Abstract: Exemplary embodiments of methods and systems for hydrogen production using an electro-activated material are provided. In some exemplary embodiments, carbon can be electro-activated and used in a chemical reaction with water and a fuel, such as aluminum, to generate hydrogen. Controlling the temperature of the reaction, and the amounts of water, aluminum and electro-activated carbon can provide hydrogen on demand at a desired rate of hydrogen generation.

Abstract: Disclosed is a process for the concurrent production of hydrogen and sulphur from a H2S-containing gas stream, with reduced, and preferably zero, emissions. The method comprises the catalytic oxidative cracking of H2S so as to form H2 and S2. Preferably, the oxidation is conducted using oxygen-enriched air, preferably pure oxygen. The process is conducted in a reaction chamber comprising a bifunctional catalyst material, so as to favor both the partial oxidation of H2S and the dissociation thereof.

Abstract: A process and a related equipment for producing ammonia synthesis gas from a hydrocarbon-containing feedstock (20), the process comprising the steps of: primary reforming with steam (21), secondary reforming with an oxidant stream (23), and purification of the effluent of said secondary reforming, said purification comprising a step of shift conversion (13) of carbon monoxide, wherein the synthesis gas (25) produced by said secondary reforming is subject to a medium-temperature shift over a copper-based catalyst, and the global steam to carbon ratio of the process is not greater than 2.

Abstract: Denitrifying bypass exhaust gases in a cement clinker producing plant. The plant comprises a rotary kiln connected to a calciner for the deacidification of raw material or to a rotary kiln riser shaft via a rotary kiln inlet chamber, and the bypass exhaust gas being drawn off in the region of the rotary kiln inlet chamber. The method comprises: cooling the bypass gas to between 260 C and 400 C in a cooling device, injecting an ammonia-, urea-, and/or ammonium-containing substance into the cooled bypass gas, introducing the cooled and mixed bypass gas into a ceramic filter system to filter out any halide and sulfate of the alkali metals and alkaline-earth metals precipitated during cooling the gas, and any nitrogen not reacted by the injected substances is chemically selectively reduced over a catalytic converter which is located in or directly downstream of the ceramic filter system.

Abstract: A marine exhaust gas scrubbing device including an enclosure having a first end and a second end, an exhaust gas inlet, at least one quencher, at least one pre-treater, at least one venturi component including a venturi inlet and a venturi outlet, an impingement basket, at least one demister, an exhaust gas outlet, and a receiver, and a process for scrubbing a marine exhaust gas including cooling the exhaust gas, pre-treating the exhaust gas, washing the exhaust gas, mixing the exhaust gas and exhausting the scrubbed exhaust gas.

Abstract: An alkaline catalyst for hydrogen generation can comprise a first metal (102), a second metal (104), and hydroxide (104). When the alkaline catalyst is added to an aqueous solution containing a hydrogen generation metal, the aqueous solution produces at least 4 L of hydrogen per 5 gram of hydrogen generation metal per 15 minutes at a production temperature of 140° F. and at a pressure of 1 atm.

Abstract: The present disclosure is directed to a hydrogen production system for creating and extracting hydrogen gas. The hydrogen production system contains a reactor vessel into which a solution and a metallic or semi-metal material may be placed. The solution is added to the reactor vessel contains both water and a caustic. When contacting the metallic or semi-metal material within the reactor vessel a chemical reaction occurs. The chemical reaction creates hydrogen gas as well as heat and other byproducts. The hydrogen gas may then flow through a hydrogen extraction point located on the reactor vessel for collection or operational use.

Abstract: The present invention relates to methods of preparing carbon monoxide (CO) and hydrogen (H2) by reacting biomass, a biomass component (e.g., lignin, ligno-cellulose, cellulose, hemiceullose or combination thereof) or a carbohydrate from any source with a polyoxometalate catalyst such as H5PV2Mo10O40, or solvates thereof, in the presence of a concentrated acid, under conditions sufficient to yield carbon monoxide (CO); followed by electrochemical release of hydrogen (H2). The carbon monoxide (CO) and hydrogen (H2) may be combined in any desired proportion to yield synthesis gas (Syngas). The present invention further relates to methods for preparing H2, CO and formic acid/formaldehyde from biomass, a biomass component and/or from carbohydrates.

Abstract: Methods of forming a diatom-based nanocomposite are provided. The methods include mixing at least one diatomic material, one or more metal precursors, and functionalized graphite oxide to form a mixture. The methods also include exfoliating the mixture in presence of hydrogen to reduce functionalized graphite oxide to graphene and reducing the one or more metal precursors to metal nanoparticles. The methods further include depositing the metal nanoparticles on the diatomic material to form the diatom-based nanocomposite.

Abstract: Provided herein are corrosion-resistant reactors that can be used for gasification, and methods of making and using the same. Some embodiments include a corrosion-resistant ceramic layer. According to some embodiments, the corrosion-resistant ceramic layer has a negative charge. At temperature above water's critical point (for example, 374 CC and at 22.1 MPa I 218 atm), water can behave as an adjustable solvent and can have tunable properties depending on temperature and pressure.

Abstract: Systems, devices, and methods combine thermally stable reactant materials and aqueous solutions to generate hydrogen and a non-toxic liquid by-product. The reactant materials can sodium silicide or sodium silica gel. The hydrogen generation devices are used in fuels cells and other industrial applications. One system combines cooling, pumping, water storage, and other devices to sense and control reactions between reactant materials and aqueous solutions to generate hydrogen. Springs and other pressurization mechanisms pressurize and deliver an aqueous solution to the reaction. A check valve and other pressure regulation mechanisms regulate the pressure of the aqueous solution delivered to the reactant fuel material in the reactor based upon characteristics of the pressurization mechanisms and can regulate the pressure of the delivered aqueous solution as a steady decay associated with the pressurization force.

Abstract: The invention relates to a process for the parallel preparation of hydrogen, carbon monoxide and a carbon-comprising product, wherein one or more hydrocarbons are thermally decomposed and at least part of the pyrolysis gas formed is taken off from the reaction zone of the decomposition reactor at a temperature of from 800 to 1400° C. and reacted with carbon dioxide to form a gas mixture comprising carbon monoxide and hydrogen (synthesis gas).

Abstract: A reactor for reforming a liquid hydrocarbon fuel, and associated processes and systems, are described herein. In one example, a two stage process is disclosed in which a first reactor is coupled to a second stage reactor having a reaction volume greater than the first reactor. In the first reactor, the liquid hydrocarbon fuel is partially reformed and thereafter is inputted into the second stage reactor for complete partial oxidation. The reaction product is at last partially synthesis gas, a mixture of carbon monoxide, hydrogen, as well as other low hydrocarbons such as methane, ethylene, ethane, and acetylene. The low hydrocarbons can be reformed further in a solid oxide fuel cell. A portion of the gaseous, rotating contents of the second stage reactor may be input into the first reactor to help generate and sustain rotation within the first reactor.

Abstract: Reactors and methods for solar thermochemical reactions are disclosed. The reactors and methods include a cascade of reduction chambers at successively lower pressures that leads to over an order of magnitude pressure decrease compared to a single-chambered design. The resulting efficiency gains are substantial, and represent an important step toward practical and efficient solar fuel production on a large scale.

Abstract: A carbonaceous substance dry powder gasification device and method, the device comprising from bottom to top a lower cooling and purification section (1), a gasification reaction section (2), a cooling reaction section (3) and an upper cooling and purification section (4); an initial cooling device is disposed at the connection between the cooling reaction section and the gasification reaction section; and a plurality of nozzles are circumferentially arranged in the gasification reaction section.

Abstract: The invention relates to mixtures comprising molecular hydrogen, hydrocarbons, and nitrogen oxides; to processes for removing at least a portion of the nitrogen oxides therefrom; to equipment useful in such processes; and to the use of such hydrocarbons for, e.g., chemical manufacturing.

Abstract: The present disclosure provides a method for preparing hydrogen-rich gas by solid organics. For example, solid organic raw materials are heated in a pyrolysis reaction device to perform pyrolysis reaction, and gaseous product generated from the pyrolysis reaction performs gasification with steam in a moving bed gasification reaction device to generate hydrogen-rich product. The present disclosure also provides a system for preparing hydrogen-rich gas by solid organics, and the system may include a solid heat carrier grading-dedusting device; a pyrolysis reaction device; a moving bed gasification reaction device; and a riser and combustion reactor. The present disclosure may operate at atmospheric pressure, and the technology is simple and suitable for the gasification and co-gasification of various high-volatile solid organics, such as raw materials containing a relatively large amount of moisture, mineral substance, and sulfur content.

Abstract: An apparatus (10) for preparation of acetylene and synthesis gas by partial oxidation of hydrocarbons with oxygen is proposed, comprising a reactor (12). The reactor (12) has a burner block (14) with a firing space for acetylene preparation, a secondary space (18) formed within the burner block (14), and an annular space (20) surrounding the secondary space (18). The burner block (14) has holes (22) for supply of a stream of a mixture of hydrocarbons and oxygen to the firing space and holes (24) for supply of a stream of auxiliary oxygen to the firing space. The holes (24) for supply of a stream of auxiliary oxygen to the firing space are connected to the secondary space (18). The secondary space (18) is connected to the annular space (20). There is a further proposal of a process for preparing acetylene and synthesis gas by partial oxidation of hydrocarbons with oxygen.

Abstract: The invention relates to a process for the parallel preparation of hydrogen, carbon monoxide and a carbon-comprising product, wherein one or more hydrocarbons are thermally decomposed and at least part of the pyrolysis gas formed is taken off from the reaction zone of the decomposition reactor at a temperature of from 800 to 1400° C. and reacted with carbon dioxide to form a gas mixture comprising carbon monoxide and hydrogen (synthesis gas).

Abstract: A process to decompose methane into carbon (graphitic powder) and hydrogen (H2 gas) without secondary production of carbon dioxide, employing a cycle in which a secondary chemical is recycled and reused, is disclosed.