Palaeoenvironmental Conditions of the Mavropigi Lignites,Ptolemais Basin,Greece: A Petrological Study

The aim of this study is to interpret the palaeoenvironmental conditions established during the formation of several lignite seams at the Mavropigi deposit, Ptolemais, Greece (corehole MAK-48). In nine representative lignite samples, ash contents, as well as the contents of the elements C, H, N, O, and S were determined. Polished block sections from the same samples were examined under the microscope. The ash contents (750°C) of the studied lignite seams range between 10–29% (on dry basis). The contents of C, H, N, and O display values between 36–55%, 2.4–4.6%, 0.7–2%, and 21–37.5%, respectively, while S contents do not exceed 1.4%. Huminite is the prevailing maceral group (87–95%). All the samples, except No. 35, display a distinct prevalence in detrohuminite maceral subgroup (up to 69 vol%, mmf). Liptinite and inertinite maceral groups show low contents, which do not exceed 9% and 7%, respectively. The Mavropigi lignites are medium to low grade coals and can be regarded as peat to lignite in terms of thermal maturity. The studied lignite seams formed in fens, possibly from herbaceous plants under limnotelmatic regime. During peat deposition, conditions were very moist and intense reducing with increased bacterial activity. The ratio of plant growth and peat accumulation versus rise of water table due to the subsidence rate was not well balanced. As a result, the petrographical composition of the Mavropigi lignites is related either to a long residence time of the organic matter in the acrotelm or to a herbaceous vegetation origin.     

Mineralogical characterization of the intraseam layers of Lofoi lignite deposits in Florina basin (western Makedonia,northwest Greece)

The mineralogical composition of intraseam layers from Lofoi lignite deposits (northwest Greece) is the subject of the present study. The samples were examined by means of X-ray diffraction (XRD), thermo-gravimetric (TG/DTG) and differential thermal analysis (DTA), and Fourier transform infrared (FT-IR) spectrometry. The clay minerals prevail in most samples, with illite-muscovite being the dominant phase, and kaolinite and chlorite being the other major clay components. No smectite was found. Quartz and feldspars, dominate in two cases. The studied materials are characterized as clays to clayey sands, showing significant similarities with the intraseam layers of the adjacent Achlada lignite deposits.     

Renewable energy sources (RES) projects and their barriers on a regional scale: The case study of wind parks in the Dodecanese islands, Greece

The increasing energy challenges faced, in particular, by isolated communities, such as insular communities, call for an integrated, flexible and easy-to-apply methodology aiming at providing a list of renewable energy sources) (RES) projects capable to reduce green house gas (GHG) emissions, satisfy future energy forecasts and reach the objectives of international/national energy directives and obligations, as, for example, the ones set by the Kyoto Protocol by 2010. The EU project EMERGENCE 2010 developed such a methodology that is implemented here in the case study of wind parks in the Dodecanese islands in Greece. The results obtained consist of a final list of financially viable RES wind projects, for which various barriers have been previously identified and assessed. The additional advantages of the proposed methodology is that besides providing as an end result a comprehensive list of RES projects adopted to specific criteria and regional priorities, it also allows space for involving – from early stages – the local community and stakeholders in the decision-making process (participatory planning); in this way, the EMERGENCE 2010 methodology may assist towards the RES promotion and public acceptance, the profitability of RES investments and the regional sustainable development.     

Tuning the alloy degree for Pd-M/Al2O3 (M=Co/ Ni /Cu) bimetallic catalysts to enhance the activity and selectivity of dodecahydro-N-ethylcarbazole dehydrogenation

Hydrogen is a promising candidate to substitute the fossil fuels. However, the efficient hydrogen storage technologies restrict the commercial applications. Developing new catalysts with high activity and selectivity is important for the dehydrogenation reaction in N-ethylcarbazole/dodecahydro-N-ethylcarbazole (NECZ/12H-NECZ) hydrogen storage system. In this work, a series of Pd-M/Al₂O₃ (M = Co, Ni and Cu) bimetallic catalysts are synthesized successfully and show good performance in the dehydrogenation reaction of 12H-NECZ than the commercial Pd/Al₂O₃ catalyst. The Pd₁Co₁/Al₂O₃ catalyst (Practical Pd content = 2.4136 wt%) showed the highest catalytic performance with 95.34% H₂ release amount, TOF of 230.5 min⁻¹ and 85.4% selectivity of NECZ. Combined with the characterization analysis, it can be proposed that the dehydrogenation performance of 12H-NECZ is dependent on the alloy phases, reasonable electronic structures and nanoparticle size of catalysts. The fine-tuned alloy degree and appropriate nanoparticle size of Pd₁Co₁/Al₂O₃ bring the 17.7% increase of H₂ release amount and 99.5% increase of NECZ selectivity than those of Pd/Al₂O₃. For the bimetallic catalysts, the enhancement of selectivity of NECZ is mainly from the increase of the kinetic constant of rate-limiting step.     

Modeling the Flow Characteristics of a Fractured Medium Overlaid by a Sedimentary Porous Medium: Application to the Borehole RCF 3 Pumping Test in Sellafield (UK)

Abstract

A numerical model was developed in order to produce more realistic simulations of the flow phenomena in fractured rock overlaid by porous sedimentary rock. This model combines the discrete fracture network (DFN) model and the equivalent porous medium (EPM) model. This coupled model was then applied to the interpretation of the RCF 3 pumping test performed in the Sellafield area of West Cumbria (UK), where crystalline fractured rock (Borrowdale Volcanic Group, BVG) is overlaid by sedimentary porous rock (Sherwood Sandstone Group, SSG).     

Behavior of the monophosphate tungsten bronzes (PO2)4(WO3)2m (m = 4 and 6) in electrochemical lithium insertion

The electrochemical lithium insertion process has been studied in the family of monophosphate tungsten bronzes (PO₂)₄(WO₃)_2m, where m = 4 and 6. Structural changes in the pristine oxides were followed as lithium insertion proceeded. Through potentiostatic intermittent technique, the different processes which take place in the cathode during the discharge of the cell were analysed. The nature of the bronzes Li_x(PO₂)₄(WO₃)_2m formed was determined by in situ X-ray diffraction experiments. These results have allowed establishment of a correlation with the reversible/irreversible processes detected during the electrochemical lithium insertion. Measurements of resistivity showed that upon lithium insertion, the metallic pristine oxides become insulating.     

A comparison study of molten-salt and solid-state method for the photoelectrochemical water splitting performance of Dion-Jacobson layers perovskite Ca2Nan-3NbnO3n+1- (n = 4, 5, and 6) nanosheets

Solar energy is one of the elements that have been used as a resource in the green energy field. Hydrogen, as an energy carrier, can be produced from many kinds of sources, including solar energy. Here, we present two-dimensional (2D)perovskite material derived from the Dion-Jacobson phase (DJ), Ca₂Na_n-3Nb_nO_3n+1^- (CNNO^?) nanosheets, with the number of layer n = 4–6 synthesized via microwave-assisted hydrothermal method. The starting material KCa₂Nb₃O₁₀ (KCNO) is made from two methods. The solid-state calcination KCNO product has more than two-phase, while the molten-salt synthesis produces a well cubic KCNO crystalline. TThe thickness of the 2D CNNO^? nanosheets is increasing, in dependence on the n value. Meanwhile, the estimated optical band gap is decreasing, in dependence on the n value. 2D CNNO^? nanosheets show the absorbance under ultraviolet (UV) light, which confirms their semiconducting nature. The capability of these 2D nanosheets to generate hydrogen is presented via photo-electrochemical (PEC) water splitting. The molten-salt fabricated CNNO^? nanosheets CNNO6 shows better performance with the highest efficiency ? up to 0.110% when applied to the PEC device.     

The catalytic effect of an inert additive (SrTiO3) on the hydrogen storage properties of 4MgH2Na3AlH6

Investigations on the catalytic effects of a non-reactive and stable additive, SrTiO₃, on the hydrogen storage properties of the 4MgH₂Na₃AlH₆ destabilized system were carried out for the first time. The Na₃AlH₆ compound and the destabilized systems used in the investigations are prepared using ball milling method. The doped system, 4MgH₂Na₃AlH₆SrTiO₃, had an initial dehydrogenation temperature of 145 °C, which 25 °C lower as compared to the un-doped system. The isothermal absorption and desorption capacity at 320 °C has increased by 1.2 wt% and 1.6 wt% with the addition of SrTiO₃ as compared to the 4MgH₂Na₃AlH₆ destabilized system. The decomposition activation energy of the doped system is estimated to be 117.1 kJ/mol. As for the XRD analyses at different decomposition stages, SrTiO₃ is found to be stable and inert. In addition to SrTiO₃, similar phases are found in the doped and the un-doped system during the decomposition and dehydrogenation processes. Therefore, the catalytic effect of the SrTiO₃ is speculated owing to its ability to modify the physical structure of the 4MgH₂Na₃AlH₆ particles through pulverization effect.