Effects of the formation of reactive chlorine species on oxidation process using persulfate and nano zero-valent iron

被引:25
|
作者
Kim, Cheolyong [1 ]
Thao, Trinh Thi [1 ]
Kim, Jae-Hyuk [1 ]
Hwang, Inseong [1 ]
机构
[1] Pusan Natl Univ, Dept Civil & Environm Engn, 2 Busandaehak Ro 63 Beon Gil, Busan 46241, South Korea
关键词
Persulfate; Nano zero-valent iron; Sulfate radical; Reactive chlorine species; SITU CHEMICAL OXIDATION; SALINE WASTE-WATER; ACTIVATED PERSULFATE; ORGANIC-COMPOUNDS; ZEROVALENT IRON; RATE CONSTANTS; HUMIC-ACID; AZO-DYE; DEGRADATION; TRANSFORMATION;
D O I
10.1016/j.chemosphere.2020.126266
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The chloride ion (Cl-) is a matrix ion that plays crucial roles in radical-based oxidation processes used to treat brackish or saline water. Here, the effects of the formation of reactive chlorine species on the performance of and reaction mechanisms involved in persulfate/nano zero-valent iron process were evaluated by investigating the reaction kinetics and performing reactive species scavenging tests. The phenol oxidation rate increased markedly in the early reaction stage in the presence of 25-200 mM of Cl-. This was because excess sulfate radicals (SO4 center dot(-)) reacted with Cl- to produce short-lived reactive chlorine species such as Cl center dot and Cl-2 center dot(-) rather than being scavenged by Fe2+ or other SO4 center dot(-). The reactive chlorine species caused Oft to form through radical propagation reactions. The total numbers of reactive species involved in phenol oxidation were higher at brackish to weakly saline Cl- concentrations than at lower and higher Cl(- )concentrations. At high Cl- concentrations (>400 mM), the phenol oxidation rate decreased because most of the SO4 center dot(- )reacted with Cl- to give large amounts of weaker oxidants such as Cl-2 center dot(-) and HOCl. Acceleration of Fe corrosion by Cl- negligibly affected the persulfate/nano zero-valent iron oxidation process. (C) 2020 Elsevier Ltd. All rights reserved.
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页数:7
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