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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Determination of Hg and Tl in environmental reference materials using slurry sampling electrothermal vaporization inductively coupled plasma mass spectrometry with permanganate as modifier and calibration against aqueous standards
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Determination of Hg and Tl in environmental reference materials using slurry sampling electrothermal vaporization inductively coupled plasma mass spectrometry with permanganate as modifier and calibration against aqueous standards

机译:以高锰酸盐为改性剂的浆料采样电热汽化电感耦合等离子体质谱法测定环境标准物质中的汞和g,并针对水标准进行校准

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摘要

A method for the determination of Hg and Tl in environmental samples by slurry sampling electrothermal vaporization inductively coupled plasma mass spectromelry is proposed. The slurry is prepared by mixing the sample, ground to a particle size of ≤50 μm, with 5% v/v nitric and 1% v/v hydrofluoric acids in an ultrasonic bath, and leaving it to stand for 40 h before analysis. The slurry was homogenized in the autosampler cup with a constant flow of argon, just before transferring an aliquot to the graphite furnace. Potassium permanganate in solution, in an untreated and a Ru-treated tube, as well as potassium and manganese in solution were studied as modifiers and carriers. Best thermal stabilization and sensitivity were obtained with KMnO_4 in an untreated tube, especially for Tl. These conditions were adopted, together with the optimized pyrolysis temperatures of 300℃ for Hg and 500℃ for Tl, and a vaporization temperature of 1000℃ for both analytes. The accuracy of the method was assured by the analysis of eight certified reference materials, using external calibration with aqueous standards prepared in the same medium as the slurries. The limits of detection in the samples were 0.18 μg g~(-1) for Hg and 0.07 μg g~(-1) for Tl. The precision found for the different samples, expressed as relative standard deviation, was 0.8-11% for Hg and 1-9% for Tl (n = 3).
机译:提出了一种通过浆液采样电热汽化电感耦合等离子体质谱法测定环境样品中汞和钛的方法。通过在超声浴中将样品与5%v / v硝酸和1%v / v氢氟酸混合,研磨至≤50μm的粒度,然后在分析前静置40小时,来制备浆料。在将等分试样转移到石墨炉之前,用恒定的氩气流量在自动进样器杯中将浆液均质化。研究了溶液中,未处理和Ru处理过的试管中的高锰酸钾以及溶液中的钾和锰作为改性剂和载体。在未经处理的试管中使用KMnO_4可获得最佳的热稳定性和灵敏度,尤其是对于T1。采用了这些条件,同时优化了Hg的热解温度为300℃,Tl的热解温度为500℃,两种分析物的最佳汽化温度为1000℃。通过使用八种标准参考物质进行分析,并使用与浆料相同的介质中制备的水性标准品进行外部校准,可以确保该方法的准确性。样品中Hg的检出限为0.18μgg〜(-1),Tl为0.07μgg〜(-1)。表示为相对标准偏差的不同样品的精密度对于Hg为0.8-11%,对于T1为1-9%(n = 3)。

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