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Ultratrace determination of cadmium(II) ions in water samples using graphite furnace atomic absorption spectrometry after separation and preconcentration using magnetic activated carbon nanocomposites

机译:磁性活性炭纳米复合物分离富集后,采用石墨炉原子吸收光谱法测定水中的痕量镉(II)离子

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The main purpose of the present study is sorption/preconcentration of trace amounts of cadmium using a magnetic activated carbon nanocomposite (MAC) as an adsorbent in various water samples using graphite furnace atomic absorption spectrometry (GFAAS). The advantages of this method include the elimination of organic solvent and easy separation of magnetic nanocomposites from the bulk solution by applying a magnet without any preliminary centrifugation and filtration steps. Initially, MAC was prepared by a sonochemical approach and characterized by FT-IR and TEM. Cadmium ions from 100 mL sample solution were then adsorbed on the prepared sorbent by batch mode at pH 7. After sedimentation of MAC, quantitative desorption occurs using 0.5 mL of 0.5 mol La?’1 HCl. The effects of various parameters on the solid-phase extraction procedure efficiency including pH, sample volume, equilibrium time, type and concentration of eluent have been thoroughly investigated and optimized. Under the optimal experimental conditions, the detection limit (LOD) based on three times the standard deviation of the blank signals (n = 8) was 4 ng La?’1. The relative standard deviation (RSD) resulting from the analysis of five replicate solutions containing 100 ng La?’1 Cd(II) was 3.5%. The effect of potentially interfering ions on the percent recovery of cadmium ions was also studied. The accuracy of the method was verified using the analysis of a certified reference material. The proposed method was successfully applied to determine Cd(II) ions in aqueous real solutions.
机译:本研究的主要目的是使用石墨炉原子吸收光谱法(GFAAS)在多种水样中使用磁性活性炭纳米复合材料(MAC)作为吸附剂吸附/富集痕量镉。该方法的优点包括无需施加任何初步离心和过滤步骤即可通过施加磁体而消除有机溶剂,并易于从本体溶液中分离出磁性纳米复合材料。最初,MAC是通过声化学方法制备的,并通过FT-IR和TEM表征。然后将来自100 mL样品溶液的镉离子通过分批模式在pH值为7的条件下吸附到制备的吸附剂上。MAC沉淀后,使用0.5 mL的0.5 mol La?1 HCl进行定量解吸。彻底研究和优化了各种参数对固相萃取过程效率的影响,包括pH,样品量,平衡时间,洗脱液的类型和浓度。在最佳实验条件下,基于空白信号标准偏差(n = 8)的三倍的检出限(LOD)为4 ng La?1。对含有100 ng La?1 Cd(II)的五个重复溶液进行分析得出的相对标准偏差(RSD)为3.5%。还研究了潜在干扰离子对镉离子回收率的影响。该方法的准确性通过使用经认证的参考物质进行了验证。所提出的方法已成功地应用于测定水溶液中的Cd(II)离子。

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