(564a) Modeling and Reduction of Carbon Dioxide Gas Formation at the Anode of a Direct Methanol Fuel Cell Using Chemically-Enhanced Solubility | AIChE

(564a) Modeling and Reduction of Carbon Dioxide Gas Formation at the Anode of a Direct Methanol Fuel Cell Using Chemically-Enhanced Solubility

Authors 

Lundin, M. D. - Presenter, University of Kansas


The production of CO2 gas at the DMFC anode leads to dramatic increases in pumping power requirements and reduced power output because of mass transfer limitations as bubble trains form in the channels of larger stacks. Experimental observations taken in a 5 cm2 DMFC test cell operated at 60ºC, 1 atm, and with a methanol/water fuel flow rates of 5-10 cc min-1 indicate that the rate of bubble formation can be reduced by increasing the fuel flow because more liquid is available for the CO2 to dissolve in. Further observations indicate that KOH and LiOH added to the fuel eliminates CO2 gas formation in situ at low concentrations because of the greatly increased solubility that results.

A mathematical model for the volumetric rate of CO2 gas production that includes effects of temperature and solubility is developed and extended to include the effects of hydroxide ions in solution. The model is used to predict the onset location of gas formation in the flow field as well as the void fraction at any point in the flow field. Predictions from the model agree very well with our experiments. Model predictions explain differences in the initial location of bubble formation for fuel solutions pre-saturated with CO2 as opposed to CO2-free solutions. Experiments with KOH and LiOH added to fuel solutions confirm the validity of the model extension that includes solubility that is enhanced by chemical reaction.

Experiments with LiOH, KOH, and ammonium hydroxide show that the long-term durability of standard Pt-Ru/Nafion/Pt membrane electrode assemblies is compromised because of the presence of lithium, potassium, and ammonium cations that interact with the Nafion membrane and result in increasing the ohmic limitations of the polymer electrolyte membrane. Experiments with Ca(OH)2, while reducing gas formation, precipitate the product CaCO3 out of solution too rapidly for downstream filtering, blocking channels in the flow field.