介孔材料
催化作用
碳纤维
化学工程
扩散
材料科学
选择性
传质
纳米技术
化学
工程类
有机化学
色谱法
复合材料
热力学
物理
复合数
作者
Shangjun Chen,Haibin Fu,Li Zhang,Ying Wan
标识
DOI:10.1016/j.apcatb.2019.02.006
摘要
This study proposes ordered mesoporous carbon nanosphere-supported gold catalysts to eliminate the diffusion limitation inside the long channels of bulk mesoporous materials. The nanospherical catalysts have a spherical morphology with a diameter of approximately 90 nm, uniform pore sizes of 2.5 nm, and high surface areas of approximately 600 m2/g; and the bulk catalysts have similar mesoporous textural properties with nanospherical catalysts but an irregular bulk shape. Metallic gold particles are both intercalated inside carbonaceous walls. The Madon-Boudart (MB) test shows that nanospherical catalysts exhibit no diffusion limitations in the reduction of nitroarenes, even for a large 2,6-dimethylnitrobenzene (2,6-DMNB) molecule. By comparison, the bulk-ordered mesoporous carbon-supported gold catalysts display distinct mass transfer inhibition. The nanospherical mesoporous carbon-supported gold catalysts are highly active and selective for the reduction of nitroarenes to corresponding amines, reaching turnover frequency (TOF) values of 13.7, 16.1, 7.6 and 26.8 min−1 for converting 4-nitrophenol (4-NP), 2-nitrophenol (2-NP), 4-(tert-butyl)-2-nitrophenol (4-TB-2-NP), and 2,6-DMNB, respectively. The catalysts are stable and can be re-used more than 15 times.
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