The present invention relates to novel sulfur-doped carbonaceous porous materials. The present invention also relates to processes for the preparation of these materials and to the use of these materials in applications such as gas adsorption, mercury and gold capture, gas storage and as catalysts or catalyst supports.

A process for the manufacturing of 3D reduced graphene oxide/Fe.sub.2O.sub.3 material includes the following steps: (i) putting in contact a graphene oxide (GO) water dispersion with an aqueous solution of iron(II) sulfate; (ii) hydrothermal treatment; and (iii) freezing the reaction product obtained in step (ii) at a temperature ≤−5° C.; and (iv) lyophilisation. A 3D reduced graphene oxide/Fe.sub.2O.sub.3 material is obtainable by the process and further relates to electrodes for CDI devices having the material. A method for removing ions from a fluid, like saline water, using the capacitive deionization device includes applying a voltage to the electrodes while supplying the fluid into the capacitive deionization device.

A process for the manufacturing of 3D reduced graphene oxide/Fe.sub.2O.sub.3 material includes the following steps: (i) putting in contact a graphene oxide (GO) water dispersion with an aqueous solution of iron(II) sulfate; (ii) hydrothermal treatment; and (iii) freezing the reaction product obtained in step (ii) at a temperature ≤−5° C.; and (iv) lyophilisation. A 3D reduced graphene oxide/Fe.sub.2O.sub.3 material is obtainable by the process and further relates to electrodes for CDI devices having the material. A method for removing ions from a fluid, like saline water, using the capacitive deionization device includes applying a voltage to the electrodes while supplying the fluid into the capacitive deionization device.

Disclosed herein are carbon doped tin disulphide (C—SnS.sub.2) and other SnS.sub.2 composites as visible light photocatalyst for CO.sub.2 reduction to solar fuels. The in situ carbon doped SnS.sub.2 photocatalyst provide higher efficiency than the undoped pure SnS.sub.2. Also disclosed herein are methods for preparing the catalysts.

Disclosed herein are carbon doped tin disulphide (C—SnS.sub.2) and other SnS.sub.2 composites as visible light photocatalyst for CO.sub.2 reduction to solar fuels. The in situ carbon doped SnS.sub.2 photocatalyst provide higher efficiency than the undoped pure SnS.sub.2. Also disclosed herein are methods for preparing the catalysts.

The present invention provides a biological morph-genetic WO3 photocatalyst and a preparation method and application thereof, and belongs to the technical field of photocatalysis The preparation method of the present invention includes the following steps: impregnating a rice husk into a tungsten source solution, and roasting an obtained solid material after solid-liquid separation to obtain the biological morph-genetic WO.sub.3 photocatalyst. The present invention utilizes the rice husk as a biological template agent; the rice husk contains a large amount of silicon dioxide, and has a silicon-carbon network structure; the rice husk is impregnated into the tungsten source solution, and after roasting, a tungsten source replicates the silicon-carbon network structure of the rice husk, forming a hierarchical structure including a micropore and a mesopore with good adsorption; at the same time, during the roasting process, the carbon of the rice husk is doped into a lattice of the WO.sub.3, which facilitates transfer between charges in the lattice of the WO.sub.3, reduces a forbidden band width of the WO.sub.3, and improves the photocatalytic reaction performance of the WO.sub.3.

A highly active hydroprocessing catalyst that comprises an inorganic oxide support particle having been impregnated with a metals-impregnation solution comprising a complexing agent and a hydrogenation metal that is further incorporated with an organic additive blend.

A highly active hydroprocessing catalyst that comprises a doped support having been impregnated with a metal-impregnation solution, comprising a complexing agent and a hydrogenation metal, and filled with an organic additive blend. The catalyst is made by providing a doped support particle followed by impregnating the doped support particle with a metal impregnation solution that contains both a hydrogenation metal component and a complexing agent component to provide a metal-impregnated doped support particle. The metal-impregnated doped support particle is dried, but not calcined, and impregnated with an organic additive blend component.

A highly active hydroprocessing catalyst that comprises a doped support impregnated with at lease one hydrogenation metal component and filled with an organic additive blend. The catalyst is made by providing a doped support particle followed by impregnating the doped support particle with a metal impregnation solution to provide a metal-impregnated doped support particle. The metal-impregnated doped support particle is dried but not calcined and impregnated with an organic additive blend component.

A chemical synthesis method to fabricate boron carbide to obtain boron carbide fine powders includes the steps of: (A) formulating a precursor solution including a boron source, a liquid organic carbon source and a catalyst; (B) subjecting the precursor solution to a pyrolytic reaction in the presence of electromagnetic radiation to obtain a boron carbide precursor; and (C) subjecting the boron carbide precursor to a thermal energy treatment in the presence of thermal energy to obtain boron carbide fine powders.