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Multielement analysis of crude oil produced water by ICP OES after acid digestion assisted by microwave

机译:微波酸消化-ICP OES法对原油采出水进行多元素分析。

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摘要

Disposing or reusing crude oil produced water is difficult because of the environmental impacts caused by the presence of high salinity and toxic components, or by the risk of obstruction on the production columns due to crust formation, which causes reduced crude oil production and huge losses to the extraction process. Thus, knowledge of the chemical composition of these waters is very important. The method proposed in this article is intended for determining trace elements (Co, Cr, Fe, Mn, Ni, Se and V) in crude oil produced water samples through inductively coupled plasma optical emission spectrometry (ICP OES) using microwave-assisted acid digestion for preparing the samples (15 g of sample and 2 mL of concentrated HNO_3). Analytical curve in 2% v/v HNO_3 was adopted as a calibration method after verifying that it is not necessary to use salinity for matrix matching. For Ni, there is no need of using internal standard, whereas for Co, Cr, Fe, Mn and V, the best results were achieved using Sc as the internal standard. For Se, the use of Y as the internal standard is recommended. The detection limits obtained were Co 0.67, Cr 1.2, Fe 2.3, Mn 0.49, Ni 1.9, Se 3.7 and V 5.5 μg L~(-1), and the limits of quantification were Co 2.2, Cr 4.0, Fe 7.7, Mn 1.6, Ni 6.5, Se 12.4 and V 18.3 μg L~(-1). Procedure accuracy was verified through recovery tests at two concentration levels (namely, 40 and 80 μg L~(-1)) and by the analysis of certified reference materials (SLEW-2 estuarine water and NASS-5 seawater). Good results were achieved from recovery tests. There was no significant difference (at 95% confidence) between the analyzed and certified values for the reference materials.
机译:由于高盐度和有毒成分的存在对环境的影响,或者由于结皮的缘故而对生产塔造成阻塞的危险,这会造成对环境的影响,从而难以处理或再利用原油生产的水,这将导致原油产量的下降和巨大的损失。提取过程。因此,了解这些水的化学组成非常重要。本文提出的方法旨在通过微波辅助酸消解-电感耦合等离子体发射光谱法(ICP OES)测定原油采出水样品中的痕量元素(Co,Cr,Fe,Mn,Ni,Se和V)。用于制备样品(15 g样品和2 mL浓HNO_3)。在确认无需使用盐度进行基质匹配后,采用2%v / v HNO_3中的分析曲线作为校准方法。对于Ni,不需要使用内标,而对于Co,Cr,Fe,Mn和V,使用Sc作为内标可获得最佳结果。对于硒,建议使用Y作为内标。检出限为Co 0.67,Cr 1.2,Fe 2.3,Mn 0.49,Ni 1.9,Se 3.7和V 5.5μgL〜(-1),定量限为Co 2.2,Cr 4.0,Fe 7.7,Mn 1.6 ,Ni 6.5,Se 12.4和V 18.3μgL〜(-1)。通过在两个浓度水平(即40和80μgL〜(-1))下的回收率测试以及通过对标准参考物质(SLEW-2河口水和NASS-5海水)的分析,验证了程序的准确性。通过恢复测试获得了良好的结果。标准物质的分析值与认证值之间没有显着差异(置信度为95%)。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2015年第5期|1154-1160|共7页
  • 作者单位

    Laboratorio de Espectrometria Atomica (LEA)/LabPetro, Departamento de Quimica, Universidade Federal do Espirito Santo, Av. Fernando Ferrari, 514, Goiabeiras, Vitoria, ES, Brazil, CEP 29.075-910;

    Laboratorio de Espectrometria Atomica (LEA)/LabPetro, Departamento de Quimica, Universidade Federal do Espirito Santo, Av. Fernando Ferrari, 514, Goiabeiras, Vitoria, ES, Brazil, CEP 29.075-910;

    Laboratorio de Espectrometria Atomica (LEA)/LabPetro, Departamento de Quimica, Universidade Federal do Espirito Santo, Av. Fernando Ferrari, 514, Goiabeiras, Vitoria, ES, Brazil, CEP 29.075-910;

    Laboratorio de Espectrometria Atomica (LEA)/LabPetro, Departamento de Quimica, Universidade Federal do Espirito Santo, Av. Fernando Ferrari, 514, Goiabeiras, Vitoria, ES, Brazil, CEP 29.075-910;

    Laboratorio de Espectrometria Atomica (LEA)/LabPetro, Departamento de Quimica, Universidade Federal do Espirito Santo, Av. Fernando Ferrari, 514, Goiabeiras, Vitoria, ES, Brazil, CEP 29.075-910;

    Laboratorio de Espectrometria Atomica (LEA)/LabPetro, Departamento de Quimica, Universidade Federal do Espirito Santo, Av. Fernando Ferrari, 514, Goiabeiras, Vitoria, ES, Brazil, CEP 29.075-910;

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  • 入库时间 2022-08-18 03:04:07

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