Availability of Seawater as A Chloride Source for UV/electro-chlorine Advanced Oxidation Process
This study reports the availability of seawater as an economical chloride (Cl−) source for the UV/electro-chlorine process from the viewpoints of advanced oxidation performance and unwanted byproduct formation of chlorate ion (ClO3−) and bromate ion (BrO3−). In the electrochemical oxidant production...
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Published in | Journal of Water and Environment Technology Vol. 19; no. 6; pp. 283 - 293 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Tokyo
Japan Society on Water Environment
2021
Japan Science and Technology Agency |
Subjects | |
Online Access | Get full text |
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Summary: | This study reports the availability of seawater as an economical chloride (Cl−) source for the UV/electro-chlorine process from the viewpoints of advanced oxidation performance and unwanted byproduct formation of chlorate ion (ClO3−) and bromate ion (BrO3−). In the electrochemical oxidant production stage, the oxidant production rate in diluted seawater containing 30 mM Cl− was 21% lower than that in the NaCl solution due to coexisting electrolytes in the seawater. The ClO3− formation during electrolysis was successfully inhibited under acidic conditions and BrO3− formation was not detected in the diluted seawater. However, ClO3− and BrO3− were steadily formed in the undiluted seawater electrolysis, even when the initial pH value was set to 3. The oxidant utilization efficiency for 1,4-dioxane removal during UV irradiation was not deteriorated in the diluted seawater but decreased under basic conditions due to the radical scavenging effect of electrochemically produced free bromine and free chlorine. As a result, the formation of BrO3− and ClO3− was enhanced under basic conditions, whereas BrO3− formation was completely inhibited at an initial pH ≤ 5. Consequently, the diluted seawater was thought to be available as a Cl− source for the UV/electro-chlorine process if an acidic condition was maintained throughout the operation. |
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ISSN: | 1348-2165 1348-2165 |
DOI: | 10.2965/jwet.21-080 |