XAS signatures of Am(III) adsorbed onto magnetite and maghemite
Publikation: Bidrag til tidsskrift › Konferenceartikel › Forskning › fagfællebedømt
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XAS signatures of Am(III) adsorbed onto magnetite and maghemite. / Finck, N.; Radulescu, L.; Schild, D.; Rothmeier, M.; Huber, F.; Lützenkirchen, J.; Rabung, T.; Heberling, F.; Schlegel, M. L.; Dideriksen, Knud; Nedel, Sorin; Geckeis, H.
I: Journal of Physics: Conference Series (Online), Bind 712, Nr. 1, 012085, 2016.Publikation: Bidrag til tidsskrift › Konferenceartikel › Forskning › fagfællebedømt
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TY - GEN
T1 - XAS signatures of Am(III) adsorbed onto magnetite and maghemite
AU - Finck, N.
AU - Radulescu, L.
AU - Schild, D.
AU - Rothmeier, M.
AU - Huber, F.
AU - Lützenkirchen, J.
AU - Rabung, T.
AU - Heberling, F.
AU - Schlegel, M. L.
AU - Dideriksen, Knud
AU - Nedel, Sorin
AU - Geckeis, H.
N1 - Conference code: 16
PY - 2016
Y1 - 2016
N2 - Trivalent americium was adsorbed on magnetite and maghemite under similar chemical conditions and the local environment probed by EXAFS spectroscopy. In both samples, partially hydrated Am(III) binds the surface but slightly different surface complexes were identified. On Fe3O4, Am(III) forms monomeric tridentate surface complexes similar to that reported for Pu(III) at the (111) surface. In contrast, the lower number of detected Fe atoms may suggest that Am(III) forms monomeric bidentate surface complexes on γ-Fe2O3. Alternatively, the lower Fe coordination number can also be due to the presence of vacancies in maghemite. XPS data imply very similar binding environments for Am at both Fe oxide surfaces.
AB - Trivalent americium was adsorbed on magnetite and maghemite under similar chemical conditions and the local environment probed by EXAFS spectroscopy. In both samples, partially hydrated Am(III) binds the surface but slightly different surface complexes were identified. On Fe3O4, Am(III) forms monomeric tridentate surface complexes similar to that reported for Pu(III) at the (111) surface. In contrast, the lower number of detected Fe atoms may suggest that Am(III) forms monomeric bidentate surface complexes on γ-Fe2O3. Alternatively, the lower Fe coordination number can also be due to the presence of vacancies in maghemite. XPS data imply very similar binding environments for Am at both Fe oxide surfaces.
U2 - 10.1088/1742-6596/712/1/012085
DO - 10.1088/1742-6596/712/1/012085
M3 - Conference article
AN - SCOPUS:84978719329
VL - 712
JO - Journal of Physics: Conference Series
JF - Journal of Physics: Conference Series
SN - 1742-6588
IS - 1
M1 - 012085
Y2 - 23 August 2015 through 28 August 2015
ER -
ID: 170765908