催化作用
氧化还原
1,2-二氯乙烷
贵金属
无机化学
色散(光学)
化学
吸附
多孔性
化学工程
材料科学
物理化学
有机化学
物理
光学
工程类
作者
Wanwan Zhou,Lin Chen,Zhaoyang Fei,Liu Qing,Mifen Cui,Xu Qiao
标识
DOI:10.1002/slct.202300340
摘要
Abstract The RuO 2 @Ce m Zr 1−m O 2 −SiO 2 catalysts were synthesized by the spontaneous deposition method. Based on the XRD patterns of various RuO 2 @Ce m Zr 1−m O 2 −SiO 2 catalysts, it was suggested that the Ru noble metal nanoparticles were distributed with high dispersion on the surface of Ce‐modified porous matrix of ZrO 2 . H 2 ‐TPR and NH 3 ‐TPD confirmed that all catalysts possessed superior redox ability as well as acidity, which were facilitated to the catalytic dichloroethane (DCE) oxidation. From the systematic study of texture structure, surface properties and catalytic activity, we knew that acid sites were shown to be favorable for adsorption as well as activation of DCE and improve the anti‐poisoning property of the catalyst, and the redox ability could facilitate the further oxidation of the intermediate. The optimized RuO 2 @Ce 0.1 Zr 0.9 O 2 −SiO 2 catalyst exhibited superior activity ( T 90 =275 °C at a space velocity of 15000 h −1 ), good stability (at 300 °C for 50 h) and outstanding tolerance towards moisture (in 5 % moisture). Our work demonstrated the important role of acidity and redox ability over these functionalized catalysts, providing guidance for the advanced catalyst design.
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