H.c. Starck Gmbh

H. C. Starck, Gmbh & Co Kg

Bayer Intellectual Property Gmbh

Umicore

H.c. Starck Tungsten Gmbh

H. C. Starck Gmbh & Co

H. C. Starch Gmbh

Covestro Deutschland Ag

Michael Erb

Gerd Maikowske

Juliane Meese-Marktscheffel

Armin Olbrich

Sven Albrecht

Viktor Stoller

Gerhard Gille

Frank Schrumpf

Matthias Jahn

Wolfgang Mathy

Dirk Naumann

Josef Schmoll

Michael Lohse

Rüdiger Zertani

Stefan Malcus

Wolfgang Kummer

Ulrich Krynitz

Astrid G&ouml;rge

Mathias Benz

Evelyn Pross

Uwe Kutzler

Klaus-Jürgen Marschall

Andreas Bulan

Rainer Weber

Ricarda Leiberich

Christoph Schild

Peter Axmann

Margret Wohlfahrt-Mehrens

Daniel Gordon Duff

Astrid Gorge

Michael Kruft

Ines Lamprecht

Frank Van Der Pütten

Anja Weiland

Johannes Poetschke

Mirja Sternberg

Petra Scholz

Dirk Paulmann

Henrik Trümpelmann

Sandra Ströbele

Wolfgang Schweda

Astrid Görge

Michael Reiss

Benno Decker

Michael Reiβ

Gerd Malkowske

Ruediger Zertani

Armin Obrich

Herbert Dittrich

Karl-Heinz Heine

Tino Sauberlich

Josef (deceased) Schmoll

Rudiger Zertani

Frank Van Der Putten

Daniel Duff

The present invention relates to β-nickel hydroxide doped with aluminum ions, in which the aluminum ions are homogeneously distributed in the crystal lattice of the β-nickel hydroxide, as well as a method for their production. The present invention further relates to the use of the β-nickel hydroxide according to the invention as a precursor material for the production of electrode material for lithium-ion batteries and nickel-metal hydride batteries and as a precursor material in the production of Raney nickel catalysts.

Beta-nickel hydroxide doped with aluminum

The present invention relates to a method for producing hard materials that are coated with a cobalt hydroxide compound and to powders that comprise the coated hard material particles, and the use thereof.

Powder comprising coated hard material particles

The invention is directed to a process for preparing a pulverulent compound of the formula NiM1M2O(OH)where M1 is Fe, Co, Zn, Cu or mixtures thereof, M2 is Mn, Al, Cr, B, Mg, Ca, Sr, Ba, Si or mixtures thereof, having the following steps:

Powered compounds, method for the production thereof, and use thereof in lithium secondary batteries

An oxygen-consuming electrode is described, more particularly for use in chloralkali electrolysis, comprising a novel catalyst coating based on silver and a finely divided silver oxide, as is an electrolysis apparatus. Also described is a production process for the oxygen-consuming electrode and the use thereof in chloralkali electrolysis or fuel cell technology.

Oxygen-consuming electrode and process for the production thereof

The invention is directed to a pulverulent compound of the formula NiM1M2O(OH)where M1 is at least one element selected from the group consisting of Fe, Co, Zn, Cu and mixtures thereof, M2 is at least one element selected from the group consisting of Mn, Al, Cr, B, Mg, Ca, Sr, Ba, Si and mixtures thereof, 0.3&#x2266;a&#x2266;0.83, 0.1&#x2266;b&#x2266;0.5, 0.01&#x2266;c&#x2266;0.5, 0.01&#x2266;x&#x2266;0.99 and 1.01&#x2266;y&#x2266;1.99, wherein the ratio of tapped density measured in accordance with ASTM B 527 to the D50 of the particle size distribution measured in accordance with ASTM B 822 is at least 0.2 g/cm&#xb7;&#x3bc;m. The invention is also directed to a method for the production of the pulverulent compound and the use as a precursor material for producing lithium compounds for use in lithium secondary batteries.

[object Object]

A process for preparing a pure ammonium perrhenate includes producing a first aqueous suspension containing an ammonium perrhenate. A stoichiometric amount of a nitric acid is added to the first aqueous suspension so as to produce a second suspension. The second suspension is introduced into a cathode space of an electrolysis cell. The electrolysis cell is divided by a cation-exchange membrane into the cathode space and an anode space. The nitric acid is cathodically reduced to a nitrous acid in the cathode space by applying an electric potential. The nitrous acid is reacted with ammonium ions of the ammonium perrhenate so as to form an aqueous perrhenic acid. Potassium ions are removed from the aqueous perrhenic acid. At least a stoichiometric amount of ammonia is added to the aqueous perrhenic acid so as to produce the pure ammonium perrhenate.

Process for producing pure ammonium perrhenate

The invention relates to a powder compound of the formula NiMO(OH), wherein M represents Co and at least one element selected from the group consisting of Fe, Zn, Al, Sr, Mg, or Ca and mixtures thereof, or M represents Co Mn and Fe, wherein 0.6&#x2266;a&#x3c;1.0, 0&#x3c;b&#x2266;0.4, 0&#x3c;x&#x2266;0.60, and 1.4&#x2266;y&#x3c;2, wherein the powder compound has a particle size distribution dvalue, measured in accordance with ASTM B 822, of &#x3c;5 &#x3bc;m, and wherein a ratio of tap density, measured in accordance with ASTM B 527, to the particle size distribution dvalue is at least 0.4 g/cm. The invention also relates to a process for preparing the compound and its uses.

Process for the production of a powdered spherical tungstic acid by acidification of an aqueous alkaline tungstate solution with mineral acid at elevated temperature, preferably in a continuous stirred tank or a cascade of at least 2 continuous stirred tanks, and tungstic acid obtainable in this way, which is characterized by a high bulk density and spherical morphology.

Tungstic acid powder consisting of spherical tungsten particles and method for producing same

The invention is directed to ammonium paratungstate decahydrate containing at least 75% of crystals having a length of at least 200 &#x3bc;m and having a ratio of length to width of less than 4.5:1.

Ammonium paratungstate hydrates and ammonium paratungstate decahydrate

A method for preparing ammonium heptamolybdate with the steps of:

Method for producing ammonium heptamolybdate

The invention is directed to a method for the production of ammonium paratungstate tetrahydrate by thermal treatment of ammonium paratungstate decahydrate in an aqueous suspension. The ammonium paratungstate tetrahydrate can be produced with high purity and high yield. The production method may furthermore be carried out in a simple and energy-efficient manner.

Method for production of ammonium paratungstate tetrahydrate and highly pure ammonium paratungstate tetrahydrate

The invention is directed to a process for the continuous preparation of ammonium paratungstate hydrate by back reextraction of a tungsten-laden organic phase with an ammonia-containing aqueous solution in a mixer-settler apparatus. The reextraction is carried out at an NH:W molar ratio of from 0.83 to 1.30, and a volume feed ratio of the tungsten-laden organic phase to the ammonia-containing aqueous solution of from 5 to 25. The above crystalline is in high purity and in high yield. The production method can be carried out in a simple and energy-efficient manner.

Method for producing ammonium paratungstate hydrates and ammonium paratungstate decahydrate

Process for the electrochemical decomposition of precursors in powder form by introducing a powder batch between two electrodes of an electrolysis cell, electrodes being designed to be liquid-permeable, and the electrolyte flowing through the powder batch perpendicularly to the electrode surfaces, and electrolysis cell suitable therefor, which is essentially characterized in that at least one electrode has a structure which consists of a supporting pierced plate (), an electrode plate () provided with perforations, and a filter cloth () arranged between the supporting pierced plate () and the electrode plate (), and in that the cathode () is shielded from the cell by means of a liquid-permeable separator ().

Process for the electrochemical decomposition of powders and electrolysis cells suitable therefor

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Goslar, Germany

Juliane Meese-Marktscheffel