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首页> 外文期刊>Journal of the Brazilian Chemical Society >Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry
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Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry

机译:分散液-液微萃取和火焰原子吸收光谱法测定铁(II)和铁(III)的形态

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摘要

An extraction method for Fe(III) from water sample before spectrometric determination was developed. Dispersive liquid-liquid microextraction (DLLME) technique was successfully used as sample preparation method for flame atomic absorption spectrometry (FAAS). In the proposed approach, 8-hydroxy quinoline (oxine) was used as chelating agent, chloroform and methanol were selected as extraction and dispersive solvents, respectively. Some factors influencing the extraction efficiency of Fe(III) and its subsequent determination were studied and optimized, including: type and volume of extraction and dispersive solvents, pH of sample solution, concentration of the chelating agent and extraction time. Under the optimized conditions, the enrichment factor of this method for Fe(III) was 462. The limit of detection for Fe(III) was 4.5 ng mL-1, and the relative standard deviation (RSD) 1.4% (n = 5, c = 400 ng mL-1).
机译:建立了一种测定水样中铁(Ⅲ)的方法。分散液-液微萃取(DLLME)技术已成功用作火焰原子吸收光谱法(FAAS)的样品制备方法。在该方法中,使用8-羟基喹啉(oxine)作为螯合剂,分别选择氯仿和甲醇作为萃取溶剂和分散溶剂。研究和优化了影响Fe(III)萃取效率及其后续测定的一些因素,包括:萃取和分散溶剂的类型和体积,样品溶液的pH值,螯合剂的浓度和萃取时间。在最佳条件下,该方法对Fe(III)的富集系数为462。Fe(III)的检出限为4.5 ng mL-1,相对标准偏差(RSD)为1.4%(n = 5)。 c = 400 ng mL-1)。

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