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Magnetic iron oxide and manganese-doped iron oxide nanoparticles for the collection of alpha-emitting radionuclides from aqueous solutions

机译:磁性氧化铁和锰掺杂的氧化铁纳米粒子用于从水溶液中收集发射α的放射性核素

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摘要

Magnetic nanoparticles are well known to possess chemically active surfaces and large surface areas that can be employed to extract a range of ions from aqueous solutions. Additionally, their superparamagnetic properties provide a convenient means for bulk collection of the material from solution after the targeted ions have been adsorbed. Herein, two nanoscale amphoteric metal oxides, each possessing useful magnetic attributes, were evaluated for their ability to collect trace levels of a chemically diverse range of alpha emitting radioactive isotopes (polonium (Po), radium (Ra), uranium (U), and americium (Am)) from a wide range of aqueous solutions. The nanomaterials include commercially available magnetite (Fe3O4) and magnetite modified to incorporate manganese (Mn) into the crystal structure. The chemical stability of these nanomaterials was evaluated in Hanford Site, WA ground water between the natural pH (~8) and pH 1. Whereas the magnetite was observed to have good stability over the pH range, the Mn-doped material was observed to leach Mn at low pH. The materials were evaluated in parallel to characterize their uptake performance of the alpha-emitting radionuclide spikes from ground water across a range of pH (from ~8 down to 2). In addition, radiotracer uptake experiments were performed on Columbia River water, seawater, and human urine at their natural pH and at pH 2. Despite the observed leaching of Mn from the Mn-doped nanomaterial in the lower pH range, it exhibited generally superior analyte extraction performance compared to the magnetite, and analyte uptake was observed across a broader pH range. We show that the uptake behavior of the various radiotracers on these two materials at different pH levels can generally be explained by the amphoteric nature of the nanoparticle surfaces. Finally, the rate of sorption of the radiotracers on the two materials in unacidified ground water was evaluated. The uptake curves generally indicate that equilibrium is obtained within a few minutes, which is attributed to the high surface areas of the nanomaterials and the high level of dispersion in the liquids. Overall, the results indicate that these nanomaterials may have the potential to be employed for a range of applications to extract radionuclides from aqueous solutions.
机译:众所周知,磁性纳米颗粒具有化学活性表面和大表面积,可用于从水溶液中提取一系列离子。另外,它们的超顺磁性质为吸附目标离子后从溶液中大量收集材料提供了一种方便的方法。在此,对两种纳米级的两性金属氧化物进行了评估,它们分别具有有用的磁性,能够收集痕量水平的化学变化范围的α放射放射性同位素(pol(Po),镭(Ra),铀(U)和meric(Am))。纳米材料包括可商购的磁铁矿(Fe3O4)和经修饰将锰(Mn)掺入晶体结构的磁铁矿。这些纳米材料的化学稳定性在华盛顿州汉福德基地的自然pH(〜8)和pH 1之间进行了评估。尽管观察到磁铁矿在pH范围内具有良好的稳定性,但观察到Mn掺杂的材料会浸出。低pH下的Mn。对材料进行了并行评估,以表征其在pH值范围(约8至2)范围内从地下水吸收α发射放射性核素钉的性能。此外,在天然pH和pH 2的哥伦比亚河水,海水和人类尿液上进行了放射性示踪剂吸收实验。尽管在较低的pH范围内观察到Mn从掺杂Mn的纳米材料中浸出,但其分析物通常表现更好与磁铁矿相比具有更高的萃取性能,并在更宽的pH范围内观察到了分析物的吸收。我们表明,这两种材料在不同pH值下,各种放射性示踪剂的吸收行为通常可以通过纳米粒子表面的两性性质来解释。最后,评估了放射性示踪剂在两种材料在未酸化的地下水中的吸附速率。吸收曲线通常指示在几分钟内获得平衡,这归因于纳米材料的高表面积和在液体中的高分散度。总体而言,结果表明这些纳米材料可能具有用于从水溶液中提取放射性核素的一系列应用领域的潜力。

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