首页> 外文期刊>Analytical methods >Synthesis and characterization of a novel nanostructured ion-imprinted polymer for pre-concentration of Y(III) ions
【24h】

Synthesis and characterization of a novel nanostructured ion-imprinted polymer for pre-concentration of Y(III) ions

机译:Y(III)离子预浓缩的新型纳米结构离子印迹聚合物的合成与表征

获取原文
           

摘要

A nanostructured Y(III) ion imprinted polymer (IIP) was synthesized by preparing a complex of Y(III) ions with 1,4-dihydroxy-9,10-anthraquinone (QZ) as a chelating agent. The Y(III) ion was found to form a 1:1 stable complex with QZ in 2-methoxyethanol solution. The prepared complex was then copolymerized with ethylene glycoldimethacrylate (cross-linking monomer), 2-hydroxyethyl methacrylate (functional monomer) and 2,2-azobis-isobutyronitrile (initiator) via a precipitation polymerization method. The imprinted Y(III) ion was removed using a 3 mol La?’1 HCl solution to obtain leached IIP nanoparticles. Non-imprinted polymer particles were similarly prepared without Y(III) ions. The polymers were characterized by Fourier transform IR spectroscopy, scanning electron microscopy (SEM), dispersive X-ray spectroscopy, thermogravimetric analysis and N2 sorptiona€“desorption isotherms. The SEM images of synthesized polymers exhibited nano-patterns. The effect of several parameters such as solution pH, sorption and desorption time, type, concentration, and volume of eluent on the extraction were investigated and optimized one variable at a time. The optimum pH for maximum sorption was 8.9. The maximum sorbent capacity of the IIP was 18.05 mg ga?’1. Following desorption, Y(III) was determined by inductively coupled plasma-atomic emission spectroscopy. A limit of detection and relative standard deviation (n = 6) of 0.9 ng mLa?’1 and 2.2%, respectively, were obtained. The method was applied in the determination of yttrium in a certified reference material and a radioyttrium sample to demonstrate the accuracy and applicability of the presented method.
机译:通过制备Y(III)离子与1,4-二羟基-9,10-蒽醌(QZ)作为螯合剂的配合物来合成纳米结构的Y(III)离子印迹聚合物(IIP)。发现Y(III)离子在2-甲氧基乙醇溶液中与QZ形成1:1稳定的络合物。然后通过沉淀聚合法将制备的络合物与乙二醇二甲基丙烯酸酯(交联单体),甲基丙烯酸2-羟乙酯(官能单体)和2,2-偶氮二异丁腈(引发剂)共聚。使用3 mol La?1 HCl溶液去除印迹的Y(III)离子,以获得浸出的IIP纳米颗粒。类似地制备不含Y(III)离子的非压印聚合物颗粒。通过傅里叶变换红外光谱,扫描电子显微镜(SEM),色散X射线光谱,热重分析和N2吸附-解吸等温线对聚合物进行了表征。合成聚合物的SEM图像显示出纳米图案。考察了溶液pH值,吸附和解吸时间,洗脱液的类型,浓度和体积等几个参数对萃取的影响,并一次优化了一个变量。最大吸附的最适pH为8.9。 IIP的最大吸附容量为18.05 mg ga?’1。解吸后,通过电感耦合等离子体原子发射光谱法确定Y(III)。检出限和相对标准偏差(n = 6)分别为0.9 ng mLa?-1和2.2%。该方法用于测定标准参考物质和放射性钇样品中的钇,以证明所提出方法的准确性和适用性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号