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Lattice oxygen activity in ceria-praseodymia mixed oxides for soot oxidation in catalysed Gasoline Particle Filters

烟灰 催化作用 氧气储存 氧气 化学工程 氮氧化物 X射线光电子能谱 惰性气体 还原气氛 化学 无机化学 惰性 材料科学 极限氧浓度 吸附 燃烧 有机化学 工程类
作者
Juan Carlos Martínez-Munuera,Mattia Zoccoli,Javier Giménez-Mañogil,Avelina Garcı́a-Garcı́a
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:245: 706-720 被引量:40
标识
DOI:10.1016/j.apcatb.2018.12.076
摘要

Two series of ceria-praseodymia catalysts with varying composition have been systematically investigated in the oxidation of soot under inert atmosphere in order to find out its potential utilization in Gasoline Particulate Filters for GDI engines. The samples have been widely characterized by XRD, Raman spectroscopy, TEM, FESEM, XPS, N2 adsorption at −196 °C and O2-TPD. The praseodymium incorporation onto the ceria enhances the oxygen mobility in the subsurface/bulk of the sample favoring higher O2 released amounts under inert atmosphere. The intermediate compositions can promote more accentuated O2 emissions at moderate temperatures (up to 500 °C). The efficiency of the own active oxygen species released from the catalyst to oxidize soot under inert atmosphere, even under loose contact mode, has been well demonstrated. The pathways of the mechanism taking place seem to be dependent on the temperature and mainly on the type of contact among soot and catalyst. Under loose contact conditions and low-medium temperatures, the O2 freshly emitted from the catalyst can oxidize soot more efficiently than a diluted O2-gas stream. Conversely, under more severe conditions (higher temperature or tight contact conditions), the soot acts as a “driving force” and the own lattice oxygen species can be transferred directly towards soot surface in an efficient way.
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