Quantifying diffusion of organic liquids in a MOF component of MOF/Polymer mixed-matrix membranes by high field NMR

被引:8
作者
Baniani, Amineh [1 ]
Rivera, Matthew P. [2 ]
Lively, Ryan P. [2 ]
Vasenkov, Sergey [1 ]
机构
[1] Univ Florida, Dept Chem Engn, Gainesville, FL 32611 USA
[2] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
基金
美国国家科学基金会;
关键词
Diffusion; PFG NMR; Liquid separations; Mixed-matrix membranes; ZIF-71; ZEOLITIC IMIDAZOLATE FRAMEWORKS; CARBON-DIOXIDE; HIGH-PERFORMANCE; GAS-SEPARATION; NANOCOMPOSITE MEMBRANES; SELF-DIFFUSION; FLEXIBILITY; ZIF-8; WATER; CO2;
D O I
10.1016/j.memsci.2021.119786
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Confinement of crystals of metal-organic frameworks (MOFs) in polymers to form MOF/polymer mixed-matrix membranes (MMMs) can lead to changes in intra-MOF diffusion. Such changes in intra-MOF diffusion were previously demonstrated for light gases, and attributed to a reduction in MOF framework flexibility. However, to our knowledge, no direct measurements of intra-MOF diffusion in MMMs and of the related MOF confinement effect on diffusion have been reported for organic liquids. In this work, C-13 pulsed field gradient (PFG) NMR was used to quantify self-diffusion of methanol, ethanol, p-xylene, and o-xylene inside MOF crystals of the type ZIF71, which were dispersed in a Torlon polymer to form MMMs. The intra-ZIF self-diffusivities in the MMMs were compared with the corresponding self-diffusivities measured in beds of ZIF-71 crystals. The observed selfdiffusivity dependencies on diffusion time were explained by crystal boundary effects. The corresponding values of intra-ZIF self-diffusivities not perturbed by such effects were found to be the same, within uncertainty, in the MMMs and ZIF-71 beds. The observed lack of an influence of the ZIF-71 confinement in Torlon on diffusion is explained, and an option to increase diffusion selectivity is discussed.
引用
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页数:10
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