An energy production device may include: a supply device for hydrocarbon gas; energy converter configured to convert the energy supplied by the H.sub.2 into electrical, thermal, and/or mechanical energy; H.sub.2 producer fluidically between the supply device and the energy converter; the H.sub.2 producer including a plasmalysis reactor configured to generate plasmalysis of the hydrocarbon gas so as to produce at least one dihydrogen directed towards the energy converter; a controller configured to generate a control instruction for the H.sub.2 producer with information on H.sub.2 present in a H.sub.2 distribution area arranged fluidically between the plasmalysis reactor and the energy converter, the H.sub.2 distribution area including a storage assembly at the plasmalysis reactor outlet and hydraulically connected to the plasmalysis reactor and energy converter, the storage assembly including a compression device, storage tank, and expander, the compression device being positioned to transfer H.sub.2 exiting the plasmalysis reactor into the storage tank.

Hydrogen purification devices and their components are disclosed. In some embodiments, the devices may include at least one foil-microscreen assembly disposed between and secured to first and second end frames. The at least one foil-microscreen assembly may include at least one hydrogen-selective membrane and at least one microscreen structure including a non-porous planar sheet having a plurality of apertures forming a plurality of fluid passages. The planar sheet may include generally opposed planar surfaces configured to provide support to the permeate side. The plurality of fluid passages may extend between the opposed surfaces. The at least one hydrogen-selective membrane may be metallurgically bonded to the at least one microscreen structure.

A burner combustion chamber (3), a reformer catalyst (4) to which burner combustion gas is fed, and a heat exchange part (13a) for heating the air fed to the burner (7) are provided. When the temperature of the reformer catalyst (4) exceeds the allowable catalyst temperature (TX) or when it is predicted the temperature of the reformer catalyst (4) will exceed the allowable catalyst temperature (TX), the air circulation route for guiding air to the burner (7) is switched from a high temperature air circulation route (13) for guiding air heated by the heat exchange part (13a) to the burner (7) to a low temperature air circulation route (14) for guiding air not flowing within the heat exchange part (13a) and lower in temperature than the air heated at the heat exchange part (13a) to the burner (7).

The system comprises a steam reforming unit to produce hydrogen from exhaust gas supplied, a hydrogen permeable membrane to allow only hydrogen produced by the steam reforming unit to pass through it, a hydrogen storage unit to absorb hydrogen supplied through the hydrogen permeable membrane and release absorbed hydrogen, a fuel cell to generate power using hydrogen supplied from the hydrogen storage unit, a gas clean-up unit to clean up residual gases delivered not passing through the hydrogen permeable membrane, and a control unit to control the hydrogen storage unit to absorb or release hydrogen depending on whether the fuel cell is supplied with sufficient hydrogen.

The disclosure relates to systems and methods to produce hydrogen (H.sub.2) gas from hydrogen sulfide (H.sub.2S). H.sub.2S is contacted with a catalyst to form H.sub.2 gas and sulfur adsorbed to the catalyst. The adsorbed sulfur is contacted with oxygen (O.sub.2) gas to convert the adsorbed sulfur to sulfur dioxide (SO.sub.2) and regenerate the catalyst

Provided is a fuel-reforming device comprising: an ammonia tank (4); a reformer (5) for reforming ammonia and generating high-concentration hydrogen gas having a hydrogen content of at least 99%; a mixing tank (7) for mixing ammonia and hydrogen for temporary storage; and a control means (10) for controlling the respective supply amounts of ammonia and high-concentration hydrogen gas that are supplied to the mixing tank (7). The control means (10) calculates the combustion rate coefficient C of mixed gas with respect to a reference fuel on the basis of equation (1). Equation (1): S.sub.0=S.sub.H?C+S.sub.A?(1?C). In equation (1), S.sub.0 is the combustion rate of the reference fuel, S.sub.H is the combustion rate of hydrogen, S.sub.A is the combustion rate of ammonia, and C is the combustion rate coefficient of mixed gas. In addition, on the basis of equation (2), the control means (10) determines the volume fractions of ammonia and hydrogen that are supplied to the mixing tank. Equation (2): C=1?exp(?A?M.sub.B). In equation (2), M is the volume fraction of hydrogen in mixed gas, and A and B are constants.

Low carbon hydrogen will play a crucial role in decarbonization of chemical complexes and manufacturing facilities. Depending on the application, different grades of low carbon hydrogen might be requiredfuel grade (90-99% H2 purity) or chemical grade (>99% H2 purity). The current invention describes a hydrogen production process based on autothermal reforming and CO2 capture to produce low carbon hydrogen with hydrogen rich offgas as part of the feedstock.

A method for enriching a synthesis gas in hydrogen is presented. The method includes adding H.sub.2O to the synthesis gas to form a synthesis gas stream that includes hydrogen, carbon monoxide, and steam. The synthesis gas stream has a steam to dry gas molar ratio, S/DG; and an oxygen to carbon molar ratio, O/C. The method includes introducing the synthesis gas stream into a water-gas shift reactor and reacting the synthesis gas stream in the water-gas shift reactor in the presence of a non-iron-based catalyst to produce a shifted synthesis gas. The method further includes controlling an outlet temperature of the synthesis gas stream to remain at or below a critical temperature or to drop to or below the critical temperature by adjusting the S/DG ratio to maintain the O/C ratio below a lower O/C limit or above an upper O/C limit.

A method for controlling a fuel reformation reaction in a fuel reformation reactor is provided. Furthermore, a non-transitory computer-readable storage medium is provided, which is configured to store a program for controlling a fuel reformation reaction in a fuel reformation reactor. In addition, a fuel reformation system for controlling a fuel reformation reaction is provided, which includes a fuel reformation reactor and a control unit.

Method and apparatus for converting waste solid sustainable carbon material to chemical products is described herein. The methods add hydrocarbon derived from fossil sources to gas derived from gasifying waste solid sustainable carbon material to enhance hydrogen availability, and in some cases carbon availability, for production of the chemical products. Biomass is used to provide energy to dry solid sustainable carbon material to form dry sustainable carbon material to gasify. Carbon dioxide made by the process is at least partially sequestered to yield a chemical manufacturing process with environmental burden substantially less than conventional processes. Use of the hydrocarbon boosts yield of final products.