A process and/or system for producing biomethane, hydrogen, or fuel, fuel intermediate, and/or chemical product from the biomethane or hydrogen. The biomethane and/or hydrogen is produced in a process that converts biomass to biomethane. In certain embodiments, the biomethane production process includes anaerobic digestion, which produces biogas and digestate. Carbon-containing material (e.g., derived from the biomass) is stored and/or used as part of at least one carbon capture and storage process, where the carbon-containing material includes (i) carbon dioxide produced from the biomethane production process (e.g., produced from anaerobic digestion), and (ii) carbon-containing material obtained or derived from residue of the biomethane production process, and optionally includes (iii) carbon dioxide produced from the hydrogen production process.

The invention relates to a method for start-up and operation of a Fischer-Tropsch reactor comprising the steps of: (a) providing a reactor with a fixed bed of reduced Fischer-Tropsch catalyst that comprises cobalt as catalytically active metal; (b) supplying a gaseous feed stream comprising carbon monoxide and hydrogen to the reactor, wherein the gaseous feed stream comprises a nitrogen-containing compound other than molecular nitrogen in an initial concentration, wherein the initial concentration in the range of from 10 to 350 ppbv based on the volume of the gaseous feed stream; (c) converting carbon monoxide and hydrogen supplied with the gaseous feed stream to the reactor into hydrocarbons at a reaction temperature and at a set reactor productivity, whilst maintaining the initial concentration of the nitrogen-containing compound and maintaining the set reactor productivity during a first time period by adjusting the reaction temperature; (d) decreasing the concentration of the nitrogen-containing compound to a second concentration in the range of from 0 to 20 ppbv, wherein the second concentration is at least 5 ppbv below the initial concentration, preferably at least 20 ppbv below the initial concentration, and maintaining the reactor productivity by adjusting the reaction temperature.

Nickel based catalyst structures are described herein that include a plurality of metal oxides formed as crystalline phases within the catalyst structures. Each metal oxide of a catalyst structure includes nickel and/or aluminum, where one or more metal oxides includes a nickel aluminum oxide, and the one or more nickel aluminum oxides is greater than 50% by weight of the catalyst structure. The catalyst structures further have surface areas of at least 13 m.sup.2/g. The catalyst structures are resistant to high concentrations of sulfur and are effective in reforming operations for converting methane and other light hydrocarbons to hydrogen and one or more other components. For example, the catalyst structures are effective in coal and biomass gasification systems for the forming and cleanup of synthetic gas.

A solar thermochemical processing system is disclosed. The system includes a first unit operation for receiving concentrated solar energy. Heat from the solar energy is used to drive the first unit operation. The first unit operation also receives a first set of reactants and produces a first set of products. A second unit operation receives the first set of products from the first unit operation and produces a second set of products. A third unit operation receives heat from the second unit operation to produce a portion of the first set of reactants.

A method and an integrated system for reducing CO.sub.2 emissions in industrial processes. The method and integrated system (100) capture carbon dioxide (CO.sub.2) gas from a first gas stream (104) with a chemical absorbent to produce a second gas stream (106) having a higher concentration of carbon monoxide (CO) gas and a lower concentration of CO.sub.2 gas as compared to first gas stream. The CO gas in the second gas stream is used to produce C.sub.5 to C.sub.20 hydrocarbons in an exothermic reaction (108) with hydrogen (H.sub.2) gas (138). At least a portion of the heat generated in the exothermic reaction is used to regenerate the chemical absorbent with the liberation of the CO.sub.2 gas (128) captured from the first gas stream. Heat captured during the exothermic reaction can, optionally, first be used to generate electricity, wherein the heat remaining after generating electricity is used to thermally regenerate the chemical absorbent.

A system for the production of synthesis gas, including a gasification apparatus configured to convert at least a portion of a gasifier feed material introduced thereto into a gasification product gas comprising synthesis gas having a molar ratio of hydrogen to carbon monoxide; at least one additional apparatus selected from the group consisting of feed preparation apparatus located upstream of the gasification apparatus, synthesis gas conditioning apparatus, and synthesis gas utilization apparatus; and at least one line fluidly connecting the at least one additional apparatus or an outlet of the gasification apparatus with the at least one vessel of the gasification apparatus, whereby a gas from the at least one additional apparatus or exiting the gasification apparatus may provide at least one non-steam component of a fluidization gas. A method of utilizing the system is also provided.

A liquid fuel product system is configured to produce liquid fuels from carbonaceous materials. The liquid fuel product system includes a plurality of feedstock delivery systems, a plurality of first stage product gas generation systems, a plurality of second stage product gas generation systems, a plurality of third stage product gas generation systems, a primary gas clean-up system, a compression system, a secondary gas clean-up system, and a synthesis system that includes one or more from the group consisting of ethanol, mixed alcohols, methanol, dimethyl ether, and Fischer-Tropsch products.

The present disclosure relates to a processes and systems for producing fuels from biomass with high carbon conversion efficiency. The processes and systems described herein provide a highly efficient process for producing hydrocarbons from biomass with very low Green House Gas (GHG) emissions using a specific combination of components, process flows, and recycle streams. The processes and systems described herein provide a carbon conversion efficiency greater than 95% with little to no GHG in the flue gas due to the novel arrangement of components and utilizes renewable energy to provide energy to some components. The system reuses water and carbon dioxide produced in the process flows and recycles naphtha and tail gas streams to other units in the system for additional conversion to syngas to produce hydrocarbon-based fuels.

Embodiments of the present invention relate to two improved catalysts and associated processes that directly convert carbon dioxide and hydrogen to liquid fuels. A catalytic system comprises two catalysts in series that are operated in tandem to directly produce synthetic liquid fuels. The carbon conversion efficiency for CO.sub.2 to liquid fuels is greater than 45%. The fuel is distilled into a premium diesel fuels (approximately 70 volume %) and naphtha (approximately 30 volume %) which are used directly as drop-in fuels without requiring any further processing. Any light hydrocarbons that are present with the carbon dioxide are also converted directly to fuels. This process is directly applicable to the conversion of CO.sub.2 collected from ethanol plants, cement plants, power plants, biogas, carbon dioxide/hydrocarbon mixtures from secondary oil recovery, and other carbon dioxide/hydrocarbon streams. The catalyst system is durable, efficient and maintains a relatively constant level of fuel productivity over long periods of time without requiring re-activation or replacement.

The present disclosure includes a method of producing a liquid FT hydrocarbon stream, an FT tail gas stream and an FT water stream using an FT reactor feed in an FT reactor under low temperature, high pressure FT operating conditions. The FT reactor feed includes syngas, the syngas having a low H.sub.2:CO ratio in the range of approximately 1.4:1 to approximately 1.8:1, and carbon dioxide at a level of at least as high as about 10 volume percent. The FT reactor has a cobalt-based, alumina-supported FT catalyst. In embodiments, a syngas preparation unit is used to produce the syngas and carbon dioxide recovered from the FT tail gas is recycled to the syngas preparation unit. Other methods, systems and apparatuses are also disclosed.