监测不同模板/单体比例在离子印迹聚合物中提取Ra(II)的效果

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2023-02-01 DOI:10.1016/j.sampre.2022.100049
Marine Boudias , Alkiviadis Gourgiotis , Charlotte Cazala , Valérie Pichon , Nathalie Delaunay
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引用次数: 2

摘要

在我们之前的论文中,首次合成了一种离子印迹聚合物(IIP),该聚合物以Ba(II)为模板离子,以乙腈/二甲基亚砜(1/1,v/v)为致孔剂,乙烯基膦酸为络合单体,苯乙烯为共聚单体,二乙烯基苯为交联剂,具有接近Ra(II)的性质,可用于提取Ra(Ⅱ)。本研究旨在研究模板离子/单体比例(1/4、1/6和1/8)对吸附剂性能的影响。将聚合物装入固相萃取(SPE)筒中进行表征。特别注意控制该比率对Ra(II)和干扰离子(即特异性)在IIP上的保留、它们的容量和它们的穿透体积的影响。尽管IIP 1/4和1/8的特异性略高于IIP 1/6,但IIP 1/4的吸附能力(0.3µmol g−1)远低于其他两种(3µmol g–1)。数据建模表明,Sips和Redlich-Peterson模型最适合,这表明与Langmuir模型相比,单层吸附过程进入不完全均匀的空腔。IIP 1/6和1/8都显示出高的穿透体积(对于在100mg吸附剂上渗透的100ng Ba(II),>80mL),并且BET实验显示单体比例对IIP 1/4、1/6和1/8的表面积没有影响。在IIP 1/6上评估了合成的可重复性。由三种独立合成的IIP 1/6得到的SPE图谱非常相似,热重和BET分析也证实了三种IIP具有相似的物理特性。IIP 1/6应用于从掺入的矿泉水(Mont-Roucous®和Volvic®)中提取Ba(II)。Ba(II)萃取回收受到基质效应的影响,但这些影响是通过使吸附剂的量与渗滤溶液的体积相适应来解决的。优化程序首次成功应用于在真实样品中使用专用IIP提取226Ra:在5 mL Mont Roucous®水中掺入226Ra和228Ra的80 mBq L−1,用作示踪剂,通过同位素稀释进行定量。提取后,使用电感耦合等离子体质谱仪测定226Ra活性(88±7 mBq L−1,覆盖因子k=2)和IIP 1/6的回收率(93%),该方法的定量限估计为19 mBq L−1(0.52 pg L−1)。
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Monitoring the benefits of varying the template/monomer proportion in the synthesis of an ion-imprinted polymer for Ra(II) extraction

In our previous paper, an ion-imprinted polymer (IIP) was for the first time synthesized for Ra(II) extraction using Ba(II) as template ion since it has properties close to Ra(II), acetonitrile/dimethylsulfoxide (1/1, v/v) as porogen, vinylphosphonic acid as complexing monomer, styrene as co-monomer, and divinylbenzene as cross-linker. The present study aims at investigating the influence of the template ion/monomer proportion (1/4, 1/6, and 1/8) on sorbents properties. Polymers were packed in solid phase extraction (SPE) cartridges for characterization. A particular attention was paid to control the impact of this ratio on the retention of Ra(II) and interfering ions (i.e. specificity) on IIPs, their capacity, and their breakthrough volume. Although the IIPs 1/4 and 1/8 tended to be slightly more specific than IIP 1/6, the adsorption capacity of the IIP 1/4 was much lower (0.3 µmol g−1) than the two others (3 µmol g−1). Data modelling indicated that Sips and Redlich-Peterson models were best fitted, sign of a monolayer adsorption process into cavities not completely homogeneous in contrast to the Langmuir model. IIPs 1/6 and 1/8 showed both high breakthrough volumes (>80 mL for 100 ng of Ba(II) percolated on 100 mg of sorbents) and BET experiments demonstrated no impact of the monomer proportion on surface area of the IIPs 1/4, 1/6, and 1/8. The repeatability of the synthesis was evaluated on the IIP 1/6. The SPE profiles resulting from three independent syntheses of the IIP 1/6 were very similar and thermogravimetric and BET analyses also confirmed that the three IIPs had similar physical characteristics. The IIP 1/6 was applied to the extraction of Ba(II) from spiked mineral waters (Mont Roucous® and Volvic®). The Ba(II) extraction recovery was subjected to matrix effects but those were solved by adapting the amount of sorbent to the volume of percolation solution. The optimized procedure has been successfully applied to extract 226Ra for the first time with a dedicated IIP in a real sample: 5 mL of Mont Roucous® water were spiked with 80 mBq L−1 of 226Ra and 228Ra which was used as tracer to perform quantification by isotope dilution. After extraction, the 226Ra activity (88 ± 7 mBq L−1, coverage factor k = 2) and recovery on IIP 1/6 (93%) were determined using an Inductively Coupled Plasma Mass Spectrometer and the limit of quantification of the method was estimated at 19 mBq L−1 (0.52 pg L−1).

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