改性NiCo2O4活化过氧单硫酸酯及其在双氯芬酸降解中的应用

Kanon Sampe , Hideyuki Katsumata , Ikki Tateishi , Mai Furukawa , Satoshi Kaneco
{"title":"改性NiCo2O4活化过氧单硫酸酯及其在双氯芬酸降解中的应用","authors":"Kanon Sampe ,&nbsp;Hideyuki Katsumata ,&nbsp;Ikki Tateishi ,&nbsp;Mai Furukawa ,&nbsp;Satoshi Kaneco","doi":"10.1016/j.nxmate.2025.100597","DOIUrl":null,"url":null,"abstract":"<div><div>Water pollution caused by pharmaceutical wastewater is becoming increasingly serious. Diclofenac (DCF), a pharmaceutical compound widely used in many medicines, is an organic pollutant that poses potential risks to ecosystems and human health. In this study, a morphologically modified NiCo<sub>2</sub>O<sub>4</sub> (NCO) catalyst was synthesized via a hydrothermal method and employed to activate peroxymonosulfate (PMS) for DCF degradation. As a result, 99.9 % of the DCF was successfully degraded within 10 min. It also succeeded in mineralizing 97.2 % of DCF after 10 min. Moreover, the NCO/PMS system was effective over a wide pH range. The degradation pathways involved both radical and non-radical mechanisms, with <sup>1</sup>O<sub>2</sub>, SO<sub>4</sub><sup>•–</sup>, and <sup>•</sup>OH identified as the primary active species. In addition, the surface hydroxyl groups on the NCO are likely to play a significant role in the degradation process. This paper presents the development of a highly efficient catalyst for the degradation of organic pollutants using PMS.</div></div>","PeriodicalId":100958,"journal":{"name":"Next Materials","volume":"8 ","pages":"Article 100597"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Activation of peroxymonosulfate by morphologically modified NiCo2O4 and application to diclofenac degradation\",\"authors\":\"Kanon Sampe ,&nbsp;Hideyuki Katsumata ,&nbsp;Ikki Tateishi ,&nbsp;Mai Furukawa ,&nbsp;Satoshi Kaneco\",\"doi\":\"10.1016/j.nxmate.2025.100597\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Water pollution caused by pharmaceutical wastewater is becoming increasingly serious. Diclofenac (DCF), a pharmaceutical compound widely used in many medicines, is an organic pollutant that poses potential risks to ecosystems and human health. In this study, a morphologically modified NiCo<sub>2</sub>O<sub>4</sub> (NCO) catalyst was synthesized via a hydrothermal method and employed to activate peroxymonosulfate (PMS) for DCF degradation. As a result, 99.9 % of the DCF was successfully degraded within 10 min. It also succeeded in mineralizing 97.2 % of DCF after 10 min. Moreover, the NCO/PMS system was effective over a wide pH range. The degradation pathways involved both radical and non-radical mechanisms, with <sup>1</sup>O<sub>2</sub>, SO<sub>4</sub><sup>•–</sup>, and <sup>•</sup>OH identified as the primary active species. In addition, the surface hydroxyl groups on the NCO are likely to play a significant role in the degradation process. This paper presents the development of a highly efficient catalyst for the degradation of organic pollutants using PMS.</div></div>\",\"PeriodicalId\":100958,\"journal\":{\"name\":\"Next Materials\",\"volume\":\"8 \",\"pages\":\"Article 100597\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-03-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Next Materials\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949822825001157\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Next Materials","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949822825001157","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

制药废水对水体的污染日益严重。双氯芬酸(DCF)是一种有机污染物,对生态系统和人类健康构成潜在风险,是一种广泛应用于多种药物的药物化合物。本研究通过水热法合成了一种形态修饰的NiCo2O4 (NCO)催化剂,并利用该催化剂激活过氧单硫酸根(PMS)降解DCF。结果,99.9 %的DCF在10 min内被成功降解。在10 min后,DCF的矿化率为97.2% %。此外,NCO/PMS体系在较宽的pH范围内有效。降解途径包括自由基和非自由基两种机制,其中1O2、SO4•-和•OH是主要活性物质。此外,NCO表面的羟基可能在降解过程中发挥重要作用。本文介绍了PMS降解有机污染物的高效催化剂的研究进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activation of peroxymonosulfate by morphologically modified NiCo2O4 and application to diclofenac degradation
Water pollution caused by pharmaceutical wastewater is becoming increasingly serious. Diclofenac (DCF), a pharmaceutical compound widely used in many medicines, is an organic pollutant that poses potential risks to ecosystems and human health. In this study, a morphologically modified NiCo2O4 (NCO) catalyst was synthesized via a hydrothermal method and employed to activate peroxymonosulfate (PMS) for DCF degradation. As a result, 99.9 % of the DCF was successfully degraded within 10 min. It also succeeded in mineralizing 97.2 % of DCF after 10 min. Moreover, the NCO/PMS system was effective over a wide pH range. The degradation pathways involved both radical and non-radical mechanisms, with 1O2, SO4•–, and OH identified as the primary active species. In addition, the surface hydroxyl groups on the NCO are likely to play a significant role in the degradation process. This paper presents the development of a highly efficient catalyst for the degradation of organic pollutants using PMS.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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