Basf Aktiengesellschaft

Basf Se Corporation

Stefan Karbach

Eberhard Ammermann

Rainer Seele

Gisela Lorenz

Hubert Sauter

Ernst-Heinrich Pommer

Reiner Kober

Ulrich Schirmer

Bernd Janssen

Barbara A Schwalge

Wolfgang Steglich

Timm Anke

Norbert Goetz

Norbert Meyer

Costin Rentzea

Hans-Gert Recker

Karl-Otto Westphalen

Bruno Wuerzer

Thomas Zierke

Wilhelm Rademacher

Thomas Kuekenhoehner

Johann Jung

Marco Thyes

Guenter Wegner

Gerhard Wagenblast

Wolfgang Rohr

Joachim Leyendecker

Walter Himmele

Torsten Mattke

Eckhard Hickmann

Matthias Zipplies

Lothar Rueb

Heinz Isak

Bernhard Zipperer

Paul S Zorner

Guenter Herrmann

Wolfgang Gerlinger

Burkhardt Dames

Gert Buerger

Gerhard Frank

Wolfgang Will

Ruediger Schmitz

Kerstin Heinen

Dale R Carlson

Hubert Smuda

Jost H Manegold

Barbara A Moore

Wolfgang Haip

Gerhard Laur

The subject of the present invention is an apparatus for the intermixing of a fluid stream with a fluid stream, which comprises a pipe through which the fluid stream is routed, at least two distributors for delivering the fluid stream being arranged inside the pipe, this arrangement of the distributors being made possible by bores in the casing of the pipe, and these distributors having a free flow cross section which is constant or decreases continuously, as seen in the main direction of flow of the fluid, and the distributors having one or more rows of holes for delivering the fluid into the fluid.

Method and apparatus for the intermixing of two fluid streams

A process for working up mother liquors resulting from the preparation of adipic acid by oxidation of cyclohexanol or cyclohexanone or mixtures thereof with nitric acid entails removal of nitric acid by azeotropic distillation with water, heating the resulting melt at from 130.degree. to 180.degree. C. and then dissolving it in water, treating the aqueous solution with cation exchangers, subsequently again evaporating off the water and heating the resulting dicarboxylic acid melt at from 200.degree. to 240.degree. C. and then obtaining a mixture of dicarboxylic acids by distillation.

Workup of mother liquors resulting from the preparation of adipic acid

Azolylmethyloxiranes of the general formula I ##STR1## where A and B are cycloalkyl, tetrahydropyranyl, tetrahydrofuranyl, dioxanyl, norbornyl, cycloalkenyl or phenyl, each of these radicals being unsubstituted or substituted, with the proviso that A and Z are not simultaneously phenyl, D is O, X is CH or N, and their plant-tolerated acid addition salts or metal complexes, and fungicides containing these compounds.

Azolylmethylcycloalkyloxiranes and their use as crop protection agents

A process for preparing .alpha.,.alpha.-dialkoxy ketones of the formula I ##STR1## where R.sup.1 and R.sup.2 are each, independently of one another, hydrogen, C.sub.1 -C.sub.20 -alkyl, C.sub.3 -C.sub.20 -cycloalkyl, C.sub.4 -C.sub.30 -cycloalkylakyl, C.sub.9 -C.sub.30 -alkylcycloalkyl, unsubstituted or C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy-, halogen-, C.sub.1 -C.sub.4 -haloalkyl-, C.sub.1 -C.sub.4 -haloalkoxy-, phenyl-, phenoxy-, halophenyl-, halophenoxy- and/or cyano-substituted aryl, C.sub.7 -C.sub.20 -aralkyl or heterocyclyl,

Preparation of .alpha.,.alpha.-dialkoxy ketones

Azolylmethyloxiranes of the general formula I ##STR1## where A and B are cycloalkyl, tetrahydropyranyl, tetrahydrofuranyl, dioxanyl, norbornyl, cycloalkenyl or phenyl, each of these radicals being unsubstituted or substituted, with the proviso that A and B are not simultaneously phenyl, D is O, X is CH or N, and their plant-tolerated acid addition salts or metal complexes, and fungicides containing these compounds.

Azolymethylcycloalkyloxiranes and therir use as crop protection agents

Vinylazoles of the general formula I ##STR1## where R.sup.1 and R.sup.2 are alkyl, cycloalkyl, tetrahydropyranyl, pyridyl, naphthyl, biphenyl or phenyl, these radicals being substituted or unsubstituted, X is CH or N, and plant-tolerated acid addition salts and metal complexes thereof, and crop protection agents containing these compounds.

Vinylazoles and the use thereof for crop protection

Azolylmethyloxiranes of the general formula I ##STR1## where R.sup.1, R.sup.2 and R.sup.3 are substituted or unsubstituted alkyl, benzyl, naphthyl, biphenyl, dioxanyl, phenyl, tetrahydropyranyl, tetrahydrofuranyl, norbornyl, C.sub.3 -C.sub.12 -cycloalkyl or C.sub.3 -C.sub.12 -cycloalkenyl, and X is CH or N, and plant-tolerated acid addition salts and metal complexes thereof, and fungicides containing these compounds.

Azolylmethyloxiranes and fungicides containing them

Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes of the general formula I ##STR1## wherein R.sup.1 and R.sup.2 are alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl,

Substituted imidazolylmethyloxiranes and substituted imidazolypropenes

Ethereal solutions of arylmethylmagnesium halides

Preparation of ethereal solutions of arylmethyl-magnesium halides

Azolylmethyloxiranes of the general formula I ##STR1## where R.sub.1 and R.sub.2 are substituted or unsubstituted alkyl, naphthyl, biphenyl, dioxanyl or phenyl,

Azolylmethyloxiranes and fungicides containing these compounds

Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes of the general formula I ##STR1## where R.sup.1 and R.sup.2 are alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl,

Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes,

Azolylmethylcyclopropanes of the formula ##STR1## where R is alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, and these radicals are substituted or unsubstituted, A is H, F, Cl or Br, and X is CH or N, their plant-tolerated acid addition salts and metal complexes, and fungicides and growth-regulating agents containing these compounds.

Azolylmethylcyclopropanes and their use as crop protection agents

N-aminotriazole derivatives of the general formulae Ia and Ib ##STR1## wherein R.sup.1 and R.sup.2 are each C.sub.1 -C.sub.8 -alkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.5 -C.sub.8 -cycloalkenyl, tetrahydropyranyl or norbornyl, or phenyl, biphenyl, naphthyl or pyridyl, and the aromatic radicals may carry from one to five halogen atoms and/or from one to three of the following groups: hydroxyl, phenoxy, nitro, amino, cyano, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy and/or C.sub.1 -C.sub.4 -alkylthio, and their salts which are environmentally compatible and tolerated by crops.

N-aminotriazole derivatives

Imidazolylmethyloxiranes of the general formula I ##STR1## where R is phenyl, pyridyl, tetrahydropyranyl, norbornyl, C.sub.3 -C.sub.12 -cycloalkyl or C.sub.5 -C.sub.8 -cycloalkenyl, these radicals being unsubstituted or substituted, and their plant-tolerated acid addition salts and metal complexes, and fungicides containing these compounds.

Fungicidal imidazolylmethyloxiranes

Thiophene compounds of the formula I ##STR1## where the substituents and the index have the following meanings: n is 0 or 1;

Thiophene compounds

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Neustadt, Germany

Stefan Karbach