Applied Catalysis B: Environment and Energy ( IF 20.2 ) Pub Date : 2020-09-28 , DOI: 10.1016/j.apcatb.2020.119585 Meimei Wang , Yunke Cui , Hongyang Cao , Ping Wei , Chen Chen , Xiuyan Li , Juan Xu , Guoping Sheng
In this study, zeolitic imidazolate framework-67 (ZIF-67) derived Co3O4/NiCo2O4 double-shelled nanocages (DSNCs) were fabricated and utilized as catalysts to activate peroxydisulfate (PDS) for bisphenol A (BPA) degradation. The results showed that Co3O4/NiCo2O4 DSNCs exhibited superior BPA degradation performance over Co3O4 NCs and NiCo2O4 NCs. PDS combined with the interfaces of both the Co3O4 inner shell and NiCo2O4 outer shell to form complex, inducing the nonradical oxidation of BPA by electron abstraction. The double-shelled hollow structure helped to increase the instantaneous concentration of reactants in the void space of Co3O4/NiCo2O4 DSNCs, thus promoting the decomposition of BPA. The Co3O4/NiCo2O4 DSNCs had high selectivity for BPA degradation and were resistant to halogens and background organic matter in wastewater. Our work indicated that metal-organic framework (MOF)-derived nanomaterials with a hollow structure have a promising application prospect for persulfate-based advanced oxidation technology.
中文翻译:
用Co 3 O 4 / NiCo 2 O 4双壳纳米笼活化过氧二硫酸盐以选择性降解双酚A –非自由基氧化过程
在这项研究中,制备了由沸石咪唑盐构架67(ZIF-67)衍生的Co 3 O 4 / NiCo 2 O 4双壳纳米笼(DSNC),并用作催化剂来活化过氧化二硫酸盐(PDS)以降解双酚A(BPA) 。结果表明,Co 3 O 4 / NiCo 2 O 4 DSNCs表现出比Co 3 O 4 NCs和NiCo 2 O 4 NCs更好的BPA降解性能。PDS结合了Co 3 O 4内壳和NiCo 2 O 4的界面外壳形成络合物,通过电子提取诱导BPA的非自由基氧化。双壳中空结构有助于增加Co 3 O 4 / NiCo 2 O 4 DSNCs空隙空间中反应物的瞬时浓度,从而促进了BPA的分解。Co 3 O 4 / NiCo 2 O 4 DSNC对BPA的降解具有很高的选择性,并且对废水中的卤素和背景有机物具有抵抗力。我们的工作表明,具有空心结构的金属-有机骨架(MOF)衍生的纳米材料在基于过硫酸盐的高级氧化技术方面具有广阔的应用前景。