| Literature DB >> 24997962 |
Angelica Bianco1, Marco Minella1, Elisa De Laurentiis1, Valter Maurino1, Claudio Minero1, Davide Vione2.
Abstract
The irradiation of L-tryptophan, L-tyrosine and 4-phenoxyphenol in aqueous solution produced compounds with similar fluorescence properties as humic substances, and with absorption spectra that were significantly extended into the UVA and visible regions compared to the starting compounds. The irradiated systems had photosensitizing properties, as proven by the photodegradation of 2,4,6-trimethylphenol and furfuryl alcohol (probes of excited triplet states and (1)O2, respectively). The described photochemical processes could constitute an additional pathway for the formation of humic substances in clear and shallow water bodies, which would be added to the complex network of reactions involving dissolved organic matter.Entities:
Keywords: Autochthonous and allochthonous organic matter; Environmental photochemistry; Excitation–emission matrix; Photoinduced transformation; Singlet oxygen; Triplet sensitizers
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Year: 2014 PMID: 24997962 DOI: 10.1016/j.chemosphere.2014.04.035
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086