甲基膦酸二甲酯
化学
金属有机骨架
分解
吸附
红外光谱学
人体净化
粉末衍射
吸收(声学)
同步加速器
化学工程
化学战剂
无机化学
神经毒剂
物理化学
有机化学
结晶学
材料科学
复合材料
酶
生化工程
核物理学
工程类
物理
乙酰胆碱酯酶
作者
Anna M. Płonka,Qi Wang,Wesley O. Gordon,Alex Balboa,Diego Troya,Weiwei Guo,Conor H. Sharp,Sanjaya D. Senanayake,John R. Morris,Craig L. Hill,Anatoly I. Frenkel
摘要
Zr-based metal organic frameworks (MOFs) have been recently shown to be among the fastest catalysts of nerve-agent hydrolysis in solution. We report a detailed study of the adsorption and decomposition of a nerve-agent simulant, dimethyl methylphosphonate (DMMP), on UiO-66, UiO-67, MOF-808, and NU-1000 using synchrotron-based X-ray powder diffraction, X-ray absorption, and infrared spectroscopy, which reveals key aspects of the reaction mechanism. The diffraction measurements indicate that all four MOFs adsorb DMMP (introduced at atmospheric pressures through a flow of helium or air) within the pore space. In addition, the combination of X-ray absorption and infrared spectra suggests direct coordination of DMMP to the Zr6 cores of all MOFs, which ultimately leads to decomposition to phosphonate products. These experimental probes into the mechanism of adsorption and decomposition of chemical warfare agent simulants on Zr-based MOFs open new opportunities in rational design of new and superior decontamination materials.
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