4.5 Article

Au/Ni/Ni(OH)2/C Nanocatalyst with High Catalytic Activity and Selectivity for m-dinitrobenzene Hydrogenation

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CATALYSIS LETTERS
卷 152, 期 2, 页码 372-382

出版社

SPRINGER
DOI: 10.1007/s10562-021-03630-8

关键词

Au/Ni/Ni(OH)(2)/C; Catalytic hydrogenation; Au islands; Ni/Ni(OH)(2) NPs; Synergy effect

资金

  1. National Natural Science Foundation of China [21763011]
  2. Natural Science Foundation of Jiangxi Province for Distinguished Young Scholars [20192BCB23015]
  3. Natural Science Foundation of Jiangxi Province of China [20202BAB203005]
  4. Youth Jinggang Scholars Program in Jiangxi Province [[2019]57]
  5. China Postdoctoral Science Foundation [2018M642597]
  6. Foundation of State Key Laboratory of Coal Conversion [J20-21-609]
  7. Research Foundation of the Education Bureau of Jiangxi Province of China [GJJ190429]
  8. Postdoctoral Science Foundation of Jiangxi Province of China
  9. Program of Qingjiang Excellent Young Talents, Jiangxi University of Science and Technology [JXUSTQJBJ2019002]
  10. Program of Technology Innovation Talents of Ganzhou

向作者/读者索取更多资源

The bimetallic nanocatalysts Au/Ni/Ni(OH)(2)/C with different Au loadings showed higher catalytic activity and selectivity compared to monometallic catalysts, with Au/Ni/Ni(OH)(2)/C-2 exhibiting the best performance.
The Au/Ni/Ni(OH)(2)/C bimetallic nanocatalysts with different Au loadings (Au/Ni/Ni(OH)(2)/C-1: 0.05 wt%Au; Au/Ni/Ni(OH)(2)/C-2: 0.46 wt%Au; Au/Ni/Ni(OH)(2)/C-3: 2.60 wt%Au) were prepared at room temperature. The characterization results proved the nanostructure of Au islands supported on the Ni/Ni(OH)(2) nanoparticles (NPs) and synergy effect of Au-, Ni- and Ni(OH)(2)-related species in Au/Ni/Ni(OH)(2)/C. These are the main reasons why their catalytic performance and selectivity to m-nitroaniline in m-dinitrobenzene hydrogenation were much higher than those of monometallic catalysts (Au/C and Ni/Ni(OH)(2)/C). Because Au/Ni/Ni(OH)(2)/C-2 was with high dispersion of Au, Au(0)/Aun+ ratio approximate to 1:1 on the surface, novel nanostructure, moderate capacity of activating and dissociating hydrogen, and synergistic effect, it had much better catalytic activity (conversion of m-dinitrobenzene-100%) and higher selectivity to m-nitroaniline (95.0%) in m-dinitrobenzene hydrogenation reaction compared to other two supported bimetallic catalysts (Au/Ni/Ni(OH)(2)/C-1 and Au/Ni/Ni(OH)(2)/C-3). Au/Ni/Ni(OH)(2)/C-2 also exhibited high stability. [GRAPHICS] .

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