Low Level Radioactivity Laboratory, Institute of Nature and Environmental Technology, Kanazawa University, Wake, Nomi, Ishikawa 923-1224, Japan.
J Environ Radioact. 2010 Mar;101(3):201-10. doi: 10.1016/j.jenvrad.2009.10.009. Epub 2009 Nov 17.
Radium isotopes in 23 Na-Cl type groundwater sampled mainly from deep wells in Niigata Prefecture, which is the site of the largest oil- and gas-fields in Japan, were measured along with U isotopes, chemical components and hydrogen and oxygen isotope ratios to elucidate the distribution and behavior of Ra in a brackish environment underground. Also analyzed were U and Th isotopes in 38 rock samples collected from outcrops at 17 locations. Ra-226 concentrations (8.86-1637 mBq kg(-1)) of groundwater samples roughly correlated with total dissolved solid (TDS) concentrations and other alkaline earth contents. Their (228)Ra/(226)Ra activity ratios (0.32-5.2) were similar to or higher than the (232)Th/(238)U activity ratios (0.6-1.7) in the rocks. The most likely transport mechanism of Ra isotopes into groundwater was due to their alpha-recoil from the solid phase, probably from the water-rock interface where Th isotopes had accumulated, and adsorption/desorption reaction based on the increase in (226)Ra contents with TDS.
在日本最大的油气田所在地新潟县,主要从深井中采集的 23Na-Cl 型地下水的镭同位素与铀同位素、化学成分以及氢氧同位素比一起进行了测量,以阐明地下咸水环境中镭的分布和行为。还分析了从 17 个露头采集的 38 个岩石样本中的铀和钍同位素。地下水样本中的镭-226 浓度(8.86-1637 mBq kg(-1)) 与总溶解固体(TDS)浓度和其他碱土金属含量大致相关。它们的(228)Ra/(226)Ra 活度比(0.32-5.2)与岩石中的(232)Th/(238)U 活度比(0.6-1.7)相似或更高。镭同位素进入地下水的最可能的迁移机制是由于它们从固相的阿尔法反冲,可能来自于钍同位素积累的水-岩界面,以及基于 TDS 增加的吸附/解吸反应。