Basf Aktiengesellschaft

Andreas Hohmann

Wolfgang Reuther

Peter Wittmer

Knut Oppenlaender

Rudolf Schuhmacher

Ulrich Riebeling

Brigitte Wegner

Enrique Freudenberg

Peter Ksoll

Arnold De Clercq

Rolf Fikentscher

Erwin Hahn

Roland Ettl

Gabriele Dralle-Voss

Theo Proll

Werner Bochnitschek

Hans-Heinrich Bechtolsheimer

Lothar Hoehr

Kurt Mayer

Gabriele Dralle-Vos

Carlos A Goncalves

Antifoams based on oil-in-water emulsions for the paper industry

Paper size mixtures

Antifoams for the paper industry are based on oil-in-water emulsions in which the oil phase accounts for from 5 to 50% by weight of the emulsion and contains

Antifoams for the paper industry, based on oil-in-water emulsions

A process for preparing carbonyl chlorides of the formula I ##STR1## where R is C.sub.1 -C.sub.30 -alkyl, C.sub.2 -C.sub.30 -alkenyl or C.sub.2 -C.sub.30 -alkynyl, from essentially equimolar amounts of a carboxylic acid of the formula II ##STR2## where R has the abovementioned meanings, and phosgene COCl.sub.2 (III), in the presence of a catalytic adduct of phosgene and N,N-disubstituted formamide or the hydrochlorides thereof, of the formula IV where R.sup.1 and R.sup.2 are each, independently of one another, C.sub.1 -C.sub.3 -alkyl or together are a C.sub.4 -C.sub.5 -alkylene chain which may be interrupted by oxygen or by nitrogen which carries C.sub.1 -C.sub.3 -alkyl or CHO, and n is 0, 1 or 2, wherein the reaction is carried out with a stationary phase of the catalytic adduct, is described.

Preparation of carbonyl chlorides

Acyl chlorides of the general formula ##STR1## where R is C.sub.8 -C.sub.30 -alkyl, C.sub.8 -C.sub.30 -alkenyl or C.sub.8 -C.sub.30 -alkynyl, are prepared from a carboxylic acid of the general formula II ##STR2## where R has the abovementioned meanings, and phosgene, COCl.sub.2 (III), in the presence of a catalyst adduct of phosgene and N,N-dialkylformamide of the general formula IV ##STR3## where R.sup.1 and R.sup.2 independently of one another are each C.sub.1 -C.sub.3 -alkyl, preferably a 1:1 adduct in excess N,N-dialkylformamide, the reaction product I being obtained by phase separation, by a process in which II and III are used in essentially equimolar amounts and the phase containing the catalyst adduct is reused.

Preparation of acyl chlorides

A process is described for the preparation of an N-alkyl- or N,N-dialkyl-1,2-diaminoethane of the general formula I ##STR1## where R.sup.1 is hydrogen or methyl, R.sup.2 is C.sub.1 - to C.sub.5 -alkyl, and R.sup.3 is hydrogen or C.sub.1 - to C.sub.5 -alkyl, with the proviso that the total number of carbon atoms in R.sup.2 and R.sup.3 is an integer from 1 to 6, by reacting an imine of the general formula II ##STR2## with an amine of the general formula III ##STR3## where R.sup.1, R.sup.2 and R.sup.3 are as defined above, which comprises carrying out the reaction in the presence of carbon dioxide at from 10.degree. to 150.degree. C. and at from 0.5 to 50 bar.

Preparation of N-alkyl- and N,N-dialkyldiaminoethanes

Stabilized aqueous C.sub.14 -C.sub.22 -alkyldiketene emulsions containing, as essential components:

Stabilized aqueous alkyldiketene emulsions

Addition salts of cysteamine with acids are prepared by reacting aziridine with an organic sulfur compound of oxidation state -2 and with a ketone and then subjecting the thiazolidine formed as an intermediate to acid hydrolysis, by a process in which aziridine and the ketone are reacted with ammonium hydrogen sulfide or with a metal hydrogen sulfide with the addition of a moderately strong or strong acid at from -10.degree. to +100.degree. C. and a pH which is greater than or equal to 8.5 is maintained.

Preparation of addition salts of cysteamine with acids

Carbonyl halides of the general formula I ##STR1## where R is an organic radical of more than 7 carbon atoms and X is chlorine or bromine, are prepared by reacting carboxylic acids of the general formula II ##STR2## where R has the abovementioned meaning, with phosphorus chlorides or bromides by treating these reaction mixtures with carboxamide/hydrochloride or hydrobromide mixtures which are not homogeneously miscible with the carbonyl halides I and then separating off the carboxamide hydrochloride or hydrobromide phase.

Preparation of carbonyl halides of more than 7 carbon atoms

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Ludwigshafen, Germany

Andreas Hohmann