001     39797
005     20190625111215.0
024 7 _ |2 DOI
|a 10.1039/A901762C
024 7 _ |2 WOS
|a WOS:000083077900031
024 7 _ |a altmetric:16806430
|2 altmetric
037 _ _ |a PreJuSER-39797
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Chemistry, Analytical
084 _ _ |2 WoS
|a Spectroscopy
100 1 _ |a Becker, J. S.
|0 P:(DE-Juel1)VDB2662
|b 0
|u FZJ
245 _ _ |a Application of double-focusing field ICP mass spectrometry with shielded torch using different nebulizers for ultratrace and isotope analysis of long-lived radionuclides
260 _ _ |a Cambridge
|b ChemSoc
|c 1999
300 _ _ |a 1493 - 1500
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Journal of Analytical Atomic Spectrometry
|x 0267-9477
|0 3023
|y 9
|v 14
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a The capability of double-focusing sector field ICP-MS with a plasma-shielded torch using different nebulizers (a Meinhard nebulizer with a Scott-type spray chamber with a solution uptake rate of 1 ml min(-1); a MicroMist microconcentric nebulizer used with a minicyclonic spray chamber with a solution uptake rate of 0.085 ml min(-1); an ultrasonic nebulizer with a solution uptake rate of 2 ml min(-1); and a direct injection high-efficiency nebulizer with a solution uptake rate of 0.085 ml min(-1)) for the introduction of radioactive sample solutions into the ICP was investigated. The total amount of analyte for each long-lived radionuclide (Ra-226, Th-230, Np-237, U-238, Pu-239 and Am-241; concentration of each was 1 ng l(-1) in the aqueous solution) using different nebulizers was 5 pg for the Meinhard nebulizer, 0.4 pg for the MicroMist microconcentric nebulizer and 10 pg for the ultrasonic nebulizer. The application of the shielded torch yielded an increase in sensitivity for all these nebulizers of up to a factor of 5 compared with the original configuration without a shielded torch. Sensitivities of about 2000 MHz ppm(-1) were measured for the radionuclides investigated (except for Ra-226) using the MicroMist microconcentric nebulizer with a shielded torch. The detection limits were in the sub-pg l(-1) range and the precision ranged from 1 to 2% RSD (n=5) for the 1 ng l(-1) concentration level (0.4 pg sample size). A further increase in sensitivity for long-lived radionuclides of nearly one order of magnitude in comparison with the MicroMist microconcentric nebulizer was observed using ultrasonic nebulization, but the amount of analyte required was significantly higher (by a factor of 25). In contrast, the direct injection high-efficiency nebulizer (DIHEN) in double-focusing sector field ICP-MS (DF-ICP-MS) with a shielded torch resulted in a decrease in sensitivity in comparison with the unshielded torch because of a higher water load due to the direct injection of aqueous solution into the plasma. At low solution uptake rates (down to several mu l min(-1)), the uranium solutions were analyzed by DIHEN-ICP-MS using a double-focusing sector field instrument with higher sensitivity than quadrupole-based ICP-MS. Flow injection was used for sample introduction to measure small sample volumes of radioactive waste solutions (20 mu l). The determination of Np-237 at a concentration of 10 ng l(-1) by flow injection DF-ICP-MS was possible with a precision of 2.0% (RSD, n=5). In order to avoid mass spectral interferences and matrix effects long-lived radionuclides (e.g., of U, Th and Tc-99) were separated from the radioactive waste matrix by liquid-liquid extraction or ion exchange. The methods developed for the precise determination of the concentration and isotopic ratios of long-lived radionuclides were applied to aqueous standard solutions and radioactive wastes by double-focusing sector field ICP-MS. The precision of Pu isotopic analysis by double-focusing ICP-MS with a shielded torch was 0.2, 2 and 14% for 1000, 100 and 10 pg l(-1) (amount of analyte: 500, 50 and 5 fg), respectively.
536 _ _ |a Entwicklung analytischer Verfahren
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588 _ _ |a Dataset connected to Web of Science
650 _ 7 |a J
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700 1 _ |a Dietze, H.-J.
|0 P:(DE-Juel1)VDB2663
|b 1
|u FZJ
773 _ _ |a 10.1039/a901762c
|g Vol. 14, p. 1493 - 1500
|p 1493 - 1500
|q 14<1493 - 1500
|0 PERI:(DE-600)1484654-8
|t Journal of analytical atomic spectrometry
|v 14
|y 1999
|x 0267-9477
856 7 _ |u http://dx.doi.org/10.1039/A901762C
909 C O |o oai:juser.fz-juelich.de:39797
|p VDB
913 1 _ |k 62.10.1
|v Entwicklung analytischer Verfahren
|l Werkstoffe der Energietechnik
|b Energietechnik
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914 1 _ |y 1999
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k ZCH
|l Zentralabteilung für Chemische Analysen
|g ZCH
|0 I:(DE-Juel1)ZCH-20090406
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980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)ZEA-3-20090406
981 _ _ |a I:(DE-Juel1)ZCH-20090406


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