Abstract: An unbalance arrangement for a compactor roller of a soil compacter includes a first unbalance mass unit rotatable around an unbalance axis of rotation having a first center of mass eccentric with respect to the unbalance axis of rotation, a second unbalance mass unit rotatable around the unbalance axis of rotation having a second center of mass eccentric with respect to the unbalance axis of rotation, an unbalance drive for jointly driving the first unbalance mass unit and the second unbalance mass unit to rotate around the unbalance axis of rotation, and a phase position adjustment unit for adjusting a phase position of the first center of mass with respect to the second center of mass around the unbalance axis of rotation. The phase position adjustment unit includes a spur gear arrangement in the torque transmission path between the unbalance drive and the first unbalance mass unit or the second unbalance mass unit.

Abstract: A soil-processing roller for a soil-processing machine includes a roller sleeve extending longitudinally in the direction of a roller axis of rotation, surrounding the roller axis of rotation, a first drive transmission element connected or connectable such that it can rotate to a rotor region of a roller drive motor for combined rotation about the roller axis of rotation, a first roller sleeve connecting element connected to the first drive transmission element by means of a plurality of first elastic suspension elements and to the roller sleeve for combined rotation about the roller axis of rotation, a second drive transmission element arranged at an axial distance to the first drive transmission element and connected by means of a drive transmission element connection arrangement to the first drive transmission element for torque transmission and a second roller sleeve connecting element connected to the second drive transmission element by means of a plurality of second elastic suspension elements and con

Abstract: An unbalance arrangement for a compactor roller of a soil compacter includes a first unbalance mass unit rotatable around an unbalance axis of rotation having a first center of mass eccentric with respect to the unbalance axis of rotation, a second unbalance mass unit rotatable around the unbalance axis of rotation having a second center of mass eccentric with respect to the unbalance axis of rotation, an unbalance drive for jointly driving the first unbalance mass unit and the second unbalance mass unit to rotate around the unbalance axis of rotation, and a phase position adjustment unit for adjusting a phase position of the first center of mass with respect to the second center of mass around the unbalance axis of rotation. The phase position adjustment unit includes a spur gear arrangement in the torque transmission path between the unbalance drive and the first unbalance mass unit or the second unbalance mass unit.

Abstract: A soil-processing roller for a soil-processing machine, comprising includes a roller sleeve extending longitudinally in the direction of a roller axis of rotation, surrounding the roller axis of rotation, a first drive transmission element connected or connectable such that it can rotate to a rotor region of a roller drive motor for combined rotation about the roller axis of rotation, a first roller sleeve connecting element connected to the first drive transmission element by means of a plurality of first elastic suspension elements and to the roller sleeve for combined rotation about the roller axis of rotation, a second drive transmission element arranged at an axial distance to the first drive transmission element and connected by means of a drive transmission element connection arrangement to the first drive transmission element for torque transmission and a second roller sleeve connecting element connected to the second drive transmission element by means of a plurality of second elastic suspension elem

Abstract: A method for detecting hydrogen peroxide wherein a sample is contacted with a peroxidase or a peroxidatively-active substance and a redox indicator of the following ##STR1## in which A and D independently of one another represent phenyl, pyridyl or imidazolyl,G represents O, CH.sub.2 or S,m represents the number zero or one, andX represents O, ##STR2## or --NR.sup.1 --NR.sup.2 -- R.sup.1 and R.sup.2, independently of one another, denote hydrogen, alkyl, cycloalkyl, aryl or aralkyl, or --NR.sup.1 R.sup.2 together represent a pyrrolidine, pyrazoline, piperidine, piperazine or morpholine radical andT denotes hydrogen, hydroxyl, alkyl, aryl, alkoxy, phenoxy, SO.sub.3 H, --COOH or ##STR3## whereby a color change is brought out if hydrogen peroxide is present.

Abstract: The present invention relates to new chromogenic amino acid esters and peptide esters of hydroxyisoquinolines and hydroxyquinolines, processes for their preparation and the use of the new esters as substrates for the analytical detection of esterolytic and/or proteolytic enzymes, for example in body fluids, the esters being incorporated into test agents, in particular test strips, in a suitable manner. The new esters are particularly used for the detection of leukocytes, in particular in urine.

Abstract: Azo dyestuffs of the formula ##STR1## wherein R.sub.1 denotes acyl,R.sub.2 denotes hydrogen, fluorine, chlorine or trifluoromethyl,R.sub.3 denotes hydrogen, optionally substituted C.sub.1 -C.sub.4 -alkyl, cyclohexyl or optionally substituted phenyl andR.sub.4 denotes hydrogen or C.sub.1 -C.sub.4 -alkyl groupare suitable for dyeing natural and synthetic fibre materials, for example for dyeing wool or polyamide fibres, in level read to violet shades with very good fastnesses to light, wet processing and perspiration, the color yield being good.

Abstract: 4-Alkyl-2-trifluoromethylanilines, in particular the 4-isopropyl derivative, are starting materials for preparing valuable azo dyestuffs. While the nonionic dyestuff types can preferably be used in transfer printing synthetic hydrophobic fibre materials, the sulpho-containing dyestuffs--in particular those based on "gamma acid"--are suitable for dyeing polyamides.

Abstract: Azo dyestuffs which contain at least one water-solubilizing group and have the formula ##STR1## wherein K stands for the radical of a coupling component,R.sub.1 stands for CN, COOX, CONXY or COZ,R.sub.2 stands for hydrogen, halogen, CN, alkyl or aryl,R.sub.3 stands for alkyl or aryl,X stands for H, alkyl, alkenyl, cycloalkyl, aryl or aralkyl andY stands for H or alkyl andZ stands for alkyl or aryl,are highly suitable for dyeing polyamide fibres. The resulting dyeings are distinguished by good all-round fastness properties.

Abstract: A composition and test device for determining the presence of an analyte selected from leukocytes, esterase and protease in a test sample. The composition comprises an ester capable of producing a detectable response upon interaction with said analyte, and a diazonium salt having the structure ##STR1## in which A.sup.- is an anion, and R same or differ, is H, lower alkyl, aryl, or both of R together form a fused ring system, and in which R' is H, OH or lower alkyl.

Abstract: Metal complexes, particularly copper and nickel complexes of azo dyes corresponding to general formula (I) are suitable as color dyes for the production of color images by the dye diffusion transfer process. The dyes are (in non-metallized form), in the form of so-called "dye-releasers", bound to a redox-active carrier radical provided with a ballast group, which dye-releasers are associated to a light-sensitive silver halide emulsion layer. During development, the metallizable dyes are image-wise released and are converted, after diffusion into a light-receiving layer, into the corresponding metal complexes ##STR1## wherein E represents an electron acceptor radical; andK represents the radical of an azo coupler component, derived from an open-chain or closed ring ketomethylene compound, a cyclic enamine compound or a phenolic compound.

Abstract: Dyes corresponding to general formula (I) are released imagewise from corresponding dye-releasers in the dye diffusion transfer process. They react with nickel ions to form lightfast, cyan dye-metal complexes having advantageous spectral properties: ##STR1## wherein Q represents the group required for completing an optionally substituted phenyl or naphthyl group;X represents --S--, --SO.sub.2 --, --SO.sub.2 --NR.degree.-- or --SO.sub.2 --O--;R.degree. represents H or alkyl; andR.sup.1 represents an aliphatic, araliphatic or a carbocyclic or heterocyclic aromatic group or, when X represents --SO.sub.2 --NR.degree.--, R.sup.1 represents hydrogen.

Abstract: Azo dyes corresponding to the formula (II): ##STR1## wherein G represents a group capable of forming a 5-membered chelate ring and R.sup.5 represents aryl or a thienyl group, combined with metal ions, in particular copper or nickel ions, to form stable azo dye-metal complexes which have advantageous spectral properties. They are therefore particularly suitable for the production of highly light-fast cyan images, e.g. by the Ink-Jet process, in which they may be used directly in the form of colored inks, or by the dye diffusion transfer process, in which they are released image-wise from corresponding dye-releasers in the course of development and transferred to a dye-absorbent layer.

Abstract: Azo dyes corresponding to the formula (I): ##STR1## wherein R.sup.1 represents a releasable group, R.sup.2 represents H, halogen or sulphonyl, R.sup.3 and R.sup.4 represent H or groups not capable of chelate formation, and Q represents a group for completing a phenyl or naphthyl group,combine with nickel ions to form stable azo dye-metal complexes which have advantageous spectral properties. They are therefore particularly suitable for the production of highly light-fast magenta images, e.g. by the ink jet process, in which they may be used directly in the form of colored inks, or by the dye diffusion transfer process, in which they are released imagewise from suitable dye-releasers in the course of development and transferred to a dye-receptive layer.

Abstract: Metal complexes, particularly copper and nickel complexes, of azo dyes corresponding to formula suitable for use as magenta-colored image dyes for the production of colored images by the dye diffusion transfer process. The dyes are linked (in non-metallized form) to a carrier radical provided with a ballast group as so-called color-providing compounds which are associated with a photosensitive silver halide emulsion layer. During development, the metallizable dyes are released imagewise and, after diffusion into an image-receiving layer, are converted into the corresponding metal complexes. ##STR1## In formula II, R.sup.1, R.sup.2, R.sup.3 and R.sup.4 represent H, F, Cl, Br, --CN, --NO.sub.2, --CF.sub.3, --OCH.sub.3, --SCF.sub.3, alkyl, alkoxy, alkylthio, acylamino, alkyl sulphonyl, aryl sulphonyl, --CO--X or --SO.sub.2 Y; or two adjacent radicals from the group of radicals R.sup.1 to R.sup.4 together represent a fused benzene ring;R.sup.

Abstract: Process for the preparation of styryl dyestuffs of the formula ##STR1## in which R.sub.1 and R.sub.2 denote hydrogen, alkyl, alkoxy or halogen andX denotes an alkylene radical,characterized in that compounds of the formula ##STR2## in which X, R.sub.1 and R.sub.2 have the meaning given for formula (I) andR denotes alkyl or aryl,are hydrolyzed by means of mineral acid to give compounds of the formula (I) and the latter are isolated.

Abstract: Azo dyes of formula II are released on development from dye releasers which are associated with a light-sensitive silver halide emulsion layer. The azo dyes are chelatable and form with metal ions blue or cyan dye-metal-complex image dyes. ##STR1## In the formula A.sup.1 and A.sup.2 represent electronegative substituents whose meta-sigma values .sigma..sub.m (according to D. H. McDaniel and H. C. Brown in J. Org. Chem. 23, 420 et seq (1958) conform to at least one of the following three relationships:1. .sigma..sub.m (A.sup.1), .sigma..sub.m (A.sup.2) +0.332. .sigma..sub.m (A.sup.1) +.sigma..sub.m (A.sup.2) +0.75;3. .sigma..sub.m (A.sup.1) +0.33 and A.sup.2 represents--SO.sub.2.sup.XX represents H, --OH, --NH.sub.

Abstract: Cyan images may be prepared by the dye diffusion transfer process, using dye-releasers which on development release diffusible dyes capable of forming light-fast cyan metal-dye-complexes particularly with copper or nickel ions. As also the dye-releasers are capable of complexation, cyan images can be prepared not only from the released dyes but also from the dye-releasers ("retained image"). Released dyes and dye-releasers of the present invention contain a chromophor of the following formula: ##STR1## wherein R.sup.1, R.sup.2, R.sup.3 and R.sup.4, which may be the same or different, each represents --H, --F, --Cl, --Br, --CN, --NO.sub.2, --CF.sub.3, --OCF.sub.3, --SCF.sub.3, alkyl, alkoxy, alkylthio, acylamino, alkylsulfonyl, arylsulfonyl, --CO--X or --SO.sub.2 --Y or two adjacent groups R.sup.1 -R.sup.4 together constitute a condensed benzene ring which may contain further substituents;R.sup.5 represents hydrogen or a substituent having an electron donor character;R.sup.

Abstract: For the production of light-fast yellow images (transfer images and retained images) by the dye diffusion transfer process dye-releasers are useful which on development release diffusible azo dyes which can complex with nickel or copper ions and which in one of their tautomeric forms correspond to the general formula: ##STR1## wherein R.sup.1 represents alkyl, alkenyl or cycloalkyl having up to 8 carbon atoms,Z represents a radical required for completing a benzene or naphthalene ring; andL represents a substituent having a group which results from the splitting from a carrier radical.

Abstract: 2-Amino-6-nitrobenzothiazole is obtained with a high selectivity if, instead of unprotected 2-aminobenzothiazole, acylation products thereof are nitrated and the acyl groups are then split off. 2-Amino-6-nitrobenzothiazole is an important intermediate product for the preparation of valuable azo dyestuffs.