Dow Corning Corporation

Other

Dow Corning Toray Company, Ltd.

Anil Kumar Tomar

William Charles Maki

Howard M Bank

Michael Wolfgang Backer

John M Gohndrone

Charles Edmund Skinner

Hongjun Yue

Eric Jude Joffre

Franck A Renauld

Takeaki Saiki

Makoto Iwai

Russell Allen Elms

Lisa Marie Boswell

Haruhiko Furukawa

Anthony Revis

Michael Salvatore Ferritto

Csilla Kollar

James Anderson Beck

Feifei Lin

Mark Keinath

Lylenette Canfield

A method of making a saccharide siloxane copolymer includes reacting an amine functional saccharide with an epoxy functional silane containing at least one condensable or hydrolysable group. This product is reacted with an oligomer to form the saccharide siloxane copolymer.

Methods of making saccharide siloxane copolymers

A novel saccharide siloxane copolymer has improved stability in the presence of water as compared to certain previously known saccharide siloxanes. The saccharide siloxane copolymer is useful in personal care compositions.

Saccharide siloxanes stable in aqueous environments and methods for the preparation and use of such saccharide siloxanes

A bis[tri(hydroxypolyalkyleneoxy)silylalkyl] polysulfide, i.e., a polysulfide that contains bonded hydroxypolyalkyleneoxy groups instead of alkoxy groups in the bis(trialkoxysilylalkyl) polysulfide; a method of manufacturing of the aforementioned polysulfide by heating a bis(trialkoxysilylalkyl) polysulfide and a polyalkyleneglycol; a tire rubber additive to a tire rubber composition that comprises a bis[tri(hydroxypolyalkyleneoxy)silylalkyl] polysulfide alone or a mixture of bis[tri(hydroxypolyalkyleneoxy)silylalkyl] polysulfide and a polyalkyleneglycol; and a tire rubber composition that contains the aforementioned additive.

Bis [tri (hydroxypolyalkyleneoxy) silylalkyl] polysulfide, method of manufacturing bis [tri (hydroxypolyalkyleneoxy) silylalkyl] polysulfide, tire rubber additive, and tire rubber composition

A method for manufacturing a bis(silatranylalkyl) polysulfide by heating a bis(trialkoxysilylalkyl) polysulfide and triethanolamine in the presence of a catalytic quantity of an alkali-metal alcoholate, thus substituting all Si-bonded alkoxy groups of the bis(trialkoxysilylalkyl) polysulfide with a (OCHCH)N group; a method for the preparation of a mixture of a bis(silatranylalkyl) polysulfide and a (silatranyalkyl)(trialkoxysilyl) disulfide or a mixture of a bis(silatranylalkyl) polysulfide, a (silatranylalkyl)(trialkoxysilyl) disulfide, and a bis(trialkoxysilylalkyl) polysulfide by heating a bis(trialkoxysilylalkyl) polysulfide and triethanolamine in the presence of a catalytic quantity of an alkali-metal alcoholate, thus substituting a part of Si-bonded alkoxy groups of the bis(trialkoxysilylalkyl) polysulfide with a (OCHCH)N group; a mixture of a bis(silatranylalkyl) polysulfide and a (silatranylalkyl)(trialkoxysilyl) disulfide; a mixture of a bis(silatranylalkyl) polysulfide, a (silatranylalkyl)(trialkoxysilyl) disulfide, and a bis(trialkoxysilylalkyl) polysulfide; and a rubber composition containing the aforementioned mixture.

Method for manufacturing a bis(silatranylalkyl) polysulfide, method for manufacturing a mixture of bis(silatranylalkyl) polysulfide etc., a mixture of bis(silatranylalkyl) polysulfide etc., and rubber composition

Silica surfaces are contacted with compositions containing organosilicon compounds to prepare modified silica fillers. The compositions contain only organosilicon compounds which are monomeric dichlorosilanes and trialkoxysilanes. The treating compositions may be (i) mixtures or blends of dialkyldichlorosilanes, and trialkoxysilanes free of hydrocarbon or organofunctional groups reactive with silica surfaces, or (ii) mixtures or blends of substituted dialkyldichlorosilanes in which the substituted dialkyldichlorosilanes are free of hydrocarbon or organofunctional groups reactive with silica surfaces, and trialkoxysilanes free of hydrocarbon or organofunctional groups reactive with silica surfaces. These mixtures and blends contain dialkyldichlorosilanes and trialkoxysilanes in a weight ratio of 1:0.1 to 1:2, respectively.

Hydrophobing silica with organosilicon compounds and blends thereof

In a first embodiment of a process for making mercaptoalkylalkoxysilanes, a pH adjusting agent and a sulfide containing compound are mixed in an aqueous phase to provide a pH of 4-9, a phase transfer catalyst is added to the aqueous phase, a haloalkylalkoxysilane is then added to the aqueous phase to form a reaction mixture containing mercaptoalkylalkoxysilanes and water soluble byproducts, and the desired mercaptoalklyalkoxysilanes are separated from the water soluble byproducts. In an alternate embodiment, the haloalkylalkoxysilane, the phase transfer catalyst, and an anhydrous pH adjusting agent such as sulfur dioxide, carbon dioxide, hydrogen sulfide, phosphoric acid, boric acid, and hydrochloric acid, are mixed, then an aqueous solution of a sulfide containing compound is added to form a reaction mixture containing mercaptoalkylalkoxysilanes and water soluble byproducts, and desired mercaptoalklyalkoxysilanes are separated from water soluble byproducts.

Method of making mercaptoalkylalkoxysilanes

Preparation of sulfur-containing organosilicon compounds using a buffered phase transfer catalysis process

Process for the preparation of sulfur-containing organosilicon compounds

This invention relates to organosilyl peroxide compounds which are stable in aqueous systems and are used for bleaching and cleaning applications. More particularly, this invention is concerned with the stability of bis(organosilyl)peroxides when formulated in aqueous and non-aqueous delivery systems. The liquid detergents containing the organosilyl peroxide compounds of this invention exhibit excellent bleaching performance and stain removal properties on fabrics at typical low wash temperatures.

Stable bleaching agents containing bis(organosilyl) peroxides

Stable bleaching agents containing bis(organosilyl)peroxides

Growing community of inventors

Midland, MI, United States of America

Anil Kumar Tomar