Process for manufacturing a hydrogen-containing synthesis gas from a natural gas feedstock, comprising the conversion of said natural gas into a raw product gas and purification of said product gas, the process having a heat input provided by combustion of a fuel; said process comprises a step of conversion of a carbonaceous feedstock, and at least a portion of said fuel is a gaseous fuel obtained by said step of conversion of said carbonaceous feedstock, and the Wobbe Index of said fuel is increased by a step of carbon dioxide removal or methanation.

Provided herein is a gas mixer for the safe mixing of a hydrocarbon containing gas with a gaseous oxidant. The gas mixer and method for mixing described includes a closed mixing vessel where bubbles of gas injected at the bottom of the vessel are mixed during their rise to the top of the vessel, forming a homogeneous mixture that can safely be removed. This simple design and method allows for safe mixing of gases and is applicable to catalytic oxidative processes such as oxidative dehydrogenation of paraffins where there is a risk of thermal runaway of reactions.

A blast furnace facility includes a process for capturing and sequestering CO2 generated from the facility process, producing hydrogen from the hot blast furnace gas, and using blast furnace gas as methanol feed. The CO2 rich streams from the facility may be sent to sequestration of some form via a sequestration compressor, thereby reducing the overall emissions from the facility. The other products generated by the facility are used as methanol feedstock and to produce hydrogen.

A blast furnace facility includes a process for capturing and sequestering CO2 generated from the facility process, generating hydrogen from hot blast furnace gas, and using blast furnace gas as methanol feed. The CO2 rich streams from the facility are sent to sequestration of some form via a sequestration compressor, thereby reducing the overall emissions from the facility. The other products generated by the facility are used as methanol feedstock and to produce hydrogen.

Provided is a method for generating hydrogen at a desired rate, using a hydrogen storage material that can be stored and transported safely and inexpensively. The method according to the present invention for producing a silanol compound and hydrogen includes subjecting a hydrosilane compound and water to a reaction with each other in the presence of a solid catalyst to give a silanol compound and hydrogen. The solid catalyst includes hydroxyapatite and gold particles supported on the hydroxyapatite, where the gold particles have an average particle size of 2.5 nm or less. The reaction in the method according to the present invention for producing a silanol compound and hydrogen is preferably performed in an air atmosphere. The reaction in the method according to the present invention for producing a silanol compound and hydrogen can be performed with application of substantially no heat and no activated energy rays.

Phase-changing fuel compositions which can generate hydrogen are provided herein. The compositions can comprise a hydrogen carrier at least partially dissolved in a polar organic solvent. The hydrogen carrier includes ammonia borane and an alkylamine borane such as methylamine borane or methylenediamine bisborane. The hydrogen carrier act as the primary fuel source in the compositions and can be present in an amount of at least 60% by weight, based on the weight of the hydrogen generation composition. The hydrogen generation compositions are a liquid at temperatures of 5° C. or greater or 25° C. or greater. Methods for the production of hydrogen from the hydrogen generation compositions are further disclosed.

A method for preparing hydrogen-rich synthesis gas by degrading waste polyolefin plastics at a low temperature includes the following steps: weighing 1 part by weight of polyolefin waste plastics and 3 parts-80 parts by weight of hydrogen peroxide containing 0.25%-6% of H.sub.2O.sub.2; feeding the polyolefin waste plastics and the hydrogen peroxide into a hydrothermal reactor, and carrying out the oxidation pretreatment reaction at a reaction temperature of 150° C.-230° C. under a reaction pressure of 0.5 MPa-2 MPa for 30 minutes-90 minutes, and obtaining an aqueous-phase product and a gas-phase product after the reaction is finished; filling another hydrothermal reactor with a mesoporous carbon supported metal-based catalyst, and then introducing the aqueous-phase product into the hydrothermal reactor for a reforming reaction to obtain a hydrogen-rich synthesis gas product. In the whole process, the H.sub.2 yield is close to 11 mol/kg plastics, and the H.sub.2 concentration in the hydrogen-rich synthesis gas is close to 55%.

A flow reactor system for providing on-demand H.sub.2 evolution at pressure from a liquid organic hydrogen carrier and/or blends thereof includes a reactor that includes a reaction vessel having an inlet and outlet. The inlet is configured to introduce reactants into the reaction vessel, and the outlet is configured to release reaction products. The reaction vessel is configured to hold therein a catalyst system capable of catalyzing the evolution of molecular hydrogen from a liquid organic hydrogen carrier. Advantageously, the reaction vessel is configured to operate at pressures greater than or equal to 50 psig (e.g., from about 50 psig to about 10500 psig. The flow reactor system also includes a source of preheated liquid organic hydrogen carrier in fluid communication with the reactor and a purification system in fluid communication with the outlet that provides purified molecular hydrogen gas for on-demand applications.

The present invention proves a hydrogen injection apparatus that is good in terms of work efficiency and sanitation at the time of maintenance and that is capable of generating hydrogen water the hydrogen content of which is flexibly adjustable. The hydrogen injection apparatus according to the present invention includes a reference vessel, on the bottom of which a particle having a material for reacting with water to generate hydrogen formed on the surface thereof is placed, the reference vessel being configured to store water for reaction with hydrogen, a communication means for fluidly connecting the interior of the upper side of the reference vessel to the storage water for drinking in the state in which the reference vessel is sealed, and an auxiliary means for increasing injection of hydrogen into the storage water for drinking from the reference vessel through the communication means.

A solids discharge system (SDS) is configured to separate solids from product gas. The system includes a solids separation device and at least one solids transfer conduit configured to receive solids from the solids separation device. The solids transfer conduit is selectively partitioned into a plurality of compartments (or “sections”) along its length by isolation valves. A gas supply conduit and a gas discharge conduits are connected to one of the sections to facilitate removal of solids. A filter in fluid communication with that section is configured to prevent solids from passing through the gas discharge conduit so that the solids can be removed from one of the sections of the solids transfer conduit. A product gas generation system incorporates first and second reactors, the latter of which receives products created by the second reactor.