Enhanced catalytic activities of natural iron ore in peroxymonosulfate activation assisted by WS2 for rapid degradation of pollutants

化学 催化作用 吸附 降级(电信) 反应速率常数 污染物 电子转移 氧化还原 硫化物 无机化学 动力学 核化学 环境化学 光化学 有机化学 物理 电信 量子力学 计算机科学
作者
Lu Chen,Chao Wang,Wenjie He,Haibo Li,Zhihong Ye,Yin Xu
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:328: 125130-125130 被引量:11
标识
DOI:10.1016/j.seppur.2023.125130
摘要

The seek for efficient and low-cost heterogeneous catalysts for peroxymonosulfate (PMS) activation holds great promise in the treatment of organic contaminants. Natural iron ore (IO) has been identified as a potential catalyst due to its low environmental risk and cost-savings. Herein, the commercial tungsten sulfide (WS2) was employed to significantly enhance the performance of IO towards PMS activation (WS2/IO/PMS) for the removal of pollutants. This system demonstrated remarkable performance, with >98.2% removal of organic pollutants in 60 min, including dyes and antibiotics, under the optimized conditions of 0.50 g/L IO, 0.10 g/L WS2, 2.0 mM PMS, and initial pH 6.0. The apparent degradation rate constant (k) of Acid Orange 7 (AO7) in WS2/IO/PMS system (0.073 min−1) was about 30.4-fold and 104.3-fold higher than that of in WS2/PMS system (0.0024 min−1) and IO/PMS system (0.0007 min−1), respectively. Mechanism insights revealed the crucial role of WS2 in boosting the degradation kinetics in the WS2/IO/PMS system. The exposed W4+ or S2− species on WS2 surface were the dominant reactive sites responsible for the promotion of Fe3+/Fe2+ redox cycles and subsequently the PMS activation. Importantly, the electrochemical analysis demonstrates that the iron ions released from IO were prone to adsorb onto the WS2 surface, forming active Fe species with high oxidative potential, which remarkably accelerated the electron transfer for Fe2+ regeneration, thereby enhancing PMS activation to generate reactive oxygen species like hydroxyl radicals (OH), sulfate radicals (SO4−) and superoxide radicals (O2−). Furthermore, the practicability of WS2/IO/PMS system was validated by treating various pollutants and investigating the interference of coexisting anions in water. Overall, this study provides a green and advanced strategy to enhance the PMS activation by natural iron ore for efficient water decontamination.
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
1秒前
1秒前
简单访卉发布了新的文献求助10
1秒前
霸气乐荷完成签到 ,获得积分10
1秒前
hxj完成签到,获得积分10
1秒前
2秒前
2秒前
selina发布了新的文献求助10
2秒前
2秒前
苹果完成签到,获得积分10
2秒前
Alice完成签到,获得积分10
2秒前
3秒前
Dihxxxx发布了新的文献求助10
3秒前
molihuakai应助标致善愁采纳,获得10
3秒前
古月完成签到,获得积分10
3秒前
tianshuai完成签到,获得积分10
3秒前
Aurora发布了新的文献求助10
4秒前
4秒前
4秒前
传奇3应助goldfish2218采纳,获得10
4秒前
未雨绸缪完成签到,获得积分10
5秒前
咕咕完成签到,获得积分10
5秒前
小马甲应助毛绒绒窝铺采纳,获得10
5秒前
苏逸发布了新的文献求助10
5秒前
Iris发布了新的文献求助10
6秒前
Jade完成签到,获得积分10
6秒前
6秒前
6秒前
Yuan完成签到,获得积分10
6秒前
7秒前
7秒前
李健应助科研小辉采纳,获得10
7秒前
一壶古酒发布了新的文献求助20
7秒前
李健应助ggfygggg采纳,获得10
7秒前
7秒前
8秒前
晨aaa完成签到,获得积分10
8秒前
未雨绸缪发布了新的文献求助10
8秒前
sikh应助hh采纳,获得10
9秒前
书羽发布了新的文献求助10
9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
The Multiple Self-States Drawing Technique 600
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Rosenblum, Global Change Biology 500
CLSI VET01S-2024 Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated From Animals (7th Ed) 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 7768753
求助须知:如何正确求助?哪些是违规求助? 9311946
关于积分的说明 20326464
捐赠科研通 7353879
什么是DOI,文献DOI怎么找? 3315828
关于科研通互助平台的介绍 2464872
邀请新用户注册赠送积分活动 2330405