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Mechanisms for the promotion and poisoning of ruthenium catalysts by sulfur

Conference · · Am. Chem. Soc., Div. Pet. Chem., Prepr.; (United States)
OSTI ID:5598516
Catalytic reactions occurring over ruthenium surfaces can be poisoned or promoted by sulfur depending on both the quantity of sulfur uptake and the specific requirements of the reaction involved. Submonolayers of surface sulfur have been shown to: (i) promote specific rates of hexene isomerization compared to bare metal, (ii) poison hydrogen adsorption sites, (iii) reduce specific rates of hexene hydrogenation, (iv) increase stretching frequencies of adsorbed carbon monoxide molecules in a fashion that depends on crystallite size, and (v) provide greater than 100-fold selectivities towards the hydrodesulfurization versus hydrogenation of thiophene. Alternatively, multi-layer sulfur uptake appears to: (i) promote irreversible hydrogen adsorption, (ii) increase specific rates of thiophene hydrogenation to match that of the HDS pathway and (iii) increase still further specific rates of hexene isomerization compared to bare or surface-sulfided metal. Conversion between the above noted sulfidization regimes, and their corresponding catalytic behaviors, can be achieved through appropriate re-sulfidization and/or annealing procedures. Reaction kinetics, microgravimetry, X-ray photoelectron spectroscopy and pulse oxygen chemisorption confirms this reversible behavior.
Research Organization:
Dept. of Chemical Engineering, Auburn Univ., Auburn, AL
OSTI ID:
5598516
Report Number(s):
CONF-860425-
Conference Information:
Journal Name: Am. Chem. Soc., Div. Pet. Chem., Prepr.; (United States) Journal Volume: 31:1
Country of Publication:
United States
Language:
English

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