159 research outputs found

    Inhibition of therapeutic protein aggregation by cyclodextrins

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    The Influence of Water-rock Reactions and O Isotope Exchange with CO2 on Water Stable Isotope Composition of CO2 Springs in SE Australia

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    Monitoring injected CO2 in CCS sites using oxygen isotopes of water has been demonstrated in field and laboratory experiments. Here, we examine natural CO2-rich springs in the Daylesford-Hepburn region, South East Australia, which show water 18O depletion compared to local precipitation. Geochemical modelling shows that water-rock reactions are unlikely to have a significant effect on the observed ÎŽ18O values, which can only be explained by isotopic exchange with CO2. The water ÎŽ18O shift can be used for monitoring CO2 impact on shallow groundwater aquifers, provided that there is sufficient CO2 and distinction between water and CO2 ÎŽ18O values exists

    The Role of Polysorbate 80 and HPÎČCD at the Air-Water Interface of IgG Solutions

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    Purpose: To test the hypothesis of surface displacement as the underlying mechanism for IgG stabilization by polysorbates and HPÎČCD against surface-induced aggregation. Methods: Adsorption/desorption-kinetics of IgG-polysorbate 80/-HPÎČCD were monitored. Maximum bubble pressure method was used for processes within seconds from surface formation. Profile analysis tensiometry was applied over long periods and to assess surface rheologic properties. Additionally, the kinetics of adsorption, desorption and surface displacement was followed by a double-capillary setup of the profile analysis tensiometer, allowing drop bulk exchange. Results: Weak surface activity for HPÎČCD vs. much higher surface activity for polysorbate 80 was shown. Protein-displacement when exceeding a polysorbate 80 concentration close to the CMC and a lack of protein displacement for HPÎČCD was observed. The drop bulk exchange experiments show IgG displacement by polysorbate 80 independent of the adsorption order. In contrast, HPÎČCD coexists with IgG at the air-water interface when the surface layer is built from a mixed IgG-HPÎČCD-solution. Incorporation of HPÎČCD in a preformed IgG-surface-layer does not occur. Conclusions: The results confirm surface displacement as the stabilization mechanism of polysorbate 80, but refute the frequently held opinion, that HPÎČCD stabilizes proteins against aggregation at the air-water interface in a manner comparable to non-ionic surfactant

    L’ AMBIANCE AU TRAVAIL ET LA PRODUCTIVITE DU PERSONNEL : Une Ă©tude menĂ©e auprĂšs des entreprises du secteur privĂ© au Cameroun

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    L’aspect climat social est un facteur dĂ©terminant de l’efficacitĂ© humaine au sein d’une organisation. De mĂȘme, le suivi de la productivitĂ© est d’une nĂ©cessitĂ© vitale pour les entreprises en vue d’apprĂ©hender en temps rĂ©el les principaux obstacles Ă  l’efficacitĂ© organisationnelle. Parmi les dĂ©terminants majeurs de cette efficacitĂ©, figure l’aspect climat social, notamment l’ambiance au travail. Beaucoup d’études ont Ă©tĂ© menĂ©es dans ce domaine du climat social des entreprises mais trĂšs peu se sont intĂ©ressĂ©es au reflet sur la productivitĂ© des hommes, des facteurs contraignants de l’ambiance gĂ©nĂ©rale au travail. Cette Ă©tude se focalise Ă  dĂ©terminer l’influence des conflits interpersonnels et de la discrimination sur la productivitĂ© du personnel dans les entreprises privĂ©es au Cameroun. Les rĂ©sultats de l’investigation menĂ©e sur un Ă©chantillon de 56 entreprises privĂ©es montrent que, dans le contexte camerounais, les pratiques discriminatoires sont nuisibles Ă  la performance humaine. Par contre, les conflits interpersonnels n’impactent pas vĂ©ritablement, du point de vue statistique, le rendement des travailleurs

    Stepping into the Same River Twice: Field Evidence for the Repeatability of a CO2 Injection Test

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    A single well characterisation test was conducted at the CO2CRC Otway storage site in Victoria, Australia, in 2011 and repeated in 2014. The near-well permeability was found to have declined nearly 60% since the 2011 test, while the residual saturation inferred from a variety of techniques was lower in 2014. There was a significant change in water chemistry, suggesting an alteration of near-well reservoir properties. Possible reasons for these changes are explored, and the implications for other field tests are discussed

    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 ÎŽ13C values are primarily controlled by the ÎŽ13C of the feedstock while ÎŽ18O 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

    Using oxygen isotopes to quantitatively assess residual CO2 saturation during the CO2CRC Otway Stage 2B Extension residual saturation test

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    Residual CO2 trapping is a key mechanism of secure CO2 storage, an essential component of the Carbon Capture and Storage technology. Estimating the amount of CO2 that will be residually trapped in a saline aquifer formation remains a significant challenge. Here, we present the first oxygen isotope ratio (ÎŽ18O) measurements from a single-well experiment, the CO2CRC Otway 2B Extension, used to estimate levels of residual trapping of CO2. Following the initiation of the drive to residual saturation in the reservoir, reservoir water ÎŽ18O decreased, as predicted from the baseline isotope ratios of water and CO2, over a time span of only a few days. The isotope shift in the near-wellbore reservoir water is the result of isotope equilibrium exchange between residual CO2 and water. For the region further away from the well, the isotopic shift in the reservoir water can also be explained by isotopic exchange with mobile CO2 from ahead of the region driven to residual, or continuous isotopic exchange between water and residual CO2 during its back-production, complicating the interpretation of the change in reservoir water ÎŽ18O in terms of residual saturation. A small isotopic distinction of the baseline water and CO2 ÎŽ18O, together with issues encountered during the field experiment procedure, further prevents the estimation of residual CO2 saturation levels from oxygen isotope changes without significant uncertainty. The similarity of oxygen isotope-based near-wellbore saturation levels and independent estimates based on pulsed neutron logging indicates the potential of using oxygen isotope as an effective inherent tracer for determining residual saturation on a field scale within a few days

    Estimating geological CO2 storage security to deliver on climate mitigation

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    Carbon capture and storage (CCS) can help nations meet their Paris CO2 reduction commitments cost-effectively. However, lack of confidence in geologic CO2 storage security remains a barrier to CCS implementation. Here we present a numerical program that calculates CO2 storage security and leakage to the atmosphere over 10,000 years. This combines quantitative estimates of geological subsurface CO2 retention, and of surface CO2 leakage. We calculate that realistically well-regulated storage in regions with moderate well densities has a 50% probability that leakage remains below 0.0008% per year, with over 98% of the injected CO2 retained in the subsurface over 10,000 years. An unrealistic scenario, where CO2 storage is inadequately regulated, estimates that more than 78% will be retained over 10,000 years. Our modelling results suggest that geological storage of CO2 can be a secure climate change mitigation option, but we note that long-term behaviour of CO2 in the subsurface remains a key uncertainty
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