507789 On the Reaction Mechanism and the Nature of the Active Site for Standard Selective Catalytic Reduction of NOx on Cu/SSZ-13 Zeolites

Fabio H. Ribeiro1, W. Nicholas Delgass1, Rajamani Gounder1, Jeffrey T. Miller1, William F. Schneider2, Aleksey Yezerets3, Atish A. Parekh1, Christopher Paolucci2, Ishant Khurana1, Jonatan D. Albarracin Caballero1, John R. Di Iorio1 and Arthur J. Shih1, (1)Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN, (2)Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, IN, (3)Cummins Inc., Columbus, IN

Cu/SSZ-13 zeolites are used commercially in mobile applications for the selective reduction of NOx with ammonia. Our data suggest that the catalytic cycle is a redox one involving Cu(I) and Cu(II) species. During preparation, the Cu(II) species are the most stable and reside preferentially on six-member rings containing two aluminum sites. The Cu(II) ions first populate 2Al sites before the other remaining unpaired sites with 1Al are populated, Cu(II)OH. These sites could be counted ex situ through vibrational and X-ray absorption spectroscopies (XAS) and chemical titrations. In spite of an apparent chemical difference, the two sites had similar standard SCR reaction turnover rates, apparent activation energies and apparent reaction orders at SCR conditions, even on zeolite frameworks other than SSZ13. Operando XAS experiments showed similar Cu(I) – Cu(II) fractions at steady state, demonstrating their similarity for SCR redox chemistry. Finally, this study also illustrates the necessity of a collaboration among experts in synthesis, characterization, kinetics and theory for a chance to understand the catalytic cycle.

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See more of this Session: 2017 Practice Award
See more of this Group/Topical: Catalysis and Reaction Engineering Division