82 research outputs found

    Energy Policy Scenarios of CCS Implementation in the Greek Electricity Sector

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    The energy balance of Greece is strongly dependent on imported oil. The rather late introduction of natural gas has increased the diversity of the energy mix while the share of renewable sources in primary energy supply still needs to increase according to the existing potential. Yet, Greece as one of the most of the EU developed countries encounters a serious task: the need to increase its electricity production of almost 5% per year but at the same time to reduce the CO2 emissions according with the National and International (20-20-20) regulations and allocation plans. Therefore reducing CO2 emissions has become a major priority for national government. In addition, from 2013, there will be the full implementation of the wholesale market in the European Trading Scheme (ETS) which is currently in the last stages of a transition phase.In Greece electricity is mainly generated from lignite, thus making the electricity sector one of the main contributors to GHG emissions with a level above 40% of the total country and higher than the corresponding average of the rest of the EU countries. The possible implementation of Carbon Capture and Storage (CCS) technologies would then become very decisive due to the large use of the lignite as fuel in the country electricity mix. CCS technology has the potential of increasing the flexibility on the achievement greenhouse gas emissions reduction by allowing to continue to use fossil fuels, which still guarantees feasibility in the energy sector. This work presents a roadmap with the modeling of the main technologies associated to the CCS and its implementation into the Greek energy system considering existing National and International Strategic energy plans under different scenarios. The implementation of CCS technologies would have a large influence on the national electrical power production, having the responsibility for large shares of the emissions reduction that can potentially achieved in this sector. For this purpose, TIMES (The Integrated MARKAL/EFOM System) has been chosen as the principal tool for building a techno-economic model of the Greek energy system and its possible evaluation over time (2040)

    Assessment of the impact of CO 2 storage in sandstone formations by experimental studies and geochemical modeling: the case of the Mesohellenic Trough, NW Greece

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    Representative sandstone samples from Mesohellenic Trough (NW Greece) were selected to investigate the geochemical reactions that occur when they come in contact with CO2 under representative in-situ conditions (T = 70 °C, P = 150 bar, 6 months reaction in batch experiments). Those sandstones consisted of predominant calcite and quartz, with lesser amounts of feldspars, chlorite, ankerite, dolomite, kaolinite, montmorillonite and muscovite. After reaction with CO2, the brine became acidic and was enriched in cations as a result of mineral dissolution. Minor mineralogical changes were observed that involved: a) the dissolution of carbonate minerals and b) the incongruent dissolution of chlorite to form clays and silica. The results related to these, have been linked with geochemical modelling using the PHREEQC code. Simulation results for a 10 ka time period predicted that chlorite was expected to dissolve completely within 100 years, leading to boehmite growth and increasing the mass of dolomite. Feldspars were expected to react at a later stage in the reaction sequence. Sensitivity tests were run to access the effect of various adjustable parameters on the outcome results. The geochemical experiments and modelling lend support to the view that Pentalofos and Tsotyli sandstone formations of the Mesohellenic Trough are suitable for the long-term storage of CO2 produced in the neighbouring lignite-fired power plants, at least in terms of mineralogy and geochemistry

    Removal of phosphate from aqueous solutions by adsorption onto Ca(OH)2 treated natural clinoptilolite

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    Phosphorus (P) recovery from wastewater is of great interest especially when the loaded adsorbent can be used in the agriculture as slow-release fertilizer. The application depends on environmental concerns related to the chemical modification of the adsorbent and the release of toxic compounds from the loaded material to the soil or the water during adsorption. The present work focused on the phosphate (PO4-P) removal from aqueous solutions under low P concentrations (0.5–10mg/L) by using Ca(OH)2-pretreated natural zeolite (CaT-Z). As activation agent, Ca(OH)2 presents benefits in terms of pretreatment costs and environmental impact of the applied adsorbent. The pretreatment of natural zeolite (clinoptilolite) with 0.25mol/L Ca(OH)2 led to an increase of P removal from 1.7 to 97.6% at initial P concentration of 10mg/L, pH 7 and 298K. Low residual concentrations of 81–238μg P/L were achieved at 298K rendering CaT-Z a promising sorbent for tertiary wastewater treatment. At 200mg P/L, the adsorption capacity was 7.57mg P/g CaT-Z. The P removal efficiency was pH-independent suggesting a beneficial use of CaT-Z under acidic and alkaline conditions. Adsorption was found to be an endothermic and slow process reaching equilibrium after 120h, whereas the half of the PO4-P was adsorbed in the first 8h. The applied kinetic models showed that both film and intraparticle diffusion contributed to phosphate removal. Phosphate sorption decreased in the presence of the anionic surfactant SDS, Fe2+, HCO3−, acetate and citrate anion. The predominant mechanisms of ligand exchange and Ca-P surface precipitation were confirmed by the IR-ATR and SEM-EDS analyses, respectively

    Stability and characterisation of spoil heaps in European surface lignite mines: a state-of-the-art review in light of new data

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    The large amount of spoil material produced during the mining process imposes a significant economic and environmental liability on lignite producers. In this context, the present paper provides an overview of the geotechnical characteristics of European lignite mine spoil heaps and discusses their significance to the stability of the heaps. In order to achieve this, samples collected from spoil heaps of Polish, Czech and Greek mines are analysed and the results are compiled with data from the literature. A major conclusion drawn is that both physical and engineering properties of spoil heaps indicate a noteworthy variability, which is larger than typical in-situ ground material. This is because of the additional factors affecting spoil heap deposition, such as the transportation and dumping method. Furthermore, failure mechanisms and case histories of large instabilities in lignite spoil heaps are critically discussed in order to better understand triggering failure mechanisms. It is concluded that classical assumptions made for natural soil slopes and relevant limit equilibrium models should be cautiously applied to spoil heaps. The challenges associated with numerical and probabilistic modelling of spoil heap stability, such as the inherent spatial variability of spoils and the time-dependent changes in their geotechnical properties, are also critically discussed. Finally, important research gaps in design and analysis of spoil heap stability, such as the absence of appropriate constitutive models developed specifically for spoil materials, are summarised

    Rapid post-disaster infrastructure damage characterisation enabled by remote sensing and deep learning technologies -- a tiered approach

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    Critical infrastructure, such as transport networks and bridges, are systematically targeted during wars and suffer damage during extensive natural disasters because it is vital for enabling connectivity and transportation of people and goods, and hence, underpins national and international economic growth. Mass destruction of transport assets, in conjunction with minimal or no accessibility in the wake of natural and anthropogenic disasters, prevents us from delivering rapid recovery and adaptation. As a result, systemic operability is drastically reduced, leading to low levels of resilience. Thus, there is a need for rapid assessment of its condition to allow for informed decision-making for restoration prioritisation. A solution to this challenge is to use technology that enables stand-off observations. Nevertheless, no methods exist for automated characterisation of damage at multiple scales, i.e. regional (e.g., network), asset (e.g., bridges), and structural (e.g., road pavement) scales. We propose a methodology based on an integrated, multi-scale tiered approach to fill this capability gap. In doing so, we demonstrate how automated damage characterisation can be enabled by fit-for-purpose digital technologies. Next, the methodology is applied and validated to a case study in Ukraine that includes 17 bridges, damaged by human targeted interventions. From regional to component scale, we deploy technology to integrate assessments using Sentinel-1 SAR images, crowdsourced information, and high-resolution images for deep learning to facilitate automatic damage detection and characterisation. For the first time, the interferometric coherence difference and semantic segmentation of images were deployed in a tiered multi-scale approach to improve the reliability of damage characterisations at different scales

    Phosphate removal by Ca(OH)2-treated natural minerals : experimental and modeling studies

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    Adsorption of phosphate phosphorus (PO4-P) from wastewater onto eco-friendly geosorbents has gained great attention aiming at recovering an essential nutrient for crop production. Notably, the literature on PO4-P adsorption kinetics is limited to the application of either empirical reaction-based models lacking a physical significance or over-simplified diffusion-based models frequently used outside their applicability area. In this study, equilibrium and kinetic experiments are presented under a wide range of phosphate concentrations (50-500 mg P/L) using sustainable and low-cost modified adsorbents. The kinetics of PO4-P adsorption from aqueous solutions onto Ca(OH)2-treated zeolite (CaT-Z) and bentonite (CaT-B) was analyzed by a dimensionless two-phase homogeneous surface diffusion model (TP-HSDM) assuming constant diffusivity and coupled with the double selectivity isotherm model (DSM). The TP-HSDM fit to the data at four initial P concentrations (50, 100, 200 and 300 mg/L) resulted in an average relative error of 14.6% and 17.4% from the experimental data for CaT-Z and CaT-B, respectively. The average surface diffusion coefficient (Ds) ranged from 2.5 × 10-10 to 8.7 × 10-10 cm2/s for CaT-Z and from 1.6 × 10-10 to 4.78 × 10-9 cm2/s for CaT-B. The external mass transfer coefficient (kf) ranged from 2.72 × 10-4 to 8.38 × 10-4 cm/s for CaT-Z and from 5.63 × 10-4 to 2.24 × 10-3 cm/s for CaT-B. The dimensionless Biot (Bi) number exhibited values in the order of magnitude of 105 indicating that intraparticle diffusion is the controlling mass transfer mechanism for both materials

    Geotechnical Characterization of Fine-Grained Spoil Material from Surface Coal Mines

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    Coal mines produce large amounts of excavated waste soils, known as spoils. These materials can cover vast areas, are typically dumped in heaps without any treatment and are difficult to exploit for engineering purposes because of their significant variability. Efficient exploitation of spoil heaps poses engineering challenges, related mainly to the involved degree of uncertainty. A small number of studies have attempted to characterize the geotechnical properties of spoil material; however, there remains a considerable gap in understanding how to deal with spoil materials in the context of sustainable development and civil infrastructure design. In this work, a systematic effort is made to quantify the uncertainty of the geotechnical properties of a particular spoil heap. Laboratory test results based on an extended investigation of a spoil material originating from lignite coal mines are gathered in one database and thoroughly analyzed. The results reveal and quantify the significant spoil material variability, which is contrasted against data for common soils, while a systematic approach is proposed for spoil material characterization
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