Atomically dispersed Ru catalysts for polychlorinated aromatic hydrocarbon oxidation

被引:5
作者
Yang, Shuai [1 ]
Li, Xinyang [1 ]
Ma, Jiawen [1 ]
Guo, Haiwei [1 ]
Chen, Yifeng [1 ]
Chen, Zhao [1 ]
Ren, Gengbo [1 ]
Ma, Xiaodong [1 ]
机构
[1] Hebei Univ Technol, Sch Energy & Environm Engn, Tianjin Key Lab Clean Energy & Pollutant Control, Tianjin 300401, Peoples R China
基金
中国国家自然科学基金;
关键词
SINGLE-ATOM CATALYSTS; SELECTIVE METHANATION; CO; HYDROGENOLYSIS; 1,3-PROPANEDIOL; GLYCEROL; SITES; WOX; PD;
D O I
10.1039/d2nr00955b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of cost-efficient catalysts with good catalytic activity is an urgent task for polychlorinated aromatic hydrocarbon (PCAH) oxidation. Herein, atomically dispersed Ru catalysts (denoted as Ru ADCs) proved by aberration corrected high-angle annular dark-field scanning transmission electron microscopy and X-ray absorption spectroscopy were synthesized for PCAH oxidation. The oxidation results showed that 0.2 Ru ADCs exhibited enhanced catalytic activity (T-50% < 250 degrees C, T-90% < 300 degrees C) compared with the T-90% > 300 degrees C on 0.2 Ru nanoparticles (NPs). Besides, 0.2 Ru ADCs demonstrated high CO2 yield with >60% CO2 ratio, along with good stability (>80% conversion for 800 mins). The better performance of 0.2 Ru ADCs was verified by kinetic experiments, in which, the apparent activation energy associated with 0.2 Ru ADCs (50.8 kJ mol(-1)) was significantly lower compared with that with 0.2 Ru NPs (80.0 kJ mol(-1)). The superior oxidation activity of 0.2 Ru ADCs was also applied to toluene oxidation. H-2 temperature-programmed reduction ensured the stronger interaction of Ru species with the supports in Ru ADCs than that in Ru NPs, thus inhibiting Ru species aggregation and favoring their higher dispersion ensured by CO temperature-programmed desorption. The present work provides a potential strategy to maximize the usage of noble metal catalysts for PCAH oxidation.
引用
收藏
页码:7849 / 7855
页数:7
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