首页|Three-dimensional lattice Boltzmann simulation of reactive transport and ion adsorption processes in battery electrodes of cation intercalation desalination cells
Three-dimensional lattice Boltzmann simulation of reactive transport and ion adsorption processes in battery electrodes of cation intercalation desalination cells
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NSTL
Cation intercalation desalination (CID) has gained great popularity in the field of water desalination because of its excellent desalination performance. Due to lack of understanding of the relationship between electrode microstructures and reactive adsorption processes in CIDs, the further development of high-performance CID electrodes has been hindered. To this end, the influences of electrode microstructures on the desalination performance of CID cells were investigated from the pore-scale level in this work. The three-dimensional microstructures of porous electrodes are first reconstructed by an improved random generation method. Based on the reconstructed porous electrodes, the flow, mass transfer and intercalation reaction processes under the constant current are simulated using the lattice Boltzmann method. The effects of applied current density, porosity and size of active particles on the change of liquid-phase sodium concentration and Na-intercalated degree in the solid phase are evaluated. The simulation results show that increasing the current density can accelerate the ion intercalation and desalination rates. During the desalination, the ion concentration is unevenly distributed in the pores of porous electrodes, and the intercalation degrees are different along the electrode thickness direction and in the particle radial direction. The increase of porosity can alleviate the concentration polarization of liquid-phase sodium ion and reduce the difference of particle intercalation degree between the front- and back-sides of the electrode. In addition, the increase of porosity can accelerate the desalination process, but cannot improve the total salt removal. Reducing particle size can shorten the time for particles to reach the sodium-rich state, but it can aggravate the polarization of sodium ion concentration in the liquid phase at both ends of the electrode. This work reveals the ion intercalation behavior in the CID and its relationship with the electrode microstructures, and may provide useful information for the design and research of CID.
NSTL
