首页> 外文期刊>Spectrochimica Acta, Part B. Atomic Spectroscopy >Extraction method based on emulsion breaking for the determination of Cu, Fe and Pb in Brazilian automotive gasoline samples by high-resolution continuum source flame atomic absorption spectrometry
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Extraction method based on emulsion breaking for the determination of Cu, Fe and Pb in Brazilian automotive gasoline samples by high-resolution continuum source flame atomic absorption spectrometry

机译:基于乳液破碎的提取方法,通过高分辨率连续源火焰原子吸收光谱法测定巴西汽车汽油样品Cu,Fe和Pb的测定

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This work reports a new method for extraction of Cu, Fe and Pb from Brazilian automotive gasoline and their determination by high-resolution continuous source flame atomic absorption spectrometry (HR-CS FAAS). The method was based on the formation of water-in-oil emulsion by mixing 2.0 mL of extraction solution constituted by 12% (w/v) Triton X-100 and 5% (v/v) HNO3 with 10 mL of sample. After heating at 90 degrees C for 10 min, two well-defined phases were formed. The bottom phase (approximately 3.5 mL), composed of acidified water and part of the ethanol originally present in the gasoline sample, containing the extracted analytes was analyzed. The surfactant and HNO3 concentrations and the heating temperature employed in the process were optimized by Doehlert design, using a Brazilian gasoline sample spiked with Cu, Fe and Pb (organometallic compounds). The efficiency of extraction was investigated and it ranged from 80 to 89%. The calibration was accomplished by using matrix matching method. For this, the standards were obtained performing the same extraction procedure used for the sample, using emulsions obtained with a gasoline sample free of analytes and the addition of inorganic standards. Limits of detection obtained were 3.0, 5.0 and 14.0 mu g L-1 for Cu, Fe and Pb, respectively. These limits were estimated for the original sample taking into account the preconcentration factor obtained. The accuracy of the proposed method was assured by recovery tests spiking the samples with organometallic standards and the obtained values ranged from 98 to 105%. Ten gasoline samples were analyzed and Fe was found in four samples (0.04-035 mg L-1) while Cu (0.28 mg L-1) and Pb (0.60 mg L-1) was found in just one sample. (C) 2018 Elsevier B.V. All rights reserved.
机译:这项工作报告了一种从巴西汽车汽油提取Cu,Fe和Pb的新方法及其通过高分辨率连续源火焰原子吸收光谱法(HR-CS FAA)的测定。该方法基于通过将2.0ml萃取溶液与10mL样品组成的12%(w / v)Triton X-100和5%(v / v)HnO 3混合的萃取溶液混合水包油乳液。在90℃下加热10分钟后,形成两个明确的相。分析了由酸化水和最初存在于汽油样品中的一部分含有提取的分析物的酸化水和乙醇的一部分含有提取的分析物的底相(约3.5mL)。使用与Cu,Fe和Pb(有机金属化合物)掺入的巴西汽油样品,优化了该方法的表面活性剂和HNO 3浓度和加热温度。研究提取效率,其范围为80%至89%。通过使用矩阵匹配方法完成校准。为此,获得了使用与汽油样品获得的乳液一起使用的乳液和加入无机标准品使用的乳液进行相同的提取方法。得到的检测限为3.0,5.0和14.0μg,分别用于Cu,Fe和Pb。考虑到获得的前浓度因子,估计这些限制估计原始样品。通过恢复试验保证了所提出的方法的准确性,这些试验掺入有机金属标准标准物的样品,所得值范围为98至105%。分析10个汽油样品,在四个样品(0.04-035mg L-1)中发现Fe,而在仅一个样品中发现Cu(0.28mg L-1)和Pb(0.60mg L-1)。 (c)2018 Elsevier B.v.保留所有权利。

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