Background effects on Faraday collectors in gas-source mass spectrometry and implications for clumped isotope measurements

被引:117
|
作者
Bernasconi, Stefano M. [1 ]
Hu, Bin [1 ,2 ]
Wacker, Ulrike [3 ]
Fiebig, Jens [3 ,4 ]
Breitenbach, Sebastian F. M. [1 ]
Rutz, Tanja [3 ]
机构
[1] Swiss Fed Inst Technol, Inst Geol, CH-8092 Zurich, Switzerland
[2] Peking Univ, Dept Geog, Beijing 100871, Peoples R China
[3] Goethe Univ Frankfurt, Inst Geosci, Dept Paleontol, D-60438 Frankfurt, Germany
[4] Biodivers & Climate Res Ctr, D-60325 Frankfurt, Germany
关键词
CARBONATE MINERALS; C-13-O-18; BONDS; PALEOTHERMOMETER; THERMOMETRY; CO2;
D O I
10.1002/rcm.6490
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RATIONALE The measurement of the abundances of minor isotopologues by mass spectrometry requires correction of subtle non-linearities in the mass spectrometer that cause deviations in the relationship between actual and measured isotope ratios. Here we show that negative backgrounds on the Faraday cups recording the minor ion beams are the cause of the observed non-linearities in the measurement of CO2 isotopologues, and propose a new correction procedure for clumped isotope measurements. METHODS We carefully investigated the cause of non-linearity effects in the measurement of the abundance of 13C18O16O, a minor isotopologue of CO2 with m/z 47, on two different mass spectrometers. By using gases of different composition with close to stochastic and with non-random distribution of isotopes we demonstrate that the apparent dependence of the excess abundance of the isotopologue of m/z 47 on the bulk isotopic composition of CO2 is due to a background interference that is linearly dependent on the partial pressure of the gas in the source of the mass spectrometer. CONCLUSIONS Background determination with gas flowing into the source of the mass spectrometer is necessary for accurate clumped isotope measurements of CO2. Background corrections can be performed accurately if the slit width of the m/z 44 Faraday cup significantly exceeds that of the one for m/z 47, using a correlation between m/z 44 signal intensity and the corresponding minimum in m/z 47 background. We propose two new correction schemes that reduce the time-consuming measurement of gases of different bulk isotopic compositions. These findings may also be relevant for the measurement of other rare isotopologues by mass spectrometry. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:603 / 612
页数:10
相关论文
共 50 条
  • [1] A modified procedure for gas-source isotope ratio mass spectrometry: the long-integration dual-inlet (LIDI) methodology and implications for clumped isotope measurements
    Hu, Bin
    Radke, Jens
    Schlueter, Hans-Juergen
    Heine, Frank Torsten
    Zhou, Liping
    Bernasconi, Stefano M.
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2014, 28 (13) : 1413 - 1425
  • [2] Methods and limitations of 'clumped' CO2 isotope (Δ47) analysis by gas-source isotope ratio mass spectrometry
    Huntington, K. W.
    Eiler, J. M.
    Affek, H. P.
    Guo, W.
    Bonifacie, M.
    Yeung, L. Y.
    Thiagarajan, N.
    Passey, B.
    Tripati, A.
    Daeron, M.
    Came, R.
    [J]. JOURNAL OF MASS SPECTROMETRY, 2009, 44 (09): : 1318 - 1329
  • [3] INTERFERENCE BY SILICONE POLYMERS IN GAS-SOURCE MASS-SPECTROMETRY
    RICHARDS, JR
    [J]. VACUUM, 1966, 16 (06) : 310 - &
  • [4] A high-resolution gas-source isotope ratio mass spectrometer
    Eiler, John M.
    Clog, Matthieu
    Magyar, Paul
    Piasecki, Alison
    Sessions, Alex
    Stolper, Daniel
    Deerberg, Michael
    Schlueter, Hans-Juergen
    Schwieters, Johannes
    [J]. INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2013, 335 : 45 - 56
  • [5] Carbonate clumped isotope analysis (Δ47) of 21 carbonate standards determined via gas-source isotope-ratio mass spectrometry on four instrumental configurations using carbonate-based standardization and multiyear data sets
    Upadhyay, Deepshikha
    Lucarelli, Jamie
    Arnold, Alexandrea
    Flores, Randy
    Bricker, Hayley
    Ulrich, Robert N.
    Jesmok, Gregory
    Santi, Lauren
    Defliese, William
    Eagle, Robert A.
    Carroll, Hannah M.
    Bateman, Jesse Bloom
    Petryshyn, Victoria
    Loyd, Sean J.
    Tang, Jianwu
    Priyadarshi, Antra
    Elliott, Ben
    Tripati, Aradhna
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2021, 35 (17)
  • [6] Determination of silicon isotopic composition in soil using gas-source isotope ratio mass spectrometry by thermal decomposition of barium hexafluorosilicate
    Zhang, Jiang-yi
    Zhang, Gui-ming
    Wang, Ya-Nan
    Liu, Wen-jing
    Xu, Zhi-fang
    [J]. MICROCHEMICAL JOURNAL, 2024, 203
  • [7] New type of filaments for improved accuracy of multiple sulfur isotope analyses by electron-impact gas-source mass spectrometry
    Cartigny, Pierre
    Bouyon, Amaury
    Bars, Hartmut
    Albrecht, Nina
    Kohl, Issaku E.
    Landais, Guillaume
    Duverger, Arnaud
    Farquhar, James
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2024, 38 (22)
  • [8] A comparison of sulfur isotope measurements of geologic materials by inductively coupled plasma and gas source mass spectrometry
    Schurr, Simon Lukas
    Genske, Felix
    Strauss, Harald
    Stracke, Andreas
    [J]. CHEMICAL GEOLOGY, 2020, 558
  • [9] Compositional and beam-size-dependent effects on pressure baseline in clumped isotope mass spectrometry
    Venturelli, Ryan A.
    Rosenheim, Brad E.
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2019, 33 (01) : 140 - 148
  • [10] Precision and accuracy in isotope ratio measurements by plasma source mass spectrometry
    Heumann, KG
    Gallus, SM
    Radlinger, G
    Vogl, J
    [J]. JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1998, 13 (09) : 1001 - 1008