Comparing the capability of collision/reaction cell quadrupole and sector field inductively coupled plasma mass spectrometers for interference removal from 90Sr, 137Cs, and 226Ra

被引:23
作者
Amr, M. A. [1 ]
Abdel-Lateef, A. M. [1 ]
机构
[1] Atom Energy Author, Dept Nucl Phys, Cent Lab Elemental & Isotop Anal, Cairo 13759, Egypt
关键词
ICP-MS; Collision/reaction cell; Sr-90; (CS)-C-137; Ra-226; NUCLEAR-FUEL SAMPLES; GAS-PHASE ION; ICP-MS; ULTRATRACE LEVEL; WATER SAMPLES; RADIONUCLIDES; SEPARATION; RESOLUTION; PERIODICITIES; REACTIVITY;
D O I
10.1016/j.ijms.2010.11.004
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Here we report a quantitative comparison of sector field inductively coupled plasma mass spectrometry (ICP-SFMS) and collision/reaction cell inductively coupled plasma quadrupole mass spectrometry (ICP-QMS) for the detection of Sr-90, Cs-137, and Ra-226 at ultra-trace levels. We observed that the identification and quantification of radioisotopes by ICP-MS were hampered by spectral (both isobaric and polyatomic ions) and non-spectral (matrix effect) interferences. ICP-QMS has been used to eliminate the isobaric Sr-90/Zr-90 interference through the addition of O-2 into the collision cell as a reactant gas. Zr+ ions were subsequently converted into ZrO+, whereas Sr+ ions were not reactive. In addition, the isobaric interference of Ba-137 on Cs-137 was eliminated by the addition of N2O gas in the cell, which led to the formation of BaO+ and BaOH+ products, whereas Cs+ remained unreactive. Furthermore, He and H-2 were used in the collision/reaction cell to eliminate polyatomic ions formed at m/z 226. A comparison of the results obtained by ICP-SFMS after a chemical separation of Sr from Zr and Cs from Ba was performed. Finally, to validate the developed analytical procedures, measurements of the same samples were performed by gamma-ray spectroscopy. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:184 / 190
页数:7
相关论文
共 32 条
[1]  
Abd El-Sabour M. F., 2007, Electronic Journal of Environmental, Agricultural and Food Chemistry, V6, P2009
[2]  
ALSAAD KA, BIOL TRACE IN PRESS, DOI DOI 10.1007/S12011-010R-R8677-2
[3]   Ultra-trace Measurements of 210Pb in natural occurring radioactive materials by ICP-MS [J].
Amr, M. A. ;
Al-Saad, K. A. ;
Helal, A. I. .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT, 2010, 615 (02) :237-241
[4]  
[Anonymous], TOX PROF RAD
[5]   Gas-phase ion-molecule reactions for resolution of atomic isobars: AMS and ICP-MS perspectives [J].
Bandura, Dmitry R. ;
Baranov, Vladimir I. ;
Litherland, A. E. ;
Tanner, Scott D. .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2006, 255 :312-327
[6]   Reaction chemistry and collisional processes in multipole devices for resolving isobaric interferences in ICP-MS [J].
Bandura, DR ;
Baranov, VI ;
Tanner, SD .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 2001, 370 (05) :454-470
[7]   Inductively coupled plasma mass spectrometry (ICP-MS) and laser ablation ICP-MS for isotope analysis of long-lived radionuclides [J].
Becker, JS .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2005, 242 (2-3) :183-195
[8]   Atomic spectrometry update. Environmental analysis [J].
Cave, MR ;
Butler, O ;
Chenery, SRN ;
Cook, JM ;
Cresser, MS ;
Miles, DL .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2001, 16 (02) :194-235
[9]   On the chemical resolution of the 87Rb+ (s0)/87Sr+ (s1) isobaric interference:: A kinetic search for an optimum reagent [J].
Cheng, Ping ;
Koyanagi, Gregory K. ;
Bohme, Diethard K. .
ANALYTICA CHIMICA ACTA, 2008, 627 (01) :148-153
[10]   Optimisation of ICPMS collision/reaction cell conditions for the simultaneous removal of argon based interferences of arsenic and selenium in water samples [J].
Darrouzes, Jerome ;
Bueno, Maite ;
Lespes, Gaetane ;
Holeman, Michel ;
Potin-Gautier, Martine .
TALANTA, 2007, 71 (05) :2080-2084