膜
渗透
制作
纳米材料
化学
背景(考古学)
纳米技术
化学工程
金属有机骨架
材料科学
选择性
有机化学
催化作用
工程类
病理
吸附
古生物学
生物
医学
替代医学
生物化学
作者
Tingting Xu,Muhammad A. Shehzad,Xin Wang,Bin Wu,Liang Ge,Tongwen Xu
标识
DOI:10.1007/s40820-020-0386-6
摘要
Abstract Metal–organic frameworks (MOFs) with angstrom-sized pores are promising functional nanomaterials for the fabrication of cation permselective membranes (MOF-CPMs). However, only a few research reports show successful preparation of the MOF-CPMs with good cation separation performance due to several inherent problems in MOFs, such as arduous self-assembly, poor water resistance, and tedious fabrication strategies. Besides, low cation permeation flux due to the absence of the cation permeation assisting functionalities in MOFs is another big issue, which limits their widespread use in membrane technology. Therefore, it is necessary to fabricate functional MOF-CPMs using simplistic strategies to improve cation permeation. In this context, we report a facile in situ smart growth strategy to successfully produce ultrathin (< 600 nm) and leaf-like UiO-66-SO 3 H membranes at the surface of anodic alumina oxide. The physicochemical characterizations confirm that sulfonated angstrom-sized ion transport channels exist in the as-prepared UiO-66-SO 3 H membranes, which accelerate the cation permeation (~ 3× faster than non-functionalized UiO-66 membrane) and achieve a high ion selectivity (Na + /Mg 2+ > 140). The outstanding cation separation performance validates the importance of introducing sulfonic acid groups in MOF-CPMs.
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