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Speciation of chromium in water samples with cloud point extraction separation and preconcentration and determination by graphite furnace atomic absorption spectrometry

机译:浊点萃取分离富集-石墨炉原子吸收光谱法测定水样中铬的形态。

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摘要

A novel method has been developed for the speciation of chromium in natural water samples based on cloud point extraction (CPE) separation and preconcentration, and determination by graphite furnace atomic absorption spectrometry (GFAAS). In this method, Cr(III) reacts with 1-phenyl-3-methyl-4-benzoylpyrazol-5-one (PMBP) yielding a hydrophobic complex, which then is entrapped in the surfactant-rich phase, whereas Cr(VI) remained in aqueous phase. Thus, separation of Cr(III) and Cr(VI) could be realized. Total chromium was determined after the reduction of Cr(VI) to Cr(III) by using ascorbic acid as reducing reagent. PMBP was used not only as chelating reagent in CPE procedure, but also as chemical modifier in GFAAS determination of chromium. The detection limit for Cr(III) was 21 ng L~(-1) with an enrichment factor of 42, and the relative standard deviation was 3.5% (n = 7, c = 10 ng mL~(-1)). The proposed method has been applied to the speciation of chromium in natural water samples with satisfactory results.
机译:开发了一种基于浊点萃取(CPE)分离和预浓缩,并通过石墨炉原子吸收光谱法(GFAAS)测定天然水样品中铬的形态的新方法。在这种方法中,Cr(III)与1-苯基-3-甲基-4-苯甲酰基吡唑-5-酮(PMBP)反应生成疏水配合物,然后将其截留在富含表面活性剂的相中,而Cr(VI)保留在水相中。因此,可以实现Cr(III)和Cr(VI)的分离。使用抗坏血酸作为还原剂将Cr(VI)还原为Cr(III)后,测定总铬。 PMBP不仅用作CPE程序中的螯合剂,还用作GFAAS测定铬中的化学改性剂。 Cr(III)的检出限为21 ng L〜(-1),富集系数为42,相对标准偏差为3.5%(n = 7,c = 10 ng mL〜(-1))。该方法已用于天然水样中铬的形态分析,结果令人满意。

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