CNRS/Université de Pau et des Pays de l'Adour, Institut Des Sciences Analytiques et de Physico-Chimie Pour L'Environnement et Les Matériaux - MIRA, UMR5254, 64000, Pau, France; Grupo Química Analítica Aplicada (QANAP), Instituto Universitario de Medio Ambiente (IUMA), Centro de Investigacións Científicas Avanzadas (CICA), Facultade de Ciencias, Universidade da Coruña, 15071 A Coruña, Spain.
CNRS/Université de Pau et des Pays de l'Adour, Institut Des Sciences Analytiques et de Physico-Chimie Pour L'Environnement et Les Matériaux - MIRA, UMR5254, 64000, Pau, France.
J Chromatogr A. 2018 Apr 27;1547:77-85. doi: 10.1016/j.chroma.2018.02.056. Epub 2018 Feb 27.
The current EU legislation lays down Environmental Quality Standards (EQS) for 45 priority substances in surface waters; among them levels for (organo)metallic species of Hg, Sn and Pb are set between ng L (for Hg and Sn) and μg L (for Pb). To date, only a few analytical methods can reach these very restrictive limits and there is thus a need for comprehensive methods able to analyze these species down to these levels in natural waters. The aim of this work was to develop an online automated pre-concentration method using large volume injections with a Programmed Temperature Vaporization (PTV) injector fitted with a sorbent packed liner coupled to GC-ICP-MS to further improve the detection limits associated to this well-established method. The influence of several parameters such as the PTV transfer temperature and time, carrier gas flow rate and amount of packing material was investigated. Finally, the maximum volume injected through single or multiple injection modes was optimized to obtain the best compromise between chromatographic resolution and sensitivity. After optimization, very satisfactory results in terms of absolute and methodological detection limits were achieved, down to the pg L level for all species studied. The potential of the method was exemplified by determining the concentrations of organometallic compounds in unpolluted river waters samples from the Adour river basin (SW France) and results were compared with conventional (splitless) GC-ICP-MS. The strength of this analytical method lies in the low detection limits reached for the simultaneous analysis of a wide group of organometallic compounds, and the potential to transfer this method to other gas chromatographic applications with inherent lower sensitivity.
目前,欧盟法规为地表水的 45 种优先物质规定了环境质量标准(EQS);其中,Hg、Sn 和 Pb 的(有机)金属物种的水平设定在 ng/L(Hg 和 Sn)和 μg/L(Pb)之间。迄今为止,只有少数分析方法能够达到这些非常严格的限制,因此需要能够在天然水中分析这些物质达到这些水平的综合方法。这项工作的目的是开发一种在线自动预浓缩方法,使用大体积进样和配备有吸附剂填充衬管的程序升温汽化(PTV)进样器与 GC-ICP-MS 联用,以进一步提高与这种成熟方法相关的检测限。研究了 PTV 传输温度和时间、载气流速和填充材料量等几个参数的影响。最后,通过单进样或多进样模式优化了最大进样体积,以在色谱分辨率和灵敏度之间取得最佳折衷。经过优化,在达到 pg/L 水平的所有研究物种的绝对和方法检测限方面取得了非常满意的结果。该方法的潜力通过测定来自法国西南部阿杜尔河流域未受污染的河水样本中的有机金属化合物浓度得到了例证,并将结果与传统的(不分流)GC-ICP-MS 进行了比较。该分析方法的优势在于可同时分析广泛的有机金属化合物,并且能够达到非常低的检测限,同时还具有将该方法转移到其他固有灵敏度较低的气相色谱应用的潜力。