State Key Laboratory of Radiation Medicine and Protection, School for Radiological and interdisciplinary Sciences (RAD-X) and Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Soochow University, Suzhou, 215123, People's Republic of China.
Department of Earth and Planetary Science, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Environ Sci Pollut Res Int. 2018 Nov;25(32):32617-32630. doi: 10.1007/s11356-018-3252-z. Epub 2018 Sep 21.
The competitive binding trends of Ni(II) and Eu(III) on montmorillonite in the absence/presence of Na-oxalate are explored by using batch sorption/desorption technique, speciation modeling, and X-ray diffraction (XRD) analysis. With a series of molar Ni:Eu ratios (i.e., 1:1, 5:1, 10:1, 1:5, and 1:10), the coexisting Ni(II) did not affect the sequestration behaviors and immobilization mechanisms of Eu(III). In contrast, the presence of Eu(III) obviously suppressed the sorption percentages of Ni(II) in the acidic pH range. Even though no obvious influence of Eu(III) on the macroscopic binding trends of Ni(II) was observed under alkaline conditions, the fraction of Ni(II) adsorbed by the inner-sphere complexation mechanism decreased and that of Ni(II) precipitation increased with rising molar Ni:Eu ratio. The coexisting Na-oxalate did not influence Eu(III) sorption, while inhibited the sorption of Ni(II). The XRD analysis indicated the potential formation of two Eu-oxalate precipitate phases (i.e., Eu(CO)·xHO(s)-1 and Eu(CO)·xHO(s)-2) at different pH values (4.0 and 6.5) and Na-oxalate concentrations (ranging from 0.5 to 5.0 mM). Interestingly, the Eu(CO)·xHO(s)-2 phase would be transformed into the Eu(CO)·xHO(s)-1 solid with the increase of Na-oxalate concentration. The research findings could provide essential data for evaluating the fate of coexistent Eu(III) and Ni(II) in the complicated aquatic environment.
采用批量吸附/解吸技术、形态建模和 X 射线衍射(XRD)分析研究了在不存在/存在草酸钠的情况下,蒙脱土对 Ni(II)和 Eu(III)的竞争结合趋势。在一系列摩尔比 Ni:Eu(即 1:1、5:1、10:1、1:5 和 1:10)下,共存的 Ni(II) 不会影响 Eu(III)的固持行为和固定机制。相比之下,在酸性 pH 范围内,Eu(III)的存在明显抑制了 Ni(II)的吸附百分比。即使在碱性条件下,Eu(III)对 Ni(II)的宏观结合趋势没有明显影响,但内配位络合机制吸附的 Ni(II)分数减少,Ni(II)沉淀的分数增加,随着摩尔比 Ni:Eu 的增加而增加。共存的草酸钠不影响 Eu(III)的吸附,但抑制了 Ni(II)的吸附。XRD 分析表明,在不同的 pH 值(4.0 和 6.5)和草酸钠浓度(0.5 至 5.0 mM)下,Eu-草酸盐可能形成两种沉淀相(Eu(CO)·xHO(s)-1 和 Eu(CO)·xHO(s)-2)。有趣的是,随着草酸钠浓度的增加,Eu(CO)·xHO(s)-2 相将转化为 Eu(CO)·xHO(s)-1 固体。研究结果可为评估共存 Eu(III)和 Ni(II)在复杂水生态环境中的归宿提供重要数据。