氧化剂
氮氧化物
钙长石
化学
解吸
柴油
吸附
氧化还原
化学工程
俘获
无机化学
催化作用
沸石
有机化学
工程类
燃烧
生态学
生物
作者
Roberta Villamaina,Umberto Iacobone,Isabella Nova,Enrico Tronconi,Maria Pia Ruggeri,Loredana Mantarosie,Jillian Collier,David Thompsett
标识
DOI:10.1016/j.apcatb.2020.119724
摘要
We have applied transient response methods to study Pd-CHA systems as Passive NOx Adsorbers (PNA) for the low-temperature NOx removal from Diesel exhausts. NO adsorption/TPD experiments were carried out at different temperatures in gaseous mixtures containing the main exhausts components (O2, CO, H2O) with the aim to clarify the mechanism determining the capability of Pd-CHA to trap and desorb NO. PdI was identified as the main NO storage site, both in mixtures containing a strong reductant like CO and in the presence of O2 only. When the oxidizing capability of the environment was enhanced, the Pd utilization, i.e. NO stored/Pdtot, dropped significantly: this loss is attributed to the competition between the NO storage on the reduced Pd sites and their re-oxidation. Pd oxidation played an important role also in the desorption phase: TPD experiments performed in gaseous mixtures with greater oxidizing strength enabled NO desorption at lower temperatures. The present data emphasize therefore the impact of the Pd redox state on the NO storage/release performances of Pd-CHA based PNAs.
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