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Quantitative Determination by 14C Analysis of the Biological Component in Fuels

Published online by Cambridge University Press:  18 July 2016

Ivo J Dijs,
Eric van der Windt,
Lauri Kaihola and
Klaas van der Borg
Ivo J Dijs*
Affiliation:
Kuwait Petroleum Research & Technology b.v., P.O. Box 545, NL-3190 AL Hoogvliet, the Netherlands
Eric van der Windt
Affiliation:
Kuwait Petroleum Research & Technology b.v., P.O. Box 545, NL-3190 AL Hoogvliet, the Netherlands
Lauri Kaihola
Affiliation:
PerkinElmer Life and Analytical Sciences, P.O. Box 10, FIN-20101 Turku, Finland
Klaas van der Borg
Affiliation:
Van de Graaff Laboratory, Utrecht University, Princetonplein 5, NL-3584 CC Utrecht, the Netherlands
*
Corresponding author. Email: ivodijs@kprt.Q8.nl.
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Abstract

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Radiocarbon analysis was performed by liquid scintillation counting (LSC) and accelerator mass spectrometry (AMS) to assess whether the content of biological components in hydrocarbon fuels could be derived. Different fuel mixtures were prepared containing bioethanol, fossil ethanol, and fossil gasoline. The specific 14C activity of these mixtures was obtained from LSC measurements and directly related to the concentration of carbon originating from the bioethanol (biocarbon). The results were checked via standardized carbon dating procedures and AMS. A good linear correlation exists between the fuel mixture's specific 14C activity and the concentration of biocarbon. Also, the biocarbon fraction of the fuel mixture (the ratio biocarbon : total carbon) and the normalized fraction of biocarbon (%M) showed good linear correlation. Therefore, both relations provide a possibility to quantitatively determine a fuel's biocarbon content by 14C analysis. When the sample composition is known (e.g. resolved by gas chromatography-mass spectroscopy [GC-MS] and nuclear magnetic resonance [NMR]), the amount of particular biological components in a fuel sample can be derived subsequently. For mixtures of bioethanol, fossil ethanol, and gasoline with bioethanol contents in the range of 0.5–2% m/m, it was found that errors in the normalized fraction of biocarbon (%M) were in the range of 25–10%, respectively. For samples with a higher bioethanol content (up to pure bioethanol), the errors in %M were <10%. Errors might be larger if substantial changes in the concentration of atmospheric 14C took place during the growth period of the biofuel feedstock. By taking into account the variation in specific 14C activity of carbon over the last decades, and by modeling simple tree-growth, it could be illustrated that this effect becomes significant only if the biofuel feedstock stopped growing more than 1 decade ago, e.g. with wood from constructions.

Information

Type
Articles
Information
Radiocarbon , Volume 48 , Issue 3 , 2006, pp. 315 - 323
Copyright
Copyright © The Arizona Board of Regents on behalf of the University of Arizona 

References

American Society for Testing and Materials [ASTM]. 2006. Standard test methods for determining the biobased content of natural range materials using radiocarbon and isotope ratio mass spectrometry analysis (Method D6866-06). Volume 8.03. West Conshohocken, Pennsylvania, USA: ASTM International.Google Scholar
Alpert, P, Niyogi, D, Pielke, RA, Eastman, JL, Xue, YK, Raman, S. 2006. Evidence for carbon dioxide and moisture synergies from the leaf cell up to global scales: implications to human-caused climate change. Global and Planetary Change. URL: http://blue.atmos.colostate.edu/publications/pdf/R-304.pdf. Accessed July 2006.Google Scholar
Berg, C. 2004. World fuel ethanol analysis and outlook. [WWW document]. Agra Informa Ltd. URL: www.distill.com/World-Fuel-Ethanol-A&O-2004.html. Accessed July 2006.Google Scholar
Boerrigter, H, Calis, HP, Slort, DJ, Bodenstaff, H, Kaandorp, AJ, Den Uil, H, Rabou, LPLM. 2004. Gas cleaning for integrated biomass gasification (BG) and Fischer-Tropsch (FT) systems. ECN Report C–04-056. URL: www.ecn.nl. Accessed July 2006.Google Scholar
Bronk Ramsey, C, Ditchfield, P, Humm, M. 2004. Using a gas ion source for radiocarbon AMS and GC-AMS. Radiocarbon 46(1):25–32.CrossRefGoogle Scholar
Buchholz, BA, Müller, CJ, Upatnieks, A, Martin, GC, Pitz, WJ, Westbrook, CK. 2004. Using carbon-14 isotope tracing to investigate molecular structure effects of the oxygenate dibutyl maleate on soot emissions from a DI diesel engine. Society of Automotive Engineers [technical paper] 2004-01-1849. UCRL-JRNL-201870.CrossRefGoogle Scholar
Chase, TO, Pielke, RA, Kittel, TGF, Zhao, M, Pitman, AJ, Running, SW, Nemani, RR. 2001. The relative climatic effects of land cover change and elevated carbon dioxide combined with aerosols: a comparison of model results and observations. Journal of Geophysical Research 106 D23:31685–31691. URL: blue.atmos.colostate.edu/publications/pdf/R-214.pdf.CrossRefGoogle Scholar
Cox, P, Chrisochoïdis, M. 2003. Directive 2003/30/EC of the European Parliament and of the Council of 8 May 2003 on the promotion of the use of biofuels or other renewable fuels for transport. Official Journal of the European Union L123:42–6.Google Scholar
Higham, T. 1999. Radiocarbon WEB-info [WWW document]. URL: www.c14dating.com. Accessed July 2006.Google Scholar
Klinedinst, DB, Currie, LA. 1999. Direct quantification of PM2.5 fossil and biomass carbon within the Northern Front Range Air Quality Study's domain. Environmental Science and Technology 33:4146–54.Google Scholar
Libby, WF. 1952. Radiocarbon Dating. Chicago: University of Chicago Press. 124 p.Google Scholar
Libby, WF. 1958. Chemistry and the atomic nucleus. American Journal of Physics 26:524–36.CrossRefGoogle Scholar
Logsdon, JE. 1994. Ethanol. In: Kroschwitz, JI, Howe-Grant, M, editors. Kirk-Othmer Encyclopedia of Chemical Technology. 4th edition. Volume 9. Wiley: New York, p 812–60.Google Scholar
Martin, GE, Noakes, JE, Alfonso, FC, Figert, DM. 1981. Liquid scintillation counting of carbon-14 for differentiation of synthetic ethanol from ethanol of fermentation. Journal of the Association of Official Analytical Chemists 64:1142–4.Google Scholar
McWeeny, DJ, Bates, ML. 1980. Discrimination between synthetic and natural ethyl alcohol in spirits and fortified wines. Journal of Food Technology 15:407–12.Google Scholar
National Diagnostics. 2004. Principles and applications of liquid scintillation counting [WWW document]. URL: www.ehs.psu.edu/radprot/LSC_Theory2.pdf. Accessed July 2006.Google Scholar
Noakes, JE. 1983. Applications of low level liquid scintillation counting. In: McQuarrie, SA, Ediss, C, Wiebe, LI, editors. Advances in Scintillation Counting. Edmonton: University of Alberta Press. p 407–19.Google Scholar
Noakes, JE, Hoffman, PG. 1980. Determination of natural product purity by radiocarbon measurement. In: Peng, C, Horrocks, DL, Alpen, EL, editors. Advances in Scintillation Counting, Recent Applications and Development. Volume II. Sample Preparation and Applications. New York: Academic Press. p 457–68.Google Scholar
Noakes, JE, Norton, G, Culp, R, Nigam, M, Dvoracek, D. Forthcoming. A comparison of analytical methods for the certification of biobased products. In: ChałSupnik, S, Schönhofer, F, Noakes, JE, editors. LSC 2005, Advances in Liquid Scintillation Spectrometry. Tucson: Radiocarbon.Google Scholar
Olsson, IU. 1968. Modern aspects of radiocarbon dating. Earth-Science Reviews 4:203.CrossRefGoogle Scholar
PerkinElmer. 2005. High performance liquid scintillation analyzers. Brochure #007204_01.Google Scholar
Rakowski, AZ, Kuc, T, Nakamura, T, Pazdur, A. 2005. Radiocarbon concentration in urban area. Geochronometria 24:63–8.Google Scholar
Ruddiman, WF. 2005. Plows, Plagues and Petroleum: How Humans Took Control of Climate. Princeton: Princeton University Press. 202 p.Google Scholar
Schönhofer, F. 1989. Determination of 14C in alcoholic beverages. Radiocarbon 31(3):777–84.Google Scholar
Shibata, Y, Yoneda, M, Tanaka, A, Uehiro, T, Morita, M, Uchida, M, Yoshinaga, J, Hirota, M. 2002. Application of accelerator mass spectrometry (AMS) to environmental researches. Proceedings of the Colloquium on Ultra-trace Analysis of Environmental Samples. Japan Atomic Energy Research Institute, p 39–44. URL: jolisf.tokai-sc.jaea.go.jp/pdf/conf/JAERI-Conf-2002-002.pdf.Google Scholar
Stuiver, M, Polach, HA. 1977. Discussion: reporting of 14C data. Radiocarbon 19(3):355–63.CrossRefGoogle Scholar
Tamers, M. 2006. Distinguishing between ‘bioethanol’ and petroleum ethanol. Ethanol Producer Magazine June:106–9.Google Scholar
United Nations Framework Convention on Climate Change [UNFCCC]. 1997. Kyoto Protocol. URL: unfccc.int/2860.php.Google Scholar
United Nations Framework Convention on Climate Change [UNFCCC]. 2005. A guide to the Climate Change Convention and the Kyoto Protocol. Rev. ed. Depledge, J, Lamb, R, editors. URL: unfccc.int/2860.php.Google Scholar