A photoreactor having computer actuated input/output ports is operated by introducing reactant through an input port and collecting product through an output port, and upon closure of the input and output ports, treating photocatalyst within the photoreactor to remove intermediates limiting performance of the photocatalyst. Once the photocatalyst is regenerated, introduction of reactant to the photoreactor through the input port and collection of product from the output port can be resumed. The automated process does not require removal of catalyst from the photoreactor and significantly improves process economics.

A photoreactor having computer actuated input/output ports is operated by introducing reactant through an input port and collecting product through an output port, and upon closure of the input and output ports, treating photocatalyst within the photoreactor to remove intermediates limiting performance of the photocatalyst. Once the photocatalyst is regenerated, introduction of reactant to the photoreactor through the input port and collection of product from the output port can be resumed. The automated process does not require removal of catalyst from the photoreactor and significantly improves process economics.

Provided is a method for producing organic molecules having at least two carbon atoms chained together by the reaction of a hydrogen-containing source, a carbon-containing source and an optional nitrogen-containing source in the presence of a nanostructure or nanostructures, wherein the reaction is initiated by heat.

Provided is a method for producing organic molecules having at least two carbon atoms chained together by the reaction of a hydrogen-containing source, a carbon-containing source and an optional nitrogen-containing source in the presence of a nanostructure or nanostructures, wherein the reaction is initiated by heat.

Processes for converting methane and/or other hydrocarbons to synthesis gas (i.e., a gaseous mixture comprising H.sub.2 and CO) are disclosed, in which at least a portion of the hydrocarbon(s) is reacted with CO.sub.2. At least a second portion of the methane may be reacted with H.sub.2O (steam), thereby improving overall thermodynamics of the process, in terms of reducing endothermicity (ΔH) and the required energy input, compared to “pure” dry reforming in which no H.sub.2O is present. Such dry reforming (reaction with CO.sub.2 only) or CO.sub.2-steam reforming (reaction with both CO.sub.2 and steam) processes are advantageously integrated with Fischer-Tropsch synthesis to yield liquid hydrocarbon fuels. Further integration may involve the use of a downstream finishing stage involving hydroisomerization to remove FT wax. Yet other integration options involve the use of combined CO.sub.2-steam reforming and FT synthesis stages (optionally with finishing) for producing liquid fuels from gas streams generated in a number of possible processes, including the hydropyrolysis of biomass.

In a broad form the present disclosure relates to a stabilized catalyst support comprising in oxide form; aluminum, zirconium, and one or more lanthanoid elements taken from the lanthanoid group of the periodic system characterized in that at least a part of the aluminum is present as transition alumina such as χ, κ, γ, δ, η, ρ and θ-alumina, characterized in the concentration of zirconium being at least 1.5 wt %, 5 wt % or 10 wt %, the concentration of lanthanoid being at least 0.5 wt %, 1.0 wt %, 2 wt % or 4 wt % and the combined concentration of zirconium and lanthanoid being at least 4 wt %, 7 wt % or 10 wt %, with the associated benefit of a support comprising transition alumina being a high surface area due to the small crystallites typical for transition alumina, and the benefit of the combined presence of oxides of zirconium and lanthanoid in the stated amounts being that at these levels these oxides stabilize the structure of the transition alumina.

Provided is a method for producing organic molecules having at least two carbon atoms chained together by the reaction of a hydrogen-containing source, a carbon-containing source and an optional nitrogen-containing source in the presence of a nanostructure or nanostructures, wherein the reaction is initiated by heat.

A catalyst suitable for use in carbon oxide conversion reactions is described, said catalyst in the form of a shaped unit formed from an oxidic catalyst powder, said catalyst comprising 30-70% by weight of copper oxide, combined with zinc oxide, alumina and silica, having a Si:AI atomic ratio in the range 0.005 to 0.15:1, and having a BET surface area >105 m.sup.2/g and a copper surface area >37 m.sup.2/g catalyst. The catalyst is prepared by a co-precipitation method using an alumina sol.

A catalyst suitable for use in carbon oxide conversion reactions is described, said catalyst in the form of a shaped unit formed from an oxidic catalyst powder, said catalyst comprising 30-70% by weight of copper oxide, combined with zinc oxide, alumina and silica, having a Si:AI atomic ratio in the range 0.005 to 0.15:1, and having a BET surface area >105 m.sup.2/g and a copper surface area >37 m.sup.2/g catalyst. The catalyst is prepared by a co-precipitation method using an alumina sol.

A hydrocarbon generation system includes a first generation apparatus configured to generate a hydrocarbon with two or more carbon atoms from a first raw material containing: at least one of carbon monoxide or carbon dioxide; and hydrogen. The hydrocarbon generation system includes a second generation apparatus configured to generate methane from a second raw material including: hydrogen; and at least one of carbon monoxide or carbon dioxide contained in the first raw material and discharged from the first generation apparatus.