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Sorption of radionuclides onto natural clay rocks

机译:放射性核素在天然粘土岩石上的吸附

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Reactions of U(VI) and Eu/Cm(III) with natural clay rock (Opalinus Clay, Switzerland, and Callovo-Oxfordian Clay, France) are investigated by batch and spectroscopic experiments as well as geochemical calculations. The aim of the Studies is to identify those minerals in the heterogeneous multiphase systems with sometimes high calcite content which control lanthanide and actinide sorption. The Outcome of batch sorption studies with natural clay rocks (2 g/L natural clay rock, 0.1 mol/L NaClO4, pH 3-11) and thermodynamic calculations is compared with experimental results using a synthetic mixture consisting of purified Na-montmorillonite and calcite (ratio 80 : 20 wt. %). Our studies show that U(VI) sorption decreases at intermediate pH (6.5-9) where dissolved U(VI) carbonate species predominate. In the high pH region (> 9) U(VI) sorption again increases by formation of tertiary hydroxo Surface complexes on the clay mineral fraction, whereby calculated U(VI) sorption overestimates experimental data for the natural rock. Complete sorption to natural clay rock and the synthetic clay/calcite mixture is observed for Eu(III) at pH > 7 for the conditions studied. Model calculations again point to the predominance of clay-sorbed species even though calculated speciation underestimates the experimentally observed sorption at pH 6-9 slightly. Preliminary time-resolved laser-fluorescence spectroscopy (TRLFS) studies using Cm(III) as fluorescent probe reveal the appearance of several Cm(III)-clay surface species in the pH range 5-11, but give no indications for the presence of calcite-bound Cm(III). We conclude that the clay minerals in the multiphasic clay rock act as main sorbents for tri- and hexavalent actinides.
机译:通过分批和光谱实验以及地球化学计算研究了U(VI)和Eu / Cm(III)与天然粘土岩石(瑞士的Opalinus Clay和法国的Callovo-Oxfordian粘土)的反应。研究的目的是确定异质多相系统中有时控制方解石和high系元素吸附的方解石含量高的那些矿物。使用由纯蒙脱土和方解石组成的合成混合物,将天然粘土岩石(2 g / L天然粘土岩石,0.1 mol / L NaClO4,pH 3-11)的批次吸附研究结果和热力学计算结果与实验结果进行了比较。 (比例80∶20重量%)。我们的研究表明,在中等pH值(6.5-9)下,溶解的U(VI)碳酸盐种类占主导地位,U(VI)的吸附降低。在高pH值区域(> 9),通过在粘土矿物级分上形成叔羟基表面复合物,U(VI)的吸附再次增加,从而计算出的U(VI)吸附高估了天然岩石的实验数据。在所研究的条件下,对于pH> 7的Eu(III),观察到了对天然粘土岩石和合成粘土/方解石混合物的完全吸附。尽管计算得出的物种略微低估了在pH 6-9下实验观察到的吸附,但是模型计算再次指出了粘土吸附物质的优势。使用Cm(III)作为荧光探针的时间分辨激光荧光光谱(TRLFS)的初步研究揭示了在pH范围5-11内几种Cm(III)-粘土表面物种的出现,但未提供方解石的存在的迹象结合的Cm(III)。我们得出的结论是,多相粘土岩石中的粘土矿物是三价和六价act系元素的主要吸附剂。

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