Nitrate reduction on surface of Pd/Sn catalysts supported by coal fly ash-derived zeolites.

In this study, we synthesized four zeolites (i.e., Zeolite-X&A9, -X&A&HS12, -X&HS15, -X&HS18) from coal fly ash (CFA), and evaluated their potential for use as support materials to fabricate novel Pd-Sn bimetallic catalysts for reactive and selective reduction of NO3- to N2. The successive transformation of zeolite (Na-A and Na-X to hydroxy sodalite (HS)) was observed with increasing crystallization time from 9 to 18 h, which resulted in different degrees of crystallinity, morphology, BET surface area, and pore volume. Compared to other monometallic and bimetallic catalysts, Pd-Sn/Zeolite-X&HS15 (crystallization time = 15 h) showed remarkable nitrate removal (100%) with the highest kinetic rate constant (k = 0.055 min-1, K' = 0.219 min-1 gcat-1, K'' = 2.922 L min-1 gPd-1) and N2 selectivity (88.1%). These results can be attributed to high surface area and stability of each of the zeolite phases (i.e., Na-X and HS). The reaction mechanism was elucidated by Energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy analyses, demonstrating the presence of Pd°, Sn°, and Sn2+ and the uniform distribution of proximate Pd-Sn ensembles on the surface. These results suggest new promising strategies for applying industrial solid waste-derived zeolites to the synthesis of novel bimetallic catalysts to ensure efficient and economical denitrification of wastewater.