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   <subfield code="a">Measurements and modelling of Pm sorption onto TiO2 and goethite</subfield>
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   <subfield code="c">[Anna-Maria Jakobsson, Yngve Albinsson, Robert S. Rundberg]</subfield>
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   <subfield code="a">The sorption of Pm (1×10-9M) onto TiO2 and goethite has been studied as a function of pH and ionic strength (0.01, 0.1M NaClO4) at ambient temperature under N2 atmosphere. For both minerals studied there is no effect of the different ionic strengths and the sorption (log Ka vs. pH) increases with a slope of ∼2. At the same pH sorption is lower on the more positively (or less negatively) charged goethite (pHpzc=8.4) than on the TiO2 (pHpzc=6.2). A comparison to other trivalent cations sorbed on different substrates (made by extracting values from %-sorbed curves and calculating these to Ka) indicate a similar pH-dependence. The results have been fitted using a 1-pK basic Stern model with FITEQL. An a priori restriction was that only one sorption reaction stoichiometry at a time was to be used to keep the number of parameters as small as possible. Outer-sphere and mono-, bi- and tri-dentate inner-sphere complexes were fitted. For each fit the value of the capacitance was varied to find the value that provided the best fit. Two different site densities were used: 1site/nm2 and 2.31sites/nm2. For the low site density the reaction which provides the best fit was: ≡SOH0.5-+Pm+3↔≡SOHPm2.5+ for both minerals. At the high site density the same reaction fits for TiO2 while there are several reactions that are equivalent in the fit for goethite.</subfield>
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   <subfield code="a">© 2004 Oldenbourg Wissenschaftsverlag GmbH</subfield>
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   <subfield code="t">Radiochimica Acta/International journal for chemical aspects of nuclear science and technology</subfield>
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