Hostname: page-component-848d4c4894-2xdlg Total loading time: 0 Render date: 2024-06-21T16:51:24.511Z Has data issue: false hasContentIssue false

The Solubility and Sorption of Radium and Tin in a Cementitious Near-Field Environment

Published online by Cambridge University Press:  26 February 2011

S Bayliss
Affiliation:
Chemistry Division, Harwell Laboratory, UKAEA, Oxfordshire, 0X11 ORA.
F. T. Ewart
Affiliation:
Chemistry Division, Harwell Laboratory, UKAEA, Oxfordshire, 0X11 ORA.
R. M. Howse
Affiliation:
Chemistry Division, Harwell Laboratory, UKAEA, Oxfordshire, 0X11 ORA.
S. A. Lane
Affiliation:
Chemistry Division, Harwell Laboratory, UKAEA, Oxfordshire, 0X11 ORA.
N. J. Pilkington
Affiliation:
Chemistry Division, Harwell Laboratory, UKAEA, Oxfordshire, 0X11 ORA.
J. L. Smith-Briggs
Affiliation:
Chemistry Division, Harwell Laboratory, UKAEA, Oxfordshire, 0X11 ORA.
S. J. Williams
Affiliation:
Chemistry Division, Harwell Laboratory, UKAEA, Oxfordshire, 0X11 ORA.
Get access

Abstract

The solubility and sorption of radium and tin have been studied for a cementitious near-field environment.

The solubility of radium was observed to be greater than 10−7M, even with the addition of IM sulphate to the cement equilibrated water. The values of Rn for radium varied from 102 to 103 ml g−1 for the cement types and initial radium concentrations studied.

The solubility of tin was observed to be about 10−4M for a range of cement equilibrated waters above tin oxides and metallic tin. The solubility of tin was observed to increase with pH. Tin solubilities were not affected by the redox conditions. Tin was present in a range of particle sizes in the sorption studies. A value of RD of 104 ml g−1 was observed for tin species less than 0.45μm.

Type
Research Article
Copyright
Copyright © Materials Research Society 1989

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

[1] Ewart, F. T. and Tasker, P W, Chemical Effects in the Near-Field. ‘Waste Management ‘87’, Tuscon, Arizona, March 1987.Google Scholar
[2] Atkinson, A.. UKAEA Report AERE R11777 (1985).Google Scholar
[3] Sharland, S M, Tasker, P W and Tweed, C J. UKAEA Report AERE R12442 (1986).Google Scholar
[4] Robinson, P. C., Hodgkinson, D P, Tasker, P W, Lever, D A, Windsor, M E, Grime, P W and Herbert, A W. UKAEA Report AERE R11854 (1988).Google Scholar
[5] Ewart, F T, Howse, R M, Thomason, H P, Williams, S J and Cross, J E. IX Symposium Scientific Basis for Nuclear Waste Management, Ed. Werne, L, Publ. Elsevier, New York (1986).Google Scholar
[6] Bayliss, S, Ewart, F T, Howse, R M, Smith-Briggs, J L, Thomason, H P and Willmott, H A. XI Symposium on Scientific Basis for Nuclear Waste Management, Ed. Apted, M J and Westerman, R L, Publ.Google Scholar
[7] Berry, J A, Hobley, J, Lane, S A, Littleboy, A K, Nash, M J, Oliver, P, Smith-Briggs, J L and Williams, S J. The solubility and sorption of protactinium in the near-field and far-field environments of a radioactive waste repository. 2nd International Conference on Nuclear and Radiochemistry, Brighton, UK, July 1988.Google Scholar
[8] Pilkington, N J, Shadbolt, P J and Wilkins, J D. Preliminary experimental measurements of the Solubilities of selected long-lived fission products, activatic products and actinide daughters under near-field conditions. UKAEA AERE R13006 (to be published).Google Scholar
[9] Baes, C F Jr. and Mesmer, R E. The Hydrolysis of Cations, John Wiley and Sons, New York, 1976.Google Scholar
[10] Cross, J E, Ewart, F T and Tweed, C J. UKAEA Report AERE R12324 (1987).Google Scholar
[11] Pourbaix, M. Atlas of Electrochemical Equilibria in Aqueous Solutions, p479. Pergamon Press (1966).Google Scholar