Lu Jue, Chen Wei, Yang Fan, Li Qiu-Li, Zhao Kui-Dong, Jiang Shao-Yong
State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Wuhan, 430074, China.
State Key Laboratory of Lithospheric and Environmental Coevolution, Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing, 100029, China; College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.
Talanta. 2025 Apr 1;285:127371. doi: 10.1016/j.talanta.2024.127371. Epub 2024 Dec 10.
Accurate in situ carbon isotopic measurements of magnesium-rich carbonates using LA-MC-ICP-MS require effective correction for isobaric interference, particularly from doubly charged Mg ions that can induce δC deviations of several permil. This study focuses on optimizing gas parameters and developing robust correction strategies to improve the accuracy of δC measurements. Experimental results demonstrate that the introduction of nitrogen gas at a flow rate of 4-6 mL/min effectively doubles signal sensitivity while optimizing low helium (0.1-0.2 L/min) and high argon (1.0-1.1 L/min) flow rates enhances the signal-to-noise ratio and minimizes Mg interference. Three correction approaches were evaluated: (1) simple peak stripping without mass bias correction, (2) peak stripping with mass bias correction using bracketed standards, and (3) iterative mass bias correction. The simple peak stripping approach is limited to samples with low Mg/C ratios (Mg/C ≤ 0.051 ‰). Bracketed standard calibration offers broader applicability but is affected by the instrumental mass bias factor (f), with long-term variations between 1.37 and 1.92 leading to δC deviations up to ∼2.35 ‰. This method performs well for carbonates with Mg/C ratios below 0.139 ‰, aligning closely with IRMS results, but introduces inaccuracies for dolomite and magnesite. The iterative correction approach yielded the most accurate δC values, consistent with IRMS results, with deviations within 0.38 ‰ and improved external reproducibility. This method negates the need for prior determination of f, offering enhanced external reproducibility. Utilizing optimal gas flow conditions and iterative correction, spatial resolution of 90 μm was achieved, with external reproducibility of 0.52 ‰ (2SD), representing a marked improvement over previous analytical methods.
使用激光烧蚀多接收电感耦合等离子体质谱仪(LA-MC-ICP-MS)对富镁碳酸盐进行准确的原位碳同位素测量,需要对同量异位素干扰进行有效校正,特别是来自双电荷镁离子的干扰,这种干扰会导致δC偏差达千分之几。本研究着重于优化气体参数并制定可靠的校正策略,以提高δC测量的准确性。实验结果表明,以4 - 6 mL/min的流速引入氮气可有效使信号灵敏度提高一倍,同时优化低氦气(0.1 - 0.2 L/min)和高氩气(1.0 - 1.1 L/min)流速可提高信噪比并使镁干扰最小化。评估了三种校正方法:(1)不进行质量偏倚校正的简单峰剥离,(2)使用括号标准进行质量偏倚校正的峰剥离,以及(3)迭代质量偏倚校正。简单峰剥离方法仅限于Mg/C比低的样品(Mg/C≤0.051‰)。括号标准校准具有更广泛的适用性,但受仪器质量偏倚因子(f)影响,长期变化在1.37至1.92之间会导致δC偏差高达约2.35‰。该方法对于Mg/C比低于0.139‰的碳酸盐表现良好,与同位素比率质谱仪(IRMS)结果紧密相符,但对白云石和菱镁矿会引入不准确结果。迭代校正方法产生了最准确的δC值,与IRMS结果一致,偏差在0.38‰以内且外部重现性得到改善。该方法无需事先确定f,具有更高的外部重现性。利用最佳气体流动条件和迭代校正,实现了90μm的空间分辨率,外部重现性为0.52‰(2SD),相较于先前的分析方法有显著改进。