掺杂氧化锰的赤泥催化剂激活过一硫酸盐过程高效降解间甲酚:性能和机理

IF 5.8 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Hongliang Chen , Qian Long , Jiancheng Shu , Fuhua Wei , Yutao Zhang
{"title":"掺杂氧化锰的赤泥催化剂激活过一硫酸盐过程高效降解间甲酚:性能和机理","authors":"Hongliang Chen ,&nbsp;Qian Long ,&nbsp;Jiancheng Shu ,&nbsp;Fuhua Wei ,&nbsp;Yutao Zhang","doi":"10.1016/j.jscs.2024.101857","DOIUrl":null,"url":null,"abstract":"<div><p>M-cresol, one of phenolics, is highly toxic, refractory, and threatens human health and ecological safety. The study on the efficient m-cresol degradation technologies is crucial and helpful to restrain its discharge into water body. A composite of MnO-doped red mud (RM) to activate peroxymonosulfate (PMS) for the m-cresol degradation was fabricated and employed, favorable to the recycling and utilization of RM. Considering the catalytic activity and cost, 0.1 M/RM@G exhibited an excellent degradation capacity attributing to strong Fe<sub>3</sub>O<sub>4</sub> and MnO synergy and was considered as the best catalyst among the investigative catalysts. 100 % of m-cresol and 71.4 % of COD could be degraded within 90 min under 2 g/L catalyst, 10 mM of PMS, 3-8 of initial pH and 50 mg/L m-cresol in the 0.1 M/RM@G/PMS system. The reaction rate constant (0.045 min<sup>−1</sup>) of 0.1 M/RM@G was much larger than RM@G (0.012 min<sup>−1</sup>), ARM (0.0048 min<sup>−1</sup>) and WRM (0.0028 min<sup>−1</sup>). Main Mn and Fe active components and abundant mesoporous structures on the catalyst surface could efficiently drove electron transfers, and further accelerated the redox cycles of Mn(III)<img>Mn(II) and Fe(III)<img>Fe(II) for activating PMS. <sup>1</sup>O<sub>2</sub> played a crucial role in degrading m-cresol. Based on the experiment data, the generation mechanism of radicals and the possible pathways of m-cresol degradation were proposed in the 0.1 M/RM@G/PMS system. This finding provides a new way for the synthesis of the efficient catalyst with RM and optimal operating strategies for the treatment of m-cresol wastewater.</p></div>","PeriodicalId":16974,"journal":{"name":"Journal of Saudi Chemical Society","volume":"28 3","pages":"Article 101857"},"PeriodicalIF":5.8000,"publicationDate":"2024-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1319610324000528/pdfft?md5=732800e5f8fd6ec5a1aa2e6640f579c0&pid=1-s2.0-S1319610324000528-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Efficient degradation of m-cresol by MnO-doped red mud catalyst activating peroxymonosulfate process: Performance and mechanism\",\"authors\":\"Hongliang Chen ,&nbsp;Qian Long ,&nbsp;Jiancheng Shu ,&nbsp;Fuhua Wei ,&nbsp;Yutao Zhang\",\"doi\":\"10.1016/j.jscs.2024.101857\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>M-cresol, one of phenolics, is highly toxic, refractory, and threatens human health and ecological safety. The study on the efficient m-cresol degradation technologies is crucial and helpful to restrain its discharge into water body. A composite of MnO-doped red mud (RM) to activate peroxymonosulfate (PMS) for the m-cresol degradation was fabricated and employed, favorable to the recycling and utilization of RM. Considering the catalytic activity and cost, 0.1 M/RM@G exhibited an excellent degradation capacity attributing to strong Fe<sub>3</sub>O<sub>4</sub> and MnO synergy and was considered as the best catalyst among the investigative catalysts. 100 % of m-cresol and 71.4 % of COD could be degraded within 90 min under 2 g/L catalyst, 10 mM of PMS, 3-8 of initial pH and 50 mg/L m-cresol in the 0.1 M/RM@G/PMS system. The reaction rate constant (0.045 min<sup>−1</sup>) of 0.1 M/RM@G was much larger than RM@G (0.012 min<sup>−1</sup>), ARM (0.0048 min<sup>−1</sup>) and WRM (0.0028 min<sup>−1</sup>). Main Mn and Fe active components and abundant mesoporous structures on the catalyst surface could efficiently drove electron transfers, and further accelerated the redox cycles of Mn(III)<img>Mn(II) and Fe(III)<img>Fe(II) for activating PMS. <sup>1</sup>O<sub>2</sub> played a crucial role in degrading m-cresol. Based on the experiment data, the generation mechanism of radicals and the possible pathways of m-cresol degradation were proposed in the 0.1 M/RM@G/PMS system. This finding provides a new way for the synthesis of the efficient catalyst with RM and optimal operating strategies for the treatment of m-cresol wastewater.</p></div>\",\"PeriodicalId\":16974,\"journal\":{\"name\":\"Journal of Saudi Chemical Society\",\"volume\":\"28 3\",\"pages\":\"Article 101857\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2024-04-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1319610324000528/pdfft?md5=732800e5f8fd6ec5a1aa2e6640f579c0&pid=1-s2.0-S1319610324000528-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Saudi Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1319610324000528\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Saudi Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1319610324000528","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

间甲酚是酚类化合物之一,毒性大,难降解,威胁人类健康和生态安全。研究高效的间甲酚降解技术对抑制间甲酚排入水体至关重要。本文制备并采用了一种掺杂氧化锰的赤泥(RM)活化过一硫酸盐(PMS)降解间甲酚的复合材料,有利于赤泥的回收和利用。从催化活性和成本方面考虑,0.1 M/RM@G 因具有较强的 Fe3O4 和 MnO 协同作用而表现出优异的降解能力,被认为是所研究催化剂中的最佳催化剂。在 2 g/L 催化剂、10 mM PMS、3-8 的初始 pH 值和 50 mg/L 间甲酚的条件下,0.1 M/RM@G/PMS 体系可在 90 分钟内降解 100 % 的间甲酚和 71.4 % 的 COD。0.1 M/RM@G 的反应速率常数(0.045 min-1)远大于 RM@G(0.012 min-1)、ARM(0.0048 min-1)和 WRM(0.0028 min-1)。催化剂表面主要的锰、铁活性组分和丰富的介孔结构可以有效地驱动电子转移,并进一步加速锰(III)锰(II)和铁(III)铁(II)活化 PMS 的氧化还原循环。1O2 在降解间甲酚的过程中发挥了关键作用。根据实验数据,提出了 0.1 M/RM@G/PMS 体系中自由基的产生机理和间甲酚降解的可能途径。这一发现为合成具有 RM 的高效催化剂以及处理间甲酚废水的最佳操作策略提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficient degradation of m-cresol by MnO-doped red mud catalyst activating peroxymonosulfate process: Performance and mechanism

M-cresol, one of phenolics, is highly toxic, refractory, and threatens human health and ecological safety. The study on the efficient m-cresol degradation technologies is crucial and helpful to restrain its discharge into water body. A composite of MnO-doped red mud (RM) to activate peroxymonosulfate (PMS) for the m-cresol degradation was fabricated and employed, favorable to the recycling and utilization of RM. Considering the catalytic activity and cost, 0.1 M/RM@G exhibited an excellent degradation capacity attributing to strong Fe3O4 and MnO synergy and was considered as the best catalyst among the investigative catalysts. 100 % of m-cresol and 71.4 % of COD could be degraded within 90 min under 2 g/L catalyst, 10 mM of PMS, 3-8 of initial pH and 50 mg/L m-cresol in the 0.1 M/RM@G/PMS system. The reaction rate constant (0.045 min−1) of 0.1 M/RM@G was much larger than RM@G (0.012 min−1), ARM (0.0048 min−1) and WRM (0.0028 min−1). Main Mn and Fe active components and abundant mesoporous structures on the catalyst surface could efficiently drove electron transfers, and further accelerated the redox cycles of Mn(III)Mn(II) and Fe(III)Fe(II) for activating PMS. 1O2 played a crucial role in degrading m-cresol. Based on the experiment data, the generation mechanism of radicals and the possible pathways of m-cresol degradation were proposed in the 0.1 M/RM@G/PMS system. This finding provides a new way for the synthesis of the efficient catalyst with RM and optimal operating strategies for the treatment of m-cresol wastewater.

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
Journal of Saudi Chemical Society
Journal of Saudi Chemical Society CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
8.90
自引率
1.80%
发文量
120
审稿时长
38 days
期刊介绍: Journal of Saudi Chemical Society is an English language, peer-reviewed scholarly publication in the area of chemistry. Journal of Saudi Chemical Society publishes original papers, reviews and short reports on, but not limited to: •Inorganic chemistry •Physical chemistry •Organic chemistry •Analytical chemistry Journal of Saudi Chemical Society is the official publication of the Saudi Chemical Society and is published by King Saud University in collaboration with Elsevier and is edited by an international group of eminent researchers.
×
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