由石墨氮化碳转化成N、O双掺杂多孔碳作为过氧单硫酸盐活化剂降解盐酸四环素

IF 2.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY New Journal of Chemistry Pub Date : 2024-12-09 DOI:10.1039/D4NJ04367G
Kang Xiong, Zhoutong Liu, Lihan Ren, De Li, Kangning Dong, Letian Yang and Xiuxia Zhang
{"title":"由石墨氮化碳转化成N、O双掺杂多孔碳作为过氧单硫酸盐活化剂降解盐酸四环素","authors":"Kang Xiong, Zhoutong Liu, Lihan Ren, De Li, Kangning Dong, Letian Yang and Xiuxia Zhang","doi":"10.1039/D4NJ04367G","DOIUrl":null,"url":null,"abstract":"<p >Graphitic carbon nitride (g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>) is a promising non-metallic material. However, its low specific surface area and chemical inertness lead to low catalytic efficiency, even in the case of non-metallic heteroatom doping. Herein, we develop a simple strategy using citric acid to convert g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> into a N and O dual-doped porous carbon material (ONPC). Compared with pristine g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>, ONPC exhibited significantly enhanced catalytic activity in peroxymonosulfate (PMS) for tetracycline hydrochloride (TC) degradation without light irradiation. In the presence of 0.3 g L<small><sup>−1</sup></small> ONPC and 2.4 mM PMS at pH 5.7, 90.75% of TC could be removed within 60 min. Singlet oxygen (<small><sup>1</sup></small>O<small><sub>2</sub></small>) and superoxide radicals (O<small><sub>2</sub></small>˙<small><sup>−</sup></small>) are the main active species, as verified by quenching experiments and electron paramagnetic resonance (EPR) analysis. Characterization results and DFT calculations confirmed the outstanding contribution of graphite N, pyridine N and carbonyl (C<img>O) to the catalytic performance of ONPC. Three possible pathways for TC degradation were proposed by high-resolution liquid chromatography–mass spectrometry (LC–MS) analysis, and the toxicity of most intermediates was lower than that of TC. Overall, this work will provide a simple approach to the design of efficient carbon catalysts with great potential in catalytic PMS for TC degradation.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 3","pages":" 855-864"},"PeriodicalIF":2.6000,"publicationDate":"2024-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"N and O dual-doped porous carbon transformed from graphitic carbon nitride as a peroxymonosulfate activator for tetracycline hydrochloride degradation†\",\"authors\":\"Kang Xiong, Zhoutong Liu, Lihan Ren, De Li, Kangning Dong, Letian Yang and Xiuxia Zhang\",\"doi\":\"10.1039/D4NJ04367G\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Graphitic carbon nitride (g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>) is a promising non-metallic material. However, its low specific surface area and chemical inertness lead to low catalytic efficiency, even in the case of non-metallic heteroatom doping. Herein, we develop a simple strategy using citric acid to convert g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> into a N and O dual-doped porous carbon material (ONPC). Compared with pristine g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>, ONPC exhibited significantly enhanced catalytic activity in peroxymonosulfate (PMS) for tetracycline hydrochloride (TC) degradation without light irradiation. In the presence of 0.3 g L<small><sup>−1</sup></small> ONPC and 2.4 mM PMS at pH 5.7, 90.75% of TC could be removed within 60 min. Singlet oxygen (<small><sup>1</sup></small>O<small><sub>2</sub></small>) and superoxide radicals (O<small><sub>2</sub></small>˙<small><sup>−</sup></small>) are the main active species, as verified by quenching experiments and electron paramagnetic resonance (EPR) analysis. Characterization results and DFT calculations confirmed the outstanding contribution of graphite N, pyridine N and carbonyl (C<img>O) to the catalytic performance of ONPC. Three possible pathways for TC degradation were proposed by high-resolution liquid chromatography–mass spectrometry (LC–MS) analysis, and the toxicity of most intermediates was lower than that of TC. Overall, this work will provide a simple approach to the design of efficient carbon catalysts with great potential in catalytic PMS for TC degradation.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":\" 3\",\"pages\":\" 855-864\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-12-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj04367g\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj04367g","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

石墨化氮化碳(g-C3N4)是一种很有前途的非金属材料。然而,其低比表面积和化学惰性导致其催化效率低,即使在非金属杂原子掺杂的情况下也是如此。在此,我们开发了一种简单的策略,使用柠檬酸将g-C3N4转化为氮氧双掺杂多孔碳材料(ONPC)。与原始g-C3N4相比,ONPC在无光照条件下对过氧单硫酸盐(PMS)降解盐酸四环素(TC)的催化活性显著增强。在0.3 g L−1 ONPC和2.4 mM PMS存在下,在pH 5.7条件下,60 min内可脱除90.75%的TC。淬灭实验和电子顺磁共振(EPR)分析证实,单线态氧(1O2)和超氧自由基(O2˙−)是主要的活性物质。表征结果和DFT计算证实了石墨N、吡啶N和羰基(CO)对ONPC催化性能的杰出贡献。通过高分辨率液相色谱-质谱(LC-MS)分析,提出了三种可能的TC降解途径,大多数中间体的毒性低于TC。总的来说,这项工作将为设计高效的碳催化剂提供一种简单的方法,在催化PMS降解TC方面具有很大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
N and O dual-doped porous carbon transformed from graphitic carbon nitride as a peroxymonosulfate activator for tetracycline hydrochloride degradation†

Graphitic carbon nitride (g-C3N4) is a promising non-metallic material. However, its low specific surface area and chemical inertness lead to low catalytic efficiency, even in the case of non-metallic heteroatom doping. Herein, we develop a simple strategy using citric acid to convert g-C3N4 into a N and O dual-doped porous carbon material (ONPC). Compared with pristine g-C3N4, ONPC exhibited significantly enhanced catalytic activity in peroxymonosulfate (PMS) for tetracycline hydrochloride (TC) degradation without light irradiation. In the presence of 0.3 g L−1 ONPC and 2.4 mM PMS at pH 5.7, 90.75% of TC could be removed within 60 min. Singlet oxygen (1O2) and superoxide radicals (O2˙) are the main active species, as verified by quenching experiments and electron paramagnetic resonance (EPR) analysis. Characterization results and DFT calculations confirmed the outstanding contribution of graphite N, pyridine N and carbonyl (CO) to the catalytic performance of ONPC. Three possible pathways for TC degradation were proposed by high-resolution liquid chromatography–mass spectrometry (LC–MS) analysis, and the toxicity of most intermediates was lower than that of TC. Overall, this work will provide a simple approach to the design of efficient carbon catalysts with great potential in catalytic PMS for TC degradation.

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
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
期刊最新文献
Back cover Crystalline coordination polymers of flavonoids with zinc: preparation, solid state structure, and functional properties Serum-stabilized Pickering emulsions as reproducible liquid SERS analyzer for direct metabolic fingerprinting A programmable multifunctional DNA hydrogel enabling integrated detection and inactivation of Staphylococcus aureus A smartphone-integrated colorimetric sensing platform for the detection of tannic acid in beverages using folic acid-functionalized copper nanoclusters nanozyme
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1