1990
DOI: 10.1016/0021-9517(90)90269-p
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Photocatalytic degradation of organic water contaminants: Mechanisms involving hydroxyl radical attack

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Cited by 1,980 publications
(958 citation statements)
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“…The photo-generated electrons react with the molecular oxygen (O 2 ) to produce superoxide radical anions (ÁO À 2 ) and then photo-generated holes react with water to produce hydroxyl (ÁOH) radicals. These reactive radicals are then responsible for the degradation of organic compounds with QDs (Turchi and Ollis 1990;Pouretedal et al 2010). In this study, at the end of each interval time, the color difference in the irradiated dye solution of both pure and ZnO/starch QDs was observed and it confirms degradation of RhB dye, whereas no observable dye degradation in RhB dye solution was found after irradiation.…”
Section: Photocatalysis Analysismentioning
confidence: 50%
“…The photo-generated electrons react with the molecular oxygen (O 2 ) to produce superoxide radical anions (ÁO À 2 ) and then photo-generated holes react with water to produce hydroxyl (ÁOH) radicals. These reactive radicals are then responsible for the degradation of organic compounds with QDs (Turchi and Ollis 1990;Pouretedal et al 2010). In this study, at the end of each interval time, the color difference in the irradiated dye solution of both pure and ZnO/starch QDs was observed and it confirms degradation of RhB dye, whereas no observable dye degradation in RhB dye solution was found after irradiation.…”
Section: Photocatalysis Analysismentioning
confidence: 50%
“…It is not a question that can be easily settled with steady-state kinetics experiments: every plausible kinetic model based on surfacebound or homogeneous reactive intermediates reacting with substrate yields kinetic information of the same form [58]. Thus, this is still a question of some dispute, though the more conventional position at this point is that most reactions occur at the surface [59].…”
Section: Isomerization Mechanisms and The Question Of Bulk Water Versmentioning
confidence: 99%
“…7 , by suitable electron scavengers, that must be present in the solution and available at the semiconductor interface. 6 On the other hand, in processes aiming at the oxidative destruction of a target organic substrate, any hole scavengers present in the same environment are potential competitors for the consumption of h + VB . 7,8 As far as electron scavenging is concerned, the most common electron scavenger, in aerated aqueous solution, is O 2 and its role has been emphasised, 1,7 including in the formation of "so-called selective oxygen species, which take part in the process of oxo functionalization of hydrocarbons".…”
Section: Introductionmentioning
confidence: 99%