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Enhanced sulfur tolerance of ceria-promoted NO x storage reduction (NSR) catalysts: Sulfur uptake, thermal regeneration and reduction with H2(g)

机译:氧化铈促进的NOx储存还原(NSR)催化剂对硫的耐受性增强:硫的吸收,热再生和H2(g)的还原

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摘要

SO x uptake, thermal regeneration and the reduction of SO x via H2(g) over ceria-promoted NSR catalysts were investigated. Sulfur poisoning and desulfation pathways of the complex BaO/Pt/CeO2/Al2O3 NSR system was investigated using a systematic approach where the functional sub-components such as Al 2O3, CeO2/Al2O3, BaO/Al2O3, BaO/CeO2/Al2O 3, and BaO/Pt/Al2O3 were studied in a comparative fashion. Incorporation of ceria significantly increases the S-uptake of Al2O3 and BaO/Al2O3 under both moderate and extreme S-poisoning conditions. Under moderate S-poisoning conditions, Pt sites seem to be the critical species for SO x oxidation and SO x storage, where BaO/Pt/Al2O3 and BaO/Pt/CeO2/Al2O3 catalysts reveal a comparable extent of sulfation. After extreme S-poisoning due to the deactivation of most of the Pt sites, ceria domains are the main SO x storage sites on the BaO/Pt/CeO2/Al2O3 surface. Thus, under these conditions, BaO/Pt/CeO2/Al 2O3 surface stores more sulfur than that of BaO/Pt/Al 2O3. BaO/Pt/CeO2/Al2O3 reveals a significantly improved thermal regeneration behavior in vacuum with respect to the conventional BaO/Pt/Al2O3 catalyst. Ceria promotion remarkably enhances the SO x reduction with H 2(g). © 2013 Springer Science+Business Media New York.
机译:研究了二氧化铈促进的NSR催化剂对SOx的吸收,热再生和H2(g)的H2(g)还原。使用系统方法研究了复杂的BaO / Pt / CeO2 / Al2O3 NSR系统的硫中毒和脱硫途径,其中功能子组分如Al 2O3,CeO2 / Al2O3,BaO / Al2O3,BaO / CeO2 / Al2O 3和以比较方式研究了BaO / Pt / Al2O3。在中等和极端的S中毒条件下,掺入二氧化铈会显着增加Al2O3和BaO / Al2O3的S吸收。在适度的S中毒条件下,Pt位点似乎是SO x氧化和SO x储存的关键物种,其中BaO / Pt / Al2O3和BaO / Pt / CeO2 / Al2O3催化剂显示出相当程度的硫酸化程度。由于大部分Pt位点失活而导致极端的S中毒后,二氧化铈域是BaO / Pt / CeO2 / Al2O3表面上的主要SO x储存位点。因此,在这些条件下,BaO / Pt / CeO2 / Al 2O3表面比BaO / Pt / Al 2O3表面存储更多的硫。与传统的BaO / Pt / Al2O3催化剂相比,BaO / Pt / CeO2 / Al2O3在真空下显示出显着改善的热再生性能。二氧化铈的促进显着增强了H 2(g)对SO x的还原作用。 ©2013纽约Springer Science + Business Media。

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