Engineering surface-exposed LaCoO3 perovskite nanotubular catalysts for catalytic combustion of toluene through acid etching†

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL
Shixing Wu, Zhan Shi, Fang Dong, Xin Song, Weiliang Han, Weigao Han, Haitao Zhang, Xiuyan Dong and Zhicheng Tang
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Abstract

Resistance to SO2 poisoning is a major technical challenge faced by catalysts in VOC oxidation. In this study, we prepared a series of nanotubular perovskite-based catalysts using electrostatic spinning technique. The catalytic activity of the prepared LaCoO3 (LCO) catalyst could be significantly enhanced by doping with a small amount of Ce. Furthermore, acid treatment significantly enhanced the adsorption of VOC molecules on the catalyst surface, thus leading to the exposure of more Co3+ on the catalyst surface. Owing to the protective effects of CeO2 and Co3O4, the acid etched Ce-doped LaCoO3 catalyst exhibited outstanding catalytic performance towards toluene, even in the presence of water vapor and SO2. The reason was that Ce addition increased the content of Co3+ and active oxygen species, and the acid treatment led to a further increase in the exposed Co3+ species on the catalyst surface. Meanwhile, Ce acted as a sacrificial site to protect Co3+ from being poisoned by SO2. The synergistic effect of Ce doping and acid etching significantly improved the catalyst's resistance to SO2. In situ FTIR confirmed that toluene primarily underwent a synergistic interaction of MvK and L–H mechanisms over the LCCO-2 catalyst. The possible reaction pathway is as follows: gaseous toluene → adsorbed toluene → benzyl alcohol → benzaldehyde → benzoate → anhydride → CO2 and H2O. Thus, this work provides innovative ideas for designing VOC catalytic combustion catalysts with excellent SO2 resistance in the future.

Abstract Image

工程表面暴露的LaCoO3钙钛矿纳米管催化剂通过酸蚀催化燃烧甲苯
抗SO2中毒是VOC氧化催化剂面临的主要技术挑战。在本研究中,我们采用静电纺丝技术制备了一系列钙钛矿基纳米管催化剂。制备的LaCoO3 (LCO)催化剂中掺入少量Ce后,催化活性明显增强。此外,酸处理显著增强了VOC分子在催化剂表面的吸附,从而导致更多的Co3+暴露在催化剂表面。由于CeO2和Co3O4的保护作用,酸蚀ce掺杂LaCoO3催化剂即使在水蒸气和SO2存在的情况下,对甲苯也表现出优异的催化性能。其原因是Ce的加入增加了Co3+和活性氧的含量,酸处理导致催化剂表面暴露的Co3+种类进一步增加。同时,Ce作为牺牲位点保护Co3+不被SO2毒害。Ce掺杂和酸蚀的协同作用显著提高了催化剂的抗SO2性能。原位FTIR证实,甲苯在LCCO-2催化剂上主要经历了MvK和L-H机制的协同相互作用。可能的反应途径为:气态甲苯→吸附甲苯→苯甲醇→苯甲醛→苯甲酸酯→酸酐→CO2和H2O。因此,本研究为未来设计抗SO2性能优异的VOC催化燃烧催化剂提供了创新思路。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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