The present disclosure provides methods for producing a regenerated hydrogenation catalyst from a fouled hydrogenation catalyst having a total surface area and at least one associated impurity. The method can include maintaining contact between the fouled hydrogenation catalyst and a flushing medium that comprises water, oxygen, and an inert or diluent gas at a regeneration temperature and a regeneration pressure sufficient to remove at least a portion of the at least one impurity from the hydrogenation catalyst to produce the regenerated hydrogenation catalyst, where the regenerated hydrogenation catalyst is characterized as retaining at least 70% of the activity of the hydrogenation catalyst.

The present disclosure provides methods for producing a regenerated hydrogenation catalyst from a fouled hydrogenation catalyst having a total surface area and at least one associated impurity. The method can include maintaining contact between the fouled hydrogenation catalyst and a flushing medium that comprises water, oxygen, and an inert or diluent gas at a regeneration temperature and a regeneration pressure sufficient to remove at least a portion of the at least one impurity from the hydrogenation catalyst to produce the regenerated hydrogenation catalyst, where the regenerated hydrogenation catalyst is characterized as retaining at least 70% of the activity of the hydrogenation catalyst.

There is provided a method for manufacturing a catalyst ink for fuel cell electrodes that allows simultaneously performing fineness of a catalyst and adjustment of viscosity of the catalyst ink. The method for manufacturing a catalyst ink for fuel cell electrodes containing a catalyst, a solvent, and an ionomer includes stirring and mixing the catalyst, the solvent, and the ionomer by a high-shear thin-film spin mixer. The ionomer contains a gel-like ionomer. The high-shear thin-film spin mixer includes a cylindrical stirring tank, a rotary vane, and a shaft. The cylindrical stirring tank has unevennesses on an inner peripheral surface. The rotary vane is concentric with the stirring tank and has an outer diameter slightly smaller than an inner diameter of the stirring tank. The shaft includes the rotary vane on an end portion and is rotatable at high speed in forward and reverse directions.

There is provided a method for manufacturing a catalyst ink for fuel cell electrodes that allows simultaneously performing fineness of a catalyst and adjustment of viscosity of the catalyst ink. The method for manufacturing a catalyst ink for fuel cell electrodes containing a catalyst, a solvent, and an ionomer includes stirring and mixing the catalyst, the solvent, and the ionomer by a high-shear thin-film spin mixer. The ionomer contains a gel-like ionomer. The high-shear thin-film spin mixer includes a cylindrical stirring tank, a rotary vane, and a shaft. The cylindrical stirring tank has unevennesses on an inner peripheral surface. The rotary vane is concentric with the stirring tank and has an outer diameter slightly smaller than an inner diameter of the stirring tank. The shaft includes the rotary vane on an end portion and is rotatable at high speed in forward and reverse directions.

A method for preparing a core-shell structure photocatalytic material includes: obtaining a titanyl sulfate solution by mixing and reacting sulfuric acid and metatitanic acid; obtaining a mixed solution by adding a porous material having a hydrophilic surface into the titanyl sulfate solution; adding an alkali into the mixed solution to obtain a precipitation product by reacting the alkali with the titanyl sulfate coated on the surface of the porous material; and filtering, washing, drying and calcining the precipitation product to obtaining a core-shell structure photocatalytic material with the porous material as a core and a mesoporous quantum titanium oxide as a shell.

A method for preparing a core-shell structure photocatalytic material includes: obtaining a titanyl sulfate solution by mixing and reacting sulfuric acid and metatitanic acid; obtaining a mixed solution by adding a porous material having a hydrophilic surface into the titanyl sulfate solution; adding an alkali into the mixed solution to obtain a precipitation product by reacting the alkali with the titanyl sulfate coated on the surface of the porous material; and filtering, washing, drying and calcining the precipitation product to obtaining a core-shell structure photocatalytic material with the porous material as a core and a mesoporous quantum titanium oxide as a shell.

The catalyst carrier structure of the present invention includes a central axis, and a plurality of fibers. The surface of each fiber is coated with a catalyst. The fibers are centered on the central axis, and are arranged around the central axis radially outward along the axial direction of the central axis. Each fiber is an independent and separate fiber set on the central axis.

The catalyst carrier structure of the present invention includes a central axis, and a plurality of fibers. The surface of each fiber is coated with a catalyst. The fibers are centered on the central axis, and are arranged around the central axis radially outward along the axial direction of the central axis. Each fiber is an independent and separate fiber set on the central axis.

A synthesis process for forming nanodendrites. The nanodendrites are utilized in a process to form a heterojunction catalyst. Nanodendrites may include PtRu.sub.8 nanodendrites that can be oxidized through annealing to form PtRuO.sub.2. One heterojunction catalyst comprises PtRuO.sub.2 on a carbon support.

Methods for producing a carbon-free, PGM-free support for PGM catalyst. The catalytic material comprises PGM metals disposed on a carbon-free support which is catalytic but free of PGM.