Authors

Abstract

Lithium promoted 2%Pt/m-ZrO2 catalysts previously observed to exhibit higher rates for the low temperature water-gas shift (LTS) were tested for the ethanol steam reforming with the aim of exploring the potential tuning of the selectivity. Characterization of catalysts having optimized Li content (0.50.75%Li) for LTS exhibited (a) weakened CH bonding of formate, a proposed intermediate in the LTS mechanism, as shown by a shift in the ?(CH) band to lower wavenumbers, (b) a relatively low extent of blocking of Pt, as measured by the ?(CO) band intensity of Pt-CO, (c) increased basicity as measured by CO2 temperature-programmed desorption with mass spectrometry, but not so high as to strongly inhibit CO2 product removal, and finally (d) no evidence of electron transfer from Li to Pt. Here, the same catalysts were tested for ethanol steam reforming (ESR). Results show that Li could likewise weaken the CC bond of the acetate intermediate, the analog of formate in LTS, and facilitate decarboxylation over decarbonylation altering the selectivity in favor of methanation. This trend was confirmed by fixed bed reaction testing, in-situ infrared spectroscopy experiments of transient ESR, and temperatureprogrammed ESR using MS. The Li-doped catalysts may be used to pre-reform ethanol prior to feeding to a methane steam reformer to increase the overall H2 selectivity of the process. DRIFTS of steady state ESR revealed that deactivation occurs through losses in the Pt-support interface, thereby hindering the turnover of the acetate intermediate.