| 1. |
- Ahlberg, E., et al.
(författare)
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The surface oxidation of pyrite in alkaline solution
- 1990
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Ingår i: Journal of Applied Electrochemistry. - 0021-891X .- 1572-8838. ; 20:6, s. 1033-1039
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Tidskriftsartikel (refereegranskat)abstract
- The collector-less flotation of pyrite has been studied by conventional techniques and is correlated to the electrochemical behaviour of pyrite in alkaline solution (1m NaClO4, pH 11). It was concluded that the initial oxidation of pyrite produces a hydrophobic sulphur rich surface together with hydrophilic iron hydroxide species. Also upon grinding, the surface is covered by hydrophilic species and therefore no significant flotation was obtained in the absence of a collector. However, collectorless flotation was readily obtained in an iron complexing solution like EDTA. This indicates that the remaining sulphur-rich layer is responsible for the floatability of pyrite under these conditions.
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| 2. |
- Alexiadis, Alessio, et al.
(författare)
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On the stability of the flow in multi-channel electrochemical systems
- 2012
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Ingår i: Journal of Applied Electrochemistry. - : Springer Science and Business Media LLC. - 0021-891X .- 1572-8838. ; 42:9, s. 679-687
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Tidskriftsartikel (refereegranskat)abstract
- The importance of the fluid dynamics in the modelling of electrochemical systems is often underestimated. The knowledge of the flow velocity pattern in an electrochemical cell, in fact, can allow us to associate certain electrochemical reactions with specific fluid patterns to maximize the yield of some reaction and, conversely, to minimize unwanted or side reactions. The correct evaluation of the convective term in the Nernst-Planck equation, however, requires the solution of the so-called Navier-Stokes equations, and computational fluid dynamics (CFD) is today the established method to numerically solve these equations. In this work, a CFD model is employed to show that the gas-liquid flow pattern can be remarkably different in a single channel or in a multi-channel gas-evolving electrochemical system. In the single channel, in fact, under certain conditions, vortices and recirculation regions can appear in the flow, which does not appear in the multi-channel case. The reason of this difference is found in the uneven distribution of the small bubbles in the two cases. Additionally, a second, simplified, model of the flow is discussed to show how a higher concentration of small bubbles in the single channel system can destabilize the flow.
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| 3. |
- Bandara, T M W J, 1968, et al.
(författare)
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Efficiency enhancement of dye-sensitized solar cells with PAN:CsI:LiI quasi-solid state (gel) electrolytes
- 2014
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Ingår i: Journal of Applied Electrochemistry. - : Springer Science and Business Media LLC. - 1572-8838 .- 0021-891X. ; 44:8, s. 917-926
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Tidskriftsartikel (refereegranskat)abstract
- While many attempts have been made in the recent past to improve the power conversion efficiencies of dye-sensitized solar cells (DSSCs), only a few reports can be found on the study of these cells using binary iodides in the gel polymer electrolyte. This paper reports the effect of using a binary mixture of (large and small cation) alkaline salts, in particular CsI and LiI, on the efficiency enhancement in DSSCs with gel polymer electrolytes. The electrolyte with the binary mixture of CsI:LiI = 1:1 (by weight) shows the highest ionic conductivity 2.9 x 10(-3) S cm(-1) at 25 A degrees C. DC polarization measurements showed predominantly ionic behavior of the electrolyte. The density of charge carriers and mobility of mobile ions were calculated using a newly developed method. The temperature dependent behavior of the conductivity can be understood as due to an increase of both the density and mobility of charge carriers. The solar cell with only CsI as the iodide salt gave an energy conversion efficiency of similar to 3.9 % while it was similar to 3.6 % for the cell with only LiI. However, the electrolyte containing LiI:CsI with mass ratio 1:1 showed the highest solar cell performance with an energy conversion efficiency of similar to 4.8 % under the irradiation of one Sun highlighting the influence of the mixed cation on the performance of the cell. This is an efficiency enhancement of 23 %.
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| 4. |
- Bandara, T M W J, 1968, et al.
(författare)
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Efficiency of 10 % for quasi-solid state dye-sensitized solar cells under low light irradiance
- 2015
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Ingår i: Journal of Applied Electrochemistry. - : Springer Science and Business Media LLC. - 0021-891X .- 1572-8838. ; 45:4, s. 289-298
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Tidskriftsartikel (refereegranskat)abstract
- Polyacrylonitrile-based gel electrolytes were prepared using tetrapropylammonium iodide salt for dye-sensitized solar cells (DSSCs). The optimized gel electrolyte exhibited an ionic conductivity of 2.6 mS cm(-1) at 25 A degrees C and the DSSC fabricated with this gel electrolyte showed open-circuit voltage, short-circuit current density, fill factor, and efficiency of 0.71 V, 11.8 mA, 51, and 4.2 %, respectively, under one sun irradiation. The efficiency of the cell increases increased with decreasing solar irradiance achieving 10 % efficiency and 80 % fill factor at 3 mW cm(-2) a low irradiance value of 3 mW cm(-2). Lower efficiencies at higher intensities were attributed to transport limitation of the redox mediators at high irradiation intensities. This work suggests that quasi-solid state DSSCs can reach efficiencies close to that of liquid electrolyte-based cells at low irradiance levels. The results open up new vistas on efficiency improvement in DSSCs by optical manipulation and control of DSSCs.
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| 5. |
- Behm, Mårten, et al.
(författare)
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Electrochemical production of polysulfides and sodium hydroxide from while liquor .2. Electrolysis in a laboratory scale flow cell
- 1997
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Ingår i: Journal of Applied Electrochemistry. - 0021-891X .- 1572-8838. ; 27:5, s. 519-528
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Tidskriftsartikel (refereegranskat)abstract
- Electrochemical production of polysulfide-containing white liquor and pure sodium hydroxide solution was investigated at 90 degrees C in a laboratory scale flow cell. A mixed iridium-tantalum oxide coated titanium electrode was used as the anode and the two electrolyte compartments were separated by a cation-exchange membrane. The process was demonstrated at current densities up to 5 kA m(-2), resulting in high current efficiencies for both products. The previously reported autocatalytic effect of polysulfide ions was confirmed, and its technical implications on the use of three-dimensional electrodes were demonstrated and discussed. The current efficiency was found to depend strongly on the degree of conversion of sulfur(-II) to sulfur(0). The anode material showed favourable properties, with respect to activity and selectivity, but suffered from limited durability.
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| 6. |
- Behm, Mårten, et al.
(författare)
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Electrochemical production of polysulfides and sodium hydroxide from white liquor .1. Experiments with rotating disc and ring-disc electrodes
- 1997
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Ingår i: Journal of Applied Electrochemistry. - 0021-891X .- 1572-8838. ; 27:5, s. 507-518
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Tidskriftsartikel (refereegranskat)abstract
- Electrochemical oxidation of white liquor in a membrane cell is a process of great potential for the pulp and paper industry. The process produces polysulfide-containing white liquor in the anode chamber, and pure sodium hydroxide solution in the cathode chamber. The anode reaction has been investigated using cyclic voltammetry at temperatures between 25 and 90 degrees C on rotating disc and ring-disc electrodes. It was further investigated using chronoamperometry on rotating disc electrodes at 90 degrees C. The experiments, which were mainly run in dilute alkaline sulfide solutions, using platinum electrodes, show that the electrochemical production of polysulfide ions, at lower anode potentials (-0.1 to +0.1 V vs SCE), proceeds via formation of elemental sulfur on the electrode surface. The sulfur is dissolved by hydrosulfide and polysulfide ions producing (longer-chain) polysulfide ions. The rate of dissolution, and thus the overall reaction rate, increases strongly with temperature. Polysulfide ions have an autocatalytic effect on the anode reaction due to their ability to dissolve adsorbed sulfur. At higher anode potentials (greater than or equal to 0.2 V vs SCE), a change of reaction mechanism is observed. In this region the reaction rate depends on electrode potential and is not catalysed by polysulfide ions.
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| 7. |
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| 8. |
- Borg, K. I., et al.
(författare)
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Effects of non-linear kinetics on free convection in an electrochemical cell with a porous separator
- 2007
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Ingår i: Journal of Applied Electrochemistry. - : Springer Science and Business Media LLC. - 0021-891X .- 1572-8838. ; 37:11, s. 1287-1302
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Tidskriftsartikel (refereegranskat)abstract
- The spatial evolution of the ionic concentration of an electrolyte in an isothermal electrochemical cell with a porous separator between the electrodes was investigated for large values of Rayleigh number. The reaction kinetics were described by the Butler-Volmer equation. The full problem, involving the coupled partial differential equations describing the velocity field, the ionic concentration, and the electric potential, was reduced by means of regular and singular perturbation theory, to a simplified evolution equation, coupled with a transcendental function for the ionic concentration and electric potential; the solution was found to agree well with the numerical solution of the full problem. In the limit of large and small cell voltages, closed analytical solutions were secured for the concentration, potential, and overall current density.
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| 9. |
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| 10. |
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