Abstract: Fuels for gasoline engines contain small amounts of polyetheramines IR.sup.1 --(OBu).sub.n --NR.sup.2 R.sup.3 (I)whereR.sup.1 is C.sub.2 -C.sub.30 -alkyl,R.sup.2 and R.sup.3, independently of one another, are each hydrogen, C.sub.1 -C.sub.8 -alkyl, aminoalkylene of the general formula II--R.sup.4 --NR.sup.5 R.sup.6 (II)or polyaminoalkylene of the general formula III--(R.sup.4 --NR.sup.5).sub.m --R.sup.6 (III)whereR.sup.4 is C.sub.2 -C.sub.10 -alkylene, R.sup.5 and R.sup.6, independently of one another, are each hydrogen or C.sub.1 -C.sub.8 -alkyl and m is from 2 to 8,Bu is a butylene radical derived from butylene oxide andn is from 12 to 28.

Abstract: In a process for preparing diamines from aminoalcohols and nitrogen compounds selected from the group consisting of ammonia and primary and secondary amines at from 80.degree. to 250.degree. C. and pressures of from 1 to 400 bar using hydrogen in the presence of a zirconium, copper, nickel catalyst, the catalytically active composition comprises from 20 to 85% by weight of oxygen-containing zirconium compounds, calculated as ZrO.sub.2, from 1 to 30% by weight of oxygen-containing compounds of copper, calculated as CuO, from 30 to 70% by weight of oxygen-containing compounds of nickel, calculated as NiO, from 0.1 to 5% by weight of oxygen-containing compounds of molybdenum, calculated as MoO.sub.3, and from 0 to 10% by weight of oxygen-containing compounds of aluminum and/or manganese, calculated as Al.sub.2 O.sub.3 and MnO.sub.2 respectively.

Abstract: A process for preparing glutaraldehyde by reaction of alkoxydihydropyrans of the general formula I ##STR1## where R is C.sub.1 -C.sub.20 -alkoxy, with water at from 0.degree. to 150.degree. C. and from 0.01 to 50 bar in the presence of a catalyst consisting essentially of a bleaching earth.

Abstract: Mixtures which are curable by heating or irradiation with actinic light contain one or more cationically curable compounds, such as an epoxy, an olefinically unsaturated monomer, amino resin or phenolic resin, and as a cationically active curing catalyst one or more N-sulfonylamino-sulfonium salts of the formula ##STR1## such as N-p-toluenesulfonyl-N-methylaminodiphenylsulfonium hexafluorophosphate with or without quinones or peroxides are suitable, inter alia, for producing moldings, coatings, relief images and resist patterns.

Abstract: Acylphosphine compounds of the formula I ##STR1## where X is oxygen, sulfur or an electron pair, R.sup.1 is R.sub.4 or OR.sup.4, R.sup.2 is --OM, where M is a monovalent cation, R.sup.3 is aryl which is substituted at least at the two positions ortho to the carbonyl group, and R.sup.4 is hydrogen, alkyl or aryl, are very effective photoinitiators for photopolymerizable materials, such as coating compositions, finishes, printing inks, unsaturated polyesters, recording media and preferably aqueous polymer dispersions or solutions.

Abstract: Photopolymerizable mixtures comprising one or more photopolymerizable, olefinically unsaturated compounds and one or more photoinitiators or photosensitizers, with or without other conventional additives and/or assistants, contain, as an activator, a tertiary amine of the general formula (I) ##STR1## wherein R.sup.1 and R.sup.2 are each an unsubstituted alkyl, cycloalkyl or phenyl radical, hydroxyl or alkoxy, or R.sup.1 and R.sup.2 are bonded together to form a cyclic alkylene radical, R.sup.3 has the same meanings as R.sup.1 or R.sup.2 and may furthermore be hydrogen, acyloxy or substituted benzoyloxy, and R.sup.4 and R.sup.5 are each an unsubstituted or substituted alkyl, cycloalkyl or phenyl radical, or R.sup.4 and R.sup.5 are bonded together to form a cyclic alkylene or alkyleneoxyalkylene radical.

Abstract: A curable composition consisting ofA. 100 parts by weight of an epoxy resin,B. from 4 to 100 parts by weight of a conventional curing agent for epoxy resins, andC. from 0.1 to 5 parts by weight of an N-acylimidazole which possesses an aromatic acyl component which is substituted at the two positions ortho to the carbonyl groupcan be used to produce moldings, coatings, finishes, adhesives and composite fiber materials.

Abstract: Acylphosphine sulfides of the formula ##STR1## where R.sup.1 is alkyl, cycloalkyl or an unsubstituted or substituted phenyl, naphthyl or heterocyclic radical; R.sup.2 has the meaning of R.sup.1 and can be identical to or different from R.sup.1, or is alkoxy, unsubstituted or substituted phenoxy or phenoxyalkyl, or R.sup.1 or R.sup.2 are linked together to form a ring, which may contain further alkyl substituents and fused-on benzene rings; R.sup.3 is alkyl, a cycloaliphatic radical, substituted phenyl, an unsubstituted or substituted naphthyl or heterocyclic radical or the group ##STR2## where X is unsubstituted or substituted phenylene or an aliphatic or cycloaliphatic divalent radical; and where one or more of R.sup.1, R.sup.2 and R.sup.3 may be olefinically unsaturated.These acylphosphine sulfides can be prepared from acylphosphines and sulfur and can be used as photoinitiators in photopolymerizable compositions.

Abstract: Acylphosphine oxides of the general formula ##STR1## where R.sup.1 is methyl or ethyl, R.sup.2 is a branched or straight-chain alkyl radical or chlorine, alkoxy or hydrogen, R.sup.3 and R.sup.4 are identical or different, and are each alkyl, alkoxy, alkylthio or chlorine and R.sup.5 is hydrogen, chlorine, alkoxy, alkylthio or alkyl, may be used as photoinitiators in photopolymerizable materials.