Methods for NH3 titration of Brønsted acid sites in Cu-zeolites that catalyze the selective catalytic reduction of NOx with NH3

• Published in: Journal of catalysis Vol. 312; pp. 26 - 36
• Main Authors: Bates, Shane A., Delgass, W. Nicholas, Ribeiro, Fabio H., Miller, Jeffrey T., Gounder, Rajamani
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier Inc 01.04.2014; Elsevier
• Subjects: Brønsted acid site; Catalysis; Chabazite; Chemistry; Copper-exchanged zeolite; Exact sciences and technology; General and physical chemistry; Ion-exchange; n-Propylamine; NH3 titration of acid sites; Selective catalytic reduction of NOx; SSZ-13; Surface physical chemistry; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Zeolites: preparations and properties; ZSM-5; Brønsted acid site; Chabazite; n-Propylamine; Selective catalytic reduction of NOx; ZSM-5; SSZ-13; Copper-exchanged zeolite; NH3 titration of acid sites; Nitrogen oxide; Catalytic reaction; Acidic site; Transition metal; Bronsted site; Chemical reduction; Ammonia; Heterogeneous catalysis; Selective catalytic reduction of NO; Brönsted acid; titration of acid sites; NH; Copper
• ISSN: 0021-9517; 1090-2694
• DOI: 10.1016/j.jcat.2013.12.020

[Display omitted] •Procedures developed for selective NH3 titration of residual H+ sites in Cu-zeolites.•NH3 and n-propylamine selectively titrate all H+ sites in Cu-ZSM-5.•n-Propylamine may titrate only a fraction of residual H+ sites in Cu-SSZ-13.•27Al MAS NMR indicates more framework Al atoms are present than H+ sites.•Standard SCR turnover rates (per Cu(II)) independent of H+ content in Cu-SSZ-13. Three methods were developed to use ammonia as a selective titrant of residual Brønsted acid sites in partially Cu-exchanged MFI (ZSM-5) and CHA (SSZ-13) zeolites that mediate the selective catalytic reduction (SCR) of NO with NH3. These methods involved saturation with gas-phase NH3 at 433K followed by purging in flowing helium, saturation with gas-phase NH3 at 323K followed by washing with deionized water, or saturation with aqueous NH4NO3 solution (353K) followed by washing with deionized water. H-ZSM-5 (Si:Altot=17–89) and Cu-ZSM-5 (Cu:Altot=0–0.27 at Si:Altot=17) samples saturated with NH3 using these three methods, and with n-propylamine titrants that react selectively with Brønsted acid sites to form C3H6 and NH3, evolved identical amounts of NH3 in temperature-programmed desorption experiments. The consistency among these four methods indicates that NH3 can be used as a selective titrant of H+ sites in the presence of Lewis acid sites on Cu-zeolites. The number of H+ sites on MFI and CHA zeolites measured by direct chemical titration was often less than the number of framework Al (Alf) atoms determined from 27Al MAS NMR spectra (H+:Alf=0.7–1.0), yet another reminder that Alf structures can be imprecise surrogates for active H+ sites on zeolites. Although n-propylamine (at 323K) titrated all H+ sites in Cu-ZSM-5, it titrated in Cu-SSZ-13 (Cu:Altot=0–0.20 at Si:Altot=4.5) only a small fraction (0–0.26) of the H+ sites that were accessible to NH3, which is the reductant in NO SCR reactions with NH3 (standard SCR). Standard SCR turnover rates on Cu-SSZ-13 samples, after normalization by the number of active Cu(II) sites, showed an apparent zero-order dependence on the number of residual H+ sites measured by NH3 titration. These data suggest that reactive NH4+ intermediates are present in excess, relative to metal-bound NOx species, under the SCR conditions studied. The methods reported herein, which titrate Brønsted acid sites selectively in the presence of Lewis acid sites, are useful in investigating the mechanistic role of H+ sites in standard SCR on small-pore Cu-zeolites and in other reactions catalyzed by metal-exchanged zeolites.