Basf Aktiengesellschaft

Basf Se Corporation

Alfred Thome

Heinz-Walter Schneider

Daniel Heineke

Rocco Paciello

Jurgen Kanand

Rolf Pinkos

Werner Bertleff

Wolfgang Rohde

Karsten Eller

Jens Scheidel

Alexander Panchenko

Manfred Stroezel

Heinz-Josef Kneuper

Arnd Garsuch

Michael Roeper

Carsten Oost

Christian Miller

Sigmar Bräuninger

Gunther Achhammer

Wilfried Berning

Sigmar BRÄUNINGER

A process is proposed for reprocessing the exhaust gas from a plant for producing hydroxylamine or hydroxylammonium salts by catalytic reduction of nitrogen monoxide with hydrogen for the purpose of utilization of at least a part of the nitrogen monoxide and if appropriate hydrogen present in the exhaust gas for producing hydroxylamine or hydroxylammonium salts, which comprises, in a first separation stage, selectively separating off nitrogen monoxide from the exhaust gas of the plant for producing hydroxylamine or hydroxylammonium salts.

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Process for working up an exhaust gas from a system for producing hydroxylamine or hydroxylammonium salts by catalytic reduction of nitrogen monoxide with hydrogen, the exhaust gas containing nitrogen monoxide, hydrogen, dinitrogen monoxide, nitrogen and ammonia. At least some of the hydrogen present in the exhaust gas is separated off from the exhaust gas by means of a gas-tight membrane-electrode assembly which comprises at least one selectively proton-conducting membrane, a retentate side, a permeate side, and, on each side of the membrane, at least one electrode catalyst, wherein, on the retentate side of the membrane, at least some of the hydrogen is oxidized to protons at the anode catalyst and the protons, after crossing the membrane, are, on the permeate side, at the cathode catalyst according to (I) reduced to hydrogen and/or (II) reacted with oxygen to form water, the oxygen originating from an oxygen-containing stream which is contacted with the permeate side.

Process for working up an exhaust gas from a system for producing hydroxylamine or hydroxylammonium salts

Method of manufacturing a hydrogenation catalyst

Preparation of n-butyraldehyde and/or n-butanol

A carbon-containing catalyst support is prepared by treating the carbon-containing catalyst support with a compound of the formula I

Preparation of a hydrogenation catalyst using M(OR).sub.m X.sub.n

A process for the preparation of a hydrogenation catalyst by reduction of platinum in an oxidation stage of not less than 2 in an aqueous medium in the presence of a carboniferous support, optionally following partial poisoning with a sulfur, arsenic, tellurium, or antimony-containing compound, using a reducing agent, in which the reducing agent used is an ammonium or phosphonium salt of the general formula I

Process for the preparation of a hydrogenation catalyst

A process for the catalytic isomerization of secondary .alpha.-alkenols of formula I ##STR1## in which R.sup.1 is a C.sub.1 -C.sub.20 alkyl group or a C.sub.2 -C.sub.2 alkenyl group and in which R.sup.2 stands for hydrogen, a halogen atom, a C.sub.1 -C.sub.10 alkoxy group, a carbonyl group, or a C.sub.1 -C.sub.20 alkyl group and in which R.sup.1 and R.sup.2 can be joined together to complete a five-membered or six-membered carbocyclic ring, to primary .alpha.-alkenols of formula II ##STR2## or for the isomerization of primary .alpha.-alkenols of formula II to secondary .alpha.-alkenols of formula I, wherein the isomerization is carried out in the presence of organotrioxorhenium(VII) compounds of formula III ##STR3## in which R.sup.3 is a C.sub.1 -C.sub.10 alkyl group, a cyclopentadienyl group substituted by from one to five C.sub.1 -C.sub.4 alkyl groups, an unsubstituted cyclopentadienyl group, a C.sub.6 -C.sub.10 aryl group, or a C.sub.7 -C.sub.11 aralkyl group, or wherein the isomerization is carried out in the presence of organotrioxorhenium(VII) compounds of formula III attached to a polymeric support.

Catalytic isomerization of .alpha.-alkenols

Octadienols are prepared by reacting 1,3-butadiene with water in the presence of a catalyst system comprising a palladium compound, a triorganophosphorus compound and carbon dioxide and in the additional presence of a triorganophosphine oxide.

Preparation of octadienols

Growing community of inventors

Speyer, Germany

Alfred Thome