Abstract

This study presents a method for high‐precision Si isotope measurement of soil and sediment reference materials using multi‐collector inductively coupled plasma‐mass spectrometry with HF‐free digestion. Potential impacts on instrumental measurement, including acid concentration, Si concentration mismatch and matrix effects, were rigorously evaluated. The acidity mismatch caused a significantly negative shift in δ30Si values when the HCl concentration ratios of the sample/standard were higher than 2. The Si concentration mismatch could result in an obvious deviation in δ30Si values when the sample/standard concentration ratios are > 1.5 or < 0.7. Matrix elements in solution did not affect Si isotope measurements when Na/Si ≤ 2, Mg/Si ≤ 2, Al/Si ≤ 0.5, K/Si ≤ 2, Ca/Si ≤ 1 and Fe/Si ≤ 2. Increasing the loading volume from 1 ml to 6 ml during chemical separation can still enable effective purification of Si and is more efficient for low Si content samples. The long‐term measurement precision of three igneous rock reference materials (BHVO‐2, BCR‐2 and AGV‐2) was better than ± 0.06‰ (2s) for δ30Si values. The δ30Si values of eighteen soil and sediment reference materials were identical in two laboratories. The values varied from −1.65‰ to −0.13‰, indicating that Si isotopes can be more widely used to study supergene processes.

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