A system and method of producing carbon nanotubes from flare gas and other gaseous carbon-containing sources.

The present disclosure relates to a process for converting syngas to C2+ alcohols, said process comprising the steps of providing a reactor, of providing a catalyst composition and one or more acidic materials within said reactor, of providing a feed stream comprising a mixture of H.sub.2 and CO; and of contacting said feed stream with said catalyst composition and said one or more acidic materials under reaction conditions to provide product stream. Said process is remarkable in that said catalyst composition comprises an active phase comprising CuFe deposited on a carbon-containing support, and the one or more acidic materials are one or more zeolites having a Si/Al molar ratio ranging between 2 and 200.

The present disclosure relates to a process for converting syngas to C2+ alcohols, said process comprising the steps of providing a reactor, of providing a catalyst composition and one or more acidic materials within said reactor, of providing a feed stream comprising a mixture of H.sub.2 and CO; and of contacting said feed stream with said catalyst composition and said one or more acidic materials under reaction conditions to provide product stream. Said process is remarkable in that said catalyst composition comprises an active phase comprising CuFe deposited on a carbon-containing support, and the one or more acidic materials are one or more zeolites having a Si/Al molar ratio ranging between 2 and 200.

A process and apparatus for producing carbon nanofibers. The process comprises two stages. The first stage involves oxidizing light hydrocarbon with carbon dioxide or water, or oxygen, or a combination thereof to a mixture of hydrogen and carbon monoxide. The second stage involves converting the produced hydrogen and the carbon monoxide to carbon nanofibers and steam. In this way, greenhouse gases may be reduced by using carbon dioxide and methane (and/or other light hydrocarbons) as reactants; and useful products may be produced, such as Carbon NanoFibers (CNF).

In some aspects and embodiments, the present application provides a wide range of porous 1-D polymeric graphitic carbon-nitride materials that are atomically doped with binary metals in different morphologies. In some embodiments, the graphitic carbon-nitride materials can be prepared with high mass production from inexpensive and natural abundant precursors. In some embodiments, the materials were used successfully for the oxidation of CO to CO.sub.2 under ambient reaction temperature in addition to the reduction of CO.sub.2 into hydrocarbons. In some embodiments, the materials can be used for practical and large-scale gas conversion for household or industrial applications.

Methods for producing a carbon-free, PGM-free support for PGM catalyst. The catalytic material comprises PGM metals disposed on a carbon-free support which is catalytic but free of PGM.

The present invention relates to a carbon-based precious metal-transition metal composite catalyst and a preparation method therefor, and more particularly, to a catalyst synthesis method in which, when preparing a high-content precious metal-transition metal composite catalyst, a catalyst having uniform particles and composition can be prepared, and cyclohexane dimethanol (CHDM) is efficiently produced by the hydrogenation reaction of cyclohexane dicarboxylic acid (CHDA) in an aqueous solution. Provided is a method for preparing a carbon-based precious metal-transition metal composite catalyst, wherein, in the carbon-based precious metal-transition metal composite catalyst, the precious metal is included in an amount of 10-20 parts by weight, and the transition metal is included in an amount of 10-20 parts by weight based on 100 parts by weight of the composite catalyst, and thus a total amount of the precious metal-transition metal is 20-40 parts by weight based on 100 parts by weight of the composite catalyst.

Disclosed is a method for preparing a ternary alloy catalyst with polydopamine coating and a ternary alloy catalyst prepared thereby. The method for preparing a ternary alloy catalyst according to the present disclosure may provide a ternary alloy catalyst with increased resistance to carbon monoxide (CO) poisoning in which polydopamine is utilized as a coating material for a ternary alloy catalyst having a core-shell structure containing platinum to suppress the growth of particles during subsequent high-temperature heat treatment, and nickel (Ni), which is a transition metal, is diffused inside to form a core, thereby effectively preventing elution of nickel under an acidic condition.

A water treatment system with a photocatalytic nanocomposite sheet, an adsorbent layer, and a fibrous filter, wherein the photocatalytic nanocomposite sheet comprises polymethylmethacrylate and silver phosphate, the adsorbent layer comprises plasma activated carbon nanotubes, and the fibrous filter is a composite of polymethylmethacrylate, polyvinylidene fluoride, and polyvinylpyrrolidone polymer fibers, with carbon nanotubes that are dispersed within the polymer fibers and silver nanoparticles that are deposited on the polymer fibers. Various embodiments of the water treatment system and methods of fabricating the photocatalytic nanocomposite sheet, the adsorbent layer, and the fibrous filter are also provided.

The present disclosure discloses a core-shell structured NiSe.sub.2@NC electrocatalytic material having a general formula of NiSe.sub.2@NC. The present disclosure also provides a preparation method and use of the catalytic material. In the present disclosure, hydrazine hydrate is used as a reducing agent, selenium powders are used as a source of selenium, and a metal-organic framework (MOF) is used as a precursor. Selective selenization of mixed-linker MOFs based on mixed ligands is carried out through a hydrothermal reaction. Then, a series of adjustable N-doped carbon-coated NiSe.sub.2 nano-octahedrons are prepared through a one-step calcination reaction. By adjusting the types of mixed ligands in the MOF, carbon-coated nickel diselenide composites doped with different pyridinic-N contents can be obtained. Corresponding electrochemical tests prove that, the electrocatalytic activity has a strong correlation with the content of pyridinic-N.