Abstract
Bimetallic FeIr/SiO{2}CO hydrogenation catalysts have been studied by temperature-programmed reduction, EXAFS, Mossbauer spectroscopy, and previously also by infrared spectroscopy of adsorbed CO. We concentrate on the structure of a freshly reduced sample, which is selective for the formation of hydrocarbons from CO+3H{2}, and a catalyst activated during 48 h of
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