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Compatibility of nonionic and anionic surfactants with persulfate activated by alkali in the abatement of chlorinated organic compounds in aqueous phase

dc.contributor.authorGarcía Cervilla, Raúl
dc.contributor.authorSantos López, Aurora
dc.contributor.authorRomero Salvador, Arturo
dc.contributor.authorLorenzo Fernández, David
dc.date.accessioned2024-01-11T09:09:13Z
dc.date.available2024-01-11T09:09:13Z
dc.date.issued2020
dc.description.abstractSurfactant Enhanced In-Situ Chemical Oxidation (S-ISCO) is an emerging technology in the remediation of sites with residual Dense Non-Aqueous Phase Liquids (DNAPLs), a ubiquitous problem in the environment and a challenge to solve. In this work, three nonionic surfactants: E-Mulse3® (E3), Tween80 (T80), and a mixture of Tween80-Span80 (TS80), and an anionic surfactant: sodium dodecyl sulfate (SDS), combined with persulfate activated by alkali (PSA) as oxidant have been investigated to remove the DNAPL generated as liquid waste in lindane production, which is composed of 28 chlorinated organic compounds (COCs). Because the compatibility between surfactants and oxidants is a key aspect in the S-ISCO effectiveness the unproductive consumption of PS by surfactants was investigated in batch (up to 864 h) varying the initial concentration of PS (84–42 mmol·L−1 ) and surfactants (0–12 g·L−1 ) and the NaOH:PS molar ratio (1 and 2). The solubilization capacity of a partially oxidized surfactant was analyzed by estimating its Equivalent Surfactant Capacity, ESC, (as mmolCOCs dissolved gsurf −1) and comparing it to the expected value for an unoxidized surfactant, ESCo. Finally, the abatement of DNAPL with simultaneous addition of surfactant and PSA was studied. At the conditions used, a negligible unproductive consumption of PS was found by SDS; meanwhile, PS consumption at 360 h ranged between 70 and 80% using the nonionic surfactants. The highest ratios of ESC/ESCo were found with SDS and E3 and these surfactants were chosen for the S-ISCO treatment. When oxidant and surfactant were simultaneously applied for DNAPL abatement the COC conversion was more than three times higher with E3 (0.6 at 360 h) than SDS. Moreover, it was obtained that the time needed for the removal of a mass of DNAPL by PSA in the absence of surfactants was notably higher than the time required when a suitable surfactant was added
dc.description.departmentDepto. de Ingeniería Química y de Materiales
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipEuropean Commission
dc.description.sponsorshipComunidad de Madrid
dc.description.sponsorshipMinisterio de Economia, Industria y ́Competitividad (España)
dc.description.statuspub
dc.identifier.citationGarcía-Cervilla, Raul, et al. «Compatibility of Nonionic and Anionic Surfactants with Persulfate Activated by Alkali in the Abatement of Chlorinated Organic Compounds in Aqueous Phase». Science of The Total Environment, vol. 751, enero de 2021, p. 141782. https://doi.org/10.1016/j.scitotenv.2020.141782.
dc.identifier.doi10.1016/j.scitotenv.2020.141782
dc.identifier.issn0048-9697
dc.identifier.officialurlhttps://doi.org/10.1016/j.scitotenv.2020.141782
dc.identifier.urihttps://hdl.handle.net/20.500.14352/92429
dc.journal.titleScience of The Total Environment
dc.language.isoeng
dc.page.initial141782
dc.publisherElsevier
dc.relation.projectID(LIFE17 ENV/ES/ 000260)
dc.relation.projectID(S2018/EMT-4317)
dc.relation.projectIDCTM2016-77151-C2- 1-R
dc.relation.projectID(ref. BES2017-081782)
dc.rights.accessRightsrestricted access
dc.subject.cdu66.0
dc.subject.keywordAspect ratio
dc.subject.keywordBiophysics
dc.subject.keywordIndium compounds
dc.subject.keywordMolar concentration
dc.subject.keywordMolar ratio
dc.subject.keywordOrganic compounds
dc.subject.keywordOxidants
dc.subject.keywordSodium dodecyl sulfate
dc.subject.keywordSodium hydroxide
dc.subject.keywordSulfur compounds
dc.subject.ucmIngeniería química
dc.subject.unesco3303 Ingeniería y Tecnología Químicas
dc.titleCompatibility of nonionic and anionic surfactants with persulfate activated by alkali in the abatement of chlorinated organic compounds in aqueous phase
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number751
dspace.entity.typePublication
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relation.isAuthorOfPublicationc9d0900f-4c0e-4a20-867d-8103d0ac678a
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relation.isAuthorOfPublication53b0ff5e-06e0-4b3f-b275-983b7944879f
relation.isAuthorOfPublication.latestForDiscovery7f7026cc-c159-4741-b75b-31514046e120

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