Loughborough University
Leicestershire, UK
LE11 3TU
+44 (0)1509 263171
Loughborough University

Loughborough University Institutional Repository

Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/3114

Title: Competitive effect of iron(III) on metal complexation by humic substances : characterisation of ageing processes
Authors: Lippold, Holger
Evans, Nicholas D.M.
Warwick, Peter
Kupsch, H.
Keywords: Humic substances
Iron (Fe)
Europium (Eu)
Issue Date: 2007
Publisher: © Elsevier
Citation: LIPPOLD, H. ... et al, 2007. Competitive effect of iron(III) on metal complexation by humic substances : characterisation of ageing processes. Chemosphere, 67 (5), pp. 1050-1056
Abstract: Aiming at an assessment of counteractive effects on colloid-borne migration of actinides in the event of release from an underground repository, competition by Fe(III) in respect of metal complexation by dissolved organic matter was investigated for the example of Eu(III) as an analogue of trivalent actinides. Complexation with different humic materials was examined in cation exchange experiments, using 59Fe and 152Eu as radioactive tracers for measurements in dilute systems as encountered in nature. Competitive effects proved to be significant when Fe is present at micromolar concentrations. Flocculation as a limiting process was attributed to charge compensation of humic colloids. Fe fractions bound to humic acids (HA) were higher than 90%, exceeding the capacity of binding sites at high Fe concentrations. It is thus concluded that the polynuclear structure of hydrolysed Fe(III) is maintained when bound to HA, which is also inferred from UV-Vis spectrometry. The competitive effect was found to be enhanced if Fe and HA were contacted before Eu was added. Depending on the time of Fe/HA pre-equilibration, Eu complexation decreased asymptotically over a time period of several weeks, the amount of bound Fe being unchanged. Time-dependent observations of UV-Vis spectra and pH values revealed that the ageing effect was due to a decline in Fe hydrolysis rather than structural changes within HA molecules. Fe polycations are slowly degraded in contact with humic colloids, and more binding sites are occupied as a consequence of dispersion. The extent of degradation as derived from pH shifts depended on the Fe/HA ratio.
Description: This article was published in the journal, Chemosphere [© Elsevier]. It is also available at: http://www.sciencedirect.com/science/journal/00456535
URI: https://dspace.lboro.ac.uk/2134/3114
ISSN: 0045-6535
Appears in Collections:Published Articles (Chemistry)

Files associated with this item:

File Description SizeFormat
Manuscript Eu-HA-Fe.pdf109.8 kBAdobe PDFView/Open


SFX Query

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.