenyl, siloxane chains of the unit formula, R a 4 SiO 4 -a/2 and mixtures thereof, where R 4 is selected from the class consisting of monovalent hydrocarbon radicals and halogenated monovalent hydrocarbon radicals, and a is from 1.5 to 2.5; and (h) neutralizing the catalyst in the reaction mixture after equilibrium has been reached.

Claim 10

A process as defined in claim 7 wherein in step (a) the amount of water is controlled such that there is formed 20% by weight of an aqueous halogen acid solution during the hydrolysis.

Claim 11

A process as defined in claim 7 wherein the catalyst is neutralized in step (h) with an ingredient selected from the class consisting of phosphoric acid and a compound of the formula, R.sub.b.sup.6 SiX.sub.4.sub.-b where R 6 is selected from the class consisting of alkyl radicals, cycloalkyl radicals, vinyl radicals and phenyl radicals, X is selected from the class consisting of bromine and chlorine and b is from 0 to 3.

Claim 12

A process as defined in claim 7 including after step (h) the step further comprising heating the reaction mixture to 150° to 200°C. at a vacuum of 1 to 100 mm Hg to remove all volatiles so as to result in the desired product.

Claim 13

A process as defined in claim 7 wherein in step (g) the reaction is carried out for a period of time varying from 1/4 hour to 10 hours.

Claim 14

A process as defined in claim 7 wherein after step (f) the tetracyclicpolysiloxanes and mixtures thereof contain less than 20 parts per million of trifunctional siloxanes, and less than 200 parts per million of monofunctional siloxanes.

Claim 15

A process as defined in claim 7 wherein R' is R 5 CH 2 CH 2 -- and R 5 is a perfluoroalkyl radical of 1 to 6 carbon atoms.