化学
氢
吸附
变压吸附
同位素分离
同位素
动力学同位素效应
量子化学
氢同位素
化学物理
量子
选择性
纳米技术
化学工程
物理化学
催化作用
分子
氘
原子物理学
有机化学
核物理学
工程类
物理
材料科学
量子力学
作者
Hyunchul Oh,Michael Hirscher
标识
DOI:10.1002/ejic.201600253
摘要
Hydrogen isotope mixtures can be separated either by confinement in small pores [i.e., “kinetic quantum sieving” (KQS)] or by strong adsorption sites [i.e., “chemical affinity quantum sieving” (CAQS)]. MOFs are excellent candidates for study of these quantum effects, due to their well‐defined, tunable pore structures and the potential to introduce strong adsorption sites directly into the framework structure. In this microreview we summarize the recent status of hydrogen isotope separation using MOFs and future strategies relating to it. Furthermore, a state‐of‐the‐art technique for the direct measurement of selectivity with regard to isotope mixtures is introduced. Experimental results relating to separation factors with different pore apertures in the case of KQS and the role of open metal sites in that of CAQS as a function of temperature and gas pressure are given. Furthermore, technologically relevant parameters such as feasible operating pressure and temperature are discussed with respect to possible applications in a temperature swing process.
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