钯
初湿浸渍
物理吸附
催化作用
苯
活性炭
吸附
苯乙烯
热液循环
环辛烯
氢
氯仿
无机化学
金属有机骨架
材料科学
化学
化学工程
有机化学
工程类
聚合物
共聚物
选择性
作者
Michal Sabo,Antje Henschel,Heidrun Fröde,Elias Klemm,Stefan Kaskel
摘要
Palladium was infiltrated into the highly porous metal–organic framework MOF-5 {[Zn4O(bdc)3], bdc = benzene-1,4-dicarboxylate} using [Pd(acac)2] (acac = acetylacetonate) as the precursor in chloroform solution via ‘incipient wetness’ impregnation. The specific surface area decreases from 2885 m2 g−1 to 958 m2 g−1 after infiltration. After reduction in hydrogen or under vacuum, the hydrogen adsorption capacity is increased from 1.15 wt% to 1.86 wt% at 1 atm and 77 K. The palladium loaded MOF-5 has a high catalytic activity in styrene hydrogenation comparable to that of palladium on activated carbon, but cis-cyclooctene hydrogenation is considerably slower. Even at room temperature, the catalyst is not stable in air due to the low hydrothermal stability of the MOF-5 support.
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