The present invention addresses to a catalyst, and the method for obtaining the same, for generating hydrogen and/or syngas. More specifically, the present invention describes a catalyst based on nickel, molybdenum and tungsten, for steam reforming processes of natural gas or other hydrocarbon streams (refinery gas, propane, butane, naphtha or any mixture thereof) that presents high resistance to deactivation by coke deposition. According to the present invention, the catalyst has NiMoW as its active phase, in bulk form and/or supported on an alumina oxide and other high surface area oxide supports, and may also contain other promoters. Furthermore, the present invention teaches the production of a catalyst whose active phase of NiMoW has high activity for hydrocarbon steam reforming reaction.

The present invention describes a processes, systems, and catalysts for the conversion of carbon dioxide and water and electricity into low carbon or zero carbon high quality fuels and chemicals. In one aspect, the present invention provides an integrated process for the conversion of a feed stream comprising carbon dioxide to a product stream comprising hydrocarbons between 5 and 24 carbon atoms in length.

A method and a system for the coproduction of hydrogen, electrical power, and heat energy. An exemplary method includes desulfurizing a feed stream to form a desulfurized feed stream, reforming the desulfurized feed stream to form a methane rich gas, and providing the methane rich gas to a membrane separator. A hydrogen stream is produced in a permeate from the membrane separator. A retentate stream from the membrane separator is provided to a solid oxide fuel cell (SOFC). Electrical power is produced in the SOFC from the retentate stream.

An apparatus for producing synthesis gas (syngas) is provided. The apparatus includes a hub, including an autothermal dry reforming of methane apparatus, configured to receive CO.sub.2 and O.sub.2, and configured to produce a first stream of syngas with low a H.sub.2/CO mole ratio; an autothermal steam reforming of methane apparatus, configured to receive steam and O.sub.2, and configured to produce a second stream of syngas with a high H.sub.2/CO mole ratio; an H.sub.2 separation apparatus, configured to receive H.sub.2 and CO.sub.2, and coupled to the autothermal dry reforming of methane apparatus to deliver CO.sub.2 thereto; and a reactor for converting CO to H.sub.2 using a water-gas shift reaction, coupled to the autothermal steam reforming of methane apparatus to receive the second stream of syngas, and coupled to the H.sub.2 separation apparatus to deliver a stream of H.sub.2 and CO.sub.2 thereto. A method for producing synthesis gas is provided. The method includes configuring an autothermal dry reforming of methane apparatus to receive CO.sub.2 from industrial emission sources and an H.sub.2 separation apparatus, which receives H.sub.2 and CO.sub.2 from a water gas shift reactor fed with a portion of the second stream of syngas from an autothermal steam reforming of methane apparatus.

Provided herein are catalyst materials and processes for processing hydrocarbons. For example, doped ceria-supported metal catalysts are provided exhibiting good activity and stability for commercially relevant dry reforming of methane as well as mixed hydrocarbon feedstocks under process conditions including low temperature and long term operation. Useful doped ceria-supported metal catalysts include nickel dispersed over Ti-doped ceria.

Systems and methods are provided for using oxycombustion to provide heat within a reverse flow reactor environment. The oxygen for the oxycombustion can be provided by oxygen stored in an oxygen storage component in the reactor. By using an oxygen storage component to provide the oxygen for combustion during the regeneration step, heat can be added to a reverse flow reactor while reducing or minimizing addition of diluents and while avoiding the need for an air separation unit. As a result, a regeneration flue gas can be formed that is substantially composed of CO.sub.2 and/or H.sub.2O without requiring the additional cost of creating a substantially pure oxygen-containing gas flow.

The present disclosure relates to a catalyst composition comprising: (a) nickel; (b) at least one promoter selected from Cu Zn, Mo, Co, Mg, Ce, Ti, Zr, Fe, Pd, Ag, Pt, or combinations thereof; and (c) a support material, wherein, the nickel loading is in the range of 6-19 wt % and the at least one promoter loading is in the range of 0.2-5 wt % with respect to the support material. The present disclosure further discloses a process for preparing a catalyst composition and a process each for the production of hydrogen gas and carbon nanotubes. Also disclosed herein, is use of a catalyst composition for obtaining hydrogen gas and carbon nanotubes.

The present subject matter relates to co-producing H-CNG and CNTs. The process comprises adding catalyst to a first reactor (110) and activating the catalyst and performing a reaction to obtain H-CNG and CNTs. At a first predetermined time after reaction has progressed in the first reactor (110), catalyst is added to a second reactor (120), activated, and then the reaction proceeds simultaneously in the first reactor (110) and second reactor (120). The use of multiple reactors with staggered start times helps in the continuous co-production of H-CNG and CNTs. Catalyst preparation process is integrated with the co-production process for efficient heat recovery. The first and second reactors are fluidized bed reactors with cantilever trays having weirs for controlling the residence time of the catalyst in the reactor and thereby controlling the purity of CNTs produced.

A pyrolysis gas reforming system is provided. The pyrolysis gas reforming system includes a pyrolysis unit configured to perform pyrolysis of waste, an oil-gas separation unit configured to separate a product generated by the pyrolysis unit into oil and gas, a pyrolysis gas purification unit configured to refine pyrolysis gas generated through the separation by the oil-gas separation unit, a pyrolysis gas reforming unit configured to generate synthesis gas by reforming the pyrolysis gas purified by the pyrolysis gas purification unit, a hydrogen gas shift reaction unit configured to convert carbon monoxide contained in the synthesis gas generated by the pyrolysis gas reforming unit into hydrogen and carbon dioxide, and a hydrogen separation unit configured to separate hydrogen from the synthesis gas discharged from the hydrogen gas shift reaction unit, wherein combustion gas generated by a burner of the pyrolysis gas reforming unit and used to supply heat to the pyrolysis gas reforming unit is used to supply heat to the pyrolysis unit.

A combined reforming apparatus is provided. The combined reforming apparatus includes a body, a first catalyst tube disposed inside the body and reacting at a first temperature to reform hydrocarbons (CA) having two or more carbon atoms into methane (CH.sub.4), a second catalyst tube disposed inside the body, connected to the first catalyst tube, and reacting at a second temperature higher than the first temperature to reform methane (CH.sub.4) into synthesis gas comprising hydrogen (H.sub.2) and carbon monoxide (CO), a combustion unit configured to supply heat to the first and second catalyst tubes, a gas supply pipe configured to supply hydrocarbon gas to the first catalyst tube, a first steam supply pipe configured to supply steam to the first catalyst tube, and a second steam supply pipe configured to supply steam to the second catalyst tube.