Dredged sediments contaminated by heavy metals and PAHs were subjected to both unenhanced and enhanced electrokinetic remediation under different operating conditions, obtained by varying the applied voltage and the type of conditioning agent used at the electrode compartments in individual experiments. While metals were not appreciably mobilized as a result of the unenhanced process, metal removal was found to be significantly improved when both the anodic and cathodic reservoirs were conditioned with the chelating agent EDTA with removal yields ranging from 28% to 84% depending on the contaminant concerned. As for the effect on organic contaminants, under the conditions tested the electrokinetic treatment displayed a poor removal capacity towards PAHs. even when a surfactant (Tween 80) was used to promote contaminant mobilization, indicating the need for further investigation on this issue. Further research on organics removal from this type of materials through electrokinetic remediation is thus required. Furthermore, a number of technical and environmental issues will also require a careful evaluation with a view to full-scale implementation of electrokinetic sediment remediation. These include controlling side effects during the treatment (such as anodic precipitation, oxidation of the conditioning agent, and evolution of toxic gases), as well as evaluating the potential ecotoxicological effects of the chemical agents used. (C) 2010 Elsevier Ltd. All rights reserved.

Enhanced electrokinetic treatment of marine sediments contaminated by heavy metals and PAHs / Antonio, Colacicco; Giorgia De, Gioannis; Aldo, Muntoni; Emmanuela, Pettinao; Polettini, Alessandra; Pomi, Raffaella. - In: CHEMOSPHERE. - ISSN 0045-6535. - 81:1(2010), pp. 46-56. (Intervento presentato al convegno 8th Symposium on Electrokinetic Remediation tenutosi a Lisbon (Portugal) nel 26-29 luglio 2009) [10.1016/j.chemosphere.2010.07.004].

Enhanced electrokinetic treatment of marine sediments contaminated by heavy metals and PAHs

POLETTINI, Alessandra
;
POMI, Raffaella
2010

Abstract

Dredged sediments contaminated by heavy metals and PAHs were subjected to both unenhanced and enhanced electrokinetic remediation under different operating conditions, obtained by varying the applied voltage and the type of conditioning agent used at the electrode compartments in individual experiments. While metals were not appreciably mobilized as a result of the unenhanced process, metal removal was found to be significantly improved when both the anodic and cathodic reservoirs were conditioned with the chelating agent EDTA with removal yields ranging from 28% to 84% depending on the contaminant concerned. As for the effect on organic contaminants, under the conditions tested the electrokinetic treatment displayed a poor removal capacity towards PAHs. even when a surfactant (Tween 80) was used to promote contaminant mobilization, indicating the need for further investigation on this issue. Further research on organics removal from this type of materials through electrokinetic remediation is thus required. Furthermore, a number of technical and environmental issues will also require a careful evaluation with a view to full-scale implementation of electrokinetic sediment remediation. These include controlling side effects during the treatment (such as anodic precipitation, oxidation of the conditioning agent, and evolution of toxic gases), as well as evaluating the potential ecotoxicological effects of the chemical agents used. (C) 2010 Elsevier Ltd. All rights reserved.
2010
chemically aided electrokinetics; pahs; heavy metals; dredged sediments
01 Pubblicazione su rivista::01a Articolo in rivista
Enhanced electrokinetic treatment of marine sediments contaminated by heavy metals and PAHs / Antonio, Colacicco; Giorgia De, Gioannis; Aldo, Muntoni; Emmanuela, Pettinao; Polettini, Alessandra; Pomi, Raffaella. - In: CHEMOSPHERE. - ISSN 0045-6535. - 81:1(2010), pp. 46-56. (Intervento presentato al convegno 8th Symposium on Electrokinetic Remediation tenutosi a Lisbon (Portugal) nel 26-29 luglio 2009) [10.1016/j.chemosphere.2010.07.004].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/124208
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