3531 results about "Water gas" patented technology

A thermally-integrated lower temperature water-gas shift reactor apparatus for converting carbon monoxide in the presence steam comprises a catalyst bed that is disposed within an outer region surrounding a waste heat recovery steam generator operating at a selected pressure corresponding to the optimum temperature for conducting the catalytic water-gas shift reaction and a process for useful recovery of the exothermic heat of reaction to generate steam that is used in a process for the conversion of hydrocarbon feedstock into useful gases such as hydrogen.

A system involving a two-step gasification of a carbonaceous source to produce bulk hydrogen that avoids the early formation of CO₂ and obviates the traditional water gas shift (WGSR) step, carbochlorination of a metallic ore the production of metals found in the ore that utilizes carbon monoxide as an oxygen sink, rather than the traditional coke, and carbon oxides management that eliminates major impediments to emission-neutral power generation and the reduction of major metals. The gasification uses a rotary kiln reactor and gas-gas cyclonic separation process to separate synthesis gas into purified hydrogen and purified carbon monoxide. Purified bulk carbon monoxide issued in metallurgical reduction, and purified bulk hydrogen as fuel for an emission-neutral hydrogen combined cycle (HCC) turbine power generation station. The carbochlorination is integrated with: a) the concurrent separation and purification of all metal-chlorides (metchlors) and capture of CO₂ for passage to the carbon oxides management system; b) the direct reduction of metchlors to nanoscale metallurgical powders and/or to dendritically-shaped particles, including metchlor reduction for the ultrahigh-performance semiconductor metals of the III-V group; and, c) the reforming of metal-oxides with improved crystalline structure from metchlors. The carbon oxides management collects, stores and directs to points of usage, carbon oxides that arise in various processes of the integrated system, and captures carbon monoxide for process enhancement and economic uses and captures carbon dioxide as a process intermediate and for economic uses.

A method of producing a carbon dioxide product stream from a synthesis gas stream formed within a hydrogen plant having a synthesis gas reactor, a water-gas shift reactor, located downstream of the synthesis gas reactor to form the synthesis gas stream and a hydrogen pressure swing adsorption unit to produce a hydrogen product recovered from the synthesis gas stream. In accordance with the method the carbon dioxide from the synthesis gas stream by separating the carbon dioxide from the synthesis gas stream in a vacuum pressure swing adsorption system, thereby to produce a hydrogen-rich synthesis gas stream and a crude carbon dioxide stream and then purifying the crude carbon dioxide stream by a sub-ambient temperature distillation process thereby to produce the carbon dioxide product. A hydrogen synthesis gas feed stream to the hydrogen pressure swing adsorption unit is formed at least in part from the hydrogen rich stream.

The invention relates to a supercritical carbon dioxide drive physical analogue device, which belongs to the technical field of petroleum engineering and technology. The device adopts two paratactic simulation core devices to be connected with an injecting system, and each simulation core device is provided with an outlet measuring system; the injecting system injects formation water, crude oil and supercritical carbon dioxide to the simulation core devices, and a temperature and pressure measuring and controlling system is adopted to control the temperature set value and the pressure value of the whole system, and the outlet measuring system is adopted to measure the volumes of the carbon dioxide, the formation water and the crude oil which pass through the simulation core devices. After the CO2 gas is cooled and liquefied, the CO2 gas is pressurized and heated up to the supercriticality, and the difficulty of the accurate measurement of the injected CO2 flow; by adopting a double-tube model, the fingering and cross flow phenomenon during the driving process of the heterogeneous reservoir CO2 can be simulated; the design pressure of the device is 0 to 40 MPa, the design temperature is 0 to 180 DEG C, and the device is mainly applied to the research on supercritical CO2 miscible drive, non-miscible drive, continues gas drive or water and gas alternate drive.

A method for separating a hydrogen-rich product stream from a feed stream comprising hydrogen and at least one carbon-containing gas, comprising feeding the feed stream, at an inlet pressure greater than atmospheric pressure and a temperature greater than 200° C., to a hydrogen separation membrane system comprising a membrane that is selectively permeable to hydrogen, and producing a hydrogen-rich permeate product stream on the permeate side of the membrane and a carbon dioxide-rich product raffinate stream on the raffinate side of the membrane. A method for separating a hydrogen-rich product stream from a feed stream comprising hydrogen and at least one carbon-containing gas, comprising feeding the feed stream, at an inlet pressure greater than atmospheric pressure and a temperature greater than 200° C., to an integrated water gas shift/hydrogen separation membrane system wherein the hydrogen separation membrane system comprises a membrane that is selectively permeable to hydrogen, and producing a hydrogen-rich permeate product stream on the permeate side of the membrane and a carbon dioxide-rich product raffinate stream on the raffinate side of the membrane. A method for pretreating a membrane, comprising: heating the membrane to a desired operating temperature and desired feed pressure in a flow of inert gas for a sufficient time to cause the membrane to mechanically deform; decreasing the feed pressure to approximately ambient pressure; and optionally, flowing an oxidizing agent across the membrane before, during, or after deformation of the membrane. A method of supporting a hydrogen separation membrane system comprising selecting a hydrogen separation membrane system comprising one or more catalyst outer layers deposited on a hydrogen transport membrane layer and sealing the hydrogen separation membrane system to a porous support.

A process for producing liquid fuel from biomass feed stock comprising feeding a biomass feedstock into a one stage atmospheric pressure thermo-catalytic plasma gasifier, contacting the feedstock with oxygen or steam or both to obtain a syngas stream; splitting the syngas stream into first and second streams; conveying the first stream to a water gas shift reactor for producing a modified syngas stream containing CO and hydrogen; the second stream bypassing the water gas shift reactor and being added to the modified syngas steam; optionally reforming natural gas by steam methane reforming to produce a synthetic gas and optionally adding the synthetic gas to the water gas shift reactor; thereby obtaining a syngas having a H₂:CO ratio of about 1:1 to about 2:1; subjecting the syngas to a Fischer Tropsch reaction thereby producing a wax product; and subjecting the product to a hydrogen cracking process to produce liquid fuel; and apparatus therefore.

The invention discloses a process for integrally heated continuous preparing biomass pyrolysis gasification gas and a rotary furnace utilized by the same. At a furnace tail cooling section, red charcoal at a temperature of 600-800 DEG C after pyrolyzing and destructive distilling reacts with steam generated by cooling spray water on the lower portion in the furnace so as to absorb large quantities of heat and simultaneously generate water gas and semi-water gas. Heat generated by burning recycled gas and air is used for maintaining pyrolysis temperature of biomass material layers and providesenough heat for further, pyrolysis, destructive distillation and steam decomposition reaction. By aid of the heat, biomass inside the furnace is pyrolyzed and destructively distilled to generate large quantities of volatile matters, and the biomass is gradually heated to decompose destructive gas with high heat value. The rotary furnace utilizes a three-section design: a first section is a furnace head preheating section, which is mainly used for preheating and drying raw materials, a second section is a rotary furnace body pyrolysis section, which is mainly used for pyrolysis and destructivedistillation and is a core operation portion of the furnace, and a third section is a furnace tail cooling section, which is mainly used for cooling charcoal. Prepared gas is high in heat value, and devices occupy small space.

The invention discloses a method for preparing low-carbon olefins from synthetic gas, and belongs to the field of olefins. In order to solve the problems that due to a backmixing phenomenon, the retention time is inconsistent, reaction products are widely distributed, and side reactions of olefin secondary reaction and water gas reaction and the like are intensified so as to influence the economy of the process in the traditional process for preparing low-carbon olefins from synthetic gas, a rotating packed bed reactor is used as a reactor, a solid Fischer-Tropsch synthesis catalyst is used or a catalyst is prepared into slurry, and the synthetic gas is converted into the low-carbon olefins. By the method, the selectivity of the low-carbon olefins can be greatly improved, and reaction heat can be quickly removed to stabilize the temperature of a reaction bed.

The invention provides a method for generating power with a gas turbine which utilizes pressure swing reforming under conditions that facilitate CO₂ capture. First a synthesis gas stream at a first pressure is produced in a pressure swing reformer. Next the synthesis gas stream is subjected to a high temperature water gas shift process to produce a CO₂ containing hydrogen enriched stream from which hydrogen and CO₂ each are separated. The separated hydrogen in turn is combusted with air to produce a gas turbine and the separated CO₂ is easily sequestered.

A process for producing synthetic hydrocarbons that reacts carbon dioxide, obtained from seawater of air, and hydrogen obtained from water, with a catalyst in a chemical process such as reverse water gas shift combined with Fischer Tropsch snthesis. The hydrogen is produced by nuclear reactor electricity, nuclear waste heat conversion, ocean thermal energy conversion, or any other source that is fossil fuel-free, such as wind or wave energy. The process can be either land based or sea based.

A homogeneous ceria-based mixed-metal oxide, useful as a catalyst support, a co-catalyst and/or a getter, is described. The mixed-metal oxide has a relatively large surface area per weight, typically exceeding 150 m<2>/g, a structure of nanocrystallites having diameters of less than 4 nm, and including pores larger than the nanocrystallites and having diameters in the range of 4 to about 9 nm. The ratio of the pore volumes, VP, to skeletal structure volumes, VS, is typically less than about 2.5, and the surface area per unit volume of the oxide material is greater than 320 m<2>/cm<3>, such that the structural morphology supports both a relatively low internal mass transfer resistance and large effective surface area for reaction activity of interest. The mixed metal oxide is made by co-precipitating a dilute metal salt solution containing the respective metals, which may include Zr, Hf, and/or other metal constituents in addition to Ce, replacing water in the co-precipitate with a water-miscible low surface-tension solvent, and relatively quickly drying and calcining the co-precipitate at moderate temperatures. A highly dispersive catalyst metal, such as Pt, may be loaded on the mixed metal oxide support from a catalyst-containing solution following a selected acid surface treatment of the oxide support. The mixed metal oxide, as catalyst support, co-catalyst or getter, is applied in various reactions, and particularly water gas shift and/or preferential oxidation reactions as associated with fuel processing systems, as for fuel cells and the like.

The present development is a catalyst for use in the water-gas-shift reaction. The catalyst includes a Group VIII or Group IB metal, a transition metal promoter selected from the group consisting of rhenium, niobium, silver, manganese, vanadium, molybdenum, titanium, tungsten and a combination thereof, and a ceria-based support. The support may further include gadolinium, samarium, zirconium, lithium, cesium, lanthanum, praseodymium, manganese, titanium, tungsten or a combination thereof. A process for preparing the catalyst is also presented. In a preferred embodiment, the process involves providing "clean" precursors as starting materials in the catalyst preparation.

The invention discloses a water-gas two-phase adsorption-desorption-seepage experimental system and method for loaded coal containing methane. The water-gas two-phase adsorption-desorption-seepage experimental system for loaded coal containing methane comprises a pressure loading part, wherein the pressure loading part comprises a tank body for containing a constant-temperature water bath, a reference pot and a coal sample holder are arranged in the tank body, the gas inlet of the reference pot is connected with a high-pressure methane delivery pipeline, the gas outlet of the reference pot is connected with the gas inlet of the coal sample holder through a connecting pipeline, and the gas outlet of the coal sample holder is connected with a water-gas separation device. The water-gas two-phase seepage experimental method for loaded coal containing methane is carried out on the basis of the experimental system. By changing different loading conditions, loading paths and experimental temperatures, adsorption-desorption experiments and methane seepage experiments for the loaded coal containing methane under the conditions of different solid-gas thermal coupling can be realized, and water-gas two-phase seepage experiments and methane adsorption-desorption experiments under the condition of different moisture contents also can be realized.

A multi-stage method and apparatus for producing methane from biomass in which the biomass is hydropyrolyzed in a reactor vessel containing molecular hydrogen and a deoxygenating catalyst, the output of which is hydrogenated using a hydroconversion catalyst. The output from the hydroconversion step is provided to a water-gas-shift process providing a mixture of H₂O and product gases including CO₂, H₂, and methane. The mixture components are separated, resulting in a product stream comprising substantially only methane.

The present invention provides a reactor, which includes: a unitary shell assembly having an inlet and an outlet; a flow path extending within the shell assembly from the inlet to the outlet, the flow path having a steam reformer section with a first catalyst and a water gas shift reactor section with a second catalyst, the steam reformer section being located upstream of the water gas shift reactor section; a heating section within the shell assembly and configured to heat the steam reformer section; and a cooling section within the shell assembly and configured to cool the water gas shift reactor section. The present invention also provides a simplified hydrogen production system, which includes the catalytic steam reforming and subsequent high temperature water gas shift of low-sulfur (<100 ppm by mass) hydrocarbon fuels followed by hydrogen purification through the pressure swing adsorption (PSA). The integrated reactor offers significant advantages such as lower heat loss, lower parts count, lower thermal mass, and greater safety than the many separate components employed in conventional and is especially well-suited to applications where less than 15,000 standard cubic feet per hour of hydrogen are required. The improved system also may be started, operated and shut down more simply and quickly than what is currently possible in conventional systems. The improved system preferably employs active temperature control for added safety of operation. The hydrogen product is of high purity, and the system may be optionally operated with a feedback control loop for added purity.

A biocomponent feedstock can be hydroprocessed using a hydrogen-containing refinery as a source of hydrogen gas. A relatively low cost catalyst, such as a water gas shift catalyst and/or spent hydrotreating catalyst, can be used as a hydrogenation catalyst for the process. The hydroprocessing can allow for olefin saturation and/or deoxygenation of the biocomponent feed by using a relatively low value refinery stream, e.g., containing from about 20 mol % to about 60 mol % hydrogen.