Bentonite has been considered as a buffer material in a deep geological repository for high-level radioactive waste (HLW). Bentonite may come into contacted with various chemical solutions during the long-term storage. In particular, solutions containing K+ can affect stability of bentonite (e.g., illitization). The bentonite can be gradually saturated with the inflow of groundwater, and the temperature can rise simultaneously due to the decay of HLW. This study aimed to evaluate the bentonite stability in contacted with very highly concentrated K+ solutions with different pHs at 150°C. Batch reaction tests using KJ-II bentonite were performed for 30–150 days in teflon-stainless steel reactors. De-ionized (DI) water (pH = 6.0) and 1 M KCl (pH = 6.0), and 1 M KOH (pH = 12.5) solutions were used as reaction solutions. After completing batch reaction tests, the reacted samples were analyzed using various analytical techniques. For DI water, chemical, mineralogical, and physicochemical properties of reacted samples were similar to those of unreacted samples. For 1 M KCl solutions, cation exchage for Ca by K and slight changes in mineralogical properties of reacted samples were observed, but there are no significant changes in the physicochemical properties. In contrast, for 1 M KOH solutions, changes in chemical, mineralogical, and physicochemical properties of reacted samples were observed. Results of X-ray diffraction (XRD) analysis indicated dissolution of montmorillonite and formation of zeolite minerals, which were confirmed by thermogravimetricdifferential thermal analysis (TGA-DTA) and fourier transform infrared (FTIR) analysis. These results suggest that highly concentrated K+ (1 M) solution combined with high pH (12.5) and high temperate (150°C) may affect bentonite alteration. These prelimiary experiments were intended to qualitatively evaluate the mechanism and influncing factors of the buffer material alteration under extreme experimental conditions, and it is revealed that the conditions do not reflect the actual repository environment.

Resveratrol (3,4',5-trihydroxy-trans-stilbene), a naturally occuring polyphenol compound which present in the skin of grapes and red wine has been considered to posses chemopreventive and antioxidant properties. However, little is known about the cellular actions by which resveratrol mediates its therapeutic effects. In this study, the effect of resveratrol on cell proliferation and induction of apoptosis in human osteogenic sarcoma (HOS) cells was investigated. IC50 value was determined to be approximately 60μg/mℓ. Chromosomal DNA framgmentation analysis showed the appearance degraded DNA in time-and dose-dependent manner upon treatment of resveratrol. In order to observe the molecular mechanism involved in resveratrol-induced apoptosis, Western blot analysis was performed. We observed the decrease in the level of procaspase-3, the zymogen form of active caspase-3 in resveratrol-treated cells. This result implies that caspase-3 is activated upon treatment of resveratrol. The activation of caspase-3 was confirmed by the cleavage of poly(ADP-ribose) polymerase. Taken together, our data demonstrate that resveratrol has anti-proliferative effect on HOS cells and induced apoptosis through activation of caspase-3 and PARP cleavage.