Abstract
A calculation method for determining the amount of Rn isotopes and daughter products at the start of measurement (CRAS) is proposed as a more accurate means of estimating the initial Rn concentration in soil gas. The CRAS utilizes the decay law between 222Rn and 220Rn isotopes and the daughter products 218Po and 216Po, and is applicable to α-scintillation counter measurements. As Rn is both inert and chemically stable, it is useful for fault investigation based on the soil gas geochemistry. However, the total number of α particles emitted by the decay of Rn has generally been considered to be proportional to the initial Rn concentration, without considering the gas condition with respect to radioactive equilibrium. The CRAS method is shown to be effective to derive Rn concentration for soil gases under both nonequilibrium conditions, in which the total number of decays increases with time, and equilibrium conditions, which are typical of normal soil under low gas flux. The CRAS method in conjunction with finite difference method simulation is applied to the analysis of two active fault areas in Japan, and it is demonstrated that this combination could detect the sharp rises in 222Rn concentrations associated with faults. The method also allows the determination of fault geometry near the surface based on the asymmetry variation of the Rn concentration distribution when coupled with a numerical simulation of 222Rn transport. The results for the new method as applied to the two case studies are consistent with the data collected from the geological survey. It implies that the CRAS method is suitable for investigating the fault system and interstitial gas mobility through fractures. The present analyses have also demonstrated that high Rn concentrations require the recent and repeated accumulation of 222Rn parents (230Th and 226Ra) in fault gouges through deep gas release during fault movement.
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