Abstract: The present invention relates to a novel liquid or crystalline methionine composition, obtained by means of biomass bioconversion by means of microorganisms that are suitable for producing methionine.

Abstract: The reaction tube for preparing hydrogen cyanide comprises a cylindrical tube composed of ceramic, a catalyst comprising platinum applied to the inner wall of the tube and also at least one insert composed of ceramic, having three or four fins pointing from the tube axis to the inner wall of the tube, which is inserted into the cylindrical tube, wherein the fins divide the tube interior space into substantially straight channels with substantially identical circle segment cross sections and wherein the mean gap between the ends of the fins and the inner wall of the tube is in the range of 0.1 to 3 mm. In the method for preparing hydrogen cyanide, ammonia and at least one aliphatic hydrocarbon having 1 to 4 carbon atoms are reacted in the reaction tube at 1000 to 1400° C.

Abstract: The present invention relates to oral care compositions comprising at least one biosurfactant and fluoride.

Abstract: The invention relates to hotmelt adhesives based on polyesters, having low VOC and fogging values. In particular, the invention relates to reactive hotmelt adhesives including polyesters containing at least 50 mole percent, based on the polycarboxylic acid components, of terephthalic acid or a derivative thereof and containing at least 40 mole percent, based on the polyol components, of diols of the formula HO—(CH2)x—OH with x?6.

Abstract: The invention relates to a process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D), A) alkoxysilano(cyclo)alkylamine is reacted with dialkyl carbonate in the presence of a basic catalyst to give alkoxysilano(cyclo)alkylurethane, B) simultaneously or successively, the catalyst is removed and/or deactivated, and low boilers, solids, salt burdens and/or high boilers are removed, C) alkoxysilano(cyclo)alkylurethane obtained after B) is thermally cleaved to release isocyanate containing alkoxysilane groups and by-product, leaving bottoms material, and D) isocyanate containing alkoxysilane groups and by-product are separated from one another and from bottoms material and collected, wherein the basic catalyst is a guanidine base.

Abstract: The invention relates to a process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D), A) alkoxysilano(cyclo)alkylamine is reacted with dialkyl carbonate in the presence of a basic catalyst to give alkoxysilano(cyclo)alkylurethane, B) simultaneously or successively, the catalyst is deactivated, and low boilers, solids, salt burdens and/or high boilers are removed, C) alkoxysilano(cyclo)alkylurethane obtained after B) is thermally cleaved to release isocyanate containing alkoxysilane groups and by-product, leaving bottoms material, and D) isocyanate containing alkoxysilane groups and by-product are separated from one another and from bottoms material and collected, pa wherein the process regime at least of steps C) to D) is continuous.

Abstract: The invention provides a process for preparing sphingolipids, compositions comprising sphingolipids and further components, and for the use of the compositions.

Abstract: The invention relates to a process for producing a porous polyurethane coatings, using a polyol ester as additives in an aqueous polymer dispersion, the process comprising the steps of a) providing a mixture comprising an aqueous polymer dispersion, a polyol ester, and an additive, b) foaming the mixture to give a homogeneous, fine-cell foam, c) adding at least one thickener to establish the desired viscosity of the wet foam, d) applying a coating of the foamed polymer dispersion to a suitable carrier, e) drying the coating. The invention further relates to a phosphorylated polyol ester.

Abstract: The invention relates to a process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D), A) haloalkylalkoxysilane is reacted with metal cyanate and alcohol to give alkoxysilanoalkylurethane, B) alkoxysilanoalkylurethane is freed of low boilers, solids, salt burdens and/or high boilers and optionally purified, C) alkoxysilanoalkylurethane obtained after B) is thermally cleaved to release isocyanate containing alkoxysilane groups and by-product, leaving bottoms material, and D) isocyanate containing alkoxysilane groups and by-product are separated from one another and from cleavage bottoms material and collected, wherein the process regime at least of steps C) to D) is continuous.

Abstract: The present invention relates to a process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D), A) alkoxysilanoalkylamine is reacted with urea in the presence of an alcohol, optionally in the presence of at least one catalyst, to give alkoxysilanoalkylurethane, B) simultaneously or successively, if used, the catalyst is removed and/or deactivated, and low boilers, medium boilers and/or high boilers are removed, C) purified alkoxysilanoalkylurethane is thermally cleaved to release isocyanate containing alkoxysilane groups and by-product, leaving bottoms material, and D) isocyanate containing alkoxysilane groups and by-product are separated from one another and from bottoms material and collected, in which, in step C), i) the bottoms material is wholly or partly discharged from the cleavage apparatus, ii) subjected to thermal treatment and/or purification and/or an aftertreatment in the presence of alcohol and iii) the material removed, after thermal treatment

Abstract: In a process for the epoxidation of propene, comprising the steps of reacting propene with hydrogen peroxide, separating propene oxide and a recovered propene stream from the reaction mixture, separating propane from all or a part of the recovered propene stream in a C3 splitter column, and passing the overhead product stream of the C3 splitter column to the epoxidation step, a propane starting material with a propane fraction of from 0.002 to 0.10 is used, the epoxidation is operated to provide a propane fraction in the reaction mixture of from 0.05 to 0.20 and the C3 splitter column is operated to provide an overhead product stream which comprises a propane fraction of at least 0.04 in order to reduce the size and the energy consumption of the C3 splitter column.

Abstract: The present invention relates to a method for heat-treating water-absorbing polymeric particles at a temperature equal to or above 150° C. in a fluidized bed dryer at a fast heat-up rate, the use of a fluidized bed dryer for heat-treating water-absorbing polymeric particles in continuous or batch mode as well as to the heat-treated polymeric particles obtained by the method of the present invention.

Abstract: In a process for the epoxidation of an olefin by continuously reacting the olefin with hydrogen peroxide in a methanol solvent on a fixed bed epoxidation catalyst comprising a titanium zeolite, the hydrogen peroxide is used as an aqueous hydrogen peroxide solution made by an anthraquinone process, the aqueous hydrogen peroxide solution is mixed with methanol to give a feed mixture and this feed mixture is filtered before being contacted with the fixed bed epoxidation catalyst.

Abstract: The invention relates to a process for producing a prepreg based on polyurethane, which is notable for high storage stability at room temperature, a two-stage reaction mechanism, and adjustable adhesion on metal surfaces. It is based on the problem of making the surface tack of the prepregs controllable during processing. The solution is to assemble the PU mixture from which the matrix originates at a later stage such that the glass transition temperature of the thermoplastic polymer is above 30° C. For this purpose, the invention proposes two basically independent but certainly synergistic measures, namely: i) use of a polyol compound or a mixture of a number of polyol compounds as binder, the OH number or mean OH number of which is above 300 mg KOH/g, ii) choice of the proportion of hardener corresponding to the co-binder in the reactive composition at greater than 2% by weight, based on the total solids content of the reactive composition.

Abstract: Described is the production of water-absorbing polymeric particles by polymerizing a monomer solution or suspension comprising a) at least one ethylenically unsaturated acid-functional monomer which is optionally at least partly present as salt, b) at least one crosslinker and c) at least one initiator, wherein the process further comprises drying the resulting polymer and also optionally grinding the dried polymer and sieving the ground polymer and also optionally surface-postcrosslinking the dried and possibly ground and sieved polymer, and wherein the polymerization is carried out in the presence of aminopolycarboxylic acids and/or salts thereof, in particular in the presence of ethylenediaminedisuccinic acid and/or a salt thereof.

Abstract: A multilayer composite containing the following layers: I. a first layer (layer I) of a molding compound containing at least 40 wt. % of the following components: 1) 60 to 99 parts by wt. of a copolyamide based on hexamethylenediamine, terephthalic acid and an aliphatic dicarboxylic acid having 8 to 19 carbon atoms and 2) 40 to 1 parts by wt. of an olefinic copolymer as impact modifier, wherein the parts by wt. of 1) and 2) sum to 100; and II. a second layer (layer II) of a molding compound containing at least 60 wt. % of thermoplastic polyester, has a high heat distortion temperature, a very good impact resistance, a high elongation at break and good layer adhesion.

Abstract: The invention relates to ahydrolysable binder based on an ABAB type polysiloxane copolymer suitable for the preparation of coating compositions with an improved anti-adhesive and/or dirt-repellent surface.

Abstract: Tertiary amine catalysts having isocyanate reactive groups capable of forming thermally stable covalent bonds able to withstand temperatures from 120° C. and higher and up to 250° C. are disclosed. These catalyst can be used to produce polyurethane foam having the following desirable characteristics: a) very low chemical emissions over a wide range of environmental conditions and isocyanate indexes (e.g., indexes as low as 65 but higher than 60); b) sufficient hydrolytic stability to maintain the catalyst covalently bound to foam without leaching of tertiary amine catalyst when foam is exposed to water or aqueous solutions even at temperatures higher than ambient (temperature range 25° C. to 90° C.

Abstract: An electrochemical method for C—C coupling a phenol and an aniline in a reaction vessel containing a suitable solvent or solvent mixture and a conductive salt to produce biaryls having both hydroxyl and amino functions, wherein the difference in the oxidation potentials ?E of the substrates ranges from 10 mV to 450 mV and the substrate with the highest oxidation potential is in excess, which method dispenses with multi-step syntheses using metallic reagents.

Abstract: The invention relates to a dispersion comprising a dispersion medium (phase I) and a disperse liquid phase II, the dispersion being characterized in that both phases I and II comprise a further dispersed phase III and this dispersed phase III comprises a release-active agent; to a process for preparing the dispersion, and to the use as or for the production of paints, inks, polymer dispersions and release agents.