Bicarbonate-enhanced transformation of phenol upon irradiation of hematite, nitrate, and nitrite
Bicarbonate enhances the transformation of phenol upon irradiation of hematite, and phenolnitration upon irradiation of both nitrate and nitrite. Hematite under irradiation is able to oxidise the carbonate ion to the CO 3 -• radical, which in turn oxidises phenol to the phenoxyl radical faster compa...
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Veröffentlicht in: | Photochemical & photobiological sciences 2009, Vol.8 (1), p.91-100 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Bicarbonate enhances the transformation of phenol upon irradiation of hematite, and phenolnitration upon irradiation of both nitrate and nitrite. Hematite under irradiation is able to oxidise the carbonate ion to the CO
3
-•
radical, which in turn oxidises phenol to the phenoxyl radical faster compared to the direct photo-oxidation of phenol by hematite. The formation of CO
3
-•
from hematite and carbonate under irradiation is supported by the detection of3,3′-dityrosine from tyrosine, added as a probe for CO
3
-•
. It is shown that Fe(III) might be an important photochemical source of CO
3
-•
in Fe-rich waters,
e.g.
waters that contain more than 1 mg L
-1
Fe. The enhancement by bicarbonate of phenolnitration upon nitrate irradiation is probably accounted for by an increased photogeneration rate of nitrogen dioxide. The process could lead to enhanced phenol photonitration by nitrate in waters rich of inorganic carbon (>10 mM bicarbonate). Bicarbonate also increases the transformation and nitration rates of phenol upon nitrite photolysis. The effect is due to the combination of basification that enhances phenol nitrosation and nitration, and of peculiar bicarbonate chemistry. It is shown that bicarbonate-enhanced phenolnitration upon nitrite photolysis could be a significant photonitration pathway, leading to the generation of toxic nitrated compounds in natural waters in which the scavenging of hydroxyl radicals by nitrite is competitive with that of Dissolved Organic Matter (DOM). |
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ISSN: | 1474-905X 1474-9092 |
DOI: | 10.1039/b807265p |