The invention relates to a photocatalytic oil-water separation material and a preparation method thereof, the method including the following steps: cleaning a base material and a metal-doped material, and drying for later use; preparing a mixed solution of an amine monomer and an acid-alkali buffer reagent, soaking the base material in the mixed solution, and reacting under an oscillation condition, to obtain the base material attached with amine monomer polymer; dissolving a soluble metal additive and an organic ligand reagent into an organic solvent, and performing ultrasonic stirring uniformly, to obtain a metal organic framework material (MOF) reaction solution with photocatalytic performance; and placing the metal-doped material, the base material attached with the amine and the MOF reaction solution into a reaction kettle for performing hydrothermal reaction, cleaning and drying the reacted base material, to obtain the photocatalytic oil-water separation material.

Disclosed is a preparation method of a nanometer metal oxide supported carrier based on anodic oxidation, comprising: Step 1: adding electrolyte to a reaction pool, and fixing the cathode and the anode oppositely, wherein the cathode is a metal plate that is identical to the nano-metal oxide, and the anode is a carrier metal material; Step 2: stirring the electrolyte at a constant speed, wherein the revolution speed is not lower than 500 rpm; Step 3: switching power on; setting the output voltage between 10 v and 50 v; and subjecting the metal plate of the anode to anodic oxidation reaction, wherein metal oxide nanotubes/nano particles are generated on the surface; under the action of stirring, the metal oxide nanotubes/nano particles on the anode surface are dissolved and shed off into the electrolyte; under the action of the electric field force, the dissolved and shed-off nano fragments migrate towards the cathode and are adhered to the surface of the cathode material, thereby forming a nano-metal oxide film. The film preparation method according to the disclosure offers advantages such as mild condition, simple instrumentation, easy operation, and low cost; the prepared film has a good load effect such that the metal oxide can hardly be shed off.

The present invention discloses a bismuth oxide (Bi.sub.2O.sub.3)/bismuth subcarbonate ((BiO).sub.2CO.sub.3)/bismuth molybdate (Bi.sub.2MoO.sub.6) composite photocatalyst, including a Bi.sub.2MoO.sub.6 photocatalyst, where Bi.sub.2O.sub.3 and (BiO).sub.2CO.sub.3 nanosheets are introduced to a surface of the Bi.sub.2MoO.sub.6 through addition of Na.sub.2CO.sub.3 and roasting. The present invention also discloses a preparation method of the Bi.sub.2O.sub.3/(BiO).sub.2CO.sub.3/Bi.sub.2MoO.sub.6 composite photocatalyst which is specifically implemented by the following steps: step 1: preparing a Bi.sub.2MoO.sub.6 photocatalyst; step 2: introducing Bi.sub.2O.sub.3 and (BiO).sub.2CO.sub.3 nanosheets to a surface of the Bi.sub.2MoO.sub.6 photocatalyst obtained in step 1 through addition of Na.sub.2CO.sub.3 and roasting to obtain the Bi.sub.2O.sub.3/(BiO).sub.2CO.sub.3/Bi.sub.2MoO.sub.6 composite photocatalyst. The photocatalyst of the present invention has no agglomeration, a wide responsive range of visible light, a significantly improved catalytic activity compared with a Bi.sub.2MoO.sub.6 alone, and excellent reusability. Moreover, the preparation method is simple with mild conditions, desired controllability and convenient operation.

Carbon dioxide can be converted into a higher energy product by contacting carbon dioxide with a polarized monocrystalline magnesium oxide producing at least in part carbon. Further a novel crystalline magnesium oxide carbon composite comprising crystalline magnesium oxide and crystalline carbon having graphene structure which are interwoven is provided.

The present invention relates to a new method for creating nanopores in single layer molybdenum disulfide (MoS.sub.2) nanosheets (NSs) by the electrospray deposition (ESD) of silver ions on a water suspension of the former. Electrospray deposited silver ions react with the MoS.sub.2 NSs at the liquid-air interface resulting in Ag.sub.2S nanoparticles (NPs) which goes into the solution leaving the NSs with holes of 3-5 nm diameter. Specific reaction with the S of MoS.sub.2 NSs leads to Mo-rich edges. Such Mo-rich defects are highly efficient for the generation of active oxygen species such as H.sub.2O.sub.2, under visible light, which causes efficient disinfection of water. The holey MoS.sub.2 NSs shows 10.sup.5 times higher efficiency in disinfection compared to normal MoS.sub.2 NSs. Developed a conceptual prototype and tested with multiple bacterial strains and a viral strain, demonstrating the utility of the method for practical applications.

A heterojunction composite material consisting of one-dimensional In.sub.2O.sub.3 hollow nanotube and two-dimensional ZnFe.sub.2O.sub.4 nanosheets and its application are disclosed. When using this material for catalytic reactions, the hollow cavity and two-dimensional nanosheets of hollow nanomaterials can not only reduce the migration distance to accelerate the electron-hole separation, but also provide a large surface area and rich active sites to promote pollution adsorption and surface catalysis. At the same time, multiple light scattering or reflection in the hollow cavity of the hollow nanomaterials can increase light absorption and utilization. In addition, the heterojunction photocatalyst constructed by growing two-dimensional semiconductor nanosheets on a tubular substrate can promote the effective separation of photogenerated electrons and photogenerated holes, thereby improving the catalytic efficiency. In terms of catalytic performance, In.sub.2O.sub.3 @ ZnFe.sub.2O.sub.4 shows effective degradation of tetracycline, and due to its ferromagnetism, it shows convenient and good separation effect and has good recycling performance.

Processes for converting an olefin reactant into a diol compound are disclosed, and these processes include the steps of contacting the olefin reactant and a supported chromium catalyst comprising chromium in a hexavalent oxidation state to reduce at least a portion of the supported chromium catalyst to form a reduced chromium catalyst, and hydrolyzing the reduced chromium catalyst to form a reaction product comprising the diol compound. While being contacted, the olefin reactant and the supported chromium catalyst can be irradiated with a light beam at a wavelength in the UV-visible spectrum. Optionally, these processes can further comprise a step of calcining at least a portion of the reduced chromium catalyst to regenerate the supported chromium catalyst.

Processes for converting an olefin reactant into a diol compound are disclosed, and these processes include the steps of contacting the olefin reactant and a supported chromium catalyst comprising chromium in a hexavalent oxidation state to reduce at least a portion of the supported chromium catalyst to form a reduced chromium catalyst, and hydrolyzing the reduced chromium catalyst to form a reaction product comprising the diol compound. While being contacted, the olefin reactant and the supported chromium catalyst can be irradiated with a light beam at a wavelength in the UV-visible spectrum. Optionally, these processes can further comprise a step of calcining at least a portion of the reduced chromium catalyst to regenerate the supported chromium catalyst.

A photocatalyst is described that is suitable for converting molecular nitrogen into ammonia. The photocatalyst comprises a layered base material comprising 1 to 100 layers, the layered base material being selected from the group consisting of molybdenum disulfide, tungsten disulfide, molybdenum telluride, tungsten telluride, molybdenum selenide and tungsten selenide, a layered base material comprising 1 to 100 layers, the layered base material being selected from the group consisting of molybdenum disulfide, tungsten disulfide, molybdenum telluride, tungsten telluride, molybdenum selenide and tungsten selenide, and 0.1-10.0% by weight, relative to the weight of the base material, of one or more Group VI, VII, VIII, IX or X transition metals. T he photocatalyst can further comprise 0.1-50.0% by weight, relative to the weight of the base material, of one or more semiconductor materials having an average particle size of 0.5-50.0 nm. The photocatalyst exhibits high catalytic efficiency without the need for high temperature and pressure. Also described is a process for the preparation of the photocatalyst, as well as uses of the photocatalyst for converting molecular nitrogen into ammonia.

The present invention relates to a method of preparing a photocatalyst composite nanofiber using coaxial electrospinning and a photocatalyst composite nanofiber prepared by the same method, and when the photocatalyst composite nanofiber is prepared by such a method, noble metal particles are located on the fiber surface and rGO surrounds the nanofiber, thereby improving photocatalytic performance and reducing costs, and being capable of being applied in various industrial fields for antibacterial treatment and deodorization.