催化作用
热解
铜
碳纤维
苯
化学
化学工程
无机化学
材料科学
有机化学
冶金
复合材料
复合数
工程类
作者
Ahsan Jalal,Yuxin Zhao,Alper Uzun
标识
DOI:10.1021/acs.iecr.1c04741
摘要
A family of carbon-embedded copper catalysts was synthesized by pyrolyzing copper benzene-1,3,5-tricarboxylate (Cu-BTC) at various temperatures ranging from 400 to 900 °C. Characterization of catalysts demonstrated that the density of defect sites on the carbon support increases with an increase in the pyrolysis temperature leading to an increase in the electron density on the copper sites. Catalytic performance tests on 1,3-butadiene hydrogenation showed that the performance becomes more stable as the pyrolysis temperature increases above 800 °C such that the catalyst prepared by pyrolysis at 900 °C provided a stable performance for more than 12 h, while the one prepared at 400 °C was deactivating by >25%. Data further demonstrated a strong dependence of the turnover frequencies to the defect site density on the carbonaceous layer. These results present a versatile approach for preparing carbon-embedded copper catalysts with tunable electronic structure and consequent catalytic properties.
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