Electroacoustic Characterization of Bidisperse Suspensions

Electroacoustic techniques are promising tools for the size determination and electrokinetic characterization of concentrated colloidal suspensions. When particles are not homogeneous in size and/or density, the dynamic mobility obtained is a kind of average of the mobilities of every particle. In this paper, we try to discern which averaging procedure provides a better description of the dynamic mobility of bidisperse suspensions consisting of a mixture of two very different types of particles. The results show that the amplitude of the sound wave induced by an applied ac field (electrokinetic sonic amplitude) is not just the sum of the amplitudes of the waves generated by every particle but has a larger contribution from the larger particles, although the small size entities considerably influence the behaviour of the latter because of their interference in the fluxes of the fluid and ions around them

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

Electrokinetic detection of the salt-free condition in colloids. Application to polystyrene latexes

Financial support from Ministerio de Ciencia, Innovación y Universidades (Spain) ( GC2018-098770-B-I00 ), and Junta de Andalucía (Spain) and European Funds for Regional Development ( BF-FQM-141-UGR18 , PI20-00233 ) is gratefully acknowledged.Financial support from Ministerio de Ciencia, Innovación y Universidades (Spain) (GC2018-098770-B-I00), and Junta de Andalucía (Spain) and European Funds for Regional Development (BF-FQM-141-UGR18, PI20-00233) is gratefully acknowledged.Because of their singular phenomenology, the so-called salt-free colloids constitute a special family of dispersed systems. Their main characteristic is that the dispersion medium ideally contains only the solvent and the ions compensating exactly the surface charge of the particles. These ions (often called released counterions) come into the solution when the surface groups responsible for the particles charge get ionized. An increasing effort is nowadays dedicated to rigorously compare theoretical model predictions for ideal salt-free suspensions, where only the released counterions are supposed to be present in solution, with appropriately devised experiments dealing with colloids as close as possible to the ideal salt-free ones. Of course, if the supporting solution is aqueous, the presence of atmospheric contamination and any other charged species different from the released counterions in the solution must be avoided. Because this is not an easy task, the presence of dissolved atmospheric CO2 and of H+ and OH− from water dissociation cannot be fully discarded in aqueous salt-free solutions (often denominated realistic in such case). Ultimately, at some point, the role of the released counterions will be comparable or even larger in highly charged concentrated colloids than that of added salts. These topics are covered in the present contribution. The model results are compared with experimental data on the dynamic mobility and dielectric dispersion of polystyrene spheres of various charges and sizes. As a rule, it is found that the model correctly predicts the significance of alpha and Maxwell-Wagner-O'Konski relaxations. Positions and amplitudes of such relaxations are well predicted, although it is necessary to assume that the released counterions are potassium or sodium instead of protons, otherwise the frequency spectra of experimental mobility and permittivity differ very significantly from those theoretically calculated. The proposed electrokinetic evaluation is an ideal tool for detecting in situ the possible contamination (or incomplete ion exchange of the latexes). A satisfactory agreement is found when potassium counterions are assumed to be in solution, mostly if one considers that the comparison is carried out without using any adjustable parameters.Ministerio de CienciaMinisterio de Ciencia, Innovación y Universidades GC2018-098770-B-I00European Regional Development Fund BF-FQM-141-UGR18, PI20-00233Junta de Andalucí