A fuel cell system includes a solid oxide fuel cell configured to receive a supply of an anode gas and a cathode gas to generate electric power. The fuel cell system includes an anode discharge passage through which an anode off-gas discharged from the fuel cell flows, a cathode discharge passage through which a cathode off-gas discharged from the fuel cell flows, a joining portion where the anode discharge passage and the cathode discharge passage join. The fuel cell system further includes a gas supply unit configured to supply a fuel gas using a fuel stored in a fuel tank into the anode discharge passage during a system stop.

Provided are boron nanoparticles. The boron nanoparticles can be made by pyrolysis of a boron precursor (e.g., a boron hydride such as, for example, diborane) using a photosensitizer and electromagnetic radiation of an appropriate wavelength. The boron nanoparticles can be functionalized. The boron nanoparticles can be hydrogen-containing boron nanoparticles (e.g., hydrogen-terminated boron nanoparticles). Also provided are methods of hydrogen generation using boron nanoparticles, an activator, and water. Examples of activators include, but are not limited to, Li, Na, K, LiH, NaH, and combinations thereof.

A chemical reactor (e.g. reformer reactor) system includes a manifold (126) for management of a flow of gaseous reaction medium thereto. Manifold (126) includes manifold housing (128) defining manifold chamber (129) and having at least one additional component selected from: a gas distributor (127); a heater; and a cavity having a seal within or adjacent to it.

An Aluminum nitride ceramic and preparation method thereof. The aluminum nitride ceramic comprises a porous aluminum nitride matrix. A ferrite is loaded on the pore surface of the porous aluminum nitride matrix; and nano nickel particles are loaded on the surface of the ferrite. The preparation method of the aluminum nitride ceramic comprises steps: sintering the aluminum nitride ceramic by pressureless sintering method, depositing the ferrite on pore surface of porous aluminum nitride matrix by hydrothermal method, and loading nano nickel particles on the surface of the ferrite by reduction method. A micro-reactor is provided. So that the technical problems: the preheating time of the micro-reactor prepared is too long, nickel particles fall off from the surface of matrix, and nano nickel particles grow up due to quick and direct temperature rise can be solved.

Hydrogen generation assemblies and methods of generating hydrogen are disclosed. In some embodiments, the method may include receiving a feed stream in a fuel processing assembly of the hydrogen generation assembly; and generating a product hydrogen stream in the fuel processing assembly from the received feed stream. Generating a product hydrogen stream may, in some embodiments, include generating an output stream in a hydrogen generating region from the received feed stream, and generating the product hydrogen stream in a purification region from the output stream. The method may additionally include receiving the generated product hydrogen stream in a buffer tank of the hydrogen generation assembly; and detecting pressure in the buffer tank via a tank sensor assembly. The method may further include stopping generation of the product hydrogen stream in the fuel processing assembly when the detected pressure in the buffer tank is above a predetermined maximum pressure.

There is described a reforming unit for hydrogen production and a power generation device incorporating at least the reforming unit for generating electricity. The reforming unit generally has a catalytic burner defining a burner cavity; a reaction assembly within the burner cavity and in thermal communication therewith, the reaction assembly including; a reactor conduit extending annularly around an axis and axially between an input port and an output port, the input port being fluidly coupled to a wet fuel source supplying wet fuel, the reactor conduit having distributed therein a plurality of catalyst elements; and a syngas conduit extending along the axis, within the reactor conduit and in thermal communication therewith, the syngas conduit having an input port fluidly coupled to the output port of the reactor conduit, and an output port; the catalytic burner having a plurality of heating devices surrounding the burner cavity.

The present invention provides a catalyst composition for producing hydrogen and preparation method and use thereof, wherein the catalyst composition comprises a catalytic component and a supporter having a pyrochlore structure. By using the catalyst composition of the present invention, carbon deposition can be reduced and the oxidative steam reforming of ethanol could be operated for a long period of time with high ethanol conversion rate and selectivity of hydrogen.

A catalyst for catalytic reactors of which the outer shape is a helix with n blades, where n is greater than or equal to 1, wherein the stack void fraction percentage is between 75% and 85% and the surface area/volume ratio is greater than 1000 square meters/square meters.

Provided is a hydrogen production reactor as a reactor producing a reforming gas including hydrogen, in which a burning unit and a reforming unit are sequentially arranged and spaced apart from each other in a concentric structure based on a raw material transfer pipe positioned at a central axis of the reactor, including a heating raw material transfer pipe supplying a raw material to the burning unit, a burning unit burning the supplied raw material and supplying heat to the reforming unit, a reforming raw material phase change pipe positioned within the burning unit and heating the supplied raw material, and a reforming unit reforming the phase-changed raw material supplied from the reforming raw material phase change pipe, wherein the reforming raw material phase change pipe is provided as a coil surrounding an outer circumferential surface of a lower end of the heating raw material transfer pipe.

The present invention relates to a process for production of hydrogen at low temperature starting from alcohols without formation of carbon using an oxyhydride material based on cerium and nickel and to the use of such a material as catalyst for transformation of alcohols to hydrogen.