Dow Silicones Corporation

Dow Global Technolgoies LLC

Rohm and Haas Company

Union Carbide Corporation

Marc-Andre Courtemanche

James Keenihan

Igor Chorvath

Keith Bruce

Sean Gaal

Jodi M Mecca

Lauren Marie Tonge

Jon Vierling Degroot, Jr

Cristina Serrat

Craig Gross

Scott Miller

Andrew Schlader

Tom Parsons

Yanhu Wei

Eun Sil Jang

Sukrit Mukhopadhyay

Arjun Raghuraman

Heather Spinney

Shawn Mealey

David Wilson

Michael Salvatore Ferritto

Shawn K Mealey

Isabelle Van Reeth

Helene Dihang

Travis Sunderland

Anne-Catherine Bedard

David D Devore

David Laitar

Hailan Guo

Emmett Malone Partain, Iii

Bethany Johnson

Zachary Wenzlick

Tian Lan

Gregoire Cardoen

Wenjun Xu

Jordan Reddel

Steven Richard Rapacki

Shane Mangold

Mike Ferritto

Emmett M Partain

Ryan Baumgartner

Andrew B Shah

Myoungbae Lee

Anne-Catherine Bédard

Shuqi Lai

Wendy Xu

Matthew Mclaughlin

Bethany K Johnson

Jon V Degroot Jr

Emmett M Iii Partain

A polymer/hydrophobic ester oil blend is provided comprising (a) a cosmetically acceptable hydrophobic ester oil; and (b) a thickening polymer powder, thickening polymer, wherein the thickening polymer is a silylated cellulose polymer, comprising a cellulose polymer functionalized with —Si(R)groups; wherein each Ris independently selected from the group consisting of a hydrogen, a Calkyl group, a Chaloalkyl group, an aryl group, a Calkylaryl group and a Chaloalkylaryl group; and wherein the cellulose polymer has a weight average molecular weight of 50,000 to 1,500,000 Daltons. Also provided are suncare formulations containing same and methods of using same.

Polymer/hydrophobic ester oil blend

A composition includes a silyl hydride (having at least one silicon-bonded hydrogen atom per molecule) and a fluorinated triarylborane Lewis acid. In the method, the Lewis acid catalyzes reaction of silicon bonded hydrogen atoms from the silyl hydride and water, thereby forming a siloxane bond in the resulting product. The composition and method can be used to form siloxane intermediates and cured networks.

Composition and method for silyl hydride reaction catalyzed by fluorinated arylborane Lewis acids

A polyfunctional organohydrogensiloxane is prepared using a fluorinated triarylborane Lewis acid as catalyst. The polyfunctional organohydrogensiloxane may be formulated into release coating compositions. Alternatively, the polyfunctional organohydrogensiloxane may be further functionalized with a curable group to form a clustered functional organosiloxane. The clustered functional organosiloxane may be formulated into thermal radical cure adhesive compositions.

Methods for making polyfunctional organosiloxanes and compositions containing same

A composition and method can be used in the preparation of various siloxanes. The composition and method employ a fluorinated triarylborane Lewis acid, a hydrocarbonoxy-functional organosilicon compound, and a silyl hydride. The fluorinated triarylborane Lewis acid catalyzes reaction of a hydrocarbonoxy moiety (from the organosilicon compound) and a silicon-bonded hydrogen atom (from the silyl hydride) to form a siloxane bond.

Composition and method for reacting an organosilicon compound and a silyl hydride catalyzed by a fluorinated arylborane Lewis acid

A personal care composition is provided, including: a cosmetically acceptable carrier; and a silicon glycan of formula (I): wherein each A comprises an independently selected saccharide moiety; wherein each W is an independently selected beta-amino alcohol moiety; wherein each Y comprises an independently selected organosilicon moiety; wherein each R is independently selected from substituted or unsubstituted hydrocarbyl groups, ether moieties, amine moieties, and H; wherein each Ris independently selected from substituted or unsubstituted hydrocarbyl groups and H; wherein each Z is an independently selected ether moiety; wherein each subscript a is independently 0 or 1; wherein subscripts x and y are each independently from ≥0 to <1; wherein subscript z is selected from >0 to 1; with the proviso that x+y+z=1; and wherein moieties indicated by subscripts x, y, and z may be in randomized or block form in the silicon glycan.

Personal care composition comprising a silicon glycan

A composition and a method for preparing a polymer composite article. The composition comprises (A) a filler in an amount of from 10 to 90 wt. The composition also comprises (B) a polymer in an amount of from 10 to 90 wt. %, wherein the (B) polymer is selected from polyolefins, polyamides, polyesters, or combinations thereof. Further, the composition comprises (C) an organopolysiloxane in an amount of from greater than 0 to 10 wt. %; the (C) organopolysiloxane having at least one silicon-bonded hydroxyl group and a viscosity of from 1,000 to 60,000 mPa·s at 25° C. The ranges for components (A)-(C) arc based on the total weight of components (A), (B) and (C) in the composition.

Composition, polymer composite article formed therewith, and method of preparing same

A polydiorganosiloxane is useful in a composition and a method for preparing a wood plastic composite article. The wood plastic composite article is useful as a building material. The polydiorganosiloxane may be added to the composition in liquid form or may form part of a solid carrier component used to make the wood plastic composite article.

Polydiorganosiloxane compositions and methods for use thereof in forming wood plastic composites

A composition contains a mixture of silyl hydride, a silanol and/or a silyl ether, and a Bridged Frustrated Lewis Pair.

Bridged frustrated Lewis pairs as thermal trigger for reactions between Si—H and Si—OR

A composition contains an alpha-beta unsaturated ester, a silyl hydride, and a Bridged Frustrated Lewis Pair.

Bridged frustrated Lewis pairs as thermal trigger for reactions between Si—H and alpha-beta unsaturated esters

A composition contains a mixture of silyl hydride, a siloxane and a Bridged Frustrated Lewis Pair and can be thermally triggered to cure.

Bridged frustrated lewis pairs as thermal trigger for reactions between Si—H and Si—O—Si

A composition contains a silylated polysaccharide, where the silylated polysaccharide is characterized by: (a) having linked fructose, galactose, anhydrogalactose, or glucose saccharide units provided that glycosidic linkages of glucose are alpha linkages and that the silylated polysaccharide is other than a silylated starch; and (b) on average 1 to 100 mole-percent of the hydroxyl groups on the polysaccharide have been silylated with a silyl group having the structure —SiRlinked to the polysaccharide through a C—O—Si bond where each R is independently selected from hydrocarbyl radicals having from one to 12 carbon atoms, provided that on average at least one R per polysaccharide has a terminally unsaturated carbon-carbon double bond.

Terminal alkenyl functional silylated polysaccharides

A composition and a method for preparing a polymer composite article. The composition comprises (A) a filler in an amount of from 10 to 90 wt. %. The composition also comprises (B) a polymer in an amount of from 10 to 90 wt. %, wherein the (B) polymer comprises a polyvinyl. Further, the composition comprises (C) an organopolysiloxane in an amount of from greater than 0 to 10 wt. %; the (C) organopolysiloxane having at least one silicon-bonded hydroxyl group and a viscosity of from 1,000 to 60,000 mPa·s at 25° C. The ranges for components (A)-(C) are based on the total weight of components (A), (B) and (C) in the composition.

A composition and a method for preparing a polymer composite article. The composition comprises (A) a filler in an amount of from 10 to 90 wt. The composition also comprises (B) a polymer in an amount of from 10 to 90 wt. %, wherein the (B) polymer is selected from polyolefins, polyamides, polyesters, or combinations thereof. Further, the composition comprises (C) an organopolysiloxane in an amount of from greater than 0 to 10 wt. %; the (C) organopolysiloxane having at least one silicon-bonded hydroxyl group and a viscosity of from 1,000 to 60,000 mPa·s at 25° C. The ranges for components (A)-(C) are based on the total weight of components (A), (B) and (C) in the composition.

A silicon glycan is provided. The silicon glycan comprises a glycoside moiety, independently selected organosilicon moieties, and beta-amino alcohol moieties joining the organosilicon moieties to the glycoside moiety. The glycoside moiety comprises independently selected saccharide moieties, which may be substituted with hydrocarbyl groups, ether moieties, and/or amine moieties. A method of preparing the silicon glycan is also provided. The method includes reacting (A) an aminoethyl polysaccharide and (B) an epoxide-functional organosilicon compound, to give the silicon glycan. The method may include preparing the aminoethyl polysaccharide (A) by first reacting (At) a hydroxyl-functional polysaccharide and (A2) an aziridinium halide compound to give the aminoethyl polysaccharide (A).

Silicon glycan and method of preparing same

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Midland, MI, United States of America

Marc-Andre Courtemanche