Abstract:
Bei einem Verfahren zum Zubereiten sowie Bereitstellen von flüssigen Lebensmitteln, insbesondere Kaffee, Tee, Suppe oder dergleichen in einem Fahrzeug (1), insbesondere PKW mit einer Vorrichtung (R) in welcher Wasser bereitgestellt wird, soll die Vorrichtung (R) zum Zubereiten sowie Bereitstellen von flüssigen Lebensmittel im Bereich des Fahrgastraumes (2) angeordnet sein, und über einen externen Wasserbehälter (5) sowie externe Steuerung (11), heisses und erwärmtes Wasser der Vorrichtung (R) zugeführt werden.
Abstract:
Bei einem Verfahren zum Zubereiten sowie Bereitstellen von flüssigen Lebensmitteln, insbesondere Kaffee, Tee, Suppe oder dergleichen in einem Fahrzeug (1), insbesondere PKW mit einer Vorrichtung (R) in welcher Wasser bereitgestellt wird, soll die Vorrichtung (R) zum Zubereiten sowie Bereitstellen von flüssigen Lebensmittel im Bereich des Fahrgastraumes (2) angeordnet sein, und über einen externen Wasserbehälter (5) sowie externe Steuerung (11), heisses und erwärmtes Wasser der Vorrichtung (R) zugeführt werden.
Abstract:
O.Z. 0050/41152 Carboxamides of the formulae Ia to Ic Ia Ib Ic where X is oxygen or sulfur; R1 is hydrogen or substituted or unsubstituted cycloalkyl or alkyl; R2 is hydroxy, alkoxy, cyanoalkyl, substituted or unsubstituted alkenyl, alkynyl, phenyl or naphthyl, a substituted or unsubstituted 5- to 6-membered heterocyctic structure or one of the groups stated for R1, or R1 and R2 together are a 4- to 7-membered chain which contains, in addition to methylene groups, one of the following groups as ring member: oxygen, sulfur, N-methyl or carbonyl; R3 and R4 are each nitro, cyano, halogen, substituted or unsubstituted amino, alkoxy, alkylthio, a substituted or unsubstituted 5- to 6-membered heterocyclic structure, substituted or unsubstituted alkenyl, alkynyl, phenyl, phenoxy or phenylthio, or one of the groups stated for R1; R5 is formyl, 4,5-dihydrooxazol-2-yl or COYR6 (Y = O,S); R6 is hydrogen, cycloalkyl, substituted or unsubstituted alkyl, alkenyl, alkynyl, cycloalkenyl or phenyl, a 5- to 6-membered heterocyclic structure, phthalimido, tetrahydrophthalimido, succinimido, maleimido, benzotriazolyl or a group -N=CR7R8, where R7 and R8 are hydrogen or alkyl, and R8 may also be cycloalkyl, phenyl, furyl or R7 and R8 together form a 4- to 7-membered alkylene chain; O.Z. 0050/41152 and if R5 is carboxyl, methoxycarbonyl or ethoxycarbonyl and R2 is hydrogen, R3 is not hydrogen and R4 is not hydrogen or methyl, and if R5 is carboxyl, methoxycarbonyl or ethoxycarbonyl and R4 is hydrogen, R3 is not hydrogen or R2 is not one of the following groups: hydrogen; C1-C4-alkyl, phenyl; 2-(3,4-dimethoxyphenyl)ethyl or 2,5-dichlorothien-3-yl; processes for the manufacture of compounds I and herbicidal agents containing them.
Abstract:
The water is prepared in a water vessel (5) located outside the passenger compartment (2). It is equipped with a supply line (4) and possibly further lines, e.g. a drain line, connecting it with remotely-located equipment, e.g. in the car boot.
Abstract:
O.Z. 0050/41776 of the Disclosure: Dicarboximides of the general formulae Ia and Ib Ia Ib where X is oxygen or sulfur, R1 is hydrogen, cycloalkyl, alkyl, hydroxyl, alkoxy, cyanoalkyl, alkenyl, alkynyl, phenyl, naphthyl or a 5-membered or 6-membered heterocyclic structure, where the stated radicals may be substituted, and R2 and R3 are each nitro, cyano, halogen, amino, mono- or dialkylamino, alkylcarbonylamino, unsubstituted or halogen-substituted alkoxy or alkylthio, alkylsulfonyl, haloalkylsulfonyl, alkenyl, alkynyl, phenyl, phenoxy or phenylthio or one of the radicals R1, with the proviso that specific compounds named in the description are excluded. Processes for the preparation of the compounds Ia and Ib and herbicides containing them.
Abstract:
False twisting of yarns uses three sets of discs of equal dimensions rotating in the same direction on three spindles, the discs of each set overlapping each other. The yarn entering the false twisting unit is angled at 10-60 degrees to the axes of the spindles on entry and/or exit. The design allows the yarn to be threaded swiftly and accurately into the false twisting unit, without operative time loss and without the difficulty of mounting a pivoted carrier plate for the precision components of the false twister.
Abstract:
Carboxamides Ia, Ib, Ic and Id (X = 0, S; R1 = H, halogen, substituted or unsubstituted alkyl, substi- tuted or unsubstituted benzyl, alkoxy, alkylthio, haloalkoxy, haloalkyl- thio, substituted or unsubstituted phenyl, substituted or unsubstituted phenoxy or phenylthio, a substituted or unsubstituted 5- or 6-membered heterocyclic radical containing one or two heteroatoms, cycloalkyl- substituted alkyl, substituted or unsubstituted alkenyl which may be epoxidized, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl or cycloalkenyl; R1' - cycloalkyl-substituted alkyl, substituted or unsubstituted alkenyl which may be epoxidized, substituted or unsubstituted cycloalkenyl; R2 = CHO, 4,5-dihydrooxazol-2- yl, COYR5, CONR6R7; Y = 0, S; R5 = H, substituted or unsubstituted alkyl, cycloalkyl, substituted or unsubstituted alkenyl, substituted or unsub- stituted cycloalkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted phenyl, a 5- or 6-membered heterocyclic radical contain- ing up to 3 heteroatoms, benzotriazole, N-phthalimido, tetrahydrophthal- imido, succinimido, maleiimido, 2,2-dimethyl-1,3-dioxolan-4-ylmethyl, 1,3-dioxolan-2-on-4-ylmethyl, and when Y = 0: one equivalent of a cation from the group of the alkali or alkaline earth metals, Mn, Cu, Fe, ammonium and substituted ammonium, a radical -N=CR8R9 or -W-Z; R8, R9 = H, substituted or unsubstituted alkyl, substituted or unsubstituted halo- alkyl, cycloalkyl, alkoxy, furanyl, substituted or unsubstituted phenyl; R8+R9 = 4-7-membered methylene chain; W = alkylene chain, ethoxyethylen e chain, butylene, butynylene chain; Z = a molecular moiety bonded to W in the .omega.-position and is the same as that linked to W in the .alpha.- position of W; R6=H, alkyl, cycloalkyl; R7=H; alkyl; -C(0-alkyl)=N-H or -C(0-alkyl)=N- alkyl; R6+R7 = 4-5-membered methylene chain; R3 = H, substituted or unsub- stituted alkyl, substituted or unsubstituted cycloalkyl; R4 = H, OH, alkoxy, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkenyl, substituted or unsub- stituted alkynyl, di-(C1-C4)-alkylamino, a substituted or unsubstituted 5- or 6-membered heterocyclic radical containing one or two heteroatoms, sub- stituted or unsubstituted phenyl, substituted or unsubstituted naphthyl; R3+R4 = 4-7-membered methylene chain which may be interrupted by 0, S o r N-CH3, or -(CH2) 3-CO-) and their environmentally tolerated salts. 40 The compounds Ia to Id are suitable as herbicides.
Abstract:
formulae Ia, Ib and Ic Dicarboximides of the (see formula Ia, Ib, Ic) where X is oxygen or sulfur, R1 is hydrogen, halogen, cyano, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, haloalkoxy, haloalkylthio, alkylsulfonyl, haloalkyl-sulfonyl, phenyl, phenylalkyl, phenoxy or phenylthio, a 5-membered or 6-membered saturated or aromatic heterocyclic radical containing one or two hetero atoms selected from the group consisting of oxygen, sulfur and nitrogen, where the stated organic radicals may be further substituted, and R2 is hydrogen, hydroxyl, alkoxy, alkyl, cycloalkyl, alkenyl, alkynyl, di-C1-C4-alkylamino, a 5-membered or 6-membered heterocyclic saturated or aromatic radical having one or two hetero atoms selected from the group consisting of oxygen, sulfur and nitrogen, phenyl or naphthyl, where the stated organic radicals may be further substituted, and plant-tolerated salts of the dicarboximides I, except for 3-methylisoxazole-4,5-dicarboximide and thiazole-4, 5-dicarboximides in which R2 is phenyl when R1 is methyl or 2-thiazolyl, and herbicides containing these compounds.