English  |  正體中文  |  简体中文  |  Items with full text/Total items : 54367/62174 (87%)
Visitors : 15177022      Online Users : 54
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTHU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    National Tsing Hua University Institutional Repository > 歷任校長 > 沈君山 (1994-1997) > 期刊論文 >  A 10-fold improvement in the precision of boron isotopic analysis by negative thermal ionization mass spectrometry

    Please use this identifier to cite or link to this item: http://nthur.lib.nthu.edu.tw/dspace/handle/987654321/80873

    Title: A 10-fold improvement in the precision of boron isotopic analysis by negative thermal ionization mass spectrometry
    Authors: J.J. Shen;C.F. You
    教師: 沈君山
    Date: 2003
    Publisher: American Chemical Society
    Relation: ANALYTICAL CHEMISTRY, American Chemical Society, Volume 75, Issue 9, MAY 1 2003, Pages 1972-1977
    Abstract: Boron isotopes are potentially very important to cosmochemistry, geochemistry, and paleoceanography. However, the application has been hampered by the large sample required for positive thermal ionization mass spectrometry (PTIMS), and high mass fractionation for negative-TIMS (NTIMS). Running as BO2-, NTIMS is very sensitive and requires only nanogram sized samples, but it has rather poor precision (similar to0.7-2.0 parts per thousand) as a result of the larger mass fractionation associated with the relatively light ion. In contrast, running as the much heavier molecule of CS2BO2+, PTIMS usually achieves better precision around 0.1-0.4 parts per thousand. Moreover, there is a consistent 10 parts per thousand offset in the B-11/B-10 ratio for NIST SRM 951 standard boric acid between the NTIMS and the certified value, but the cause of this offset is unclear. In this paper, we have adapted a technique we developed earlier to measure the La-138/La-139 using LaO+1 to improve the NTIMS technique for BO2. We were able to correct for instrumental fractionation by measuring BO2- species not only at masses of 42 and 43, but also at 45, which enabled us to normalize (BO2)-B-45 /(BO2)-B-43 to an empirical O-18/O-16 value. We found that both I-45/I-42 = ((BOO)-B-11-O-16-O-18/(BPO)-B-10-P-16-O-16) and (I-43/I-42)(C) = ((BOO)-B-11-O-16-O-16/(BOO)-B-10-O-16-O-16) vary linearly with (I-45/I-43)C x 0.5 = ((BOO)-B-11-O-16-O-18/(BPO)-B-11-P-16-O-16) x 0.5 = O-18/O-16. In addition, different activators and different chemical forms of B yield different slopes for the fractionation lines. After normalizing (BOO)-B-11-O-16-O-18/(BPO)-B-11-P-16-O-16 x 0.5 to a fixed O-18/O-16 value, we obtained a mean B-11/B-10 value of NIST SRM 951 that matches the NIST certified value at 4.0430 +/- 0.0015 (+/- 0.36parts per thousand, n = 11). As a result, our technique can achieve precision and accuracy comparable to that of PTIMS with only 1parts per thousand of the sample required. This new NTIMS technique for B isotopes is critical to the studies of early solids in the solar system and individual foraminifera in sediments that require both high sensitivity and precision.
    Relation Link: http://pubs.acs.org/
    URI: http://nthur.lib.nthu.edu.tw/dspace/handle/987654321/80873
    Appears in Collections:[沈君山 (1994-1997)] 期刊論文
    [物理系] 期刊論文

    Files in This Item:

    File SizeFormat


    SFX Query


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback