环加成
催化作用
反应性(心理学)
固碳
金属有机骨架
化学
多孔性
金属
有机合成
路易斯酸
组合化学
有机化学
吸附
二氧化碳
医学
替代医学
病理
作者
Jin‐Mi Noh,Youngik Kim,Hyojin Park,Ji‐Hyun Lee,Minyoung Yoon,Myung Hwan Park,Youngjo Kim,Min Kim
标识
DOI:10.1016/j.jiec.2018.04.010
摘要
A variety of metal-organic frameworks (MOFs) have been reported as efficient catalysts for CO2 fixation reactions, such as cycloaddition to cyclic carbonates. The permanent porosity of the frameworks and the Lewis acidity of the MOF metal sites have been considered as the major contributors to the catalytic activity in the cycloaddition of CO2. In this study, we have, instead, focused on the effects of the organic functional groups for effective catalytic ability. A total of eight different functionalized Zr-based MOFs were tested. It was revealed that the non-functionalized pristine UiO-66 MOF (UiO = University of Oslo) showed the best conversion at low temperature (77% at 50 °C), whereas the hydroxy-functionalized UiO-66-OH MOF displayed the best conversion at high temperature (91% at 140 °C). The Zr-MOF could be recycled up to four times without a significant decrease in the reactivity.
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