Abstract: A process for producing a thermoformable polymer/fiber composite using a fibrous substrate, an organic di- or polyisocyanate compound and a dispersion polymer.

Abstract: A process for producing a thermoformable and/or -embossable fiber/polymer composite using a fibrous lignocellulosic substrate S and a polymer P, which contains i) homogeneously mixing the substrate S and the polymer P, then ii) converting the substrate S/polymer P mixture to a fiber web, and then iii) compacting the resultant fiber web at a temperature not less than the glass transition temperature of the polymer P [TgP] to give a thermoformable and/or -embossable fiber/polymer composite, wherein a) the substrate S comprises acetylated lignocellulosic fibers, and b) the polymer P is thermoplastic and has a TgP?20° C. The invention relates to a fiber/polymer molding obtainable by the process and a component in motor vehicle construction, in built structures and in furniture which contains the fiber/polymer molding.

Abstract: Described herein are aqueous binder formulations including organic compounds including acryloyloxy groups and carboxylic acid hydrazides.

Abstract: A process for producing a thermoformable polymer/fiber composite using a fibrous substrate, an organic di- or polyisocyanate compound and a dispersion polymer.

Abstract: A process for producing a thermoformable and/or -embossable fiber/polymer composite using a fibrous lignocellulosic substrate S and a polymer P, which contains i) homogeneously mixing the substrate S and the polymer P, then ii) converting the substrate S/polymer P mixture to a fiber web, and then iii) compacting the resultant fiber web at a temperature not less than the glass transition temperature of the polymer P [TgP] to give a thermoformable and/or -embossable fiber/polymer composite, wherein a) the substrate S comprises acetylated lignocellulosic fibers, and b) the polymer P is thermoplastic and has a TgP?20° C. The invention relates to a fiber/polymer molding obtainable by the process and a component in motor vehicle construction, in built structures and in furniture which contains the fiber/polymer molding.

Abstract: A process for the preparation of 4-acetals of butene-1,4-dial of the formula ##STR1## where R is an alkyl, alkenyl, cycloalkyl or aralkyl radical of 1 to 12 carbon atoms which may contain alkoxy groups, or the two radicals R together form an alkylene or alkenylene radical of 2 to 10 carbon atoms which may contain alkoxy groups, and R.sup.1 is an alkyl, alkenyl or alkynyl radical of 1 to 12 carbon atoms which may be substituted by cycloaliphatic, aromatic or heterocyclic radicals or by hydroxyl, ether, thioether, acyl, alkylamino, carboxyl or carbalkoxy groups, or is an unsubstituted or substituted aryl radical or an alkoxy, alkylthio or acyloxy group, wherein a glyoxal monoacetal of the formula ##STR2## is reacted with an aldehyde of the formulaR.sup.1 --CH.sub.2 --CHO IIIat up to 150.degree. C., and novel acetals of butene-1,4-dial.

Abstract: Motor fuel compositions contain alkoxylation products of oxo oils or their fractions or esters thereof, which are alkoxylated with propene oxide and/or butene oxides and/or not more than minor aomunts of ethene oxide.

Abstract: Cyclopentenones of the formula I ##STR1## where each of R.sup.1 to R.sup.4 is independently of the others hydrogen or an organic radical, are prepared by converting a carboxylic ester of the formula IIa, IIb or IIcR.sup.1 CH.dbd.CR.sup.2 --CHR.sup.3 --CHR.sup.4 --CO.sub.2 R.sup.5 (IIa) and/orR.sup.1 CH.sub.2 --CR.sup.2 .dbd.CR.sup.3 --CHR.sup.4 --CO.sub.2 R.sup.5(IIb) and/orR.sup.1 CH.sub.2 --CHR.sup.2 --CR.sup.3 .dbd.CR.sup.4 --CO.sub.2 R.sup.5(IIc),where each of R.sup.1 to R.sup.4 is as defined above and R.sup.5 is C.sub.1 -C.sub.8 -alkyl, over an acidic heterogeneous catalyst at 50.degree.-800.degree. C. and 0.001-50 bar.

Abstract: Olefinically unsaturated carboxylic esters having a terminal ester group and of the general formulae Ia and IbR.sup.1 --CH.sub.2 --CH.dbd.CH--(CH.sub.2).sub.r--1 --COOR.sup.2 (Ia)R.sup.1 --CH.dbd.CH--(CH.sub.2).sub.r --COOR.sup.2 (Ib)and, if desired, further double bond isomers, where R.sup.1 is hydrogen or an organic radical, R.sup.2 is C.sub.1 -C.sub.8 -alkyl and r is from 1 to 20, are prepared by a process in which an .alpha.-substituted .alpha.,.omega.-(n-alkylenedicarboxylic ester) of the general formula II ##STR1## where R.sup.1 and R.sup.2 and r have the abovementioned meanings and R.sup.3 is C.sub.1 -C.sub.8 -alkyl, is converted over an acidic heterogeneous catalyst at from 150.degree. to 800.degree. C. and under from 0.01 to 50 bar.

Abstract: 2-Substituted 4-acyloxy-2-butenals of the general formula I ##STR1## where R.sup.1 is alkyl of 1 to 12 carbon atoms which may be substituted by cycloalphatic, aromatic or heterocyclic radicals, by alkenyl or alkynyl or by hydroxyl, ether, thioether, acetoxy acyl, alkylamino, carboxyl or carbalkoxy, and R.sup.2 is acyloxy, are prepared by reacting a monosubstituted acetaldehyde of the general formula II ##STR2## where R.sup.2 has the abovementioned meaning, with an aldehyde of the general formula III ##STR3## where R.sup.1 has the abovementioned meaning, in the presence of a linear or cyclic secondary amine and of an organic acid at from 20.degree. to 100.degree. C.