Molybdenum Carbide Catalyst Enables Efficient Conversion of Chlorinated Volatile Organic Waste into Syngas through Catalytic Steam Reforming

被引:1
|
作者
Lin, Feng [1 ]
Chen, Zezhi [1 ]
Gong, Huijuan [1 ,2 ]
Wang, Xiaoshu [2 ]
Qin, Yong [2 ]
机构
[1] Nanjing Univ, Sch Environm, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Peoples R China
[2] Nanjing Univ, Ctr Mat Anal, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
CVOCs; catalytic steam reforming; molybdenumcarbide; gamma-Al2O3; dechlorination; HYDROGEN-PRODUCTION; HYDRODECHLORINATION; ETHANOL; 1,2-DICHLOROETHANE; PHASE; OXIDE; CO;
D O I
10.1021/acsami.4c10695
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Catalytic steam reforming offers a groundbreaking approach for converting industrial chlorinated volatile organic compound (CVOC) waste into valuable syngas (H-2 and CO) and recovering HCl. However, the lack of C-Cl bond activation ability in traditional transition metal catalysts results in their insufficient reforming activity toward CVOCs. Herein, a novel molybdenum carbide (beta-Mo2C) catalyst is developed and loaded onto a gamma-Al2O3 support synthesized through a self-assembly method. The gamma-Al2O3 support provides abundant unsaturated coordinated Al3+ ions, which effectively anchor and disperse beta-Mo2C nanoparticles. In the catalytic steam reforming reaction at 600 degrees C, the beta-Mo2C/gamma-Al2O3 catalyst achieves a conversion efficiency higher than 95% and syngas yields of 82.4-92.3% for various typical industrial CVOCs. The mechanistic research reveals that the coordination between C and Mo atoms in beta-Mo2C leads to a slightly electron-deficient state of the Mo sites, accompanied by a high density of unoccupied 4d orbitals. These characteristics are highly advantageous for the adsorption and dechlorination of CVOC molecules. The produced nonchlorinated intermediates can subsequently be oxidized to CO and H-2 by hydroxyl radicals on adjacent Mo sites.
引用
收藏
页码:61868 / 61876
页数:9
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