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
聚合物
工程类
作者
Yunbin Xia,Yuanyuan Yang,Mingli Li,Ziyue Lan,Yinghao Chu,Ganxue Wu,Dexin Fang,Zhenxin Zeng,Hong Xiao,Shihuai Deng,Yaoqiang Chen
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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