Processes, systems, and methods for producing combustible gas from wet biomass are provided. In one aspect, for example, a process for generating a combustible gas from a wet biomass in a closed system is provided. Such a process may include growing a wet biomass in a growth chamber, moving at least a portion of the wet biomass to a reactor, heating the portion of the wet biomass under high pressure in the reactor to gasify the wet biomass into a total gas component, separating the gasified component into a liquid component, a non-combustible gas component, and a combustible gas component, and introducing the liquid component and non-combustible gas component containing carbon dioxide into the growth chamber to stimulate new wet biomass growth.

Methods and systems of the present disclosure can function to capture flue gas and convert the flue gas to a synthesis gas, which can be further processed to other components such as liquid fuels. Aspects of the present disclosure provide for a process designed to capture flue gas from large scale (i.e. ˜GW), fossil based power plants in a 24/7 continuous operation. In addition, the method and system can convert the flue gas to a synthesis gas (mainly carbon monoxide and hydrogen), which will be processed into high quality liquid fuels, like diesel.

A light absorbing member includes a ceramic composite having a plurality of first ceramic particles exhibiting positive resistance temperature characteristics in a first ceramics having an open porosity of 5% or lower.

A system including a gas production device including (a) a solid containing compartment configured to contain a solid, (b) at least one fluid channel with an inlet and an outlet comprising an opening along at least a portion of its length, the opening facing the solid, (c) a solution compartment configured to contain a solution, the solution compartment: (1) being in fluid communication with the fluid channel inlet and outlet, (2) located along a fluid pathway in between the fluid channel outlet and inlet, and (3) at least one hydrogen gas outlet, (d) a fluid flow driver in fluid communication with the fluid pathway, and (e) a fluid flow rate regulator connected to the fluid flow driver. Disclosed is also a method for producing a gas (e.g., hydrogen).

A submerged plasma generator includes: a reactor inside of which a flow path, through which a working fluid passes, is formed along a lengthwise direction; and a dielectric insert which is disposed in the flow path so as to define the flow path into one space and the other space, and has formed therein a through-hole to generate micro-nano bubbles by cavitation in the working fluid fed into the one space of the flow path, and includes, a metallic catalyst which undergoes friction with the working fluid flowing through the through-hole and releases electric charges of the same polarity to the micro-nano bubbles to collapse the micro-nano bubbles and generate plasma; in which the other space of the flow path in which the working fluid ionized by exposure to the plasma travels is formed in an oval structure.

A submerged plasma generator includes: a reactor inside of which a flow path, through which a working fluid passes, is formed along a lengthwise direction; and a dielectric insert which is disposed in the flow path so as to define the flow path into one space and the other space, and has formed therein a through-hole to generate micro-nano bubbles by cavitation in the working fluid fed into the one space of the flow path, and includes, a metallic catalyst which undergoes friction with the working fluid flowing through the through-hole and releases electric charges of the same polarity to the micro-nano bubbles to collapse the micro-nano bubbles and generate plasma; in which the other space of the flow path in which the working fluid ionized by exposure to the plasma travels is formed in an oval structure.

A porous carbon-based metal catalyst, a preparation method and application thereof are provided. The preparation method includes: successively performing activation, surface corrosion, nitrogen-doping treatment and graphitization treatment on washed micro-grade porous carbon, then performing sensitization treatment, and subsequently carrying out loading, reduction and other treatments of catalytic metal, so as to finally obtain the porous carbon-based metal catalyst. The porous carbon-based metal catalyst provided by the present application has excellent catalytic performance, is especially suitable for producing hydrogen by efficiently catalytically decomposing ammonia borane, is not prone to inactivation, and is easy to regenerate after inactivation. Meanwhile, the preparation method is environmental-friendly, is suitable for large-scale production and has a wide application prospect in the fields such as hydrogen fuel batteries.

A porous carbon-based metal catalyst, a preparation method and application thereof are provided. The preparation method includes: successively performing activation, surface corrosion, nitrogen-doping treatment and graphitization treatment on washed micro-grade porous carbon, then performing sensitization treatment, and subsequently carrying out loading, reduction and other treatments of catalytic metal, so as to finally obtain the porous carbon-based metal catalyst. The porous carbon-based metal catalyst provided by the present application has excellent catalytic performance, is especially suitable for producing hydrogen by efficiently catalytically decomposing ammonia borane, is not prone to inactivation, and is easy to regenerate after inactivation. Meanwhile, the preparation method is environmental-friendly, is suitable for large-scale production and has a wide application prospect in the fields such as hydrogen fuel batteries.

Methods and devices for generating power using PEM fuel cell power systems comprising a rotary bed reactor for hydrogen generation are disclosed. Hydrogen is generated by the hydrolysis of fuels such as lithium aluminum hydride and mixtures thereof Water required for hydrolysis may be captured from the fuel cell exhaust. Water is preferably fed to the reactor in the form of a mist generated by an atomizer. An exemplary 750 We-h, 400 We PEM fuel cell power system may be characterized by a specific energy of about 550 We-h/kg and a specific power of about 290 We/kg.

A chemical looping process for the production of hydrogen and the co-production of carbon dioxide comprising: a first redox loop that comprises: feeding of a first solid oxygen carrier to a first reaction zone (R1) in which a first carbonaceous fuel is also fed, which reacts with the first solid oxygen carrier fed at its maximum oxidising state (fully-oxidised form), leading to the formation of the combustion products carbon dioxide and water and the solid oxygen carrier at a lower oxidising state (reduced form); and feeding of the first solid oxygen carrier in reduced form to a second reaction zone (R2) into which air is also fed, obtaining, from the oxidation of the first solid oxygen carrier, heat and the solid oxygen carrier in fully-oxidised form to be recycled to the first reaction zone (R1); and a second redox loop that comprises: feeding of a second solid oxygen carrier to a third reaction zone (R3) in which a second carbonaceous fuel is also fed, which reacts with the second solid oxygen carrier fed at its an intermediate oxidising state (oxidised form), leading to the formation of the combustion products carbon dioxide and water and the solid oxygen carrier at a lower oxidising state (reduced form); and feeding of the second solid oxygen carrier in reduced form to a fourth reaction zone (R4) into which steam is also fed, which reacts with the reduced form of the solid oxygen carrier, producing hydrogen and the solid oxygen carrier at an intermediate oxidising state (oxidised form) to be recycled to the third reaction zone (R3) and/or the first reaction zone (R1), wherein the first reaction zone (R1) and the third reaction zone (R3) are interconnected allowing transfer of at least a portion of the first solid oxygen carrier from the first reaction zone (R1) to the third reaction zone (R3).