Abstract: The ink mixture contains at least one organosilane and optionally at least one hydrophobic silicic acid. The ink mixture can be used as a printing ink, especially as an ink for ink-jet printing.

Abstract: A process for the enantioselective epoxidation of C═C double bonds and use of the epoxides. The present invention provides a process for the enantioselective epoxidation of compounds of the formula I by means of a diastereomer and enantiomer enriched homopolyamino acid and an oxidizing agent. The epoxides prepared according to the invention are used as intermediates in organic syntheses.

Abstract: The acid-catalyzed intermolecular etherification of mono- or polyhydric alcohols and acid-catalyzed ether cleavage in the presence of water may be improved if etherification or ether cleavage is carried out in the presence of an acid catalyst and, additionally, a hydrogenation catalyst under a hydrogen atmosphere. The process relates in particular to the etherification of diols, triols and tetrols with the formation of hydroxyethers.

Abstract: A process for producing, on a metallic substrate, a geometric metal structure having a precise contour, including the steps of: solder coating a solder paste onto the substrate by screen printing to create the geometric metal structure, the solder paste comprising an organic binder system, and 80 to 95 weight % of a mixture of a nickel-based solder and a pulverulent alloy of nickel with at least one member selected from the group consisting of chromium, molybdenum, tungsten, manganese and iron, provided as a higher-melting metallic filler, wherein a weight ratio of solder to filler is 2-6:1, an average grain size of the solder is between 10 and 50 &mgr;m, and a grain size ratio of solder to filler, relative to the average grain size is from 0.5-2.5:1; drying the structure; decomposing the organic binder system present in the solder paste, without leaving a reside, by a heat treatment; and raising the temperature until the resulting solder material liquifies.

Abstract: An aqueous aluminium silicate suspension having a content of aluminium silicate of at least 30 wt. % is prepared by liquefaction of the aluminium silicate filter cake or by dispersion of aluminium silicate powder in water with the addition of aluminium silicate powder, surfactant and aluminium sulfate. It can be employed in papermaking.

Abstract: Measurement of density and mass flow of disperse systems with a gas as fluid phase flowing through a pipe is carried out by introducing sound in the frequency range 20-2,000 Hz in the middle of the cross-section of the pipe. The sound has a wavelength which is at least half the pipe diameter. The speed propagation of sound waves in the flowing disperse system is is measured in the axial direction of flow over at least two transit sections of differing length; and the speed propagation of sound waves in the flowing disperse system is also measured in a direction contrary to the axial direction of flow over at least two transit sections of differing length. The fill level of a reception member in communication with a line of the disperse system is calculated from the measured mass flow rate over a period of time.

Abstract: The invention relates to L-lysine-producing strains of corynebacteria with amplified lysE gene (lysine export carrier gene), in which strains additional genes chosen from the group comprising the dapA gene (dihydrodipicolinate synthase gene), the lysC gene (aspartate kinase gene), the dapB gene (dihydrodipicolinate reductase gene) and the pyc gene, but especially the dapA gene and the lysC gene (aspartate kinase gene), are amplified and, in particular, overexpressed, and to a process for the preparation of L-lysine.

Abstract: A process for the preparation of mixtures of organosilicon disulfanes with a high disulfane content includes first reacting finely divided sodium and sulfur in an organic solvent, and then reacting the resulting Na2Sx, product further with a halogenoalkylalkoxysilane to give the desired product.

Abstract: Chlorine-free tetraalkoxysilanes of formula (I) (R1O)4Si  (I) wherein R1 is, independently in each instance, an unbranched, branched, and/or cyclic C1-6 hydrocarbon group is continuously manufactured by a process, comprising: reacting metallic silicon powder with a monohydric alcohol in the presence of a basic catalyst comprising a mixture of: (a) at least one compound of formula (II) [R2O—(R3O)m]nSi)OR1)4-n  (II) (b) at least one compound of formula (III) R2O—(R3O)m—M, and  (III) (c) at least one compound of formula (IV) R2O—(R3O)m—H  (IV) wherein R1 is as defined above; R2 represents, independently in each instance, a C1-10 hydrocarbon group, or hydrogen; R3 represents, independently in each instance, a C1-4 hydrocarbon group; M represents an alkali metal selected from the group consisting of Li, Na, and K; m is zero or a number in the range of 1-20; and n is zero or a number in the range of 1-4; further comprisin

Abstract: A partially hydrophobic precipitated silica having a methanol wettability of 10 to 49%, in particular with a DBP uptake on a dry basis of greater than 250 g/100 g and a mean particle size of 1 to 12 &mgr;m and/or a carbon content of 0.3 to 1.85% and/or a loss on drying of 2.6 to 10.0% and/or a pH value of 5.5 to 10.0, is prepared by mixing the amount of water-repellent agent with the precipitated silica suspension at very short residence time and low pH value, filtering off the solid substance, washing free of salt, drying, post-treating thermally and milling. The partially hydrophobic precipitated silica can be used in active substance formulations and active substance formulations of hydrolysis-sensitive substance and in defoaming agents.

Abstract: A process for joining two solid bodies, in particular of silicon. via the substantially smooth surfaces that have first of all been coated with a monomolecular layer of a sulfur-containing organosilane, and the resultant solid bodies, which may be used in microelectronics or micromechanics.

Abstract: A method for the production of D-pantothenic acid by the fermentation of microorganisms of the family Enterobacteriacae producing D-pantothenic acid which is characterized in that strains are used which a) Contain the plasmid pFV31 and/or pFV202 and that b) A panD gene and optionally other nucleotide sequences coding for aspartate-1-decarboxylase are enhanced, especially overexpressed in these microorganisms, c) The pantothenic acid is enriched in the medium or in the cells of the microorganisms and d) The pantothenic acid formed is isolated.

Abstract: The invention is a method for the production of D-pantothenic acid by the fermentation of microorganisms in which at least the panD gene is enhanced (overexpressed), optionally in combination with the panB and/or panC gene, to provide for the enrichment of the pantothenic acid in the medium or the cells of the microorganisms.

Abstract: The invention discloses three polynucleotide sequences for the fermentative production of D-pantothenic acid. These polynucleotide sequences are genes named panB, encoding a ketopantoate hydroxymethyltransferase, panC, encoding pantothenate synthase, and ilvD, encoding dihydroxy-acid dehydratase. The genes panB and panC are found on the same operon, panBC, while the gene ilvD is found in a separate operon. These genes can be used separately or together to enhance the production of D-pantothenic acid in microorganisms, especially in Corynebacterium.

Abstract: A process of operating a nitrogen oxides storage catalyst of an exhaust gas treatment system is described. The process relates to the cycling of the normalized air/fuel ratio &lgr;-value of the exhaust gas exiting the engine, in which a lambda value greater than 1 represents oxygen-rich, lean burn conditions in which a sorption phase for the sorption of nitrogen oxides takes place; and in which a lambda value less than 1 represents oxygen-poor, rich burn conditions in which a desorption and conversion phase for the desorption and conversion of nitrogen oxides takes place. The &lgr;-value of the exhaust gas downstream from the storage catalyst is monitored during the desorption and conversion phase to determine the end of the desorption and conversion phase based on the &lgr;-value falling below a predetermined threshold value.

Abstract: A platinum alloy catalyst on an electrically conductive carbon support which contains an alloy of 40 to 60 atom-% of platinum, 10 to 20 atom-% of rhodium and 20 to 50 atom-% of iron in the form of finely divided alloy particles. The catalyst is characterised in that the average particle size of the alloy particles is less than 10 nm.

Abstract: Cyanide-free electroplating baths for deposition of gold and gold alloy coatings, using sulphurous gold complexes that are stable for a relatively long time, can be used with current density over 1 A/dm.sup.2 and are practically odor-free, are obtained when the sulphurous compounds used are mercaptosulfonic acids, dye sulfide sulfonic acids or salts thereof.

Abstract: Paints and printing inks are disclosed which contain carbon black as the pigment. The dispersion and storage stability of printing inks and paints may be improved by using carbon blacks containing silicon. The rheological behavior of the paints is improved by silicon-doping of the carbon blacks used. Paints having a reduced solvent content are consequently obtainable.

Abstract: Quadridentate Cu.sup.II and Zn.sup.II phenoxyl complexes and phenoxyl radical complexes thereof, in which one ligand L is bonded to each metal atom and H.sub.2 L stands for the general formula ##STR1## in which the bridge-unit Q stands for --S--, --O--, --N(R.sup.3)--, --P(R.sup.4)--, or ortho-NH--C.sub.6 H.sub.4 --NH-- and R.sup.1 and R.sup.2 stand for radical-stabilizing residues.Preferred radical complexes include ##STR2## The radical complexes are oxidation catalysts for oxidizing organic substrates with O.sub.2 in the course of which H.sub.2 O.sub.2 is also formed.

Abstract: A cyclic anthraquinone process for producing hydrogen peroxide using at least two differently substituted 2-alkylanthraquinones and/or their tetrahydro derivatives. The working solution to be used contains (i) at least one reaction carrier from the series 2-(4-methyl-3-pentenyl) anthraquinone (IHEAQ), 2-(4-methylpentyl) anthraquinone (IHAQ) and their di- and tetrahydro derivatives such as, in particular 2-(4-methylpentyl)-.beta.-tetrahydroanthraquinone (THIHAQ), and (ii) at least one reaction carrier from the series of the 2-(C.sub.1 - to C.sub.5)-alkylanthraquinones, especially 2-ethylanthraquinone (EAQ), and their tetrahydro derivatives. The reaction carriers according to (i) make up 5 to 95 molar %, especially 20 to 50 molar % of all reaction carriers. The method is distinguished by greater H.sub.2 O.sub.2 capacity, improved hydrogenation kinetics and lesser susceptibility to disturbances. A method for making THIHAQ is also disclosed.