Influence of photochemical reactions on the complexation of humic acid with europium(III)

Citation
Jm. Monsallier et al., Influence of photochemical reactions on the complexation of humic acid with europium(III), J PHOTOCH A, 138(1), 2001, pp. 55-63
Citations number
33
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
ISSN journal
10106030 → ACNP
Volume
138
Issue
1
Year of publication
2001
Pages
55 - 63
Database
ISI
SICI code
1010-6030(20010101)138:1<55:IOPROT>2.0.ZU;2-V
Abstract
Photochemical reactions in the Eu(III)-humic acid system are investigated b y fluorescence spectroscopy. For comparison, humic acid without europium is also studied. Irradiation is performed by high energy laser beam and a low pressure mercury lamp. The impact of photodegradation on spectroscopic pro perties, size and decomposition of humic acid is monitored by steady state and time-resolved fluorescence spectroscopy, W-Vis spectroscopy, gel permea tion chromatography (GPC), dissolved organic carbon (DOC) analysis and ultr afiltration. The different indicators for photodegradation show different s ensitivity. The decrease in DOC content with increasing irradiation dose is lower than the decrease in UV/Vis absorption. The highest impact is found for the fluorescence intensity. At 3 kJ/mg humic acid absorbed energy and i n absence of europium, fluorescence diminishes by more than 90%. In the pre sence of Eu(III), however, fluorescent groups are partly stabilized in this range of absorbed energy. Results from GPC show changes in the chemical st ructure, especially generation of smaller entities. The photodegradation of the humic acid leads to a decrease of the europium-humate complexation con stant. Furthermore, europium is reduced to the divalent state. The present study shows that for metal ion humic acid complexation studies by laser flu orescence spectroscopy, great care is needed to avoid significant experimen tal artifacts, such as photodegradation and metal ion redox reactions. (C) 2001 Published by Elsevier Science B.V.