Abstract: A process for producing one or more alkoxysiloxanes by thermal reaction of at least one siloxane parent structure with at least one alkali metal alkoxide and at least one alcohol, where the process includes mixing, while heating, the at least one siloxane parent structure with the at least includes one alcohol and the at least one alkali metal alkoxide to form a reaction mixture, neutralizing the reaction mixture by addition of at least one Brønsted acid and optionally with addition of at least one solvent, and subsequently isolating the one or more alkoxysiloxanes by thermal separation of volatile compounds. Potentially occurring water is not removed from the reaction mixture and the reaction mixture does not include solvents which form an azeotrope with water and/or further dehydrating agents.

Abstract: A process for producing alkoxysiloxanes by thermal reaction of at least one waste silicone with at least one alkali metal alkoxide and at least one alcohol. The process includes a first step of reacting the at least one waste silicone by mixing with at least one alcohol and at least one alkali metal alkoxide with heating, but without removing any potentially occurring water from the reaction mixture, and a second step of neutralizing the reaction mixture resulting from this reaction using at least one Brønsted acid and separating the solid constituents, and subsequently isolating the alkoxysiloxane by thermal separation of volatile compounds.

Abstract: Spherical amorphous, non-porous silicas are useful for oral compositions. A method of making the spherical amorphous, non-porous silicas is also provided.

Abstract: Processes may produce alkoxysiloxane(s) by reaction of siloxane parent structure(s) with alkali metal alkoxide(s). Such processes may include reacting siloxane parent structure(s) by mixing with alkali metal alkoxide(s) with heating and optionally adding silicon dioxide, but without adding alcohol and without removal of any potentially occurring water from the reaction mixture; and neutralizing the resulting reaction mixture by adding Brønsted acid(s), optionally solvent(s), and preferably separating solid constituents; and subsequently isolating the alkoxysiloxane(s) by thermally separating volatile compounds. The siloxane parent structure(s) may be a hexamethylcyclotrisiloxane (D3), octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5), dodecamethylcyclohexasiloxane (D6), mixture of cyclic branched D/T type siloxanes, silicone oils preferably including at least 100 D units, polydimethylsiloxanediol(s), and/or ?,?-divinylsiloxane(s).

Abstract: The present invention relates to a process for the preparation of methionine comprising the step of contacting a solution or suspension comprising 2-amino-4-(methylthio)butanenitrile and/or 2-amino-4-(methylthio)butaneamide with water in the presence of a catalyst to give a methionine comprising mixture, wherein the catalyst comprises CeO2 comprising particles, wherein the CeO2 comprising particles have a BET surface area of from 175 to 300+/?10% m2/g measured according to DIN ISO 9277-5 (2003), a mean maximum Feret diameter xFmax, mean of from 3+/?10% to 40+/?10% nm and a mean minimum Feret diameter xFmin, mean of from 2+/?10% to 30+/?10% nm, both measured according to DIN ISO 9276-6 (2012).

Abstract: In a method for producing hydrogen cyanide by passing a feed mixture comprising ammonia and methane through reaction tubes, coated on the inner surface with a catalyst comprising platinum, at a reaction temperature of 1000° C. to 1400° C., operated for a time period of at least 100 h, the concentration difference between the ammonia concentration and the methane concentration in the product gas mixture is maintained in a range of from 1.05 % by volume to 3.0% by volume for at least 80% of the time.

Abstract: A method for the preparation of homo- and copolymers of alkyl (meth)acrylates having a low residual monomer content involves preparing a reaction mixture containing monomers, charging the reaction mixture, heating the reaction mixture, adding an additional monomer after initial monomer conversion, and optional further processing of the reaction mixture. The homo- and copolymers of alkyl (meth)acrylates obtained by this method as useful in lubricant applications.

Abstract: The present invention relates to a new structural class of phenalkamine, phenalkamine curing agent compositions, methods of making such phenalkamine, and methods of making such compositions. The phenalkamine curing agent compositions of the present invention can be prepared by reacting cardanol with an aldehyde compound and a mixture of methylene bridged poly(cycloaliphatic-aromatic)amines. These curing-agent compositions may be used to cure, harden, and/or crosslink an epoxy resin.

Abstract: A process for purifying ethylene cyanohydrin involves incubating an industrial grade ethylene cyanohydrin product with at least one titanium(IV)alkoxide. Ethylene cyanohydrin products with purities of >99% contain less than 0.05% of ethylene glycol (EG), and/or contain a water content of less than 1000 ppm.

Abstract: Nanoparticle compositions contain a graphene-based material. A preparation process involves providing several components and milling a mixture. The nanoparticle compositions can be used as a lubricant additive to improve tribological performance, in particular to improve anti-friction and anti-wear performance on metal parts. A corresponding lubricant composition contains these nanoparticle compositions.

Abstract: Mixture compositions contain A) crosslinked organopolysiloxanes having organopolysiloxane units linked by a building block containing polyether groups, and B) crosslinked organopolysiloxanes having organopolysiloxane units bridged by a bridging siloxane. The mixture compositions are useful, for example, as an emulsifier, for stabilizing formulations, and for dispersion of solid pigments.

Abstract: A process for the recovery of a light boiler and a heavy boiler from a vapor stream, where the process includes: A1) introducing a vapor stream containing a light boiler and a heavy boiler into a column at a point at the bottom of the column, A2) withdrawing a vapor stream, enriched in the light boiler, from the top of the column, A3) withdrawing a liquid stream, enriched in the heavy boiler, from the bottom of the column, and splitting the stream into a partial stream and a partial stream, A4) recycling the stream back into the column at a point above the column, wherein the stream is kept essentially adiabatically during the recycling, A5) withdrawing a stream, enriched in a middle boiler, from the middle section of the column and splitting the stream into a partial stream and a partial stream, A6) cooling the partial stream in the heat exchanger to provide the cooled stream and recycling the stream as stream back into the column at an introduction point below the top of the column, and A7) withdrawing the

Abstract: An in vitro method can be used for screening of the bioactivity of a compound by a synthetic mixed culture resembling a skin microbiome.

Abstract: A method for separating butenes from C4 hydrocarbon streams containing butanes and butenes involves extractive distillation with a suitable solvent. The method also involves heat integration, which makes it possible to use the heat of the solvent in order to heat various streams.

Abstract: The invention relates to a method for preparation of (meth)acrylic acid esters from (meth)acrylic acid anhydrides. The method involves: reacting a (meth)acrylic acid anhydride of Formula (I): wherein R1 is a hydrogen atom or a methyl group; with a substrate in the presence of a first catalyst to form a product mixture comprising the (meth)acrylic acid ester; and wherein: the substrate is selected from the group consisting of: primary alcohols; secondary alcohols; tertiary alcohols; and phenols; and the first catalyst comprises a salt of magnesium or of a rare earth element.

Abstract: A process for the production of functionalized particle foam mouldings based on a thermoplastic base material with a glass transition temperature of at least 100° C. involves functionalization of base particles.

Abstract: The present invention refers to a method for producing hydroxylated fatty acids by oxidizing at least one unsaturated fatty acid by at least one lipoxygenase and thereafter reducing the obtained compound by at least one peroxidase and/or heating. Furthermore, the present invention refers to the compound obtained by said method.

Abstract: A composition contains at least one aldehyde (A), at least one phenolic compound (B), and at least one amine (C) bearing at least two amino groups selected from primary and secondary amino groups. At least one of these compounds bears at least one (meth)acrylate group. A fibre-reinforced composition contains the composition. The compositions can be cured in a process, and fibre composite materials/thermosets are obtainable by the process.

Abstract: An improved process can be used for the acid hydrolysis of polylaurolactam with sulfuric acid. An especially suitable starting material is polylaurolactam which is intended for recycling and which is characterized by a low laurolactam content.

Abstract: A process for making propene oxide involves reacting propene with hydrogen peroxide in the presence of methanol, a titanium zeolite epoxidation catalyst, and nitrogen containing compounds present in an amount of from 100 to 3000 mg/kg of hydrogen peroxide. Non-reacted propene is separated from the reaction mixture; the propene depleted reaction mixture is continuously distilled in a distillation column providing an overhead product stream containing propene oxide and methanol and a bottoms product stream; and propene oxide is separated from the overhead product stream. An acid is added to the propane depleted reaction mixture and/or to the distillation column at the same level or above the feed point for the propene depleted reaction mixture and/or contacted to the feed to the distillation column to provide an apparent pH in the bottoms product stream of from 3 to 4.5, which reduces the nitrogen content of the separated propene oxide.