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Determination of total contents and volatile and non-volatile fractions of nickel and vanadium in gasohol by graphite furnace atomic absorption spectrometry after extraction induced by emulsion-breaking

机译:破乳萃取石墨炉原子吸收光谱法测定汽油中镍和钒的总含量及挥发性和非挥发性成分。

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摘要

The determination of the total contents and volatile and non-volatile fractions of nickel and vanadium in gasohol by graphite furnace atomic absorption spectrometry (GF AAS) after extraction induced by emulsion-breaking (EIEB) is proposed. In the extraction procedure, a 0.5 mL aliquot of 6% (v/v) Triton X-114 solution diluted in 10% (v/v) HNO3 was added to 5.0 mL of a gasohol sample. The system was subjected to an ultrasonic bath for 10 min. The emulsion formed was broken at 90 degrees C, and the hydroalcoholic phase was collected for analysis. The determination of the total contents and non-volatile and volatile (by difference) fractions of nickel and vanadium was carried out by assessing the differences in the thermal behavior of the species during the pyrolysis step. Because the extracted phase was less complex than the original matrix, it was possible to use pyrolysis temperatures at 300 and 200 degrees C, in the presence of Pd(NO3)(2), to determine the total contents of V and Ni, respectively. The thermostable (non-volatile) fractions were determined without the use of a modifier at higher pyrolysis temperatures (1700 and 1500 degrees C for V and Ni, respectively). For vanadium, the limits of detection, precision (% RSD, n = 8, 10 mu g L-1) and values for the recovery test were 1.1 and 0.42 mu g L-1, 5.8 and 3.4% and 96-108 and 100-108% for the total content and non-volatile fraction, respectively. For the nickel, the limits of detection, precision (% RSD, n = 8, 10 mu g L-1) and values for the recovery test were 3.5 and 1.7 mu g L-1, 9.6 and 2.0%, and 86-101 and 91-109% for the total content and non-volatile fraction, respectively. Enrichment factors between 2.5 and 5.0 times were found for both metals. This method was applied to the determination of the total contents (3.70-31.98 and 15.71-126.1 mu g L-1), non-volatile fractions (2.16-14.33 and 2.00-10.99 mu g L-1) and volatile fractions (1.54-20.54 and 13.71-115.1 mu g L-1) of vanadium and nickel, respectively, in gasohol samples.
机译:提出了通过破乳诱导萃取(EIEB)后石墨炉原子吸收光谱法(GF AAS)测定汽油中镍和钒的总含量以及挥发性和非挥发性部分的方法。在萃取程序中,将0.5 mL等份的10%(v / v)HNO3稀释的6%(v / v)Triton X-114溶液添加到5.0 mL的汽油样品中。使系统经受超声浴10分钟。在90℃下将形成的乳液破碎,并收集水醇相用于分析。镍和钒的总含量以及非挥发性和挥发性(通过差异)馏分的测定通过评估热解步骤中物质的热行为差异来进行。由于提取的相比原始基质复杂,因此可以在存在Pd(NO3)(2)的情况下使用300和200摄氏度的热解温度分别测定V和Ni的总含量。在较高的热解温度下(V和Ni分别为1700和1500摄氏度),无需使用改性剂即可测定热稳定(非挥发性)馏分。对于钒,检出限,精密度(%RSD,n = 8,10μg L-1)和回收率测试值分别为1.1和0.42μg L-1、5.8和3.4%以及96-108和100总含量和非挥发分分别为-108%。对于镍,检出限,精密度(%RSD,n = 8,10μg L-1)和回收率测试值分别为3.5和1.7μg L-1、9.6%和2.0%,以及86-101总含量和不挥发分分别为91和109%。两种金属的富集系数均为2.5至5.0倍。该方法用于测定总含量(3.70-31.98和15.71-126.1μg L-1),非挥发性组分(2.16-14.33和2.00-10.99μgL-1)和挥发性组分(1.54-汽油样品中的钒和镍分别为20.54和13.71-115.1微克L-1)。

著录项

  • 来源
    《Fuel》 |2019年第15期|479-486|共8页
  • 作者单位

    Univ Fed Bahia, Inst Quim, Dept Quim Analit, Campus Univ Ondina, BR-40170115 Salvador, BA, Brazil|Inst Fed Educ Ciencia & Tecnol Baiano, Campus Santa Ines, BR-45320000 Santa Ines, BA, Brazil;

    Univ Fed Bahia, Inst Quim, Dept Quim Analit, Campus Univ Ondina, BR-40170115 Salvador, BA, Brazil|Univ Fed Bahia, Inst Quim, INCT Energia & Ambiente, Campus Univ Ondina, BR-40170115 Salvador, BA, Brazil;

    Univ Fed Bahia, Inst Quim, Dept Quim Analit, Campus Univ Ondina, BR-40170115 Salvador, BA, Brazil|Univ Fed Bahia, Inst Quim, INCT Energia & Ambiente, Campus Univ Ondina, BR-40170115 Salvador, BA, Brazil;

    Univ Estadual Sudoeste Bahia, Lab Quim Analit, BR-45206190 Jequie, BA, Brazil;

    Univ Estadual Sudoeste Bahia, Lab Quim Analit, BR-45206190 Jequie, BA, Brazil;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Gasohol; Vanadium; Nickel; Speciation; Extraction induced by emulsion breaking; GF AAS;

    机译:汽油;钒;镍;形态;破乳诱导萃取;GF AAS;

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