One-step synthesis of Mn-doped MIL-53(Fe) for synergistically enhanced generation of sulfate radicals towards tetracycline degradation

催化作用 电子顺磁共振 化学 激进的 X射线光电子能谱 核化学 傅里叶变换红外光谱 水溶液 腐植酸 降级(电信) 吸热过程 化学工程 无机化学 吸附 物理化学 有机化学 工程类 物理 电信 核磁共振 计算机科学 肥料
作者
Jun Yu,Jian Cao,Zhaohui Yang,Weiping Xiong,Zhengyong Xu,Peipei Song,Meiying Jia,Saiwu Sun,Yanru Zhang,Juan Zhu
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:580: 470-479 被引量:117
标识
DOI:10.1016/j.jcis.2020.07.045
摘要

Herein, Mn-doped MIL-53(Fe) were fabricated via one-pot solvothermal method and used for peroxymonosulfate (PMS) activation towards tetracycline (TC) degradation from aqueous solution. The characterizations of SEM, FTIR and XRD were utilized to reveal the morphology and structure of the materials. The results showed that Mn-MIL-53(Fe)-0.3 displayed the optimal catalytic performance, the removal efficiency of TC could reach 93.2%. Moreover, the catalytic activity of Mn-MIL-53(Fe) towards TC under different initial pH values, co-existing anions (Cl-,CO32- and SO42-) and humic acid (HA) were investigated. The results of thermodynamic experiment suggested that the catalytic process was endothermic. In addition, integrated with capture experiments results and the characterization results of electron paramagnetic resonance (EPR), which revealed that SO4·- and HO- were the reactive radicals involving in the reaction. More importantly, the possible activation mechanism was discussed in detail based on the X-ray photoelectron spectroscopy results. The active species were generated by the active sites of Fe(II) and Mn(II) on Mn-MIL-53(Fe) effectively activated PMS. Furthermore, the degradation intermediates and possible degradation pathway were investigated by LC-MS. Finally, the catalyst also showed good performance in actual wastewater and demonstrated good recyclability. The Mn-MIL-53(Fe)/PMS system exhibited a promising application prospect for antibiotic-containing waste water treatment.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
棒槌发布了新的文献求助10
1秒前
1秒前
2秒前
宣孤菱发布了新的文献求助10
3秒前
xiaoxiao发布了新的文献求助20
3秒前
4秒前
一减完成签到 ,获得积分0
5秒前
DaBin发布了新的文献求助20
5秒前
6秒前
哈哈客完成签到,获得积分10
6秒前
万能图书馆的应助被长生采纳,获得10
7秒前
7秒前
8秒前
打打的应助被网友采纳,获得10
11秒前
时鹏飞发布了新的文献求助10
11秒前
烟花的应助被网友采纳,获得10
11秒前
刻苦的阁的应助被网友采纳,获得10
11秒前
上官若男的应助被网友采纳,获得10
11秒前
科研通AI6.2的应助被网友采纳,获得10
11秒前
Ali的应助被网友采纳,获得10
11秒前
万能图书馆的应助被网友采纳,获得10
12秒前
秋风的应助被网友采纳,获得10
12秒前
领导范儿的应助被网友采纳,获得10
12秒前
CipherSage的应助被19采纳,获得30
12秒前
白佳坤发布了新的文献求助10
12秒前
宣孤菱完成签到,获得积分10
13秒前
11完成签到,获得积分10
14秒前
16秒前
香蕉觅云的应助被网友采纳,获得10
18秒前
Jasper的应助被网友采纳,获得10
18秒前
万能图书馆的应助被网友采纳,获得10
18秒前
科研通AI6.4的应助被网友采纳,获得10
18秒前
小二郎的应助被网友采纳,获得10
18秒前
脑洞疼的应助被网友采纳,获得10
18秒前
18秒前
科研通AI6.4的应助被网友采纳,获得10
18秒前
科研通AI6.2的应助被网友采纳,获得10
18秒前
科目三的应助被网友采纳,获得10
19秒前
CodeCraft的应助被fjg采纳,获得10
19秒前
弥七的应助被网友采纳,获得10
19秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
自動車の空力技術 800
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Issues in Task-Based Language Teaching 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7783638
求助须知:如何正确求助?哪些是违规求助? 9322927
关于积分的说明 20392349
捐赠科研通 7372274
什么是DOI,文献DOI怎么找? 3320727
关于科研通互助平台的介绍 2468728
邀请新用户注册赠送积分活动 2336951