Hostname: page-component-848d4c4894-r5zm4 Total loading time: 0 Render date: 2024-06-23T08:02:23.607Z Has data issue: false hasContentIssue false

The initial dissolution rates of simulated UK Magnox–ThORP blend nuclear waste glass as a function of pH, temperature and waste loading

Published online by Cambridge University Press:  02 January 2018

N. Cassingham
Affiliation:
Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK
C.L. Corkhill*
Affiliation:
Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK
D.J. Backhouse
Affiliation:
Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK
R.J. Hand
Affiliation:
Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK
J.V. Ryan
Affiliation:
Energy and Environment Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA
J.D. Vienna
Affiliation:
Energy and Environment Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA
N.C. Hyatt*
Affiliation:
Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The first comprehensive assessment of the dissolution kinetics of simulant Magnox–ThORP blended UK high-level waste glass, obtained by performing a range of single-pass flow-through experiments, is reported here. Inherent forward rates of glass dissolution were determined over a temperature range of 23 to 70°C and an alkaline pH range of 8.0 to 12.0. Linear regression techniques were applied to the TST kinetic rate law to obtain fundamental parameters necessary to model the dissolution kinetics of UK high-level waste glass (the activation energy (Ea), pH power law coefficient (η) and the intrinsic rate constant (k0)), which is of importance to the post-closure safety case for the geological disposal of vitreous products. The activation energies based on B release ranged from 55 ± 3 to 83 ± 9 kJ mol–1, indicating that Magnox–THORP blend glass dissolution has a surface-controlled mechanism, similar to that of other high-level waste simulant glass compositions such as the French SON68 and LAW in the US. Forward dissolution rates, based on Si, B and Na release, suggested that the dissolution mechanism under dilute conditions, and pH and temperature ranges of this study, was not sensitive to composition as defined by HLW-incorporation rate.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
Copyright © The Mineralogical Society of Great Britain and Ireland 2015. This is an open access article, distributed under the terms of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2015

References

Abraitis, P.K., Livens, F.R., Monteith, J.E., Small, J.E., Trivedi, D.P., Vaughan, D.J. and Wogelius, R.A. (2000a) The kinetics and mechanisms of simulated British Magnox waste glass dissolution as a function of pH, silicic acid activity and time in low-temperature aqueous systems. Applied Geochemistry, 15, 13991416.CrossRefGoogle Scholar
Abraitis, P.K., McGrail, B.P., Trivedi, D.P., Livens, F.R. and Vaughan, D.J. (2000b) Single-pass flow-through experiments on a simulated glass in alkaline media at 40°C. I. Experiments conducted at variable solution flow rate to glass surface area. Journal of Nuclear Materials, 280, 196205.CrossRefGoogle Scholar
Abraitis, P.K., McGrail, B.P., Trivedi, D.P., Livens, F.R. and Vaughan, D.J. (2000c) Single-pass flow-through experiments on a simulated glass in alkaline media at 40°C. II. Experiments conducted with buffer solutions containing controlled quantities of Si and Al. Journal of Nuclear Materials, 280, 206215.CrossRefGoogle Scholar
ASTM (1994) Standard Test Methods for determining the chemical durability of nuclear waste glasses: The Product Consistency Test (PCT). ASTM C1285-94, Annual Book of ASTM Standards, Philadelphia, USA.Google Scholar
Brady, P.V. and House, W.A. (1996) Surface-controlled dissolution and growth of minerals. Pp. 225-306 in: Physics and Chemistry of Mineral Surfaces (P.V. Brady, editor). CRC Press, New York.Google Scholar
Cassingham, N.J., Stennett, M.C., Bingham, P.A. and Hyatt, N.C. (2011) The structural role of Zn in nuclear waste glasses. International Journal of Applied Glass Science, 2, 343353.CrossRefGoogle Scholar
Corkhill, C.L., Cassingham, N.J., Heath, P.G. and Hyatt, N.C. (2013) Dissolution of UK high-level waste glass under simulated hyperalkaline conditions of a co-located geological disposal facility. International Journal of Applied Glass Science, 4, 341356.CrossRefGoogle Scholar
Connelly, A.J., Hyatt, N.C., Travis, K.P., Hand, R.J., Maddrell, E.R. and Short, R.J. (2011) The structural role of Zr within alkali borosilicate glasses for nuclear waste immobilisation. Journal of Non-Crystalline Solids, 357, 16471656.CrossRefGoogle Scholar
Curti, E., Crovisier, J.L., Morvan, G., and Karpoff, A.M. (2006) Long-term corrosion of two nuclear waste reference glasses (MW and SON68): A kinetic and mineral alteration study. Applied Geochemistry, 21, 11521168.CrossRefGoogle Scholar
Della Mea, G., Gasparatto, A., Bettinelli, M., Montenero, A. and Scaglioni, R. (1986) Chemical durability of zinc-containing glasses. Journal of Non-Crystalline Solids, 84, 443451.CrossRefGoogle Scholar
Dove, P.M. (1994) The dissolution kinetics of amorphous silica into sodium chloride solutions: effects of temperature and ionic strength. American Journal of Science, 294, 665712.CrossRefGoogle Scholar
Gin, S., Beaudoux, X., Angeli, F., Jegou, C. and Godon, N. (2012) Effect of composition on the short-term and long-term dissolution rates often borosilicate glasses of increasing complexity from 3 to 30 oxides. Journal of Non-Crystalline Solids, 358, 25592570.CrossRefGoogle Scholar
Gin, S., Abdelouas, A., Criscenti, L.J., Ebert, W.L., Ferrand, K., Geisler, T., Harrison, M.T., Inagaki, Y., Mitsui, S., Mueller, K.T., Marra, J.C., Pantano, C.G., Pierce, E.M., Ryan, IV, Schofield, J.M., Steefel, C.I and Vienna, J.D. (2013a) An international initiative on long-term behavior of high-level nuclear waste glass. Materials Today, 16, 243248.CrossRefGoogle Scholar
Gin, S., Frugier, P., Jollivet, P., Bruguier, F. and Curti, E. (2013b) New insight into the residual rate of borosilicate glasses: Effect of s/v and glass composition. International Journal of Applied Glass Science, 4, 371382.CrossRefGoogle Scholar
Harrison, M.T., Steele, C.J. and Riley, A.D. (2012) The effect on long term aqueous durability of variations in the composition of UK vitrified HLW product. Glass Technology: European Journal of Glass Science and Technology A, 53, 211216.Google Scholar
Hyatt, N.C., Taylor, K.J., Gibb, F.G. and Lee, W.E. (2004) Crystallisation of Magnox waste glass under conditions of very high temperature, very deep, geological disposal. Glass Technology, 45, 6870.Google Scholar
Icenhower, J.P. and Dove, P.M. (2000) The dissolution kinetics of amorphous silica in sodium chloride solutions: effects of temperature and ionic strength. Geochimica et Cosmochimica Acta, 64, 41934203.CrossRefGoogle Scholar
Icenhower, J.P. and Steefel, C.I. (2013) Experimentally determined dissolution kinetics of SON68 glass at 90°C over a silica saturation interval: Evidence against a linear rate law. Journal of Nuclear Materials, 439, 137147.CrossRefGoogle Scholar
Icenhower, IP, Strachan, D.M., McGrail, B.P., Scheele, R.D., Rodriguez, E.A., Steele, J.L. and Legore, V.L. (2006) Dissolution kinetics of pyrochlore ceramics for the disposition of plutonium. American Mineralogist, 91, 3953.CrossRefGoogle Scholar
Icenhower, IP, McGrail, B.P., Shaw, W.J., Pierce, E.M., Nachimuthu, P., Shuh, D.K., Rodriguez, E.A. and Steele, J.L. (2008) Experimentally determined dissolution kinetics of Na-rich borosilicate glass at far from equilibrium conditions: Implications for Transition State Theory. Geochimica et Cosmochimica Acta, 72, 27672788.CrossRefGoogle Scholar
Jollivet, P., Gin, S. and Schumacher, S. (2012) Forward dissolution rate of silicate glasses of nuclear interest in clay-equilibrated groundwater. Chemical Geology, 330-331, 207-217.Google Scholar
Lasaga, A.C. (1981) Transition state theory. Pp. 135-168 in: Kinetics of Geochemical Processes (A.C Lasaga and R.J. Kirkpatrick, editors). Reviews in Mineralogy, 8, Mineralogical Society of America, Washington DC.Google Scholar
Lasaga, A.C. (1995) Fundamental approaches in describing mineral dissolution and weathering rates. Pp. 23-86 in: Chemical Weathering Rates of Silicate Minerals (A.F. White and S.L. Brantley, editors). Reviews in Mineralogy, 31, Mineralogical Society of America, Washington DC.Google Scholar
Marsal, F., De Windt, L. and Pellegrini, D. (2007) Modelling of long term geochemical evolution of the bentonite buffer of KBS-3 repository. Institute de Radioprotection et de Sûreté Nucléaire, Report DSU/ SSIAS number 3.Google Scholar
Material Characterisation Centre (MCC) (1981) Nuclear Waste Materials Handbook, DOE/TIC 11400, Pacific Northwest Laboratory, Richmond, Washington, USA.Google Scholar
McGrail, B.P. and Peeler, D.K (1995) Evaluation of the single-pass flow-through test to support a low-activity waste specification. PNL-10746, Pacific Northwest Laboratory, Richmond, Washington, USA.Google Scholar
McGrail, B.P., Ebert, W.L., Bakel, A.J. and Peeler, D.K. (1997) Measurement of kinetic rate law parameters on a Na-Ca-Al borosilicate glass for low-activity waste. Journal of Nuclear Materials, 249, 175189.CrossRefGoogle Scholar
Nuclear Decommissioning Authority (2014) 2013 UK Radioactive Waste Inventory: Waste Quantities from all Sources. NDA Report NDA/ST/STY(14)0010, February 2014.Google Scholar
Pierce, E.M., Icenhower, J.P., Serne, R.J. and Catalano, J. (2005) Experimental determination of UO2(cr) dissolution kinetics: effects of solution saturation state and pH. Journal of Nuclear Materials, 345, 206218.CrossRefGoogle Scholar
Pierce, E.M., Rodriguez, E.A., Calligan, L.J., Shaw, W.J. and McGrail, B.P. (2008) An experimental study of the dissolution rates of simulated aluminoboro silicate waste glasses as a function of pH and temperature under dilute conditions. Applied Geochemistry, 223, 25592573.CrossRefGoogle Scholar
Pierce, E.M., Reed, L.R., Shaw, W.J., McGrail, B.P., Icenhower, J.P., Windisch, C.F., Cordova, E.A. and Borady, J. (2010) Experimental determination of the effect of the ratio of B/Al on glass dissolution along the nepheline (NaAlSiO4) - malinkoite (NaBSiO4) join. Geochimica et Cosmochimica Acta, 74, 26342654.CrossRefGoogle Scholar
Utton, C.A., Swanton, S.W., Schofield, J., Hand, R.J., Clacher, A. and Hyatt, N.C. (2012) Chemical durability of vitrified wasteforms: effects of pH and solution composition. Mineralogical Magazine, 76, 29192930.CrossRefGoogle Scholar
Vernaz, E. and Dussossoy, L.J. (1992) Current state of knowledge of nuclear waste glass corrosion mechanisms: the case of R7T7 glass. Applied Geochemistry, 1, 1322.Google Scholar
Wellman, D.M., Icenhower, J.P., Gamerdinger, A.P. and Forrester, S.W. (2006) Effects of pH, temperature and aqueous organic material on the dissolution kinetics of meta-autunite materials, (Na, Ca)2_! [(UO2)(PO4)]2-3H2O. American Mineralogist, 91, 143158.CrossRefGoogle Scholar
Wolff-Boenisch, D., Gislason, S.R., Oelkers, E.H. and Putnis, C. (2004) The dissolution rates of natural glasses as a function of their composition at pH 4 and 10.6, and temperatures from 25 to 74°C. Geochimica et Cosmochimica Acta, 68, 48434858.CrossRefGoogle Scholar
Zapol, P., He, H., Kwon, K.D. and Crisenti, L.J. (2013) First-principles study of hydrolysis reaction barriers in a sodium borosilicate glass. International Journal of Applied Glass Science, 4, 395407.CrossRefGoogle Scholar
Zhang, H., Corkhill, C.L., Heath, P.G., Hand, R.J., Stennett, M.C. and Hyatt, N.C. (2015) Effect of Zn-and Ca-oxides on the structure and chemical durability of simulant alkali borosilicate glasses for immobilisation of UK high level wastes. Journal of Nuclear Materials, 462, 321328.CrossRefGoogle Scholar