Abstract: A reaction composition contains (a) an allyl polyether having the following formula: CH2=CHCH2O-Aa-B where, (i) subscript a is 2 to 170; (ii) A is selected from: —CH2CH2O—; —CH2CH(CH3)O—; —CH(CH3)CH2O—, CH2CH(CH2CH3)O—; —CH(CH2CH3)CH2O, —CH2CF(CF3)O—, —CF(CF3)CF2O— and —CF2CF(CF3)O—; and (iii) B is selected from —H, —CH3, —CH2CH3, —CH2CH2CH3, —CH2CH2CH2CH3, —C(O)CH3, and —CF2CF2CF3; (b) A silyl hydride functional siloxanc comprising the following siloxane units [R2HSiO1/2]m[R2SiO2/2]d[R2SiO3/2]t[SiO4/2]q wherein d+t+q is one or more and wherein: (i) R is selected from hydrocarbyl groups liaing from one to 8 carbon atoms; (ii) subscript m is 2 or more; (iii) subscript d is zero to 20; (iv) subscript t is zero to 2; (v) subscript q is zero to 2; and (c) a platinum-based hydrosilylation catalyst; where there are at least 4 molar equivalents of silyl hydride functionalities relative to allyl functionalities in the reaction composition.

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.

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.