dc.contributor.author | Sokmen, M | |
dc.contributor.author | Allen, DW | |
dc.contributor.author | Clench, MK | |
dc.contributor.author | Hewson, AT | |
dc.date.accessioned | 2019-07-27T12:10:23Z | |
dc.date.accessioned | 2019-07-28T10:24:33Z | |
dc.date.available | 2019-07-27T12:10:23Z | |
dc.date.available | 2019-07-28T10:24:33Z | |
dc.date.issued | 2002 | |
dc.identifier.issn | 1203-8407 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12418/11570 | |
dc.description | WOS: 000181723900002 | en_US |
dc.description.abstract | The 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.iso | eng | en_US |
dc.publisher | SYCAMORE GLOBAL PUBLICATIONS LLC | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.title | GC-MS characterisation of products of oxidation of thiophenes using the Fenton and related reagents | en_US |
dc.type | article | en_US |
dc.relation.journal | JOURNAL OF ADVANCED OXIDATION TECHNOLOGIES | en_US |
dc.contributor.department | Sheffield Hallam Univ, Div Chem, Sheffield S1 1WB, S Yorkshire, England -- Cumhuriyet Univ, Dept Chem, TR-58140 Sivas, Turkey | en_US |
dc.identifier.volume | 5 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.endpage | 21 | en_US |
dc.identifier.startpage | 11 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |