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Automated Sample Combustion and CO2 Collection System with IRMS for 14C AMS in Yamagata University, Japan

Published online by Cambridge University Press:  26 July 2016

Kazuhiro Kato*
Affiliation:
Faculty of Science, Yamagata University, Japan
Fuyuki Tokanai
Affiliation:
Faculty of Science, Yamagata University, Japan
Minoru Anshita
Affiliation:
Faculty of Science, Yamagata University, Japan
Hirohisa Sakurai
Affiliation:
Faculty of Science, Yamagata University, Japan
Mami S Ohashi
Affiliation:
JASCO International Co., Ltd., Japan
*
2. Corresponding author. Email: [email protected].

Abstract

Accelerator mass spectrometry (AMS) was introduced at Yamagata University in 2010, including the measurement of radiocarbon. In the Yamagata University laboratory (YU-AMS), the application of 14C AMS is aimed at microdose pharmacokinetics investigation and the development of improved sample preparation techniques. The lab also measures environmental samples. With the installation of this AMS system, a new automated sample production system was installed, which is composed of an elemental analyzer, a glass vacuum line, and an isotope ratio mass spectrometer (IRMS). In this system, it is also possible to measure stable isotopes (δ13C, δ15N, and δ34S) of the sample gas using a mass spectrometer. To increase the amount of CO2 gas introduced into the glass vacuum line, the gas mass flow introduced into the MS was reduced, and the change of δ13C accompanying this reduction was monitored. The sample gas split was changed to set the glass vacuum line (GVL):isotope ratio mass spectrometer (IRMS) ratio to 5:5, 8:2, and 9:1, and δ13C was measured for each ratio. It was confirmed that there was no effect on the isotopic fractionation accompanying the change in the sample gas split ratio. To prioritize the use of gas in the production of graphite, the GVL:IRMS ratio of 9:1 was chosen for this setup. The components are connected on-line, and up to 20 samples can be processed automatically.

Type
Articles
Copyright
Copyright © 2014 by the Arizona Board of Regents on behalf of the University of Arizona 

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References

Aerts-Bijma, AT, Meijer, HAJ, van der Plicht, J. 1997. AMS sample handling in Groningen. Nuclear Instruments and Methods B 123(1–4):221–5.CrossRefGoogle Scholar
Gagnon, AR, McNichol, AP, Donoghue, JC, Stuart, DR, von Reden, K, NOSAMS. 2000. The NOSAMS sample preparation laboratory in the next millenium: progress after the WOCE program. Nuclear Instruments and Methods in Physics Research B 172(1–4):409–15.CrossRefGoogle Scholar
Hong, W, Park, JH, Kim, KJ, Woo, HJ, Kim, JK, Choi, HW, Kim, GD. 2010. Establishment of chemical preparation methods and development of an automated reduction system for AMS sample preparation at KIGAM. Radiocarbon 52(3):1277–87.CrossRefGoogle Scholar
Kato, K, Tokanai, F, Anshita, M, Sakurai, H. 2012. Automatic sample combustion and CO2 collection system for AMS-14C. Radioisotopes 61(9):469–73.CrossRefGoogle Scholar
Tokanai, F, Kato, K, Anshita, M, Izumi, A, Sakurai, H, Saito, T. 2011. Compact AMS system at Yamagata University. AIP Conference Proceedings 1336:70–4.CrossRefGoogle Scholar
Tokanai, F, Kato, K, Anshita, M, Sakurai, H, Izumi, A, Toyoguchi, T, Kobayashi, T, Miyahara, H, Ohyama, M, Hoshino, Y. 2013. Present status of the YU-AMS system, Yamagata University. Radiocarbon 55(2):251–9.Google Scholar
Wacker, L, Němec, M, Bourquin, J. 2009. A revolutionary graphitisation system: fully automated, compact and simple. Nuclear Instruments and Methods in Physics Research B 268(7–8):931–4.Google Scholar