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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Speciation of chromium in river water samples contaminated with leather effluents by flame atomic absorption spectrometry after separation/preconcentration by cloud point extraction
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Speciation of chromium in river water samples contaminated with leather effluents by flame atomic absorption spectrometry after separation/preconcentration by cloud point extraction

机译:浊点萃取分离富集后火焰原子吸收光谱法测定皮革废水污染的河水样品中铬的形态

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In the present work, a cloud point extraction (CPE) system has been proposed for determination of species de chromium in the natural water samples, Cr(III) and Cr(VI). The procedure was based on the reaction of Cr(Ill) with 1-(2-pyridilazo)-2-naphtol (PAN) in a surfactant solution (Triton X-114) yielding a hydrophobic complex, which then is entrapped "in situ" in the surfactant micelles. When the temperature of the system was higher than the cloud point of Triton X-114, the complex of Cr(III)-PAN entered the surfactant-rich phase and thus separation of the analyte from the matrix was achieved. Separation of the two phases was accomplished by centrifugation for 15 min at 2500 rpm. The Cr(VI) assay is based on its reduction to Cr(III) by ascorbic acid which subsequently reacts with PAN in a similar manner. The main factors affecting the cloud point extraction, such as complexation pH (7.7), buffer concentration (0.025 mol L-1) and microwave irradiation time (10 min) were optimized by response surface methodology (RSM) using Box-Behnken design. Under the optimized conditions, the preconcentration system (50 mL sample) permitted an enrichment factor of 48, linear range of 2.5-80 mu g L-1, limit of detection and quantification of 0.7 and 2.5 mu g L-1. respectively, and the relative standard deviation (n = 10) of 2.0% for 50 mu g L-1 Cr(III) solution and (n = 10) 5.5% for 10 mu g L-1. The proposed procedure was applied to the speciation of chromium in river water samples. The procedure affords recoveries of 84-115% and a relative standard deviation lower than 4.2%. The analytical results of total chromium in the river water samples under study agreed well with those by electrothermal atomic absorption spectrometry (ETAAS). It is proved that the procedure can be successfully employed as an alternative to the commonly used preconcentration and speciation analytical techniques.
机译:在目前的工作中,已经提出了一种浊点萃取(CPE)系统来测定天然水样品中的铬(III)和铬(VI)中的铬。该程序基于Cr(III)与1-(2-吡啶并偶氮)-2-萘酚(PAN)在表面活性剂溶液(Triton X-114)中的反应,产生疏水性络合物,然后将其“原位”截留。在表面活性剂胶束中。当系统温度高于Triton X-114的浊点时,Cr(III)-PAN的络合物进入表面活性剂富集相,从而实现了分析物与基质的分离。通过以2500 rpm离心15分钟来完成两相的分离。 Cr(VI)测定基于抗坏血酸将其还原为Cr(III)的作用,随后抗坏血酸以类似方式与PAN反应。使用Box-Behnken设计,通过响应面法(RSM)优化了影响浊点提取的主要因素,例如络合pH(7.7),缓冲液浓度(0.025 mol L-1)和微波辐照时间(10分钟)。在最佳条件下,预浓缩系统(50 mL样品)的富集系数为48,线性范围为2.5-80μg L-1,检出限和定量限为0.7和2.5μgL-1。 50μg L-1 Cr(III)溶液的相对标准偏差(n = 10)为2.0%,10μg L-1的相对标准偏差(n = 10)5.5%。拟议的程序被应用于河流水样中铬的形态分析。该方法的回收率为84-115%,相对标准偏差低于4.2%。所研究的河流水样中总铬的分析结果与电热原子吸收光谱法(ETAAS)的结果吻合良好。事实证明,该方法可成功替代常用的预浓缩和形态分析技术。

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