Dissolution of Basaltic Glass in Seawater : Experiments and Thermodynamic Modelling

1985 ◽  
Vol 50 ◽  
Author(s):  
J. L. Crovisier ◽  
B. Fritz ◽  
B. Grambow ◽  
J. P. Eberhart

The reaction of basalt glasses with natural waters were proposed as analog systems to the long-term alteration of nuclear waste glasses in the geosphere [1].

1985 ◽  
Vol 50 ◽  
Author(s):  
B. Grambow ◽  
M. J. Jercinovic ◽  
R. C. Ewing ◽  
C. D. Byers

AbstractLaboratory experiments alone cannot be used to verify models for the long-term release of radionuclides from nuclear waste glasses. Basalt glasses have been proposed as an appropriate natural analogue for the long-term validation of release models [1]. Their analogous behavior has been demonstrated in laboratory experiments in which both types of glasses display similar reaction rates, alteration products and surface layer morphologies [2,3]. This paper illustrates how empirical data from natural occurrences of basalt glass can be interpreted by a model which is developed to describe the reaction progress of the corrosion of nuclear waste form borosilicate glass [4,5].


1984 ◽  
Vol 44 ◽  
Author(s):  
C. D. Byers ◽  
M. J. Jercinovic ◽  
R. C. Ewing ◽  
K. Keil

AbstractThe long-term stability of nuclear waste form borosilicate glasses can be evaluated by understanding the processes that effect the long-term alteration of glass and by comparing laboratory alteration of synthetic basalt and borosilicate glasses with the observed stability of naturally occurring basaltic glasses in diverse geologic environments. This paper presents detailed electron microprobe analyses of naturally altered basaltic glasses (with maximum ages of 10,000 to 20 million years) from low-temperature environments. These results are compared to laboratory data on the corrosion of a synthetic basaltic glass in MCC-1 tests (90°C, a SA/V of 0.1 cm−1 and time periods up to 182 days), MCC-2 tests (190°C, a SA/V of 0.1 cm−1 and time periods up to 210 days) and hydration tests in saturated water vapor (240°C, an estimated SA/V of ∼ 106 cm−1 and time periods up to 63 days). Additionally, laboratory induced hydration alteration of synthetic basalt and borosilicate glasses is compared. These preliminary experiments provide evidence that the alteration processes observed for natural basalt glasses are relevant to understanding the alteration of nuclear waste glass, as both appear to react via similar processes.


Nature ◽  
1985 ◽  
Vol 314 (6008) ◽  
pp. 252-255 ◽  
Author(s):  
W. Lutze ◽  
G. Malow ◽  
R. C. Ewing ◽  
M. J. Jercinovic ◽  
K. Keil

Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 135
Author(s):  
Justyna Topolska ◽  
Bartosz Puzio ◽  
Olaf Borkiewicz ◽  
Julia Sordyl ◽  
Maciej Manecki

Although vanadinite (Pb5(VO4)3Cl) occurs in abundance in various terrestrial geochemical systems of natural and anthropogenic origin and is seriously considered as a potential nuclear waste sequestering agent, its actual application is severely limited by a lack of understanding of its basic thermodynamic parameters. In this regard, the greatest challenge is posed by its incongruent dissolution, which is a pivotal hurdle for effective geochemical modeling. Our paper presents an universal approach for geochemical computing of systems undergoing incongruent dissolution which, along with unique, long-term experiments on vanadinites’ stability, allowed us to determine the mineral solubility constant. The dissolution experiments were carried out at pH = 3.5 for 12 years. Vanadinite has dissolved incongruently, continuously re-precipitating into chervetite (Pb2V2O7) with the two minerals remaining in mutual equilibrium until termination of the experiments. The empirically derived solubility constant Ksp,V,298 = 10–91.89 ± 0.05 of vanadinite was determined for the first time. The proposed modeling method is versatile and can be adopted to other mineral systems undergoing incongruent dissolution.


1993 ◽  
Vol 333 ◽  
Author(s):  
A. Abdelouas ◽  
J. L. Crovisier ◽  
W. Lutze ◽  
R. Müller ◽  
W. Bernotat

ABSTRACTThe R7T7 and synthetic basaltic glasses were submitted to corrosion in a saline MgCl2dominated solution at 190°C. For both glasses, the early alteration product is a hydrotalcite-like compound in which HPO42-, SO4-2and Cl-substitutes to CO32. The measured d003spacing is 7.68 Å for the hydrotalcite formed from R7T7 glass and 7.62 Å for the hydrotalcite formed from basaltic glass which reflect the high aluminium content. Chemical microanalyses show that the hydrotalcite is subsequently covered by a silica-rich gel which evolves into saponite after few months.


1997 ◽  
Vol 506 ◽  
Author(s):  
F. Angeli ◽  
P. Faucon ◽  
T. Charpentier ◽  
J.C. Petit ◽  
J. Virlet

ABSTRACTThe local cation environments in a borosilicate glass (containing the main components of the French nuclear waste glass, R7T7) and of basaltic-like glass are presented on the basis of17A1 and23Na Multi-Quanta Magic-Angle Spinning Nuclear Magnetic Resonance (MQ-MAS NMR) spectroscopies. The chemical and geometrical environment of each nucleus is characterized. Moreover, qualitative information about the distribution of these parameters, characteristic of the disorder level in the structure, is obtained. These results are presented with the characteristics of the Al and Na dissolution in water at 100°C. The relation between the local environments of these cations and their mass loss in solution is discussed.


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