Th. Goldschmidt Ag

Goldschmidt Ag

Goldschmidt Ag & Gdf Gesellschaft Fur Dentale Forschung U. Innovationen

Th. Goldschmidt Ag & Gdf Gesellschaft Fur Dentale Forschung U.

Jurgen Fock

Eberhard Esselborn

Dietmar Schaefer

Dietmar Schedlitzki

Eckehard Schamberg

Arno Knebelkamp

Gotz Koerner

Georg Burkhart

Hans-Ferdi Fink

Ulrich Holtschmidt

Werner Schafer

Volker Mohring

Gunter Hahn

Helmut Buhler

Volker Zellmer

Helmut Lammerting

Karl-Heinz Reichert

Hans Rott

Otto Klocker

Wernfried Heilen

Manfred Schmuck

Alfred Walter

Hans-Heinrich Schlons

Gunter Wagenknecht

Stephan Fengler

Roland Smolin

Michael Barkowsky

Wolfgang Hoffmann

Gunther Hahn

Wilhelm Ahrens

Gunter Wagerknecht

Holger Wacker

.alpha., .omega.-polymethacrylate glycols of the general formula ##STR1## are prepared and a method for their synthesis and their use as only or partial glycol component for the preparation of polyesters and polyurethanes and for the modification of alkyd and epoxide resins are described.

.alpha., .omega.-polymethacrylate glycols, methods for their synthesis

Polyacrylate esters having an average molecular weight of 1500 to 20,000 and being obtainable by the transesterification of alkyl polyacrylates, obtained by free radical polymerization and containing 1 to 4 carbon atoms in the alkyl group, with

Use of polyacrylate esters as dispersants

Disclosed are polymethacrylic esters of the central formula ##STR1## in which the radicals R.sup.1 are identical or different and are alkyl radicals having 1 to 8 carbon atoms, perfluoroalkyl radicals or dialkylaminoalkyl radicals, and

Polymethacrylic esters whose ester groups in position and differ from

.alpha.,.omega.-polymethacrylate dicarboxylic acids of the general formula ##STR1## wherein R.sup.1 is an optionally halogenated alkyl group with 1 to 22 carbon atoms, wherein the R1 group can assume different meanings in the polymer molecule, R.sup.2 is the group of a known chain transfer agent, which has a terminal --COOH croup and a has a value not less than 4. The invention furthermore relates to the synthesis of these compounds and their use as sole or partial components for the synthesis or modification of polyepoxides, polyesters, polyamides, alkyd resins or polyurethanes.

.alpha., .omega.-polymethacrylate dicarboxylic acids, their synthesis

Novel polymethacrylate esters are prepared; the ester groups of which in the .alpha. and optionally also in the .omega. position differ from the ester groups in the chain. The invention furthermore relates to a method for the synthesis of these compounds by transesterification under selected method conditions.

Polymethacrylate esters, the ester groups of which in the .alpha. and

Novel polymethacrylate esters are prepared; the ester groups of which in the .alpha. and optionally also in .omega. the position differ from the ester groups in the chain. The invention furthermore relates to a method for the synthesis of these compounds by transesterification under selected method conditions.

Polyolefins, polyolefin blends and elastomer-modified polyolefins containing additives to increase the surface polarity are prepared. They contain AB block copolymers as additives. A method for preparation of polyolefins, polyolefin blends and elastomer-modified polyolefins with a polar surface is defined as well as the method of preparing the polyolefins articles.

Polyolefins, polyolefin blends and elastomer-modified polyolefins with

Inventive block copolymers are prepared, and their synthesis is described. These inventive block copolymers act as polymeric surfactants, especially as emulsifiers and surfactants, and as compounds having antistatic properties.

Polymethacrylate-polymethacrylic acid block copolymers

The invention relates to polymethacrylate ester/polysiloxane block copolymer of the ABA or AB type, A being a polymethacrylate ester block and B a polysiloxane block. The invention furthermore relates to a method for the synthesis of such block copolymers as well as to a method to modify synthetic resins, particularly those based on (meth)acrylates, by adding an effective amount of the inventive block copolymer. The invention also relates to the block copolymer as additives for organic lacquer and varnish systems.

Polymethacrylate ester/polysiloxane block co-polymers method for

A mixed block copolymer of the A-B type is prepared. The A block of the block copolymer is formed by the polymerization of compounds having vinyl groups and the B block of which is a polyoxyalkylene block, obtainable by polymerizing, first of all, monomers having vinyl groups at temperatures of 60.degree. to 150.degree. C. by a free radical mechanism in the presence of sufficient amounts of an initiator and an amount, which corresponds to the desired chain length, of a chain-length regulator, which carries, aside from a mercapto group, a further functional group having at least one active hydrogen and adding alkylene oxide, optionally in the presence of a known addition reaction catalyst, in an addition reaction at 20.degree. to 180.degree. C. onto the polymer so modified, until the desired molecular weight of block B is reached.

Polyvinyl-polyoxyalkylene block copolymers

A poly(meth) acrylic acid dispersion with an organic solvent as outer phase, the dispersed phase particles having a low polydispersity is obtained by the free radical polymerization of (meth) acrylic acid and optionally co-monomers, which bring about a cross-linking of the poly(meth) acrylic acid, in a nonpolar, organic solvent in the presence of stabilizers, costabilizers, and initiators. The stabilizer is a block copolymer.

(meth) acrylic acid polymer dispersion

Polyacrylate esters with long-chain hydrocarbon and polyoxyalkylene groups are disclosed, which are prepared by transesterification of polyacrylate alkyl esters, the alkyl groups of which have 1 to 4 carbon atoms and which were obtained by free radical polymerization, wherein the transesterification is carried out with a mixture of selected alcohols and polyoxyalkylene monools. Compared to products obtained by copolymerization, the transesterification products are largely free of undesirable low molecular weight components, have a narrow molecular weight distribution and exhibit excellent surfactant properties. They are useful especially as W/O emulsifiers for natural and synthetic oils.

Polyacrylate esters with long-chain hydrocarbon and polyoxyalkylene

Polyacrylate esters with long-chain alkoxylated hydrocarbonoxy groups are disclosed which can be obtained by the transesterification of polyacrylate esters with polyoxyalkylene monools, wherein the polyacrylate esters, up to 50% of which can be replaced by the corresponding methacrylate esters, have been obtained by free radical polymerization and wherein the polyoxyalkylene monools have the average formula

Polyacrylate ester with long-chain alkoxylated hydrocarbonoxy groups and

Polyacrylate esters with ammonium salt groups obtained by the transesterification of alkyl polyacrylates produced by free radical polymerization are disclosed, wherein the alkyl groups of the acrylate esters have 1 to 8 carbon atoms, up to 50% of the acrylate esters can be replaced by the corresponding methacrylate esters and the transesterification is carried out with

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Dusseldorf, Germany

Jurgen Fock