Abstract

Short chain carbon-14 (14C) containing organic compounds can be formed by abiotic oxidation of carbides and impurities within nuclear fuel cladding. During fuel reprocessing and subsequent waste storage there is potential for these organic compounds to enter shallow subsurface environments due to accidental discharges. Currently there is little data on the persistence of these compounds in such environments. Four 14C-labelled compounds (acetate; formate; formaldehyde and methanol) were added to aerobic microcosm experiments that contained glacial outwash sediments and groundwater simulant representative of the Sellafield nuclear reprocessing site, UK. Two concentrations of each electron donor were used, low concentration (10−5 M) to replicate predicted concentrations from an accidental release and high concentration (10−2 M) to study the impact of the individual electron donor on the indigenous microbial community in the sediment. In the low concentration system only ∼5% of initial 14C remained in solution at the end of experiments in contact with atmosphere (250–350 h). The production of 14CO2(g) (measured after 48 h) suggests microbially mediated breakdown is the primary removal mechanism for these organic compounds, although methanol loss may have been partially by volatilisation. Highest retention of 14C by the solid fractions was found in the acetate experiment, with 12% being associated with the inorganic fraction, suggesting modest precipitation as solid carbonate. In the high concentration systems only ∼5% of initial 14C remains in solution at the end of the experiments for acetate, formate and methanol. In the formaldehyde experiment only limited loss from solution was observed (76% remained in solution). The microbial populations of unaltered sediment and those in the low concentration experiments were broadly similar, with highly diverse bacterial phyla present. Under high concentrations of the organic compounds the abundance of common operational taxonomic units was reduced by 66% and the community structure was dominated by Proteobacteria (particularly Betaproteobacteria) signifying a shift in community structure in response to the electron donor available. The results of this study suggest that many bacterial phyla that are ubiquitous in near surface soils are able to utilise a range of 14C-containing low molecular weight organic substances very rapidly, and thus such substances are unlikely to persist in aerobic shallow subsurface environments.

Highlights

  • Low molecular weight organic (LMWO) substances have long been considered a potential source of future carbon-14 (14C) release from deep subsurface environments due to the predicted accumulation of 14CH4 in underground repositories (Jefferies, 1990; Jackson and Yates, 2011; Limer et al, 2011, 2013; Marshall et al, 2011)

  • The high concentration tests exhibited a lag phase lasting between 1 and 4 days with no significant 14C removal observed it is likely that the indigenous microbial population utilised these electron donors at the same rate as the low concentration tests, but due to the higher overall concentration of LMWO substances, this had little impact on the proportion of the initial 14C-organic remaining in solution

  • This study shows there is minimal persistence of 14C-labelled LMWO substances in solution in the presence of sediment with an active microbial population under aerobic conditions

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Summary

Introduction

Low molecular weight organic (LMWO) substances have long been considered a potential source of future carbon-14 (14C) release from deep subsurface environments due to the predicted accumulation of 14CH4 in underground repositories (Jefferies, 1990; Jackson and Yates, 2011; Limer et al, 2011, 2013; Marshall et al, 2011). There is concern that corrosion of activated fuel and fuel cladding may form a range of LMWO substances as a by-product (Wieland and Hummel, 2015) providing a source for it's potential release to shallow subsurface environments from storage ponds. At greater depth the oxygen penetration is minimal and corrosion of readily oxidised metals, such as magnesium, uranium and iron, leads to chemically reducing conditions forming within storage ponds (Equations (1)–(3))

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