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Electrodialytic remediation of soil fines (<63 μm) in suspension-Influence of current strength and L/S

datacite.subject.sdg11:Cidades e Comunidades Sustentáveispt_PT
dc.contributor.authorJensen, P. E.
dc.contributor.authorOttosen, Lisbeth M.
dc.date.accessioned2023-06-30T13:16:37Z
dc.date.available2023-06-30T13:16:37Z
dc.date.issued2007
dc.description.abstractCurrent treatment of the remaining soil fines from soil wash is onerous and expensive, and therefore, in this work, we investigated the feasibility of electrodialytic remediation (EDR) as an alternative treatment. The study focuses on EDR efficiency as a function of current strength, liquid-tosolid-ratio (L/S), pH and time. We found out that during the experiments, Pb was easily dissolved by the acidification resulting from water splitting at the anion-exchange membrane. When higher currents and/or higher L/S ratios were applied, it was found that water splitting occurring at the cation-exchange membrane increased the pH, and this resulted in decreased remediation efficiency. It was shown that complete remediation of the soil-fines is possible, with the majority of the Pb being transported into the catholyte and precipitated at the cathode. Based on the results it is recommended that EDR is implemented using a number of reactors in series, where the initial reactor works at the highest possible removal rate, and the final reactor works at the target Pb-concentration.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.electacta.2006.03.116pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.2/14152
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.subjectElectrodialysispt_PT
dc.subjectPbpt_PT
dc.subjectSoil remediationpt_PT
dc.subjectSoil washingpt_PT
dc.subjectWater splittingpt_PT
dc.titleElectrodialytic remediation of soil fines (<63 μm) in suspension-Influence of current strength and L/Spt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage3419pt_PT
oaire.citation.startPage3412pt_PT
oaire.citation.titleElectrochimica actapt_PT
rcaap.rightsrestrictedAccesspt_PT
rcaap.typearticlept_PT

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