Electrically enhanced adsorption and green regeneration for fluoride removal using Ti(OH)4-loaded activated carbon electrodes
An electrically enhanced fluoride removal method was developed that blended the merits of electrosorption and adsorbent adsorption. This method has the advantages of high adsorption selectivity and capacity for fluoride. The saturated adsorption capacity of Ti(OH)4 for fluoride in the electrode of T...
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Published in | Chemosphere (Oxford) Vol. 200; pp. 554 - 560 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.06.2018
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Subjects | |
Online Access | Get full text |
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Summary: | An electrically enhanced fluoride removal method was developed that blended the merits of electrosorption and adsorbent adsorption. This method has the advantages of high adsorption selectivity and capacity for fluoride. The saturated adsorption capacity of Ti(OH)4 for fluoride in the electrode of Ti(OH)4-loaded activated carbon reached 115.2 mg/g when a voltage of +1.2 V was applied to the electrode. The electrode was easily and cleanly regenerated in a short time in aqueous solution with high fluoride concentrations when a voltage of −1.6 V was applied. The adsorption capacity of the Ti(OH)4-loaded electrode for fluoride did not decrease after multiple cycles of electrically enhanced adsorption and regeneration. Excellent adsorption selectivity for fluoride was achieved. The electrically enhanced adsorption method showed potential for fluoride removal.
•An electrically enhanced adsorption method for fluoride removal was developed.•.The Ti-AC electrode had high adsorption selectivity for fluoride.•The fluoride adsorption capacity reached 115.2 mg/g at +1.2 V.•The Ti-AC electrode was easily and cleanly regenerated at −1.6 V.•.Fluoride adsorption capacity did not decrease after serval cycles. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0045-6535 1879-1298 |
DOI: | 10.1016/j.chemosphere.2018.02.112 |