Temperature effects on energy production by salinity exchange

This is an unedited version of this paper. The publisher version can be reached in this URL: http://pubs.acs.org/doi/abs/10.1021/es500634fIn recent years, the capacitance of the interface between charged electrodes and ionic solutions (the electric double layer) has been investigated as a source of clean energy. Charge is placed on the electrodes either by means of ion-exchange membranes or of an external power source. In the latter method, net energy is produced by simple solution exchange in open circuit, due to the associated decrease in the capacitance of the electric double layer. In this work, we consider the change in capacitance associated with temperature variations: the former decreases when temperature is raised, and, hence, a cycle is possible in which some charge is put on the electrode at a certain potential and returned at a higher one. We demonstrate experimentally that it is thus viable to obtain energy from electric double layers if these are successively contacted with water at different temperatures. In addition, we show theoretically and experimentally that temperature and salinity variations can be conveniently combined to maximize the electrode potential increase. The resulting available energy is also estimated.Departamento de Física AplicadaThe research leading to these results received funding from the European Union 7th Frame-work Programme (FP7/2007-2013) under agreement No. 256868. Further Financial supports from Junta de Andalucía, project FQM 694, and Ministerio de Economía y Competitividad (Spain), project FIS2013-47666-C3-1-R

Effect of Solution Composition on the Energy Production by Capacitive Mixing in Membrane-Electrode Assembly

The final edited version of the paper can be found at: http://pubs.acs.org/articlesonrequest/AOR-c9UMxSzGY3eiU5SENNgT The complete citation is: Ahualli, S.; et al. Effect of Solution Composition on the Energy Production by Capacitive Mixing in Membrane-Electrode Assembly. Journal of Physical Chemistry, 118(29): 15590-15599 (2014). DOI:10.1021/jp504461mOpen access in the Journal on May 26, 2015In this work we consider the extent to which the presence of multi-valent ions in solution modifies the equilibrium and dynamics of the energy production in a capacitive cell built with ion-exchange membranes in contact with high surface area electrodes. The cell potential in open circuit (OCV) is controlled by the difference between both membrane potentials, simulated as constant volume charge regions. A theoretical model is elaborated for steady state OCV, first in the case of monovalent solutions, as a reference. This is compared to the results in multi-ionic systems, containing divalent cations in concentrations similar to those in real sea water. It is found that the OCV is reduced by about 25 % (as compared to the results in pure NaCl solutions) due to the presence of the divalent ions, even in low concentrations. Interestingly, this can be related to the “uphill” transport of such ions against their concentration gradients. On the contrary, their effect on the dynamics of the cell potential is negligible in the case of highly charged membranes. The comparison between model predictions and experimental results shows a very satisfactory agreement, and gives clues for the practical application of these recently introduced energy production methods.The research leading to these results received funding from the European Union 7th Framework Programme (FP7/2007-2013) under agreement No. 256868. Further financial support from Junta de Andalucia, Spain (PE2012-FQM 694) is also acknowledged. One of us, M.M.F., received financial support throughan FPU grant from the Universityof Granada

Influence of ionic strength and polyelectrolyte concentration on the electrical conductivity of suspensions of soft colloidal polysaccharides

International audienceTile electrokinetic properties of carboxymethyldextran, a soft and anionic polysaccharide, were analysed in aqueous NaNO3 solutions through measurements of the electrical conductivity of the suspensions. The results, which furnish new experimental support for the structure of soft polysaccharides in electrolyte solution show that the polyion concentration governs the conductance behavior of the suspension as the ionic strength decreases. This is particularly evident for large polymer concentrations, for which electrical double layer overlap is more likely. In contrast, the electrical conductivity of the suspension at high ionic strength reduces to the contribution of the ions in solution, as screening of the polyion charges is more efficient in such conditions. The applicability of Ohshima's general conductivity expression to these electrical conductivity measurements was examined, and a major discrepancy against the theory was observed. The calculated values of the electrical conductivity deduced on the basis of this theory were found to be lower than the experimental ones. Possible reasons for this discrepancy are discussed and a numerical model, based on the use of a cell approach to account for hydrodynamic and electrical interactions between particles, has shown to be a good description of the experimental electrokinetic data