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Relationships between radium and radon occurrence and hydrochemistry in fresh groundwater from fractured crystalline rocks, North Carolina (USA)

机译:美国北卡罗来纳州裂隙结晶岩中新鲜地下水中镭和ra的发生与水化学的关系

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Naturally-occurring radionuclides (uranium, radium, and radon), major dissolved constituents, and trace elements were investigated in fresh groundwater in 117 wells in fractured crystalline rocks from the Piedmont region (North Carolina; USA). Chemical variations show a general transition between two water types: (1) slightly acidic (pH 5.0-6.0), oxic, low-total dissolved solids (TDS) waters, and (2) near neutral, oxic to anoxic, higher-TDS waters. The uranium, radium, and radon levels in groundwater associated with granite (Rolesville Granite) are systematically higher than other rock types (gneiss, metasedimentary, and metavolcanic rocks). Water chemistry plays a secondary role on radium and radon distributions as the ~(222)Rn/~(226)Ra activity ratio is correlated with redox-sensitive solutes such as dissolved oxygen and Mn concentrations, as well as overall dissolved solids content including major divalent cations and Ba. since ~(224)Ra/~(228)Ra activity ratios in groundwater are close to 1, we suggest that mobilization of Ra and Rn is controlled by alpha recoil processes from parent nuclides on fracture surfaces, ruling out Ra sources from mineral dissolution or significant long-distance Ra transport. Alpha recoil is balanced by Ra adsorption that is influenced by redox conditions and/or ion concentrations, resulting in an approximately one order of magnitude decrease (-20,000 to -2000) in the apparent Ra distribution coefficient between oxygen-saturated and anoxic conditions and also across the range of dissolved ion concentrations (up to ~ 7 mM). Thus, the U and Th content of rocks is the primary control on observed Ra and Rn activities in groundwater in fractured crystalline rocks, and in addition, linked dissolved solids concentrations and redox conditions impart a secondary control.
机译:在皮埃蒙特地区(北卡罗来纳州;美国)破裂的结晶岩中的117口井中,对新鲜地下水中的天然放射性核素(铀,镭和ra),主要溶解成分和微量元素进行了研究。化学变化显示了两种水之间的一般过渡:(1)弱酸性(pH 5.0-6.0),有氧,低总量溶解固体(TDS)水,以及(2)中性,有氧至无氧,高TDS水。与花岗岩(Rolesville花岗岩)相关的地下水中的铀,镭和ra水平系统地高于其他岩石类型(片麻岩,准沉积岩和中火山岩)。水化学在镭和ra的分布中起次要作用,因为〜(222)Rn /〜(226)Ra活性比与氧化还原敏感的溶质(例如溶解氧和Mn浓度)以及包括主要成分在内的总溶解固体含量相关二价阳离子和钡。由于地下水中〜(224)Ra /〜(228)Ra的活度比接近1,我们建议Ra和Rn的动员是由裂缝表面母核的α反冲过程控制的,排除了矿物溶解或溶解产生的Ra来源远距离Ra运输。阿尔法后坐力受氧化还原条件和/或离子浓度影响的Ra吸附平衡,导致氧饱和和缺氧条件之间的表观Ra分布系数降低大约一个数量级(-20,000到-2000)溶解离子浓度范围内(最高〜7 mM)。因此,岩石中的U和Th含量是控制裂缝结晶岩石中地下水中Ra和Rn活性的主要控制因素,此外,相关的溶解固体浓度和氧化还原条件可以提供辅助控制作用。

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