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Approach to the Characterization of Monolithic Catalysts Based on La Perovskite-like Oxides and Their Application for VOC Oxidation under Simulated Indoor Environment Conditions

催化作用 钙钛矿(结构) 材料科学 化学工程 无机化学 X射线光电子能谱 堇青石 陶瓷 化学 有机化学 冶金 工程类
作者
Ornel Padilla,Jessica Múnera-Jaramillo,Jaime Gallego,Alexander Santamarı́a
出处
期刊:Catalysts [Multidisciplinary Digital Publishing Institute]
卷期号:12 (2): 168-168 被引量:11
标识
DOI:10.3390/catal12020168
摘要

Catalysts are very important in controlling the pollutant emissions and are used for hundreds of chemical processes. Currently, noble metal-based catalysts are being replaced for other kinds of materials. In this study, three lanthanum-based perovskite-like oxides were synthesized (LaCo, LaCoMn, and LaMn) by the glycine-combustion method. The powder catalysts obtained were supported onto cordierite ceramic monoliths using an optimized washcoating methodology to obtain the subsequent monolithic catalysts (LaCo-S, LaCoMn-S, and LaMn-S). Sample characterization confirmed the formation of the perovskite-like phase in the powder materials as well as the presence of the perovskite phase after supporting it onto the monolithic structure. The XPS analysis showed a general decrease in lattice oxygen species for monolithic catalysts, mainly caused by the colloidal silica used as a binder agent during the washcoating process. Additionally, some variations in the oxidation state distribution for elements in Co-containing systems suggest a stronger interaction between cordierite and such catalysts. The catalytic activity results indicated that powder and monolithic catalysts were active for single-component VOC oxidation in the following order: 2-propanol > n-hexane ≅ mixture > toluene, and there was no evidence of loss of catalytic activity after supporting the catalysts. However, LaMn-S had a better catalytic performance for all VOC tested under dry conditions, achieving oxidation temperatures between 230–420 °C. The oxidation efficiency for the VOC mixture was strongly affected by the presence of moisture linking the oxidation efficiency at wet conditions to the VOC chemical nature. Additionally, for higher VOC concentrations, the catalyst efficiency decreased due to the limited number of active sites.
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