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dc.contributor.authorSokmen, M
dc.contributor.authorAllen, DW
dc.contributor.authorClench, MK
dc.contributor.authorHewson, AT
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:24:33Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:24:33Z
dc.date.issued2002
dc.identifier.issn1203-8407
dc.identifier.urihttps://hdl.handle.net/20.500.12418/11570
dc.descriptionWOS: 000181723900002en_US
dc.description.abstractThe oxidative degradation of thiophene, 2-methyl- and 3-methyl-thiophene, and their intermediate oxidation products, by the Fenton and related reagents, has been studied. Hydroxylated thiophenes were the main intermediate oxidation products, but a range of other apparently radical-derived oxidation products was also characterized. The ease of oxidisability was established as thiophene > 2-methylthiophene > 3-methylthiophene. Of the metal ion-hydrogen peroxide reagents studied, the Fenton system (Fell) was generally the most effective and the range of oxidation products formed was largely independent of the reagent used.en_US
dc.language.isoengen_US
dc.publisherSYCAMORE GLOBAL PUBLICATIONS LLCen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleGC-MS characterisation of products of oxidation of thiophenes using the Fenton and related reagentsen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF ADVANCED OXIDATION TECHNOLOGIESen_US
dc.contributor.departmentSheffield Hallam Univ, Div Chem, Sheffield S1 1WB, S Yorkshire, England -- Cumhuriyet Univ, Dept Chem, TR-58140 Sivas, Turkeyen_US
dc.identifier.volume5en_US
dc.identifier.issue1en_US
dc.identifier.endpage21en_US
dc.identifier.startpage11en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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