LAUSR

Diesel oxidation catalysts Pt-Pd-(y)ZrO2-(z)WO3/CeZrOx-Al2O3 with total Pt & Pd loading of only 0.68 wt.% were prepared and investigated for oxidation activity and stability of CO, C3H6, and NO. Introduction of ZrO2 greatly improved low-temperature activities and retained stability especially for CO and C3H6 oxidation after treated at 800 °C. With the optimal loading amount of 6 wt% ZrO2, 2 wt% WO3 was introduced to the system and showed higher activity. Reaction temperature for 50% CO and C3H6 conversion declined to 160 and 181 °C, and the maximal NO conversion increased to 50%. By using XRD, TEM, CO chemisorption, XPS, and H2-TPR analysis, it was found that ZrO2 could inhibit aggregation of Pt and Pd, improve metal dispersion, and increase surface-chemisorbed oxygen after high-temperature treatment, accounting for promoted performance. Also, there were more reducible oxide species in ZrO2-doped catalysts. ZrO2 could induce reduction of noble metal oxides and surface ceria by weakening Pt-O-Ce interaction, which increased the ability to dissociate H2 and spillover effect of dissociated hydrogen to ceria. Doping WO3 increased metal dispersion of fresh samples and brought more Pt0 species that were active sites for oxidation reactions. Thus, ZrO2 and WO3 could be effective additives for oxidation catalysts to synergistically improve their activities and thermal stability.