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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:离子印迹氨基官能化介孔吸附剂,用于镉的选择性小柱预富集和GFAAS测定

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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 (3Sb), 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-凝胶共缩聚法制备了具有镉(II)和表面活性剂胶团双重印迹的氨基官能化介孔吸附剂。该材料用于微量柱(MCs)中镉离子的高选择性预富集,并通过石墨炉原子吸收光谱法(GFAAS)在超痕量水平上对其进行测定。为了进行比较,通过SEM,FTIR和氮气吸附-脱附对离子印迹(II)和非印迹(NI)固体进行了表征。为了优化吸附-洗脱过程,进行了包括pH影响,吸附容量和吸附动力学在内的分批实验。 II显示出比NI吸附剂更大的吸收能力,分别为122 mg g?1和67 mg g?1,这与Langmuir等温线方程一致。在MC动态条件下对两种吸附剂测试并优化了样品和洗脱流速,样品和洗脱液的体积以及最合适的洗脱液的选择。在优化的条件下,II填充物的预浓系数(PCF)为50,而NI的预浓系数为10。当比较水样品中常见的干扰阳离子和阴离子的最大容许限量(MTL)时,II填充剂的选择性更高,对于所有测试的伴随产品,II的MTL比NI的MTL高100到200倍。固体II的主要优点为:检出限为0.0011 ng mL?1(3Sb),线性范围为0.01–20 ng mL?1,RSD%为2(n = 6; 0.05 ng mL 1)。另外,在动态条件下进行操作以及使用少量的样品和洗脱液,可以使吸附剂II的使用寿命超过700个循环,而不会降低灵敏度或无需重新填充。该方法已成功用于渗透和自来水中痕量Cd(II)的测定,回收率为98.8–101.3%。将提供完整的讨论,包括与文献中已报道的其他方法的比较。

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