Construction of unique oxygen vacancy defect through various metal-doping (Cu, Mn, Zr) of Ce2Co1Ox nanoparticles towards boosting the catalytic oxidation toluene performance

甲苯 催化作用 催化氧化 氧化还原 材料科学 马来酸酐 氧气 空间速度 化学工程 无机化学 化学 有机化学 选择性 共聚物 工程类 聚合物
作者
Yunbin Xia,Yuanyuan Yang,Mingli Li,Ziyue Lan,Yinghao Chu,Ganxue Wu,Dexin Fang,Zhenxin Zeng,Hong Xiao,Shihuai Deng,Yaoqiang Chen
出处
期刊:Separation and Purification Technology [Elsevier]
卷期号:342: 126993-126993 被引量:8
标识
DOI:10.1016/j.seppur.2024.126993
摘要

Achievement of catalytic oxidation of volatile organic compounds (VOCs) at low temperature is still a challenge to be addressed. Promoting catalytic activity via constructing oxygen vacancy defect is an attractive strategy in heterogeneous catalysis. Herein, a series of Ce2Co1M1 (M = Cu, Mn, Zr) catalysts were prepared by modified co-precipitation method and their catalytic oxidation performance of toluene was measured. Activity results suggested that the introduction of doping-metals significantly enhanced the catalytic performance of Ce2Co1Ox, with Ce2Co1Cu1 possessed the optimal catalytic activity (T90 = 210 ℃), robust stability, water resistance, GHSV tolerance and anti-aging ability. It has been demonstrated that Cu-doping resulted in the formation of Cu-Ce solid solution and constructed a Cu2+-O-Ce4+ complex active site. Benefiting from this, the redox and gaseous oxygen molecule capture & activation capabilities of the catalyst are tremendously improved via constructing abundant oxygen vacancies. The in-situ DRIFTS results revealed that Ce2Co1Cu1 exhibited a better C=C breaking of aromatic rings ability, a faster consumption rate of benzoate and maleic anhydride, and is less prone to accumulation of by-products, the above account for its enhanced low-temperature catalytic performance for toluene. This work may provide a new strategy to design the high-efficiency toluene oxidation catalysts.

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