Abstract: Active compound mixtures comprising ipconazole and at least one further fungicidally active compound are highly suitable for protecting industrial materials against colonization and destruction by microorganisms.

Abstract: Primary isocyanates are produced by reacting the corresponding primary amine(s) with phosgene at a temperature above the boiling temperature of the amine(s) in a tube reactor with a reaction space. In this tube reactor, at least one educt stream P containing phosgene and at least one educt stream A containing the amine(s) are fed to the reaction space via a nozzle arrangement. The nozzle arrangement includes a number of n?1 nozzles aligned parallel to the axis of rotation of the tube reactor and a free space surrounding the nozzles. One of the educt streams A or P is fed to the reaction space via the nozzles and the other educt stream is fed to the reaction space via the free space surrounding the nozzles. The reaction space contains at least one moving mixing device.

Abstract: Meta-toluene-diisocyanate is produced by reacting meta-toluenediamine with phosgene in the gas phase. The meta-toluenediamine to be vaporized for use in this phosgenation process must contain less than 0.5 wt. % of toluenediamine residue, a total of less than 0.2 wt. % of ammonia and cycloaliphatic amines, and less than 20 ppm of heavy metals. At least 0.1 wt. % of the liquid meta-toluenediamine being to be vaporized must not be vaporized. This non-vaporized content of the meta-toluenediamine must not be fed to the phosgenation reactor.

Abstract: Aromatic isocyanates are produced by reacting one or more aromatic primary amines with phosgene in the gas phase. The phosgene and primary aromatic amine(s) are reacted at a temperature above the boiling temperature of the amine(s) in a reactor having a reaction space which is essentially rotationally symmetric to the direction of flow. The flow fate, averaged over the cross-section, of the reaction mixture along the axis of the essentially rotationally symmetric reaction space in the section of the reaction space in which the conversion of the amine groups into isocyanate groups is between 4 and 80 % is not more than 8 m/sec. The flow rate averaged over the cross-section of the reaction mixture along the axis of the essentially rotationally symmetric reaction space in the section of the reaction space in which the conversion of the amine groups into isocyanate groups is 4 to 80 % is always below the flow rate averaged over the cross-section at the start of this section.

Abstract: The novel process for preparing substituted azoles allows compounds of the general formula (I) and/or their salts and/or their acid addition compounds in which the substituents R1 and R2, A and B are as defined in the description to be prepared in good yield and in a simple, economically favourable manner.

Abstract: Isocyanates are produced by reaction of primary amines with phosgene in the gas phase. In this process, the reaction is terminated by guiding the reaction mixture from the reaction chamber through a cooling stretch into which liquids are injected. Direct cooling takes place in the cooling stretch in one stage in two or more cooling zones connected in series.

Abstract: Synergistically effective mixtures comprising prochloraz and tebuconazole and fungicidal compositions based thereon are highly suitable for protecting industrial materials, in particular wood and timber products, against attack, damage and/or destruction by biological pests.

Abstract: Aromatic diisocyanates are produced by reacting in the gas phase the corresponding primary aromatic diamine with phosgene. The phosgene and the primary aromatic diamine are reacted within a mean residence time of from 0.05 to 15 seconds. The aromatic diamine used contains less than 0.05 mole % overall of aliphatic amine containing no keto groups, per mole of primary amino groups.

Abstract: The active compound prochloraz and fungicidal compositions based on prochloraz are highly suitable for protecting wood and timber products against attack and/or destruction by soft-rot fungi.

Abstract: An isocyanate is produced by reacting a primary amine with phosgene in the gas phase above the boiling point of the amine over an average contact time of 0.05 to 15 seconds under adiabatic conditions.

Abstract: Device for holding a load on a load support of an industrial truck with the following characteristics: a support device on a lifting scaffold of the industrial truck, adjustable in its height by a shifting drive, extending approximately horizontally above the load support, at least one sack-shaped container, made of flexible, air-impermeable material, which is hanged up on the support device and which is filled with granular material, wherein the flexible material and the granular material are constituted such that the bottom side of the container adapts itself to the surface contour of the load, when the container is lowered onto the load, and an aspirating device, connectable with the interior of the container, for generating a negative pressure in the container.

Abstract: Processes comprising providing an amine reactant, and reacting the amine reactant with a stream of phosgene in a reaction zone to form a product comprising a corresponding isocyanate, wherein the phosgene stream has a CO content of 0.5% by weight or more.

Abstract: The compounds of the formula (I) in which R1 represents cycloalkyl, and its stereoisomers and any mixtures thereof are highly suitable as microbicides for protecting plants and materials.

Abstract: The compounds of the formula (I) in which R1 represents hydrogen or in each case optionally substituted alkyl, alkenyl, alkynyl or phenyl are highly suitable as microbicides for protecting plants and materials.

Abstract: Using synergistically effective mixtures comprising triadimefon and/or triadimenol and at least one further known fungicidally active compound, it is possible to protect industrial materials, in particular wood, against attack, damage and/or destruction by biological pests, in particular by wood-destroying fungi.

Abstract: Chlorine is prepared by catalytic oxidation of a hydrogen chloride stream having a content of sulfur in elemental or bonded form of less than 100 ppm, preferably less than 50 ppm, more preferably less than 5 ppm, most preferably less than 1 ppm, based on the weight of the hydrogen chloride stream.

Abstract: Isocyanates are produced by reaction of primary amines with phosgene in the gas phase. In this process, the reaction is terminated by guiding the reaction mixture from the reaction chamber through a cooling stretch into which liquids are injected. Direct cooling takes place in the cooling stretch in one stage in two or more cooling zones connected in series.

Abstract: An isocyanate is produced by reacting a primary amine with phosgene in the gas phase above the boiling point of the amine over an average contact time of 0.05 to 15 seconds under adiabatic conditions.

Abstract: Active compound mixtures comprising ipconazole and at least one further fungicidally active compound are highly suitable for protecting industrial materials against colonization and destruction by microorganisms.

Abstract: The compound of the formula (I) its metal salts or acid addition compounds are highly suitable for protecting industrial materials against attack and/or destruction by insects.