C08G77/10

TWO COMPONENT (2K) COMPOSITION BASED ON MODIFIED EPOXY RESINS

The present invention is directed to a two component (2K) composition comprising: (A) a first component comprising: a) at least one epoxy resin different from said resin b); and, b) at least one elastomer modified epoxy resin; (B) a second component comprising: c) a curative which consists of at least one compound possessing at least two epoxide reactive groups per molecule, said curative being characterized by comprising at least one alkoxy-containing aminofunctional silicone resin,
wherein said composition is characterized in that it is free of catalysts.

UPCYCLING PROCESS FOR PROCESSING SILICONE WASTES

Upcycling process for producing acidic, end-equilibrated siloxanes bearing acetoxy groups and having chain lengths of greater than 3 silicon atoms from end-of-life silicones by thermal digestion in an acidic reaction medium comprising acetic anhydride, acetic acid and at least one further Brønsted acid having a pKa of <4, the digestion taking place in a reactor having a volume of at least 1 liter.

METHOD FOR PREPARING POLY(DIORGANO/ORGANOHYDROGEN)SILOXANE COPOLYMERS
20230331920 · 2023-10-19 ·

A method for preparing a poly(diorgano/organohydrogen)siloxane copolymer is provided. The method includes use of a vibrational spectroscopy technique.

METHOD FOR PREPARING POLY(DIORGANO/ORGANOHYDROGEN)SILOXANE COPOLYMERS
20230331920 · 2023-10-19 ·

A method for preparing a poly(diorgano/organohydrogen)siloxane copolymer is provided. The method includes use of a vibrational spectroscopy technique.

Acetoxy systems

Reaction system for preparing acetoxy function-bearing siloxanes having chain lengths of more than 3 silicon atoms, comprising silanes and/or siloxanes bearing alkoxy groups, silanes and/or siloxanes bearing acetoxy groups, silanes and/or siloxanes bearing hydroxy groups and/or simple siloxane cycles and/or DT cycles, and also a reaction medium comprising acetic anhydride, Brønsted acid and acetic acid, wherein Brønsted acids having a pKa ≤−1.30 are used, and wherein the acetic acid is present in the reaction system in amounts of 0.4 to 15.0 percent by weight, based on the reaction system, wherein the molar ratio of Brønsted acid used to acetic acid is in a defined range, with the proviso that either the sole use of trifluoromethanesulfonic acid and also of trifluoromethanesulfonic acid and acetic acid is excluded, and/or that the Brønsted acid used at least in part has a pKa between −1.3 and >−13.5.

Acetoxy systems

Reaction system for preparing acetoxy function-bearing siloxanes having chain lengths of more than 3 silicon atoms, comprising silanes and/or siloxanes bearing alkoxy groups, silanes and/or siloxanes bearing acetoxy groups, silanes and/or siloxanes bearing hydroxy groups and/or simple siloxane cycles and/or DT cycles, and also a reaction medium comprising acetic anhydride, Brønsted acid and acetic acid, wherein Brønsted acids having a pKa ≤−1.30 are used, and wherein the acetic acid is present in the reaction system in amounts of 0.4 to 15.0 percent by weight, based on the reaction system, wherein the molar ratio of Brønsted acid used to acetic acid is in a defined range, with the proviso that either the sole use of trifluoromethanesulfonic acid and also of trifluoromethanesulfonic acid and acetic acid is excluded, and/or that the Brønsted acid used at least in part has a pKa between −1.3 and >−13.5.

SiOC-based polyethersiloxanes

Branched SiOC-linked polyethersiloxanes have the following formula (I) ##STR00001##
where R.sup.1 is an alkyl radical having 1 to 4 carbon atoms or a phenyl radical, but preferably 90% of the radicals R.sup.1 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 R.sup.2 denotes identical or different polyether radicals, but at least one radical R.sup.2 is a structural element radical of formula (II): ##STR00002##
where p=at least 2, preferably p=2-6, particularly preferably p=3.

Method for condensation polymerization of hydroxyl-terminated polydiorganosiloxanes

A method for making long chain hydroxyl terminated polydiorganosiloxanes with low cyclics content via condensation polymerization employs a selective catalyst. The catalyst includes a salt-anion complex and a free acid.

Method for condensation polymerization of hydroxyl-terminated polydiorganosiloxanes

A method for making long chain hydroxyl terminated polydiorganosiloxanes with low cyclics content via condensation polymerization employs a selective catalyst. The catalyst includes a salt-anion complex and a free acid.

METHOD FOR CONDENSATION POLYMERIZATION OF HYDROXYL-TERMINATED POLYDIORGANOSILOXANES

A method for making long chain hydroxyl terminated polydiorganosiloxanes with low cyclics content via condensation polymerization employs a selective catalyst. The catalyst includes a salt-anion complex and a free acid.