Pacific Northwest National Laboratory, PO Box 999, Richland, WA 99352, USA.
Analyst. 2017 Sep 8;142(18):3333-3340. doi: 10.1039/c7an00777a.
Solid sampling and analysis methods, such as laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), are challenged by matrix effects and calibration difficulties. Matrix-matched standards for external calibration are seldom available and it is difficult to distribute spikes evenly into a solid matrix as internal standards. While isotopic ratios of the same element can be measured to high precision, matrix-dependent effects in the sampling and analysis process frustrate accurate quantification and elemental ratio determinations. Here we introduce a potentially general solid matrix transformation approach entailing chemical reactions in molten ammonium bifluoride (ABF) salt that enables the introduction of spikes as tracers or internal standards. Proof of principle experiments show that the decomposition of uranium ore in sealed PFA fluoropolymer vials at 230 °C yields, after cooling, new solids suitable for direct solid sampling by LA. When spikes are included in the molten salt reaction, subsequent LA-ICP-MS sampling at several spots indicate that the spikes are evenly distributed, and that U-235 tracer dramatically improves reproducibility in U-238 analysis. Precisions improved from 17% relative standard deviation for U-238 signals to 0.1% for the ratio of sample U-238 to spiked U-235, a factor of over two orders of magnitude. These results introduce the concept of solid matrix transformation (SMT) using ABF, and provide proof of principle for a new method of incorporating internal standards into a solid for LA-ICP-MS. This new approach, SMT-LA-ICP-MS, provides opportunities to improve calibration and quantification in solids based analysis. Looking forward, tracer addition to transformed solids opens up LA-based methods to analytical methodologies such as standard addition, isotope dilution, preparation of matrix-matched solid standards, external calibration, and monitoring instrument drift against external calibration standards.
固体取样和分析方法,如激光烧蚀电感耦合等离子体质谱(LA-ICP-MS),受到基质效应和校准困难的挑战。外部校准用基体匹配标准品很少可用,且难以将内标均匀分布到固体基体中。虽然可以高精度测量同一元素的同位素比值,但采样和分析过程中的基质依赖性效应会阻碍准确的定量和元素比测定。在这里,我们介绍了一种潜在的通用固体基质转化方法,该方法涉及在熔融双氟铵(ABF)盐中的化学反应,从而可以将内标作为示踪剂或内标引入。原理验证实验表明,在 230°C 下将铀矿石密封在 PFA 氟聚合物小瓶中分解,冷却后得到新的固体,适合通过 LA 直接进行固体取样。当在熔融盐反应中加入内标时,随后在几个点进行的 LA-ICP-MS 取样表明,内标均匀分布,并且 U-235 示踪剂极大地提高了 U-238 分析的重现性。U-238 信号的相对标准偏差从 17%提高到样品 U-238 与加标 U-235 比值的 0.1%,提高了两个数量级以上。这些结果介绍了使用 ABF 的固体基质转化(SMT)的概念,并为将内标引入 LA-ICP-MS 固体的新方法提供了原理验证。这种新方法 SMT-LA-ICP-MS 为基于固体的分析中的校准和定量提供了改进的机会。展望未来,向转化固体中添加示踪剂为基于 LA 的方法开辟了新的途径,例如标准加入、同位素稀释、制备基体匹配的固体标准品、外部校准以及使用外部校准标准监测仪器漂移。