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Synthesis and higher catalytic property of the novel bimetallic Ni–Fe/SiO2 microspheres with mesoporous structure
- Source :
- Journal of Materials Research. 32:766-774
- Publication Year :
- 2017
- Publisher :
- Springer Science and Business Media LLC, 2017.
-
Abstract
- Bimetallic catalyst Ni–Fe/SiO2 microspheres were obtained by reducing bimetallic (Ni,Fe2+)3Si2O5(OH)4 microspheres with controllable morphology structure in situ under the hydrogen atmosphere at 650 °C, which are synthesized via one-step self-template method under hydrothermal conditions. The TEM images indicate the formation process of the different morphology and the synthesis conditions of bimetallic Ni–Fe silicate were obtained. Bimetallic catalyst Ni–Fe/SiO2 (reduced) hollow microspheres had the smaller surface area and the bigger pore diameter than that of (Ni,Fe2+)3Si2O5(OH)4 (unreduced) hollow microspheres because the reduction reaction under high temperature may make part pores in nanosheets collapsing and metal particles aggregating easily for the strong magnetism. For synergistic effect of nickel ion and iron ion, the reaction conditions of the chosen catalyst with higher activity were decreased from 140 °C–24 h + 180 °C −12 h for iron silicate hydroxide to 140 °C–12 h. Ni–Fe/SiO2 core-shell microspheres exhibited excellent catalytic activity with a conversion of nitrobenzene reaching 94% within 2 h, which is 82% higher than Fe/SiO2.
- Subjects :
- Materials science
Mechanical Engineering
02 engineering and technology
010402 general chemistry
021001 nanoscience & nanotechnology
Condensed Matter Physics
01 natural sciences
Redox
Hydrothermal circulation
0104 chemical sciences
Catalysis
Metal
Nitrobenzene
chemistry.chemical_compound
Chemical engineering
chemistry
Mechanics of Materials
visual_art
visual_art.visual_art_medium
Hydroxide
General Materials Science
0210 nano-technology
Mesoporous material
Bimetallic strip
Subjects
Details
- ISSN :
- 20445326 and 08842914
- Volume :
- 32
- Database :
- OpenAIRE
- Journal :
- Journal of Materials Research
- Accession number :
- edsair.doi...........8c53fa718a9ade127c28d9253774453e