According to one or more embodiments presently disclosed, a catalyst for converting hydrocarbons may include catalytic oxidized metal materials comprising oxidized iron, oxidized cobalt, and oxidized copper. At least 95 wt. % of the catalytic oxidized metal materials may be a combination of oxidized iron, oxidized cobalt, and oxidized copper. The catalyst may additionally include a mesoporous support material comprising pores having an average pore diameter of from 2 nm to 50 nm. At least 95 wt. % of the mesoporous support material may comprise alumina. At least 95 wt. % of the catalyst may be the combination of the catalytic oxidized metal materials and the mesoporous support material. Additional embodiments are included, such as methods for making the presently disclosed catalysts.

Melamine is calcined to obtain melem; melem, perylene tetracarboxylic dianhydride and a solvent are mixed to obtain a mixture, and the mixture is subjected to a solvothermal reaction in an inert atmosphere to obtain perylene imide; and the perylene imide is dispersed in an aqueous solution containing a bismuth source and a tungsten source, and is subjected to a hydrothermal reaction to obtain a perylene imide/bismuth tungstate composite photocatalytic material. By means of constructing an organic-inorganic composite photocatalytic material, the introduction of the organic photocatalytic material that responds to visible light may enable the composite material to have a wider spectral response range; and the introduction of an inorganic semiconductor catalyst enables the composite material to produce more oxidizing active free radicals, thereby enhancing the photocatalytic degradation performance of the composite material on organic pollutants. The constructed organic-inorganic composite photocatalytic material has an excellent catalytic performance.

The present disclosure provides a preparation method of a monometallic or bimetallic nanoparticle-supported catalyst. The synthesis of metal nanoparticles with different shapes, sizes, and atomic structures is affected by nucleation and growth rates. In the present disclosure, by changing a ratio of strong and weak reducing agents, a suitable double reducing agent is provided for metal nanoparticles with different reduction potentials, where the strong reducing agent is used for rapid nucleation and the weak reducing agent is used for the growth of metal nanoparticles. Accordingly, modulation and control of the nucleation and growth rates can be realized during the synthesis of nanoparticles. In addition, through multiple actions of a combination of reducing agents with different reduction intensities, monometallic/bimetallic nanoparticles of different sizes, shapes, and atomic structures are controllably prepared, which are then supported with a carrier to obtain the monometallic or bimetallic nanoparticle-supported catalyst.

A molybdenum sulfide powder according to the invention contains molybdenum disulfide having a 3R crystal structure. A heavy-metal adsorbent according to the invention contains molybdenum sulfide particles, and the molybdenum sulfide particles have a median diameter Dso of 10 nm to 1,000 nm obtained by a dynamic light scattering type particle diameter distribution measuring device. A photothermal conversion material according to the invention contains a material containing molybdenum sulfide particles and generates heat by absorbing light energy.

A method for using a natural attapulgite is disclosed. The method includes using the natural attapulgite as a natural nano mineral enzyme. The results of the examples show that the natural attapulgite has peroxidase-like activity, catalase-like activity or superoxide dismutase-like activity, and good biocompatibility. Compared with protease, the natural attapulgite has the advantages such as large reserves, easy to obtain, low cost, high temperature resistance and wide range of pH value. Compared with a developed artificial nano enzymes, the natural attapulgite further has the advantages such as multi-function, natural non-toxic (from nature, no heavy metals), good biocompatibility, easy to obtain, no complex processing, and huge surface area which provides a place for cell growth and proliferation.

In one aspect, the disclosure relates to relates to CO.sub.2-free methods of co-producing hydrogen and solid forms of carbon via methane decomposition. The methods are efficient, self-sustaining, and environmentally sound. In a further aspect, the disclosure relates to recyclable and recoverable catalysts supported by solid forms of carbon and methods for recycling the catalysts. In some aspects, the disclosure relates to catalysts that do not require support by solid forms of carbon. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.

A nickel-based MOF film photocatalyst grown in-situ on a foamed nickel surface, a preparation method therefor, and an application thereof. The nickel-based MOF film photocatalyst grown in-situ on a foamed nickel surface is prepared by first immersing foamed nickel in a diluted acid and performing ultrasonic processing, then cleaning the foamed nickel with deionized water, and drying the foamed nickel to obtain surface-activated foamed nickel; immersing the surface-activated nickel foam in a mixture of an imidazole compound, sodium formate, and a solvent and reacting at 100° C. to 180° C. to obtain an unactivated nickel-based MOFs film on the surface of the foamed nickel, and after cooling to room temperature, removing same and soaking in an organic solvent to activate, and then drying the obtained product. The film photocatalyst synthesized in-situ on the foamed nickel can increase the specific surface area of the material to facilitate the adsorption and diffusion of VOCs, and can expose more catalytic sites, so that the VOCs can be effectively degraded under the action of sunlight.

A transformational energy efficient technology using ionic liquid (IL) to couple with monoethanolamine (MEA) for catalytic CO.sub.2 capture is disclosed. [EMmim.sup.+][NTF.sub.2.sup.−] based catalysts are rationally synthesized and used for CO.sub.2 capture with MEA. A catalytic CO.sub.2 capture mechanism is disclosed according to experimental and computational studies on the [EMmim.sup.+][NTF.sub.2.sup.−] for the reversible CO.sub.2 sorption and desorption.

The present disclosure discloses a method of preparing a Ni active site-loaded C—Si aerogel catalyst, and a product and use thereof, belonging to the technical field of catalyst preparation. The method includes the following steps: (1) dissolving absolute ethanol, trimethoxymethylsilane, cetyltrimethylammonium bromide and HCl in deionized water, conducting hydrolysis to obtain a hydrolyzate, followed by adjusting a pH value of the hydrolyzate to 7 to 8.5, and drying to obtain a C—Si aerogel; and (2) in the absolute ethanol, mixing NiCl.sub.2.6H.sub.2O with the C—Si aerogel obtained in step (1) uniformly, and conducting ultrasonication, impregnation and drying, followed by calcination to obtain the Ni active site-loaded C—Si aerogel catalyst. In the present disclosure, the prepared Ni active site-loaded C—Si aerogel catalyst is capable of conducting catalytic degradation of aromatic volatile organic compounds (VOCs) at room temperature.

A process for synthesis of PtNi high surface area core/shell particles. The processing including formation of PtNi nanoparticles, exposure of the PtNi nanoparticles to oxygen to form a nickel oxide coating on the nanoparticles at the same time the segregation of Ni to surface induces a Pt-skin with PtNi core structure, removal of the nickel oxide coating to form PtNi core/Pt shell (or Pt-skin) structure.