Oxy-Anionic Doping: A New Strategy for Improving Selectivity of Ru/CeO2 with Synergetic Versatility and Thermal Stability for Catalytic Oxidation of Chlorinated Volatile Organic Compounds

催化作用 化学 二氯甲烷 氧化还原 兴奋剂 无机化学 热稳定性 催化氧化 选择性 金属 激进的 有机化学 材料科学 光电子学 溶剂
作者
Kai Shen,Biao Gao,Hangqi Xia,Wei Deng,Jiaorong Yan,Xiaohan Guo,Yanglong Guo,Xingyi Wang,Wangcheng Zhan,Qiguang Dai
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:56 (12): 8854-8863 被引量:68
标识
DOI:10.1021/acs.est.2c00942
摘要

Understanding the formation and inhibition of more toxic polychlorinated byproducts from the catalytic oxidation elimination of chlorinated volatile organic compounds (Cl-VOCs) and unveiling efficient strategies have been essential and challenging. Here, RuOx supported on CePO4-doped CeO2 nanosheets (Ru/Pi-CeO2) is designed for boosting catalytic oxidation for the removal of dichloromethane (DCM) as a representative Cl-VOC. The promoted acid strength/number and sintering resistance due to the doping of electron-rich and thermally stable CePO4 are observed along with the undescended redox ability and the exposed multi-active sites, which demonstrates a high activity and durability of DCM oxidation (4000 mg/m3 and 15,000 mL/g·h, stable complete-oxidation at 300 °C), exceptional versatility for different Cl-VOCs, alkanes, aromatics, N-containing VOCs, CO and their multicomponent VOCs, and enhanced thermal stability. The suppression of polychlorinated byproducts is determined over Ru/Pi-CeO2 and oxy-anionic S, V, Mo, Nb, or W doping CeO2, thus the oxy-anionic doping strategy is proposed based on the quenching of the electron-rich oxy-anions on chlorine radicals. Moreover, the simple mechanical mixing with these oxy-anionic salts is also workable even for other catalysts such as Co, Sn, Mn, and noble metal-based catalysts. This work offers further insights into the inhibition of polychlorinated byproducts and contributes to the convenient manufacture of monolithic catalysts with superior chlorine-poisoning resistance for the catalytic oxidation of Cl-VOCs.
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