• Energy Research
• 2016-2025close
• European Commission close
• 7. Clean energy close

The energy considered as waste heat in industrial furnaces owing to inefficiencies represents a substantial opportunity for recovery by means of thermal energy storage (TES) implementation. Although conventional systems based on sensible heat are used extensively, these systems involve technical limitations. Latent heat storage based on phase change materials (PCMs) results in a promising alternative for storing and recovering waste heat. Within this scope, the proposed PCM-TES allows for demonstrating its implementation feasibility in energy-intensive industries at high temperature range. The stored energy is meant to preheat the air temperature entering the furnace by using a PCM whose melting point is 885 °C. In this sense, a heat transfer model simulation is established to determine an appropriate design based on mass and energy conservation equations. The thermal performance is analysed for the melting and solidification processes, the phase transition and its influence on heat transference. Moreover, the temperature profile is illustrated for the PCM and combustion air stream. The obtained results prove the achievability of very high temperature levels (from 700 to 865 °C) in the combustion air preheating in a ceramic furnace; so corroborating an energy and environmental efficiency enhancement, compared to the initial condition presenting an air outlet at 650 °C.

Abstract This paper aims to present a feasibility study of the innovative plant for methanol synthesis from carbon dioxide-sequestered by fossil fuel power plant and hydrogen, which is produced by water electrolyzer employing the over-production on the electrical grid. The thermo-economic analysis is performed in the framework of the MefCO2 H2020 EU project and it is referred to the German economic scenario, properly taking into account the real market costs and cost functions for different components of the plant. Three different plant capacities for methanol production (4000 10,000 and 50,000 ton/year) have been investigated, assuming an average cost for electrical energy to feed electrolysers and analyzing the influence of the most significant parameters (oxygen selling option, methanol selling price and electrolysers’ capital cost) on the profitability of the plant. The analysis has been performed in W-ECoMP, software for the thermo-economic analysis and plant optimization developed by the University of Genoa.

Biofuels have been identified as a mid-term GHG emission abatement solution for decarbonising the transport sector. This study examines the techno-economic analysis of biofuel production via biomass fast pyrolysis and subsequent bio-oil upgrading via zeolite cracking. The aim of this study is to compare the techno-economic feasibility of two conceptual catalyst regeneration configurations for the zeolite cracking process: (i) a two-stage regenerator operating sequentially in partial and complete combustion modes (P-2RG) and (ii) a single stage regenerator operating in complete combustion mode coupled with a catalyst cooler (P-1RGC). The designs were implemented in Aspen Plus® based on a hypothetical 72 t/day pine wood fast pyrolysis and zeolite cracking plant and compared in terms of energy efficiency and profitability. The energy efficiencies of P-2RG and P-1RGC were estimated at 54% and 52%, respectively with corresponding minimum fuel selling prices (MFSPs) of £7.48/GGE and £7.20/GGE. Sensitivity analysis revealed that the MFSPs of both designs are mainly sensitive to variations in fuel yield, operating cost and income tax. Furthermore, uncertainty analysis indicated that the likely range of the MFSPs of P-1RGC (£5.81/GGE  £11.63/GGE) at 95% probability was more economically favourable compared with P-2RG, along with a penalty of 2% reduction in energy efficiency. The results provide evidence to support the economic viability of biofuel production via zeolite cracking of pyrolysis-derived bio-oil.

Spinel LiNi0.5Mn1.5O4 as one of the high-energy positive electrode materials for next generation Li-ion batteries has attracted significant interest due to its economic and environmental advantages. However, the sensitivity of this type of material upon short to long term ambient storage conditions and the impact on the electrochemical performances remains poorly explored. Nevertheless, this remains an important aspect for practical large-scale synthesis, storage and utilization. Herein, we study and compare the evolution of surface chemistry, bulk crystal structure and elemental content evolution and distribution of LiNi0.5Mn1.5O4 using a variety of characterization techniques including XPS and STEM-EDS-EELS, as well as electrochemical analysis. We show that Mn species dominate the outer surface (0–5 nm), while Ni and Li are preferentially located further away and in the bulk. The studied LiNi0.5Mn1.5O4 material is found to be stable, with minor changes in surface or bulk characteristics detected, even after 12 months of storage under ambient air conditions. The low surface reactivity to air also accounts for the minor changes to the electrochemical performance of the air-exposed LiNi0.5Mn1.5O4, compared to the pristine material. This study provides guidance for the appropriate storage, handling and processing of this high-performance cathode material.

Optimization of all numerical codes ported in the infrastructure and used for supercapacitors, PV and batteries. The scope of deliverable D3.2 is to report the new advances in the field of materials for energy that comes from the search of new methodologies and models that could be more efficient on the new generation of computer hardware for exascale. In this respect, deliverable D3.2 is a transversal deliverable that report the new advances related to activities described in task T3.2, T3.3 and T3.4. H2020

A membrane assisted process for green hydrogen production from a bioethanol derived feedstock is here developed and evaluated, starting from the conventional Steam Methane Reforming (SMR) process. Such a process is suitable for centralized hydrogen production, and is here analyzed for a large-scale H2 production unit with the capacity of 40.000 Nm3/h. The basic Steam Ethanol Reforming (SER) process scheme is modified in a membrane assisted process by integrating the Pd-membrane separation steps in the most suitable reaction steps. The membrane assisted process, configured in three alternative architectures (Open architecture, Membrane Reactor and Hybrid architecture) was evaluated in terms of efficiencies and hydrogen yields, obtaining a clear indication of improved process performance. The alternative membrane assisted process architectures are compared to the basic SER process and to the benchmark SMR process fed by natural gas, for an overall comparative assessment of the efficiency and specific CO2 emissions and for an economic analysis based on the operating expenditures.