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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Multielemental determination in oil matrices diluted in xylene by ICP-MS with a dynamic reaction cell employing methane as reaction gas for solving specific interferences
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Multielemental determination in oil matrices diluted in xylene by ICP-MS with a dynamic reaction cell employing methane as reaction gas for solving specific interferences

机译:ICP-MS采用动态反应池,以甲烷为反应气体,通过二甲苯稀释的石油基体中的多种元素测定,以解决特定的干扰

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摘要

The analysis of organic samples by ICP-MS is still a challenge due to the occurrence of non-spectral and spectral interferences, which usually requires time-consuming sample preparation procedures for their minimization. In this work, results are presented on the direct multielemental determination in oil samples after simple dilution in xylene. The solutions were introduced into the plasma by a sample introduction system especially suited for organics, and the operational conditions of the plasma and the dynamic reaction cell were optimized. A central composite design showed that the nebulizer and the auxiliary gas flow rates had a significant influence on interference formation, monitored by Ba~(++) and LaO~+ intensities. The compromised plasma conditions were: RF power of 1300 W and gas flow rates of 0.42 L min~(-1) for the nebulizer (Ar), 1.1 L min~(-1) for the auxiliary gas (Ar), and 0.1 L min~(-1) of O_2 used as an additional gas. In order to minimize spectral interferences on Ca, Cr, Fe and Mg, the operational conditions of the dynamic reaction cell, working with methane as reaction gas, were optimized for ~(56)Fe, ~(52)Cr, ~(40)Ca and ~(24)Mg. Two certified reference materials, NIST 1634c (used fuel oil) and NIST 1085b (lubricating oil), were analyzed and the recoveries were in the range of 90% to 110% for most elements, being the sample detection limits between 0.2 μg kg~(-1) (Cr) and 40 ug kg~(-1) (Zn). Reliability of the data was also tested by comparing the results for a set of biodiesel samples with those determined by ICP OES and good agreement was obtained for most elements. Differences in the elemental compositions of biodiesel samples produced from different raw materials were observed, suggesting that elemental fingerprinting may be used for source identification.
机译:由于非光谱和光谱干扰的发生,通过ICP-MS分析有机样品仍然是一个挑战,这通常需要耗时的样品制备程序才能将其最小化。在这项工作中,给出了在二甲苯中简单稀释后直接在油样中进行多元素测定的结果。通过特别适用于有机物的样品引入系统将溶液引入等离子体,并优化了等离子体和动态反应池的操作条件。中央复合设计表明,雾化器和辅助气体流速对干扰形成有显着影响,并通过Ba〜(++)和LaO〜+强度进行监测。折衷的等离子体条件为:1300 W的RF功率和雾化器(Ar)的气体流速为0.42 L min〜(-1),辅助气体(Ar)的1.1 L min〜(-1)和0.1 L将min〜(-1)的O_2用作附加气体。为了最大程度地减少对Ca,Cr,Fe和Mg的光谱干扰,针对〜(56)Fe,〜(52)Cr,〜(40)优化了以甲烷为反应气体的动态反应池的工作条件Ca和〜(24)Mg。分析了两种经认证的参考物质NIST 1634c(废燃料油)和NIST 1085b(润滑油),大多数元素的回收率在90%至110%范围内,即样品检出限在0.2μgkg〜( -1)(Cr)和40 ug kg〜(-1)(Zn)。通过将一组生物柴油样品的结果与ICP OES测定的结果进行比较,还测试了数据的可靠性,并且大多数元素均获得了良好的一致性。观察到由不同原料生产的生物柴油样品的元素组成存在差异,这表明元素指纹可用于来源鉴定。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2012年第8期|p.1280-1286|共7页
  • 作者单位

    Departamento de Quimica, Pontificia Universidade Catolica do Rio de Janeiro (PUC-Rio), Rua Marques de Sao Vicente 225, 22451-900 Rio de Janeiro, RJ, Brazil;

    Departamento de Quimica, Pontificia Universidade Catolica do Rio de Janeiro (PUC-Rio), Rua Marques de Sao Vicente 225, 22451-900 Rio de Janeiro, RJ, Brazil Departamento de Quimica, Universidade Federal Fluminense, Outeiro Sao Jodo Batista sin, 24020-150 Niteroi, RJ, Brazil;

    Centro de Pesquisas Leopoldo A. Miguez de Mello da Petrobras (CENPES), Brazil;

    Departamento de Quimica, Pontificia Universidade Catolica do Rio de Janeiro (PUC-Rio), Rua Marques de Sao Vicente 225, 22451-900 Rio de Janeiro, RJ, Brazil;

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