Patent classifications
C01B2203/1241
PROCESS FOR H2 AND SYNGAS PRODUCTION
A process for producing syngas that uses the syngas product from a partial oxidation reactor to provide all necessary heating duties, which eliminates the need for a fired heater. Soot is removed from the syngas using a dry filter to avoid a wet scrubber quenching the syngas stream and wasting the high-quality heat. Without the flue gas stream leaving a fired heater, all of the carbon dioxide produced by the reforming process is concentrated in the high-pressure syngas stream, allowing essentially complete carbon dioxide capture.
CATALYST FOR PREPARING A SYNTHESIS GAS, A METHOD FOR PREPARING THE SAME, AND A METHOD FOR PREPARING A SYNTHESIS GAS USING THE SAME
A catalyst for preparing a synthesis gas includes: a mesoporous Al.sub.2O.sub.3 support including mesopores having a pore size of about 1 nm to about 30 nm; metal nanoparticles supported in the mesopores of the mesoporous Al.sub.2O.sub.3 support wherein the metal nanoparticles have a particle size of less than or equal to about 20 nm; and a metal oxide coating layer including particles wherein the metal oxide coating layer is coated on the surface of the mesoporous Al.sub.2O.sub.3 support and includes mesopores having a pore size of about 2 nm to about 50 nm.
Hydrogen production with membrane reformer
A system and method for producing hydrogen from hydrocarbon and steam, including a membrane reformer with multiple membrane reactors each having a tubular membrane. The bore of the tubular membrane is the permeate side for the hydrogen. The region external to the tubular membrane is the retentate side for carbon dioxide. A sweep gas flows through the bore to displace hydrogen in a direction countercurrent to flow of hydrocarbon and steam in the region external to the tubular membrane. The method includes discharging hydrogen as permeate with the sweep gas from the bore, and discharging carbon dioxide in the region external to the tubular membrane as retentate from the membrane reactor.
Low steam/carbon revamp of a plant comprising a steam reforming section and a water-gas shift section
The present invention relates to a revamp method for increasing the front-end capacity of a plant comprising a reforming section, wherein a feed is reformed in at least one reforming step to a reformed stream comprising CH.sub.4, CO, CO.sub.2, H.sub.2 and H.sub.2O a shift section wherein the reformed stream is shifted in a shift reaction in at least a high temperature shift step,
said method comprising the steps of In the High temperature shift step exchanging an original Fe-based catalyst with a non-Fe-based catalyst Increasing the feed flow to the reforming section, and The HTS step is carried out at a reduced steam/dry-gas ratio (S/DG) compared to an original S/DG in the original HTS step with the original Fe-based catalyst.
Nickel-containing catalyst composition having enhanced acidity for dry reforming processes
Modified red mud catalyst compositions, methods for production, and methods of use in dry reforming, the composition comprising: red mud material produced from an alumina extraction process from bauxite ore; and nickel oxide, the nickel oxide present at between about 5 wt. % to about 40 wt. % of the modified red mud catalyst composition.
Production of hydrogen-rich fuel-gas with reduced CO.SUB.2 .emission
An H.sub.2-rich fuel gas stream can be advantageously produced by reforming a hydrocarbon/steam mixture in to produce a reformed stream, followed by cooling the reformed stream in a waste-heat recovery unit to produce a high-pressure steam stream, shifting the cooled reformed stream a first shifted stream, cooling the first shifted stream, shifting the cooled first shifted stream to produce a second shifted stream, cooling the second shifted stream, abating water from the cooled second shifted stream to obtain a crude gas mixture stream comprising H.sub.2 and CO.sub.2, and recovering a CO.sub.2 stream from the crude gas mixture stream. The H.sub.2-rich stream can be advantageously combusted to provide thermal energy needed for residential, office, and/or industrial applications including in the H.sub.2-rich fuel gas production process. The H.sub.2-rich fuel gas production process can be advantageously integrated with an olefins production plant comprising a steam cracker.
SYSTEMS AND METHODS FOR POWER PRODUCTION WITH INTEGRATED PRODUCTION OF HYDROGEN
The present disclosure relates to systems and methods useful for power production. In particular, a power production cycle utilizing CO.sub.2 as a working fluid may be configured for simultaneous hydrogen production. Beneficially, substantially all carbon arising from combustion in power production and hydrogen production is captured in the form of carbon dioxide. Further, produced hydrogen (optionally mixed with nitrogen received from an air separation unit) can be input as fuel in a gas turbine combined cycle unit for additional power production therein without any atmospheric CO.sub.2 discharge.
PRE-COMBUSTION CO2 REMOVAL IN A NATURAL GAS FED STEAM METHANE REFORMER (SMR) BASED HYDROGEN PLANT
In a hydrocarbon-fed steam methane reformer hydrogen-production process and system, carbon dioxide is recovered in a pre-combustion context, and optionally additional amounts of carbon dioxide are recovered in a post-combustion carbon dioxide removal, to provide the improved carbon dioxide recovery or capture disclosed herein.
System and method for methanol production using energy mix systems
A system and a method for methanol production is described. The method includes gasifying coal to produce a coal gas comprising hydrogen and carbon monoxide; transferring heat from the coal gas to a natural gas reforming mixture including water and methane; reforming the natural gas reforming mixture to form a reformed natural gas; mixing the coal gas, the reformed natural gas, and a recycled gas including hydrogen and carbon monoxide to form a synthesis gas; reacting the synthesis gas to form methanol and a waste gas; separating the methanol and the waste gas; removing hydrogen from the waste gas to produce a dehydrogenated waste gas; and subjecting the dehydrogenated waste gas to a water-gas shift reaction to produce the recycled gas.
ENDOTHERMIC REACTION OF A FEED GAS HEATED BY RESISTANCE HEATING
Array including a first and a second monolith of a structured catalyst for carrying out an endothermic reaction of a feed gas, wherein: a) the first and second monolith include a macroscopic structure of a first and second electrically conductive material; b) each of said first and second monoliths has a number of flow channels formed therein for conveying feed gas through the monoliths; c) the array includes at least a first and a second conductor electrically connected to said first and second monoliths, respectively, and to an electrical power supply, d) the first and second monolith are electrically connected by a monolith bridge; e) the array is configured to direct an electrical current to run from the first conductor through the first monolith to a second end, then through the bridge, and then through the second monolith to the second conductor.