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!

Generation and identification of 1O2 in catalysts/peroxymonosulfate systems for water purification

催化作用 单线态氧 化学 价(化学) 金属 纳米技术 生化工程 氧气 材料科学 有机化学 工程类
作者
Qianzhen Fang,Hailan Yang,Shujing Ye,Peng Zhang,Mingyang Dai,Xinjiang Hu,Yanling Gu,Xiaofei Tan
出处
期刊:Water Research [Elsevier]
卷期号:245: 120614-120614 被引量:148
标识
DOI:10.1016/j.watres.2023.120614
摘要

Catalysts for peroxymonosulfate (PMS) activation are appealing in the purification of organic wastewater. Singlet oxygen (1O2) is widely recognized as a crucial reactive species for degrading organic contaminants in catalysts/PMS systems due to its adamant resistance to inorganic anions, high selectivity, and broad pH applicability. With the rapid growth of studies on 1O2 in catalysts/PMS systems, it becomes necessary to provide a comprehensive review of its current state. This review highlights recent advancements concerning 1O2 in catalysts/PMS systems, with a primary focus on generation pathways and identification methods. The generation pathways of 1O2 are summarized based on whether (distinguished by the geometric structures of metal species) or not (distinguished by the active sites) the metal element is included in the catalysts. Furthermore, this review thoroughly discusses the influence of metal valence states and metal species with different geometric structures on 1O2 generation. Various potential strategies are explored to regulate the generation of 1O2 from the perspective of catalyst design. Identification methods of 1O2 primarily include electron paramagnetic resonance (EPR), quenching experiments, reaction in D2O solution, and chemical probe tests in catalysts/PMS systems. The principles and applications of these methods are presented comprehensively along with their applicability, possible disagreements, and corresponding solutions. Besides, an identifying procedure on the combination of main identification methods is provided to evaluate the role of 1O2 in catalysts/PMS systems. Lastly, several perspectives for further studies are proposed to facilitate developments of 1O2 in catalysts/PMS systems.
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
PDF的下载单位、IP信息已删除 (2025-6-4)

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
富贵发布了新的文献求助10
1秒前
47gongjiang发布了新的文献求助10
2秒前
热情怡发布了新的文献求助10
3秒前
5秒前
李健应助去月球数星星采纳,获得10
6秒前
10秒前
科研通AI6应助闾丘剑封采纳,获得10
10秒前
WangLu2025完成签到 ,获得积分10
11秒前
jasonjiang完成签到 ,获得积分0
11秒前
summerer发布了新的文献求助10
11秒前
pluto应助UUU采纳,获得10
13秒前
领导范儿应助11采纳,获得10
13秒前
16秒前
科研通AI6应助mxtmxt采纳,获得10
18秒前
李海发布了新的文献求助10
19秒前
我是老大应助紧张的毛衣采纳,获得30
20秒前
Forez发布了新的文献求助10
23秒前
25秒前
aa完成签到,获得积分20
30秒前
31秒前
senli2018发布了新的文献求助10
32秒前
Owen应助科研通管家采纳,获得10
37秒前
慕青应助科研通管家采纳,获得50
37秒前
爆米花应助科研通管家采纳,获得30
37秒前
orixero应助科研通管家采纳,获得10
37秒前
慕青应助科研通管家采纳,获得10
37秒前
CipherSage应助科研通管家采纳,获得10
37秒前
李健应助科研通管家采纳,获得10
37秒前
科目三应助科研通管家采纳,获得10
37秒前
酷波er应助科研通管家采纳,获得10
37秒前
小马甲应助科研通管家采纳,获得10
37秒前
38秒前
希望天下0贩的0应助nono采纳,获得10
47秒前
李海完成签到,获得积分10
49秒前
49秒前
神勇元瑶完成签到,获得积分20
59秒前
1分钟前
1分钟前
踏实的老四完成签到,获得积分10
1分钟前
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
Introduction to Early Childhood Education 1000
List of 1,091 Public Pension Profiles by Region 921
Aerospace Standards Index - 2025 800
Identifying dimensions of interest to support learning in disengaged students: the MINE project 800
流动的新传统主义与新生代农民工的劳动力再生产模式变迁 500
Historical Dictionary of British Intelligence (2014 / 2nd EDITION!) 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5431945
求助须知:如何正确求助?哪些是违规求助? 4544768
关于积分的说明 14193772
捐赠科研通 4463994
什么是DOI,文献DOI怎么找? 2446920
邀请新用户注册赠送积分活动 1438241
关于科研通互助平台的介绍 1415027