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6.21 Conservation of energy once more           189

            specific entropy, which is defined as ds = de + pdν in thermodynamics. The reason for
            introducing the specific entropy is that thermodynamics gives

                                            c p     α
                                       ds =    dT −   dp                      (6.321)
                                             T
            where c p is the heat capacity at constant pressure, T is the absolute temperature in kelvin
            and α is the thermal expansibility (see Notes 6.15, 6.16 and 6.17). The temperature
            equation for a single phase medium is therefore
                                DT       Dp                     ∂v i
                              c p   − αT    =∇ · (λ∇T ) + S + σ ij            (6.322)
                                 dt      dt                     ∂x j
            which includes a term for the rate of change of pressure. This term can normally be ignored
            as justified by Exercise 6.33.
              The derivation above generalizes to a multicomponent system, like a porous rock satu-
            rated by a fluid, by expressing the internal energy (E), the kinetic energy (K) and the work
            done on the system (W) as sums over each component. The derivation above is then car-
            ried out for each component, where the continuity equation and Newton’s second law are
            used separately for each component to simplify the expression. The only difference is that
            the density   is now replaced by φ k   k , where φ k and   k are the volume fraction and the
            density of each component, respectively. The term Q =−λ∇T for heat conduction is not
            written as a sum over each component, because it is a bulk property. The heat generation S
            is also treated as a bulk property, but it could have been divided between each component
            as S = φ k S k . The multicomponent version of the single component equation (6.322)is
            then

                                   DT                              ∂v i
                           φ k   k c k   −∇ · (λ∇T ) = S +    σ ij     .      (6.323)
                                    dt                           ∂x j
                         k              k                  k          k
            The subscript k on the material derivative says that the velocity of component k is used.
            This is exactly the same temperature equation as equation (6.11), except for the last term
            on the right-hand side that involves the work done on the system per unit time for each
            component. The temperature equation for a fluid saturated porous rock is
                        DT                                      ∂v i
                      b c b  +   f c f v D ·∇T −∇ · (λ∇T ) = S + σ ij         (6.324)
                         dt                                     ∂x j
                                                                    s
            by introducing the bulk properties from equation (6.12) and the Darcy flux from equa-
            tion (6.14). (The subscript b denotes the bulk and the subscript f the fluid.) The material

            derivative of equation (6.324) is with respect to the solid velocity. The term (σ ∂v i /∂x j ) s
                                                                          ij
            represents the work per unit time in the solid phase, and the corresponding term in the fluid
            phase is ignored.
            Note 6.15 Entropy can be taken as a function of temperature and pressure, s = s(T, p),
            and the increment ds is
                                           ∂s           ∂s

                                ds(T, p) =       dT +        dp.              (6.325)
                                           ∂T          ∂p
                                               p           T
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