首页> 外文期刊>International journal of environmental analytical chemistry >A green solventless temperature-assisted homogeneous liquid-liquid microextraction method based on 8-hydroxyquinoline simultaneously as complexing agent and extractant for preconcentration of cobalt and nickel from water and fruit juice samples
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A green solventless temperature-assisted homogeneous liquid-liquid microextraction method based on 8-hydroxyquinoline simultaneously as complexing agent and extractant for preconcentration of cobalt and nickel from water and fruit juice samples

机译:基于8-羟基喹啉同时作为络合剂和萃取剂的绿色无溶剂温度辅助均相液-液微萃取方法,用于从水和果汁样品中预富集钴和镍

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摘要

A green, simple, rapid and efficient solventless temperature-assisted homogeneous liquid-liquid microextraction based on 8-hydroxyquinoline as complexing agent and extractant, followed by flame atomic absorption spectrometry was developed for the extraction, enrichment, and determination of trace amounts of nickel and cobalt in aqueous samples. For this purpose, first, a specified amount of 8-hydroxyquinoline is added to the analytes solution. Then the temperature of the solution is increased to melt 8-hydroxyquinoline and form a homogeneous solution. Then, it is cooled to room temperature and a cloudy solution is formed due to decreasing 8-hydroxyquinoline solubility. The solution is then centrifuged, and 8-hydroxyquinoline particles containing the produced complexes (8-hydroxyquinoline-cation) are collected at the bottom of the tube. They are removed and dissolved in a suitable solvent and injected to the detection system. The main parameters affecting the extraction efficiency, such as the amount of 8-hydroxyquinoline, solvent nature, pH, extraction temperature and heating time were investigated. Under optimum conditions, linear ranges for Co(II) and Ni(II) were 1-100 and 0.5-75 mu g L-1, respectively. Relative standard deviations for intra- and inter-day precisions calculated from six repeated determinations at three different concentrations of Co(II) and Ni(II) were = 5.2 %. Moreover, the obtained detection limits of the analytes were 0.35 and 0.20 mu g L-1 for Co(II) and Ni(II), respectively. The accuracy of the developed procedure was checked by analysing SPS-WW2 Batch 108 water as a certified reference material. Finally, the developed method was successfully applied for the determination of the selected cations in water and fruit juice samples.
机译:建立了以8-羟基喹啉为络合剂和萃取剂的绿色,简单,快速,高效的无溶剂温度辅助均相液-液微萃取方法,然后采用火焰原子吸收光谱法进行了痕量镍和痕量镍的萃取,富集和测定。水溶液样品中的钴。为此,首先将指定量的8-羟基喹啉添加到分析物溶液中。然后升高溶液的温度以熔融8-羟基喹啉并形成均匀溶液。然后,将其冷却至室温,并且由于降低的8-羟基喹啉溶解度而形成浑浊溶液。然后将溶液离心,并在管的底部收集包含产生的复合物(8-羟基喹啉-阳离子)的8-羟基喹啉颗粒。将它们除去并溶解在合适的溶剂中,然后注入检测系统。研究了影响萃取效率的主要参数,如8-羟基喹啉的用量,溶剂性质,pH,萃取温度和加热时间。在最佳条件下,Co(II)和Ni(II)的线性范围分别为1-100和0.5-75μgL-1。在三种不同浓度的Co(II)和Ni(II)进行六次重复测定后得出的日内和日间精度的相对标准偏差<= 5.2%。此外,对于Co(II)和Ni(II),分析物的检出限分别为0.35和0.20μg L-1。通过分析作为认证参考材料的SPS-WW2批次108的水,检查了所开发程序的准确性。最终,该方法成功地用于测定水和果汁样品中选定的阳离子。

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