Details
Original language | English |
---|---|
Pages (from-to) | 966-976 |
Number of pages | 11 |
Journal | Dalton Transactions |
Volume | 44 |
Issue number | 3 |
Publication status | Published - 24 Nov 2014 |
Abstract
Non-selective luminescence spectroscopy and luminescence line-narrowing spectroscopy were used to study the retention of UO22+ on titanium dioxide (TiO2), synthetic calcium silicate hydrate (C-S-H) phases and hardened cement paste (HCP). Non-selective luminescence spectra showed strong inhomogeneous line broadening resulting from a strongly disordered UO22+ bonding environment. This problem was largely overcome by using luminescence line-narrowing spectroscopy. This technique allowed unambiguous identification of three different types of UO22+ sorbed species on C-S-H phases and HCP. Comparison with spectra of UO22+ sorbed onto TiO2 further allowed these species to be assigned to a surface complex, an incorporated species and an uranate-like surface precipitate. This information provides the basis for mechanistic models describing the UO22+ sorption onto C-S-H phases and HCP and the assessment of the mobility of this radionuclide in a deep geological repository for low and intermediate level radioactive waste (L/ILW) as this kind of waste is often solidified with cement prior to storage. This journal is
ASJC Scopus subject areas
- Chemistry(all)
- Inorganic Chemistry
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In: Dalton Transactions, Vol. 44, No. 3, 24.11.2014, p. 966-976.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - A luminescence line-narrowing spectroscopic study of the uranium(vi) interaction with cementitious materials and titanium dioxide
AU - Tits, Jan
AU - Walther, Clemens
AU - Stumpf, Thorsten
AU - Macé, Nathalie
AU - Wieland, Erich
PY - 2014/11/24
Y1 - 2014/11/24
N2 - Non-selective luminescence spectroscopy and luminescence line-narrowing spectroscopy were used to study the retention of UO22+ on titanium dioxide (TiO2), synthetic calcium silicate hydrate (C-S-H) phases and hardened cement paste (HCP). Non-selective luminescence spectra showed strong inhomogeneous line broadening resulting from a strongly disordered UO22+ bonding environment. This problem was largely overcome by using luminescence line-narrowing spectroscopy. This technique allowed unambiguous identification of three different types of UO22+ sorbed species on C-S-H phases and HCP. Comparison with spectra of UO22+ sorbed onto TiO2 further allowed these species to be assigned to a surface complex, an incorporated species and an uranate-like surface precipitate. This information provides the basis for mechanistic models describing the UO22+ sorption onto C-S-H phases and HCP and the assessment of the mobility of this radionuclide in a deep geological repository for low and intermediate level radioactive waste (L/ILW) as this kind of waste is often solidified with cement prior to storage. This journal is
AB - Non-selective luminescence spectroscopy and luminescence line-narrowing spectroscopy were used to study the retention of UO22+ on titanium dioxide (TiO2), synthetic calcium silicate hydrate (C-S-H) phases and hardened cement paste (HCP). Non-selective luminescence spectra showed strong inhomogeneous line broadening resulting from a strongly disordered UO22+ bonding environment. This problem was largely overcome by using luminescence line-narrowing spectroscopy. This technique allowed unambiguous identification of three different types of UO22+ sorbed species on C-S-H phases and HCP. Comparison with spectra of UO22+ sorbed onto TiO2 further allowed these species to be assigned to a surface complex, an incorporated species and an uranate-like surface precipitate. This information provides the basis for mechanistic models describing the UO22+ sorption onto C-S-H phases and HCP and the assessment of the mobility of this radionuclide in a deep geological repository for low and intermediate level radioactive waste (L/ILW) as this kind of waste is often solidified with cement prior to storage. This journal is
UR - http://www.scopus.com/inward/record.url?scp=84919390942&partnerID=8YFLogxK
U2 - 10.1039/c4dt02172j
DO - 10.1039/c4dt02172j
M3 - Article
AN - SCOPUS:84919390942
VL - 44
SP - 966
EP - 976
JO - Dalton Transactions
JF - Dalton Transactions
SN - 1477-9226
IS - 3
ER -