已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Recent trends on the catalytic activation of peroxymonosulfate for the abatement of organic dyes in waters

催化作用 环境化学 化学 环境科学 有机化学
作者
Enric Brillas
出处
期刊:Journal of environmental chemical engineering [Elsevier]
卷期号:12 (4): 113191-113191 被引量:5
标识
DOI:10.1016/j.jece.2024.113191
摘要

Peroxymonosulfate (HSO5−, PMS) is a well-known oxidant for water treatment. It needs to be activated to form strong oxidizing agents of organic pollutants like sulfate radical (SO4●−), hydroxyl radical (●OH), superoxide ion radical (O2•−), and the non-radical singlet oxygen (1O2). Recently, the removal of synthetic organic dyes from waters by PMS upon homogeneous and heterogeneous catalysts has received a great research attention due to their high effectiveness and oxidation rate determined by simple treatments centered at bench scale in the laboratory. The present review summarizes and analyzes the recent trends of this topic over the period 2020-2023. Homogeneous catalysts with transition metal ions like iron ions and Cu2+, and heterogeneous catalysts with single or mixed transition metals such as Co, Cu, Fe, and Mn, MOFs, and carbonaceous and other materials, have been examined. The action of these catalysts has been detailed for the generation of oxidizing agents from PMS activation. Selected examples describe the discoloration rate of synthetic waters contaminated with organic dyes and the influence of the operating variables on process performance. The production of oxidants via radical and non-radical mechanisms of PMS reduction has been confirmed by specific scavengers and EPR analysis. In some cases, the effect of the aqueous matrix on the dye discoloration has been analyzed and the detection of its by-products has been described with proposal of pathways for the degradation/mineralization of dyes to better know their oxidation process. A final section proposes the future development of dyes remediation with catalytic activators of PMS.

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
科研通AI6应助无限猫咪采纳,获得10
4秒前
昵称完成签到,获得积分0
6秒前
8秒前
斯文败类应助科研通管家采纳,获得10
10秒前
今后应助科研通管家采纳,获得10
10秒前
科研通AI2S应助科研通管家采纳,获得10
10秒前
科研通AI2S应助科研通管家采纳,获得10
10秒前
顾矜应助科研通管家采纳,获得10
10秒前
华仔应助科研通管家采纳,获得10
10秒前
11秒前
moon完成签到 ,获得积分10
11秒前
子车茗应助望远Arena采纳,获得30
12秒前
临子完成签到,获得积分10
16秒前
111完成签到 ,获得积分10
17秒前
小龙完成签到,获得积分10
19秒前
20秒前
奋斗慕凝完成签到 ,获得积分10
21秒前
英俊的铭应助杨杨杨采纳,获得10
26秒前
小姚姚完成签到,获得积分10
26秒前
Neyou发布了新的文献求助10
26秒前
纪富完成签到 ,获得积分10
29秒前
31秒前
hehe完成签到,获得积分20
32秒前
大鼻子的新四岁完成签到,获得积分10
35秒前
yuan完成签到,获得积分10
35秒前
三千完成签到,获得积分10
37秒前
hehe发布了新的文献求助10
37秒前
酷波er应助kk采纳,获得10
43秒前
搬砖王发布了新的文献求助10
44秒前
45秒前
小葛完成签到,获得积分10
46秒前
de完成签到,获得积分10
47秒前
Heaven完成签到,获得积分10
49秒前
可爱的函函应助三千采纳,获得10
51秒前
53秒前
Criminology34应助悦耳的易梦采纳,获得10
56秒前
kk发布了新的文献求助10
58秒前
害羞的天真完成签到 ,获得积分10
1分钟前
eing关注了科研通微信公众号
1分钟前
qifei完成签到 ,获得积分10
1分钟前
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
Basic And Clinical Science Course 2025-2026 3000
《药学类医疗服务价格项目立项指南(征求意见稿)》 880
花の香りの秘密―遺伝子情報から機能性まで 800
Stop Talking About Wellbeing: A Pragmatic Approach to Teacher Workload 500
Terminologia Embryologica 500
Silicon in Organic, Organometallic, and Polymer Chemistry 500
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5616976
求助须知:如何正确求助?哪些是违规求助? 4701321
关于积分的说明 14913230
捐赠科研通 4747317
什么是DOI,文献DOI怎么找? 2549156
邀请新用户注册赠送积分活动 1512289
关于科研通互助平台的介绍 1474049