Abstract: The loom contains a weaving station, at which warp yarns can be interwoven by at least one weft yarn, a device for supplying the warp yarns, and a device for supplying the at least one weft yarn. A shedding device for forming a shed from the warp yarns, and a weft insertion needle for inserting a weft yarn loop into the shed, are also present. The weft yarn loop is tied off with a knitting needle and beaten with a reed. A take-down device serves to draw off the woven fabric that is produced. In order to produce a profiled woven article, the weaving station is assigned a fabric holder with a shaping aperture whose opening cross section corresponds substantially to the cross section of the profiled woven article that is to be produced with a round or polygonal cross section.

Abstract: The loom contains a weaving station, at which warp yarns can be interwoven by means of at least one weft yarn, a device for supplying the warp yams, and a device for supplying the at least one weft yam. A shedding device for forming a shed from the warp yarns, and a weft insertion needle for inserting a weft yarn loop into the shed, are also present. The weft yam loop is tied off with a knitting needle and beaten with a reed. A take-down device serves to draw off the woven fabric that is produced. In order to produce a profiled woven article, the weaving station is assigned a fabric holder with a shaping aperture whose opening cross section corresponds substantially to the cross section of the profiled woven article that is to be produced with a round or polygonal cross section.

Abstract: A crosslinkable hot-melt adhesive for coating and/or laminating sheeting materials is described, whereby the hot-melt adhesive is an amino-terminated copolyamide and the crosslinking agent belongs to the chemical class of multifunctional acrylic acid esters and/or multifunctional acrylamides.

Abstract: A process and a composition for the production of crosslinkable hotmelts for the coating and/or lamination (bonding) of substrates are described, whereby the hotmelt is an amine-terminated copolyamide and the crosslinker belongs to the class of multifunctional acrylates and/or multifunctional acrylamides.

Abstract: Water-soluble, biologically decomposable carbonic acid polyesters having the general formula (I): ##STR1## in which R.sub.1 represents a straight- or branched-chain, saturated or monounsaturated alkyl residue having from 6 to 22 carbon atoms;R.sub.2 represents a hydrogen or methyl group;R.sub.3 represents hydrogen or the group: ##STR2## n is an integer between 0 and 10; m is an integer between 5 and 16, andz is an integer between 1 and 3 are disclosed.The use of these compounds for preparation and lubricating agents for synthetic fibers is also disclosed.

Abstract: The invention relates to a process for the preparation of .alpha.,.beta.-unsaturated N-substituted carboxylic acid amides, novel .alpha.,.beta.-unsaturated N-substituted carboxylic acid amides, a process for the polymerization of these novel .alpha.,.beta.-unsaturated N-substituted carboxylic acid amides, including the polymers, and the use of these polymers as sedimentation, flocculating, dewatering and retention aids, as additives for mineral oils, and as ion exchangers.The .alpha.,.beta.-unsaturated N-substituted carboxylic acid amides are prepared by transamidation of .beta.-hydroxy or .beta.-alkoxy carboxylic acid amides with primary amines and heating of the N-substituted .beta.-hydroxy or .beta.-alkoxy carboxylic acid amides obtained as intermediate products in the vapor phase in the presence of catalysts. Primary amines are preferably used in the conversion which have no hydrogen beta to the amino group.These .alpha.,.beta.

Abstract: The invention relates to a process for the preparation of .alpha., .beta.-unsaturated N-substituted carboxylic acid amides, novel .alpha., .beta.-unsaturated N-substituted carboxylic acid amides, a process for the polymerization of these novel .alpha., .beta.-unsaturated N-substituted carboxylic acid amides, including the polymers, and the use of these polymers as sedimentation, flocculating, dewatering and retention aids, as additives for mineral oils, and as ion exchangers.The .alpha., .beta.-unsaturated N-substituted carboxylic acid amides are prepared by transamidation of .beta.-hydroxy or .beta.-alkoxy carboxylic acid amides with primary amines and heating of the N-substituted .beta.-hydroxy or .beta.-alkoxy carboxylic acid amides obtained as intermediate products in the vapor phase in the presence of catalysts. Primary amines are preferably used in the conversion which have no hydrogen beta to the amino group.These .alpha.,.beta.

Abstract: The invention relates to a process for the preparation of N-substituted acrylamides of the general formula ##STR1## wherein Y denotes a bivalent straight - or branched chain radical with 2 to 30, preferably 2 to 18, and particularly 2 to 6 carbon atom-, preferably a group of the formula (Y.sub.1).sub.m -(Y.sub.2).sub.n -(Y.sub.3).sub.t, in whichY.sub.1, Y.sub.2 and Y.sub.3 each stands for an alkylene group or the radical of a cyclic organic ring system with 5 or 6 carbon atoms, and the sum of m, n, and t is 2 or 3, and R.sub.1 denotes hydrogen or the radical of an amine of the formula N(R.sub.2) (R.sub.3),whereinR.sub.2 and R.sub.3 stand for alkyl radicals with 1 to 4 carbon atoms, which method is characterized in that dihydracrylic acid amide of the general formula ##STR2## is transmitted with amines of the general formulaH.sub.2 N--(Y)--R.sub.1 (III)with elimination of ammonia and the resulting N-substituted .beta.

Abstract: Process for the manufacture of .alpha.,.beta.-unsaturated N-substituted carboxylic acid amides of the general formula ##STR1## in which R.sup.1 represents H or CH.sub.3R.sup.2 represents H or CH.sub.3, andY represents a divalent straight-chain or branched organic radical having 2-30 carbon atoms, andR.sup.3 represents H or the radical of an amine of the formula --N(R.sup.4)(R.sup.5), in which R.sup.4 and R.sup.5 represent alkyl radicals having 1 to 4 carbon atoms,by reacting .beta.-substituted carboxylic acid amides of the formula ##STR2## in which Z represents OH or the radical R.sup.6 O--, in which R.sup.6 is an alkyl radical having 1 to 4 carbon atoms,with amines of the general formulaH.sub.2 N--(Y)--R.sub.3 IIIat temperatures in the range of 100.degree. to 200.degree. C., preferably 120.degree. to 175.degree. C., with the elimination of ammonia, and heating the resulting N-substituted .beta.-hydroxycarboxylic or .beta.