The invention provides a catalyst system and method for the deoxygenation of hydrocarbons, such as bio-oil, using a sulphide-sulfate or an oxide-carbonate (LDH) system. The invention extends to a pyrolysis process of a carbonaceous bio-mass wherein a first combustion zone is carried out in one or more combustion fluidised beds in which a particulate material including chemically looping deoxygenation catalyst particles is fluidised and heated, and a second pyrolysis zone carried out in one or more pyrolysis fluidised beds in which the hot particles, including the catalyst particles, heated in the combustion zone are used for pyrolysis of the bio-mass, said combustion zone being operated at a temperature of from 250 C. to 1100 C., typically around 900 C., and the pyrolysis zone being operated at a temperature of from 250 C. to 900 C., typically 450 C. to 600 C., said catalyst particles being oxygenated in the pyrolysis zone in the presence of oxygenates in the pyrolysis oil and regenerated in the combustion zone either by calcining to drive off the carbon oxides, such as CO.sub.2, or by reduction to its form which is active for deoxygenation of the pyrolysis oil.

The invention provides a catalyst system and method for the deoxygenation of hydrocarbons, such as bio-oil, using a sulphide-sulfate or an oxide-carbonate (LDH) system. The invention extends to a pyrolysis process of a carbonaceous bio-mass wherein a first combustion zone is carried out in one or more combustion fluidised beds in which a particulate material including chemically looping deoxygenation catalyst particles is fluidised and heated, and a second pyrolysis zone carried out in one or more pyrolysis fluidised beds in which the hot particles, including the catalyst particles, heated in the combustion zone are used for pyrolysis of the bio-mass, said combustion zone being operated at a temperature of from 250 C. to 1100 C., typically around 900 C., and the pyrolysis zone being operated at a temperature of from 250 C. to 900 C., typically 450 C. to 600 C., said catalyst particles being oxygenated in the pyrolysis zone in the presence of oxygenates in the pyrolysis oil and regenerated in the combustion zone either by calcining to drive off the carbon oxides, such as CO.sub.2, or by reduction to its form which is active for deoxygenation of the pyrolysis oil.

Provided herein are compositions comprising cadmium sulfide quantum dot photocatalysts and methods and systems utilizing as much (e.g., for the reduction of a nitrobenzene to an aniline).

Provided herein are compositions comprising cadmium sulfide quantum dot photocatalysts and methods and systems utilizing as much (e.g., for the reduction of a nitrobenzene to an aniline).

According to an example aspect of the present invention, there is provided a synthesis method for producing furoic acid from a monoacid containing five carbons in the presence of pressure, heat, solvent and catalyst.

According to an example aspect of the present invention, there is provided a synthesis method for producing furoic acid from a monoacid containing five carbons in the presence of pressure, heat, solvent and catalyst.

Photoactive catalyst and methods of producing H.sub.2 by photocatalytic water splitting. The photoactive catalyst includes an upconverting material, a photocatalyst material, and plasmonic metal nanostructures deposited on the surface of the photocatalyst material. The upconverting material is not embedded in or coated by the photocatalyst material. The upconverting material is capable of emitting light at a first wavelength that has an energy equal to or higher than the band gap of the photocatalyst material and at a second wavelength that can be absorbed by the plasmonic metal nanostructures.

Photoactive catalyst and methods of producing H.sub.2 by photocatalytic water splitting. The photoactive catalyst includes an upconverting material, a photocatalyst material, and plasmonic metal nanostructures deposited on the surface of the photocatalyst material. The upconverting material is not embedded in or coated by the photocatalyst material. The upconverting material is capable of emitting light at a first wavelength that has an energy equal to or higher than the band gap of the photocatalyst material and at a second wavelength that can be absorbed by the plasmonic metal nanostructures.

A hydroprocessing catalyst has been developed. The catalyst is a poorly crystalline transition metal tungstate material or a metal sulfide decomposition product thereof. The hydroprocessing using the crystalline ammonia transition metal tungstate material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

The disclosure relates to a photocatalytic structure. The photocatalytic structure includes a carbon nanotube structure, a photocatalytic active layer coated on the carbon nanotube structure, and a metal layer including a plurality of nanoparticles located on the surface of the photocatalytic active layer. The carbon nanotube structure comprises a plurality of intersected carbon nanotubes and defines a plurality of openings, and the photocatalytic active layer is coated on the surface of the plurality of carbon nanotubes. The metal layer includes a plurality of nanoparticles located on the surface of the photocatalytic active layer.