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Ultratrace arsenic determination through hydride trapping on oxidized multiwall carbon nanotubes coupled to electrothermal atomic absorption spectrometry

机译:氢化物捕集-氧化多壁碳纳米管上的氢化物捕集-电热原子吸收光谱法测定痕量砷

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摘要

Arsenic determination in natural waters is an issue of current research. This article reports a novel hydride generation (HG) approach developed for As determination with electrothermal atomic absorption spectrometry (ETAAS) detection. The HG process was interfaced with ETAAS through hydride trapping onto a carbon nanotubes microcolumn. To this end a homemade gas-liquid separator was used, allowing arsine formation and its flow throughout the CNT microcolumn. The retention process involved thus a solid phase extraction from the gas phase to the solid support. Once arsine generation was completed, the elution was carried out with nitric acid directly onto the dosing hole of the graphite furnace. Outstanding sensitivity with detection limit of 1 ng L~(-1) quantification limit of 5 ng L~(-1) and the characteristic mass, 5.8 ± 0.4 pg could be achieved. A satisfactory correlation between concentration of As and absorbance {R = 0.9993) from, the limit of quantification up to 500 ng L~(-1), with a relative standard deviation of 6.3% were obtained. A sensitive enhancement factor of 38 was reached when 2 mL of sample were processed and 50 uL of HNO_3 were used as eluent. The system was successfully applied to the analysis of a standard reference material, QC LL2 metals in natural waters. In addition tap water analysis provided an As concentration of 0.29 ± 0.03 ng L~(-1).
机译:天然水中的砷测定是当前研究的一个问题。本文报道了一种新的氢化物发生(HG)方法,该方法用于电热原子吸收光谱法(ETAAS)检测中的砷测定。 HG过程通过氢化物捕集到碳纳米管微柱上与ETAAS接触。为此,使用了自制的气液分离器,以使砷化氢的形成及其在整个CNT微柱中的流动。因此,保留过程涉及从气相到固体载体的固相萃取。砷化氢生成完成后,直接用硝酸洗脱到石墨炉的定量孔上。灵敏度极高,检测限为1 ng L〜(-1),定量限为5 ng L〜(-1),特征质量为5.8±0.4 pg。从定量限至500 ng L〜(-1),As的浓度与吸光度之间具有令人满意的相关性(R = 0.9993),相对标准偏差为6.3%。当处理2 mL样品并将50 uL HNO_3用作洗脱液时,达到38的敏感增强因子。该系统已成功应用于天然水中标准参考物质QC LL2金属的分析。另外,自来水分析提供了0.29±0.03 ng L〜(-1)的As浓度。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2013年第6期|916-922|共7页
  • 作者单位

    Instituto de Quimica de San Luis (CCT-San Luis)- Area de Quimica Analitica, Facultad de Quimica Bioquimica y Farmacia, Universidad National de San Luis, Ejercito de los Andes 950, San Luis, CP5700, Argentina;

    Instituto de Quimica de San Luis (CCT-San Luis)- Area de Quimica Analitica, Facultad de Quimica Bioquimica y Farmacia, Universidad National de San Luis, Ejercito de los Andes 950, San Luis, CP5700, Argentina;

    Instituto de Quimica de San Luis (CCT-San Luis)- Area de Quimica Analitica, Facultad de Quimica Bioquimica y Farmacia, Universidad National de San Luis, Ejercito de los Andes 950, San Luis, CP5700, Argentina;

    Instituto de Quimica de San Luis (CCT-San Luis)- Area de Quimica Analitica, Facultad de Quimica Bioquimica y Farmacia, Universidad National de San Luis, Ejercito de los Andes 950, San Luis, CP5700, Argentina;

    Instituto de Quimica de San Luis (CCT-San Luis)- Area de Quimica Analitica, Facultad de Quimica Bioquimica y Farmacia, Universidad National de San Luis, Ejercito de los Andes 950, San Luis, CP5700, Argentina;

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