选择性
纳米材料基催化剂
催化作用
甲醇
蒸发
铜
材料科学
化学工程
双金属片
化学
无机化学
冶金
有机化学
热力学
工程类
物理
作者
Zhiqiao Wang,Zhong‐Ning Xu,Siyan Peng,Ming‐Jian Zhang,Gang Lü,Qingsong Chen,Yumin Chen,Guo‐Cong Guo
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2015-06-08
卷期号:5 (7): 4255-4259
被引量:235
标识
DOI:10.1021/acscatal.5b00682
摘要
Cu-based nanocatalysts have been widely used for CO2 hydrogenation, but their poor stability is the bottleneck for further industrial applications. A high-performance and long-lived Cu/SiO2 nanocatalyst was synthesized by an ammonia-evaporation method for CO2 hydrogenation. The conversion of CO2 reaches up to 28%, which is close to the equilibrium conversion of CO2 (30%), and the selectivity to methanol is 21.3%, which is much higher than the equilibrium selectivity (6.6%) at 320 °C and 3.0 MPa. Furthermore, after 120 h of evaluation, the conversion can be still maintained at a high value (27%), which is much better than a Cu/SiO2 catalyst prepared by traditional impregnation. The Cu+ species has been demonstrated to be the active component for the activation and conversion of CO2. The higher ratio of Cu+/(Cu0 + Cu+) and interaction between the metal and support deriving from copper phyllosilicate are mainly responsible for the high catalytic activity and excellent stability, respectively.
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