Patent classifications
C01B2203/1252
Method for producing synthesis gas
A method for producing synthesis gas may involve introducing a hydrocarbon-containing coke-oven gas and a carbon dioxide-containing converter gas into a first reaction zone where hydrogen present in the hydrocarbon-containing coke-oven gas reacts at least partly with carbon dioxide to form water, which reacts thermally with hydrocarbon to form synthesis gas containing carbon monoxide and hydrogen. The method may further involve introducing an oxygen-containing gas in a second reaction zone, and using the oxygen-containing gas and some hydrogen from the first reaction zone to produce thermal energy. Still further, the method may involve supplying the thermal energy produced in the second reaction zone to the first reaction zone.
Method of chemical looping reforming at low temperatures with hydrogen from water splitting
Chemical looping reform methods comprising heating an oxygen carrier in the presence of a catalyst and plasma radicals to react the oxygen carrier with a fuel to provide a reduced oxygen carrier; and contacting the reduced oxygen carrier with water or carbon dioxide to produce hydrogen or carbon monoxide, respectively, and regenerate the oxygen carrier. The chemical looping reform methods are carried out at low temperatures such as from 150° C. to 1000° C., preferably from 150° C. to 500° C. Catalyst used in the chemical looping reform methods include a sintered rare earth metal oxide oxygen carrier and perovskite. Methods of preparing the catalyst are also provided.
Integrated process plant having a biomass reforming reactor using a fluidized bed
An interconnected set of two or more stages of reactors to form a bio-reforming reactor that generates syngas for a number of different liquid fuel or chemical processes is discussed. A first stage includes a circulating fluidized bed reactor that is configured to cause a chemical devolatilization of the biomass into its reaction products of constituent gases, tars, chars, and other components, which exit through a reactor output from the first stage. A second stage of the bio-reforming reactor has an input configured to receive a stream of some of the reaction products that includes the constituent gases and at least some of the tars as raw syngas, and then chemically reacts the raw syngas within a vessel of the second stage to make the raw syngas from the first stage into a chemical grade syngas by further cracking the tars, excess methane, or both.
Compositions and Methods of Using Fine Mineral Matter as a Catalyst for Chemical Recycling
The presently disclosed embodiments relate to the utilization of coal-derived fine mineral matter in chemical recycling of plastics or of solid mixed plastic waste. The instantly disclosed mineral based catalyst benefits the processes of catalytic cracking, gasification and steam reforming to maximize carbon utilization and production of plastics of original quality from recycled or renewable feedstocks while reducing the plastic pollution in the environment. The catalyst can be based on inorganic fine mineral matter, a natural ancient mineral mixture found in coal deposits and containing a plurality of transition metals, such as iron, copper, and manganese, as well as calcium, barium, magnesium, potassium, sodium, which can act as co-catalysts. Addition of the catalyst can convert plastic to syngas at a faction of the energy of conventional technologies.
Combustion of spent adsorbents containing HPNA compounds in a membrane wall partial oxidation gasification reactor
A process for the economical and environmentally acceptable disposal of spent adsorbent recovered from an adsorption column used to remove HPNA compounds and HPNA precursors from hydrocracking unit bottoms and/or recycle streams includes removing the liquid hydrocarbon oil from the spent adsorbent material by a combination of solvent flushing, and/or heating and vacuum treatment, grinding the dried adsorbent material containing the HPNA compounds and HPNA precursors to produce free-flowing particles of a predetermined maximum size, and introducing the particulate adsorbent material into a membrane wall partial oxidation gasification reactor to produce hydrogen and carbon monoxide synthesis gas, or syngas, which can be further processed by the water-gas shift reaction to increase the overall hydrogen recovered from the initial feed to the gasifier.
HYDROGEN SUPPLY SYSTEM
A hydrogen supply system supplying hydrogen, the hydrogen supply system including: a dehydrogenation reaction unit acquiring a hydrogen-containing gas by performing a dehydrogenation reaction of a raw material containing a hydride; and a control unit controlling the hydrogen supply system, in which in a case in which generation of the hydrogen-containing gas in the dehydrogenation reaction unit stops, the control unit causes the hydrogen supply unit to supply hydrogen to the dehydrogenation reaction unit, and the hydrogen supply unit supplies at least one of the hydrogen-containing gas between the dehydrogenation reaction unit and a vapor-liquid separating unit separating a dehydrogenation product from the hydrogen-containing gas and the hydrogen-containing gas separated by the vapor-liquid separating unit separating a dehydrogenation product from the hydrogen-containing gas to the dehydrogenation reaction unit.
METHOD OF CHEMICAL LOOPING REFORMING AT LOW TEMPERATURES WITH HYDROGEN FROM WATER SPLITTING
Chemical looping reform methods comprising heating an oxygen carrier in the presence of a catalyst and plasma radicals to react the oxygen carrier with a fuel to provide a reduced oxygen carrier; and contacting the reduced oxygen carrier with water or carbon dioxide to produce hydrogen or carbon monoxide, respectively, and regenerate the oxygen carrier. The chemical looping reform methods are carried out at low temperatures such as from 150 C. to 1000 C., preferably from 150 C. to 500 C. Catalyst used in the chemical looping reform methods include a sintered rare earth metal oxide oxygen carrier and perovskite. Methods of preparing the catalyst are also provided.
Fuel upgrading by reforming and dehydrocracking
Zn-promoted and/or Ga-promoted cracking catalysts, such as cracking catalysts comprising an MSE framework zeolite or an MFI framework zeolite can provide unexpectedly superior conversion of branched paraffins when used as part of a catalyst during reforming of a hydrocarbon fuel stream. The conversion and reforming of the hydrocarbon fuel stream can occur, for example, in an internal combustion engine. The conversion and reforming can allow for formation of higher octane compounds from the branched paraffins.
Tar reforming furnace
Syngas is alternatingly introduced by a syngas alternating lead-in system through either of one- and the other-end-side heat storage bodies into flow passages in a primary reforming furnace, and oxidant is alternatingly supplied to the syngas by a primary-oxidant alternating supply system. The syngas derived from the primary reforming furnace by a syngas alternating lead-out system is introduced into a secondary reforming furnace to which connected is a secondary-oxidant supply system for supply of oxidant only at alternation in the syngas alternating lead-in and -out systems.
Catalyst support, recycle reactor and method for releasing hydrogen
A catalyst support may be provided that comprises: an inner core, which includes at least one phase change material; a coating layer around the inner core, which includes at least one metal oxide; a catalytically active layer, which is positioned in interstices of the coating layer and/or lying on the coating layer, wherein at least one catalytically active substance is included in the catalytically active layer; and a supporting layer which is positioned under the coating layer. A recycle reactor may be provided comprising a reservoir for accommodating a chemical hydrogen storage substance; the catalyst support; a screw conveyor for input and transport of the catalyst support; and a heating device with which the catalyst support can be heated. A method for releasing hydrogen from a chemical hydrogen storage substance may be provided.