Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil.
Talanta. 2010 Dec 15;83(2):364-9. doi: 10.1016/j.talanta.2010.09.030. Epub 2010 Sep 25.
A microwave-induced combustion (MIC) procedure was applied for coal digestion for subsequent determination of As, Cd and Pb by inductively coupled plasma mass spectrometry (ICP-MS) and Hg using cold vapor (CV) generation coupled to ICP-MS. Pellets of coal (500 mg) were combusted using 20 bar of oxygen and ammonium nitrate as aid for ignition. The use of nitric acid as absorbing solution (1.7, 3.5, 5.0, 7.0 and 14 mol L(-1)) was evaluated. For coal samples with higher ash content, better results were found using 7.0 mol L(-1) HNO(3) and an additional reflux step of 5 min after combustion step. For coal samples with ash content lower than 8%, 5.0 mol L(-1) nitric acid was suitable to the absorption of all analytes. Accuracy was evaluated using certified reference material (CRM) of coal and spikes. Agreement with certified values and recoveries was better than 95 and 97%, respectively, for all the analytes. For comparison of results, a procedure recommended by the American Society of Testing and Materials (ASTM) was used. Additionally, a conventional microwave-assisted digestion (MAD) in pressurized vessels was also performed. Using ASTM procedure, analyte losses were observed and a relatively long time was necessary for digestion (>6h). By comparison with MAD procedure, higher sample mass can be digested using MIC allowing better limits of detection. Additionally, the use of concentrated acids was not necessary that is an important aspect in order to obtain low blank levels and lower limits of detection, respectively. The residual carbon content in digests obtained by MAD and MIC was about 15% and <1%, respectively, showing the better digestion efficiency of MIC procedure. Using MIC it was possible to digest completely and simultaneously up to eight samples in only 25 min with relatively lower generation of laboratory effluents.
采用微波诱导燃烧(MIC)法对煤样进行消解,随后采用电感耦合等离子体质谱法(ICP-MS)测定砷(As)、镉(Cd)和铅(Pb),采用冷蒸气(CV)发生法与 ICP-MS 联用测定汞(Hg)。使用 20 巴氧气和硝酸铵作为助燃剂对 500mg 煤样进行燃烧。评估了使用硝酸作为吸收液(1.7、3.5、5.0、7.0 和 14mol/L)的效果。对于灰分含量较高的煤样,在燃烧后再加入 7.0mol/L HNO3 并进行 5 分钟回流,可获得更好的结果。对于灰分含量低于 8%的煤样,5.0mol/L 硝酸适合所有分析物的吸收。使用煤的认证参考物质(CRM)和加标物来评估准确性。所有分析物的回收率均在 95%以上,与认证值的一致性均在 97%以上。为了比较结果,采用了美国测试材料协会(ASTM)推荐的程序。此外,还采用了加压容器中的常规微波辅助消解(MAD)法。使用 ASTM 程序时,观察到分析物损失,且消解需要较长时间(>6h)。与 MAD 程序相比,MIC 可消化更多的样品,从而获得更好的检测限。此外,使用浓酸并非必需,这是获得低空白水平和更低检测限的重要方面。MAD 和 MIC 获得的消解物中残留的碳含量分别约为 15%和<1%,表明 MIC 程序的消解效率更高。使用 MIC 可以在 25 分钟内同时完全消解多达 8 个样品,并且产生的实验室废液相对较少。