The invention relates to a composition that contains a first semiconductor SC1, particles that comprise one or more element(s) M in the metal state selected from among an element of groups IVB, VB, VIB, VIIB, VIIIB, IB, IIB, IIIA, IVA and VA of the periodic table, and a second semiconductor SC2 that comprises cerium oxide, with said first semiconductor SC1 being in direct contact with said particles that comprise one or more element(s) M in the metal state, with said particles being in direct contact with said second semiconductor SC2 that comprises cerium oxide in such a way that the second semiconductor SC2 covers at least 50% of the surfaces of the particles that comprise one or more element(s) M in the metal state. The invention also relates to its preparation method as well as its application of photocatalysis.

The invention relates to a reactor comprising a plasma source and a catalyst comprising a mesoporous support. The invention also relates to a process comprising feeding methane to said reactor in order to obtain one or more of ethene, hydrogen and carbon as well as downstream products derived from ethene thus obtained. The invention relates to a reactor comprising as reactor parts: a. a housing and in said housing; b. a plasma source; and c. a catalyst, wherein said catalyst comprises as catalyst parts: i) a mesoporous support; ii) a metal selected from the group Pd, Ni, Ag or at least two thereof, wherein the metal is carried by said mesoporous support; wherein at least a part of said plasma source is located in said housing upstream of said catalyst.

Sulfur-tolerant reforming catalysts that include bulk alumina in the catalyst support are provided. The sulfur-tolerant reforming catalysts can include a sulfur-tolerant catalytic metal to facilitate reforming. The catalyst can further include a support material that includes at least some alumina as bulk alumina and/or octahedrally coordinated alumina. The sulfur-tolerant reforming catalysts can be regenerated, such as periodically regenerated, under relatively mild conditions that allow the catalysts to maintain reforming activity in the presence of 1 vppm to 1000 vppm of sulfur in the feed for reforming.

Embodiments of the present disclosure are directed to a diesel reforming system comprising: a diesel autothermal reformer; a liquid desulfurizer disposed upstream of the diesel autothermal reformer and configured to remove sulfur compounds from diesel fuel prior to feeding to the diesel autothermal reformer; a combustor in communication with the liquid desulfurizer and configured to provide heat for the liquid desulfurizer; a regulating valve in communication with the liquid desulfurizer and the combustor, the regulating valve being configured to control diesel fuel feeds to the liquid desulfurizer and the combustor; and a post-reformer disposed downstream of the diesel autothermal reformer.

The present disclosure relates to yolk-shell structured catalysts having compositions that can be particularly useful in the dry reforming of methane. These catalysts can demonstrate long-term stability that would be an advantage in industrial applications such as mitigating fossil fuel plant emissions. Example catalysts can include a yolk containing nickel (Ni) or nickel oxide (NiO), platinum (Pt) or platinum oxide (PtO.sub.2), and a third material (M3) such as a cerium oxide (CeO.sub.x). The shell can be formed of a ceramic such as silica and is generally a porous material that can support the yolk.

The present invention relates to a steam reforming catalyst for hydrogen production. More specifically, the present invention provides a novel catalysts support for sustainable hydrogen production by steam reforming process using bio-based materials feedstock such as ethanol, glycerol, n-butanol and ethylene glycol. The said improved support catalyst and metal doped catalysts therefrom, are comprising of combination of crystalline Mesoporous cellular foam (MCF) silica and basic site assistant for enhancing catalytic activity of doped active metals thereon and lower coke formation. The benefits of present invention is in the cost efficient steam reforming process for hydrogen production, wherein the said catalysts are efficiently providing a high reactant conversion at lower temperature, no coke formation, high thermal stability for longer time and effective catalytic performance for multiple cycles.

The present disclosure relates generally to portable energy generation devices and methods. The devices are designed to covert formic acid into released hydrogen, alleviating the need for a hydrogen tank as a hydrogen source for fuel cell power. In particular, an electricity generation device for powering a battery comprising a formic acid reservoir containing a liquid consisting of formic acid; a reaction chamber capable of using a catalyst and heat to convert the formic acid to hydrogen and carbon dioxide; a fuel cell that generates electricity; a delivery system for moving converted hydrogen into the fuel cell; and a battery powered by electricity generated by the fuel cell is provided.

A process for producing syngas and olefins includes the steps of feeding a catalytic partial oxidation (CPO) reactant mixture having oxygen, first hydrocarbons, and optionally steam to a CPO reaction zone having a CPO catalyst such that at least a portion of the CPO reactant mixture reacts, via an exothermic CPO reaction, to produce syngas having hydrogen (H.sub.2), carbon monoxide (CO), carbon dioxide (CO.sub.2), water, and unreacted first hydrocarbons. The syngas is characterized by a molar ratio M defined as (H.sub.2−CO.sub.2)/(CO+CO.sub.2). The method further includes feeding a cracking zone feed having second hydrocarbons to a cracking zone such that at least a portion of the second hydrocarbons undergoes an endothermic cracking reaction to produce a cracking zone product stream having olefins, hydrogen, and unreacted second hydrocarbons; and cooling the CPO reaction zone by heating the cracking zone while cooling the CPO reaction zone via heat transfer between the CPO reaction zone and the cracking zone.

A catalyst composition suitable for the ethanol reforming process at low temperature with enhanced stability on long term, comprises a noble metal, such as platinum or rhodium, and a transition non-noble metal, such as nickel or cobalt, supported by a carrier comprising, cerium, zirconium, optionally aluminium, supplemented with potassium. It is provided also a method for the stable production of hydrogen from an ethanol containing gas stream, comprising subjecting the gas stream to catalytic ethanol reforming as to form a rich H2 stream, using the catalyst as defined above.

A highly compact heat integrated fuel processor, which can be used for the production of hydrogen from a fuel source, suitable to feed a fuel cell, is described. The fuel processor assembly comprises a catalytic reforming zone (29) and a catalytic combustion zone (28), separated by a wall (27). Catalyst able to induce the reforming reactions is placed in the reforming zone and catalyst able to induce the combustion reaction is placed in the combustion zone, both in the form of coating on a suitable structured substrate, in the form of a metal monolith. Fe—Cr—Al—Y steel foils, in corrugated form so as to enhance the available area for reaction, can be used as suitable substrates. The reforming and the combustion zones can be either in rectangular shape, forming a stack with alternating combustion/reforming zones or in cylindrical shape forming annular sections with alternating combustion/reforming zones, in close contact to each other. The close placement of the combustion and reforming catalyst facilitate efficient heat transfer through the wall which separates the reforming and combustion chambers.