Generation of dichloroacetonitrile with the co-presence of g-C3N4 and chloride in peroxymonosulfate/Vis system: Impacts and mechanism

被引:1
|
作者
Zhao, Zhiwei [1 ,2 ]
Li, Yu [1 ]
Wang, Fei [1 ]
Xu, Zhitao [1 ]
Zhang, Sai [1 ]
Li, Li [1 ]
Fan, Junyu [3 ]
Liu, Jie [3 ]
机构
[1] Chongqing Univ, Coll Environm & Ecol, Key Lab Ecoenvironm Three Gorges Reservoir Reg, Minist Educ, Chongqing 400045, Peoples R China
[2] Guangdong Univ Technol, Sch Civil & Transportat Engn, Guangzhou 510006, Peoples R China
[3] PLA Army Serv Acad, Dept Mil Facil, Chongqing 401311, Peoples R China
基金
中国国家自然科学基金;
关键词
Dichloroacetonitrile; Peroxymonosulfate; Photocatalytic degradation; Phenol; Formation mechanism; GRAPHITIC CARBON NITRIDE; BY-PRODUCTS; VALENT IRON; DEGRADATION; ACTIVATION; OXIDATION; KINETICS; SULFATE; PHOTOCATALYSTS; ANTIBIOTICS;
D O I
10.1016/j.cej.2024.149541
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Monitoring and regulating the formation of toxic byproducts in advanced oxidation processes (AOPs) is of great significance for their practical application in water treatment. In this work, we found that dichloroacetonitrile (DCAN), a common N-containing byproduct in chloramination disinfection, can be formed with the co-presence of g-C3N4 and chloride in a peroxymonosulfate (PMS) system. The measured value was 12.01 mu M within 12 h under the given conditions. Structure analysis of raw and used g-C3N4 demonstrated that g-C3N4 decomposition indeed occurred, and C = N bonds acted as primary active sites, releasing N resources for subsequent DCAN formation. Additionally, multiple parameters, including the reactant (i.e., g-C3N4, PMS, Cl-, phenol) dose and solution pH, were observed to remarkably affect the yield of DCAN. Phenol was identified as the organic precursor of DCAN and may cooperate with inorganic chloramine to promote DCAN formation via the decarboxylation pathway. This study highlights the generation of DCAN in N-involved catalyst-based AOPs and improves understanding of the DCAN formation mechanism.
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页数:9
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