Mass spectrometry of long-lived radionuclides

被引:104
作者
Becker, JS [1 ]
机构
[1] Forschungszentrum Julich, Cent Div Analyt Chem, D-52425 Julich, Germany
关键词
environmental monitoring; glow discharge mass spectrometer; inductively coupled plasma mass spectrometry; isotope ratios; laser ablation ICP-MS; long-lived radionuclides; radioactive waste; trace analysis;
D O I
10.1016/S0584-8547(03)00156-3
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The capability of determining element concentrations at the trace and ultratrace level and isotope ratios is a main feature of inorganic mass spectrometry. The precise and accurate determination of isotope ratios of long-lived natural and artificial radionuclides is required, e.g. for their environmental monitoring and health control, for studying radionuclide migration, for age dating, for determining isotope ratios of radiogenic elements in the nuclear industry, for quality assurance and determination of the burn-up of fuel material in a nuclear power plant, for reprocessing plants, nuclear material accounting and radioactive waste control. Inorganic mass spectrometry, especially inductively coupled plasma mass spectrometry (ICP-MS) as the most important inorganic mass spectrometric technique today, possesses excellent sensitivity, precision and good accuracy for isotope ratio measurements and practically no restriction with respect to the ionization potential of the element investigated-therefore, thermal ionization mass spectrometry (TIMS), which has been used as the dominant analytical technique for precise isotope ratio measurements of long-lived radionuclides for many decades, is being replaced increasingly by ICP-MS. In the last few years instrumental progress in improving figures of merit for the determination of isotope ratio measurements of long-lived radionuclides in ICP-MS has been achieved by the application of a multiple ion collector device (MC-ICP-MS) and the introduction of the collision cell interface in order to dissociate disturbing argon-based molecular ions, to reduce the kinetic energy of ions and neutralize the disturbing noble gas ions (e.g. of Xe-129(+) for the determination of I-129). The review describes the state of the art and the progress of different inorganic mass spectrometric techniques such as ICP-MS, laser ablation ICP-MS vs. TIMS, glow discharge mass spectrometry, secondary ion mass spectrometry, resonance ionization mass spectrometry and accelerator mass spectrometry for the determination of long-lived radionuclides in quite different materials. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:1757 / 1784
页数:28
相关论文
共 153 条
[1]   DETERMINATION OF URANIUM AND THORIUM CONCENTRATIONS IN SOILS - COMPARISON OF ISOTOPE-DILUTION SECONDARY ION MASS-SPECTROMETRY AND ISOTOPE-DILUTION THERMAL IONIZATION MASS-SPECTROMETRY [J].
ADRIAENS, AG ;
FASSETT, JD ;
KELLY, WR ;
SIMONS, DS ;
ADAMS, FC .
ANALYTICAL CHEMISTRY, 1992, 64 (23) :2945-2950
[2]   Verification of the long term stability of uranium reference solutions of low concentration [J].
Agarande, M ;
Mayer, K ;
DeBievre, P .
JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY-ARTICLES, 1996, 207 (02) :395-400
[3]  
Aggarwal SK., 1997, INTRO MASS SPECTROME
[4]   CHARACTERIZATION OF SPENT NUCLEAR-FUEL DISSOLVER SOLUTIONS AND DISSOLUTION RESIDUES BY INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY [J].
ALONSO, JIG ;
THOBYSCHULTZENDORFF, D ;
GIOVANONNE, B ;
GLATZ, JP ;
PAGLIOSA, G ;
KOCH, L .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1994, 9 (11) :1209-1215
[5]   Determination of long-lived radioisotopes using electrothermal vaporization-inductively coupled plasma mass spectrometry [J].
Alvarado, JS ;
Erickson, MD .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1996, 11 (10) :923-928
[6]   The use of secondary ion mass spectrometry in radiotoxicology [J].
Amaral, A ;
Cossonnet, C ;
Galle, P .
RADIATION PROTECTION DOSIMETRY, 1998, 79 (1-4) :137-140
[7]   Perspectives of uranium and plutonium analysis in urine samples by secondary ion mass spectrometry [J].
Amaral, A ;
Galle, P ;
Cossonnet, C ;
Franck, D ;
Pihet, P ;
Carrier, M ;
Stephan, O .
JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY, 1997, 226 (1-2) :41-45
[8]  
[Anonymous], ENCY ANAL CHEM
[9]   DETERMINATION OF URANIUM AND THORIUM IN BASALTS AND URANIUM IN AQUEOUS-SOLUTION BY INDUCTIVELY-COUPLED PLASMA-MASS SPECTROMETRY [J].
BAILEY, EH ;
KEMP, AJ ;
RAGNARSDOTTIR, KV .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1993, 8 (04) :551-556
[10]   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