Uranium Micro-isotopic Analysis of Weathered Rock by a Sensitive High Resolution Ion Microprobe (SHRIMP II)

Tsutomu Sato*, Nobuyuki Yanase, Ian S. Williams, William Compston, Myint Zaw, Timothy E. Payne, Peter L. Airey

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    7 Citations (Scopus)

    Abstract

    The SHRIMP II was used to measure the 234U/238U isotope ratios in weathered rock from the Koongarra uranium (U) deposit in Northern Australia. The results were compared with data obtained using sequential extraction (SE) procedures. The key attribute of the SHRIMP measurement is that sensitive isotopic data can be obtained without dissolution of the sample, and associated loss of textural relationships. The SHRIMP provides spot- by-spot isotopic ratios in individual mineral phases, and has not been previously applied to measurements of 234U/238U ratios. The SHRIMP measurements of 234U/238U activity ratios in the accumulated iron (Fe)-materials were closer to unity than in the chemically extracted amorphous Fe-oxide fraction, the primitive phase of all Fe-minerals. This indicates an approach to secular equilibrium subsequent to the deposition of U with the amorphous precursor phases. The activity ratios of 234U/238U in kaolinite were significantly lower than the ratios obtained for residual mineral phases in the SE study, although being higher than unity. This suggests that the extremely high 234U/238U ratio of the residual phase in the SE study was mainly derived from other minerals, presumably the abundant quartz rather than the kaolinite. Activity ratios exceeding unity were found in all kaolinites studied, regardless of their proximity to U-rich phases and grain boundaries. Individually, the SE procedure and SHRIMP analysis are useful techniques for measuring isotopes within mineral phases. However, in contrast to the SHRIMP, the SE procedure does not provide spatial or textural information, and quantifies isotopes in individual extractable fractions. On the other hand, the SHRIMP is not suitable for phases with very small gram size or low U content. By the parallel use of SE procedures and the SHRIMP, samples can be analyzed both quantitatively and with high spatial resolution.

    Original languageEnglish
    Pages (from-to)335-340
    Number of pages6
    JournalRadiochimica Acta
    Volume82
    Issue number1
    DOIs
    Publication statusPublished - 1 Dec 1998

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