Page 277 - The Combined Finite-Discrete Element Method
P. 277

260    FLUID COUPLING

            the chamber; the detonation gas expands until the rigid chamber is completely filled
            with the detonation gas. Because the chamber is rigid, no mechanical work is done by
            the expanding gas. The chamber walls being impermeable to the flow of heat (adiabatic
            walls) means that no heat transfer between the chamber walls and gas takes place. The
            detonation gas expands into the chamber, and when all the transient motion has ceased
            the gas reaches equilibrium. In this process the gas has done no mechanical work, and
            no energy in the form of heat has been exchanged. As a result, no change in the internal
            energy of detonation gas occurs.
              In a state of thermodynamic equilibrium, the internal energy of the unit mass of deto-
            nation gas, u, depends only upon the thermodynamic state of the gas, which in this case
            is completely described by the specific volume v and temperature T . Consequently, any
            change in u is given by

                                          ∂u          ∂u
                                   du =        dT +         dv                    (8.8)
                                          ∂T  v       ∂v  T
            where any changes in u depend only upon the initial and final states, and not on the path
            (for instance, changing v at constant T and then changing T at constant v yields the same
            u as changing T at constant v and then changing v at constant T ).
              With an additional assumption that the internal energy per unit mass of the detonation
            gas at a given temperature does not depend upon the specific volume, any change in
            internal energy can be given in terms of the temperature only:
                                             ∂u

                                      du =        dT = c v dT                     (8.9)
                                            ∂T
                                                 v
            where c v is the heat capacity per unit mass of the detonation gas at constant volume.
              The heat capacity per unit mass of the detonation gas is in general a function of the
            temperature of the detonation gas. However, for the sake of simplicity it is assumed that
            c v is constant and calculated in such a way that the internal energy of the detonation gas
            at maximum temperature is accurately represented. In other words, c v is such that the
            specific explosive energy of the explosive is accurately represented.
              No change in internal energy implies no change in temperature, and consequently the
            temperature of the detonation gas after the expansion is completed and equilibrium state
            is reached is equal to the temperature of the detonation gas before the expansion, i.e.
            expansion is also isothermal and

                                         u c = u 0 ;  T c = T 0                  (8.10)

            where subscripts o and c indicate equilibrium states before and after the expansion.
              From the equation of state, it follows that

                                         p o                p c
                               T 0 =            = T c =                          (8.11)
                                              b
                                                                 b
                                    R(ρ o + aρ o )     R(ρ c + aρ c )
            which yields the expression for the pressure of the detonation gas after expansion, p c ,as
            function of the density of detonation gas after expansion:
                                 b           b−1            b−1      b−1
                    p c  ρ c + aρ c  ρ c 1 + aρ c  ρ c 1 + aρ o  (ρ c /ρ o )
                       =          =              =                               (8.12)
                    p o  ρ o + aρ o b  ρ o 1 + aρ o b−1  ρ o  1 + aρ o b−1
   272   273   274   275   276   277   278   279   280   281   282