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Geochemistry of the rare-earth elements and uranium in the acidic Berkeley Pit lake, Butte, Montana

机译:蒙大拿州比尤特市酸性Berkeley Pit湖中稀土元素和铀的地球化学

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Filtered (0.45 mum) and nonfiltered concentrations of rare-earth elements (REE), U, Zr, Th, Ba, Sc, and Y were measured as a function of depth in the Berkeley Pit lake, a large acidic mining lake in Butte, MT. The REE show very little variation with depth, apart from a slight concentration near the surface, presumably due to evaporation. The REE profiles of the pit waters show a depletion in light REE when normalized against NASC and the host Butte Quartz Monzonite (BQM), and a possible enrichment in middle REE vs. heavy REE when normalized against BQM. All of the REE partitioned weakly into secondary ferric precipitates formed by aging of deep Berkeley Pit water. The measured distribution coefficients increased across the lanthanide series from La (K-d = 7.7) to Nd (K-d = 10.3), and then decreased steadily to Lu (K-d = 1.4). Under the conditions of the Berkeley Pit lake, the aqueous speciation of REE and U is dominated by sulfate complexes. Because the stability constants of REE-sulfate complexes show very little variation across the lanthanide series, the observed trends in Kd cannot be explained by aqueous complexation. Despite high concentrations of dissolved REE (e.g., 1.1 mg/l Ce) and U (0.85 mg/l), saturation indices for all solid phases were strongly negative, due to the low pH of the Berkeley Pit lake (2.3-2.6). The mobility of REE and U is more likely constrained by adsorption or co-precipitation with strengite, jarosite, schwertmannite, or other secondary minerals forming in the lake. (C) 2003 Elsevier Science B.V. All rights reserved. [References: 63]
机译:在Butte的一个大型酸性采矿湖Berkeley Pit湖中,测量了经过过滤(0.45毫米)和未过滤的稀土元素(REE),U,Zr,Th,Ba,Sc和Y的浓度与深度的关系。公吨。 REE显示出随深度的变化很小,除了可能是由于蒸发引起的表面附近的少量浓度外。井水的REE分布图相对于NASC和宿主的Butte Quartz Monzonite(BQM)归一化显示轻REE减少,而相对于BQM归一化的重REE可能富集。所有的REE都微弱地分成由伯克利深坑水老化形成的二次铁沉淀。镧系元素的测量分布系数从La(K-d = 7.7)到Nd(K-d = 10.3)逐渐增加,然后稳定地下降到Lu(K-d = 1.4)。在伯克利坑湖的条件下,稀土元素和铀的水形态以硫酸盐配合物为主。由于稀土元素硫酸盐配合物的稳定性常数在整个镧系元素上几乎没有变化,因此观察到的Kd趋势无法用水络合来解释。尽管溶解的REE(例如1.1 mg / l Ce)和U(0.85 mg / l)的浓度很高,但由于伯克利·皮特湖的pH较低(2.3-2.6),所有固相的饱和指数都强烈地为负。 REE和U的流动性更可能受到与湖泊中形成的硬石膏,黄钾铁矾,schwertmannite或其他次生矿物的吸附或共沉淀的限制。 (C)2003 Elsevier Science B.V.保留所有权利。 [参考:63]

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