同位素
分析化学(期刊)
化学
闪锌矿
磁黄铁矿
微量分析
黄铜矿
质谱法
硫化物
同位素分馏
电感耦合等离子体质谱法
放射化学
矿物学
铜
分馏
黄铁矿
环境化学
物理
色谱法
量子力学
有机化学
作者
Yantong Feng,Wen Zhang,Zhaochu Hu,Tao Luo,Qinglin Li,Jinyu Liu
摘要
S‐Fe‐Cu isotope systems are powerful tracers for revealing geochemical processes. However, the microanalysis of S‐Fe‐Cu isotopes is critically limited by the lack of suitable reference materials. Herein, we present three potential reference materials Ll‐Cpy (chalcopyrite), Ll‐Po (pyrrhotite) and Ll‐Sp (sphalerite) for in situ S‐Fe‐Cu isotope measurements. Numerous in situ S‐Fe‐Cu isotope measurements were performed over two years to assess isotopic homogeneity. The bulk S isotopic compositions were determined independently in seven laboratories by isotope ratio mass spectrometry (IRMS); the preferred δ 34 S V‐CDT for Ll‐Cpy, Ll‐Po, Ll‐Sp are 6.13 ± 0.37‰ (2 s ), 6.42 ± 0.37‰ (2 s ) and 6.28 ± 0.38‰ (2 s ), respectively. The bulk Fe isotope ratios in Fe‐bearing Ll‐Cpy and Ll‐Po were determined using solution nebulisation multi‐collector inductively coupled plasma‐mass spectrometry, and the obtained δ 56 Fe IRMM‐014 values are 0.57 ± 0.07‰ (2 s ) and ‐0.62 ± 0.07‰ (2 s ), respectively. The mean bulk δ 65 Cu NIST SRM 976 value of Ll‐Cpy is 0.57 ± 0.06‰ (2 s ). All the bulk values are in good agreement with the long‐term statistical results of laser ablation‐MC‐ICP‐MS and proposed as the recommended values. These sulfides are well characterised and isotopically homogeneous (at 30–40 μm spatial resolution), and can be used as potential calibration materials for in situ S‐Fe‐Cu isotope measurements.
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