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integration of solid oxide fuel cells and ... - Ea Energianalyse

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3.12. Solid Oxide Fuel Cell - SOFC<br />

Current <strong>and</strong> power<br />

The electric current will be proportional to the mole flow <strong>of</strong> the reacted<br />

Hydrogen, the number <strong>of</strong> electrons per mole Hydrogen, <strong>and</strong> Faraday’s<br />

constant. And the current becomes:<br />

I SOFC =ṅ H2 ,c 2F (3.90)<br />

i d = I SOFC<br />

A cell<br />

(3.91)<br />

The electrical gross power <strong>of</strong> the cell will then be:<br />

Ẇ SOFC = V SOFC I SOFC (3.92)<br />

A control volume is put around the SOFC component, <strong>and</strong> the first law<br />

<strong>of</strong> thermodynamics is applied on this. Potential <strong>and</strong> kinetic energy is<br />

neglected, so the energy balance becomes as follows:<br />

Ḣ i − Ḣ o −Ẇ SOFC − ˙Q loss = 0 (3.93)<br />

Ḣ i <strong>and</strong> Ḣ o are the total enthalpy flow rates for in- <strong>and</strong> out-lets (cathode<br />

plus anode). Hereby the enthalpy <strong>and</strong> hence temperature at the outlet<br />

can be determined. ˙Q loss is the heat lost directly to the surroundings.<br />

Pressure losses<br />

The pressure losses in the anode <strong>and</strong> cathode can be different, <strong>and</strong> are set<br />

by the parameters ∆p a <strong>and</strong> ∆p c .<br />

p a,o =p a,i + ∆p SOFC ,a (3.94)<br />

p c,o =p c,i + ∆p SOFC ,c (3.95)<br />

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