Abstract
Several reactions representing important categories of catalytic systems have been studied on chemically modified single crystal surfaces. These reactions are methanation of CO and CO 2 , hydrogenolysis of ethane, hydrogenation of ethylene, and cyclopropane ring-opening and hydrogenolysis. Poisoning of the above reactions by ordered, submonolayer coverages of sulfur show large nonlinear effects for sulfur coverages versus reactivity attenuation. These data together with related chemisorption results are reviewed with emphasis on the author's own work. These studies suggest that the dominant effect in poisoning by sulfur is an electronic one and extends over distances larger than the atomic radius. Related studies have addressed the role of potassium promoters in nickel catalysts for methanation. Potassium decreases the rate of methane formation and increases the rate of higher hydrocarbons relative to the clean nickel surface. Similar results have been reported for supported nickel catalysts suggesting that support effects play a small role in catalytic promotion by potassium.
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