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Characterization of Al2O3 Supported Nickel Catalysts Derived from RF Non-thermal Plasma Technology

Authors :
Chengdu Liang
Steven H. Overbury
Ben W Jang
Viviane Schwartz
Chunkai Shi
Michael J Helleson
Adam J. Rondinone
Source :
Topics in Catalysis. 49:145-152
Publication Year :
2008
Publisher :
Springer Science and Business Media LLC, 2008.

Abstract

Catalysts derived from non-thermal plasma techniques have previously shown unusual and highly advantageous catalytic properties including room temperature reduction, unusual metal particle structure and metal-support interactions, and enhanced selectivity and stability. This study focuses on the characterization of Al2O3 supported Ni catalysts derived from the RF non-thermal plasma technique with in-situ XRD, TPR-MS and STEM and on relating the results to the enhanced activity and stability of benzene hydrogenation. The results suggest that catalysts with plasma treatments before impregnation are relatively easier to be reduced and result in better activities under mild reduction conditions. These plasma treatments stabilize the nickel particle sizes of air(B) and H2(B) catalysts at 600 °C by slowing down the sintering process. Plasma treatments after the impregnation of precursors, on the other hand, tend to delay the growth of nickel particles below 600 °C, forming smaller Ni particles, but with a sudden increase in particle size near 600 °C. It suggests that the structure of Ni nitrate and the metal-support interaction have been altered by the plasma treatments. The reduction patterns of plasma treated catalysts are, therefore, changed. The catalyst with a combination plasma treatment demonstrates that the effect of a combination plasma treatment is larger than either the plasma treatment before or after the impregnation alone. Both plasma treatments before and after the impregnation of metal precursor play important roles in modifying supported metal catalysts.

Details

ISSN :
15729028 and 10225528
Volume :
49
Database :
OpenAIRE
Journal :
Topics in Catalysis
Accession number :
edsair.doi...........0e41c2b6a42f678029f91ffd46161d79