Synthesis and Characterization of Copper-Exchanged Zeolite Catalysts and Kinetic Studies on NOx Selective Catalytic Reduction with Ammonia

Arthur Jayang Shih, Purdue University

Abstract

Although Cu-SSZ-13 zeolites are used commercially in diesel engine exhaust after-treatment for abatement of toxic NOx pollutants via selective catalytic reduction (SCR) with NH3, molecular details of its active centers and mechanistic details of the redox reactions they catalyze, specifically of the Cu(I)  Cu(II) oxidation half-reaction, are not well understood. A detailed understanding of the SCR reaction mechanism and nature of the Cu active site would provide insight into their catalytic performance and guidance on synthesizing materials with improved low temperature (< 473 K) reactivity and stability against deactivation (e.g. hydrothermal, sulfur oxides). We use computational, titration, spectroscopic, and kinetic techniques to elucidate (1) the presence of two types of Cu2+ ions in Cu-SSZ-13 materials, (2) molecular details on how these Cu cations, facilitated by NH3 solvation, undergo a reduction-oxidation catalytic cycle, and (3) that sulfur oxides poison the two different types of Cu2+ ions to different extents at via different mechanisms. Copper was exchanged onto H-SSZ-13 samples with different Si:Al ratios (4.5, 15, and 25) via liquid-phase ion exchange using Cu(NO3)2 as the precursor. The speciation of copper started from the most stable Cu2+ coordinated to two anionic sites on the zeolite framework to [CuOH]+ coordinated to only one anionic site on the zeolite framework with increasing Cu:Al ratios. The number of Cu2+ and [CuOH]+ sites was quantified by selective NH3 titration of the number of residual Brønsted acid sites after Cu exchange, and by quantification of Brønsted acidic Si(OH)Al and CuOH stretching vibrations from IR spectra. Cu-SSZ-13 with similar Cu densities and anionic framework site densities exhibit similar standard SCR rates, apparent activation energies, and orders regardless of the fraction of Z2Cu and ZCuOH sites, indicating that both sites are equally active within measurable error for SCR. The standard SCR reaction uses O2 as the oxidant (4NH3 + 4NO + O2  6H2O + 4N2) and involves a Cu(I)/Cu(II) redox cycle, with Cu(II) reduction mediated by NO and NH3, and Cu(I) oxidation mediated by NO and O2. In contrast, the fast SCR reaction (4NH3 + 2NO + 2NO2  6H2O + 4N2) uses NO2 as the oxidant. Low temperature (437 K) standard SCR reaction kinetics over Cu-SSZ-13 zeolites depend on the spatial density and distribution of Cu ions, varied by changing the Cu:Al and Si:Al ratio. Facilitated by NH3 solvation, mobile Cu(I) complexes can dimerize with other Cu(I) complexes within diffusion distances to activate O2, as demonstrated through X-ray absorption spectroscopy and density functional theory calculations. Monte Carlo simulations are used to define average Cu-Cu distances. In contrast with O2-assisted oxidation reactions, NO2 oxidizes single Cu(I) complexes with similar kinetics among samples of varying Cu spatial density. These findings demonstrate that low temperature standard SCR is dependent on Cu spatial density and requires NH3 solvation to mobilize Cu(I) sites to activate O2, while in contrast fast SCR uses NO2 to oxidize single Cu(I) sites.

Degree

Ph.D.

Advisors

Ribeiro, Purdue University.

Subject Area

Energy

COinS