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
硼
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
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI