1572results about "Carbon monoxide" patented technology

An apparatus for thermal conversion of one or more reactants to desired end products includes an insulated reactor chamber having a high temperature heater such as a plasma torch at its inlet end and, optionally, a restrictive convergent-divergent nozzle at its outlet end. In a thermal conversion method, reactants are injected upstream from the reactor chamber and thoroughly mixed with the plasma stream before entering the reactor chamber. The reactor chamber has a reaction zone that is maintained at a substantially uniform temperature. The resulting heated gaseous stream is then rapidly cooled by passage through the nozzle, which "freezes" the desired end product(s) in the heated equilibrium reaction stage, or is discharged through an outlet pipe without the convergent-divergent nozzle. The desired end products are then separated from the gaseous stream.

The invention provides a system designed for the complete conversion of carbonaceous feedstock into syngas and slag. The system comprises a primary chamber for the volatilization of feedstock generating a primary chamber gas (an offgas); a secondary chamber for the further conversion of processed feedstock to a secondary chamber gas (a syngas) and a residue; a gas-reformulating zone for processing gas generated within one or more of the chambers; and a melting chamber for vitrifying residue. The primary chamber comprises direct or indirect feedstock additive capabilities in order to adjust the carbon content of the feedstock. The system also comprises a control system for use with the gasification system to monitor and regulate the different stages of the process to ensure the efficient and complete conversion of the carbonaceous feedstock into a syngas product.

Use of physical vapor deposition methodologies to deposit nanoscale gold on activating support media makes the use of catalytically active gold dramatically easier and opens the door to significant improvements associated with developing, making, and using gold-based, catalytic systems. The present invention, therefore, relates to novel features, ingredients, and formulations of gold-based, heterogeneous catalyst systems generally comprising nanoscale gold deposited onto a nanoporous support.

The present invention relates to processes for preparing gaseous products, and in particular methane, via the hydromethanation of a carbonaceous feedstock in the presence of steam, syngas, a hydromethanation catalyst and an oxygen-rich gas stream.

By using catalytic partial oxidation or autothermal reforming process, a catalytic oxidizer installed in the engine's Exhaust Gas Recycle (EGR) line can be used to produce from fossil fuels or bio-fuels a reformate gas containing H2 and CO for an IC engine or a gas turbine. Thus, a system consisting of an EGR Oxidizer and an IC engine / gas turbine can be used by itself as a driving device, or can be combined with an electric generator and a battery bank to produce, store and transmit electricity to be used in stationary or mobile power generation, transportation and utility etc.The Oxidizer can also be used to provide reducing gases to regenerate the NOx or diesel particulate traps, so that the traps can continuously be used for reducing emissions from IC engine, diesel truck, gas turbine, power plant etc.

A process and apparatus for producing a synthesis gas for use as a gaseous fuel or as feed into a Fischer-Tropsch reactor to produce a liquid fuel in a substantially self-sustaining process. A slurry of particles of carbonaceous material in water, and hydrogen from an internal source, are fed into a hydro-gasification reactor under conditions whereby methane rich producer gases are generated and fed into a steam pyrolytic reformer under conditions whereby synthesis gas comprising hydrogen and carbon monoxide are generated. A portion of the hydrogen generated by the steam pyrolytic reformer is fed through a hydrogen purification filter into the hydro-gasification reactor, the hydrogen therefrom constituting the hydrogen from an internal source. The remaining synthesis gas generated by the steam pyrolytic reformer is either used as fuel for a gaseous fueled engine to produce electricity and / or process heat or is fed into a Fischer-Tropsch or similar reactor under conditions whereby a liquid fuel is produced.

The invention discloses a dehydrogenation catalyst for feed gas containing carbon monoxide, a preparation method and an application method thereof. The catalyst takes alumina as a carrier, palladium and / or platinum as an active component and 2 to 4 MOxes as an additive, M is sodium, potassium, magnesium, titanium, zirconium, vanadium, manganese, iron, nickel, cobalt, copper, molybdenum, tungsten or cerium, and components of the catalyst (calculated by carrier mass) are: 0.01 to 2 percent of the palladium and / or 0.01 to 1 percent of the platinum, and 1 to 2 percent of MOxes. The preparation method for the catalyst comprises the following steps that: firstly, an additive metal salt solution is used to impregnate the carrier; a palladium and / or platinum salt solution is used to impregnate the carrier after the carrier is dried and roasted; and the impregnated carrier is roasted at a temperature of between 450 and 850 DEG C to obtain the catalyst. Before the use, H2-N2 mixed gas containing more than 10 percent of hydrogen or pure hydrogen is activated by the catalyst at a temperature of between 450 and 650 DEG C. The catalyst can perform deep removal on less than 5 percent of hydrogen in the feed gas with the CO content of between 10 and 99 percent, the using temperature is between 100 and 300 DEG C, the space velocity is between 500 and 9,000h<-1>, the dehydrogenation rate is more than 99 percent, the content of outlet hydrogen is less than 100 ppm, and the loss of the carbon monoxide is less than 0.5 percent.

This invention relates to an apparatus, comprising: at least one process microchannel having a height, width and length, the height being up to about 10 mm, the process microchannel having a base wall extending in one direction along the width of the process microchannel and in another direction along the length of the process microchannel; at least one fin projecting into the process microchannel from the base wall and extending along at least part of the length of the process microchannel; and a catalyst or sorption medium supported by the fin.

A method for activating chemical reactions using a non-thermal capillary discharge plasma (NT-CDP) unit or a non-thermal slot discharge plasma (NT-SDP) unit (collectively referred to as “NT-CDP / SDP”). The NT-CDP / SDP unit includes a first electrode disposed between two dielectric layers, wherein the first electrode and dielectric layers having at least one opening (e.g., capillary or a slot) defined therethrough. A dielectric sleeve inserted into the opening, and at least one second electrode (e.g., in the shape of a pin, ring, metal wire, or tapered metal blade) is disposed in fluid communication with an associated opening. A non-thermal plasma discharge is emitted from the opening when a voltage differential is applied between the first and second electrodes. Chemical feedstock to be treated is then exposed to the non-thermal plasma. This processing is suited for the following exemplary chemical reactions as (i) partial oxidation of hydrocarbon feedstock to produce functionalized organic compounds; (ii) chemical stabilization of a polymer fiber (e.g., PAN fiber precursor in carbon fiber production; (iii) pre-reforming of higher chain length petroleum hydrocarbons to generate a feedstock suitable for reforming; (iv) natural gas reforming in a chemically reducing atmosphere (e.g., ammonia or urea) to produce carbon monoxide and Hydrogen gas; or (v) plasma enhanced water gas shifting.

Supported perovskite-type oxides are described. The perovskite-type oxides have the general formula of AxA′x′ByB′y′O3−δ, wherein A is an ion of a metal of Group IIIa or IIIb of the periodic table of elements or mixtures thereof; A′ is an ion of a metal of Groups Ia or IIa of the periodic table or mixtures thereof; B and B′ are ions of a d-block transition metal of the periodic table or mixtures thereof; x, x′, y and y′ vary from 0 to 1; 0.95<x+x′<1.05; 0.95<y+y′<1.05; δ is the deviation from ideal oxygen stoichiometry. This invention also provides for the selection of support materials and the shapes of supported perovskite-type oxides as well as the methods for making them.

The carbon dioxide reduction method of the present invention is a method including steps of: bringing an electrode (working electrode) containing a carbide of at least one element selected from Group V elements (vanadium, niobium, and tantalum) into contact with an electrolytic solution; and introducing carbon dioxide into the electrolytic solution to reduce the introduced carbon dioxide by the electrode. The material contained in the electrode, that is, the material containing a carbide of at least one element selected from Group V elements (vanadium, niobium, and tantalum) is the carbon dioxide reduction catalyst of the present invention.