A method of preparing large-size high-porosity Fe-doped photocatalytic porous magnetic microspheres, including: dissolving a soluble macromolecule in a distilled water to obtain a solution A having a concentration of 0.5-1.5 wt %; adding a photocatalyst to the solution A, and uniformly stirring the solution A to obtain a suspension B; mixing a saturated soluble ferric salt solution with the suspension B, and uniformly stirring the mixture to obtain a suspension C; dropwise adding the suspension C to a high-concentration alkali solution by a syringe equipped with a suitable needle size to form microspheres; ageing the reaction system and drying the formed microspheres after adding; calcining the dried microspheres at 600-1100 C.; cooling the calcined microspheres to obtain the large-size high-porosity Fe-doped photocatalytic porous magnetic microspheres.

Provided is a fabrication method of a photocatalytic material in which a single layer of a carbon-based participate is formed on a surface of each of titanium dioxide particle. The method includes (a) loading titanium dioxide particles into an electric furnace comprising a mechanism for rotating a core tube; (b) heating an inside of the core tube of the electric furnace into which the titanium dioxide particles have been loaded to a temperature of not less than 400 C. and not more than 800 C., while an inert gas is introduced into the inside of the core tube; (c) supplying a hydrocarbon gas to the inside of the core tube in addition to the inert gas; and (d) performing a thermal CVD on each of the titanium dioxide particles in a fluidized state inside the core tube, while the core tube is rotated, to form a single layer of a carbon-based precipitate containing graphene on a surface of each of the titanium dioxide particles. A photocatalyst material is provided.

An embodiment of the present specification provides a method for preparing a catalyst for preparing a carbon nanotube, comprising: (a) dissolving a main catalyst precursor, a support precursor, a cocatalyst precursor and a precipitation inhibitor in a solvent to prepare a precursor solution; and (b) pyrolyzing the precursor solution by spraying the precursor solution into a reactor, wherein a mole fraction of the precipitation inhibitor to the cocatalyst precursor is 0.1 to 1.5.

A porous composite includes a porous base material and a porous collection layer provided on a collection surface of the base material. The collection layer includes particles deposited in pores of the collection surface. In a plan view of the collection surface, the proportion of the area of a covered region that is covered with the collection layer out of the collection surface is less than or equal to 70%, and the proportion of the area of a pore region out of a non-covered region that is not covered with the collection layer is less than or equal to 15%.

The present invention relates to a process for production of high yield of hydrogen by carrying out the dry reforming of the dry gas generated from the process itself by utilizing the same catalyst for cracking and producing high yield of light olefins such as ethylene, propylene and butylenes from residue feedstocks.

A mesoporous ozonation catalyst including a cerium-titanium-zirconium composite oxide. The catalyst is in the form of a solid spherical particle having a diameter of between 0.7 and 1.2 mm. The solid spherical particle exhibits lattice fringes under transmission electron microscope, and the lattice fringes have a spacing between 0.332 and 0.339 nm.

Provided is a catalyst for oxidative dehydrogenation, a method of preparing the catalyst, and a method of performing oxidative dehydrogenation using the catalyst. The catalyst for oxidative dehydrogenation has improved durability and fillability by including a porous support coated with a metal oxide (AB.sub.2O.sub.4) according to Equation 1 of the present invention, wherein the metal oxide exhibits activity during oxidative dehydrogenation. Therefore, when the catalyst is used in oxidative dehydrogenation of butene, the conversion rate of butene and the selectivity and yield of butadiene may be greatly improved.

The invention discloses a composite material used for catalyzing and degrading nitrogen oxide and its preparation method and application thereof. The invention of the hollow g-C.sub.3N.sub.4 nanospheres/reduced graphene oxide composite-polymer carbonized nanofiber material is prepared as follow: 1) the preparation of silica nanospheres; 2) the preparation of hollow g-C.sub.3N.sub.4 nanospheres; 3) the preparation of graphene oxide; 4) the preparation of surface modified hollow g-C.sub.3N.sub.4 nanoparticles preparation; 5) the preparation of composites; 6) the preparation of composite-polymer carbon nanofiber material. The raw materials used in the process is low cost and easy to get; the operation of the invention is simple and convenient without the use of expensive equipment in the whole process; the composite has high adsorption efficiency of ppb level nitrogen oxide with good repeatability.

The present invention provides amorphous bi-functional catalytic aluminum metallic glass particles having an aluminum metallic glass core and 2 or more transition metals disposed on the surface of the aluminum metallic glass core to form amorphous bi-functional aluminum metallic glass particles with catalytic activity.

An object of the present invention is to provide a method for regenerating a catalyst for butadiene production, for removing a coke-like substance which is generated by oxidative dehydrogenation of n-butene in the presence of a catalyst for butadiene production and which is attached to the catalyst and the inside of a reactor. After the catalyst is used in oxidative dehydrogenation of butenes, the catalyst regeneration method of the present invention removes a coke-like substance in a reactor which is charged with the catalyst for butadiene production, the catalyst having a prescribed composition before being used in the oxidative dehydrogenation.