电泳剂
亲核细胞
环境修复
化学
分解
钼
催化作用
反应性(心理学)
反应中间体
同种类的
多相催化
环境化学
光化学
无机化学
污染
有机化学
物理
病理
热力学
生物
替代医学
医学
生态学
作者
Yibing Sun,Hongchao Li,Shengli Zhang,Ming Hua,Jieshu Qian,Bingcai Pan
出处
期刊:ACS ES&T water
[American Chemical Society]
日期:2022-02-02
卷期号:2 (2): 376-384
被引量:32
标识
DOI:10.1021/acsestwater.1c00459
摘要
Heterogeneous peroxymonosulfate (PMS)-based advanced oxidation processes (AOPs) are under extensive investigation for their great potential in water remediation. The understanding of the PMS activation mechanism is crucial but still debatable. Here, we describe a thorough investigation of the mechanism involved in PMS activation by using molybdenum disulfide (MoS2) as a catalyst. This MoS2/PMS system exhibited intriguing target-dependent reactivity. Further comprehensive experimental results excluded the major contributions of various possible species, including HO•, SO4•–, O2•–, 1O2, homogeneous Mo(VI), and heterogeneous Mo(VI). We then proposed a surface ≡Mo–OOSO3– complex as the major reactive species, while SO4•– derived from the decomposition of ≡Mo–OOSO3– acted as the secondary reactive species for pollutant removal. This complex could oxidize pollutants through the oxygen-atom-transfer mechanism and perform both nucleophilic and electrophilic attacks. This work provides novel perspectives for the mechanistic understanding of heterogeneous PMS-based AOPs for water remediation.
科研通智能强力驱动
Strongly Powered by AbleSci AI