2018
DOI: 10.1007/s10967-018-6149-x
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Improved protactinium spike calibration method applied to 231Pa–235U age-dating of certified reference materials for nuclear forensics

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Cited by 11 publications
(14 citation statements)
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“…Radiochronometry analyses at LLNL use ultra-high purity acids and water purified to > 18.2 MΩ for labware cleaning and analytical dilutions. The procedure used in this study follows the method outlined in detail in Treinen et al [6].…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Radiochronometry analyses at LLNL use ultra-high purity acids and water purified to > 18.2 MΩ for labware cleaning and analytical dilutions. The procedure used in this study follows the method outlined in detail in Treinen et al [6].…”
Section: Methodsmentioning
confidence: 99%
“…Th and Pa concentrations were measured on the same aliquot via isotope dilution mass spectrometry. Weighed sample aliquots were spiked with a high-purity nuclear forensic reference material (NFRM) 229 Th spike [7] and a 233 Pa spike that is produced by separation of 233 Pa from a 20-60 mg 237 Np parent solution; the resulting 233 Pa spike is calibrated with a 231 Pa high purity standard [8] before use (see [6] for a more detailed discussion of 233 Pa spike production and calibration). Th and Pa are then separated using a series of anion, TEVA, and silica gel purifications to produce analytical aliquots free of uranium (key for protactinium analyses, where the continual production of 233 U from decay of the 233 Pa spike must be minimized for accurate results).…”
Section: Methodsmentioning
confidence: 99%
“…Ketika bahan nuklir dimurnikan saat proses produksi, kotoran dihilangkan (termasuk isotop anak luruhnya), setelah itu produk peluruhan mulai tumbuh dalam bahan melalui peluruhan radioaktif. [8], [9].…”
Section: Pendahuluanunclassified
“…After this step, the protactinium was again dissolved in HF (Seastar Chemicals Inc., Vancouver, Canada) 2 and a subsample containing 2 mg protactinium was dried first in perchloric acid and then dried two times in concentrated HNO 3 (Seastar Chemicals Inc., Vancouver, Canada). An additional separation was then performed on this sample using a silica gel column chemistry technique described in Treinen et al [17]. A subsample of this purified material (approximately 125 μg of 231 Pa) was prepared as the M solution by diluting the 231 Pa in a mixed solution of 2 mol L −1 HNO 3 and 0.1 mol L −1 HF.…”
Section: Materials Preparationmentioning
confidence: 99%
“…A batch of 233 Pa IDMS spike was prepared by separation from a high-purity 237 Np solution (65 mg of 237 Np in HCl). This separation was performed using an AG MP-1 M anion exchange resin followed by a silica gel separation, as described in [17]. The purification procedure was completed at 22:50 UTC on 27 June 2017.…”
Section: Materials Preparationmentioning
confidence: 99%