Understanding the chemistry during the preparation of Pd/SSZ-13 for the low-temperature NO adsorption: The role of NH4-SSZ-13 support

[Display omitted] •Improvement effect of NH4-SSZ-13 support on Pd2+ ions dispersion was investigated.•Pd(NO3)2 precursor transformed to Pd(NH3)x2+ intermediate during calcination.•Pd(NH3)x2+ converted to Pd2+ ions by oxidizing NH3 ligands to N2.•Formation of Pd(NH3)x2+ is critical for achieving high...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2021-03, Vol.282, p.119611, Article 119611
Hauptverfasser: Zhao, Huawang, Chen, Xiaoyin, Bhat, Adarsh, Li, Yongdan, Schwank, Johannes W.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:[Display omitted] •Improvement effect of NH4-SSZ-13 support on Pd2+ ions dispersion was investigated.•Pd(NO3)2 precursor transformed to Pd(NH3)x2+ intermediate during calcination.•Pd(NH3)x2+ converted to Pd2+ ions by oxidizing NH3 ligands to N2.•Formation of Pd(NH3)x2+ is critical for achieving high Pd2+ ions dispersion.•Pd2+ ions might be reduced to metallic Pd during calcination without O2. The chemistry during the preparation of Pd/SSZ-13, including impregnation and calcination process, was investigated, using Pd(NO3)2 as precursor and NH4-SSZ-13 as the support. Special attention was paid on analyzing the improvement effect of NH4-SSZ-13 support on Pd2+ ions dispersion. The Pd(NO3)2 precursor remained intact after impregnation and transformed to Pd(NH3)x2+ during calcination at 200−290 °C, and then converted to Pd2+ ions occupying the ion-exchange sites by oxidizing the NH3 ligands to N2 at 290−450 °C. The formation of Pd(NH3)x2+ intermediates is a critical factor for achieving high Pd2+ dispersion, probably due to the fact that NH3 ligands give the intermediates high mobility, facilitating their movement to the ion-exchange sites. The PdO formation might be related to the excessive reduction of Pd2+ sites to metallic Pd, when catalyzing the oxidation of NH3 ligands and the NH4+ on the Brønsted acid sites.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2020.119611