Modelling and simulation of H2-H2O bubbly flow through a stack of three cells in a pre-pilot filter press electrocoagulation reactor

被引:23
作者
Sandoval, Miguel A. [1 ,2 ]
Fuentes, Rosalba [1 ]
Perez, Tzayam [1 ]
Walsh, Frank C. [3 ]
Nava, Jose L. [4 ]
Ponce de Leon, Carlos [3 ]
机构
[1] Univ Guanajuato, Dept Ingn Quim, Norial Alta S-N, Guanajuato 36050, Mexico
[2] Univ Santiago Chile USACH, Fac Quim & Biol, Dept Quim Mat, Lab Electroquim Medio Ambiental LEQMA, Casilla 40,Correo 33, Santiago, Chile
[3] Univ Southampton, Energy Technol Res Grp, Electrochem Engn Lab, Engn Sci, Southampton SO17 1BJ, Hants, England
[4] Univ Guanajuato, Dept Ingn Geomat & Hidraul, Av Juarez 77, Guanajuato 36000, Mexico
关键词
Biphasic turbulent flow; Current distribution; Euler-Eulerian approach; Hydrogen evolution reaction; Multi-electrode stack;
D O I
10.1016/j.seppur.2020.118235
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Computational fluid dynamics simulations were carried out to describe the hydrodynamic characteristics of a two-phase bubbly flow in a filter-press flow reactor stack of three cells, which is typically used in electrocoagulation (EC). The hydrogen evolution reaction (HER) took place at the cathode; dissolution of aluminium occurred at the anode. The fundamental transport equations of momentum and electrical potential were simultaneously solved to simulate the H-2-H2O flow. Continuous (H2O) and dispersed phase (H-2) velocity fields were modelled via the Euler-Eulerian approach, using the biphasic Reynolds Averaged Navier-Stokes (RANS) equations and the standard k - epsilon turbulence model. The influence of volumetric flow rate (1.7 <= Q <= 15 cm(3) s(-1)) and applied current density (-28 <= j <= -5 mA cm(-2)) was systematically addressed to calculate the fraction of dispersed phase and current distribution along the electrodes. The evolved H-2 bubbles were transported away from the electrode by the liquid flow. The dispersion of H-2 through the electrode gap showed a modest bubble curtain profile due to the liquid flow rate. A homogeneous current distribution along the electrode length was experienced due to the geometrical design of the electrochemical cell and the low degree of H-2 dispersion. The velocity profiles of the H-2-H2O mixture were different in each cell due to the change of flow direction. H-2 bubbles increased the velocity of the liquid phase but the gas fraction of such bubbles resulted in a higher pressure drop. Good agreement between theoretical and experimental residence time distribution curves was achieved; the experimental aluminium dose released by the anode agreed well with the simulations.
引用
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页数:12
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