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Inagaki, Yaohiro*; Sakatani, Keiichi*; Yamamura, Yuki*; Mitsui, Seiichiro; Noshita, Kenji*; Miura, Yoshiyuki*; Kanehira, Norio*; Ochi, Eiji*; Mukunoki, Atsushi*; Chiba, Tamotsu*
Dai-7-Kai Saishori, Risaikuru Bukai Semina Tekisuto, p.136 - 137, 2011/01
Conventional static test methods are not appropriate to evaluate glass dissolution behavior at an arbitrarily-fixed condition due to compositional change of the solution with glass dissolution. In this study, we applied a newly-devised micro-channel flow-through test method to measurement of the initial dissolution rates of Japanese simulated waste glasses, JAEA-P0798 and JNFL-KMOC, at arbitrarily-fixed conditions and we evaluated temperature and pH dependence of glass dissolution. The results showed that the initial dissolution rate increased with temperature and had "V-shaped" pH dependence at each temperature.
Miki, Takahito*; Sasamoto, Hiroshi; Chiba, Tamotsu*; Inagaki, Manabu*; Yui, Mikazu
JNC TN8400 2000-007, 32 Pages, 2000/01
This report presents a summary of literature survey about geochemical reactions which are important to evaluate the redox conditions in the near field rock mass and buffer. The results of literature survey are summarized as follows; (1)Minerals including ferrous iron and organic materials in the rock mass are important reductants. Initial stage after closure of repository, oxygen will be consumed by pyrite, because the reaction rate between pyrite and oxygen is relatively fast. (2)It is possible to estimate the redox capacity for reductants by rock (mineral)-water iteraction experiment in a laboratory. And it is expected that the ferrous iron-rich rock and higher porosity rock may have bigger redox capacity. (3)It is possible to estimate the oxygen consumption rate by reductants such as minerals including ferrous iron. The rate law and rate constant for the oxidation reaction of ferrous iron in the solution are also determined. As a conclusion, it seems that we can evaluate kinetically the evolution of geochemical conditions in the near field rock mass and buffer by excavation of drifts, based on data derived from these existing literatures.
Chiba, Tamotsu*; Sasamoto, Hiroshi; Miki, Takahito*; Inagaki, Manabu*; Yui, Mikazu
JNC TN8400 99-027, 144 Pages, 1999/06
It is planned that high level radioactive waste is going to be disposed under deep geological environment. It is believed that the chemical condition of deep groundwater is generally anoxic and reducing. However, during construction and operation phase of repository, oxygen will diffuse some distance into the surrounding rock mass, and diffused oxygen may remain in the surrounding rock mass even after repository closure. In such a case, the transitional redox condition around the drift is not preferable in view point of safety assessment for HLW disposal. Hence, it is very important to evaluate evolution of redox conditions in the near field. This report describes results of preliminary analysis for evolution of redox conditions in the near field rock mass and buffer after repository closure based on the model developed by Chiba et al. (1999). The results of preliminary analysis are summalized as follows : (1)The decrease of oxygen in the near field rock mass and buffer are affected by pH of groundwater and surface area of iron-bearing minerals. (2)The decrease of oxygen in the near field rock mass takes place at time scales lower than 500 years in considering the hypothetical reference groundwater pH range for H12 report. It is implicated that the redox conditions in the near field rock mass will recover to reducing conditions. (3)The decrease of oxygen in the buffer takes place at time scales lower several tens years under neutral to weakly alkaline pH values of porewater in the buffer, even if it is assumed that residual oxygen in the near field rock mass after repository closure will diffuse into the buffer. On the other hand, under weakly acid pH values of porewater in the buffer, it may be presumed that oxygen remain in the buffer at time scale more than 500 years.
Sasamoto, Hiroshi; Yui, Mikazu; Chiba, Tamotsu*; Miki, Takahito*; Inagaki, Manabu*
JNC TN8400 99-019, 30 Pages, 1999/02
Deep underground is thought to be a potential place for high level radioactive waste repository. It is believed that the chemical condition of deep groundwater is generally anoxic and reducing. However, during construction and operation phase of repository, oxygen will diffuse some distance into the surrounding rock mass, and diffused oxygen may remain in the surrounding rock mass even after repository closure. In such a case, the transitional redox condition around the drift is not preferable in view point of safety assessment for HLM disposal. Hence, it is very important to evaluate evolution of redox conditions in the near field. This report describes the status of model development to evaluate evolution of redox conditions in the near field. We use the commercial solver to equate the mathematical equations which mean evolution of redox condition in the near field. The target area modeled in this report are near field rock mass and engineered barrier (buffer). In case of near field rock mass, we consider the following two geological media : (1) porous media for sedimentary rock, (2)fractured media for crystalline rock. In case of the engineered barrier, we the regard buffer as porous media. We simulate the behavior of dissolved oxygen and Fe in groundwater during evolution of redox condition in the near field rock mass and the buffer. In case of the porous media, we consider diffusion of chemical species as dominant transport mechanism. On the other hand, in case of the fractured media, we consider diffusion of chemical species in rock matrix and advection of that (only dissolved oxygen considered in this model) in fracture as transport mechanism. We also use the rate raw of iron oxidation reaction and dissolution of Fe-bearing minerals in this model besides.
Ikeda, Takao*; Amaya, Takayuki*; Chiba, Tamotsu*
PNC TJ1281 97-004, 42 Pages, 1997/03
It is very important to explain the sorption mechanisms of relevant radionuclides, for the performance assessment of geological disposal and for the technical development of engineering barrier system. In the previous studies 1993-1996, these tests were carried out to understand sorption mechanism of SN; -solubility tests -sorption tests onto bentonite, pure montmorillonite, A-FEO(OH) -extraction tests from these minerals -sorption tests onto tuff as a next step, these tests were carried out ragarding SN in this study; -diffusion tests (in-diffusion) -tests for effect of SN concentration and ionic strength on sorption -sorption tests onto granite -tests for effect of coexistent ions on solubility
Amaya, Takayuki*; Suzuki, Kazunori*; Chiba, Tamotsu*; Oda, Chie; Yoshikawa, Hideki; Yui, Mikazu
Materials Research Society Symposium Proceedings, Vol.465, p.751 - 758, 1997/00
None
Chiba, Takanori*; Sato, Seichi*; Kozaki, Tamotsu*; Miyauchi, Yoshihiro*; Kozai, Naofumi; Onuki, Toshihiko
no journal, ,
Redistribution behavior of C in acetate between rock and water have been examined in anaerated condition. In the presence of nitrate salt
C prefer to transport in air.
Tanaka, Shingo; Sato, Haruo; Niizato, Tadafumi; Amano, Kenji; Nohara, Tsuyoshi; Iwatsuki, Teruki; Murakami, Hiroaki; Sugita, Yutaka; Nakayama, Masashi; Abe, Hironobu; et al.
no journal, ,
The sorption distribution coefficients of cesium and iodine onto the soil are studied. The batch sorption experiments were conducted onto the 24 specimens obtained from 11 sites (12 geoslicers) at each two different depth compartment. The experiments were based on the way standardized by Atomic Energy Society of Japan. The Kd values of cesium ranged from 1,000 to 100,000 ml/g, corresponding to the result that most of the cesium in the investigation sites are stayed in the surface of the ground. On the other hand, the Kd values of iodine ranged from 0.4 to 150 ml/g. It is likely that the difference of Kd values is affected by not only the chemical form of the elements between cesium and iodine, but also mineral composition, cation and anion exchange capacities, content of organic matter, and so on. This investigation initially focuses on varieties of soil, such as sandy or clayey soil, and soil colors.
Chiba, Takanori*; Yokochi, Takuya*; Kozaki, Tamotsu*; Sato, Seichi*; Miyauchi, Yoshihiro*; Kozai, Naofumi; Onuki, Toshihiko
no journal, ,
Partitioning behavior of acetic C in sedimentary rock has been studied in anaerobic atomosphere condition. Addition of nitrate salt in the solution showed good correlation between increase of oncentration of
C in air and decrease of concentration of nitate salts. These results suggest that respiration of nitrifying bacteria result in the transformation of
C.
Ebashi, Takeshi; Kawamura, Makoto; Inagaki, Manabu; Shibata, Masahiro; Chiba, Tamotsu*
no journal, ,
no abstracts in English