Abstract: Modified silicas, having the following physicochemical parameters: a CTABmod of <200 m2/g, a BETMP of 50-500 m2/g, a CTABmod-BETMP of <0 m2/g, a carbon content of >0.5% by weight, a modemod from CPS particle size determination of >50 nm, a d75mod from CPS particle size determination of 20-150 nm, a Rmin from Hg pore size determination, pressurized of <10 nm, and a sulfur content of ?1.50% by weight.

Abstract: A composition containing 2-ethylhexyl silicate, is produced by heating a reaction mixture of ethyl silicate with an excess amount of 2-ethylhexanol in the presence of titanium tetrabutoxide as catalyst to a temperature below the boiling point of 2-ethylhexanol while mixing, allowing the reaction mixture to react and, after the reaction, removing ethanol and excess 2-ethylhexanol from the reaction mixture by distillation and obtaining the composition containing 2-ethylhexyl silicate.

Abstract: A novel compound, which is 3-glycidyloxypropyltri(-2-propylheptoxy)silane. A process for producing a 3-glycidyloxypropyltrialkoxysilane having long-chain alkoxy groups of formula (I) or of formula (II) where m=1 or 2, n=0 or 1, p=3, 4, 5, 6, 7, 8, 9 or 10, where the method includes heating 3-glycidyloxypropyltrimethoxysilane or 3-glycidyloxypropyltriethoxysilane, with a stoichiometric amount or an excess of a longer-chain alcohol from the group of the C5- to C16-alcohols, in the presence of titanium tetrabutoxide as catalyst, with stirring to a temperature of not more than 225° C., reacting, and then following the reaction by removing methanol/ethanol and excess reactant alcohol from the product mixture by distillation, optionally under reduced pressure. A method of using the 3-glycidyloxypropyltri(-2-propylheptoxy)silane for functionalization of rubber and using the rubber in treads for reducing rolling resistance in tires.

Abstract: A composition containing 2-propylheptyl silicate is obtained by heating ethyl silicate with an amount of 2-propylheptanol used in excess in the presence of titanium tetrabutoxide as catalyst to a temperature of not more than 220° C. while mixing, allowing them to react and, after the reaction, removing ethanol and excess 2-propylheptanol from the reaction mixture by distillation and obtaining the product, to obtain the composition comprising 2-propylheptyl silicate.

Abstract: A composition containing 2-ethylhexyl silicate, is produced by heating a reaction mixture of ethyl silicate with an excess amount of 2-ethylhexanol in the presence of titanium tetrabutoxide as catalyst to a temperature below the boiling point of 2-ethylhexanol while mixing, allowing the reaction mixture to react and, after the reaction, removing ethanol and excess 2-ethylhexanol from the reaction mixture by distillation and obtaining the composition containing 2-ethylhexyl silicate.

Abstract: A composition containing organosilicon compounds having the formula I and/or II wherein R is ethyl, R1 is a mixture such that the proportion of one component of the mixture is 10 to 50 mol % and is the same or different C9-C30 branched or unbranched monovalent alkyl, and R2 is a branched or unbranched, saturated or unsaturated, aliphatic, aromatic or mixed aliphatic/aromatic divalent C1-C30 hydrocarbon is produced by reacting silanes having the formula III with mixtures of alcohols having the general formula R1—OH, with elimination of R—OH, and R—OH is continuously separated off from the reaction mixture by distillation. The organosilicon compounds can be used in rubber compounds.

Abstract: Organosilicon compounds of the general formula I and/or II are produced by reacting silanes of the general formula III with alcohols of the general formula R?—OH, with elimination of R—OH, wherein R—OH may be continuously separated from the reaction mixture by distillation. The organosilicon compounds may be used in rubber mixtures. Compounds, such as rubbers, produced using such organosilicon compounds.

Abstract: Organosilicon compounds having the formula I and/or II wherein R1 is a mixture and the proportion of one component of the mixture is 10 to 50 mol %, are produced by reacting silanes having the formula III with mixtures of alcohols having the general formula R1—OH, with elimination of R—OH, and R—OH is continuously separated off from the reaction mixture by distillation. The organosilicon compounds can be used in rubber compounds.

Abstract: Siloxane oligomers of the general formula I or II wherein at least one functionalized alkyl group is present per oligomer molecule. The siloxane oligomers are produced by oligomerization of halogenalkyltrihalogensilanes, and co-optionally co-oligomerized with (C1-C18)-alkyl-, phenyl-, aryl- or aralkyl-trihalogensilanes and/or silicon tetrachloride, in the presence of alcohol and water, following which the halogenalkyl function is optionally modified in a further step. The siloxane oligomers can be used as coupling agents in rubber mixtures or as building preservation agents.

Abstract: Organosilicon compounds of the general formula I and/or II are produced by reacting silanes of the general formula III with alcohols of the general formula R?—OH, with elimination of R—OH, wherein R—OH may be continuously separated from the reaction mixture by distillation. The organosilicon compounds may be used in rubber mixtures. Compounds, such as rubbers, produced using such organosilicon compounds.

Abstract: Organosilicon compounds of the general formula I and/or II are produced by reacting silanes of the general formula III with alcohols of the general formula R?—OH, with elimination of R—OH, wherein R—OH may be continuously separated from the reaction mixture by distillation. The organosilicon compounds may be used in rubber mixtures. Compounds, such as rubbers, produced using such organosilicon compounds.

Abstract: Siloxane oligomers of the general formula I or II 1

Abstract: Sulfur-functional polyorganosiloxanes corresponding to the general formula I with substituents as described in the specification, corresponding to the general formula I They can be used in rubber mixtures.

Abstract: Oligomeric organosilanes useful in rubber mixtures are built up from the two structural units A and B, according to formula I The oligomeric organosilanes are produced by mixing and then co-oligomerizing the monomeric compounds of the structure types I and II

Abstract: Abstract Organosilicon compounds having the formula I and/or II 1

Abstract: Blocked mercaptosilanes, having the following general formula I

Abstract: Organosilicon compounds of the general formula I and/or II 1

Abstract: Oligomeric organosilanes useful in rubber mixtures are built up from the two structural units A and B, according to formula I 1

Abstract: Sulfur-functional polyorganosiloxanes corresponding to the general formula I with substituents as described in the specification, corresponding to the general formula I 1

Abstract: Process for the production of yellow bis(3-[trialkoxy-silyl]alkyl)polysulfanes with an iodine color index of ≦10 mg iodine/100 ml, in which an organic acid is added to neutral chloroalkyltrialkoxysilane and then reacted with sodium polysulfide (NPS) or sodium sulfide (Na2S) and sulfur or sodium polysulfide (NPS) and Na2S in alcohol.