Jason B. Truscott, Lee Bromley, Phil Jones, E. Hywel Evans, Justine Turner and Ben Fairman
An on-line solid phase extraction method has been developed for the determination of 238U and 232Th biological certified reference material using inductively coupled plasma mass spectrometry (ICP-MS). Absolute detection limits were 2.7 pg and 3.1 pg for the determination of 238U and 232Th respectively, both being blank limited. The result for the determination of 238U in NASS-4 Open Ocean Sea Water was 2.13±0.28 ng ml–1 compared with a certified value of 2.68±0.12 ng ml–1. The results for the determination of 238U in SLRS-3 River Water was 0.043±0.002 ng ml–1 compared with an indicative value of 0.045 ng ml–1. Results for the determination of 238U and 232Th in NIST 1575 Pine Needles were 14.6±3.4 ng g–1 and 28.3±4.5 ng g–1 respectively compared with certified values of 20±4 ng g–1 and 37±3 ng g–1, using a dry and wet ashing sample preparation method. Results for the determination of 238U and 232Th in NIST 1566a oyster tissue were 121±21 ng g–1 and 29±8 ng g–1 for 238U and 232Th compared to certified and indicative values of 132±12 ng g–1 and 40 ng g–1, using the same method. When a lithium metaborate fusion method was used, results for 238U and 232Th were 23.3±2.0 ng g–1 and 36.2±5.6 ng g–1 respectively in NIST 1575 Pine Needles. The application of electrothermal vaporisation ICP-MS (ETV-ICP-MS) to NASS-4 Open Ocean Sea Water gave 2.81±0.54 ng ml–1 and SLRS-3 River Water 0.045±0.004 ng ml–1 for 238U. When the fused NIST 1575 samples were analysed using ETV-ICP-MS, results for 238U and 232Th were 19.5±1.7 ng g–1 and 38.8±2.2 ng g–1 respectively. Absolute detection limits for ETV-ICP-MS were 30 fg and 9 fg for 238U and 232Th respectively, both being blank limited.