Systems and methods are provided for performing hydrocarbon reforming within a reverse flow reactor environment (or another reactor environment with flows in opposing directions) while improving management of CO.sub.2 generated during operation of the reactor. The improved management of CO.sub.2 is achieved by making one or more changes to the operation of the reverse flow reactor. The changes can include using an air separation unit to provide an oxygen source with a reduced or minimized content of nitrogen and/or operating the reactor at elevated pressure during the regeneration stage. By operating the regeneration at elevated pressure, a regeneration flue gas can be generated that is enriched in CO.sub.2 at elevated pressure. The CO.sub.2-enriched stream can include primarily water as a contaminant, which can be removed by cooling while substantially maintaining the pressure of the stream. This can facilitate subsequent recovery and use of the CO.sub.2.

An engine system for internal combustion and reformation of a fuel includes an engine, and a reforming reactor. The engine comprising an intake manifold for receiving a first fuel and an exhaust manifold for releasing an exhaust gas. The reforming reactor includes a first end portion, a second end, a wall having an outer surface and an inner surface. The inner surface defines an interior cavity for receiving the first fuel, a second fuel, reactants for the first fuel, or combinations thereof. The exhaust manifold of the system is sized and shaped for receiving a portion of the reforming reactor such that the exhaust gas flows along a surface of the reforming reactor within the exhaust manifold.

A catalyst for the pyrolysis of a hydrocarbon, such as methane or natural gas, includes a pile of waste-product configured to facilitate the decomposition of the hydrocarbon into hydrogen and carbon. The waste-product is one of bauxite residue, mill scale, or slag. The pile of waste product may be broken down into a powder or piece-meal form.

A catalyst for the pyrolysis of a hydrocarbon, such as methane or natural gas, includes a pile of waste-product configured to facilitate the decomposition of the hydrocarbon into hydrogen and carbon. The waste-product is one of bauxite residue, mill scale, or slag. The pile of waste product may be broken down into a powder or piece-meal form.

The invention comprises a process for obtaining a gas from a fluid fuel and an oxidising fluid, said process comprising steps in which the incoming fluid is subjected to temperature, photocatalytic action and reaction with catalysts, all this within a device with a tubular structure which the incoming fluid circulates through in a spiral manner, between a fixed bed attached to the walls of the duct and a circulating bed with an ionised gas stream that occupies a central position of the duct, producing a gas obtained.

The disclosure provides a system and method for synthesizing ultra-pure hydrogen from biomass waste. The present invention comprises a gasifier, an oils and tars filter, a steam generator, a water gas shift reactor (“WGS”), a heat-exchange two-phase water separator, a scrubber, a hydrogen separator, and fluid conduits in fluid communication with the various system components, which together convert hydrocarbon-based biomass, e.g., woodchips, into ultra-pure hydrogen gas. Fluid conduits connect the gasifier and the steam generator, separately, to the WGS, the WGS to the two-phase separator, the two-phase separator to the scrubber, and the scrubber to the hydrogen separator, which further comprises an outlet port through which hydrogen gas may flow free of carbon monoxide. The hydrogen may flow to a device that utilizes hydrogen to generate energy, such as a hydrogen fuel cell or to an internal combustion engine.

Catalysts for converting carbon dioxide and methane to synthesis gas include an alumina supported copper-nickel alloy composition having the formula Ni.sub.xCu.sub.y. The catalyst comprises about 70% to about 98% by weight of alumina in the catalyst, wherein x is an atomic percentage nickel content and y is an atomic percentage copper content, and wherein a ratio of x to y is about 3:1 to about 10:1. In one embodiment, the Ni—Cu catalyst composition according to the present disclosure is derived by state of the art electronic structure calculations based on Density Functional Theory (DFT).

The present invention refers to processes for obtaining steam reforming catalysts containing nickel, cerium, lanthanum and copper oxides, free from potassium or alkali metals, preferably with the oxide layer being located externally with a thickness of less than 0.5 mm on the support particle, preferably the support being based on alumina, magnesium aluminate, hexaaluminates or mixtures thereof. The catalysts according to present invention show high activity, resistance to thermal deactivation and resistance to coke accumulation in the steam reforming reaction of hydrocarbons.

Provided are a structured catalyst for CO shift or reverse shift that can realize a long life time by suppressing the decline in function, a method for producing the same, a CO shift or reverse shift reactor, a method for producing carbon dioxide and hydrogen, and a method for producing carbon monoxide and water. The structured catalyst for CO shift or reverse shift (1) includes a support (10) of a porous structure composed of a zeolite-type compound, and at least one CO shift or reverse shift catalytic substance (20) present in the support (10), the support (10) has channels (11) connecting with each other, and the CO shift or reverse shift catalytic substance (20) is present at least in the channels (11) of the support (10).

A reactor suitable for a reaction containing an exothermic reaction is provided. The reactor includes the following components. A reaction channel has an inlet and an outlet, and has a front-end reaction zone, middle-end reaction zones, and a back-end reaction zone from the inlet to the outlet. A front-end catalyst support and a front-end catalyst are located in the front-end reaction zone, a middle-end catalyst support and a middle-end catalyst are respectively located in the middle-end reaction zones, and a back-end catalyst support and a back-end catalyst are located in the back-end reaction zone. The concentration of the front-end catalyst is less than the concentration of the back-end catalyst, and the concentration of the middle-end catalyst is decided via a computer simulation of reaction parameters. The reaction parameters include size and geometric shape of the reaction channel.