Suppr超能文献

构建核壳结构 FeO@GO-CoPc 光-Fenton 催化剂以实现四环素的高效去除:GO 在促进 HO 向 •OH 转化中的作用。

Construction of core-shell FeO@GO-CoPc photo-Fenton catalyst for superior removal of tetracycline: The role of GO in promotion of HO to •OH conversion.

机构信息

Department of Environmental Science and Engineering, College of Environment and Resources, Xiangtan University, Xiangtan, 411105, China.

Hunan Non-ferrous Metals Holding Group Co., Ltd, Changsha, 410000, China.

出版信息

J Environ Manage. 2022 Apr 15;308:114613. doi: 10.1016/j.jenvman.2022.114613. Epub 2022 Feb 3.

Abstract

A novel core-shell structured FeO@GO-CoPc magnetic catalyst, which is with magnetite (FeO) as the core, graphene oxide (GO) as the interlayer and cobalt-phthalocyanine (CoPc) as the shell, was successfully prepared and used as a heterogeneous photo-Fenton catalyst for tetracycline (TC) degradation in this work. The core-shell structure of the catalyst was confirmed by XRD, FTIR, SEM and TEM. BET and magnetic hysteresis loops measurements indicated that FeO@GO-CoPc catalyst owned large specific surface area and could be easily recovered under an external magnetic field. Meanwhile, the experimental results of TC degradation demonstrated that the photo-Fenton efficiency of FeO@GO-CoPc was excellent. When the reaction time was 120 min, TC could be degraded almost completely in the photo-Fenton system with FeO@GO-CoPc. The high photo-Fenton catalytic activity of FeO@GO-CoPc could be resulted from the effective transfer of photo-generated electrons between CoPc and FeO by GO. Moreover, the main reaction species, •OH, O•-, O and h, were verified by the analysis of active species in this system. Finally, the mechanism analyses and quantitative analysis results of active species indicated that the introduction of GO accelerated the cycle between Fe(II) and Fe(III) as well as improved the effective utilization of HO (the efficiency of conversion of HO to •OH).

摘要

一种新型核壳结构的 FeO@GO-CoPc 磁性催化剂,以磁铁矿 (FeO) 为核,氧化石墨烯 (GO) 为夹层,钴酞菁 (CoPc) 为壳,成功制备并用作非均相光芬顿催化剂,用于降解四环素 (TC)。催化剂的核壳结构通过 XRD、FTIR、SEM 和 TEM 得到证实。BET 和磁滞回线测量表明,FeO@GO-CoPc 催化剂具有较大的比表面积,并可在外磁场下轻易回收。同时,TC 降解实验结果表明,FeO@GO-CoPc 的光芬顿效率非常优异。当反应时间为 120 min 时,在 FeO@GO-CoPc 的光芬顿体系中,TC 几乎可完全降解。GO 有效促进了 CoPc 和 FeO 之间光生电子的转移,从而使 FeO@GO-CoPc 具有较高的光芬顿催化活性。此外,通过分析该体系中的活性物质,验证了 •OH、O•-、O 和 h 等主要反应物质。最后,通过对活性物质的机制分析和定量分析结果表明,GO 的引入加速了 Fe(II)和 Fe(III)之间的循环,提高了 HO 的有效利用效率 (HO 转化为 •OH 的效率)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验