Nylon-MOF Composites through Postsynthetic Polymerization

被引:171
作者
Kalaj, Mark [1 ]
Denny, Michael S. [1 ]
Bentz, Kyle C. [1 ]
Palomba, Joseph M. [1 ]
Cohen, Seth M. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
关键词
chemical warfare agents; hybrid materials; metal-organic frameworks; polymers; METAL-ORGANIC FRAMEWORKS; MIXED-MATRIX MEMBRANES; POLYMOFS; NANOCOMPOSITES; HYDROLYSIS; REMOVAL; SURFACE;
D O I
10.1002/anie.201812655
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hybridization of metal-organic frameworks (MOFs) and polymers into composites yields materials that display the exceptional properties of MOFs with the robustness of polymers. However, the realization of MOF-polymer composites requires efficient dispersion and interactions of MOF particles with polymer matrices, which remains a significant challenge. Herein, we report a simple, scalable, bench-top approach to covalently tethered nylon-MOF polymer composite materials through an interfacial polymerization technique. The copolymerization of a modified UiO-66-NH2 MOF with a growing polyamide fiber (PA-66) during an interfacial polymerization gave hybrid materials with up to around 29 weight percent MOF. The covalent hybrid material demonstrated nearly an order of magnitude higher catalytic activity for the breakdown of a chemical warfare simulant (dimethyl-4-nitrophenyl phosphate, DMNP) compared to MOFs that are non-covalently, physically entrapped in nylon, thus highlighting the importance of MOF-polymer hybridization.
引用
收藏
页码:2336 / 2340
页数:5
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