Overlooked interaction between redox-mediator and bisphenol-A in permanganate oxidation

IF 14 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Honglong Zhang , Qiaoqiao Zhao , Kangbao Zhong , Ruopeng Bai , Jiaojiao Dong , Jun Ma , Jing Zhang , Timothy J. Strathmann
{"title":"Overlooked interaction between redox-mediator and bisphenol-A in permanganate oxidation","authors":"Honglong Zhang ,&nbsp;Qiaoqiao Zhao ,&nbsp;Kangbao Zhong ,&nbsp;Ruopeng Bai ,&nbsp;Jiaojiao Dong ,&nbsp;Jun Ma ,&nbsp;Jing Zhang ,&nbsp;Timothy J. Strathmann","doi":"10.1016/j.ese.2024.100421","DOIUrl":null,"url":null,"abstract":"<div><p>Research efforts on permanganate (Mn(VII)) combined with redox-mediator (RM), have received increasing attention due to their significant performance for bisphenol-A (BPA) removal. However, the mechanisms underpinning BPA degradation remain underexplored. Here we show the overlooked interactions between RM and BPA during permanganate oxidation by introducing an RM—N-hydroxyphthalimide (NHPI). We discovered that the concurrent generation of MnO<sub>2</sub> and phthalimide-<em>N</em>-oxyl (PINO) radical significantly enhances BPA oxidation within the pH range of 5.0–6.0. The detection of radical cross-coupling products between PINO radicals and BPA or its derivatives corroborates the pivotal role of radical cross-coupling in BPA oxidation. Intriguingly, we observed the formation of an NHPI-BPA complex, which undergoes preferential oxidation by Mn(VII), marked by the emergence of an electron-rich domain in NHPI. These findings unveil the underlying mechanisms in the Mn(VII)/RM system and bridge the knowledge gap concerning BPA transformation via complexation. This research paves the way for further exploration into optimizing complexation sites and RM dosage, significantly enhancing the system's efficiency in water treatment applications.</p></div>","PeriodicalId":34434,"journal":{"name":"Environmental Science and Ecotechnology","volume":null,"pages":null},"PeriodicalIF":14.0000,"publicationDate":"2024-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666498424000358/pdfft?md5=94f0e165188da85406483c76afe9cbdc&pid=1-s2.0-S2666498424000358-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Science and Ecotechnology","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666498424000358","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Research efforts on permanganate (Mn(VII)) combined with redox-mediator (RM), have received increasing attention due to their significant performance for bisphenol-A (BPA) removal. However, the mechanisms underpinning BPA degradation remain underexplored. Here we show the overlooked interactions between RM and BPA during permanganate oxidation by introducing an RM—N-hydroxyphthalimide (NHPI). We discovered that the concurrent generation of MnO2 and phthalimide-N-oxyl (PINO) radical significantly enhances BPA oxidation within the pH range of 5.0–6.0. The detection of radical cross-coupling products between PINO radicals and BPA or its derivatives corroborates the pivotal role of radical cross-coupling in BPA oxidation. Intriguingly, we observed the formation of an NHPI-BPA complex, which undergoes preferential oxidation by Mn(VII), marked by the emergence of an electron-rich domain in NHPI. These findings unveil the underlying mechanisms in the Mn(VII)/RM system and bridge the knowledge gap concerning BPA transformation via complexation. This research paves the way for further exploration into optimizing complexation sites and RM dosage, significantly enhancing the system's efficiency in water treatment applications.

Abstract Image

高锰酸盐氧化过程中被忽视的氧化还原介质与双酚 A 之间的相互作用
高锰酸盐(Mn(VII))与氧化还原介质(RM)的研究工作因其在去除双酚-A(BPA)方面的显著效果而受到越来越多的关注。然而,人们对双酚 A 降解的机理仍未充分探究。在这里,我们通过引入 RM-N-hydroxyphthalimide (NHPI),展示了在高锰酸盐氧化过程中 RM 与双酚 A 之间被忽视的相互作用。我们发现,在 pH 值为 5.0-6.0 的范围内,同时生成 MnO2 和邻苯二甲酰亚胺-N-氧自由基(PINO)可显著增强双酚 A 的氧化作用。PINO 自由基与双酚 A 或其衍生物之间的自由基交叉偶联产物的检测证实了自由基交叉偶联在双酚 A 氧化过程中的关键作用。耐人寻味的是,我们观察到 NHPI-BPA 复合物的形成,该复合物会优先被 Mn(VII)氧化,其标志是 NHPI 中出现了一个富电子域。这些发现揭示了 Mn(VII)/RM 系统的基本机制,弥补了有关双酚 A 通过络合转化的知识空白。这项研究为进一步探索优化络合位点和 RM 用量铺平了道路,从而大大提高了该系统在水处理应用中的效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
20.40
自引率
6.30%
发文量
11
审稿时长
18 days
期刊介绍: Environmental Science & Ecotechnology (ESE) is an international, open-access journal publishing original research in environmental science, engineering, ecotechnology, and related fields. Authors publishing in ESE can immediately, permanently, and freely share their work. They have license options and retain copyright. Published by Elsevier, ESE is co-organized by the Chinese Society for Environmental Sciences, Harbin Institute of Technology, and the Chinese Research Academy of Environmental Sciences, under the supervision of the China Association for Science and Technology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信