摘要
The determination of trace lead in a CaCO3 matrix by isotope dilution coupled anion-exchange and quadrupole-based inductively coupled plasma-mass spectrometry was established. The matrix of CaCO3 seriously affected the determination by clogging the cones of the instrument was removed by the anion-exchange resin column. Effects such as dead time, mass bias, dwell time and the amount of isotopic agent spiked were discussed and corrected. The detection limit estimated by 3 x standard deviation of the procedure blank was 2.94 ng g(-1). The results indicated that the lead concentration in all samples tested was far less than 3%, the legislated limit. The recovery mostly ranged from 90 to 110%. The relative standard deviation was found to be <1%.
- 出版日期2004-4-29
- 单位国家海洋局第一海洋研究所; 厦门大学; 集美大学