Evonik Degussa Gmbh

Evonik Operations Gmbh

Other

Huels Aktiengesellschaft

Roehm Gmbh Chemische Fabrik

Kaneka Belgium N.v.

Dirk Hoppe

Emmanouil Spyrou

Stephan Kohlstruk

Manfred Kreczinski

Christoph Nacke

Hans-Dieter Zagefka

Andre Raukamp

Rainer Lomölder

Michael Ferenz

Frank Schubert

Clemens Auschra

Gerhard Hoerpel

Monika Berweiler

Holger Loesch

Gerd Loehden

Joachim Venzmer

Rainer Lomoelder

Hinnerk Gordon Becker

Friedrich Georg Schmidt

Axel Hengstermann

Dirk Kuppert

Anne Rittsteiger

Hans Guenther Wey

Alexander Martin Rüfer

Hans-Werner Michalczak

Jan Hendrik Schattka

Annegret Lilienthal

Marita Kaufmann

Sven Schneider

Stefan Röder

Sabrina Sowka

Winfried Belzner

Evelyn Albrecht

Rainer Spittka

Markus Galle

Norbert Schlüter

Martin Schuster

Martin Kothe

Melanie Sajitz

Michael Wolff

Gerd Löhden

Horst Hoffmann

Jutta Stiehl

Alexander Martin RÜFER

Hans Günther Wey

A process for preparing trimers and/or oligomers of diisocyanates is disclosed along with a composition of trimers and/or oligomers formed from diisocyanates and monomeric diisocyanates obtainable by reaction of I. 5-94.999% by weight of A) at least one diisocyanate having a boiling point of less than 250&#xb0; C. (at standard pressure) and/or

Process for preparing trimers and/or oligomers of diisocyanates

The present invention relates to a process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D),

Process for preparing isocyanates containing alkoxysilane groups

The invention relates to a process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D),

The present invention relates to a process for hydrogenating nitrile compounds to amino compounds, in which the cross-sectional loading of the reactor during the hydrogenation is less than or equal to 4.0 kg/m*s, based on the liquid phase.

Process for preparing amino compounds from nitrile compounds

The invention relates to the use of polyolefins modified with one or more silanes as adhesion promoters for the production of flat glass/glass, glass/plastic, or plastic/plastic laminates, to corresponding laminates, and to displays containing the laminates according to the invention.

Use of silane-modified polyolefins as adhesion promoters for the production flat laminates

The invention relates to water-soluble or water-dispersible, hydrophilic polyisocyanates and polyisocyanate mixtures, to a process for preparing them, and to their use as a starting component in the production of polyurethane polymers, more particularly as crosslinkers for water-soluble or water-dispersible film-forming binders, adhesives binders, or sealant binders or binder components with or without groups which are reactive towards isocyanate groups.

Hydrophilic polyisocyanates

The invention relates to a battery comprising an electrode separator arrangement filled with an electrolyte, characterized in that the electrode separator arrangement is at least partially covered with a casting compound (FIG.). The invention also relates to a method for producing such a battery.

Lithium cells and batteries with improved stability and safety, method for the production thereof, and application in mobile and stationary electrical energy accumulators

The invention relates to plastisols which even without the addition of adhesion promoters exhibit high adhesion to metallic and cathodically deposition-coated substrates.

Adhesive agents for plastisols

The invention relates to high-reactivity polyurethane compositions containing uretdione groups and intended for use in the plastics sector.

Highly reactive polyurethane compositions containing uretdione groups

The invention relates to high-reactivity polyurethane compositions. The invention further relates to low temperature curable polyurethane compositions which contain uretdione groups, particularly useful for polyurethane powder coating compositions and adhesive compositions, and to processes for preparing and using the same.

Low temperature curable polyurethane compositions containing uretdione groups

A thermoplastic compound useful in filling pores and voids in wooden materials, particularly edge regions, wherein the thermoplastic compound comprises a blend of two copolyesters and optionally fillers, wherein the first copolyester has a melting point of 140&deg; C. to 260&deg; C. and a glass transition temperature of &minus;10&deg; C. to 80&deg; C., and wherein the second copolyester has a melting point of 120&deg; C. to 190&deg; C. and a glass transition temperature of &minus;70&deg; C. to 10&deg; C. Also, a method of filling pores in a wooden material comprising using a thermoplastic compound having a softening point of 140&deg; C. to 200&deg; C., an open time of 2 to 15 seconds, and a viscosity number of 30 to 150 ml/g, with the thermoplastic compound preferably being a blend of two different copolyesters, wherein the application of such thermoplastic compounds enable the surfaces of chipboard panels and the like to be smoothed in a continuous one-pass process. In particular, immediate aftertreatment such as milling is possible through the use of the thermoplastic compounds.

Thermoplastic compound for filling pores in wooden materials

A coating formulation comprises (A) a base polyester consisting of the copolymerization product of at least one aliphatic, cycloaliphatic and/or aromatic polybasic acid and/or anhydride thereof or at least one hydroxycarboxylic acid or derivative thereof and at least one diol, and (B) an additive polyester resin prepared by condensing at least one unsaturated dicarboxylic acid and optionally at least one saturated dicarboxylic acid monomer with at least one diol and/or triol, wherein the proportion of unsaturated additive polyester to base polyester ranges from 0.1-15 parts to 99.9-85 parts.

Coatings based on thermoplastic polyesters with addition of an

New oligoesters made from a tricyclic diol with 8 to 20 carbon atoms, a dicarboxylic acid with 4 to 20 carbon atoms, and an aliphatic alcohol with 1 to 30 carbon atoms are useful as lubricants, hydraulic oils and compressor oils for mobile field use in forestry and agriculture, in construction, in mining and in transport. The oligoesters have a kinematic viscosity of 50 to 50,000 mm.sup.2 /s at 40.degree. C. and are biodegradable.

Biodegradable oligoesters suitable as lubricants

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Nottuln, Germany

Dirk Hoppe