Experimental determination of the speciation, partitioning, and release of perrhenate as a chemical surrogate for pertechnetate from a sodalite-bearing multiphase ceramic waste form

• Published in: Applied geochemistry Vol. 42; pp. 47 - 59
• Main Authors: Pierce, E.M., Lukens, W.W., Fitts, J.P., Jantzen, C.M., Tang, G.
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier Ltd 01.03.2014; Elsevier
• Subjects: Aluminosilicates; Aluminum silicates; Ceramics; Earth sciences; Earth, ocean, space; Engineering and environment geology. Geothermics; Exact sciences and technology; Geochemistry; Multiphase; Nuclear waste; Pollution, environment geology; Sodalite; Wastes; Weathering; rhenium; technetium; ion exchange; fine-grained materials; nosean; X-rays; cycles; aluminum; radionucleids; storage; Earth; aluminosilicates; silicates; framework silicates; anions; waste management; synthesis; cations; absorption; oxidation; weathering; concentration; sodalite; speciation; sodium; materials; nepheline
• ISSN: 0883-2927; 1872-9134
• DOI: 10.1016/j.apgeochem.2013.12.017

[Display omitted] •Multiphase ceramic waste form is composed of primarily of nepheline, nosean, and sodalite.•Rhenium is in the 7+ oxidation state and has partitioned to a mixed Re-bearing sodalite phase.•Mechanism of corrosion for the multiphase matrix is similar to other silicate minerals.•A mixed-anion sodalite phases controls Re release in the multiphase waste forms. A key component to closing the nuclear fuel cycle is the storage and disposition of nuclear waste in geologic systems. Multiphase ceramic waste forms have been studied extensively as a potential host matrix for nuclear waste. Understanding the speciation, partitioning, and release behavior of radionuclides immobilized in multiphase ceramic waste forms is a critical aspect of developing the scientific and technical basis for nuclear waste management. In this study, we evaluated a sodalite-bearing multiphase ceramic waste form (i.e., fluidized-bed steam reform sodium aluminosilicate [FBSR NAS] product) as a potential host matrix for long-lived radionuclides, such as technetium (99Tc). The FBSR NAS material consists primarily of nepheline (ideally NaAlSiO4), anion-bearing sodalites (ideally M8[Al6Si6O24]X2, where M refers to alkali and alkaline earth cations and X refers to monovalent anions), and nosean (ideally Na8[AlSiO4]6SO4). Bulk X-ray absorption fine structure analysis of the multiphase ceramic waste form, suggest rhenium (Re) is in the Re(VII) oxidation state and has partitioned to a Re-bearing sodalite phase (most likely a perrhenate sodalite Na8[Al6Si6O24](ReO4)2). Rhenium was added as a chemical surrogate for 99Tc during the FBSR NAS synthesis process. The weathering behavior of the FBSR NAS material was evaluated under hydraulically unsaturated conditions with deionized water at 90°C. The steady-state Al, Na, and Si concentrations suggests the weathering mechanisms are consistent with what has been observed for other aluminosilicate minerals and include a combination of ion exchange, network hydrolysis, and the formation of an enriched-silica surface layer or phase. The steady-state S and Re concentrations are within an order of magnitude of the nosean and perrhenate sodalite solubility, respectively. The order of magnitude difference between the observed and predicted concentration for Re and S may be associated with the fact that the anion-bearing sodalites contained in the multiphase ceramic matrix are present as mixed-anion sodalite phases. These results suggest the multiphase FBSR NAS material may be a viable host matrix for long-lived, highly mobilie radionuclides which is a critical aspect in the management of nuclear waste.