双金属片
化学
单线态氧
金属有机骨架
纳米片
激进的
电子顺磁共振
光化学
金属
催化作用
氧气
无机化学
有机化学
吸附
物理
核磁共振
作者
Qiao Wang,Jiahong Lu,Yan Jiang,Shurong Yang,Yang Yang,Wenjun Wang
标识
DOI:10.1016/j.cej.2022.136483
摘要
Singlet oxygen (1O2) and superoxide radicals (O2•–) are active species that can selectively oxidize organic pollutions. A two-dimensional FeCo-based bimetallic metal organic framework (MOF) nanosheet was rationally designed to activate peroxymonosulfate (PMS) for selective oxidation of organics in water. The FeCo MOF nanosheets (FeCo-BDC) achieved a 99.1% degradation efficiency of RhB in 5 min, showing a high kinetic constant of 0.884 min−1 that is 1.6 and 294.7 times higher than those of the monometallic MOFs, i.e., Co-BDC and Fe-BDC. Radical scavenging experiments and electron paramagnetic resonance measurements revealed that 1O2 and O2•– are predominant reactive oxygen species in the FeCo-BDC/PMS system. These nanosheets thus preferentially oxidize organics with electron donating groups (e.g., –NH2, –OH and -NR2), whereas having low reaction activities towards substances with electron withdrawing groups (e.g., –NO2). The oxidation process also proved to resist interference from co-existing dissolved species in water, such as Cl−, SO42- and humic acids.
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