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Determination of lead isotope ratios in Mn–Fe-rich nodules by laser ablation multi-collector inductively coupled plasma mass spectrometry.

Authors :
Bao, Zhian
Zong, Chunlei
Chen, Lu
Lei, Danbo
Chen, Kaiyun
Yuan, Honglin
Source :
JAAS (Journal of Analytical Atomic Spectrometry). Dec2018, Vol. 33 Issue 12, p2143-2152. 10p.
Publication Year :
2018

Abstract

In this study, Pb isotope ratios in ferromanganese nodules were determined with good repeatability and minimum laboratory bias using laser ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS). One certified ferromanganese nodule reference material, NOD-A-1, in the form of pressed powder pellets (PPPs) produced upon ultrafine processing, was homogeneous enough to be used as an in-house matrix-matched standard or quality control sample for Pb isotopic microanalysis. The Tl normalization exponential law correction method with CTl-NIST SRM 997/CTl-sample≥ 15 (method 1) and the standard-sample-bracketing (SSB) method (method 2) were utilized to determine Pb isotope ratios with good repeatability and laboratory bias. In situ measurements of the Pb isotopes yielded a good relative standard deviation (2RSD) of <0.036% for 207,208Pb/206Pb and <0.066% for 206,207,208Pb/204Pb. In addition, the matrix effect was insignificant when the silicate glass reference material was employed as the external standard in the ferromanganese nodules using these two methods, resulting in relative errors (RE) of <0.064% for 206,207,208Pb/204Pb, and <0.046% for 207,208Pb/206Pb. The in situ Pb isotopic compositions of three Chinese ferromanganese nodules, GBW07249, GBW07295, and GBW07296, were in good agreement with those obtained by solution nebulization MC-ICP-MS (SN-MC-ICP-MS) within 2s (standard deviation) measurement uncertainties, demonstrating the reliability and robustness of our proposed analytical protocol. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02679477
Volume :
33
Issue :
12
Database :
Academic Search Index
Journal :
JAAS (Journal of Analytical Atomic Spectrometry)
Publication Type :
Academic Journal
Accession number :
133267755
Full Text :
https://doi.org/10.1039/c8ja00302e