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   <subfield code="a">Effect of humic acid on the sorption of Cm(III) onto γ-Al2O3 studied by the time-resolved laser fluorescence spectroscopy</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[X. K. Wang, Thomas Rabung, Horst Geckeis, Petra J. Panak, R. Klenze, Thomas Fanghänel]</subfield>
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   <subfield code="a">Sorption of Cm(III) onto γ-alumina coated with humic acid (HA) is studied by the Time Resolved Laser Fluorescence Spectroscopy (TRLFS). The experiments are performed at 0.1M NaClO4, 0.44g/L γ-Al2O3, 10mg/L HA and at a metal ion concentration of 2×10-7mol/L. At the investigated pH range (4 to 10) HA is completely sorbed to γ-Al2O3. The excitation spectrum of Cm(III) bound to HA/γ-Al2O3 in the wavelength range 370-400nm exhibits broad flat bands very different from those obtained for the Cm(III) aquo ion and the Cm(III)-γ-Al2O3 surface complex, respectively. The spectrum, lacking distinctive structure due to intramolecular energy transfer processes, points to the predominant binding of the Cm(III) to surface-bound HA. TRLFS experiments performed at two different excitation wavelengths (λex=355 and 396.6nm) allow for a differentiation of humic-bound and non-humic-bound Cm(III). Differences in fluorescence spectra obtained at the different excitation wavelengths are found at pH&lt;6.9. They are due to the presence of the non-complexed Cm(III) aquo ion which is not detected in the indirect excitation mode (λex=355nm). At pH≥7, the fluorescence spectra obtained by indirect and direct excitation become congruent and again point to the existence of only humic-bound Cm(III) species. Comparison of peak maxima and fluorescence lifetimes for Cm(III)-HA and Cm(III)-HA/γ-Al2O3, however, reveal differences. The results clearly indicate a contribution of the γ-Al2O3 surface to the Cm(III) binding and, thus, suggest the formation of ternary complexes such as &gt;Al-O-Cm(III)(HA).</subfield>
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