Page 94 - High Temperature Solid Oxide Fuel Cells Fundamentals, Design and Applications
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Thermodynamics  71

            HPF has to be supplied reversibly with the work \i’tHpFrev  that is equal to the
          exergy eFFC of the fuel with the thermodynamic state of the fuel cell and the heat
          qHpFrev from the environment

              WtHPFrev   eFFC  = ~;FC - TO ’ S$FC  = (hFFC - hF0) - TO ’ (SFFC - SFO)   (73)






            In the right-hand part of Eq. (73) the definition of  the exergy of  the fuel with
          the thermodynamic state of the fuel cell is now worked out in more detail. Similar
          processes are used for the reversible heating of the air and the reversible cooling
          of the flue gas. The reversible air heating needs the work wtHPA


              WfHPArev = PA ’ eAFC = PA ’ (h&C  - TO . s2FC)                (75)
          and the reversible heat engine HEG for the cooling of  the flue gas G delivers the
          work WtHEGrev

              WtHEGrev = --(PA f 1) ’ eGFC  = --(PA  f 1) ’ (h&c - TO . Sipc).   (76)

            The total work of the reversible fuel cell-heat  engine system is defined  by

              Wtsystrev = WtFCrev f WtCCrcv f WtHPFrev f WtHPdrev f WtHEGrev   (77)

            UsingEqs. (S),  (70), (73) and(75)-(77) weget

              Wtsystrev = A‘HO  - T~ . A‘SO   = A‘GO                        (78)

            The reversible work wtsystrev of any fuel cell-heat  engine system is independent
          of  the state of the cell and is equal to the free enthalpy of the reaction A‘GO  at the
          ambient state [3]. The standard condition is assumed to be the ambient state to
          keep the argument simple.
            It is useful to define a simplified process for further analysis, because the three
          reversible heat engines HPA, HPF and HEG  do really nothing else than to heat
          fuel and air by cooling the flue gas - their total reversible work is negligible. Thus
          the simplified process uses a heat exchanger system for the heat recovery instead
          of HPA, HPF and HEG, as shown in Figure 3.9. But this simplified reference cycle
          is generally not reversible [5]. This is caused by the changes of  the specific heat
          capacities  of  the  different  substances  with  the  reaction  temperature  T  that
          change the reaction enthalpy ArH(T,p). A (small) amount of the waste heat of FC
          must be used to heat the reactants completely. We lose this amount of  heat for
          further reversible use in the Carnot cycle CC.
            The simplified fuel cell-heat  engine hybrid cycle as a reference cycle fits the
          reversible system well; the deviation at 1000°C is -0.76%  only for the hydrogen
          oxidation. Figure 3.10 shows the applications of this cycle. The left-hand side of
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