184 research outputs found

    Inherent tracers for carbon capture and storage in sedimentary formations: composition and applications

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    Inherent tracers - the “natural” isotopic and trace gas composition of captured CO₂ streams – are potentially powerful tracers for use in CCS technology. This review outlines for the first time the expected carbon isotope and noble gas compositions of captured CO₂ streams from a range of feedstocks, CO₂-generating processes and carbon capture techniques. The C-isotope composition of captured CO₂ will be most strongly controlled by the feedstock, but significant isotope fractionation is possible during capture; noble gas concentrations will be controlled by the capture technique employed. Comparison with likely baseline data suggests that CO₂ generated from fossil fuel feedstocks will often have δ13C distinguishable from storage reservoir CO₂. Noble gases in amine-captured CO₂ streams are likely to be low concentration, with isotopic ratios dependant on the feedstock, but CO₂ captured from oxyfuel plants may be strongly enriched in Kr and Xe which are potentially valuable subsurface tracers. CO₂ streams derived from fossil fuels will have noble gas isotope ratios reflecting a radiogenic component that will be difficult to distinguish in the storage reservoir, but inheritance of radiogenic components will provide an easily recognisable signature in the case of any unplanned migration into shallow aquifers or to the surface

    Lunar exploration: opening a window into the history and evolution of the inner Solar System

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    The lunar geological record contains a rich archive of the history of the inner Solar System, including information relevant to understanding the origin and evolution of the Earth-Moon system, the geological evolution of rocky planets, and our local cosmic environment. This paper provides a brief review of lunar exploration to-date, and describes how future exploration initiatives will further advance our understanding of the origin and evolution of the Moon, the Earth-Moon system, and of the Solar System more generally. It is concluded that further advances will require the placing of new scientific instruments on, and the return of additional samples from, the lunar surface. Some of these scientific objectives can be achieved robotically, for example by in situ geochemical and geophysical measurements and through carefully targeted sample return missions. However, in the longer term, we argue that lunar science would greatly benefit from renewed human operations on the surface of the Moon, such as would be facilitated by implementing the recently proposed Global Exploration Roadmap

    Predominantly Non-Solar Origin of Nitrogen in Lunar Soils

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    Simultaneous static-mode mass spectrometric measurements of nitrogen, carbon, helium, neon, and argon, extracted from the same aliquot of sample by high-resolution stepped combustion, have been made for a suite of five lunar soils. Noble gas isotope ratios show that the majority of noble gases are derived from a solar wind source; for example, at peak release temperatures of 500–600 °C,21Ne/22Ne = 0.0313 ± 0.0007 to 0.0333 ± 0.0007, and 20Ne/22Ne = 11.48 ± 0.05 to 12.43 ± 0.07, with values at the lowest temperature steps less fractionated during implantation from, and therefore even closer to, solar values (21Ne/22NeSW = 0.03361 ± 0.00018 and 20Ne/22NeSW = 14.001 ± 0.042 (Pepin et al., 2012)). Despite the co-release of nitrogen and solar wind argon, measured nitrogen isotopic signatures at each temperature step, whilst variable, are significantly more enriched in 15N compared to the measured solar wind nitrogen value from the Genesis mission. Therefore, mixing between a 15N-enriched non-solar planetary nitrogen source with solar wind nitrogen is required to explain the measured isotopic values from the stepped combustion analysis of lunar soils. Binary mixing calculations, made under different assumptions about the degree of loss of solar wind 36Ar, reveal that the majority (up to 98%) of the nitrogen released is derived from a non-solar source. The range of modelled non-solar end-member nitrogen compositions required to satisfy the measuredδ15N values varies between samples and temperature steps from +5‰ up to +300‰, or between +87‰ and +160‰ for bulk samples. This range of modelled isotopic compositions for the non-solar source of nitrogen encompasses measured values for several different groups of carbonaceous chondrite, as well as IDPs

    Search for anomalously heavy isotopes of helium in the Earth's atmosphere

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    Motivated by the theoretical hypotheses on the existence of heretofore unobserved stable elementary particles and exotic nuclear states, we searched for doubly-charged particles, as anomalously heavy isotopes of helium, in the Earth's atmoshpere using a sensitive laser spectroscopy technique. The concentration of noble-gas-like atoms in the atmosphere and the subsequent very large depletion of the light He-3,4 isotopes allow us to set stringent limits on th abundance: 10^-13 to 10^-17 per atom in the solar system, over the mass range of 20 to 10,000 amu.Comment: 13 pages, 4 figure

    Recycled gabbro signature in hotspot magmas unveiled by plume–ridge interactions

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    Lavas erupted within plate interiors above upwelling mantle plumes have chemical signatures that are distinct from midocean ridge lavas. When a plume interacts with a mid-ocean ridge, the compositions of both their lavas changes, but there is no consensus as to how this interaction occurs1–3. For the past 15 Myr, the Pacific–Antarctic mid-ocean ridge has been approaching the Foundation hotspot4 and erupted lavas have formed seamounts. Here we analyse the noble gas isotope and trace element signature of lava samples collected from the seamounts. We find that both intraplate and on-axis lavas have noble gas isotope signatures consistent with the contribution from a primitive plume source. In contrast, nearaxis lavas show no primitive noble gas isotope signatures, but are enriched in strontium and lead, indicative of subducted former oceanic lower crust melting within the plume source5–7. We propose that, in a near-ridge setting, primitive, plumesourced magmas formed deep in the plume are preferentially channelled to and erupted at the ridge-axis. The remaining residue continues to rise and melt, forming the near-axis seamounts. With the deep melts removed, the geochemical signature of subduction contained within the residue becomes apparent. Lavas with strontium and lead enrichments are found worldwide where plumes meet mid-ocean ridges6–8, suggesting that subducted lower crust is an important but previously unrecognised plume component

    The Inherent Tracer Fingerprint of Captured CO2.

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    Carbon capture and storage (CCS) is the only currently available technology that can directly reduce anthropogenic CO2 emissions arising from fossil fuel combustion. Monitoring and verification of CO2 stored in geological reservoirs will be a regulatory requirement and so the development of reliable monitoring techniques is essential. The isotopic and trace gas composition - the inherent fingerprint - of captured CO2 streams is a potentially powerful, low cost geochemical technique for tracking the fate of injected gas in CCS projects; carbon and oxygen isotopes, in particular, have been used as geochemical tracers in a number of pilot CO2 storage sites, and noble gases are known to be powerful tracers of natural CO2 migration. However, the inherent tracer fingerprint in captured CO2 streams has yet to be robustly investigated and documented and key questions remain, including how consistent is the fingerprint, what controls it, and will it be retained en route to and within the storage reservoir? Here we present the first systematic measurements of the carbon and oxygen isotopes and the trace noble gas composition of anthropogenic CO2 captured from combustion power stations and fertiliser plants. The analysed CO2 is derived from coal, biomass and natural gas feedstocks, using amine capture, oxyfuel and gasification processes, from six different CO2 capture plants spanning four different countries. We find that δ13C values are primarily controlled by the δ13C of the feedstock while δ18O values are predominantly similar to atmospheric O2. Noble gases are of low concentration and exhibit relative element abundances different to expected reservoir baselines and air, with isotopic compositions that are similar to air or fractionated air. The use of inherent tracers for monitoring and verification was provisionally assessed by analysing CO2 samples produced from two field storage sites after CO2 injection. These experiments at Otway, Australia, and Aquistore, Canada, highlight the need for reliable baseline data. Noble gas data indicates noble gas stripping of the formation water and entrainment of Kr and Xe from an earlier injection experiment at Otway, and inheritance of a distinctive crustal radiogenic noble gas fingerprint at Aquistore. This fingerprint can be used to identify unplanned migration of the CO2 to the shallow subsurface or surface
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