A method for producing a multiphase mixed-oxide catalyst including at least one active phase based on bismuth molybdate and one co-catalyst based on iron molybdate and at least one amongst the two elements cobalt and nickel, includes the following steps:

preparing a mixture of the precursors of said-mixed oxides in a solvent,

making said precursors react through a microwave-assisted hydrothermal reaction, and

isolating the mixed oxides to obtain the catalyst.

A catalyst and a catalytic system prepared in this manner are related to the method as well as the uses of this catalyst and of this catalytic system, in particular in the oxidation of propene into acrolein.

Disclosed is a method for producing a photocatalyst for air cleaning. The present production method comprises the steps of: preparing titanium dioxide (TiO.sub.2); attaching platinum to a surface of the titanium dioxide; and attaching fluoro to the platinum-attached surface of the titanium dioxide to obtain surface-modified titanium dioxide.

The invention aims to provide a copper mesh coated with manganese molybdate and application thereof in the separation of oil-water emulsion and degradation of organic pollutants in water. A large amount of nano-scale manganese molybdates are grown on the surface of a copper mesh through a two-step hydrothermal method. Thereby, a multifunctional composite material is prepared, which can effectively separate oil-water emulsion and degrade organic pollutants in water. The copper mesh has good recyclability. Most of all, the product is suitable for industrial production to achieve the purpose of treating water pollution.

A nanoparticle comprises an internal D/A heterojunction, wherein the nanoparticle comprises a HER rate of 64,426±7022 μmolh.sup.−1g.sup.−1 under broadband visible light illumination. Measured EQEs of the nanoparticle throughout a visible spectrum exceed 5% at 660 to 700 nm. Methods may include fabricating a nanoparticle comprising: preparing individual stock solutions of PTB7-TH and EH-IDTBR in chloroform; heating the individual stock solutions to a complete dissolution; filtering the individual stock solutions; preparing a nanoparticle precursor solution from the filtered individual stock solutions by mixing the individual stock solutions in a ratio of 0-100% EH-IDTBR adding a portion of the nanoparticle precursor solution to a solution of surfactant (SDS or TEBS) in water and mixing to form a pre-emulsion; sonicating the pre-emulsion to form a mini-emulsion; heating the mini-emulsion to remove the chloroform to thereby form a surfactant stabilized nanoparticle dispersion; and filtering the nanoparticle.

This invention relates to a method for preparing a bimetallic titania-based catalyst for use in hydrodesulfurization reactions.

The present invention is directed to the synthesis of novel delaminated layered zeolite precursor materials prepared by fluoride/chloride anion-promoted exfoliation. The method comprises, for example, using a combination of fluoride and chloride anions at a mild pH in aqueous solution to affect delamination of a layered zeolite precursor. The method can also comprise using a combination of fluoride and chloride anions in a non-aqueous solution comprising an organic solvent. The method may be used in conjunction with either acidification or sonication, or both. The resulting delaminated zeolite precursors are then isolated. Precursors that are then isolated lack amorphous silica content. The UCB-1 product is an example of such a novel oxide material and is obtained in yields in excess of 90% without the need for sonication.

According to embodiments, methods for the production of boron-silicalite-1 are disclosed. In embodiments, the method may include combining a mineralizer agent, a templating agent, water, and boric acid in a first microwave unit; heating the first microwave unit to form a boron-zeolite; calcining the boron-zeolite to form an alkali-zeolite; combining the alkali-zeolite with ammonium nitrate to produce an ion-exchanged zeolite; heating the ion-exchanged zeolite to form a protonated zeolite; and calcining the protonated zeolite to form the boron-silicalite-1. In embodiments, the method may include combining a templating agent, water, and boric acid in a first hydrothermal unit; heating the first microwave unit to form a boron-zeolite; calcining the boron-zeolite to form an alkali-zeolite; combining the alkali-zeolite with ammonium nitrate to produce an ion-exchanged zeolite; heating the ion-exchanged zeolite to form a protonated zeolite; and calcining the protonated zeolite to form the boron-silicalite-1. The boron-silicalite-1 may be microscale or nanoscale.

A process for treating metal oxide catalysts includes activating one or more lasers to produce laser light. The process also includes exposing at least a portion of the metal oxide catalyst to the laser light to increase hydrophobicity of the metal oxide catalyst. The metal oxide catalyst may include a plurality of metal oxide particles or a metal oxide film.

Methods and apparatuses to produce graphene and nanoparticle catalysts supported on graphene without the use of reducing agents, and with the concomitant production of heat, are provided. The methods and apparatuses employ radiant energy to reduce (deoxygenate) graphite oxide (GO) to graphene, or to reduce a mixture of GO plus one or more metals to produce nanoparticle catalysts supported on graphene. Methods and systems to generate and utilize heat that is produced by irradiating GO, graphene and their metal and semiconductor nanocomposites with visible, infrared and/or ultraviolet radiation, e.g. using sunlight, lasers, etc. are also provided.

The present disclosure provides a catalyst product having particular three-dimensional plate-like shape and comprising catalyst nanoparticles and a method for manufacturing same. The present product may be useful in fuel cells or battery applications. In certain embodiments the present catalysts show good catalytic activity and durability even at low catalyst loads.