A composition for treating dye wastewater and method of synthesizing said composition, is disclosed. The composition is a catalyst composition used for ultrasound irradiation process. The composition comprises a copper sulfide and cobalt ferrite (Cu.sub.2S/CoFe.sub.2O.sub.4) nanocomposite material, and hydrogen peroxide (H.sub.2O.sub.2). Further, the present invention also discloses a method for treating dye wastewater using said nanocomposite catalyst composition. The composition according to the present invention, provides a novel, eco-friendly and economical method for the complete degradation of the organic dye pollutants from the industrial wastewater. Further, the sonocatalyst has enough stability, as its structure and degradation ability does not change even after multiple use. Further, the sonocatalyst could be easily separated and reused from a waste water, without any need for complex separation process.

Embodiments of the present disclosure provide for IrO.sub.2 catalysts, methods of making IrO.sub.2 catalysts, methods of using IrO.sub.2 catalysts to make methanol, formaldehyde, and/or ethylene from CH.sub.4, systems for using IrO.sub.2 catalysts, and the like.

Embodiments of the present disclosure provide for IrO.sub.2 catalysts, methods of making IrO.sub.2 catalysts, methods of using IrO.sub.2 catalysts to make methanol, formaldehyde, and/or ethylene from CH.sub.4, systems for using IrO.sub.2 catalysts, and the like.

The invention relates to a catalyst comprising a support, at least one noble metal M, tin, phosphorus and at least one lanthanide group element, the content of phosphorus element being comprised between 0.4 and 1% by weight, and the content of lanthanide group element(s) being less than 1% by weight with respect to the weight of the catalyst. The invention also relates to the process for the preparation of the catalyst and the use thereof in reforming.

Provided is a methanation catalyst processing method capable of suppressing degradation of a catalyst performance. A methanation catalyst processing method of the present disclosure includes oxidizing nickel through a heat treatment of a methanation catalyst by supplying an oxygen gas containing oxygen to a reactor, the reactor housing the methanation catalyst containing the nickel as a catalyst component. In the oxidizing, the oxygen gas is supplied to the reactor such that the oxygen is supplied to 1 g of the methanation catalyst at a supply rate in a range of from 0.0213 mmol-O.sub.2/sec.Math.g-cat. to 0.0638 mmol-O.sub.2/sec.Math.g-cat., and a time period of the heat treatment of the methanation catalyst by supplying the oxygen gas to the reactor is set to 30 minutes or more.

Provided is a methanation catalyst processing method capable of suppressing degradation of a catalyst performance. A methanation catalyst processing method of the present disclosure includes oxidizing nickel through a heat treatment of a methanation catalyst by supplying an oxygen gas containing oxygen to a reactor, the reactor housing the methanation catalyst containing the nickel as a catalyst component. In the oxidizing, the oxygen gas is supplied to the reactor such that the oxygen is supplied to 1 g of the methanation catalyst at a supply rate in a range of from 0.0213 mmol-O.sub.2/sec.Math.g-cat. to 0.0638 mmol-O.sub.2/sec.Math.g-cat., and a time period of the heat treatment of the methanation catalyst by supplying the oxygen gas to the reactor is set to 30 minutes or more.

Improved catalytic materials for and methods of oxidative dehydrogenation (ODH) of short chain alkanes or ethylbenzene to the corresponding olefins are disclosed. The disclosed methods use catalysts made by impregnating boron onto the surface of oxidized amorphous carbon, and result in higher selectivity and a lower induction period than methods using conventional ODH catalysts.

Improved catalytic materials for and methods of oxidative dehydrogenation (ODH) of short chain alkanes or ethylbenzene to the corresponding olefins are disclosed. The disclosed methods use catalysts made by impregnating boron onto the surface of oxidized amorphous carbon, and result in higher selectivity and a lower induction period than methods using conventional ODH catalysts.

A method is described for preparing an eggshell catalyst comprising the steps of: (i) preparing a calcined shaped alkaline earth metal aluminate catalyst support, (ii) treating the calcined shaped alkaline earth metal aluminate support with a gas containing water vapour to form a hydrated support, (iii) with or without an intervening drying step, impregnating the hydrated support with an acidic solution containing one or more catalytic metal compounds and drying the impregnated support, (iv) calcining the dried impregnated support, to form a calcined catalyst having a catalytic metal oxide concentrated at the surface of the support and (v) optionally repeating steps (ii), (iii) and (iv).

A method of manufacturing a catalyst material includes the steps of: providing a body having an open-porous foam structure and comprising at least a first metal or alloy; providing particles, each of which particles comprising at least a second metal or alloy; distributing the particles on the body; forming a structural connection between each of at least a subset of the particles and the body; and forming an oxide film on at least the subset of the particles and the body, wherein the oxide film has a catalytically active surface.