The invention describes phospho-amino pincer-type ligands, metal complexes thereof, and catalytic methods comprising such metal complexes for conversion of carbon dioxide to methanol, conversion of aldehydes into alcohols, conversion of aldehydes in the presence of a trifluoromethylation agent into trifluorinated secondary alcohols, cycloaddition of carbon dioxide to an epoxide to provide cyclic carbonates or preparation of an amide from the combination of an alcohol and an amine.

The invention relates to a process for preparing isocyanate containing alkoxysilane groups, in which, in the sequence of steps A) to D), A) alkoxysilano(cyclo)alkylamine is reacted with dialkyl carbonate in the presence of a basic catalyst to give alkoxysilano(cyclo)alkylurethane, B) simultaneously or successively, the catalyst is removed and/or deactivated, and low boilers, solids, salt burdens and/or high boilers are removed, C) alkoxysilano(cyclo)alkylurethane obtained after B) is thermally cleaved to release isocyanate containing alkoxysilane groups and by-product, leaving bottoms material, and D) isocyanate containing alkoxysilane groups and by-product are separated from one another and from bottoms material and collected, wherein the basic catalyst is a guanidine base.

This application is in the field of technologies for desulfurization and demercaptanization of gaseous hydrocarbons. The device includes a catalytic reactor loaded with a catalyst solution in an organic solvent, a means of withdrawal sulfur solution from the reactor into the sulfur-separating unit, and a sulfur-separating unit. The said device has at least means of supplying gaseous hydrocarbon medium to be purified and oxygen-containing gas into the reactor, and a means of outletting the purified gas from the reactor. The sulfur-separation unit includes a means of sulfur extraction. The reactor design and the catalyst composition provide conversion of at least 99.99% of hydrogen sulfide and mercaptans into sulfur and disulfides. The catalyst is composed of mixed-ligand complexes of transition metals. The technical result achieved by use of claimed invention is single-stage purification of gaseous hydrocarbons from hydrogen sulfide and mercaptans with remaining concentration of SH down up to 0.001 ppm.

This invention relates to aprocess for the preparation of glycerolcarbonate from the reaction of glycerol and a dialkyl-carbonate, for example dimethyl carbonate, or a cyclic alkylene carbonate. More specifically, the invention relates to a process where the synthesis of glycerolcarbonate is conducted in the presence of a homogeneous transesterificationcatalyst and involves the partial reaction of a glycerol reactant stream and a dialkyl carbonateor cyclic alkylene carbonate reactant stream and an intermediate step of alcohol by-product separation before further reaction in order to improve glycerol conversion and glycerol carbonate selectivity and yield.

Disclosed are processes and intermediates for the preparation of compound (X), which is currently being investigated for the treatment of prostate cancer.

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The present invention relates to a catalyst composition and a process for preparing thereof, wherein the catalyst composition is specifically active for hydro-conversion of LCO involving mainly the partial ring opening of multi-ring aromatics leading to the production of petrochemical feedstock. The catalyst composition comprises of a carrier comprising ultra-stable Y zeolite and binder alumina, group VIB and VIIIB metal species, and organic additives. The carrier is impregnated with metal solution to form active sites of WS.sub.2 slabs of dimensions in the range of 35-45 .

This invention relates to a polymerization catalyst system comprising group 8 or 9 containing non-coordinating anion activator, a polymerization catalyst compound, optional support, and optional scavenger. Preferably, the activator comprises a compound represented by the formula: H.sub.s(L).sub.mM where M is a group 8 or 9 metal, s is 0 or 1, m 1, 2, 3, or 4, each L ligand is independently CO, NR.sub.3, PR.sub.3, where each R, independently is halogen, haloalkyl, or haloaryl) or optionally two or more L ligands may together form a multiply-valent ligand complex. Further, this invention relates to anon-coordinating anion activator represented by the formula: [Z.sub.d].sup.+[H.sub.sL.sub.mM].sup.d, where M, s, m, L, are as defined above, d is 1, 2, or 3 and Z is (L-H) or a reducible Lewis acid; L is a neutral Lewis base; H is hydrogen, and (L-H) is a Bronsted acid. This invention also relates to a process for making a polymeric product comprising contacting a C2-C40 alpha-olefin feed with the polymerization catalyst system to obtain a polymerization reaction mixture; and obtaining a polymer product from the polymerization reaction mixture.

The invention describes phospho-amino pincer-type ligands, metal complexes thereof, and catalytic methods comprising such metal complexes for conversion of carbon dioxide to methanol, conversion of aldehydes into alcohols, conversion of aldehydes in the presence of a trifluoromethylation agent into trifluorinated secondary alcohols, cycloaddition of carbon dioxide to an epoxide to provide cyclic carbonates or preparation of an amide from the combination of an alcohol and an amine.

The present disclosure provides a process for preparing a hydrocarbon fuel from waste rubber. The process involves admixing, in a reaction vessel, at least one fluid medium with the waste rubber to obtain a slurry; wherein the concentration of the waste rubber in the slurry ranges from 45% to 70%. A reactor is charged with the slurry and a predetermined amount of at least one catalyst composition to obtain a mixture, followed by introduction of hydrogen to the reactor to attain a predetermined pressure and heating the mixture at a predetermined temperature, to attain an autogenously generated pressure, and for a predetermined time period to obtain a reaction mass comprising the hydrocarbon fuel. This reaction mass comprising the hydrocarbon fuel is then cooled to obtain a cooled reaction mass. The hydrocarbon fuel is then separated from the cooled reaction mass.

A transformational energy efficient technology using ionic liquid (IL) to couple with monoethanolamine (MEA) for catalytic CO.sub.2 capture is disclosed. [EMmim.sup.+][NTF.sub.2.sup.?] based catalysts are rationally synthesized and used for CO.sub.2 capture with MEA. A catalytic CO.sub.2 capture mechanism is disclosed according to experimental and computational studies on the [EMmim.sup.+][NTF.sub.2.sup.?] for the reversible CO.sub.2 sorption and desorption.