A composition comprising a supported hydrogenation catalyst comprising palladium and a support, wherein the supported hydrogenation catalyst is capable of selectively hydrogenating highly unsaturated hydrocarbons to unsaturated hydrocarbons; and a dopant comprising a fluorene structure. A method of making a selective hydrogenation catalyst including contacting a support with a palladium-containing compound to form a supported-palladium composition; contacting the supported-palladium composition with a dopant comprising a fluorene structure group to form a selective hydrogenation catalyst precursor; and reducing the selective hydrogenation catalyst precursor to form the selective hydrogenation catalyst. A method of selectively hydrogenating highly unsaturated hydrocarbons to an unsaturated hydrocarbon enriched composition by contacting a supported catalyst comprising palladium and a dopant comprising a fluorene structure with a feed comprising highly unsaturated hydrocarbon under conditions suitable for hydrogenating at least a portion of the highly unsaturated hydrocarbon feed to form the unsaturated hydrocarbon enriched composition.

A composition comprising a supported hydrogenation catalyst comprising palladium and a support, wherein the supported hydrogenation catalyst is capable of selectively hydrogenating highly unsaturated hydrocarbons to unsaturated hydrocarbons; and a dopant comprising a fluorene structure. A method of making a selective hydrogenation catalyst including contacting a support with a palladium-containing compound to form a supported-palladium composition; contacting the supported-palladium composition with a dopant comprising a fluorene structure group to form a selective hydrogenation catalyst precursor; and reducing the selective hydrogenation catalyst precursor to form the selective hydrogenation catalyst. A method of selectively hydrogenating highly unsaturated hydrocarbons to an unsaturated hydrocarbon enriched composition by contacting a supported catalyst comprising palladium and a dopant comprising a fluorene structure with a feed comprising highly unsaturated hydrocarbon under conditions suitable for hydrogenating at least a portion of the highly unsaturated hydrocarbon feed to form the unsaturated hydrocarbon enriched composition.

Provided is an antimicrobial photoreactive composition comprising a photocatalytic multijunction composite that is photoreactive in ordinary room lighting and comprises at least one photocatalytic heterojunction that is primarily carbon based. The composition further comprises at least one surface-coupling material, optionally at least one additive selected from a charge-transfer augmenting material, a light-capturing augmenting material, an antimicrobial augmenting material(s), or a combination thereof, and a carrier. The composition can be coupled to a surface or embedded in a cationic polymer matrix to form an antimicrobial film that is removable. Further provided is a method of disinfecting a surface comprising applying the antimicrobial photoreactive composition to a surface.

The present invention provides a photolatent Ti-chelate catalyst formulation, comprising (i) at least one compound of the formula (I) wherein R.sub.1 is C.sub.1-C.sub.20alkyl or C.sub.2-C.sub.20alkyl which is interrupted by one or more non-consecutive O-atoms; Y is formula (II) or optionally substituted phenyl; Y.sub.1 is formula (III) or optionally substituted phenyl; Y.sub.2 is formula (IV) or optionally substituted phenyl; Y.sub.3 is formula (V) or optionally substituted phenyl; R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10, R.sub.11, R.sub.12 and R.sub.13 independently of each other are hydrogen, halogen, optionally substituted C.sub.1-C.sub.20alkyl, or R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10, R.sub.11, R.sub.12 and R.sub.13 independently of each other are optionally substituted C.sub.6-C.sub.14aryl, provided that only one of R.sub.2, R.sub.3, R.sub.4 is hydrogen and only one of R.sub.5, R.sub.6, R.sub.7 is hydrogen and only one of R.sub.8, R.sub.9, R.sub.10 is hydrogen and only one of R.sub.11, R.sub.12, R.sub.13 is hydrogen; and (ii) at least one chelate ligand compound of the formula IIa, IIb or IIc, wherein Y is formula (VI) or formula (VII); Y.sub.1 is formula (VIII) or formula (IX); R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6 and R.sub.7 independently of each other have on of the meanings as given for R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10, R.sub.11, R.sub.12 and R.sub.13; and R.sub.14, R.sub.15 and R.sub.16 independently of each other have on of the meanings as given for R.sub.14, R.sub.15 and R.sub.16. ##STR00001##

The invention provides a method of treating waste comprising the steps of: providing an electrochemical cell comprising a cathode, and an anode; supplying a waste stream comprising an organic compound which is a liquid or dissolved in a solvent and contacting the anode and cathode with the waste stream; electrochemically oxidising the organic compound at the anode; supplying oxygen to the cathode; electrochemically reducing the oxygen at the cathode; wherein the cathode comprises a poison resistant oxygen reduction catalyst.

The present invention discloses a composite catalyst for the photocatalytic isomerization of norbornadiene to prepare quadricyclane, comprising: a solid photocatalyst, selected from the group consisting of TiO.sub.2, Ti-MCM-41, Ti-SBA-15, ZnO, WO.sub.3, Ta.sub.2O.sub.5 or SrTiO.sub.3; and an organic photo-sensitizer loaded on the surface or in the channel of said solid photocatalyst, selected from benzophenone, acetophenone, Michler's Ketone, tetraethyl Michler's Ketone, and diethyl Michler's Ketone, where the organic photo-sensitizer is present in the solid photocatalyst in an amount of 0.5% to 20% by weight. The catalyst of the invention can catalyze a target reaction under the condition that no solvent is used, and the yield of the target product quadricyclane is higher. Furthermore, the catalyst of the invention has a stable activity, and it can be recycled. The invention further discloses a process for preparing the composite catalyst.

A hydroprocessing catalyst or catalyst precursor has been developed. The catalyst is a unique transition metal tungsten oxy-hydroxide material. The hydroprocessing using the transition metal tungsten oxy-hydroxide material or the decomposition product thereof may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

A hydroprocessing catalyst has been developed. The catalyst is a unique transition metal tungsten oxy-hydroxide material. The hydroprocessing using the transition metal tungsten oxy-hydroxide material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

Layered double hydroxides having a high surface area (at least 125 m.sup.2/g) and the formula (I)
[M.sup.z+.sub.1?xM.sup.y+.sub.x(OH).sub.2].sup.a+(X.sup.n?).sub.a/n.sub.+bH.sub.2O.c(AMO-solvent)(I)
wherein M and M are different and each is a charged metal cation (and must be present), z=1 or 2; y=3 or 4, 0<x<0.9, b is 0 to 10, c=0 to 10, X is an anion, n is the charge on the anion, and a=z(1?x)+xy?2; AMO-solvent is aqueous miscible organic solvent, may be prepared by a method which comprises a) precipitating a layered double hydroxide having the formula
[M.sup.z+.sub.1?xM.sup.y+.sub.x(OH).sub.2].sup.a+(X.sup.n?).sub.a/n.sub.+bH.sub.2O wherein M, M, z, y, x, a, b and X are as defined above from a solution containing the cations of the metals M and M and the anion X.sup.n?; b) ageing the layered double hydroxide precipitate obtained in step a) in the original solution; c) collecting, then washing the layered double hydroxide precipitate; d) dispersing the wet layered double hydroxide in an AMO solvent so as to produce a slurry of the layered double hydroxide in the solvent; e) maintaining the dispersion obtained in step d); and f) recovering and drying the layered double hydroxide. The high surface area products have low particle size and are particularly suitable for use as catalysts, catalyst supports, sorbents and coatings.

Embodiments of the invention relate to a method for preparing a hydroprocessing catalyst including supporting a carrier with one or more hydrogenation metal components selected from the group consisting of VIB, VIIB, and VIII group metals of the periodic table; drying and calcining the supported carrier having the hydrogenation metal components; supporting the supported carrier having the hydrogenation metal components with an organic compound, and drying and calcining the supported carrier having the hydrogenation metal components and the organic compound. The hydrogenation metal components and the organic compound are supported in the carrier. The organic compound is selected from the group consisting of methyl acetoacetate, ethyl acetoacetate and a mixture thereof. The hydrogenation metal components supported in the carrier is sulfide. An amount of the organic compound is 15 wt % to 90 wt % based on the total amount of the hydroprocessing catalyst.