The effect of chloride ion on the reinforcement of zero-valent copper activated peroxysulphate

被引:0
|
作者
Xu, Peng [1 ]
Li, Na
Zhu, Pengfei
Wu, Ruoxi
机构
[1] Hunan Univ, Coll Civil Engn, Hunan Engn Res Ctr Water Secur Technol & Applicat, Changsha 410082, Peoples R China
关键词
Cl /Cu(0)/PS; Sulfate radical; Hydroxyl radical; Reactive chlorine species; PERSULFATE ACTIVATION; DEGRADATION; OXIDATION; TETRACYCLINE; MECHANISMS; KINETICS; REMOVAL; COMPLEX; CU(I); WATER;
D O I
10.1016/j.jwpe.2025.107409
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The use of the zero-valent copper activated peroxysulphate system (Cu(0)/PS system) has been widely studied for pollutant degradation. However, the presence of Cu(I) in the Cu(0)/PS system was limited due to the interaction of Cu(I) with O2 and the occurrence of disproportionation reaction, which greatly reduced the effectiveness of the Cu(0)/PS system. To solve this problem, chloride ion (Cl ) were introduced into the Cu(0)/PS system (Cl /Cu (0)/PS system). When 10 mM Cl was added to the Cu(0)/PS system, the degradation rate of tetracycline (TC) was enhanced from 48.5 % to 81.0 % within 8 min, while the reaction rate was also increased by about 2.5 times. The results indicated that the presence of Cl significantly restricted the disproportionation and ineffective oxidation of Cu(I) by forming a stable Cu-Cl complex with Cu(I). This ultimately enhanced the utilization of Cu (I). Furthermore, Cl facilitated the reaction between Cu(0) and Cu(II) to produce CuCl, thereby establishing the Cu(II)/Cu(I) cycle, which was more conducive to the production of Cu(I). The main reactive species in the Cl /Cu (0)/PS system were sulfate radicals (SO4 center dot ), hydroxyl radicals (center dot OH), and reactive chlorine species (RCS). Overall, Cl incorporation is a viable facilitator for the Cu(0)/PS system.
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页数:5
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