化学
铈
催化作用
锆
金属有机骨架
水溶液
介孔材料
水解
降级(电信)
无机化学
核化学
金属
立体化学
有机化学
吸附
电信
计算机科学
作者
Elham Geravand,Faezeh Farzaneh,Rodrigo Gil-San-Millán,Francisco J. Carmona,Jorge A. R. Navarro
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2020-11-05
卷期号:59 (22): 16160-16167
被引量:48
标识
DOI:10.1021/acs.inorgchem.0c01434
摘要
A series of Ce/Zr mixed-metal–organic frameworks with different topology/connectivity, namely, Ce/Zr-UiO-66 (U01, U02, and U03) (fcu (12-c)), Ce/Zr-DUT-67-PZDC (D01 and D02) (reo (8-c)), and Ce/Zr-MOF-808 (M01, M02, and M03) (spn (6-c)) were evaluated toward the detoxification of toxic nerve agent model diisopropylfluorophosphate (DIFP) at room temperature in unbuffered aqueous solution. Noteworthily, the catalytic rate for P–F bond cleavage increased with increasing Ce/Zr molar ratio. A further increase in catalytic activity can be achieved by Mg(OMe) 2 doping of the mixed-metal MOFs as exemplified with M01@Mg(OMe) 2 and M02@Mg(OMe) 2 systems. The results show that Mg(OMe) 2 incorporation into the mesoporous cavities of M01 and M02 give rise to P–F hydrolytic degradation half-lives of nearly 5 and 2 min with 100% degradation of DIFP after 55 and 65 min for M01@Mg(OMe) 2 1:2 and M02@Mg(OMe) 2 1:4, respectively.
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