A Multi-Fluid Model for Water and Methanol Transport in a Direct Methanol Fuel Cell
TL;DR: In this paper , a three-dimensional, steady-state, two-phase, multi-component and non-isothermal direct-methanol fuel cell (DMFC) model is presented, which can account for gas and liquid transport in porous media subject to mixed wettability.
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Abstract: Direct-methanol fuel cell (DMFC) systems are comparatively simple, sometimes just requiring a fuel cartridge and a fuel cell stack with appropriate control devices. The key challenge in these systems is the accurate determination and control of the flow rates and the appropriate mixture of methanol and water, and fundamental understanding can be gained by computational fluid dynamics. In this work, a three-dimensional, steady-state, two-phase, multi-component and non-isothermal DMFC model is presented. The model is based on the Eulerian approach, and it can account for gas and liquid transport in porous media subject to mixed wettability, i.e., the simultaneous presence of hydrophilic and hydrophobic pores. Other phenomena considered are variations in surface tension due to water–methanol mixing and the capillary pressure at the gas diffusion layer–channel interface. Another important aspect of DMFC modeling is the transport of methanol and water across the membrane. In this model, non-equilibrium sorption–desorption, diffusion and electro-osmotic drag of both species are included. The DMFC model is validated against experimental measurements, and it is used to study the interaction between volume porosity of the anode gas diffusion layer and the capillary pressure boundary condition at the anode, and how it affects performance and limiting current density.
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Citations
New insights for the methanol transport properties within anode gas diffusion layer of direct methanol fuel cell
Yajing Wen,Ruili Sun,Zinan Zhang,WEI WEI,Xinlong Xu,Feng Ji,Shaorong Wang +6 more
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TL;DR: In this paper, the surface tension of aqueous solutions of methanol, ethanol, 1-propanol, and 2propanols was measured over the entire concentration range at temperatures of 20-50 C. The experimental values were correlated with temperature and with mole fraction.
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