Tan Xijuan
Laboratory of Mineralization and Dynamics, College of Earth Sciences and Land Resources, Chang'an University, 126 Yanta Road, Xi'an 710054, China.
Molecules. 2025 Mar 31;30(7):1552. doi: 10.3390/molecules30071552.
In this paper, the quantitative feasibility of time-of-flight secondary ion mass spectrometry (tof-SIMS) for major and minor elements in spodumene was evaluated in terms of calibration method with a matrix-matched or non-matrix-matched standard and an internal standard element using Al or Si. The matrix-matched standard calibration method was studied using spodumene 503R as the external standard and unknown sample, with signal intensities collected under positive ion mode using 100 µm of raster size. The sensitivities of Li, Na, Al, Si, Mn, and Fe were obtained by applying the sample-standard bracketing method, and the corresponding concentrations were given as the division of signal intensities by sensitivities. It was found that there were no significant differences between concentration results using Al and Si as the internal standard element. After 100% normalization, the concentrations at a 95% confidence level of matrix LiO, AlO, and SiO in oxide form were found to be 7.62 ± 0.27%, 27.68 ± 0.10%, and 64.32 ± 0.29%, respectively, which agreed with those from LA-ICPMS measurements and/or EPMA analyses. The comparison of the minor components including NaO, MnO, and FeO showed that the contents from tof-SIMS were consistent with references from LA-ICPMS, giving ratios within 0.98-1.02. Furthermore, the element behavior investigation of NIST SRM 610 showed that the ionization efficiencies differentiated among the studied elements, resulting in far lower sensitivities of Li, Na, Mn, and Fe in spodumene than the values from the proposed matrix-matched standard calibration method. Thus, the matrix-matched standard calibration method for element determination of spodumene by tof-SIMS was recommended. The successful determination of major and minor elements in spodumene also promises the future application of tof-SIMS to trace element quantification.
本文从采用基体匹配或非基体匹配标准以及使用铝或硅作为内标元素的校准方法方面,评估了飞行时间二次离子质谱法(tof-SIMS)对锂辉石中主次元素进行定量分析的可行性。采用锂辉石503R作为外标和未知样品,研究了基体匹配标准校准方法,在正离子模式下使用100 µm的光栅尺寸收集信号强度。通过应用样品-标准夹心法获得了锂、钠、铝、硅、锰和铁的灵敏度,并将相应浓度表示为信号强度除以灵敏度。结果发现,以铝和硅作为内标元素时,浓度结果没有显著差异。经过100%归一化后,氧化物形式的基体LiO、AlO和SiO在95%置信水平下的浓度分别为7.62±0.27%、27.68±0.10%和64.32±0.29%,这与激光烧蚀电感耦合等离子体质谱(LA-ICPMS)测量结果和/或电子探针微区分析(EPMA)结果一致。对包括NaO、MnO和FeO在内的次要成分的比较表明,tof-SIMS的含量与LA-ICPMS的参考值一致,比值在0.98 - 1.02之间。此外,对美国国家标准与技术研究院(NIST)标准物质610的元素行为研究表明,所研究元素的电离效率存在差异,导致锂辉石中锂、钠、锰和铁的灵敏度远低于所提出的基体匹配标准校准方法的值。因此,推荐采用基体匹配标准校准方法通过tof-SIMS测定锂辉石中的元素。锂辉石中主次元素的成功测定也为tof-SIMS未来在微量元素定量分析中的应用带来了希望。