Abstract: The present invention relates to a process for preparing 3-cyano-3,5,5-trimethylcyclohexanone (isophoronenitrile) by reacting isophorone with hydrogen cyanide in the presence of a base as a catalyst to obtain a crude isophoronenitrile product, and subsequently distilling the crude isophoronenitrile product, with the addition before distillation of at least one specific sulfonic acid or specific carboxylic acid. In addition, the present invention relates to the use of a specific sulfonic acid or of a specific carboxylic acid as a neutralizing agent before distillation of a crude isophoronenitrile product which has been obtained by reacting isophorone with hydrogen cyanide in the presence of a base as a catalyst, in order to avoid precipitates in the neutralization of the base used as a catalyst with an acid.

Abstract: The present invention relates to the use, for stabilizing polymers, in particular polyolefins, with respect to exposure to UV radiation, of fine-particle polymer powders comprising at least one UV absorber. The present invention further relates to stabilizer mixtures for stabilizing polymers with respect to exposure to UV radiation, oxygen and heat, which, inter alia, comprise these polymer powders, and to a process for stabilizing polymers, in particular polyolefins, with respect to exposure to UV radiation, oxygen and heat, which comprises adding, to the polymers, in particular to the polyolefins, an effective amount of these stabilizers.

Abstract: Aqueous formulations are prepared by a process wherein at least one cyclic compound of the formula I is heated in the presence of water and of an acidic catalyst and, during or after the heating, H—X—R3 is at least partially separated off, where, in formula I, X is selected from oxygen, sulfur and N—R6, R3 and R6 are identical or different and are selected from C1-C12-alkyl, C3-C12-cycloalkyl, substituted or unsubstituted, C7-C13-aralkyl, C6-C14-aryl, substituted or unsubstituted, formyl, CO—C1-C12-alkyl, CO—C3-C12-cycloalkyl, substituted or unsubstituted, CO—C7-C13-aralkyl, CO—C6-C14-aryl, where, if X is N—R6, R3 and R6 may be linked to one another with formation of a ring; R1, R2 and R4 are identical or different and are selected from hydrogen, C1-C12-alkyl, C3-C12-cycloalkyl, substituted or unsubstituted, C7-C13-aralkyl, C6-C14-aryl, substituted or unsubstituted, it being possible in each case for two neighboring radicals to be linked to one another with formation of a ring; n is an integer from 1

Abstract: The invention relates to a method for continuously returning an olefin which has not been reacted with hydroperoxide in order to form oxiranes during the epoxidation of olefins. Said olefin is contained in the flow of waste gas which is produced during epoxidation. Said method is characterised by the following steps: (i) compressing and cooling the flow of waste gas, (ii) separating the olefin from the flow of waste gas obtained in step (i) by distillation,(iii) epoxidating the olefin separated in (ii) with hydroperoxide.

Abstract: Aqueous polymer dispersions comprising a) 50-70% by weight of polymer particles composed of at least two different (co)polymers having glass transition temperatures each above 50° C. and synthesized from at least 80% by weight of at least one principal monomer, 0.1-10% by weight of at least one auxiliary monomer, and 0-3% by weight of at least one crosslinker molecule, the difference in the glass transition temperatures (Tg) of the different polymers being at least 10° C., and b) 30-50% by weight of at least one polyfunctional (meth)acrylate, the dispersion a) being subjected to physical and/or chemical deodorization.

Abstract: The invention relates to the use of copolymers as gas hydrate inhibitors, whereby these copolymers are synthesized from: 40 to 99.5% by weight of at least one ethylenically unsaturated cyclic lactam A; 0.5 to 60% by weight of monomers B having a solubility in water of less than 10 parts by weight of monomers in 100 parts by weight of water, and; 0 to 50% by weight of other monomers C.

Abstract: The present invention relates to a process for the preparation of hydrogen peroxide from oxygen or oxygen-delivering substances and hydrogen or hydrogen-delivering substances in the presence of at least one catalyst containing a metal-organic framework material, wherein said framework material comprises pores and a metal ion and an at least bidentate organic compound, said bidentate organic compound being coordinately bound to the metal ion. The invention further relates to a novel material consisting of said metal organic framework material wherein the material is brought in contact with at least one additional metal.

Abstract: Pyrimidines of the formula I in which Ln is as defined in the description and the substituents R1, R2 and R3 are as defined below: R1 is C1-C10-alkyl, C2-C10-alkenyl, C2-C10-alkynyl, C3-C12-cycloalkyl, C3-C10-cycloalkenyl, phenyl or a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which is attached via carbon and contains one to four heteroatoms from the group consisting of O, N and S; R2 is halogen, cyano, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C1-C4-alkoxy, C3-C4-alkenyloxy or C3-C4-alkynyloxy, where the alkyl, alkenyl and alkynyl radicals of R2 may be substituted by halogen, cyano, nitro, C1-C2-alkoxy or C1-C4-alkoxycarbonyl; R3 is a five- or six-membered saturated, partially unsaturated or aromatic mono- or bicyclic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S; and processes and intermediates for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi are

Abstract: Rylene derivatives of the general formula I where the variables have the following meanings: R is hydrogen or substituted or unsubstituted C1-C30-alkyl, aryl or hetaryl; R1 is hydrogen or bromine; R2 is hydrogen or C1-C6-alkyl; R3 is hydrogen, C1-C18-alkyl or substituted or unsubstituted aryl or hetaryl; and n is 2 or 3.

Abstract: The invention relates to a method for producing 2-keto-L-gulonic acid-C4-C10 alkyl ester by esterifying 2-keto-L-gulonic acid (KGS) with an unsaturated, branched or unbranched C4-C10 alcohol. The inventive method is characterized by the fact that an aqueous KGS solution is reacted with a C4-C10 alcohol up to an esterification degree of 20 to 70 percent in a pre-esterification process carried out under acidic catalysis conditions; and the obtained product is dehydrogenated with an unsaturated, branched or unbranched C4-C10 alcohol in a continuous rectification device, whereby the esterification reaction continues, n-butanol preferably being used as the alkyl alcohol. In a preferred embodiment, the aqueous KGS solution is concentrated up to or beyond the limit of solubility prior to the esterification process, preferably by catalyzing a homogeneous or heterogeneous catalyst, especially sulfonic acid, at temperatures of 50 to 120 ° C.

Abstract: The invention relates to a mixture, comprising (A) 10 to 90 wt. % of at least one C6 to C18 alkyl ester, or C5 to C8 cycloalkyl ester of 2-cyano-3,3-diphenylacrylic acid and (B) 90 to 10 wt. % of at least one further compound, with at least one UV absorption maximum in the range 280 to 450 nm and structurally different from compound (A). Said mixture is suitable for the protection of human skin from damaging UV radiation and for the protection of coloured textile materials from colour fading.

Abstract: A process for preparing (meth)acrylic acid, in which a saturated hydrocarbon precursor compound is conducted through a catalyst charge which consists of two spatially successive catalyst beds I, II in the flow direction of the reaction mixture, each of which contains different catalysts and has different reaction-selectivity behavior.

Abstract: The invention relates to phosphacyclohexanes of general formulae I and II, wherein the following designations, among others, apply: R can represent hydrogen, C1-100-alkyl, C7-20-aralkyl, C7-20-alkaryl, and C6-12-aryl: R1 to R10 can independently represent hydrogen, C1-20-alkyl, C7-20-aralkyl, C7-20-alkaryl, and C6-12-aryl: W, W? can independently represent single bonds or bridges comprising 1 to 20 carbon atoms, which can form part of a cyclic or aromatic group and can be interrupted by heteroatoms. Said phosphacyclohexanes are used as ligands in transition metal complexes of transition metals belonging to groups VIII to X of the periodic table.

Abstract: The invention relates to the use of liquid colouring preparations, containing at least one pigment and 0.5 to 10 wt. % of at least one dye, based on the pigment, for the decorative colouring of derived timber products.

Abstract: Disclosed is a method for jointly producing (i) formic acid (III); (ii) a carboxylic acid comprising at least two carbon atoms (II) and/or the derivatives thereof; and (iii) a carboxylic acid anhydride (VII). According to said method, (a) a formic acid ester (I) is transesterfied to formic acid (III) and the corresponding carboxylic acid ester (IV) by means of a carboxylic acid comprising at least two carbon atoms (II); (b) at least one portion of the carboxylic acid ester (IV) formed in step (a) is carbonylated in order to obtain the carboxylic acid anhydride (V); and (c) at least one portion of the carboxylic acid anhydride (V) formed in step (b) is further dehydrated by means of a carboxylic acid (VI) so as to form a carboxylic acid anhydride (VII) and the carboxylic acid (II).

Abstract: Isocyanates are prepared by reacting primary amines with phosgene in a reactor by a process in which a reaction discharge is present in the form of a suspension which contains the isocyanate to be prepared, as a liquid, and carbamyl chlorides as a solid, and the suspension is worked up in a film evaporator, and this process is carried out in a production plant.

Abstract: In the polymer of transition-metal-bridged units of the formula (I) where A is an m-valent organic radical, T independently of one another are O or NH, Q independently of one another are CHR1—CH2 where R1 is H or optionally substituted C1-6-alkyl, R independently of one another are H, 2-pyridyl, 2-imidazolinyl, 2-imidazolyl, 2-thiazolinyl, 2-thiazolyl, 2-pyridazyl, 2-pyrimidyl, carboxyl, carboxylic ester radical, carboxamide radical, carboxylate, phosphonate, where at least one of the radicals R is different from H, M is Fe2+, Fe3+, Co2+, Co3+, Zn2+, Ru2+, Os2+, Ni2+, Z is SO42?, CH3OO?, BF4?, SF6?, Cl?, I?, PF6?, perchlorate, n is 1 to 10 000, m is 2 to 100, p is a number which corresponds to the charge balance within the polymer, the average molecular weight of the polymer is at least 15 000.

Abstract: The present invention relates to a process for preparing at least one alkoxylate, which comprises bringing at least one alkylene oxide selected from the group consisting of ethylene oxide, propylene oxide, butylene oxide, pentylene oxide and decene oxide into contact with at least one starter compound in the presence of at least one double metal cyanide compound, with the reaction being carried out at a temperature of from 130° C. to 155° C., to the alkoxylates, in particular ethoxylates, themselves and to the use of such ethoxylates as emulsifier, foam regulator or as wetting agents for hard surfaces.

Abstract: Mercury is removed from solutions contaminated with mercury by filtration through a carbon filter consisting of electrode graphite.

Abstract: The invention relates to processes for the preparation of alkylarylsulfonates by a) reaction of a C4-olefin mixture over a metathesis catalyst to prepare an olefin mixture comprising 2-pentene and/or 3-hexene and optional removal of 2-pentene and/or 3-hexene, b) dimerization of the 2-pentene and/or 3-hexene obtained in stage a) in the presence of a dimerization catalyst to give a mixture comprising C10-12-olefins and optional removal of the C10-12-olefins, c) reaction of the C10-12-olefin mixtures obtained in stage b) with an aromatic hydrocarbon in the presence of an alkylation catalyst to form alkyl aromatic compounds, where, prior to the reaction, additional linear olefins may be added, d) sulfonation of the alkyl aromatic compounds obtained in stage c) and neutralization to give alkylarylsulfonates, where, prior to the sulfonation, linear alkylbenzenes may additionally be added, e) optional mixing of the alkylarylsulfonates obtained in stage d) with linear alkylarylsulfonates.