过氧化氢驱动的NH2和石墨- n掺杂稻渣碳对e- /h+介导的对乙酰氨基酚和双氯芬酸的降解

IF 8.1 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Larissa Crestani , Camila Abreu Teles , Gabriela Carvalho Collazzo , Guilherme Luiz Dotto , Yasmin Vieira
{"title":"过氧化氢驱动的NH2和石墨- n掺杂稻渣碳对e- /h+介导的对乙酰氨基酚和双氯芬酸的降解","authors":"Larissa Crestani ,&nbsp;Camila Abreu Teles ,&nbsp;Gabriela Carvalho Collazzo ,&nbsp;Guilherme Luiz Dotto ,&nbsp;Yasmin Vieira","doi":"10.1016/j.chemosphere.2025.144641","DOIUrl":null,"url":null,"abstract":"<div><div>This study presents a novel, sustainable, and metal-free photocatalyst based on nitrogen-doped carbon derived from pre-carbonized rice residue (CRHN) for the visible-light degradation of acetaminophen (ACT) and diclofenac (DC). Synthesized via urea-assisted pyrolysis, the material incorporated NH<sub>2</sub> and graphitic-N groups, enhancing surface basicity and reduced the band gap from 2.5 to 2.16 eV. Under optimal conditions (85 W, 0.1 g L<sup>−1</sup>, pH 7), CRHN achieved mineralization efficiencies of 97% for DC and 70% for ACT within 30 min, outperforming the undoped material. Kinetic modeling followed a pseudo-second-order model, with rate constants of 0.022 and 0.002 L mg<sup>−1</sup> min<sup>−1</sup> for DC and ACT, respectively. Scavenger experiments confirmed the dominant role of <span><math><mrow><msup><mi>e</mi><mo>−</mo></msup><mo>/</mo><mi>h</mi><mmultiscripts><mo>+</mo></mmultiscripts></mrow></math></span> pairs, supported by •OH radicals in a peroxide-driven mechanism. Moreover, adsorption was negligible due to the low dosage of CRHN needed in the experiments. These findings highlight CRHN as a high-performance and eco-friendly photocatalyst for pharmaceutical degradation, promoting sustainable water treatment and agro-industrial waste valorization.</div></div>","PeriodicalId":276,"journal":{"name":"Chemosphere","volume":"386 ","pages":"Article 144641"},"PeriodicalIF":8.1000,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Peroxide-driven activation on NH2 and graphitic-N doped rice-residue carbon for e−/h+ mediated degradation of acetaminophen and diclofenac\",\"authors\":\"Larissa Crestani ,&nbsp;Camila Abreu Teles ,&nbsp;Gabriela Carvalho Collazzo ,&nbsp;Guilherme Luiz Dotto ,&nbsp;Yasmin Vieira\",\"doi\":\"10.1016/j.chemosphere.2025.144641\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study presents a novel, sustainable, and metal-free photocatalyst based on nitrogen-doped carbon derived from pre-carbonized rice residue (CRHN) for the visible-light degradation of acetaminophen (ACT) and diclofenac (DC). Synthesized via urea-assisted pyrolysis, the material incorporated NH<sub>2</sub> and graphitic-N groups, enhancing surface basicity and reduced the band gap from 2.5 to 2.16 eV. Under optimal conditions (85 W, 0.1 g L<sup>−1</sup>, pH 7), CRHN achieved mineralization efficiencies of 97% for DC and 70% for ACT within 30 min, outperforming the undoped material. Kinetic modeling followed a pseudo-second-order model, with rate constants of 0.022 and 0.002 L mg<sup>−1</sup> min<sup>−1</sup> for DC and ACT, respectively. Scavenger experiments confirmed the dominant role of <span><math><mrow><msup><mi>e</mi><mo>−</mo></msup><mo>/</mo><mi>h</mi><mmultiscripts><mo>+</mo></mmultiscripts></mrow></math></span> pairs, supported by •OH radicals in a peroxide-driven mechanism. Moreover, adsorption was negligible due to the low dosage of CRHN needed in the experiments. These findings highlight CRHN as a high-performance and eco-friendly photocatalyst for pharmaceutical degradation, promoting sustainable water treatment and agro-industrial waste valorization.</div></div>\",\"PeriodicalId\":276,\"journal\":{\"name\":\"Chemosphere\",\"volume\":\"386 \",\"pages\":\"Article 144641\"},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2025-08-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemosphere\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0045653525005880\",\"RegionNum\":2,\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemosphere","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0045653525005880","RegionNum":2,"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

摘要

本研究提出了一种新型的、可持续的、无金属的光催化剂,该催化剂基于来自预碳化稻渣(CRHN)的氮掺杂碳,用于可见光降解对乙酰氨基酚(ACT)和双氯芬酸(DC)。通过尿素辅助热解合成,该材料加入了NH2和石墨- n基团,提高了表面碱性,并将带隙从2.5 eV减小到2.16 eV。在最佳条件下(85 W, 0.1 g L−1,pH 7), CRHN在30分钟内实现了97%的DC矿化效率和70%的ACT矿化效率,优于未掺杂材料。动力学建模遵循伪二阶模型,DC和ACT的速率常数分别为0.022和0.002 L mg−1 min−1。清道夫实验证实了在过氧化物驱动机制中由•OH自由基支持的e−/h+对的主导作用。此外,由于实验中所需的CRHN用量较低,吸附作用可以忽略不计。这些发现强调了CRHN作为一种高性能和环保的光催化剂,可用于药物降解,促进可持续水处理和农业工业废物的增值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Peroxide-driven activation on NH2 and graphitic-N doped rice-residue carbon for e−/h+ mediated degradation of acetaminophen and diclofenac

Peroxide-driven activation on NH2 and graphitic-N doped rice-residue carbon for e−/h+ mediated degradation of acetaminophen and diclofenac
This study presents a novel, sustainable, and metal-free photocatalyst based on nitrogen-doped carbon derived from pre-carbonized rice residue (CRHN) for the visible-light degradation of acetaminophen (ACT) and diclofenac (DC). Synthesized via urea-assisted pyrolysis, the material incorporated NH2 and graphitic-N groups, enhancing surface basicity and reduced the band gap from 2.5 to 2.16 eV. Under optimal conditions (85 W, 0.1 g L−1, pH 7), CRHN achieved mineralization efficiencies of 97% for DC and 70% for ACT within 30 min, outperforming the undoped material. Kinetic modeling followed a pseudo-second-order model, with rate constants of 0.022 and 0.002 L mg−1 min−1 for DC and ACT, respectively. Scavenger experiments confirmed the dominant role of e/h+ pairs, supported by •OH radicals in a peroxide-driven mechanism. Moreover, adsorption was negligible due to the low dosage of CRHN needed in the experiments. These findings highlight CRHN as a high-performance and eco-friendly photocatalyst for pharmaceutical degradation, promoting sustainable water treatment and agro-industrial waste valorization.
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
Chemosphere
Chemosphere 环境科学-环境科学
CiteScore
15.80
自引率
8.00%
发文量
4975
审稿时长
3.4 months
期刊介绍: Chemosphere, being an international multidisciplinary journal, is dedicated to publishing original communications and review articles on chemicals in the environment. The scope covers a wide range of topics, including the identification, quantification, behavior, fate, toxicology, treatment, and remediation of chemicals in the bio-, hydro-, litho-, and atmosphere, ensuring the broad dissemination of research in this field.
×
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:604180095
Book学术官方微信