The present invention discloses a method of quickly desorbing phosgene from a catalyst in a phosgene synthesizing tower when the catalyst in the phosgene synthesizing tower is replaced. The method is carried out by first purging out easily-desorbed phosgene from the catalyst activated carbon in the phosgene synthesizing tower with nitrogen gas, then purging with ammonia gas, and the ammonia gas is reacted with the hardly-desorbed phosgene in the catalyst of the phosgene synthesizing tower. Then the phosgene synthesizing tower is rinsed with a water gun and then dried with hot gas. The phosgene content at an outlet of the phosgene synthesizing tower after purging is below 0.5 ppm, which can significantly save the time of the phosgene synthesizing tower for purging the phosgene, greatly reduce the amount of nitrogen gas consumed, and improve the safety of the process operation.

The present invention discloses a method of quickly desorbing phosgene from a catalyst in a phosgene synthesizing tower when the catalyst in the phosgene synthesizing tower is replaced. The method is carried out by first purging out easily-desorbed phosgene from the catalyst activated carbon in the phosgene synthesizing tower with nitrogen gas, then purging with ammonia gas, and the ammonia gas is reacted with the hardly-desorbed phosgene in the catalyst of the phosgene synthesizing tower. Then the phosgene synthesizing tower is rinsed with a water gun and then dried with hot gas. The phosgene content at an outlet of the phosgene synthesizing tower after purging is below 0.5 ppm, which can significantly save the time of the phosgene synthesizing tower for purging the phosgene, greatly reduce the amount of nitrogen gas consumed, and improve the safety of the process operation.

The present invention provides a photocatalyst particle comprising titanium dioxide particles, a zeolite particle, and a carbon layer. The titanium dioxide particles are adsorbed on a part of an external surface of the zeolite particle. The carbon layer coats a part of an external surface of the zeolite particle other than the part of the external surface of the zeolite particle on which the titanium dioxide particles are adsorbed. The carbon layer is in contact with a part of surfaces of the titanium dioxide particles. At least a part of the other part of the surfaces of the titanium dioxide particles is not coated with the carbon layer and are exposed on a surface of the photocatalyst particle. The present invention provides a photocatalyst particle used even in an alkaline aqueous solution.

A method can include incorporating graphene oxide (GO) in a solution, reducing the graphene oxide (GO) by refluxing carbon nitride (C.sub.3N.sub.4) in the solution to form carbon-nitride refluxed-graphene-oxide (C.sub.3N.sub.4-rGO) composites, and incorporating ruthenium ions into the C.sub.3N.sub.4-rGO composites to form C.sub.3N.sub.4-rGO-Ru complexes.

A method can include incorporating graphene oxide (GO) in a solution, reducing the graphene oxide (GO) by refluxing carbon nitride (C.sub.3N.sub.4) in the solution to form carbon-nitride refluxed-graphene-oxide (C.sub.3N.sub.4-rGO) composites, and incorporating ruthenium ions into the C.sub.3N.sub.4-rGO composites to form C.sub.3N.sub.4-rGO-Ru complexes.

A method of producing a catalytic carbon fiber may include: providing a carbon fiber and an aminated macrocycle, mixing the carbon fiber and the aminated macrocycle with a solvent; and reacting the carbon fiber and the aminated macrocycle to form an amide bond between the carbon fiber and the aminated macrocycle thereby forming the catalytic carbon fiber.

A method of producing a catalytic carbon fiber may include: providing a carbon fiber and an aminated macrocycle, mixing the carbon fiber and the aminated macrocycle with a solvent; and reacting the carbon fiber and the aminated macrocycle to form an amide bond between the carbon fiber and the aminated macrocycle thereby forming the catalytic carbon fiber.

The present specification relates to a carrier-nanoparticle complex, a method for preparing the same, and a catalyst comprising the same.

The invention relates to a method of preparing a catalytic composition comprising at least one non-noble metal from group VIII and at least one metal from group VIB of the periodic table. The invention also relates to the catalytic composition thus produced, which has a high specific activity in reactions involving the hydroprocessing of light and intermediate fractions, preferably in reactions involving the hydrotreatment of hydrocarbon streams, including hydrodesulphurisation (HDS), hydrodenitrogenation (HDN) and hydro-dearomatisation (HDA).

A protein template is added to a solution in which metal ions of iron and copper are dissolved to introduce the metal ions into the protein template; the protein template is separated from metal ions that have not been incorporated in the protein template; the metal ions that have been incorporated in the protein template are reduced to obtain a protein containing alloy nanoparticles of iron and copper; a sol or gel in which a co-continuous body is dispersed is frozen; the frozen sol or gel is dried in a vacuum to obtain a porous body; the porous body is allowed to support the alloy nanoparticle containing protein; and the protein is removed.