表面改性
吸附
X射线光电子能谱
材料科学
胺气处理
金属
金属有机骨架
化学工程
中子衍射
比表面积
核化学
无机化学
有机化学
化学
晶体结构
催化作用
冶金
工程类
作者
Xiao Su,Lev Bromberg,Vladimir Martis,Fritz Simeon,Ashfia Huq,T. Alan Hatton
标识
DOI:10.1021/acsami.7b02471
摘要
Postsynthetic functionalization of magnesium 2,5-dihydroxyterephthalate (Mg-MOF-74) with tetraethylenepentamine (TEPA) resulted in improved CO2 adsorption performance under dry and humid conditions. XPS, elemental analysis, and neutron powder diffraction studies indicated that TEPA was incorporated throughout the MOF particle, although it coordinated preferentially with the unsaturated metal sites located in the immediate proximity to the surface. Neutron and X-ray powder diffraction analyses showed that the MOF structure was preserved after amine incorporation, with slight changes in the lattice parameters. The adsorption capacity of the functionalized amino-Mg-MOF-74 (TEPA-MOF) for CO2 was as high as 26.9 wt % versus 23.4 wt % for the original MOF due to the extra binding sites provided by the multiunit amines. The degree of functionalization with the amines was found to be important in enhancing CO2 adsorption, as the optimal surface coverage improved performance and stability under both pure CO2 and CO2/H2O coadsorption, and with partially saturated surface coverage, optimal CO2 capacity could be achieved under both wet and dry conditions by a synergistic binding of CO2 to the amines as well as metal centers.
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