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]
卷期号:328: 125130-125130 被引量:4
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
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
2秒前
lingjuanwu发布了新的文献求助10
3秒前
清脆寒香发布了新的文献求助10
3秒前
3秒前
小九不太乖完成签到,获得积分10
3秒前
淡定蓝发布了新的文献求助10
4秒前
5秒前
hrt完成签到,获得积分20
5秒前
5秒前
7秒前
Alita完成签到 ,获得积分10
8秒前
CodeCraft应助吴迪采纳,获得10
8秒前
8秒前
btutou发布了新的文献求助10
10秒前
烟花应助淡定蓝采纳,获得10
11秒前
程程程完成签到,获得积分20
12秒前
12秒前
玊尔发布了新的文献求助10
13秒前
小白完成签到,获得积分10
13秒前
追寻的秋玲应助CC采纳,获得10
16秒前
勤劳的沅发布了新的文献求助10
17秒前
18秒前
可爱的函函应助刘RJ采纳,获得10
19秒前
勤劳的辉辉完成签到,获得积分10
19秒前
小白发布了新的文献求助10
19秒前
Orange应助洛依1213采纳,获得10
19秒前
20秒前
好奇宝宝完成签到,获得积分10
20秒前
科研通AI2S应助kjding采纳,获得10
21秒前
22秒前
戏言121发布了新的文献求助30
25秒前
不好发布了新的文献求助10
26秒前
27秒前
ps完成签到 ,获得积分10
28秒前
猫咪也疯狂应助鲁轶祎采纳,获得10
29秒前
223完成签到,获得积分10
30秒前
31秒前
muzi发布了新的文献求助10
31秒前
张兮兮发布了新的文献求助10
33秒前
lc关注了科研通微信公众号
34秒前
高分求助中
The ACS Guide to Scholarly Communication 2500
Sustainability in Tides Chemistry 2000
Microlepidoptera Palaearctica, Volumes 1 and 3 - 13 (12-Volume Set) [German] 1122
The Data Economy: Tools and Applications 1000
Diamonds: Properties, Synthesis and Applications 800
PraxisRatgeber Mantiden., faszinierende Lauerjäger. – Buch gebraucht kaufen 700
Mantiden - Faszinierende Lauerjäger – Buch gebraucht kaufen 700
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3097793
求助须知:如何正确求助?哪些是违规求助? 2749704
关于积分的说明 7605682
捐赠科研通 2401576
什么是DOI,文献DOI怎么找? 1274203
科研通“疑难数据库(出版商)”最低求助积分说明 616015
版权声明 599016