Porous boron nitride micro-nanotubes efficiently anchor CoFe2O4 as a magnetic recyclable catalyst for peroxymonosulfate activation and oxytetracycline rapid degradation

单线态氧 羟基自由基 催化作用 氮化硼 降级(电信) 化学 化学工程 热液循环 材料科学 氧气 激进的 有机化学 电信 计算机科学 工程类
作者
Lingyun Jing,Wenhan Yang,Tong Wang,Jingquan Wang,Xiuqin Kong,Suyun Lv,Xinyong Li,Rui Quan,Hao Zhu
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:290: 120925-120925 被引量:33
标识
DOI:10.1016/j.seppur.2022.120925
摘要

In order to further enhance the activation performance of peroxymonosulfate (PMS), an efficient and recyclable ferromagnetic catalyst was successfully fabricated by co-precipitation and hydrothermal methods. We designed commercial hexagonal sheet boron nitride (C-BN) and boron nitrogen micro-nanotubes (BNMTs) to anchor CoFe2O4 nanoparticles ([email protected]2O4/[email protected]2O4). Compared with smooth hexagonal C-BN, BNMTs were rich in pores and oxygen-containing groups. This could effectively immobilize CoFe2O4 to a certain extent, increase the loading of CoFe2O4 and enrich the active sites. Under optimal conditions, [email protected]2O4/PMS system could rapidly and efficiently degrade 92.7% of oxytetracycline (OTC) within 5 min. In addition, the strong binding force between BNMTs and CoFe2O4 enabled favorable regeneration efficiency after 5 cycles (87.6%). [email protected]2O4 activated PMS to generate hydroxyl radical (·OH), sulfate radical (SO4•-), superoxide radical (·O2–) and singlet oxygen (1O2) to further attack OTC, SO4•- and 1O2 were the main activities species. Meanwhile, there was also a non-radical mechanism for the activation of PMS by [email protected]2O4, and OTC achieved a rapid and efficient degradation process through electron transfer. Our survey results were expected to provide new insights for the rational design and application of boron nitride-based materials and transition metal/PMS systems for environmental remediation.
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