Mechanisms behind pH changes during electrocoagulation
Autor: | Morten Lykkegaard Christensen, Søren Fredberg Weiss, Mads Koustrup Jørgensen |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Flocculation
Electrolysis Environmental Engineering Chemistry General Chemical Engineering medicine.medical_treatment surface water water treatment Pulp and paper industry Ph changes Electrocoagulation law.invention electrochemical processes law flocculation electrolysis iron chemistry medicine Water treatment SDG 6 - Clean Water and Sanitation SDG 12 - Responsible Consumption and Production Surface water Biotechnology |
Zdroj: | Weiss, S F, Christensen, M L & Jørgensen, M K 2021, ' Mechanisms behind pH changes during electrocoagulation ', AIChE Journal, vol. 67, no. 11, e17384 . https://doi.org/10.1002/aic.17384 |
DOI: | 10.1002/aic.17384 |
Popis: | Electrocoagulation is a promising method for removing pollutants from surface water and industrial wastewater. The coagulation efficiency is dependent on pH but it is not fully understood how electrocoagulation affects pH of the treated water. Three series of experiments have been conducted to study how (1) chloride and sulfate anions, (2) negatively charged organic macromolecules, and (3) carbonate influence pH during electrocoagulation. It is found that dissolved carbonate has a significant influence on the pH change as CO2 is stripped off during electrocoagulation due to formation of H2 microbubbles at the cathode. The pH increased by (Formula presented.) 1 pH unit, which may significantly affect coagulation efficiency of iron. The pH increase depended strongly on the initial pH and the concentration of carbonate in the water. A secondary contribution to pH change was found to be ion exchange by sulfate and chloride ions into Fe(OH)3 flocs, whereby OH− was released into solution but only minor pH change was observed, not enough to affect the coagulation. The presence of charged organic macromolecules did not have any significant effect on pH. |
Databáze: | OpenAIRE |
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