The present invention relates to carbon fiber composites and a method for producing the same. By reducing specific transition metal ions with a specific concentration, the method for producing the carbon fiber composites can form nanoparticles of a transition metal on an outer surface of a titanium dioxide layer encapsulating a carbon fiber to produce the carbon fiber composites. The nanoparticles of the transition metal directionally contact the titanium dioxide layer, so that the carbon fiber composites have synergistically photocatalytic activity.

A process for preparing a catalyst comprises coating substantial internal surfaces of porous inorganic powders with titanium oxide to form titanium oxide-coated inorganic powders. After the coating, an extrudate comprising the titanium oxide-coated inorganic powders is formed and calcined to form a catalyst support. Then, the catalyst support is impregnated with a solution containing one or more salts of metal selected from the group consisting of molybdenum, cobalt, and nickel.

There is provided an ammoxidation catalyst for propylene having a structure in which molybdenum (Mo) oxide is supported first, and an oxide of heterogeneous metals including bismuth (Bi) is supported later. Related methods of making and using the catalyst are also provided.

In a method, device, catalyst and a method for producing a catalyst for the catalytic conversion of a substance mixture containing glycerol to propanol in a fixed-bed reactor, substrates of the catalyst have inorganic materials and/or metal oxides. The substrates have a pore diameter at the surface of between 10 and 25 angstroms, preferably between 12 and 20 angstroms, particularly preferably 15 angstroms.

Embodiments of the present invention relates to two improved catalysts and associated processes that directly converts carbon dioxide and hydrogen to liquid fuels. The catalytic converter is comprised of two catalysts in series that are operated at the same pressures to directly produce synthetic liquid fuels or synthetic natural gas. The carbon conversion efficiency for CO.sub.2 to liquid fuels is greater than 45%. The fuel is distilled into a premium diesel fuels (approximately 70 volume %) and naphtha (approximately 30 volume %) which are used directly as “drop-in” fuels without requiring any further processing. Any light hydrocarbons that are present with the carbon dioxide are also converted directly to fuels. This process is directly applicable to the conversion of CO.sub.2 collected from ethanol plants, cement plants, power plants, biogas, carbon dioxide/hydrocarbon mixtures from secondary oil recovery, and other carbon dioxide/hydrocarbon streams. The catalyst system is durable, efficient and maintains a relatively constant level of fuel productivity over long periods of time without requiring re-activation or replacement.

The invention discloses a catalyst for propane dehydrogenation to propylene and a preparation method and application thereof. The catalyst comprises a support, an active component and promoters supported on the carrier. Among them, the carrier is alumina ball, the active component is platinum group metal, the promoters include three kinds: rare earth elements (Y, La, Ce, Pr, Nd), tin, and alkali metal elements (Li, Na, K). When the catalyst is used for propane dehydrogenation to propylene, higher propane conversion and propylene selectivity are obtained.

Monodisperse polystyrene microspheres are self-assembled on a conductive surface of FTO glass by vertical deposition method to prepare three-dimensional ordered photonic crystal opal template; the three-dimensional ordered photonic crystal opal template is immersed in a solution containing rhodium source, titanium source and strontium source, and is then calcined to prepare a rhodium doped strontium titanate inverse opal material; and the rhodium doped strontium titanate inverse opal material is added to water containing pollutants, and is then subjected to illumination and/or ultrasonic treatment to complete the removal of the pollutants in the water. The three-dimensional ordered macroporous rhodium doped strontium titanate inverse opal material may be applied in the field of photocatalysis. Under the action of external force, a built-in electric field formed by the spontaneous polarization of the material may effectively separate the photo-induced carriers, which may thus enhance the photocatalytic performance and improve the photocatalytic efficiency.

A catalyst for wastewater treatment is disclosed. The catalyst includes a porous carrier, iron oxide impregnated into the pores of the porous carrier, and platinum impregnated into the pores and mixed with the iron oxide in the pores. Also disclosed are a method for preparing the catalyst and a method for wastewater treatment using the catalyst.

Methods for fabricating thermally stable reducible metal oxide catalyst support structures on a base material using a multi-step incipient wetness impregnation (IWI) process are disclosed. For example, reducible metal oxide catalyst support structures having high surface area and high thermal stability may be formed using a multi-step IWI process, where the support structure is generated through high-temperature calcination between IWI steps. The metal or metal oxide catalysts fabricated using the methods are also disclosed. The generation of engineered surface defects on reducible metal oxides using a gas reduction process to serve as anchoring sites for metal or metal oxide catalysts is also disclosed. Generating engineered defects through a gas reduction process may be a relatively low-cost and scalable process suitable for fabricating efficient catalysts using a wide range of materials.

Embodiments of the present invention relates to two improved catalysts and associated processes that directly converts carbon dioxide and hydrogen to liquid fuels. The catalytic converter is comprised of two catalysts in series that are operated at the same pressures to directly produce synthetic liquid fuels or synthetic natural gas. The carbon conversion efficiency for CO.sub.2 to liquid fuels is greater than 45%. The fuel is distilled into a premium diesel fuels (approximately 70 volume %) and naphtha (approximately 30 volume %) which are used directly as “drop-in” fuels without requiring any further processing. Any light hydrocarbons that are present with the carbon dioxide are also converted directly to fuels. This process is directly applicable to the conversion of CO.sub.2 collected from ethanol plants, cement plants, power plants, biogas, carbon dioxide/hydrocarbon mixtures from secondary oil recovery, and other carbon dioxide/hydrocarbon streams. The catalyst system is durable, efficient and maintains a relatively constant level of fuel productivity over long periods of time without requiring re-activation or replacement.