A hybrid dehydrogenation reaction system includes: an acid aqueous solution tank having an acid aqueous solution; an exothermic dehydrogenation reactor including a chemical hydride of a solid state and receiving the acid aqueous solution from the acid aqueous solution tank for an exothermic dehydrogenation reaction of the chemical hydride and the acid aqueous solution to generate hydrogen; an LOHC tank including a liquid organic hydrogen carrier (LOHC); and an endothermic dehydrogenation reactor receiving the liquid organic hydrogen carrier from the LOHC tank and generating hydrogen through an endothermic dehydrogenation reaction of the liquid organic hydrogen carrier by using heat generated from the exothermic dehydrogenation reactor.

The disclosure relates to methods, systems, and apparatus arranged and designed for converting non-methane hydrocarbon gases into multiple product gas streams including a predominately hydrogen gas stream and a predominately methane gas steam. Hydrocarbon gas streams are reformed, cracked, or converted into a synthesis gas stream and methane gas stream by receiving a volume of flare gas or other hydrocarbon liquid or gas feed, where the volume of hydrocarbon feed includes a volume of methane and volume of nonmethane hydrocarbons. The hydrogen contained in the syngas may be separated into a pure hydrogen gas stream. A corresponding gas conversion system can include a super heater to provide a hydrocarbon feed/steam mixture, a heavy hydrocarbon reactor for synthesis gas formation, and a hydrogen separator to recover the hydrogen portion of the synthesis gas.

A looping reaction hydrogen production system includes a reduction reaction device, a primary separation device, a hydrogen production reaction device, a secondary separation device, a primary heat transfer device and a cooling purification device. Based on looping combustion reaction mechanism, the system makes MeO/Me circularly flow between the hydrogen production reaction device and the reduction reaction device to respectively generate a reduction/oxidation chemical reaction, and to convert the conventional carbon-based solid fuel into the high-purity clean hydrogen energy. Compared with the conventional hydrogen production technology from water-gas shift reaction of syngas, the system reduces water consumption, energy consumption and environmental pollution of the hydrogen production process; converts conventional carbon-based fuel into clean hydrogen energy by use of renewable energy sources, such as solar energy; and achieves efficient capture and storage of gaseous CO.sub.2.

A method is provided for rapidly switching a metal-catalysed steam methane reforming reaction of a feed gas from a first steady-state reaction condition (A) to a second steady-state reaction condition (B) or vice-versa. After applying a given voltage and/or feed gas flow, the system can work towards a thermal equilibration to reach steady state without any additional operator input.

A process is proposed for producing synthesis gas with reduced steam export by catalytic steam reforming of a hydrocarbonaceous feed gas with steam in a multitude of reformer tubes in a burner-heated reformer furnace to form a steam reforming flue gas. This process includes a configuration of the reformer tubes as reformer tubes with internal heat exchange and the use of a structured catalyst. For amounts of export steam between 0 and 0.8 kg of export steam per m.sub.N.sup.3 of hydrogen produced, these features interact synergistically when particular steam reforming conditions are selected.

Embodiments of the invention relate to systems and methods for cracking hydrocarbons into hydrogen gas and carbon using heating of a fluidized bed. The systems and methods utilize electrically conductive carbon or graphite particles as a fluidized bed material for heating hydrocarbon feedstock to at least a pyrolysis temperature. The electrically conductive carbon, graphite, or other particles may be heated by electrically powered sources that include induction heating, microwave heating, millimeter wave heating, joule heating and/or plasma heating. Combustion heating may also be employed in varying amounts with varying combinations of electrically powered heating sources.

Process for cracking hydrocarbon gases, wherein the hydrocarbon gas is passed through a flow channel of an absorptive receiver reactor (1, 30, 40), characterized in that cracking takes place during the passing through the receiver reactor (1, 30, 40), wherein in a first region (21) of the flow channel (2) the hydrocarbon gas is heated to its cracking temperature, in an adjoining second, downstream flow region (22) is heated to beyond its cracking temperature and in a third, further downstream region (23) of the flow channel is heated yet further and is brought therein into physical contact, over the cross-section of said region, with a reaction accelerator, after which the stream of products downstream of the reaction accelerator is discharged from the receiver reactor (1, 30, 40), and wherein the heating of the hydrocarbon gas to above its cracking temperature is achieved by absorption of blackbody radiation (20) which is given off by the reaction accelerator heated by solar radiation (7) incident thereupon to the hydrocarbon gas flowing towards it, in such a way that the hydrocarbon gas in the flow channel (2) and extending up to the reaction accelerator forms disc-shaped, consecutive temperature zones (60 to 67) of ever-increasing temperature extending transversely to the flow channel (2).

A micro-reactor for a reforming process has a cold side and a hot side opposite the cold side. Inlets are defined in the cold side, the inlets configured for receiving reagents. An outlet is defined in the cold side, the outlet configured for exiting reforming products. A reforming chamber is in the hot side, the reforming chamber having a catalyst, the reforming chamber configured for reforming the reagents into the reforming products, the reforming chamber including channels extending toward an end surface on the hot side of the reforming chamber, and a return plenum. A reagent path is from the inlets to the reforming chamber, the reagent path configured to feed the plurality of channels with reagents. A reforming product path is from the reforming chamber to the outlet, the reforming product path configured to receive products from the return plenum.

Embodiments include a method for converting renewable energy source electricity and a hydrocarbon feedstock into a liquid fuel by providing a source of renewable electrical energy in communication with a synthesis gas generation unit and an air separation unit. Oxygen from the air separation unit and a hydrocarbon feedstock is provided to the synthesis gas generation unit, thereby causing partial oxidation reactions in the synthesis gas generation unit in a process that converts the hydrocarbon feedstock into synthesis gas. The synthesis gas is then converted into a liquid fuel.

This disclosure relates installed or new synthesis gas (Syngas) production units and potential modifications to those units to reduce the firing requirements and significant emissions of CO.sub.2 from those units with affordable capital expenditures.