氮氧化物
烟灰
催化作用
化学吸附
燃烧
氮氧化物
化学
无机化学
镧
氧化物
铜
化学工程
有机化学
工程类
作者
Virginia Alcalde‐Santiago,Arantxa Davó‐Quiñonero,Esther Bailón‐García,Dolores Lozano‐Castelló,Agustín Bueno‐López
出处
期刊:Chemcatchem
[Wiley]
日期:2020-09-28
卷期号:12 (24): 6375-6384
被引量:11
标识
DOI:10.1002/cctc.202001187
摘要
Abstract The individual and simultaneous removal of NOx by Storage and Reduction with H 2 (H 2 ‐NSR) and combustion of soot have been studied for La and CuLa catalysts. The NOx storage capacity of pure lanthanum oxide is improved either by copper addition or by using a colloidal crystal hard template for the synthesis of a macroporous structure. Although the NOx storage capacity of the CuLa macroporous material is around ten times lower regarding conventional PtBa catalysts, the kinetics of the H 2 ‐NSR cycles are fast enough to allow high NOx removal (until 90 % removal). Lanthanum oxide catalyst prepared with uncontrolled structure has no activity for soot combustion, but the activity increases for a macroporous counterpart prepared using the colloidal crystal template because the macroporous structure improves the soot‐catalyst contact and allows the nitrogen‐oxygen surface groups yielded upon NOx chemisorption to oxidize soot. The soot combustion activity of lanthanum catalysts is also enhanced upon copper loading, because copper improves the NO 2 ‐assisted soot combustion mechanism and favors the chemisorption of NOx, enhancing soot oxidation by nitrogen‐oxygen surface species. Finally, it is demonstrated that the simultaneous removal of NOx by H 2 ‐NSR and soot combustion can be carried out with a CuLa catalyst at 450 °C. The simultaneous removal does not affect the combustion of soot and only has a small effect in NOx removal.
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