Abstract: The present invention teaches a new process to produce novel, hard, optically clear, impact-resistant polyurethane polymers that are characterized by excellent thermo mechanical properties and chemical resistance, and the polymers made as a result of such a process. The polyurethanes are made by reacting a) a prepolymer made by reacting a polyisocyanate with a primary amine-terminated polyether with an amine functionality of about 2 and a molecular weight of >1000, and in which the free —NCO content of the resulting prepolymer is >18% by weight; with b) (i) a polyol having an average hydroxyl functionality greater than or equal to 2 and an average hydroxyl equivalent weight of from about 300 to about 1,000, and (ii) a curing agent that has isocyanate reactive groups, a functionality of 2 to 3 and a molecular weight of <400.

Abstract: This invention discloses hydrophilic additives in polysiloxane gels, elastomers and coatings, and novel processes for producing them. The process comprises:(a) redistributing into polysiloxane-polyether copolymers an unsaturated silane or siloxane,(b) adding to the mixture of reagents a catalytically effective amount of a basic catalyst; and(c) heating the reaction mixture to effect reaction.Novel siloxane structures of unsaturated aliphatic modified polyerther siloxane copolymers are also taught.

Abstract: Dissolved silanes, silicones and silicates from solvents used in the slurry phase Direct Synthesis of alkoxysilanes are removed by adding a carboxylic acid such as formic acid to generate filterable precipitates and reusable solvent. The solvents are thereby remediated and made suitable for reuse in Direct Synthesis processes. Foaming is reduced with the remediated solvent and silicon conversion rates are higher. The precipitates are easily filtered and retain negligible quantities of solvent.

Abstract: Polyester polyols which contain at least one dihydrazide linkage --C(.dbd.O)--NHNH--C(.dbd.O)-- reduce the incidence of scorching when used as a reactant in the manufacture of polyurethane foam. Also disclosed are compounds of structures (2) and (3):D--HN(--NH--C(.dbd.O)--R--C(.dbd.O)NH).sub.0-1 --NH--D (2)(A--C(.dbd.T)--NH)--.sub.

Abstract: Emulsions comprising a water insoluble or semi-soluble silane or mixtures of such silanes have been found useful when used alone or formulated into aqueous primer systems to improve the adhesion of sealants, adhesives or coatings to a variety of substrates. These aqueous primers are suitable for both inorganic and organic substrates having either porous or non-porous surfaces. In many cases they have been found to outperform solvent based primers. Primers of this type can be used with a variety of waterborne or solvent based sealants, adhesives or coatings including acrylic or polyurethane latexes, high solid polyurethanes, epoxies and silicones. When used with waterborne systems, it is not necessary to wait for the primer to dry before application of the sealant, adhesive or coating.

Abstract: A process for hydrosilation reactions between olefins and hydrosilanes or hydrosiloxanes wherein a portion of the reactor output is recycled continuously to the reactor.

Abstract: The instant invention provides a method for improving the miscibility of the lower molecular weight unsaturated siloxane-polyether copolymers with the .alpha., .omega.-divinylpolysiloxanes without loss of storage stability, or delay of cure at the vulcanization temperature, or loss of permanent hydrophilicity or other desirable features of the cured polysiloxane. The compositions of the present invention comprise one or more .alpha., .omega.-divinylpolysiloxanes, unsaturated polysiloxane-polyether copolymers having from 2 to 5 silicon atoms per molecule which are preferably trisiloxanes, and a compatibilizing additive. The permanently hydrophilic, rapidly wettable polysiloxane compositions yield static water contact angles <50.degree. dynamic advancing contact angles of less than about 100.

Abstract: Disclosed is a process for making isocyanatoorganosilane by adding a carbamatoorganosilane of the general formula to an inert liquid medium and holding the mixture thus formed at a temperature and pressure effective to convert said carbamatoorganosilane to isocyanatoorganosilane.

Abstract: The present invention discloses blends of silanes and specific silicas, characterized in that when the blend is compounded into a rubber formulation even after 4 months of storage following formation of the blend, an unexpectedly high proportion of the silane present is available as a coupling and reinforcing agent for the rubber formulation. Over 80% and even over 90% of the silica can be extracted or described from the blend even 4 months after formation of the blend, and rubber formulation properties indicate high availability of the silane for coupling and reinforcement.

Abstract: Sealant compositions comprising a latex polymer and an epoxysilane of the formula ##STR1## in which R.sup.1 is a difunctional alkyl bridge with 2 to 6 carbon atoms,each R.sup.2 group is the same or different and each is a C.sub.1 to C.sub.12 alkyl or aryl group, or a C.sub.1 to C.sub.6 alkoxy groupeach R.sup.3 group is the same or different and each is a C.sub.2 to C.sub.6 alkyl group,n is 2 or 1,R.sup.4, R.sup.5, and R.sup.6 are each hydrogen or a C.sub.1 to C.sub.6 alkyl group,R.sup.7 is an alkyl group having from one to four carbon atoms, or aralkyl, or an aryl group having six to ten carbon atoms, andc has a value of zero or one;wherein the epoxysilane is added to the polymer neat or as a non-aqueous solution.

Abstract: The present invention relates to diesel fuel and lubrication oil defoaming agents, and crude oil demulsifiers, as well as methods for using same. In particular, the defoaming agents and demulsifiers are comprised of copolymers which have structures constituting a backbone of polysiloxane onto which is grafted an organic group. These structures comprise a polymer of the formula MD.sub.x D'.sub.y D".sub.z M, where M is O.sub.0.5 Si(CH.sub.3).sub.3, D is a OSi(CH.sub.3).sub.2, D' is OSi(CH.sub.3)R, D" is OSi(CH.sub.3)R', R is a polyhydric C.sub.6 -C.sub.28 organic group, R' is a phenol derivative or a long chain aliphatic group or polyethers, z is between 0 and 80, x+y+z is between 10-200, x/z is .gtoreq.1, and x/(y+z) is between about 1 and about 5, or formula M'D.sub.a M' where M' is O.sub.0.5 Si(CH.sub.3).sub.2 R, a is between 4-10, and R and D are the same as defined above.

Abstract: Certain members of the class of N-silylalkyl-aspartic acid esters, when used to endcap polyurethane polymers, offer moisture curable, one-part sealant formulations having significantly improved physical property improvements over other members of the same class of organofunctional silanes. More specifically, polyurethane polymers terminated with either the dibutyl or diethyl maleate/primary aminoalkyl silane addition product offer sealants which substantially outperform comparative sealants obtained using polymers endcapped with other olefinic carboxylate ester (dimethyl maleate, dimethyl crotonate) or nitrile (acrylonitrile)/primary aminoalkyl silane addition products. Additionally, sealant formulations incorporating the dibutyl or diethyl maleate/primary aminoalkyl silane terminated polymers demonstrate unexpected improvements in both elongation and tensile strength performance. The dibutyl maleate and dimethyl maleate based polymers give significant increase in tear resistance.

Abstract: Disclosed are aqueous polyurethane dispersions prepared from polyester polyols having 0.95 to 1.5 equivalents of carboxylic functionality thereon per equivalent of polyol, the dispersions also containing a nonionic surfactant component wherein the ratio by weight of said carboxylic functionality to said nonionic surfactant component is 1:2.5 to 1:0.5. The dispersions are particularly adapted to the formation of thin wall articles exhibiting greatly improved properties.

Abstract: It has been discovered that organoamine modified siloxane alkoxylates overcome the antagonism associated with nonionic trisiloxane alkoxylates on pesticide uptake in plants. The organoamine modified siloxane alkoxylates of the present invention have the average general formula: AMe.sub.2 SiO[(Me).sub.2 SiO].sub.x [MeSi(Z)O].sub.y SiMe.sub.2 A, wherein x=0 to 1, y=0 to 2, with the proviso than when y=0, A is Z, A=is Z or Me, Z=RO(R.sup.1).sub.n R.sup.2 N(R.sup.3).sub.2, R is a divalent organic group having from 2 to 4 carbon atoms, R.sup.1 is an alkyleneoxide group containing 2 to 4 carbon atoms, R.sup.2 is a divalent organic group containing 2 to 6 carbons, R.sup.3 may be hydrogen, an alkyl radical with 1 to 4 carbons, an amino alkyl of one to four carbons, or an alkyl of 2 to 4 carbon atoms which may have hydroxy substitutions thereon. Each R.sup.3 may be the same or different.When R.sup.1 is oxyethylene, n is from 1 to 10, preferably 2 to 5. When R.sup.

Abstract: Silylated polyurethanes exhibiting a superior combination of mechanical properties and which cure in reasonable time to a low-tack sealant, without excessive viscosity, are prepared by reacting a polyol component having terminal unsaturation of less than 0.2 meq/g with a diisocyanate component to form a hydroxyl-terminated prepolymer, and endcapping the prepolymer with an isocyanate silane of the formula OCN--R--Si--(X).sub.m (--OR.sup.1).sub.3-m wherein m is 0, 1 or 2, each R.sup.1 is alkyl containing 1 to 4 carbon atoms, each X is alkyl containing 1 to 4 carbon atoms, and R is a difunctional organic group.

Abstract: Disclosed are antifoam emulsions useful in control of foam in aqueous foaming systems which comprise:(A) polydiorganosiloxane;(B) fine solid particles of inorganic oxide, bearing on the surface thereof a polydiorganosiloxane component; wherein the total amount of polydiorganosiloxane present in components (A) and (B) comprises 5 wt % to 60 wt % of the emulsion and the weight ratio of the total amount of polydiorganosiloxane present in components (A) and (B) to the amount of said inorganic oxide is 10:1 to 200:1;(C) an organic surfactant dispersing agent selected from the group consisting of non-ionic tetrafunctional block copolymers terminating in primary or secondary hydroxyl groups and mixtures thereof, which agent comprises 0.

Abstract: This Invention discloses the use of ascorbic and citric acid, their salts, ethers, acid esters and mixtures thereof in a method for the prevention of peroxide formation, and/or for decomposing peroxides already formed in polyethers. Hereby, the polyethers are made reactive to hydrosilylation by silanes and hydrosiloxanes. When the polyether treatment is done with mixtures of ascorbic acid and sodium ascorbate and allyl polyethers, the hydrosilylation product contains reduced levels of propanal. The copolymers prepared using the treated polyethers are efficient stabilizers of flexible polyurethane foams and rigid polyurethane and polyisocyanurate foams.

Abstract: Disclosed are aqueous dispersions of polyurethane polymers from which films can be formed which have enhanced hydrophilicity. The enhanced hydrophilicity is provided by hydrophilic moieties chemically incorporated in the polymer network.

Abstract: Disclosed is a continuous process for producing silicone copolymers using a series of at least one stirred-tank reactor, the last of which reactors in said series has crude product stream feeding into at least one plug flow reactor, wherein this crude product stream is sufficiently homogeneous that this stream which undergoes further reaction in the plug flow reactor does not undergo phase separation.

Abstract: The present invention discloses non-hydrolyzable, block, (AB).sub.n A type, copolymers comprising alternating units of polysiloxane and amino-polyalkyleneoxide and provides a method for the preparation of these copolymers. Also provided is the use of these copolymers as softeners, in particular durable, hydrophilic textile softeners, which improve tactile properties of the textiles substrates treated with the commercial soil release finishes, without substantially detracting from their properties. The copolymers of the present invention have alternating units of polysiloxane [X(C.sub.a H.sub.2a O).sub.b R.sup.2 [(SiO(R.sup.1).sub.2 ].sub.c Si(R.sup.1).sub.2 R.sup.2 (C.sub.a H.sub.2a O).sub.b X] and polyalkyleneoxides [YO(C.sub.a H.sub.2a O).sub.d Y] wherein R.sup.1 is a C.sub.1 to C.sub.4 alkyl, preferably methyl, R.sup.