Exploring the Synergistic Performance of a Pt-Rh/γ-Al2O3 Catalyst for the Reduction of NO with H2

Monday, November 17, 2008: 12:55 PM
Room 103-A (Pennsylvania Convention Center)

Paul S. Dimick, Chemical Engineering, Lehigh University, Bethlehem, PA
Richard G. Herman, Chemistry, Lehigh University, Bethlehem, PA
Charles E. Lyman, Materials Science and Engineering, Lehigh University, Bethlehem, PA

The performance of two bimetallic Pt-Rh catalysts Pt(95%)-Rh(5%)/γ-Al2O3 (95/5) and Pt(90%)-Rh(10%)/γ-Al2O3 (90/10) was compared to Pt/γ-Al2O3 and Rh/γ-Al2O3 for the reduction of NO with H2 resulting in the following order of relative activity: 95/5 > Pt/γ-Al2O3 ≈ 90/10 > Rh/γ-Al2O3. A conditioning step, equilibrating the catalyst to reaction conditions at 250°C for 10 h, was necessary to observe the maximum synergistic performance of 95/5, a five-fold increase over the activity of Pt/γ-Al2O3. Prior to conditioning, 95/5 had similar activity to Pt/γ-Al2O3. The prepared catalysts were characterized with in-situ FTIR spectroscopy and electron microscopy to gain insight into the difference in performance between 95/5 and 90/10. In-situ FTIR studies were conducted using NO and NO + H2 as probes to qualitatively examine the surfaces of the supported Pt-Rh alloy nanoparticles. Results indicate that metallic Pt and Rh are both present on the surface of 95/5, while the surface of 90/10 contains oxidized Rh in addition to metallic Pt. The non-synergistic performance of 90/10 is attributed to the presence of oxidized Rh and/or an increased surface fraction of Rh.
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