Abstract: The invention relates to an ethylene polymer having an intrinsic viscosity of at least 4 dl/g, which has a maximum draw ratio of at least 20, is pulverulent, has a bulk density of at most 300 kg/m.sup.3 and has an amount of catalyst residues of less than 50 ppm. The invention also relates to a method for the preparation of a pulverulent ethylene polymer having an intrinsic viscosity of at least 4 dl/g through polymerization of ethylene or of a mixture of ethylene and not more than 2 mol% higher olefins at a temperature below 80.degree. C. and an ethylene pressure below 0.2 MPa in the presence of a catalyst having a specific surface area of at most 150 m.sup.2 /g. It further relates to articles composed of the ethylene polymer.

Abstract: The invention relates to a composite web comprising one elongated flat composite layer of mutually parallel fibers in a matrix, in which the fibers run at an angle .alpha. (differing from 0.degree.) relative to the lengthwise direction of the web, and which in the lengthwise direction is made up of joined-up and connected web parts. This composite web can be used for continuously producing multi-layer composites. The composite layer of the composite web has no areas with overlap or gaps when placed in a multi-layer composite. The invention also relates to a method for the production of this composite web and of multi-layer composites.

Abstract: The present invention relates to a process and apparatus for the preparation of urea, and in particular for urea obtained from ammonium carbamate formulated from carbon dioxide and ammonia at a pressure of about 125 bar to about 350 bar in a urea synthesis solution in a urea reactor. The reactor defines a horizontally arranged condensation zone and contains a heat exchanger. According to this process, NH.sub.3 and CO.sub.2 are supplied to the reactor and are largely absorbed into the urea synthesis solution. A substantial portion of the heat formed in the condensation is discharged by means of the heat exchanger. The residence time of the urea synthesis solution in the reactor preferably is selected so that at least about 85% of the theoretically obtainable amount of urea is prepared. Thereafter, the urea synthesis solution can be processed into a urea solution or solid urea.

Abstract: A process for the incorporation of silica into a polymer in latex in which a silica is treated with an organo silicon compound coupling agent in aqueous suspension to form a compatibilized silica and then contacting a polymer latex with the compatibilized silica whereby the silica becomes substantially uniformly distributed throughout the latex and can be recovered when the latex is coagulated to yield little residual silica in the liquid residue from the latex. Also described is a process for preparing the compatibilized silica.

Abstract: The invention relates to a binder composition for powder coatings. The binder composition is substantially based on a mixture of an unsaturated polyester and an oligomer having a plurality of allyl groups and further having at least either ether and ester groups or urethane and optionally ether groups.The oligmer is preferably an allyl ether ester being more preferably the ester of trimethylolpropane diallyl ether or pentaerythritol triallyl ether and a polycarboxylic acid (anhydride).

Abstract: The invention relates to a polymer composition comprising 5 to 79 wt. % of a graft copolymer of vinyl aromatic monomer units and monomer units chosen from the group of C.sub.1 -C.sub.4 alkyl methacrylates, C.sub.1 -C.sub.4 alkyl acrylates, methacrylonitrile and acrylonitrile on a rubber, 90 to 20 wt. % of a thermoplastic polymer with polar groups, and 1 to 50 wt. % of a terpolymer comprising a vinyl aromatic monomer, at least one monomer chosen from the group of C.sub.1 -C.sub.4 alkyl methacrylates, C.sub.1 -C.sub.4 alkyl acrylates, methacrylonitrile and acrylonitrile, and 0.2 to 5 mol % of an .alpha.,.beta.-unsaturated compound containing dicarboxylic anhydride, the wt. % of components (A), (B) and (C) being relative to the total weight of components (A), (B) and (C), characterized in that the molar mass of component (C) is comprised between 160,000 g/mol and 230,000 g/mol. The polymer composition has excellent mechanical properties, in particular a high impact resistance at low temperatures.

Abstract: Process for the preparation of pure (S,S)-N-(1-ethoxycarbonyl-3-phenylpropyl) alanine,in which impure (S,S)-N-(1-ethoxycarbonyl-3-phenylpropyl)alanine is suspended in water, dissolved by heating to the boiling point and separated from insoluble impurities by filtration and the desired end product is then precipitated by cooling, filtered off and dried.

Abstract: The invention relates to a process for the preparation of an alkyl benzene by catalytic dehydrogenation of the corresponding alkenyl cyclohexene in the gas phase in the presence of a diluent. A characteristic feature is that at least a part of the alkyl cyclohexane in the reaction product is used as diluent. Hydrogen can be used as an additional diluent according to the invention.

Abstract: The invention relates to the use of a hydroxyl functional polyester having a glass transition temperature of at least 40.degree. C., a hydroxylnumber between 5 and 150 mg KOH/gram resin, a molecular weight (Mn) between 800 and 10.000 and a molecular weight (Mw) between 8000 and 100.000 in the preparation of coatings for the interior of can ends. The polyester has to be crosslinked with for example an amino resin or an epoxy resins.

Abstract: A process for the preparation of carboxylic acid succinimidyl esters by reaction of N-hydroxysuccinimide with a carboxylic acid and a halophosphoric acid ester of the formula ##STR1## is desired, in which R.sub.1 and R.sub.2 are identical or different and are a C.sub.2 - to C.sub.6 -alkyl radical or a phenyl radical, or R.sub.1 and R.sub.2 The process is carried out in the presence of a base in a diluent at a temperature of 0.degree. C. up to 100.degree. C. with isolation of the corresponding carboxylic acid succinimidyl ester.

Abstract: A plugging compound for chemical fastening technology is based on a free-radically polymerizable resin and a free-radical initiator spatially separated therefrom. The plugging compound in question is a self-supporting and storage-stable material which can be inserted in that form directly into a drill-hole.

Abstract: A binder composition for thermosetting powder paints comprising (i) a polymer that is capable of reacting with epoxy groups and (ii) a crosslinker that contains epoxy groups, wherein the crosslinker comprises at least one C.sub.5 to C.sub.26 linear or branched aliphatic chain with the proviso that epoxy groups are carried on at least one aliphatic chain. In order to function as a crosslinker the amount of oxirane-oxygen originating from the crosslinker in the binder composition is higher than 0.1 meq/gram. The crosslinker is, for example, an epoxydized oil, a modified epoxydized oil or an epoxydized alkyd resin. A powder paint comprising the binder composition can contain a suitable catalyst and, optionally, an additional curing agent.

Abstract: The invention relates to a method for preparing an .alpha.-alkylcinnamaldehyde via aldol concensation of a benzaldehyde and an alkanal, with pyrrolidine being employed as a catalyst. The method is suitable, in particular, for preparing .alpha.-hexylcinnamaldehyde by aldol condensation of benzaldehyde and n-octanal, in particular for preparing .alpha.-hexylcinnamaldehyde of olfactory quality, since it was found that, in the method according to the invention, relatively little .alpha.-hexyldecenal, the aldol condensation product of n-octanal, is formed. Preferably, the aldol condensation is carried out without a solvent in the presence of an acid, and the alkanal is metered in over time to a mixture which contains pyrrolidine and benzaldehyde.

Abstract: A copolymer having an RSV less than 0.6 and a process for its preparation in which ethylene, at least one other 1-alkene and, optionally, an aliphatic or alicyclic polyunsaturated monomer are polymerized in the presence of a catalyst system containing (1) a compound of vanadium, (2) at least one alkyl aluminum halide, (3) an .alpha.-halo, ketoaromatic promoter and (4) a chain transfer agent in which the molar ratio of alkyl groups of the alkyl aluminum halide to halogen atoms is at least 1.5.

Abstract: A process for preparing high-purity calcium pyruvate or its hydrates by reacting an aqueous solution of pyruvic acid with an inorganic calcium compound with the pH being set to 2 to 7, preferably 2.5 to 4, which comprises reacting an up to 10% strength aqueous solution of pyruvic acid with the calcium compound, in the presence or absence of a stabilizer or complexing agent, and mixing the resulting solution with an organic diluent at temperatures of 0.degree. to 30.degree. C. and isolating the resulting precipitate of calcium pyruvate or its hydrate from the solution.

Abstract: Process for the preparation of pure 4,6-dichloropyrimidine by reaction of 4,6-dihydroxypyrimidine with an excess of phosphorus oxychloride at 20.degree. C. up to reflux temperature, in the presence of a trialkylamine as acid scavenger and catalyst.

Abstract: A process for separating and recovering waste carpet material components, especially face fiber material, includes removing adhesive material from the waste carpet material feedstock to obtain a mixture containing face fiber material which is passed with a liquid medium to a hydrocyclone, where the solids in the mixture are separated on the basis of specific gravity, and recovered. The recovered components can then be processed into desired products.

Abstract: An additive compositon comprising a graft and aminederivatized copolymer prepared from ethylene and at least one (C.sub.3 -C.sub.10) alpha-monoolefin and, optionally, a polyene selected from non-conjugated dienes and trienes comprising from about 15 to 80 mole percent of ethylene, from about 20 to 85 mole percent of said (C.sub.3 -C.sub.10) alpha-monoolefin and from about 0 to 15 mole percent of said polyene, said copolymer having a number average molecular weight ranging from about 5,500 to 50,000 and having grafted thereon at least 1.8 molecules of a carboxylic acid acylating function per molecule of said copolymer and reacting said grafted copolymer with an amino alcohol compound selected from the group consisting of a 2-Anilinoalcohol, a (2-hydroxyalkyl) pyrridine, a 4-(2-hydroxyalkyl) morpholine, a 1-(2-hydroxyalkyl) piperazine, a 1-(2-pyrrolidine and a 1-(2-hydroxyalkyl) 2-pyrrolidine.

Abstract: The invention relates to a process for the preparation of 5-formylvaleric acid or the corresponding 5-formylvalerate by hydroformylation of 3-pentenoic acid or 3-pentenoate ester with carbon monoxide and hydrogen in the presence of a catalyst comprising of rhodium and a phosphite ligand, wherein the phosphite ligand is represented by the following general formula ##STR1## where R.sup.1 and R.sup.2 are the same or different aromatic organic groups and where A is an n-valent group or atom and where n is an integer chosen upwards of 2 and where the respective ?--O--P(OR.sup.1)(OR.sup.2)! group may be the same group or different groups and where the phosphite forms a chelate-type complex with rhodium.

Abstract: Process for the preparation of .epsilon.-caprolactam starting from an aldehyde compound comprising at least one member from among 5-formylvaleric acid, ester or amide in which the aldehyde compound is allowed to react in the presence of ammonia and hydrogen and a subsequent cyclization of the reaction products thus formed (.epsilon.-caprolactam-precursors) to .epsilon.-caprolactam is performed in the presence of water, involved the combination of steps(a) contacting the 5-formylvaleric acid, ester or amide with ammonia and water under non-hydrogenation conditions,(b) contacting the resulting mixture of step (a) with hydrogen in the presence of ammonia under hydrogenation conditions, wherein the water content is greater than 10 wt. %,(c) heating the resulting mixture of step (b) at a temperature between 200.degree. and 350.degree. C. in order to convert the reaction products of step (b) to .epsilon.-caprolactam.