首页> 外文期刊>International journal of environmental analytical chemistry >Co-microprecipitation/flotation of trace amounts of cadmium from environmental samples through its complexation with iodide and neutralization with cetyltrimethylammonium bromide in the presence of perchlorate ions
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Co-microprecipitation/flotation of trace amounts of cadmium from environmental samples through its complexation with iodide and neutralization with cetyltrimethylammonium bromide in the presence of perchlorate ions

机译:通过与碘化物络合并在高氯酸根离子存在下用十六烷基三甲基溴化铵中和,从环境样品中共微量沉淀/浮选痕量镉

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摘要

A fast, cost-effective and reliable method is presented for separation and preconcentration of trace amounts of cadmium based on co-precipitation and flotation prior to its flame atomic absorption (AAS) spectrometric determination. Cadmium (II) was complexed with iodide and neutralized with cetyltrimethylammonium bromide (CTAB) in the presence of perchlorate ions. This resulted in the formation of a bulky precipitate containing the ternary complex of CdI4(CTA)(2), floating on the top of the solution. The aqueous layer was then simply drained out, the floated layer was dissolved in 1.0 mL of acetonitrile, and its Cd content was determined by flame atomic absorption spectrometry. The parameters affecting the designed separation method such as KI, CTAB, and ClO4- concentration, pH, ionic strength, volumes of sample and dissolving solvent, and extraction time were studied and optimized. For preconcentration of 200 mL of the sample, the calibration graph was linear in the range of 1-30 mu g L-1 of cadmium with a correlation coefficient of 0.9997, enhancement factor of 194 and a limit of detection of 0.18 mu g L-1. The relative standard deviation for seven replicate determinations at 20 mu g L-1 levels of cadmium was found to be 2.1%. The effect of the presence of different common cations and anions on the separation and determination of Cd(II) by the developed method was studied. The method was successfully applied to the determination of trace amounts of Cd(II) ions in different types of real samples including tap water, polluted industrial wastewater, dust, and soil with the recoveries in the range of 95.3 to 103.4.
机译:提出了一种快速,经济高效且可靠的方法,用于在火焰原子吸收(AAS)光谱测定之前基于共沉淀和浮选分离和预富集痕量镉。在高氯酸根离子存在下,将镉(II)与碘化物络合,并用十六烷基三甲基溴化铵(CTAB)中和。这导致形成大块的沉淀物,其中含有CdI4(CTA)(2)的三元复合物,漂浮在溶液顶部。然后将水层简单地排干,将浮层溶解在1.0 mL乙腈中,并通过火焰原子吸收光谱法测定其Cd含量。研究和优化了影响设计分离方法的参数,如KI,CTAB和ClO4-的浓度,pH,离子强度,样品和溶解溶剂的体积以及萃取时间。对于200mL样品的预浓缩,校正曲线在1-30μgL-1的镉范围内呈线性,相关系数为0.9997,增强因子为194,检出限为0.18μgL-。 1。发现在20μg L-1镉水平下进行7次重复测定的相对标准偏差为2.1%。研究了不同常见阳离子和阴离子的存在对分离和测定Cd(II)的影响。该方法成功地用于测定不同类型的实际样品中的痕量Cd(II)离子,包括自来水,污染的工业废水,粉尘和土壤,回收率在95.3至103.4之间。

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