Effect of ferric salt addition on UV/electro-chlorine advanced oxidation process

被引:0
作者
Kishimoto, Naoyuki [1 ]
Nakamura, Kenjiro [1 ,2 ,3 ]
机构
[1] Ryukoku Univ, Fac Adv Sci & Technol, 1-5 Yokotani,Setaoe Cho, Otsu 520-2194, Japan
[2] Ryukoku Univ, Fac Sci & Technol, Otsu, Japan
[3] Sanki Engn Co Ltd, 7-10-1 Chuorinkan, Yamato, Kanagawa 2420007, Japan
基金
日本学术振兴会;
关键词
Advanced oxidation process; chlorine photolysis; 1,4-dioxane; ferric photolysis; UV/chlorine process; HYDROXYL RADICALS; RATE CONSTANTS; BY-PRODUCTS; 1,4-DIOXANE; PHOTOLYSIS; DEGRADATION; COMPLEXES; WATER;
D O I
10.1080/09593330.2023.2283800
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study discussed the effect of ferric salt addition on UV/electro-chlorine advanced oxidation process using a train of electrolytic and UV flow cells with an ozone-free low-pressure mercury vapour lamp (total irradiance:0.60 W at 254 nm). Ferric salt addition enhanced 1,4-dioxane degradation at an electrolytic current of 0.100 A. By contrast, an inhibitory effect of ferric salt addition was observed at a current of 0.500 A. The enhanced accumulation of free chlorine at a current of 0.500 A directly decreased the 1,4-dioxane degradation rate by scavenging reactive radicals like HO. and Cl-.. However, at an electrolytic current of 0.100 A, UV irradiance was relatively excessive for electrochemical chlorine production. The excess UV energy enhanced the photoreduction of FeOH2+, followed by the Fenton-type reaction of Fe2+ and HOCl, which produced HO. and consumed free chlorine. As a result, the free chlorine concentration decreased, and the reaction efficiency between the reactive radicals and 1,4-dioxane improved. Thus, the addition of ferric salt to a UV/electro-chlorine system is recommended when the UV irradiance in the system is excessive compared to the electrochemical chlorine supply. [GRAPHICS]
引用
收藏
页码:5074 / 5082
页数:9
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