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000138578 037__ $$aFZJ-2013-04677
000138578 1001_ $$0P:(DE-Juel1)144040$$aBrandt, Felix$$b0$$eCorresponding author$$ufzj
000138578 1112_ $$aGoldschmidt Conference 2013$$cFirenze$$d2013-08-25 - 2013-08-30$$wItaly
000138578 245__ $$aSolid solution formation and uptake of Radium in the presence of barite
000138578 260__ $$c2013
000138578 3367_ $$0PUB:(DE-HGF)6$$2PUB:(DE-HGF)$$aConference Presentation$$bconf$$mconf$$s1382439850_8542$$xOther
000138578 3367_ $$033$$2EndNote$$aConference Paper
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000138578 520__ $$aThe phase relations in the BaSO4-RaSO4-H2O system may determine the solubility of radium in natural waters due to the formation of a solid solution. In the near-field of nuclear waste repositories for spent fuel, radium may enter a system in which barite is in equilibrium with the aqueous solution. Thermodynamically, a RaxBa1-xSO4 solid solution is expected to form as solubility controlling phase rather than RaSO4. However, due to a lack of reliable data, the solid solution system RaSO4-BaSO4-H2O is currently not considered in long term safety assessments for nuclear waste repositories. The solubility product of the pure RaSO4 endmember is poorly constrained between pKRaSO4 = 10.26 to 10.41 by only very few experimental data [1,2]. Published interaction parameters WBaRa of the RaSO4-BaSO4-H2O system varies varies in different studies [3, 4] between 0.9 and 3.9 - 6.5 kJ/mol.
In this study we have combined experimental data, atomistic calculations and thermodynamic modeling to study in detail how a radium containing solution will equilibrate with solid BaSO4 under repository relevant conditions. Batch sorption experiments at close to equilibrium conditions indicate the formation of a RaxBa1-xSO4 solid. Our first principles calculations based on the single defect method [5] indicate a value of WBaRa = 2.5 ± 1.0 kJ/mol, implying a non-ideal solid solution. Thermodynamic assessment calculations indicate that the final experimental Ra(aq) concentration at room temperature and 90 °C can be matched with
WBaRa ≈ 1.5 kJ/mol and pKRaSO4 ≈ 10.41.
[1] Lind, S. C., et al (1918). J Am Chem Soc 40, 465-472. [2] Paige, C. R. et al.(1998). Geochim. Cosmochim. Acta 62, 15-23. [3] Zhu, C., 2004. Geochim. Cosmochim. Acta 68, 3327-3337. [4] Curti, E., et al. (2010). Geochim. Cosmochim. Acta 74, 3553-3570. [5] Sluiter & Kawazoe (2002) Europhys Lett. 57, 526-532.
000138578 536__ $$0G:(DE-HGF)POF2-142$$a142 - Safety Research for Nuclear Waste Disposal (POF2-142)$$cPOF2-142$$fPOF II$$x0
000138578 536__ $$0G:(EU-Grant)269688$$aSKIN - Slow processes in close-to-equilibrium conditions for radionuclides in water/solid systems of relevance to nuclear waste management (269688)$$c269688$$fFP7-Fission-2010$$x1
000138578 7001_ $$0P:(DE-Juel1)130364$$aKlinkenberg, Martina$$b1$$ufzj
000138578 7001_ $$0P:(DE-Juel1)144348$$aVinograd, Victor$$b2$$ufzj
000138578 7001_ $$0P:(DE-Juel1)144076$$aRozov, Konstantin$$b3$$ufzj
000138578 7001_ $$0P:(DE-Juel1)130324$$aBosbach, Dirk$$b4$$ufzj
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000138578 9131_ $$0G:(DE-HGF)POF2-142$$1G:(DE-HGF)POF2-140$$2G:(DE-HGF)POF2-100$$3G:(DE-HGF)POF2$$4G:(DE-HGF)POF$$aDE-HGF$$bEnergie$$lNukleare Sicherheitsforschung$$vSafety Research for Nuclear Waste Disposal$$x0
000138578 9141_ $$y2013
000138578 9201_ $$0I:(DE-Juel1)IEK-6-20101013$$kIEK-6$$lNukleare Entsorgung und Reaktorsicherheit$$x0
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