Preparation method of core-shell-structured catalyst for low-temperature catalytic oxidation of toluene
A core-shell structure, low-temperature catalysis technology, used in metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, chemical instruments and methods, etc., can solve the problem of size increase, activity decline, and uneven dispersion. and other problems, to achieve the effect of good low temperature, solving sintering growth, good catalytic activity and stability
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[0029] The present invention is used for the preparation method of the core-shell structure catalyst of low-temperature catalytic oxidation of toluene, comprises the following steps:
[0030] First, prepare a solution of chloroauric acid into a certain concentration and heat it in a water bath to a specific temperature, then add an appropriate amount of reducing agent to reduce Au 4+ After reacting for a certain period of time, the resulting solution was centrifuged, washed and dried to obtain Au NPs.
[0031] Then, Au NPs were uniformly dispersed in an appropriate amount of surfactant solution, a certain amount of copper nitrate solution was added to the above solution, and after stirring evenly, the Cu adsorbed on the surface of Au NPs was reduced in situ with a strong reducing agent. 2+ , after reacting for a certain period of time, the resulting solution is centrifuged, washed and dried to obtain the gold intermediate product Au@Cu 2 O.
[0032] Finally, the Au@Cu 2 O i...
Embodiment 1
[0035] ①First, heat the prepared 0.25mmol / L chloroauric acid solution in a water bath to 100°C, then add 7.5ml of 0.1mol / L sodium citrate solution, and stir magnetically for 30 minutes, then centrifuge, wash, and Gold nanoparticles (Au NPs) can be obtained by drying.
[0036]②Then, the obtained Au NPs were uniformly dispersed in 1 g of polyvinylpyrrolidone solution, 50 ml of 0.1 mol / L copper nitrate solution was added to the above solution, and after stirring evenly, the Cu adsorbed on the surface of Au NPs was reduced in situ with water and hydrazine solution. 2 + , after reacting for 30min, the resulting solution was centrifuged, washed and dried to obtain the intermediate product Au@Cu 2 O.
[0037] ③Au@Cu 2 O was added to the mixed solution of 20ml tert-butanol and 1ml 1.71mol / L sodium chloride after drying, and Au@Cu 2 After O is dispersed evenly, add 0.15 mol / L hydrochloric acid acidified potassium permanganate solution (0.158 mol / L) to oxidize Au@Cu in situ 2 O, th...
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