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Arthur, R. C,*; Savage, D.*; Sasamoto, Hiroshi; Shibata, Masahiro; Yui, Mikazu
JNC TN8400 2000-005, 61 Pages, 2000/01
JNC-TN8400-2000-005.pdf:2.83MB
Kinetic data, including rate constants, reaction orders and activation energies, are compiled for 34 hydrolysis reactions involving feldspars, sheet silicates, zeolites, oxides, pyroxenes and amphiboles, and for similar reactions involving calcite and pyrite. The data are compatible with a rate law consistent with surface reaction control and transition-state theoly, which is incorporated in the geochemieal software package EQ3/6 and GWB. Kinetic data for the reactions noted above are strictly compatible with the transition-state rate law only under far-from-equilibrium conditions. It is possiblethat the data are conceptually consistent with this rate law under both far-from-equilibrium and near-to-equilibrium conditions, but this should be confirmed whenever possible through analysis of original experimental results, Due to limitations in the availability of kinetic data for mineral-water reactions, and in order to simplify evaluations of geochemical models of groundwater evolution, it is convenient to assume local-equilibrium in such models whenever possible. To assess whether this assumption is reasonable, a modeling approach accounting for coupled fluid flow and water-rock interaction is described that can be used to estimate spatial and temporal scale of local equiliblium. The approach is demonstrated for conditions involving groundwater flow in fractures at JNC's Kamaishi in-situ tests site, and is also used to estimate the travel time necessary for oxidizing surface waters to migrate to the level of a HLW repository in crystalline rock. The question of whether local equilibrium is a reasonable assumption must be addressed using an appropriate modeling approach. To be appropriate for conditions at the Kamaishi site using the modeling approach noted above, the fracture fill must closely approximate a porous medium, groundwater flow must be purely advective and diffusion of solutes across the fracture-host rock boundary must not occur. Moreover, the ...
Sasamoto, Hiroshi; Yui, Mikazu; Randolph C Arthu*
JNC TN8400 99-074, 84 Pages, 1999/12
Hydrochemical investigation of Tertiary sedimentary rocks at JNC's Tono in-situ tests site indicate the groundwaters are: (1)meteoric in origin, (2)chemically reducing at depths greater than a few tens of meters in the sedimentary rock, (3)relatively old [carbon-14 ages of groundwaters collected from the lower part of the sedimentary sequence range from 13,000 to 15,000 years BP (before present)] (4)Ca-Na-HCO
type solutions near the surface, changing to Na-HCO type groundwaters with increasing depth. The chemical evolution of the groundwaters is modeled assuming local equilibrium for selected mineral-fluid reactions, taking into account the rainwater origin of these solutions. Results suggest it is possible to interpret approximately the "real" groundwater chemistry (i.e., pH, Eh, total dissolved concentrations of Si, Na, Ca, K, Al, carbonate and sulfate) if the following assumptions are adopted: (1)CO
concentration in the gas phase contacting pore solutions in the overlying soil zone = 10
bar, (2)minerals in the rock zone that control the solubility of respective elements in the groundwater include; chalcedony (Si), albite (Na), kaolinite (Al), calcite (Ca and carbonate), muscovite (K) and pyrite (Eh and sulfate). It is noted, however, that the available field data may not be sufficient to adequately constrain parameters in the groundwater evolution model. In particular, more detailed information characterizing certain site properties (e.g., the actual mineralogy of "plagioclase", "clay" and "zeolite") are needed to improve the model. Alternative conceptual models of key reactions may also be necessary. For this reason, a model that accounts for ion-exchange reactions among clay minerals, and which is based on the results of laboratory experiments, has also been evaluated in the present study. Further improvements of model considering ion-exchange reactions are needed in future, however.
Sasaki, Yuji; *; *; *; *
Chikyu Kagaku, 23, p.97 - 103, 1989/00
no abstracts in English
Iyatomi, Yosuke; Ishibashi, Masayuki; Matsui, Hiroya; Uyama, Masao*; Hitomi, Takashi*
no journal, ,
no abstracts in English
Iyatomi, Yosuke; Ishibashi, Masayuki; Matsui, Hiroya; Uyama, Masao*; Hitomi, Takashi*
no journal, ,
no abstracts in English
