Dow Corning Corporation

Michigan State University

Mizu Systems, Inc.

Bioplastic Polymers and Composites, LLC

Other

Virginia Commonwealth University

University of South Australia

University of New York

Bio-materials Universe Company

Daniel Graiver

Robert E Kalinowski

Arnold W Lomas

Ramani Narayan

Kenneth W Farminer

Binh Thanh Nguyen

Aaron Quoc Khieu

Udo C Pernisz

Arthur James Tselepis

Gary T Decker

Nedeljko V Gvozdic

Mohamed Samy El-Shall

Phuong T Tran

Dwight E Williams

Israel Cabasso

Michael James Owen

Shedric Oneal Glover

Osamu Tanaka

Stephen Ross Clarke

Janis Gunars Matisons

Tam Tran, Legal Representative

Toshiyuki Okada

Samir D Serrano

John Donald Blizzard

Antony P Wright

Vahid Sendijarevic

Alan L Freiberg

James McVie

Thomas F Lim

Yoshito Ikada

Sudhanwa D Dewasthale

Howard Franklin Stewart

Steven E Cray

Kelly James Wall

Eric J Hough

Jani G Matisons

Arthur Provatas

Jenny L Gilles

Edward Thomas Rasmussen, Jr

Gary A Dahlbeck

Madhusudhan Srinivasan

Elodie Hablot

Sho-kyu Gen

Siva Rama Krishna Chalasani

Preparation and use of organopolysiloxanes having carbinol groups that are bonded to the silicon atom through carbamate-containing groups. These hydrophilic polysiloxanes can be made to completely dissolve in water or behave as amphoteric surfactants by controlling the concentration of the carbinol radicals and the molecular weight of the polysiloxane.

Hydrophilic polysiloxane compositions containing carbinol groups

Polyol compositions containing methane linkages derived from amino acids. The polyols are obtained from the reaction of the carbonate with the cadres in the amino acids. Individual amino acids or mixtures of amino acids that are prepared from the hydrolysis of the proteins can be used.

Polyols from biomass and polymeric products produced therefrom

Fuel oxygenates comprised of fatty acid or fatty acid ester derivatives which have been reacted with ozone; a base; and a lower alkanol (1 to 8 carbon atoms) are described. The oxygenates comprise ester groups at a point of cleavage by the ozone which provide oxygen in the oxygenate.

Bio-based oxygenated esters and diesters and method of preparation thereof

A process for the preparation of new polyols and polyesters from a natural oil or other unsaturated fatty acid esters is described. The process involves ozone cleavage of double bonds in the fatty acid chains of the oils along with coupling of a hydroxylated compound such as a mono-alcohol, a diol, or a polyol to the cleaved ends of the molecules resulting from the cleavage with a base. The resulting polyols and polyesters are as intermediates for polymers.

Modified fatty acid esters and method of preparation thereof

A moisture-curable, silane-modified oil is disclosed. The silane-modified oil includes an unsaturated oil having at least one unsaturated aliphatic hydrocarbon chain per molecule of the unsaturated oil, and at least one hydrolysable silyl group grafted to the unsaturated aliphatic hydrocarbon chain. The silane-modified oil has a degree of unsaturation that is substantially similar that of the unsaturated oil. A process for forming the moisture-curable, silane-modified oil according to the disclosure includes reacting the unsaturated oil with an unsaturated hydrolysable silane in the presence of a free radical initiator. Also disclosed is a cured silane-modified oil which includes the reaction product of the silane-modified oil and water. Compositions according to the disclosure have relatively low viscosities (facilitating their application to a substrate) and have relatively high levels of silane grafting (resulting in non-leaching cured compositions with a high gel content).

Moisture curable oil and fat compositions and processes for preparing the same

A method for lubrication by supplying a liquid lubricant to moving metal parts, more than fifty percent by weight of the liquid lubricant being a triglyceride vegetable oil having a saturated fatty acid content of less than nine percent by weight of the triglyceride vegetable oil and a polyunsaturated fatty acid content of more than seventy percent by weight of the triglyceride vegetable oil, the triglyceride vegetable oil having an American Petroleum Institute Thermo-Oxidation Engine Oil Simulation Test rod residue weight of less than thirty five milligrams and a pour point of less than minus twenty degrees Celsius.

Triglyceride based lubricant

A process for the preparation of new polyols from a natural oil is described. The process involves ozone cleavage of double bonds in the fatty acid chains of the oils along with coupling of a di or polyol to the cleaved ends of the molecules resulting from the cleavage with a base. The resulting polyols are as intermediates for polymers.

Triglycerides and method of preparation thereof

Biodiesel additive and method of preparation thereof

Nanoparticles of silicon oxide alloys (i.e., oxides of SiMo, SiPt, and SiAl) are produced by laser vaporization of a silicon target and a target of a metal (i.e., Mo, Pt, or Al), in an oxygen containing atmosphere in a diffusion cloud chamber, where the target metal vapors aggregate into novel three-dimensional porous web structures. The structures have a homogeneous composition with a uniform ratio of silicon to the metal.

Nanoparticles of silicon oxide alloys

Substrates are rendered water repellent by applying to the substrate a hyperbranched polymer containing a silicon atom made by polymerizing a derivatized aminofunctional organosilicon monomer which is the reaction product of an amine functional silane monomer precursor or an amine functional polysiloxane monomer precursor and a derivative of carbonic acid or a cyclic lactone.

Method of rendering substrates water repellent using hyperbranched

What is disclosed herein are new and novel hydrogel soaps and a process for obtaining them which comprises providing surface active agents in a pre-hydrogel mixture, and then forming the hydrogel. The process affords solid soaps which do not change significantly in size during use, have wide varying mechanical properties including high strengths in spite of the very high water content of the soaps, and moreover, unexpectedly provide uniform release of the surfactants and/or detergents slowly over a long period of time.

Hydrogel soap

A process for manufacturing high molecular weight, alternating polysiloxane copolymers, by solid-liquid phase, nonaqueous, interfacial polymerization. The copolymers consist of alternating siloxane repeating units of the (AB).sub.m type, such as diphenylsiloxane units and dimethylsiloxane units, alternately polymerized together to form the copolymer. The solid-liquid phase interfacial polymerization process is fast, proceeds smoothly at room temperature, and is not reversible, i.e., no cyclic siloxane species are generated. The resulting polysiloxanes can be formed into thermoplastic elastomers which are suitable for use as sealants, fillers, and films.

Solid-liquid phase interfacial polymerization

An exchange reaction of hydroxyl and alkoxysilane is used as a polymerization avenue yielding hyperbranched polymers. A monomer containing hydroxy alcohol functionality and alkoxy functionality attached to a silicon atom in the monomer is employed, and a simple exchange reaction with driving off of alcohol by-product leads to the desired hyperbranched polymerization and materials.

Hyperbranched polymers containing silicon atoms

Dialkali metal organosilanolate and dialkali metal organosiloxanolate salts are manufactured from cyclic siloxanes or linear silicone polymers using a heterogeneous interfacial reaction process. A stoichiometric excess of an alkali metal hydroxide such as potassium hydroxide or an alkali metal oxide as a solid or dissolved or dispersed in a compatible solvent, is prepared and used as a first phase. The cyclic siloxane or linear silicone polymer is placed in a second phase either dissolved or dispersed in another solvent which is immiscible with the first phase. The resulting silanolate and siloxanolate salts can be used as monomers for solid-liquid phase and liquid-liquid phase interfacial polymerization or in a polycondensation process for the synthesis of alternating siloxane polymers. They can also be used as ring opening initiators for the base catalyzed polymerization of cyclic siloxanes.

Method of making dialkali metal silanolates and siloxanolates

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Midland, MI, United States of America

Daniel Graiver