Proposed are a process and a plant for producing a synthesis gas product stream having an adjustable H.sub.2/CO ratio and a pure hydrogen stream, wherein it is provided according to the invention that a substream of a deacidified synthesis gas stream is supplied to a membrane separation plant fitted with a hydrogen-selective membrane and the remaining substream is supplied to a pressure swing adsorption plant, wherein the latter affords a pure hydrogen stream and a fuel gas stream. The hydrogen-enriched permeate stream obtained from the membrane separation is likewise supplied to the pressure swing adsorption plant, thus enhancing the yield of pure hydrogen. The hydrogen-depleted retentate stream obtained from the membrane separation is discharged as a synthesis gas product stream and if of a suitable composition may be utilized as oxo gas.

The invention is directed to a process to prepare a char product by pyrolysis or mild gasification of a solid biomass feed thereby obtaining a gaseous fraction comprising hydrogen, carbon monoxide and a mixture of gaseous organic compounds and a solid fraction comprising of char particles having a reduced atomic hydrogen over carbon ratio and a reduced oxygen over carbon ratio relative to the solid biomass feed. The solid biomass feed are pellets of a solid torrefied biomass feed. The pyrolysis or mild gasification is performed at a temperature of between 500 and 800° C. and at a solid residence time of between 10 and 60 minutes.

The invention is directed to a process to prepare a char product by pyrolysis or mild gasification of a solid biomass feed thereby obtaining a gaseous fraction comprising hydrogen, carbon monoxide and a mixture of gaseous organic compounds and a solid fraction comprising of char particles having a reduced atomic hydrogen over carbon ratio and a reduced oxygen over carbon ratio relative to the solid biomass feed. The solid biomass feed are pellets of a solid torrefied biomass feed. The pyrolysis or mild gasification is performed at a temperature of between 500 and 800° C. and at a solid residence time of between 10 and 60 minutes.

A process for converting carbon dioxide and hydrogen into a product stream comprising carbon monoxide, water and hydrogen by introducing carbon dioxide, hydrogen and oxygen into a reaction vessel, and performing a reverse water gas shift reaction at elevated temperature, wherein (a) no catalyst is present in vessel (b) gas stream comprising carbon dioxide, a hydrogen and an oxygen rich gas stream are introduced into the vessel in separate feed streams, (c) the hydrogen and oxygen rich gas stream being introduced in close vicinity of each other, via burner comprising coaxial channels wherein gases gas undergo a combustion reaction, providing the heating energy required for the reverse water-gas shift reaction; and (d) the temperature in vessel is in the range of 1000 to 1500° C. by varying the molar ratio of hydrogen to oxygen.

It is useful in reducing the carbon footprint of certain industrial technologies, and in production of synthesis gas.

A process for converting carbon dioxide and hydrogen into a product stream comprising carbon monoxide, water and hydrogen by introducing carbon dioxide, hydrogen and oxygen into a reaction vessel, and performing a reverse water gas shift reaction at elevated temperature, wherein (a) no catalyst is present in vessel (b) gas stream comprising carbon dioxide, a hydrogen and an oxygen rich gas stream are introduced into the vessel in separate feed streams, (c) the hydrogen and oxygen rich gas stream being introduced in close vicinity of each other, via burner comprising coaxial channels wherein gases gas undergo a combustion reaction, providing the heating energy required for the reverse water-gas shift reaction; and (d) the temperature in vessel is in the range of 1000 to 1500° C. by varying the molar ratio of hydrogen to oxygen.

It is useful in reducing the carbon footprint of certain industrial technologies, and in production of synthesis gas.

A reactor includes a reaction-side flow passage through which a reaction fluid being a fluid constituting a reaction object flows; a temperature controller (heat-medium side flow passage) configured to heat or cool the reaction fluid from outside the reaction-side flow passage; and a catalyst configured to promote a reaction of the reaction fluid, the catalyst provided in the reaction-side flow passage so that a contact area with the reaction fluid is larger on a downstream side than on an upstream side in the reaction-side flow passage.

A fuel cell system comprising a fuel cell stack, an evaporator for evaporating a mixture of methanol and water to be forwarded through a catalytic reformer for producing portions of free hydrogen. The fuel cell stack being composed of a number of proton exchange membrane fuel cells each featuring electrodes in form of an anode and a cathode for delivering an electric current. The system provides an enhanced system for evaporating the liquid fuel using a pre-evaporator, which partly evaporates the fuel, followed by a nozzle, which atomizes the fuel into a fine mist, before being passed to the final evaporation zone. This configuration ensures minimal fuel accumulation in the system and fast load transition's.

Disclosed is a lanthanide oxide coated catalyst, and methods for its use, that includes a supported catalyst comprising a support material, a catalytic material, and a lanthanide oxide, wherein the lanthanide oxide is attached to at least a portion of the surface of the supported catalyst.

Provided is a catalyst structure for a liquid organic hydrogen carrier (LOHC) dehydrogenation reactor, including a support, a plurality of channels formed on the support in such a manner that the LOHC may flow therethrough, and an LOHC dehydrogenation catalyst that is coated on the inner surfaces of the channels and is in contact with the LOHC to carry out LOHC dehydrogenation, wherein the hydrogen gas generated from the dehydrogenation is discharged along the channels so that the contact area between the LOHC and the LOHC dehydrogenation catalyst may be increased.

The invention relates to an improved method for chemical-looping combustion of a solid hydrocarbon-containing feed using a particular configuration of the reduction zone with: a first reaction zone R1 operating under dense fluidized bed conditions; a second reaction zone R2; a fast separation zone S3 for separation of the unburnt solid feed particles, of fly ashes and of the oxygen-carrying material particles within a mixture coming from zone R2; fumes dedusting S4; a particle stream division zone D7, part of the particles being directly recycled to first reaction zone R1, the other part being sent to an elutriation separation zone S5 in order to collect the ashes through a line 18 and to recycle the dense particles through a line 20 to first reaction zone R1. The invention also relates to a chemical-looping combustion plant allowing said method to be implemented.