The synthesis route of 10Al2O3·2B2O3 (10A2B) and effect of additives were studied to use this compound as a thermally stable support material for Pd catalysts. The preparation by reverse coprecipitation was found to have a beneficial effect on the BET surface area of 10A2B and thus Pd metal dispersion, compared to other preparation routes via solid-state reaction and hydrolysis of metal alkoxides. The addition of 3 wt % BaO suppressed the sintering of 10A2B and Pd during thermal aging at 900 °C in a stream of air containing 10% H2O. Although direct interactions between Pd and the support material were not detected by EXAFS, the catalytic performance for NO–CO–C3H6–O2–H2O reactions under modulated air-to-fuel ratio (A/F) conditions was strongly influenced by the Ba additive. The activity for NO and C3H6 in a rich region (A/F < 14.6) was especially enhanced in the presence of Ba because of accelerated elemental reactions including NO–CO and NO–C3H6. In situ FT-IR of CO suggested that the Pd electronic state changed by electrostatic effect of Ba additives would activate NO and weaken the self-poisoning effect of C3H6.
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