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An ion imprinted amino-functionalized mesoporous sorbent for the selective minicolumn preconcentration of cadmium ions and determination by GFAAS

机译:一种离子印记的氨基官能化的中孔吸附剂,用于镉离子的选择性小聚丙烯前浓缩和GFAAs的测定

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摘要

An amino-functionalized mesoporous sorbent with double imprinting of Cd(ii) and surfactant micelles was prepared via the sol-gel co-condensation method. The material was employed for the highly selective preconcentration of cadmium ions in minicolumns (MCs) and their determination at ultratrace levels by graphite furnace atomic adsorption spectroscopy (GFAAS). For comparative purposes ion-imprinted (II) and non-imprinted (NI) solids were characterized by SEM, FTIR and nitrogen gas adsorption-desorption. Batch experiments including pH influence, sorption capacity and adsorption kinetics were carried out in order to optimize the adsorption-elution process. II showed a greater absorption capacity than the NI sorbent being 122 mg g(-1) and 67 mg g(-1) respectively, consistent with the Langmuir isotherm equation. Sample and elution flow rates, volumes of the sample and eluent and the choice of the most suitable eluent were tested and optimized under MC dynamic conditions for both sorbents. Under optimized conditions, the II filling showed a preconcentration factor (PCF) of 50 whilst that of NI was 10. The higher selectivity of filler II was revealed when comparing the maximum tolerable limit (MTL) of interfering cations and anions commonly found in water samples, the MTL for II being 100 to 200 times higher than that for NI for all the tested concomitants. The main figures of merit found for solid II are: a limit of detection of 0.0011 ng mL(-1) (3S(b)), a linear range of 0.01-20 ng mL(-1), and RSD% of 2 (n = 6; 0.05 ng mL(-1)). Additionally, the operation under dynamic conditions together with the employment of low volumes of the sample and eluent allowed a large lifetime of sorbent II of more than 700 cycles with no loss of sensitivity or need for refilling. The method was successfully applied to the determination of traces of Cd(ii) in osmosis and tap water with recoveries of 98.8-101.3%. A full discussion will be provided, including a comparison with other methods already reported in the literature.
机译:通过溶胶 - 凝胶共缩法制备具有CD(II)和表面活性剂胶束双压印的氨基官能化的介孔吸附剂。该材料用于小聚母标(MCS)中镉离子的高度选择性前浓缩,并通过石墨炉原子吸附光谱(GFAAS)在超rastrace水平的测定。对于对比目的,通过SEM,FTIR和氮气吸附 - 解吸来表征离子印迹(II)和非印记(Ni)固体。进行包括pH影响,吸附能力和吸附动力学的批次实验,以优化吸附洗脱过程。 II分别表现出比Ni吸附剂分别为122mg g(-1)和67mg g(-1)的更大吸收能力,与Langmuir等温线等式一致。样品和洗脱流量,样品和洗脱液的体积以及选择最合适的洗脱液,并在MC动态条件下针对两种吸附剂进行了优化。在优化的条件下,II填充显示了Ni的50的前浓度因子(PCF)。当比较干扰阳离子和水样中常见的阴离子的最大耐受极限(MTL)时,揭示了填料II的选择性较高的选择性,II的MTL为100至200倍,对于所有测试的伴随剂,NI高于NI。用于固体II的主要图形是:0.0011ng ml(-1)的检测限,线性范围为0.01-20ng ml(-1),rsd%2( n = 6; 0.05 ng ml(-1))。另外,在动态条件下的操作以及在低体积的样品和洗脱液中的使用允许大量的吸附剂II,其吸附剂II的寿命超过700次循环,并且没有敏感性的损失或需要重新填充。该方法成功地应用于渗透和自来水中的CD(II)痕量的测定,回收率为98.8-101.3%。将提供全面的讨论,包括与文献中已报道的其他方法的比较。

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  • 来源
    《Analytical methods》 |2018年第44期|共8页
  • 作者单位

    Univ Buenos Aires Fac Ciencias Exactas &

    Nat DQIAQF Lab Trazas INQUIMAE Ciudad Univ Pab 2 C1428EHA Buenos Aires DF Argentina;

    Univ Buenos Aires Fac Ciencias Exactas &

    Nat DQIAQF Lab Trazas INQUIMAE Ciudad Univ Pab 2 C1428EHA Buenos Aires DF Argentina;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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