Wacker-chemie Gmbh

Consortium Fur Elektrochemische Industrie Gmbh

Rudolf Kaufmann

Karl-Heinrich Wegehaupt

Norman Haberle

Karl Huhn

Hermann Braunling

Peter Huber

Franz X Wimmer

Karl Braunsperger

Johann Muller

Wolfgang Deinhammer

Johann Bindl

Gunter Von Au

Reinhard Muller

Juurgen Burkhardt

The invention relates to a cleaner and/or conditioner for glass-ceramic surfaces which contains epoxide funcitonal organopolysiloxanes. The cleaner and/or conditioner may additionally contain other components, such as non-reactive organopolysiloxanes, surfactants, organic solvents, scouring agents, acid, additional additives and water, the composition being present as an oil-in-water or a water-in-oil emulsion.

Cleaner and/or conditioners containing organopolysiloxanes for

Novel organopolysiloxanes are described in which the organopolysiloxanes are terminated by units of the formula R.sub.3 SiO.sub.1/2 and comprise units of the formulas RR.sup.1 SiO, RR.sup.2 SiO, RR.sup.3 SiO, RHSiO and R.sub.2 SiO, where R represents the same or different alkyl radicals having from 1 to 4 carbon atoms per radical, or phenyl radicals, R.sup.1 represents the same or different alkyl radicals having at least 6 carbon atoms per radical, R.sup.2 represents the same or different aralkyl radicals and R.sup.3 represents the same or different, SiC-bonded, monovalent organic radicals having at least one vicinal epoxy group per radical. These organopolysiloxanes are preferably prepared by reacting organopolysiloxanes which contain units of the formulas R.sub.3 SiO.sub.1/2 and RHSiO and optionally units of the formula R.sub.2 SiO, wherein R is the same as above, with an organic compound that has a terminal C.dbd.C-bond and at least one vicinal epoxy group per molecule, at least one alkene having at least 6 carbon atoms per molecule, and at least one aralkene in the presence of a catalyst which promotes the addition of Si-bonded hydrogen to the aliphatic C.dbd.C bond. These organopolysiloxanes may be applied simultaneously with a polymer having perfluoroalkyl groups with at least 3 carbon atoms per alkyl group to fibers to render them oil and water repellent.

Organopolysiloxanes having Si-bonded hydrogen and SiC-bonded epoxy

A method for preparing diorganopolysiloxanes containing fluoroalkyl and/or fluoroalkyloxyalkyl groups which comprises hydrolyzing dichlorosilanes containing fluororalkyl and/or fluoroalkyloxyalkyl groups and thereafter equilibrating the hydrolyzed product in the presence of a compound having the formula

Method for preparing diorganopolysiloxanes containing fluoroalkyl groups

A method for stabilizing organopolysiloxanes containing phosphonitrile chlorides or their reaction products which promote the condensation and/or equilibration of organopolysiloxanes which comprises reacting at least one compound containing at least one epoxy group per molecule with the phosphorus compounds present in the organopolysiloxanes.

Method for stabilizing organopolysiloxanes

Organopolysiloxanes having substituted carbamoyloxy groups (.tbd.SiOCO--NH--) bonded to silicon via oxygen, which are prepared by reacting an organopolysiloxane containing Si-bonded hydroxyl groups with an organic isocyanate in the presence of an organic tin compound. The stability of the organopolysiloxanes containing carbamoyloxy groups may be improved if the organopolysiloxane having Si-bonded hydroxyl groups is reacted with an organic isocyanate in the presence of an organic tin compound which is supported on a solid carrier and then the reaction product is filtered under anhydrous conditions to remove the supported organic tin compound.

Process for the preparation of organopolysiloxanes

A process for the production of substituted furans of the general formula ##STR1## wherein R is a member of the group consisting of alkoxy radicals having from 1-6 C-atoms, a substituted aryloxy radical, an unsubstituted aryloxy radical and an alkyl radical, R.sub.1 is a alkyl or aryl radical with 1-6 C-atoms, preferably methyl, R.sub.2 and/or R.sub.3 is an alkyl radical with 1-6 C-atoms or hydrogen by reacting a .beta.-dicarbonyl compound with an .alpha.-chlorocarbonyl compound in the presence of a compound capable of combining with the hydrochloric acid formed, at temperatures between 30.degree. and 100.degree. C., the reaction being carried out at pH values between 2 and 7, preferably between 3.5 and 6, with the addition of equimolar amounts of an alkaline earth carbonate.

Process for the production of substituted furans

A process for the manufacture of furancarboxylic acid anilides of the general formula ##STR1## in which R.sub.1 represents an aryl group or an alkyl group, R.sub.2 and R.sub.3 each represent an alkyl group or hydrogen, by a ring-closure reaction of a .beta.-ketoester with an .alpha.-haloaldehyde or .alpha.-haloketone, in the presence of a stoichiometric amount of a halide-binding substance to form a furancarboxylic acid ester, and by subsequent anilidation, the reaction being performed in two stages, the ring-closure reaction being carried out in the presence of a mixture of alkaline earth metal carbonates and pyridine in a ratio of from 1000 to 5:1 Val, based on the hydrohalic acid liberated, at temperatures between 50.degree. and 100.degree. C.; and after separation in said second stage, the furancarboxylic ester is reacted while stirring with aniline in up to 20 times molecular excess, in the presence of equimolar amounts based on the furancarboxylic acid, of magnesium dianilide and/or aluminum trianilide in liquid phase or in suspension at temperatures between 20.degree. and 180.degree. C., under normal pressure. The furancarboxylic acid anilides have an outstanding pesticidal action.

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Burghausen, Germany

Rudolf Kaufmann