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A systematic series of binary and ternary copper catalysts was investigated using the methanol synthesis reaction at atmospheric pressure. Strong metal-support interactions between copper and zinc oxide induced by strongly reducing conditions were probed by the adsorption of carbon monoxide, which was monitored qualitatively and quantitatively by a combination of microcalorimetry, temperature-programmed desorption experiments and Fourier transform infrared spectroscopy. For the zinc oxide-containing catalysts, the pretreatment in flowing carbon monoxide at 493 K resulted in a severe decoration of the copper metal particles with ZnOx adspecies, whereas after methanol synthesis at 493 K the state of the copper was essentially identical to that seen after hydrogen reduction. Copper was always found to be present in its zero-valent state.
d’Alnoncourt et al. (Sun,) studied this question.