Patent classifications
C01B3/025
METHOD FOR MIXING AT LEAST TWO GASES
A method of co-producing a nitrogen containing stream and a methanol stream, including producing at least an oxygen enriched stream and a nitrogen enriched stream in an air separation unit, introducing at least a portion of the oxygen enriched stream into an oxygen-based reformer, thereby producing a first syngas stream, introducing at least a portion of the first syngas stream into a methanol synthesis reactor, thereby producing at least a hydrogen containing stream and a methanol containing stream, introducing at least a portion of the methanol containing stream into a methanol distillation system, thereby producing a methanol product stream, introducing at least a portion of the nitrogen enriched stream, at least a portion of the first enriched hydrogen containing stream, and at least a portion of the second enriched hydrogen containing stream into an ammonia synthesis reactor, thereby producing an ammonia product stream.
Process and plant for the combination production of a mixture of hydrogen and nitrogen and also of carbon monoxide by cryogenic distillation and cryogenic scrubbing
Process for the combined production of a mixture of hydrogen and nitrogen, and of carbon monoxide by cryogenic distillation and cryogenic scrubbing, wherein a methane-rich liquid is introduced at a first intermediate level of a scrubbing column as first scrubbing liquid and at least one nitrogen-rich liquid is introduced at a level higher than the first level of the scrubbing column as second scrubbing liquid and a mixture of hydrogen and nitrogen is drawn off as overhead gas from the scrubbing column.
PROCESS FOR PRODUCING A HYDROGEN-CONTAINING SYNTHESIS GAS
Process including the production of a hydrogen-containing synthesis gas by conversion of a hydrocarbon feedstock, wherein said process has a heat input provided by combustion of a plurality of process fuel streams and said plurality of process fuel streams comprises at least one fuel stream of ammonia. Combustion of said at least one fuel stream of ammonia is performed non-catalytically in at least one fired equipment.
Urea process with controlled excess of CO.SUB.2 .and/or NH.SUB.3
A process for producing urea with controlled excess of CO.sub.2 and/or NH.sub.3. The process includes the steps of: reforming the hydrocarbon feed gas, thereby obtaining a synthesis gas comprising CH.sub.4, CO, CO.sub.2, H.sub.2 and H.sub.2O, shifting the synthesis gas, removing CO.sub.2 from the synthesis gas, removing residual H.sub.2O and/or CO.sub.2 from the synthesis gas, removing CH.sub.4, CO, Ar and/or He, and adding stoichiometric nitrogen to produce NH.sub.3 to the synthesis gas, synthesizing NH.sub.3 to obtain a NH.sub.3 product, and adding at least part of the product CO.sub.2 and at least part of the NH.sub.3 product to a urea synthesis step to make a urea product. The amount of excess CO.sub.2 and/or NH.sub.3 is controlled by adjusting the steam/carbon in the reforming step and/or the H.sub.2O addition upstream the shift step and/or adjusting the inlet temperature to at least one or more shift steps.
Carbon capture, waste upgrade, and chemicals production using improved flexicoking
Systems and methods are provided for integrating a fluidized coking operation, a reverse osmosis operation, a coke gasification operation and/or processes for production of compounds from the synthesis gas generated during the coke gasification. Conventional FLEXICOKING™ processes may produce carbon dioxide emissions and low Joule Flexigas, as well as waste water containing metals and poor quality coke containing metals, which may be expensive to process, or may require sending to other facilities for further processing. The systems and methods described herein address these issues in an advantageous and economical manner, with improved carbon capture, waste upgrade and chemicals production, while providing high value ash (e.g., for recovery of metals such as vanadium, nickel, sodium, iron, and mixtures thereof) and upgraded coke streams.
Bioreactors with Integrated Catalytic Nitrogen Fixation
Nitrogen in a form suitable for feeding a population of microbes in a bioreactor is produced by reacting nitrogen gas and hydrogen gas to form ammonia plus an unreacted gas stream under conditions favorable to having little unreacted nitrogen gas in the unreacted gas stream. The ammonia, or a compound derived from the ammonia is fed to the microbes and the unreacted gas stream is optionally fed back into the reaction, or fed into the bioreactor. Oxygen can be produced, such as by electrolysis, and also provided to the microbes. Hydrogen from the electrolysis can be added to the hydrogen being reacted with nitrogen gas, and/or can be added to the bioreactor. Where nitrogen gas is produced from air separation, the residual gases can be another source of oxygen.
METHOD FOR PRODUCING SYNGAS, AS WELL AS SYNGAS COOLING ASSEMBLY AND USE
A method of producing synthesis gas in a dual pressure level ammonia plant having a first synthesis section operated in once through fashion at a first relatively lower high pressure and having a second synthesis section operated in recirculating fashion at a second relatively higher high pressure. In the first synthesis section downstream of an OT reactor of the first synthesis section the synthesis gas is cooled using cooling medium at a pressure below the first high pressure, wherein the cooling medium is provided at a pressure below the first high pressure level by means of a medium pressure steam generator or wherein the cooling is effected by means of the medium pressure steam generator. The disclosure further relates to a synthesis gas cooling assembly in such a dual pressure level ammonia plant and at least one plant component for providing or for utilizing the cooling medium.
TRANSITION METAL CARBIDE CHEMICAL LOOPING REFORMING
A process for producing syngas including at least H.sub.2 and CO. The process includes the steps of a) generating a transition metal carbide by reacting a corresponding transition metal oxide with a fuel to produce a stream of syngas; and b) combining the transition metal carbide with oxygen to oxidize the transition metal carbide to regenerate the corresponding transition metal oxide, thereby producing a gas output comprising at least one or more oxidized carbon compounds and heat for autothermal operation.
OXYGEN TRANSPORT REACTORS FOR CO-GENERATING AMMONIA AND POWER
A system for co-generating ammonia and power is described. The system includes oxygen transport reactors having an ion transport membrane (ITM) that separates a feed side and a permeate side. The feed side includes a feed inlet and a feed outlet, and the permeate side includes a permeate inlet and a permeate outlet. A first feed inlet receives water vapor to be converted into hydrogen and first oxygen, and a second feed inlet receives air to be split into nitrogen and second oxygen. The ITM selectively allows permeation of the first oxygen and the second oxygen to respective permeate side to support oxy-combustion process. A first feed outlet discharges hydrogen and a second feed outlet discharges nitrogen, where the hydrogen and the nitrogen are combined in a catalytic converter to form ammonia. Combustion gases from the oxygen transport reactors are used to run a gas turbine to extract power.
Process for producing ammonia synthesis gas and a method for revamping a front-end of an ammonia plant
A process for producing ammonia make-up synthesis gas and a procedure for revamping a front-end of an ammonia plant for producing ammonia make-up synthesis gas are disclosed, wherein the make-up synthesis gas is produced by means of steam reforming of a hydrocarbon gaseous feedstock; said front-end includes a primary reformer, a secondary reformer, a shift conversion section, a CO2 removal section and optionally a methanation section; a shell-and-tube gas-heated reformer is installed after said secondary reformer, and a portion of the available feedstock is reformed in the tubes of said gas-heated reformer, and heat is provided to the shell side of said gas-heated reformer by at least a portion of product gas leaving the secondary reformer, possibly mixed with product gas leaving the tubes of said gas-heated reformer.