C08K5/3467

HIGH TEMPERATURE STABLE THERMALLY CONDUCTIVE MATERIALS

Disclosed herein are compositions, preparation methods, and use of thermally conductive materials comprising silicone composition curable by hydrosilylation, thermally conductive fillers, and phthalocyanine. The novel composition retains its desirable pliability after cure even when kept at an elevated temperature for an extended period.

INK COATING FORMULATIONS AND POLYMERIZABLE SYSTEMS FOR PRODUCING THE SAME

Ink and coating compositions, printing and coating processes, and printed and coated substrates utilizing a polymerizable composition comprising one or more di-activated vinyl compounds, with the proviso that said a di-activated vinyl compound is not a cyanoacrylate. Exemplary compositions include methylene malonates, methylene -ketoesters, methylene -diketones, dialkyl disubstituted vinyls, and dihaloalkyl disubstituted vinyls. Exemplary compositions are polymerizable at ambient temperatures.

PVB film with low-migration UV protection
09604433 · 2017-03-28 · ·

Polyvinylacetal films exhibiting high UV absorbance, freedom from cloudiness, and low tendency for UV stabilizer migration use, as a UV absorber, one or more UV absorbers of the formulae (1a), (1b), (2) or (3) in films formed from plasticizer-containing polyvinyl acetal ##STR00001##

PVB film with low-migration UV protection
09604433 · 2017-03-28 · ·

Polyvinylacetal films exhibiting high UV absorbance, freedom from cloudiness, and low tendency for UV stabilizer migration use, as a UV absorber, one or more UV absorbers of the formulae (1a), (1b), (2) or (3) in films formed from plasticizer-containing polyvinyl acetal ##STR00001##

PVB film with low-migration UV protection
09604433 · 2017-03-28 · ·

Polyvinylacetal films exhibiting high UV absorbance, freedom from cloudiness, and low tendency for UV stabilizer migration use, as a UV absorber, one or more UV absorbers of the formulae (1a), (1b), (2) or (3) in films formed from plasticizer-containing polyvinyl acetal ##STR00001##

High temperature stable thermally conductive materials

Disclosed herein are compositions, preparation methods, and use of thermally conductive materials comprising silicone composition curable by hydrosilylation, thermally conductive fillers, and phthalocyanine. The novel composition retains its desirable pliability after cure even when kept at an elevated temperature for an extended period.

High temperature stable thermally conductive materials

Disclosed herein are compositions, preparation methods, and use of thermally conductive materials comprising silicone composition curable by hydrosilylation, thermally conductive fillers, and phthalocyanine. The novel composition retains its desirable pliability after cure even when kept at an elevated temperature for an extended period.

Liquid hardening

Curing agents for air-drying alkyd-based resins, coatings, such as paint, varnish or wood stain, inks and linoleum floor coverings, based on an iron/manganese complex containing tetradentate, pentadentate or hexadentate nitrogen donor ligands are disclosed.

Liquid hardening

Curing agents for air-drying alkyd-based resins, coatings, such as paint, varnish or wood stain, inks and linoleum floor coverings, based on an iron/manganese complex containing tetradentate, pentadentate or hexadentate nitrogen donor ligands are disclosed.

Drier for auto-oxidisable coating compositions

A drier for air-drying an auto-oxidizable resin composition, said drier comprising: 1,4,7-trialkyl-1,4,7-triazacyclononane (L); a manganese salt having the general formula Mn.sup.2+[X].sub.n, wherein anion X is selected from PF.sub.6.sup., SbF.sub.6.sup., AsF.sub.6.sup., BF.sub.4.sup., B(C.sub.6F.sub.5).sub.4.sup., Cl.sup., Br.sup., I.sup., NO.sub.3, or R.sub.2COO.sup. in which case n=2, or the anion X is SO.sub.4.sup.2 in which case n=1, and wherein R.sub.2 is C.sub.1-C.sub.20 alkyl optionally substituted with heteroatoms, C.sub.6-C.sub.20) aryl optionally substituted with heteroatoms, or a polymeric residue; wherein the 1,4,7-trialkyl-1,4,7-triazacyclononane (L) is present in the mixture in an amount such that the molar ratio of Mn:L is at least 1.25:1 and preferably at least 1.5:1.