Department of Earth Science and Engineering, Imperial College London, South Kensington Campus, London, SW7 2AZ, United Kingdom.
Department of Earth Sciences, University College London, Gower Street, London, WC1E 6BT, United Kingdom.
Anal Chem. 2020 Aug 18;92(16):11232-11241. doi: 10.1021/acs.analchem.0c01780. Epub 2020 Aug 10.
The application of Pb isotopes to marine geochemistry is currently hindered by challenges associated with the analysis of Pb isotopes in seawater. The current study evaluates the performance of multiple collector inductively coupled plasma mass spectrometry (MC-ICP-MS) measurements of seawater Pb isotope compositions following Pb separation by either solid-phase extraction with Nobias Chelate PA-1 resin or coprecipitation with Mg(OH) and using either a Pb double spike or external normalization to Tl for mass bias correction. The four analytical combinations achieve results of similar quality when measuring 1-7 ng of seawater Pb, with reproducibilities (two standard deviations, 2SD) of 100-1200 ppm for Pb/Pb and Pb/Pb and 300-1700 ppm for ratios involving the minor Pb isotope. All four procedures enable significantly improved sample throughput compared to an established thermal ionization mass spectrometry (TIMS) double-spike method and produce unbiased seawater Pb isotope compositions with similar or improved precision. Nobias extraction is preferable to coprecipitation due to its greater analytical throughput and suitability for analyses of large seawater samples with high Si(OH) contents. The most accurate Pb isotope data are produced following Nobias extraction and double-spike correction as such analyses are least susceptible to matrix effects. However, Nobias extraction with Tl normalization constitutes an attractive alternative as, unlike the double-spike procedure, only a single mass spectrometric measurement is required, which improves analytical throughput and optimizes Pb consumption for analysis. Despite the advantages of solid-phase extraction, coprecipitation represents a useful Pb separation technique for samples with low to moderate Si contents as it is inexpensive, simple to implement, and the data are only marginally less accurate, especially when combined with a Pb double spike for mass bias correction.
铅同位素在海洋地球化学中的应用目前受到海水铅同位素分析相关挑战的阻碍。本研究评估了固相萃取(Nobias Chelate PA-1 树脂)或共沉淀(Mg(OH))分离后,采用多接收电感耦合等离子体质谱仪(MC-ICP-MS)测量海水铅同位素组成的性能,使用 Pb 双标或外部 Tl 归一化进行质量偏差校正。当测量 1-7ng 海水 Pb 时,这四种分析组合的结果质量相似,Pb/Pb 和 Pb/Pb 的重现性(两个标准差,2SD)为 100-1200ppm,涉及次要铅同位素的比值为 300-1700ppm。与建立的热电离质谱(TIMS)双标法相比,所有四种程序都能显著提高样品通量,并产生具有相似或改善精度的无偏海水铅同位素组成。与共沉淀相比,Nobias 萃取由于其更高的分析通量和适用于高 Si(OH)含量的大体积海水样品分析而更具优势。在 Nobias 萃取和双标校正后,可获得最准确的铅同位素数据,因为这种分析最不易受基质效应的影响。然而,由于仅需要进行一次质谱测量,因此与双标程序相比,采用 Tl 归一化的 Nobias 萃取构成了一种有吸引力的替代方法,这提高了分析通量并优化了分析用 Pb 的消耗。尽管固相萃取具有优势,但共沉淀对于 Si 含量低至中等的样品来说仍是一种有用的 Pb 分离技术,因为它成本低廉、易于实施,并且数据的准确性仅略有降低,尤其是当与 Pb 双标结合用于质量偏差校正时。