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得益于氯苯催化销毁的铈改性铁锰复合氧化物的高产率合成。

High-yield synthesis of Ce modified Fe-Mn composite oxides benefitting from catalytic destruction of chlorobenzene.

作者信息

Li Anqi, Long Hongming, Zhang Hongliang, Li Haijin

机构信息

School of Metallurgical Engineering, Anhui University of Technology Ma'anshan Anhui 243002 China.

Key Laboratory of Metallurgical Emission Reduction & Resource Recycling (Anhui University of Technology), Ministry of Education Ma'anshan Anhui 243002 PR China

出版信息

RSC Adv. 2020 Mar 10;10(17):10030-10037. doi: 10.1039/c9ra10489e. eCollection 2020 Mar 6.

DOI:10.1039/c9ra10489e
PMID:35498593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9050221/
Abstract

Ce-Fe-Mn catalysts were prepared by an oxalic acid assisted co-precipitation method. The influence of Ce doping and calcination temperature on the catalytic oxidation of chlorobenzene (as a model VOC molecule) was investigated in a fixed bed reactor. The MnO phase was formed in Ce-Fe-Mn catalysts at low calcination temperatures (<400 °C), which introduced more chemisorbed oxygen, and enhanced the mobility of O atoms, resulting in an improvement of the reduction active of MnO and FeO. Additionally, CeO has strong redox properties, and Ce would oxidize Mn and Fe . Therefore, the interaction of Ce, Fe and Mn can improve the content of surface chemisorbed oxygen. As compared with Fe-Mn catalysts, the catalytic conversion of chlorobenzene over Ce(5%)-Fe-Mn-400 was about 99% at 250 °C, owing to high specific surface area, MnO phase, and Ce doping. However, with the increase in roasting temperature, the performance of the catalysts for the catalytic combustion of chlorobenzene was decreased, which probably accounts for the formation of the MnO phase in Ce-Fe-Mn-500 catalysts, leading to a decrease in the specific surface area and concentration of chemically adsorbed oxygen. As a result, it can be expected that the Ce-Fe-Mn catalysts are effective and promising catalysts for chlorobenzene destruction.

摘要

采用草酸辅助共沉淀法制备了Ce-Fe-Mn催化剂。在固定床反应器中研究了Ce掺杂和煅烧温度对氯苯(作为典型挥发性有机化合物分子)催化氧化的影响。在较低煅烧温度(<400°C)下,Ce-Fe-Mn催化剂中形成MnO相,引入了更多化学吸附氧,增强了O原子的迁移率,导致MnO和FeO还原活性提高。此外,CeO具有很强的氧化还原性能,Ce会氧化Mn和Fe。因此,Ce、Fe和Mn之间的相互作用可以提高表面化学吸附氧的含量。与Fe-Mn催化剂相比,由于高比表面积、MnO相和Ce掺杂,Ce(5%)-Fe-Mn-400在250°C下对氯苯的催化转化率约为99%。然而,随着焙烧温度的升高,催化剂对氯苯催化燃烧的性能下降,这可能是由于Ce-Fe-Mn-500催化剂中形成了MnO相,导致比表面积和化学吸附氧浓度降低。因此,可以预期Ce-Fe-Mn催化剂是用于氯苯销毁的有效且有前景的催化剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6933/9050221/b24091bb5aac/c9ra10489e-f7.jpg
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本文引用的文献

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Catalytic oxidation of chlorobenzene over noble metals (Pd, Pt, Ru, Rh) and the distributions of polychlorinated by-products.贵金属(Pd、Pt、Ru、Rh)催化氧化氯苯及多氯副产物的分布。
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