Abstract: Branched SiOC-linked polyethersiloxanes have the following formula (I) where R1 is an alkyl radical having 1 to 4 carbon atoms or a phenyl radical, but preferably 90% of the radicals R1 are methyl radicals; b has a value of from 1 to 10; a has a value of from 1 to 200, preferably 10 to 100, a value of from 3 to 70 when b is ?1 and ?4, or a value of from 3 to 30 when b is >4; and R2 denotes identical or different polyether radicals, but at least one radical R2 is a structural element radical of formula (II): where p=at least 2, preferably p=2-6, particularly preferably p=3.

Abstract: A process for the recycling of silicones, especially silicone rubber and/or silicone oils, by the chemical transformation thereof to silanes and/or siloxanes having acetoxy groups is described, wherein silicone rubber and/or silicone oils are subjected to a heat treatment in digestion systems comprising acetic anhydride and/or acetoxysiloxane, and at least one Brønsted acid, with addition of acetic acid.

Abstract: Processes are described for purifying acidic, preferably superacidic, in particular trifluoromethanesulfonic acid-acidified, end-equilibrated acetoxysiloxanes, wherein the acidic, preferably superacidic, in particular trifluoromethanesulfonic acid-acidified, acetic anhydride-containing and optionally acetic acid-containing equilibrated, preferably end-equilibrated acetoxysiloxane, which is optionally dissolved in an inert solvent, is contacted with a base, the precipitate is filtered off thereafter and then the filtrate obtained is optionally purified by distillation.

Abstract: Process for producing PU foams by reacting at least one polyol component with at least one isocyanate component in the presence of one or more catalysts that catalyse the isocyanate-polyol and/or isocyanate-water reactions and/or isocyanate trimerization, and optionally one or more chemical or physical blowing agents, with use of SiOC-bonded polyether siloxanes having branching in the siloxane moiety, prepared from branched siloxanes bearing acetoxy groups, wherein a sufficient amount of the SiOC-bonded polyether siloxane having branching in the siloxane moiety is added that the proportion by mass of this polyether siloxane (e) based on the finished PU foam is from 0.0001% to 10% by weight.

Abstract: SiOC-based polyethersiloxanes are prepared based on linear ?,?-hydroxy group-bearing siloxanes. In a first step, ?,?-acetoxy group-bearing linear polysiloxanes are prepared. In a second step, the ?,?-acetoxy group-bearing linear polysiloxanes are converted into the desired organosiloxane units, preferably shorter organosiloxane units, wherein the thus converted organosiloxane units have ?,?-acetoxy groups. In a third step, the ?,?-acetoxy group-bearing linear polysiloxanes from step 2 react with polyetherols to give SiOC-based polyethersiloxanes.

Abstract: Described is a process for producing SiOC-bonded polyether siloxanes branched in the siloxane portion from cyclic branched siloxanes of the D/T type, wherein said process comprises in a first step reacting the mixtures of cyclic branched siloxanes of the D/T type with acetic anhydride optionally in admixture with simple siloxane cycles under acid catalysis to afford acetoxy-bearing branched siloxanes, in a second step performing the equilibration of the acetoxy-modified branched siloxane with superacid, preferably with addition of acetic acid and in a third step reacting the superacid-treated acetoxysiloxane with polyetherols optionally in the presence of bases and optionally in the presence of an inert solvent.

Abstract: Described is a process for producing SiOC-bonded polyether siloxanes branched in the siloxane portion from cyclic branched siloxanes of the D/T type, wherein said process comprises in a first step reacting the mixtures of cyclic branched siloxanes of the D/T type with acetic anhydride optionally in admixture with simple siloxane cycles under acid catalysis to afford acetoxy-bearing branched siloxanes, in a second step performing the equilibration of the acetoxy-modified branched siloxane with superacid, preferably with addition of acetic acid and in a third step reacting the superacid-treated acetoxysiloxane with polyetherols optionally in the presence of bases and optionally in the presence of an inert solvent.

Abstract: Described is a process for producing preferably trifluoromethanesulfonic acid-acidified, end-equilibrated, acetoxy-bearing siloxanes which comprises reacting cyclic siloxanes, in particular comprising D4 and/or D5, and/or cyclic branched siloxanes of the D/T type with acetic anhydride using preferably trifluoromethanesulfonic acid as catalyst and with addition of acetic acid, wherein the cyclic branched siloxanes of the D/T type are mixtures of cyclic branched siloxanes of the D/T type which contain not only siloxanes comprising D and T units but also siloxanes comprising Q units.

Abstract: Described is a process for producing preferably trifluoromethanesulfonic acid-acidified, end-equilibrated, acetoxy-bearing siloxanes which comprises reacting cyclic siloxanes, in particular comprising D4 and/ or D5, and/or cyclic branched siloxanes of the D/T type with acetic anhydride using preferably trifluoromethanesulfonic acid as catalyst and with addition of acetic acid, wherein the cyclic branched siloxanes of the D/T type are mixtures of cyclic branched siloxanes of the D/T type which may contain not only siloxanes comprising D and T units but also siloxanes comprising Q units.

Abstract: Described is a process for producing SiOC-bonded polyether siloxanes branched in the siloxane portion from cyclic branched siloxanes of the D/T type, wherein said process comprises in a first step reacting the mixtures of cyclic branched siloxanes of the D/T type with acetic anhydride optionally in admixture with simple siloxane cycles under acid catalysis to afford acetoxy-bearing branched siloxanes, in a second step performing the equilibration of the acetoxy-modified branched siloxane with trifluoromethanesulfonic acid, preferably with addition of acetic acid, and in a third step reacting the trifluoromethanesulfonic acid-treated acetoxysiloxane with polyetherols optionally in the presence of bases and optionally in the presence of an inert solvent.

Abstract: Mixtures of cyclic branched siloxanes having exclusively D and T units, with the proviso that the cumulative proportion of the D and T units having Si-alkoxy and/or SiOH groups that are present in the siloxane matrix, determinable by 29Si NMR spectroscopy, is less than 2.0 and preferably less than 1.0 mole percent, are described, as are branched organomodified siloxanes obtainable therefrom.

Abstract: Mixtures of cyclic branched siloxanes having exclusively D and T units and having no functional groups, with the proviso that the cumulative proportion of the D and T units having Si-alkoxy and/or SiOH groups that are present in the siloxane matrix, determinable by 29Si NMR spectroscopy, is ?2 mole percent, are described, as are branched organo-modified siloxanes obtainable therefrom.

Abstract: Described is a process for producing trifluoromethanesulfonic acid-acidified, end-equilibrated, acetoxy-bearing siloxanes which comprises reacting cyclic siloxanes, in particular comprising D4 and/or D5, and/or cyclic branched siloxanes of the D/T type with acetic anhydride using trifluoromethanesulfonic acid as catalyst and with addition of acetic acid.

Abstract: The production of SiOC-bonded, linear polydimethylsiloxane-polyoxyalkylene block copolymers comprising repeating (AB) units by reaction of polyether diols with trifluoromethanesulfonic acid-acidified, equilibrated ?,?-diacetoxypolydimethylsiloxanes is described, wherein the reaction is undertaken by adding a solid, liquid or gaseous base, optionally using inert solvents.

Abstract: The invention relates to a method for producing siloxanes that have glycerin modifications and, at the same time, hydrophobic substituents. The invention further relates to a siloxane that has glycerin modifications and also hydrophobic side chains, wherein at least some of the glycerin modifications bear ketal groups, and to the use of said new siloxanes.

Abstract: A process for producing SiOC-bonded polyether siloxanes by transesterification of alkoxysiloxanes with polyetherols in the presence of zinc acetylacetonate as catalyst is described.

Abstract: Mixtures of cyclic branched siloxanes having exclusively D and T units and having no functional groups, with the proviso that the cumulative proportion of the D and T units having Si-alkoxy and/or SiOH groups that are present in the siloxane matrix, determinable by 29Si NMR spectroscopy, is ?2 mole percent, are described, as are branched organomodified siloxanes obtainable therefrom.

Abstract: Described is a method for synthesizing polymer compounds (P), preferably polysiloxanes, comprising at least one carboxylic ester group, in particular (meth)acrylate-containing polysiloxanes, said method being carried out in the presence of conversion products (U) of metal salts, in particular chromium(III) salts, and conversion products of aldehydes and primary amines.

Abstract: Mixtures of cyclic branched siloxanes having exclusively D and T units, with the proviso that the cumulative proportion of the D and T units having Si-alkoxy and/or SiOH groups that are present in the siloxane matrix, determinable by 29Si NMR spectroscopy, is greater than 2 and less than 10 mole percent, are described, as are branched organomodified siloxanes obtainable therefrom.

Abstract: The invention relates to a method for producing siloxanes that have glycerin modifications and, at the same time, hydrophobic substituents. The invention further relates to a siloxane that has glycerin modifications and also hydrophobic side chains, wherein at least some of the glycerin modifications bear ketal groups, and to the use of said new siloxanes.