选择性
吸附
复合数
催化作用
空间速度
化学
相(物质)
材料科学
化学工程
核化学
复合材料
有机化学
工程类
作者
Qian Zhang,Sen Wang,Xuerong Shi,Mei Dong,Jiangang Chen,Juan Zhang,Jianguo Wang,Weibin Fan
标识
DOI:10.1016/j.apcatb.2024.123748
摘要
Direct conversion of CO2 into higher alcohols (C2+OH) is highly desirable, but rather challenging due to requiring the synergetic action of C-C coupling and CO insertion. Here, we developed a new K-CuZnAl/Zr-CuFe composite, which gave CO2 conversion and C2+OH selectivity of 40.6% and 22.4% respectively, while CO selectivity is only 10.3% at 320 °C, 4 MPa and 6000 mL gcat−1 h−1. The C2+OH STY can reach 195.1 mg gcat–1 h–1, and is well maintained within 200 h at higher GHSV of 24000 mL gcat−1 h−1. Introduction of K-CuZnAl and decrease of the contact distance of K-CuZnAl and Zr-CuFe boost the formation and subsequent conversion of CO* intermediate. In addition, doping small amounts of Zr into CuFe catalyst hinders the phase separation of Cu and Fe species by enhancing their interface interaction. As a result, the CHx * species generated on iron carbide through CO* dissociative activation quickly reacts with the non-dissociative adsorbed CO* on adjacent Cu to produce more C2+OH.
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