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首页> 外文期刊>Spectrochimica Acta, Part B. Atomic Spectroscopy >Novel extraction induced by microemulsion breaking for Cu, Ni, Pb and V determination in ethanol-containing gasoline by graphite furnace atomic absorption spectrometry
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Novel extraction induced by microemulsion breaking for Cu, Ni, Pb and V determination in ethanol-containing gasoline by graphite furnace atomic absorption spectrometry

机译:通过石墨炉原子吸收光谱法测定Cu,Ni,Pb和V测定乙醇汽油中微乳液诱导的新型提取

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摘要

This paper describes a detailed study on the determination of Cu, Ni, Pb, and V in ethanol-containing Brazilian commercial gasoline by graphite furnace atomic absorption spectrometry (GF AAS) after application of the novel extraction induced by microemulsion breaking (EIMB) for the extraction of analytes from the sample. EIMB is based on the formation and breaking of microemulsions with the sample and an extractant acid solution (typically HNO3 solution) in the presence of a dispersant agent (typically a short-chain alcohol). After microemulsion breaking, the following two phases are formed: (i) a top phase containing the remaining gasoline and (ii) a bottom phase containing the extracted metals in a medium composed of water, the dispersant agent, and ethanol, which was already present in the Brazilian gasoline. The bottom phase is collected and used for metal quantification by GF AAS. Several parameters that could affect the performance of the method were evaluated. Under optimized conditions, the microemulsion was prepared by mixing 4.6 mL of the sample with 0.35 mL of 1-propanol and 0.05 mL of a 3.5 mol L-1 HNO3 solution. The microemulsion was shaken for 5 min at 110 rpm to enhance the extraction and was then disrupted by the addition of 0.40 mL of a 3.5 mol L-1 HNO3 solution. The bottom phase formed under these conditions was taken for metal determination by GF AAS. The limits of detection of the method for Cu, Ni, Pb and were 0.7, 0.1, 0.8 and 1.6 mu g L-1, respectively. The method was applied in the analysis of five Brazilian gasoline samples, which presented concentrations of Cu, Ni, Pb, and V in the range of 7.1-63 mu g L-1, 1.6-2.8 mu g L-1, 5.3-9.7 mu g L-1, and 24-44 mu g L-1, respectively. Recovery tests were performed to assess the accuracy of the proposed method, with observed satisfactory recovery percentages of 87-116%.
机译:本文通过石墨炉原子吸收光谱法(GF AAS)在施用通过微乳液破碎(EIMB)诱导的新萃取后,对含乙醇的巴西商业汽油中Cu,Ni,Pb和V的测定的详细研究从样品中提取分析物。 EIMB基于在分散剂(通常是短链醇)存在下用样品和萃取剂酸溶液(通常是HNO 3溶液)的微乳液的形成和破碎。在微乳液破碎后,形成以下两相:(i)含有剩余汽油和(ii)在已经存在的水,分散剂和乙醇组成的培养基中含有萃取金属的底部相的顶部阶段在巴西汽油。收集底相并通过GF AAS用于金属定量。评估了几种可能影响该方法性能的参数。在优化的条件下,通过将4.6ml样品混合在0.35ml 1-丙醇和0.05mL 3.5mol L-1 HNO 3溶液中混合4.6ml样品来制备微乳液。将微乳液在110rpm下摇动5分钟,以增强萃取,然后通过添加0.40ml 3.5mol L-1 HNO 3溶液而破坏。在这些条件下形成的底相被GF AAS用于金属测定。分别检测Cu,Ni,Pb和0.7,0.1,0.8和1.6μg1-1的方法的限制。该方法应用于五种巴西汽油样品的分析,其呈现浓度的Cu,Ni,Pb和V的浓度为7.1-63μgl-1,1.6-2.8μgl-1,5.3-9.7 MU G L-1和24-44μgl-1分别。进行恢复试验以评估所提出的方法的准确性,观察到的令人满意的恢复百分比为87-116%。

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