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Selective solid phase extraction of copper using a new Cu(II)-imprinted polymer and determination by inductively coupled plasma optical emission spectroscopy (ICP-OES)

机译:使用新型Cu(II)印迹聚合物选择性固相萃取铜并通过电感耦合等离子体发射光谱法(ICP-OES)测定

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摘要

This work reports the preparation of a novel Cu(II)-ion imprinted polymer using 2-thiozylmethacrylamide (TMA) for on-line preconcentration of Cu(II) prior to its determination by inductively coupled optical emission spectroscopy (ICP-OES). Cu(II)-TMA monomer (complex) was synthesized and copolymerized via bulk polymerization method in the presence of ethyleneglycoldimethacrylate cross-linker. The resulting polymer was washed with 5% (v/v) HNO3 to remove Cu(II) ions and then with water until a neutral pH. The ion imprinted polymer was characterized by FT-IR and scanning electron microscopy. The experimental conditions were optimized for on-line preconcentration of Cu(II) using a minicolumn of ion imprinted polymer (IIP). Quantitative retention was achieved between pH 5.0 and 6.0, whereas the recoveries for the non-imprinted polymer (NIP) were about 61%. The IIP showed about 30 times higher selectivity to Cu(II) in comparison to NIP. The IIP also exhibited excellent selectivity for Cu(II) against the competing transition and heavy metal ions, including Cd, Co, Cr, Fe, Mn, Ni, Pb and Zn. Computational calculations revealed that the selectivity of IIP was mediated by the stability of Cu(II)-TMA complex which was far more stable than those of Co(II), Ni(II) and Zn(II) that have similar charge and ionic radii to Cu(II). A volume of 10 mL sample solution was loaded onto the column at 4.0 mL min−1 by using a sequential injection system (FIALab 3200) followed by elution with 1.0 mL of 2% (v/v) HNO3. The relative standard deviation (RSD) and limit of detection (LOD, 3s) of the method were 3.2% and 0.4 μg L−1, respectively. The method was successfully applied to determination of Cu(II) in fish otoliths (CRM 22), bone ash (SRM 1400) and coastal seawater and estuarine water samples.
机译:这项工作报告了在使用电感耦合光发射光谱法(ICP-OES)测定之前,使用2-巯基甲基丙烯酰胺(TMA)在线预浓缩Cu(II)制备新型Cu(II)离子印迹聚合物。合成了Cu(II)-TMA单体(配合物),并在乙烯甲基丙烯酸二甲基丙酯交联剂的存在下,通过本体聚合法进行了共聚。将所得聚合物用5%(v​​ / v)HNO3洗涤以除去Cu(II)离子,然后用水洗涤直至中性pH。通过FT-IR和扫描电子显微镜对离子印迹聚合物进行表征。使用离子印迹聚合物(IIP)的小柱对Cu(II)的在线预浓缩进行了优化的实验条件。在pH 5.0和6.0之间实现了定量保留,而非印迹聚合物(NIP)的回收率约为61%。与NIP相比,IIP对Cu(II)的选择性高出约30倍。 IIP还显示出对Cu(II)对抗竞争性过渡离子和重金属离子(包括Cd,Co,Cr,Fe,Mn,Ni,Pb和Zn)的出色选择性。计算结果表明,IIP的选择性是由Cu(II)-TMA络合物的稳定性所介导的,该稳定性远比具有相似电荷和离子半径的Co(II),Ni(II)和Zn(II)稳定。到Cu(II)。使用顺序进样系统(FIALab 3200),以4.0 mL min -1 的体积将10 mL样品溶液上样到色谱柱上,然后用1.0 mL 2%(v / v)HNO3洗脱。该方法的相对标准偏差(RSD)和检出限(LOD,3s)分别为3.2%和0.4μgL -1 。该方法已成功地用于测定鱼耳石(CRM 22),骨灰(SRM 1400)以及沿海海水和河口水样品中的Cu(II)。

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