TY - JOUR
T1 - Evolution and revolution in instrumentation for plasma-source mass spectrometry
AU - Hieftje, Gary M.
AU - Barnes, James H.
AU - Grøn, Ole A.
AU - Leach, Andrew M.
AU - McClenathan, Denise M.
AU - Ray, Steven J.
AU - Solyom, David A.
AU - Wetzel, William C.
AU - Denton, M. Bonner
AU - Koppenaal, David W.
N1 - Funding Information:
This research was supported in part by the U.S. Department of Energy through grant 40159-A9E, by the Leco Corporation, and by ICI Technologies, UK. Support for this work was also provided by the U.S. Department of Energy, Office of Nonproliferation Research and Engineering. Pacific Northwest National Laboratory is operated by Battelle Memorial Institute for the Department of Energy under contract DE-AC06-76RLO-1830.
PY - 2001
Y1 - 2001
N2 - Plasma-source mass spectrometry, usually in the form of inductively coupled plasma mass spectrometry (ICP-MS), has matured into a widely accepted method for ultra-trace multielemental analysis. However, the method exhibits shortcomings. For example, it does not provide adequate precision for isotope ratio measurements if many isotopes are to be determined. Moreover, isobaric overlaps (spectral interferences) can be very troublesome in some situations. Similarly, matrix interferences can adversely affect many determinations. Yet, it is in the area of high-speed transient measurements that ICP-MS perhaps suffers its greatest weakness. When sampling devices such as flow injection, laser ablation, electrothermal vaporization, or chromatography are employed, the user must choose between broad elemental or isotopic coverage and signal-to-noise ratio (S/N). In turn, compromised S/N means lower precision or poorer detection limits. Here, new instrumentation aimed at overcoming these limitations will be described. One system, based on a time-of-flight mass spectrometer, provides excellent detection limits, resolving power better than commercial quadrupole mass filters, precision of at least 0.02% rsd in a ratioing mode, and extraordinarily high speed for use with transient sampling devices. The second instrument is based on a sector-field mass spectrometer but, unlike other such units, is equipped with a focal-plane array detector. So equipped, the system can detect a broad mass range at once.
AB - Plasma-source mass spectrometry, usually in the form of inductively coupled plasma mass spectrometry (ICP-MS), has matured into a widely accepted method for ultra-trace multielemental analysis. However, the method exhibits shortcomings. For example, it does not provide adequate precision for isotope ratio measurements if many isotopes are to be determined. Moreover, isobaric overlaps (spectral interferences) can be very troublesome in some situations. Similarly, matrix interferences can adversely affect many determinations. Yet, it is in the area of high-speed transient measurements that ICP-MS perhaps suffers its greatest weakness. When sampling devices such as flow injection, laser ablation, electrothermal vaporization, or chromatography are employed, the user must choose between broad elemental or isotopic coverage and signal-to-noise ratio (S/N). In turn, compromised S/N means lower precision or poorer detection limits. Here, new instrumentation aimed at overcoming these limitations will be described. One system, based on a time-of-flight mass spectrometer, provides excellent detection limits, resolving power better than commercial quadrupole mass filters, precision of at least 0.02% rsd in a ratioing mode, and extraordinarily high speed for use with transient sampling devices. The second instrument is based on a sector-field mass spectrometer but, unlike other such units, is equipped with a focal-plane array detector. So equipped, the system can detect a broad mass range at once.
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U2 - 10.1351/pac200173101579
DO - 10.1351/pac200173101579
M3 - Article
AN - SCOPUS:0035742494
SN - 0033-4545
VL - 73
SP - 1579
EP - 1588
JO - Pure and Applied Chemistry
JF - Pure and Applied Chemistry
IS - 10
ER -