Th. Goldschmidt Ag

Evonik Degussa Gmbh

Evonik Goldschmidt Corporation

Goldschmidt Ag

Goldschmidt Gmbh

Evonik Operations Gmbh

Volker Zellmer

Georg Burkhart

Andreas Weier

Rolf-Dieter Langenhagen

Matthias Lobert

Wilfried Knott

Michael Ferenz

Frank Schubert

Volker Mohring

Melanie Roessing

Hans-Heinrich Schlons

Andreas Sellmann

Jurgen Fock

Tammo Boinowitz

Anke Lewin

Bastian Matthias Brugger

Rainer Ziegler

Ralf Hoffmann

Hans-Heinrich Schl&ouml;ns

Gerhard Kettenbach

Thomas Reibold

Bernd-Jurgen Klietsch

Felix M&uuml;ller

Anja Brösgen

Peter Cramers

Andreas Weir

Anette Brune-Fischer

Anette Brune

Irina Neisius-Sellmann, Legal Representative

Andrea Villa

Gerrit Wienhöfer

Described are a process for producing hydrosilylable polyoxyalkylene ethers, comprising the steps of (1) alkoxylation of at least one terminally unsaturated alcohol with alkylene oxides to afford a polyoxyalkylene ether, (2) etherification of the polyoxyalkylene ether from step (1) and (3) neutralization of the product from step (2) under buffered conditions, and hydrosilylable polyoxyalkylene ether mixtures.

Process for producing hydrosilylable polyoxyalkylene ethers

The invention relates to alkoxylation products, their preparation, compositions comprising the alkoxylation products of the invention, and the use thereof as or for producing adhesives and sealants.

Modified alkoxylation products which have alkoxysilyl groups and contain urethane groups, and their use

Alkoxylation products, their preparation, compositions comprising these alkoxylation products, and the use thereof as or for producing adhesives and sealants.

Modified alkoxylation products having at least one non-terminal alkoxysilyl group and a plurality of urethane groups, and their use

The invention relates to a process for preparing polyethers of the formula (I)R&#x2014;(CHRCHR&#x2014;O)&#x2014;H&#x2003;&#x2003;(I)

Process for alkoxylation with DMC catalysts in a loop reactor with ejector

The invention relates to a process for simultaneously performing two chemically successive reactions in a loop reactor, specifically reaction I) an optionally catalyzed equilibrium reaction between high-boiling liquid reactants, in which essentially one high boiler is formed as an intermediate and at least one low boiler as a by-product, and reaction II) a substantially diffusion-controlled reaction in which the liquid intermediate is reacted with at least one gaseous reactant to give the end product, wherein reactions (I) and (II), optionally after a start phase, are allowed to proceed simultaneously in the same apparatus, specifically loop reactor, and the loop reactor has a connectable gas-liquid circulation system coupled via an ejector mixing nozzle, in which circulated liquid phase is mixed in the ejector mixing nozzle with newly supplied gaseous reactant of reaction (II) () and/or gaseous reactant of reaction (II) aspirated by means of the ejector from the reactor via a connectable condenser (), and fed to the reactor by a liquid jet ejector () for the reaction, the low-boiling by-product(s) of reaction (I) and also any low-boiling solvent being condensed and discharged in the condenser continuously over the duration of the process. In particular, the invention relates to a process for etherifying high-boiling polyether alcohols.

Equilibrium reaction and gas/liquid reaction in a loop reactor

The invention relates to the use of metal salts of ricinoleic acid or solutions thereof in water or in organic solvents in producing polyurethane foams.

Use of metal salts of ricinoleic acid in producing polyurethane

The invention relates to a method for the production of high resilience polyurethane foams by reacting a mixture of highly reactive polyols, which usually have an average molecular weight of between about 4800 and 6500 g/mole and at least 70% primary hydroxyl groups and optionally contain fillers, polyfunctional isocyanates, amine activators, cross-linking agents, tin catalysts, blowing agents and stabilizers, compounds of the general formula ##STR1## being used as stabilizers, in which R.sup.1 is the same or different in the average molecule and represents a methyl group or a group of the general formula --CH.sub.2 --CH.sub.2 --(CH.sub.2).sub.a --C.sub.6 H.sub.3 (R.sup.2).sub.2 (a=0 or 1; R.sup.2 =--O--CH.sub.3), with the proviso that at least one R.sup.1 group is a group having the formula --CH.sub.2 --CH.sub.2 --(CH.sub.2)a--C.sub.6 H.sub.3 (R.sup.2).sub.2

Method for producing cold polyurethane foams

The invention relates to polysiloxanes with 1) at least two polyether groups A and B, polyoxyalkylene group, with an average molecular weight of 600 to 5,500, consisting of 20 to 100% by weight of oxyethylene units and of 80 to 0% by weight of oxypropylene units and the polyoxyalkylene group B, with an average molecular weight of 700 to 5,000, consisting of 0 to &lt;20% by weight of oxyethylene units and of 100 to 80% by weight of oxypropylene units, and with 2) hydrocarbon groups with 6 to 30 carbon atoms, linked to silicon. The invention further relates to the synthesis of these polysiloxanes and their use as additives for hair cosmetics, particularly as additives for hair shampoos to improve the handle and the combability of the hair.

Polysiloxane-polyoxyalkylene block copolymers and their use as additives

High resilience polyurethane foams are produced by reacting a mixture of highly reactive polyols having a weight average molecular weight between about 4800 and 6500 g/mole and containing at least 70% primary hydroxyl groups and optionally fillers, polyfunctional isocyanates, amine activators, cross-linking agents, tin catalysts, blowing agents and stabilizers. The inventive stabilizers can be used universally in high resilience slabstock foam systems as well as in high resilience molded foam systems and in formulations based on pure TDI, TDI/MDI mixtures as well as on pure MDI in combination with appropriate polyols.

Polysiloxane-polyoxyaikylene block copolymers, which are intended for the production of polyurethane foams, are prepared. The foams obtained have an improved, finer cell structure and the collapse of the foams is reduced. It is essential for the invention that a mixture of polyoxyalkylene groups is present in the polysiloxane-polyoxyalkylene block copolymers. Further particulars are laid down for selecting the different polyoxyalkylene groups with regard to the respective molecular weights and the ratio of polyoxyalkylene groups to one another.

Polysiloxane-polyoxyalkylene block copolymers with different

Polysiloxane-polyoxyalkylene block copolymers, which are intended for the production of polyurethane foams, are prepared. The foams obtained have an improved, finer cell structure and the collapse of the foams is reduced. It is essential for the invention that a mixture of polyoxyalkylene groups is present in the polysiloxane-polyoxyalkylene block copolymers. Further particulars are laid down for selecting the different polyoxyalkylene groups with regard to the respective molecular weights and the ratio of polyoxyalkylene groups to one another.

Polysiloxane-polyoxyalkylene block copolymers having different polyoxyalkylene blocks in the average molecule are prepared. The mixture of the polyoxyalkylene blocks consists of at least one polyoxyalkylene group A and at least one polyoxyalkylene group B and/or at least one polyoxyalkylene group C, each polyoxyalkylene group A having an average molecular weight of 600 to 5,500 and consisting of 20 to 90% by weight of oxyethylene units and 80 to 10% by weight of oxypropylene units, polyoxyalkylene group B having an average molecular weight of 500 to 5,000 and consisting of 2 to 19% by weight of oxyethylene units and 98 to 81% by weight of oxypropylene units, polyoxyalkylene group C having an average molecular weight of 1,500 to 4,500 and consisting of oxypropylene units. Up to 20% by weight of the oxypropylene units is replaceable by oxybutylene units and the molar ratio of polyoxyalkylene groups A to the sum of the polyoxyalkylene groups B and C is 1:4 to 4:1. The block copolymers are highly effective stabilizers for the production of flexible polyurethane foams with an excellent ratio of cell fineness of the foam to air permeability of the foam.

A method for the preparation of highly elastic foams of reduced compression hardness and having urethane groups is disclosed, in which the reaction of the polyurethane-forming materials is carried in the presence of 0.01 to 5% by weight, based on the polyol, of a compound, which has at least one polyoxyalkylene group and at least one anionic group in the molecule. The use of fluorocarbons to decrease the compression hardness can reduced appreciably by the use of this compound.

Method for the preparation of highly elastic forms of reduced

A method for the preparation of flexible foams containing urethane groups and having a reduced hardness is disclosed. Polyethers, having at least two hydroxyl groups and a molecular weight of 400 to 12,000 are reacted with polyisocyanates in the presence of catalysts and water and, optionally, in the presence of emulsifiers, stabilizers, cross linking agents, blowing agents and conventional auxiliaries and additives. The method is carried out in the presence of 0.01 to 1.0 parts by weight, based on 100 parts by weight of the polyol, of the alkali salt or the alkaline earth metal salt of a hydroxycarboxylic acid. The method enables the use of chlorofluorocarbons to be omitted largely or completely as physical blowing agents.

Method for the preparation of flexible polyurethane foams with reduced

A method is disclosed for the preparation of flexible polyester polyurethane foam by reaction of at least difunctional polyesterols with at least difunctional organic isocyanates in the presence of catalysts and a stabilizer mixture of organic and organosilicon compounds, water, optionally blowing agents and optionally conventional additives, wherein the stabilizer mixture used comprises

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Bottrop, Germany

Volker Zellmer