Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/10726
DC FieldValueLanguage
dc.contributor.authorSilva, Eliana-
dc.contributor.authorPereira, Mariette M.-
dc.contributor.authorBurrows, Hugh D.-
dc.contributor.authorAzenha, M. E.-
dc.contributor.authorSarakha, Mohamed-
dc.contributor.authorBolte, Michèle-
dc.date.accessioned2009-07-17T12:18:53Z-
dc.date.available2009-07-17T12:18:53Z-
dc.date.issued2003-11-25-
dc.identifier.citationPhotochemical & Photobiological Sciences. 3 (2004) 200-204en_US
dc.identifier.issn1474-905X-
dc.identifier.urihttps://hdl.handle.net/10316/10726-
dc.description.abstractThe photosensitised degradation of 4-chlorophenol (4-CP) by iron meso-tetrakis(2,6-dichloro-3-sulfophenyl)porphyrin (FeTDCPPS) has been studied in aerated aqueous solution, and is shown to lead to formation of p-benzoquinone (BQ) and p-hydroquinone (HQ) as main photoproducts. In deaerated solution no p-benzoquinone was formed. The photolysis products were identified by high performance liquid chromatography (HPLC) and UV-visible spectroscopy. The photodegradation in aerated solution was also carried out in the presence of sodium azide (NaN3) as a singlet oxygen [1O2(1g)] quencher, and showed a significant decrease in the rate of photolysis, suggesting under these conditions, that Type II sensitisation is one of the dominant mechanisms of 4-CP degradation. Support for this comes from laser flash photolysis and time-resolved singlet oxygen phosphorescence measurements. However, these also show direct reaction between the excited porphyrin and 4-CP, indicating that there are two mechanisms involved in the chlorophenol photodegradation.en_US
dc.description.sponsorshipClermont-Ferrand; ICCTI/GRICES; CNRS; FCT; POCTI; FEDERen_US
dc.language.isoengen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsopenAccesseng
dc.titlePhotooxidation of 4-chlorophenol sensitised by iron meso-tetrakis(2,6-dichloro-3-sulfophenyl)porphyrin in aqueous solutionen_US
dc.typearticleen_US
dc.identifier.doi10.1039/b308975d-
uc.controloAutoridadeSim-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
crisitem.author.deptFaculty of Sciences and Technology-
crisitem.author.parentdeptUniversity of Coimbra-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0003-4958-7677-
crisitem.author.orcid0000-0003-3127-2298-
crisitem.author.orcid0000-0002-9495-2592-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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