A sulfur-resistant, high activity methane oxidation catalyst for use in removing methane from gas streams having a concentration of methane by oxidizing the methane. The methane oxidation catalyst is especially useful in processing gas streams that also have a concentration of a sulfur compound. The sulfur-resistant methane oxidation catalyst includes a unique multi-crystalline zirconia as a support for a platinum component and a ruthenium component. The multi-crystalline zirconia contributes to the excellent properties of the catalyst. The platinum and ruthenium components can be included in the methane oxidation catalyst in a specific weight ratio that also contributes to the enhanced properties of the catalyst. The sulfur-resistant methane oxidation catalyst may also include a chloride component that contributes to enhanced properties of the catalyst.

A catalyst used for dehydrogenation of an organic hydrogen-storage material to generate hydrogen, a support for the catalyst, and a preparation process thereof are presented. A hydrogen-storage alloy and a preparation process thereof are also provided. A process for providing high-purity hydrogen, a high-efficiently distributed process for producing high-purity and high-pressure hydrogen, a system for providing high-purity and high-pressure hydrogen, a mobile hydrogen supply system, and a distributed hydrogen supply apparatus are also described.

Process for fixed-bed reforming of a hydrocarbon-based feedstock comprising n-paraffinic, naphthenic and aromatic hydrocarbons, at a temperature of between 400 and 700° C., a pressure of between 0.1 and 4 MPa, and a mass flow of feedstock treated per unit mass of catalyst and per hour of between 0.1 and 10 h.sup.−1, by bringing said feedstock into contact with a catalyst comprising platinum, a promoter metal selected from the group consisting of rhenium and iridium, a halogen selected from the group consisting of fluorine, chlorine, bromine and iodine, and a porous alumina support in the form of an extrudate characterized by a length “l” of between 1 and 10 mm, a section comprising four lobes, the largest diameter “D” of the cross section of said extrudate being between 1 and 3 mm.

A battery includes an electrode group including an air electrode and a negative electrode stacked with a separator therebetween, and an accommodating bag accommodating the electrode group along with an alkali electrolyte solution. The air electrode includes a catalyst for an air secondary battery. This catalyst for an air secondary battery is produced by a method for producing a catalyst for an air secondary battery, the method including a precursor preparation step of preparing a bismuth-ruthenium oxide precursor, a calcination step of calcining the bismuth-ruthenium oxide precursor obtained in this precursor preparation step to form a bismuth-ruthenium oxide, and a nitric acid treatment step of immersing the bismuth-ruthenium oxide obtained by this calcination step in a nitric acid aqueous solution.

A bi-modal radial flow reactor comprising a cylindrical outer housing surrounding at least five cylindrical, concentric zones, including at least three annulus vapor zones and at least two catalyst zones. The at least two catalyst zones comprise an outer catalyst zone and an inner catalyst zone. The at least three annulus vapor zones comprise an outer annulus vapor zone, a middle annulus vapor zone, and a central annulus vapor zone, wherein the central annulus vapor zone extends along a centerline of the bi-modal radial flow reactor. The outer catalyst zone is intercalated with the outer annulus vapor zone and the middle annulus vapor zone, and the inner catalyst zone is intercalated with the middle annulus vapor zone and the central annulus vapor zone. A removable head cover can be fixably coupled to a top of the cylindrical outer housing to seal a top of the bi-modal radial flow reactor.

A process of making an aromatization catalyst comprising: (a) mixing a zeolite, a binder, and water to form a mixture; (b) extruding the mixture to form a green extrudate; (c) drying the green extrudate to form a dried green extrudate; (d) calcining the dried green extrudate to form a support, wherein calcining the dried green extrudate is the only calcination step in the process; (e) washing the support to form a washed support; (f) drying the washed support to form a dried washed support; (g) impregnating the dried washed support with a Group 8-10 transition metal compound and at least one halide-containing compound to form a metalized-halided material; and (h) vacuum drying the metalized-halided material to form a dried metalized-halided material which is the aromatization catalyst.

A process of making an aromatization catalyst comprising: (a) mixing a zeolite, a binder, and water to form a mixture; (b) extruding the mixture to form a green extrudate; (c) drying the green extrudate to form a dried green extrudate; (d) calcining the dried green extrudate to form a support, wherein calcining the dried green extrudate is the only calcination step in the process; (e) washing the support to form a washed support; (f) drying the washed support to form a dried washed support; (g) impregnating the dried washed support with a Group 8-10 transition metal compound and at least one halide-containing compound to form a metalized-halided material; and (h) vacuum drying the metalized-halided material to form a dried metalized-halided material which is the aromatization catalyst.

Process for hydroformylation of olefins using Pt and iodine.

Provided herein a method for forming one or more intramolecular disulfide bonds.

The present disclosure provides a process for preparing a reforming catalyst, said process comprising: (a) impregnating at least one support with at least one promoter metal and at least one active metallic component to obtain a second catalytic precursor; (b) contacting the second catalytic precursor with at least one non-metallic component to obtain a third catalytic precursor; (c) coating the third catalytic precursor with at least one silanizing agent to obtain a coated third catalytic precursor; and (d) drying the coated third catalytic precursor to obtain a dried third catalytic precursor followed by calcination of the dried third catalytic precursor to obtain the reforming catalyst. The present disclosure also provides a reforming catalyst and the process for catalytically reforming a hydrocarbon feed stream by using the reforming catalyst.