Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/1943
DC FieldValueLanguage
dc.contributor.authorChoi, Hyeok-
dc.contributor.authorPelaez, Miguel A.-
dc.contributor.authorAntoniou, Maria G.-
dc.date.accessioned2013-01-21T08:21:26Zen
dc.date.accessioned2013-05-16T06:25:25Z-
dc.date.accessioned2015-12-02T09:40:45Z-
dc.date.available2013-01-21T08:21:26Zen
dc.date.available2013-05-16T06:25:25Z-
dc.date.available2015-12-02T09:40:45Z-
dc.date.issued2007-
dc.identifier.citationEnvironmental science and technology, 2007, vol. 41, no. 21, pp. 7530-7535.en_US
dc.identifier.issn0013936X-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/1943-
dc.description.abstractThe presence of the harmful cyanobacterial toxins in water resources worldwide drives the development of an innovative and practical water treatment technology with great urgency. This study deals with two important aspects: the fabrication of mesoporous nitrogen-doped TiO2 (N-TiO2) photocatalysts and their environmental application for the destruction of microcystin-LR (MC-LR) under visible light. In a nanotechnological sol-gel synthesis method, a nitrogen-containing surfactant(dodecylammonium chloride) was introduced as a pore templating material for tailor-designing the structural properties of TiO2 and as a nitrogen dopant for its visible light response. The resulting N-TiO2 exhibited significantly enhanced structural properties including 2-8 nm mesoporous structure (porosity 44%) and high surface area of 150 m2/g. Red shift in light absorbance up to 468 nm, 0.9 eV lower binding energy of electrons in Ti 2p state, and reduced interplanar distance of crystal lattices proved nitrogen doping in the TiO 2 lattice. Due to its narrow band gap at 2.65 eV, N-TiO2 efficiently degraded MC-LR under visible spectrum above 420 nm. Acidic condition (pH 3.5) was more favorable for the adsorption and photocatalytic degradation of MC-LR on N-TiO2 due to electrostatic attraction forces between negatively charged MC-LR and +6.5 mV charged N-TiO2. Even under UV light, MC-LR was decomposed 3-4 times faster using N-TiO2 than control TiO2. The degradation pathways and reaction intermediates of MC-LR were not directly related to the energy source for TiO2 activation (UV and visible) and nature of TiO2 (neat and nitrogen-doped). This study implies a strong possibility for the in situ photocatalytic remediation of contaminated water with cyanobacterial toxins and othertoxic compounds using solar light, a sustainable source of energy.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofEnvironmental Science & Technologyen_US
dc.rights© American Chemical Societyen_US
dc.subjectIrradiationen_US
dc.subjectPhotocatalysisen_US
dc.subjectTitanium dioxideen_US
dc.subjectNitrogenen_US
dc.subjectMicrocystinsen_US
dc.subjectElectronsen_US
dc.titleMesoporous nitrogen-doped TiO2 for the photocatalytic destruction of the cyanobacterial toxin microcystin-lr under visible light irradiationen_US
dc.typeArticleen_US
dc.affiliationUniversity of Cincinnatien
dc.collaborationUniversity of Cincinnatien_US
dc.journalsSubscriptionen_US
dc.countryGreeceen_US
dc.subject.fieldEngineering and Technologyen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1021/es0709122en_US
dc.dept.handle123456789/54en
dc.relation.issue21en_US
dc.relation.volume41en_US
cut.common.academicyear2007-2008en_US
dc.identifier.spage7530en_US
dc.identifier.epage7535en_US
item.languageiso639-1en-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
crisitem.author.deptDepartment of Chemical Engineering-
crisitem.author.facultyFaculty of Geotechnical Sciences and Environmental Management-
crisitem.author.orcid0000-0003-0738-6068-
crisitem.author.parentorgFaculty of Geotechnical Sciences and Environmental Management-
crisitem.journal.journalissn1520-5851-
crisitem.journal.publisherAmerican Chemical Society-
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