Hostname: page-component-8448b6f56d-gtxcr Total loading time: 0 Render date: 2024-04-24T02:03:47.869Z Has data issue: false hasContentIssue false

Biogenic Carbon Fraction of Biogas and Natural Gas Fuel Mixtures Determined with 14C

Published online by Cambridge University Press:  26 July 2016

Sanne W L Palstra*
Affiliation:
Centre for Isotope Research, ESRIG, University of Groningen, Nijenborgh 4, 9747 AG Groningen, the Netherlands
Harro A J Meijer
Affiliation:
Centre for Isotope Research, ESRIG, University of Groningen, Nijenborgh 4, 9747 AG Groningen, the Netherlands
*
2. Corresponding author. Email: s.w.l.palstra@rug.nl.

Abstract

This study investigates the accuracy of the radiocarbon-based calculation of the biogenic carbon fraction for different biogas and biofossil gas mixtures. The focus is on the uncertainty in the 14C reference values for 100% biogenic carbon and on the 13C-based isotope fractionation correction of the measured 14C values. The separately (AMS) measured CO2 and CH4 fractions of 8 different biogas samples showed 14C values between 102‰ and 116% (pMC). The δ13C values of these samples varied between –6‰ and +31‰ for the CO2 fraction and between –28‰ and –62‰ for the CH4 fraction. The uncertainty in calculated biogenic carbon fractions due to uncertainty in the 14C reference values depends on the available information about the origin of the used biogenic materials. It varies between ±0.5% and ±3.5% (absolute) depending on the type of biogas. A method is proposed to minimize this uncertainty for different groups of biogases. The calculated biogenic carbon fraction deviates up to ±2.5% for biofossil gas mixtures, if the applied isotope fractionation correction is based on the δ13C value of the mixed biofossil sample instead of the biogenic δ13C value. Combination of both error sources shows that the uncertainty in the calculated biogenic carbon fraction varies between ±0.7% and ±4.5%, depending on the type of biogas in the sample.

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

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

European Commission. 2003. 2003/87/EC. Establishing a scheme for greenhouse gas emission allowance trading within the Community and Amending Council Directive 96/61/EC, Directive of the European Parliament and of the Council, Official Journal of the European Union, L275, 25.10.2003. p 3246.Google Scholar
Aerts-Bijma, AT, Meijer, HAJ, van der Plicht, J. 1997. AMS sample handling in Groningen. Nuclear Instruments and Methods in Physics Research B 123(1–4):221–5.Google Scholar
ASTM. 2012. ASTM D6866-12. Standard test methods for determining the biobased content of solid, liquid and gaseous using radiocarbon analysis. ASTM International, West Conshohocken, Pennsylvania, USA.Google Scholar
Bergamaschi, P, Lubina, C, Königstedt, R, Fisher, H. 1998. Stable isotopic signatures (δ13C, δD) of methane from European landfill sites. Journal of Geophysical Research 103(D7):8251–65.CrossRefGoogle Scholar
Cabral, AR, Capanema, MA, Gebert, J, Moreira, JF, Jugnia, LB. 2010. Quantifying microbial methane oxidation efficiencies in two experimental landfill biocovers using stable isotopes. Water, Air, & Soil Pollution 209(1–4):157–72.CrossRefGoogle Scholar
Conrad, R. 2005. Quantification of methanogenic pathways using stable isotopic signatures: a review and a proposal. Organic Geochemistry 36(5):739–52.Google Scholar
de Rooij, M, van der Plicht, J, Meijer, HAJ. 2008. Sample dilution for AMS 14C analysis of small samples (30–150 μg C). Radiocarbon 50(3):413–36.Google Scholar
Dijs, IJ, van der Windt, E, Kaihola, L, van der Borg, K. 2006. Quantitative determination by 14C analysis of the biological component in fuels. Radiocarbon 48(3):315–23.Google Scholar
Fellner, J, Rechberger, H. 2009. Abundance of 14C in biomass fractions of wastes and solid recovered fuels. Waste Management 29(5):1495–503.Google Scholar
Fuex, AN. 1977. The use of stable carbon isotopes in hydrocarbon exploration. Journal of Geochemical Exploration 7:155–88.Google Scholar
Gonfiantini, R. 1984. Stable Isotope Reference Samples for Geochemical and Hydrological Investigations. Vienna: IAEA. 77 p.Google Scholar
Hsueh, DY, Krakauer, NY, Randerson, JT, Xu, X, Trumbore, SE, Southon, JR. 2007. Regional patterns of radiocarbon and fossil fuel-derived CO2 in surface air across North America. Geophysical Research Letters 34: L02816, doi:10.1029/2006GL027032.Google Scholar
Hua, Q, Barbetti, M, Rakowski, AZ. 2013. Atmospheric radiocarbon for the period 1950–2010. Radiocarbon 55(4):2059–72.Google Scholar
Hut, G, Begemann, MJS, Weerkamp, HR. 1984. Determination of isotope ratios in the natural gas components CH4 and N2 separated by gas chromatography. Chemical Geology 46(1):7583.Google Scholar
ISO. 2012. ISO/FDIS 13833. Stationary source emissions – Determination of the ratio of biomass (biogenic) and fossil-derived carbon dioxide – Radiocarbon sampling and determination. [This standard is still under construction.] ISO, Geneva, Switzerland.Google Scholar
Krzycki, JA, Kenealy, WR, DeNiro, MJ, Zeikus, JG. 1987. Stable carbon isotope fractionation by Methanosarcina barkeri during methanogenesis from acetate, methanol, or carbon dioxide-hydrogen. Applied and Environmental Microbiology 53(10):2597–9.Google Scholar
Laukenmann, S, Polag, D, Heuwinkel, H, Greule, M, Gronauer, A, Lelieveld, J, Keppler, E. 2010. Identification of methanogenic pathways in anaerobic digesters using stable carbon isotopes. Engineering in Life Sciences 10(6):509–14.Google Scholar
Levin, I, Kromer, B. 2004. The tropospheric 14CO2 level in mid-latitudes of the Northern Hemisphere (1959–2003). Radiocarbon 46(3):1261–72.CrossRefGoogle Scholar
Levin, I, Bergamanschi, P, Dörr, H, Trapp, D. 1993. Stable isotopic signature of methane from major sources in Germany. Chemosphere 26(1–4):161–77.Google Scholar
Levin, I, Graul, R, Trivett, NBA. 1995. Long-term observations of atmospheric CO2 and carbon isotopes at continental sites in Germany. Tellus B 47(1–2):2334.Google Scholar
Levin, I, Kromer, B, Schmidt, M, Sartorius, H. 2003. A novel approach for independent budgeting of fossil fuels CO2 over Europe by 14CO2 observations. Geophysical Research Letters 30(23):2194.Google Scholar
Mann, WB. 1983. An international reference material for radiocarbon dating. Radiocarbon 25(2):519–27.Google Scholar
Meijer, HAJ, van der Plicht, J, Gislefoss, JS, Nydal, R. 1995. Comparing long-term atmospheric 14C and 3H records near Groningen, The Netherlands with Fruholmen, Norway and Izaña, Canary Islands 14C stations. Radiocarbon 37(1):3950.Google Scholar
Milkov, AV. 2005. Molecular and stable isotope compositions of natural gas hydrates: a revised global dataset and basic interpretations in the context of geological settings. Organic Geochemistry 36(5):681702.Google Scholar
Mohn, J, Szidat, S, Fellner, J, Rechberger, H, Quartier, R, Buchmann, B, Emmenegger, L. 2008. Determination of biogenic and fossil CO2 emitted by waste incineration based on 14CO2 and mass balances. Bioresource Technology 99(14):6471–9.CrossRefGoogle ScholarPubMed
Mohn, J, Szidat, S, Zeyer, K, Emmenegger, L. 2012. Fossil and biogenic CO2 from waste incineration based on a yearlong radiocarbon study. Waste Management 32(8):1516–20.Google Scholar
Mook, WG. 1980. The effect of fossil fuel and biogenic CO2 on the 13C and 14C content of atmospheric carbon dioxide. Radiocarbon 22(2):392–7.Google Scholar
Mook, WG. 2000. Environmental Isotopes in the Hydrological Cycle. Volume 1, Introduction, Principles, Methods. Vienna: UNESCO/IAEA. 255 p.Google Scholar
Mook, WG, van der Plicht, J. 1999. Reporting 14C activities and concentrations. Radiocarbon 41(3):227–39.Google Scholar
Norton, GA, Devlin, SL. 2006. Determining the modern carbon content of biobased products using radiocarbon analysis. Bioresource Technology 97(16):2084–90.CrossRefGoogle ScholarPubMed
Palstra, SWL, Meijer, HAJ. 2010. Carbon-14 based determination of the biogenic fraction of industrial CO2 emissions – application and validation. Bioresource Technology 101(10):3702–10.Google Scholar
Palstra, SWL, Karstens, U, Streurman, H-J, Meijer, HAJ. 2008. Wine ethanol 14C as a tracer for fossil fuel CO2 emissions in Europe: measurements and model comparison. Journal of Geophysical Research 113: D211302, doi:10.1029/2008JD010282.Google Scholar
Rosenfeld, WD, Silverman, SR. 1959. Carbon isotope fractionation in bacterial production of methane. Science 130(3389):1658–9.Google Scholar
Schoell, M. 1980. The hydrogen and carbon isotopic composition of methane from natural gases of various origins. Geochimica et Cosmochimica Acta 44(5):649–61.Google Scholar
Staber, W, Flamme, S, Fellner, J. 2008. Methods for determining the biomass content of waste. Waste Management & Research 26(1):7887.Google Scholar
Stuiver, M. 1983. International agreements and the use of the new oxalic acid standard. Radiocarbon 25(2):793–5.Google Scholar
Stuiver, M, Polach, HA. 1977. Discussion: reporting of 14C data. Radiocarbon 19(3):355–63.Google Scholar
van der Plicht, J, Wijma, S, Aerts, AT, Pertuisot, MH, Meijer, HAJ. 2000. Status report: the Groningen AMS facility. Nuclear Instruments and Methods in Physics Research B 172(1–4):5865.Google Scholar
Weiland, P. 2010. Biogas production: current state and perspectives. Applied Microbiology and Biotechnology 85(4):849–60.Google Scholar
Whiticar, MJ, Faber, E, Schoell, M. 1986. Biogenic methane formation in marine and freshwater environments: CO2 reduction vs. acetate fermentation—isotope evidence. Geochimica et Cosmochimica Acta 50(5):693709.Google Scholar
Wijma, S, Aerts, AT, van der Plicht, J, Zondervan, A. 1996. The Groningen AMS facility. Nuclear Instruments and Methods in Physics Research B 113(1–4):465–9.Google Scholar
Zyakun, AM, Muravyev, AI, Baskunov, BP, Laurinavichius, KS, Zakharchenko, VN, Peshenko, VP, Lykov, IN, Shestakova, GA. 2010. Estimation of microbial methane generation and oxidation rates in the municipal solid waste landfill of Kaluga city, Russia. Isotopes in Environmental and Health Studies 46(1):7890.Google Scholar