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Title: Catalytic carbon dioxide methanation by alumina-supported mono- and polynuclear ruthenium carbonyls

Journal Article · · Inorg. Chem.; (United States)
DOI:https://doi.org/10.1021/ic00230a018· OSTI ID:5645076

The catalytic activity and selectivity toward methanation of carbon dioxide using several alumina-supported ruthenium-cluster-derived catalysts have been studied over the temperature range 180-250 /sup 0/C. The ruthenium clusters used in these investigations include Ru/sub 3/(CO)/sub 12/, KHRu/sub 3/(CO)/sub 11/, (PPN)(HCO/sub 2/Ru/sub 3/(CO)/sub 10/), H/sub 4/Ru/sub 4/(CO)/sub 12/, KH/sub 3/Ru/sub 4/(CO)/sub 12/, (PPN)(H/sub 3/Ru/sub 4/(CO)/sub 12/), and Ru/sub 6/-C(CO)/sub 17/ (PPN = bis(triphenylphosphine)nitrogen(1+)). Comparative studies were made with the mononulcear complexes RuCl/sub 3/ and Ru(CO)/sub 5/. The latter species provides a low-valent, organometallic, mononuclear ruthenium source. Catalysts were supported by impregnation over alumina (partially dehydroxylated at 150 /sup 0/C in vacuo) and activated in hydrogen at 200/sup 0/C. Catalyst characterization included diffuse-reflectance infrared spectroscopy, surface area determination, oxygen chemisorption, and electron microscopy. 38 references, 9 figures, 3 tables.

Research Organization:
Texas A and M Univ., College Station
OSTI ID:
5645076
Journal Information:
Inorg. Chem.; (United States), Vol. 25:10
Country of Publication:
United States
Language:
English