A process and a plant for cooling a synthesis gas produced by catalytic steam reformation of a hydrocarbonaceous feed gas, which is cooled by heat exchange with boiler feed water for its conversion into steam, by separating the resulting aqueous condensate, wherein the further cooling is effected in that the gas passes through several series-connected cooling stages and comprises the heat exchange with the feed gas, with degassed and non-degassed boiler feed water for generating the steam required for the steam reformation, and with ambient air, and wherein condensate obtained after the last cooling stage is separated from the gas and the gas is discharged for the further treatment, wherein at least after a further cooling stage upstream of the last cooling stage a hot aqueous condensate is separated from the gas.

A method for generating energy in mobile applications, such as water vehicles, wherein hydrogen is produced by at least partially dehydrogenating a hydrogenated liquid organic hydrogen carrier (LOHC) in a chemical reactor, where electricity and water are generated in at least one fuel cell and heat for the chemical reactor is generated in a heating device from the produced hydrogen, and where the hydrogen produced by the chemical reactor is first conducted through the at least one fuel cell and then supplied to the heating device, such that the at least one fuel cell can therefore be operated under partial load and thus with better efficiency than if the hydrogen for the heating device is branched off before the fuel cell.

Among other things, the present invention encompasses the applicant's recognition that epoxide carbonylation can be performed industrially utilizing syngas streams containing hydrogen, carbon monoxide and varying amounts carbon dioxide. Contrary to expectation, the epoxide carbonylation reaction proceeds selectively in the presence of these mixed gas streams and incorporates excess CO in the syngas stream into valuable chemical precursors, resulting in hydrogen streams substantially free of CO. This is economically and environmentally preferable to performing WSGR which releases the excess carbon as CO2. The integrated processes herein therefore provide improved carbon efficiency for processes based on coal or biomass gasification or steam methane reforming.

Provided is a novel production system that does not involve, or can minimize, the transport of liquid ammonia in the production of an organic compound or the production of a microorganism by microbial fermentation. A production system for an organic compound or a microorganism includes: an ammonia synthesis apparatus in which an ammonia-containing gas is synthesized by reaction of a source gas containing hydrogen and nitrogen in the presence of a supported ruthenium catalyst; and a culture apparatus that cultures a microorganism having organic compound productivity using ammonia originating from the ammonia-containing gas obtained by using the ammonia synthesis apparatus.

A system and method for processing unconditioned syngas first removes solids and semi-volatile organic compounds (SVOC), then removes volatile organic compounds (VOC), and then removes at least one sulfur containing compound from the syngas. Additional processing may be performed depending on such factors as the source of syngas being processed, the products, byproducts and intermediate products desired to be formed, captured or recycled and environmental considerations.

A method of generating a hydrogen or hydrocarbon fuel from a feedstock via a centrifuge reactor that includes introducing a flow of feedstock to a centrifuge reactor with a centrifuge assembly having a reaction chamber and configured to rotate about a central rotational axis X, rotating the centrifuge assembly about the central rotational axis X at a tip speed of 100 m/s to 1000 m/s to generate an acceleration gradient from the central rotational axis X and from the first reaction chamber end to the second reaction chamber end; and generating reaction conditions in the reaction chamber, including pressure of 5 MPa to 500 MPa and temperature within a range of 200 C. to 1000 C., the reaction conditions and acceleration gradient causing a separation of products from a reaction of the feedstock within the reaction chamber.

According to an embodiment of the present disclosure, petrochemicals may be produced from crude oil by a process which includes passing the crude oil and hydrogen into a hydroprocessing reactor, separating the hydrotreated oil into a lesser boiling point fraction and a greater boiling point fraction, passing the lesser boiling point fraction to a pyrolysis section of a steam cracker to produce a pyrolysis effluent comprising olefins, aromatics, or both, passing the greater boiling point fraction to a gasifier, where the gasifier produces hydrogen, and passing at least a portion of the hydrogen produced by the gasifier to the hydroprocessing reactor.

Process for debottlenecking a plant that produces hydrogen including reforming of hydrocarbons, then conversion of CO, purification of hydrogen by PSA-H2 for the production of a high-pressure gaseous stream of ultra-pure hydrogen with associated production of a low-pressure residue, the two major constituents of which are carbon dioxide and hydrogen, the debottlenecking of the plant is carried out by installing, level with the PSA residue, an EHS electrochemical cell for supplying, from the PSA residue, hydrogen and a hydrogen-depleted residue, the additional hydrogen stream recovered in the EHS cell is compressed and sent to the inlet of the PSA unit thus increasing the hydrogen production of the plant while keeping the purity of the hydrogen produced by the PSA unchanged. The invention also relates to a process and a plant for producing hydrogen having an optimized hydrogen yield.

In a process for the production of ammonia synthesis gas from a hydrocarbon-containing feedstock, comprising steam reforming of the feedstock and treatment of the synthesis gas obtained, the shift of the synthesis gas comprises two shift steps, both including stable catalysts, whereby the formation of hazardous by-products is avoided or at least reduced to an acceptable low level. The two shift steps can both be HTS, or they can be one HTS and one LTS or one HTS and one MTS. The catalyst used in the HTS and the LTS steps is based on zinc oxide and zinc aluminum spinel, and the catalyst used in the MTS and the LTS steps can be based on copper.

In various aspects, systems and methods are provided for operating a molten carbonate fuel cell, such as a fuel cell assembly, with increased production of syngas while also reducing or minimizing the amount of CO.sub.2 exiting the fuel cell in the cathode exhaust stream. This can allow for improved efficiency of syngas production while also generating electrical power.