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Effect of ruthenium precursor on hydrogen-treated active carbon supported ruthenium catalysts for ammonia synthesis
Authors:Zhi-hua Zhong  Ken-ichi Aika  
Institution:

Department of Environmental Chemistry and Engineering, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226, Japan

Abstract:Active carbon (A.C.), after treatment at 1123 K with hydrogen for more than 24 h, was found to be very effective as a support for ruthenium catalysis in ammonia synthesis. The activity of barium promoted Ru catalysts supported on this treated A.C. is affected remarkably by the Ru precursor. Ru3(CO)12 was found previously to be the most effective Ru precursor for oxide supports such as Al2O3, MgO, and CeO2 in ammonia synthesis. However, in this study, the Ru---Bao/A.C. catalyst prepared from Ru(acac)3 was found to yield the highest activity, while the catalyst prepared from Ru3(CO)12 resulted in the lowest activity among several precursors. Transmission electron microscopy and hydrogen chemisorption showed that the particle size of Ru obtained from the decomposition of Ru(acac)3 on hydrogen-treated A.C. is smaller than the particle size of Ru obtained from the decomposition of Ru3(CO)12. Additionally, RuCl3 was found to be an effective precursor for Ru/A.C. catalyst. It has been suggested that chlorine ions can be removed easily from A.C. by hydrogen reduction at 773 K, and that this results in the high activity.
Keywords:Ruthenium complexes  Active carbon supported complexes  Ammonia synthesis  Catalysis
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