Photocatalytic degradation of geosmin: Reaction pathway analysis
| Autor: | Evans M.N. Chirwa, Emomotimi Bamuza-Pemu |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2012 |
| Předmět: |
Bicyclic molecule
photocatalysis geosmin 2-methylisoborneol (2-MIB) taste and odour degradation intermediates chemistry.chemical_element Management Monitoring Policy and Law Photochemistry Applied Microbiology and Biotechnology Geosmin Reaction rate chemistry.chemical_compound chemistry Chlorine Photocatalysis Degradation (geology) Organic chemistry Hydroxyl radical Dehydrogenation Waste Management and Disposal Water Science and Technology |
| Zdroj: | Water SA; Vol 38, No 5 (2012); 689-696 |
| ISSN: | 0378-4738 |
| Popis: | The presence of geosmin in drinking water imparts a musty odour which leads to consumer complaints. Geosmin and other unwanted organics can be treated using photocatalysis. However, the intermediates formed during the photocatalytic degradation process and their degradation pathways have not previously been described. In this study, the degradation profile, as well as the intermediates formed during the photocatalytic degradation of geosmin was monitored in an effort to obtain a better understanding of the degradation kinetics and pathway. Photocatalytic degradation of geosmin in the presence of radical scavengers was shown to be inhibited, as evidenced by the reduction in reaction rate coefficient (kf) from 0.055 to 0.038 min-1. The hydroxyl radical reaction was thus shown to be the predominant process over direct photolysis by incident UV energy. Results from mass spectrum analysis of degradation intermediates indicate rapid fission of sp3„Ÿsp3 (C„ŸC) bonds resulting in ring opening of the cyclic geosmin structure. Bicyclic compounds that could be expected from dehydration and dehydrogenation of geosminfs ringed structure were not found among the detected intermediate products. Intermediates identified consisted of acyclic unsaturated alkenes, carbonyl compounds and some organic acids. Although the identified degradation products are not seen to be directly harmful, chlorine disinfection of water containing thesecompounds could produce potentially harmful halogenated hydrocarbons |
| Databáze: | OpenAIRE |
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