Dow Corning Corporation

University of Florida Research Foundation, Incorporated

Gary T Burns

Gregg A Zank

James Richard Hahn

Clifford Carlton Reese

Aroop K Roy

Qin Deng

Chandan K Saha

Ronald H Baney

William H Atwell

Debora F Bergstrom

Patricia A Giwa-Agbomeirele

Chi-long Lee

Kenneth Boone Wagener

Russell Keith King

Arthur James Tselepis

Gary T Decker

Linda Denise Kennan

Carl J Bilgrien

Paul P Lu

Lawrence D Fiedler

Michael Robert Reiter

Ronald S Reaoch

Jeffrey Allen Ewald

Leslie D Fontaine

Krystyna Regina Brzezinska

Ronald J Keller

The present invention is neutral-aged hydrophobic organosilicate-modified silica gels and a method for their preparation. The method comprises three steps, where in the first step an organosilicate-modified silica hydrosol is contacted with a strong mineral acid at a pH less than about 1 to form an organosilicate-modified silica hydrogel. In the second step the organosilicate-modified silica hydrogel is aged at a pH within a range of about pH 3.5 to pH 8. In the third step the neutral-aged organosilicate-modified silica hydrogel is contacted with an organosilicon compound in the presence of a catalytic amount of a strong acid to effect hydrophobing of the organosilicate-modified silica hydrogel to form a hydrophobic organosilicate-modified silica hydrogel having a surface area within a range of about 100 m.sup.2 /g to 750 m.sup.2 /g in the dry state. In a preferred process the hydrophobic organosilicate-modified silica hydrogel is contacted with a sufficient quantity of a water-immiscible organic solvent to convert the hydrophobic organosilicate-modified silica hydrogel into a hydrophobic organosilicate-modified silica organogel.

Neutral-aged hydrophobic organosilicate-modified silica gels

A method for preparing an .alpha.,.omega.-silyl terminated branched polyalkenylenes and polyolefins is provided. The method involves:

Synthesis of functional silyl terminated branched polyalkenylenes and

The present invention is hydrophobic organosilicate-modified silica gels and a method for their preparation under neutral conditions. The method comprises two steps, where in the first step the pH of an organosilicate-modified silica hydrosol is adjusted with a base to within a range of about pH 3 to pH 7 to facilitate formation of an organosilicate-modified silica hydrogel. In the second step the organosilicate-modified silica hydrogel is contacted with an organosilicon compound in the presence of a catalytic amount of a strong acid to effect hydrophobing of the organosilicate-modified silica hydrogel to form a hydrophobic organosilicate-modified silica gel having a surface area within a range of about 100 m.sup.2 /g to 850 m.sup.2 /g in the dry state. In a preferred process the hydrophobic organosilicate-modified silica hydrogel is contacted with a sufficient quantity of a water-immiscible organic solvent to convert the hydrophobic organosilicate-modified silica hydrogel into a hydrophobic organosilicate-modified silica organogel. A water soluble compound of cerium or iron may be added in the second step to improve the heat stability of the hydrophobic organosilicate-modified silica gel.

Method for making hydrophobic organosilicate-modified silica gels under

A method for the preparation of hydrophobic silica gels which are useful as reinforcing fillers in rubber compositions. The method comprises two steps, where in the first step a silica hydrosol is contacted with a sufficient concentration of a strong mineral acid at a pH less than about pH 1 to form a silica hydrogel. In the second step the silica hydrogel is contacted with described organosilicon compounds in the presence of a catalytic amount of a strong acid to effect hydrophobing of the silica hydrogel thereby forming a hydrophobic silica gel having a surface area within a range of about 100 m.sup.2 /g to 750 m.sup.2 /g as measured in the dry state. In a preferred method the hydrophobic silica hydrogel is contacted with a sufficient quantity of a water-immiscible organic solvent to convert the hydrophobic silica hydrogel into a hydrophobic silica organogel.

Method for preparing hydrophobic silica gels

The present invention is hydrophobic organosilicate-modified silica gels and a method for their preparation. The method comprises two steps, where in the first step an organosilicate-modified silica hydrosol is heat treated in the presence of a strong mineral acid at a pH less than about pH 1 to form an organosilicate-modified silica hydrogel. In the second step the organosilicate-modified silica hydrogel is contacted with an organosilicon compound in the presence of a catalytic amount of a strong acid to effect hydrophobing of the organosilicate-modified silica hydrogel thereby forming a hydrophobic organosilicate-modified silica hydrogel having a surface area within a range of about 100 m.sup.2 /g to 750 m.sup.2 /g as measured in the dry state. In a preferred method the hydrophobic organosilicate-modified silica gel is contacted with a sufficient quantity of a water-immiscible organic solvent to convert the hydrophobic organosilicate-modified silica hydrogel into a hydrophobic organosilicate-modified silica organogel.

Hydrophobic organosilicate-modified silica gels

The present invention is hydrophobic silica gels and a method for their preparation under neutral conditions. The method comprises two steps, where in the first step the pH of a silica hydrosol is adjusted with a base to within a range of about pH 3 to pH 7 to facilitate formation of a silica hydrogel. In the second step the silica hydrogel is contacted with an organosilicon compound in the presence of a catalytic amount of a strong acid to effect hydrophobing of the silica hydrogel. In a preferred method, in a third step the hydrophobic silica gel is contacted with a sufficient quantity of a water-immiscible organic solvent to convert the hydrophobic silica hydrogel into a hydrophobic silica organogel.

Method for making hydrophobic silica gels under neutral conditions

An optically clear platinum-group metal curable liquid silicone rubber composition having good physical properties. The composition comprises a vinyldimethylsiloxy-terminated polydimethyl(diphenyl)siloxane copolymer comprising about 1 to 20 mole percent diphenylsiloxy units and having a viscosity within a range of about 20,000 mPa.multidot.s to 100,000 mPa.multidot.s at 25.degree. C., vinyldimethylsiloxy-terminated polydimethyl(diphenyl)siloxane copolymer comprising about 1 to 20 mole percent diphenylsiloxy units and having a viscosity within a range of about 50 mPa.multidot.s to 10,000 mPa.multidot.s at 25.degree. C. and optionally comprising up to about 3 mole percent vinyldimethylsiloxy units, a treated reinforcing silica filler, and curing agents.

Optically clear liquid silicone rubber

A method of hydrophobing fillers such as inorganic pigments, metal oxides, metal hydroxides, and silicate minerals, involves contacting a filler with an oxa-silacycloalkane, until hydroxyl functionality on the filler is replaced with carbinol functionality (i.e. .tbd.C--OH). The preferred oxa-silacycloalkane is 2,2,4-trimethyl-1-oxa-2-silacyclopentane.

Treatment of fillers with oxa-silacycloalkanes

This invention relates to the preparation of a highly densified boron carbide ceramic body by the pyrolysis of a mixture comprising boron carbide powder and a preceramic organosilicon polymer selected from the group consisting of polysiloxanes, polysilazanes, polysilanes, metallopolysiloxanes and metallopolysilanes. Such highly densified ceramic bodies can be prepared by sintering under pressure or by utilizing a pressureless process.

Preparation of high density boron carbide ceramics with preceramic

A method for preparing in situ reinforced silicone elastomers and the compositions prepared by the method. The method comprises forming a mixture comprising an end-functional diorganopolysiloxane; a stoichiometric excess of a hydrolyzable siloxane having hydrolyzable functionality described by formula--R.sup.2 SiQ.sub.3-b R.sub.b, were each R is independently selected from a group consisting of alkyls comprising one to six carbon atoms, alkenyls comprising two to six carbon atoms, and aryls, R.sup.2 is a divalent hydrocarbon radical comprising one to 12 carbon atoms, each Q is independently selected from a group consisting of hydroxy, acyloxys comprising one to six carbon atoms, alkoxys comprising one to six carbon atoms, and substituted alkoxys comprising one to six carbon atoms, and b=0 to 2; and a tin salt catalyst and contacting the mixture with water to effect curing. The resulting silicone elastomers are in situ reinforced to provide high strength.

In-situ reinforced silicone elastomer using resin precursor

A method for preparing in situ reinforced silicone elastomers and the compositions prepared by the method. The method comprises forming a mixture comprising a diorganosiloxane polymer having reactive end-terminal functionality, a stoichiometric excess of a reactive siloxane selected from a group consisting of triorganosilyl endblocked reactive siloxanes and reactive cyclosiloxanes, and a tin salt catalyst and contacting the mixture with water to effect curing. The resulting silicone elastomers are in situ reinforced to provide high strength.

Method of preparing in situ reinforced silicone elastomer

The present invention is a method for the preparation of carbinol-functional organosiloxanes and carbinol-functional organosiloxane resins. The method comprises contacting a cyclic silyl ether with an organosiloxane or an organosiloxane resin at a temperature within a range of about 25.degree. C. to 150.degree. C. The method may be conducted in the presence of an inert organic solvent to facilitate dissolution and contact of the reactants.

Method for preparation of carbinol-functional siloxanes

This invention provides polyorganooxothiazenes exhibiting levels of molecular weight and properties not heretofore achieved by similar polymers reported in the prior art. The sulfonimidates that are condensed to form the polymers are prepared using a novel reaction between an N-triorganosilylsulfonamide and a triorganodihalophosphorane to form the corresponding N-triorganosilylsulfonimidoyl halide that is subsequently reacted with a fluorinated alcohol or phenol to form the N-triorgano-silylsulfonimidate.

Polyorganooxothiazenes and method for preparing same

This invention relates to the preparation of highly densified ceramic bodies by the pyrolysis of a mixture comprising a preceramic borosiloxane, silicon carbide powder, a curing agent for the borosiloxane, a crosslinking agent for the borosiloxane and, optionally, additional components to facilitate sintering. Such highly densified ceramic bodies can be prepared by sintering under pressure or by a pressureless sintering process.

High density silicon carbide sintered bodies from borosiloxanes

A method is disclosed for the preparation of ceramic materials or articles by the pyrolysis of preceramic polysilanes wherein the preceramic polysilanes are rendered infusible prior to pyrolysis by exposure to ultraviolet irradiation in the presence of a reactive gas selected from the group consisting of ethylene, 1,3-butadiene, 2-methyl-1,3-butadiene, 1,4-pentadiene, silane, chlorosilane, dichlorosilane, boron trichloride, oxygen and water mixture, acetylene, and tetravinylsilane. This method is especially suited for the preparation of ceramic fibers. The ceramic fiber's surface properties can be modified by the practice of this invention; for example, a ceramic fiber with a carbon rich surface layer can be obtained when 1,3-butadiene is used as the reactive gas.

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Midland, MI, United States of America

Gary T Burns