Dow Corning Corporation

Dow Silicones Corporation

Other

Air Products and Chemicals, Inc.

Dow Toray Co., Ltd.

Colgate Palmolive Company

Dow Global Technolgoies LLC

Dow Corning Toray Company, Ltd.

Dow Corning (China) Holding Co., Ltd

Lenin J Petroff

David Joseph Romenesko

Kimmai Thi Nguyen

Robert A Ekeland

Kenneth Edward Zimmerman

Michael Ward Skinner

Qian Jane Feng

Michael Allen Stanga

James Darryl Thornsberry

David Robert Battice

Eric Jude Joffre

Seiki Tamura

Igor Chorvath

Koji Nakanishi

Paul Joseph Vincenti

Wei Chen

William James Schulz, Jr

Edwin P Plueddemann

Nanguo Liu

Anthony J Esposito

Heng Cai

Morton L Barr

Shizhong Zhang

John Herbert Frey

Bhalchandra D Moghe

Kenneth Michael Lee

Michael S Mendolia

Thomas Schamper

Richard Leroy Rabe

Bradley C Bahr

Katherine S Clement

Zuchen Lin

Kaoru Aou

Brian Harkness

Richard Michael Wehmeyer

Arjun Raghuraman

Kenneth Christopher Fey

Michael Salvatore Ferritto

Gerald Lawrence Witucki

Michael Stephen Starch

Jeffrey A Kosal

Grish Chandra

Koichi Aizawa

Juan Carlos Medina

Robert H Whitmarsh

Severine Cauvin

Zachary Wenzlick

Michael Kang-Jen Lee

Tsunehito Sugiura

Leon Neal Cook

Eric E Joffre

Robert L Oldinski

James B McGee

Dawei Li

Yongjun Lee

Douglas W King

Jay Brian Rose

Joel Freundlich

Scott Miller

Isabelle Van Reeth

Frances Marie Fournier

Travis Sunderland

Ching-min Kimmy Wu

Christopher Michael Brewer

Joseph S Steger

Diane Elizabeth Swarthout

Dennis J Colwell

James W Young, Jr

Wanda Wells Rauscher

Guodong Shen

Fernando Vazquez

Martin K Severance

Sachit Goyal

Joan E Sudbury-Holtschlag

Alix Schmidt

Krunoslav Muha

Karla Asuncion Sabram

Keiichi Akinaga

Doris Jean Brecht

Michael S Ferrito

Michael K Lee

Jean-Luc Garaud

Ryan Baumgartner

Maria R Pretzer

Paula Michele Bauer

Julie Ann Hayes

Jodi Lynnette Jibben

By John Ollinger, Legal Representative

William J Ollinger, Deceased

Hiroaki Shoji

Hortense Baillet

David J Romensko

Takeshi Yoshizawa

Michal Hrebicik

Thomas D Bekemeier

Brian Deeth

Zachary R Wenzlick

Robert Whitmarsh

Kenneth Lee

A coated article, such as a proppant, includes a base substrate and one or more polyurethane based coatings on an outer surface of the base substrate. The one or more polyurethane based coatings including the reaction product of an isocyanate component that has at least one isocyanate and an isocyanate-reactive component that has one or more simple polyols and one or more polyether monols at a ratio from 1:18 to 18:1. An isocyanate index is greater than 0.2 and less than 1.0.

Polyurethane based proppant coatings

A detergent composition comprises a trisiloxane having at least one carbinol functional group. The trisiloxane comprises the reaction product of (A) an initial trisiloxane and (B) an organic compound. Component (A) has a pendant silicon-bonded functional group selected from a hydrogen atom, an epoxy-containing group, an ethylenically unsaturated group, and an amine group. Typically, component (A) is free of certain terminal silicon-bonded functional groups and is free of polyoxyalkylene groups. Component (B) has a functional group reactive with the pendant silicon-bonded functional group of component (A), and has at least one hydroxyl functional group. The trisiloxane may be of the following general formula (I): (RSiO)(RRSiO)(RSiO) (I). In formula (I), each Ris an independently selected hydrocarbyl group. Rmay be selected from the groups (i) to (x) described herein, each of the groups having at least one carbinol group. Typically, the trisiloxane has 1-6 carbinol groups.

Detergent composition comprising a carbinol functional trisiloxane

A silicone material is provided. The silicone material is an organopolysiloxane or acid-neutralized salt thereof that contains a side-chain bonded hydrophilic group having a tertiary-amine structure and represented by the general formula:&#x2014;CH&#x2014;O&#x2014;CH&#x2014;CH(OH)&#x2014;CH&#x2014;N(R)(R)wherein q is a number ranging from 1 to 6, and wherein each of Rand Ris independently a halogen-substituted or non-substituted monovalent hydrocarbon group or an alkanol group. At least one of Rand Rhas a hydroxyl group, provided the total number of hydroxyl groups in Rand Ris at most three (3). Any of Rand Rdoes not have a nitrogen atom in the group. The silicone material has a number of beneficial properties.

Organopolysiloxane, acid-neutralized salt thereof, and applications thereof

The present disclosure relates to cosmetic compositions comprising an organosilane (A) having the formula:(R)(RO)SiRO(CHCHO)(CHO)Rwhere

Cosmetic composition comprising hydrophilic organosilanes

The present disclosure relates to compositions comprising: an organosilane having the formula: (R)(3-n) (RO)SiRO(CHCHO)(CHO)Rwherein: n is 1 or 2; a&#x2265;1, b may vary from 0 to 30, with the proviso a&#x2265;b; Ris a hydrocarbon group containing 1 to 12 carbon atoms; Ris hydrogen or an alkyl group containing 1 to 6 carbon atoms; Ris a divalent hydrocarbon group containing 2 to 12 carbon atoms; and Ris hydrogen, R, or an acetyl group; and at least one of a thermoplastic resin, a thermoset resin, and an elastomer. The present organosilane compositions may be useful for treating various surfaces to render them, among other things, more hydrophilic.

Hydrophilic organosilanes

Provided in various embodiments are compositions for topical application to the skin of a mammal, methods for their preparation, and their uses in skin care compositions to reduce adhesion of unwanted particles to the skin. When a hydrophobic non-volatile solvent and a hydrophobic non-volatile high melting point material with a melting point in the range of 60&#xb0; C. and 100&#xb0; C. are combined with a hydrophobic volatile solvent which compatibilizes the hydrophobic non-volatile solvent and the hydrophobic non-volatile high melting point material and the hydrophobic non-volatile high melting point material is selected to be at least partially incompatible with the hydrophobic non-volatile solvent in the absence of the hydrophobic volatile solvent, the resulting composition may be applied to skin to reduce adhesion of unwanted particles to the skin.

Compositions for application to the skin for reducing adhesion of pollution particles on skin and methods of preparing same

A lithography method includes the steps of: A) filling a mold having a patterned surface with a phase change composition at a temperature above the phase change temperature of the phase change composition; B) hardening the phase change composition to form a patterned feature; C) separating the mold and the patterned feature; optionally D) etching the patterned feature; optionally E) cleaning the mold; and optionally F) repeating steps A) to D) reusing the mold. The PCC may include an organofunctional silicone wax.

Lithography processes using phase change compositions

A method of treating textiles with a silicone block copolymer containing polyether-amide units is disclosed. Textiles treated with the silicone block copolymer have a feel or hand comparable to conventional hydrophobic silicones, but do not negatively impact the hydrophilicity of the textile.

Treating textiles with silicone polyether-amide block copolymers

Silicone block copolymers containing polyether-amide units, processes to prepare such silicone block copolymers, and their use in various personal care, cosmetic, household care, and healthcare formulations are disclosed.

Silicone polyether-amide block copolymers

A phase change composition comprises: a matrix comprising an organofunctional silicone wax, and a thermally conductive filler. The composition can be used as a thermal interface material in electronic devices. The composition is formulated to have any desired phase change temperature.

Thermally conductive phase change materials

There are disclosed silicone polyether compositions, methods for making them and their uses. The compositions are based on polyethers initiated by non-isomerizing alkenyl or alkynyl alcohols.

Certain silicone polyethers, methods for making them and uses

Siloxane-based polyamide elastomers can be prepared by heating a reaction mixture containing an olefinic acid and an organic amine to form an organic amide, and reacting the organic amide with a hydride functional polyorganosiloxane in the presence of a hydrosilylation catalyst to form the siloxane-based polyamide elastomer. The hydride functional polyorganosiloxane contains at least one pendant hydrogen. The elastomers are useful additives in personal care products and can be applied to the hair, the skin, or the underarm. They can also be used to modify thermoplastic nylons, and for treating woven and non-woven textiles, such as air bags, carpeting, and apparel.

Method of making siloxane-based polyamide elastomers

Methods for making silicone-organic copolymers are disclosed involving the manipulation of polymerization chain terminators allowing for polymer molecular weight control.

Methods for making silicone-organic copolymers

Thermoplastic silicone elastomers from compatibilized polyamide resins

Growing community of inventors

Bay County, MI, United States of America

Lenin J Petroff