Page 67 - Air pollution and greenhouse gases from basic concepts to engineering applications for air emission control
P. 67

2.1 Gas Kinetics                                                41

              Assume one molecule collides with the wall only once during Dt; then the
            number of collisions is the same as the number of molecules within the volume
            formed by Dx and A. Then, the number of collisions is expressed as the corre-
            sponding number of molecules that collide with the wall during Dt

                                       n c ¼ C N c x ADt                 ð2:53Þ

            where C N is the number of molecules per unit volume of gas, which is defined in
            Eq. (2.49). From this equation, we can get the number of molecules colliding with
                                              2
            the wall per unit area per unit time (1=sm )
                                           n c
                                      j x ¼   ¼ C N c x                  ð2:54Þ
                                          ADt
              Then, the total number of collisions considering the molecule speed distribution
            is determined by integration, assuming constant molecule number concentration C N
            at steady state,
                                  Z 1             Z 1
                              J x ¼  j x fc x       c x fc x             ð2:55Þ
                                                       ðÞdc x
                                      ðÞdc x ¼ C N
                                  0               0
              Using the Maxwell-Boltzmann distribution described in Eq. (2.2), the integration
            part in Eq. (2.55) can be manipulated following
                              1              1
                                          1                1
                             Z              Z
                                  ðÞdc x ¼
                                               c x ðÞdc x ¼   c x
                               c x fc x        jjfc x                    ð2:56Þ
                                          2                2
                             0              1
            where   c x is the average of the absolute value of c x . Then Eq. (2.55) becomes
                 jj
                                            1
                                        J x ¼ C N   c x                  ð2:57Þ
                                            2
              A step further from the Boltzmann distribution, we can relate   c x with average
                                                                jj
            molecular speed that can be calculated from Eq. (2.2)
                      Z 1           Z 1
                                         m           mc x       1
                                             3=2       2
                           ðÞdc x ¼
                    c x ¼  c x fc x            exp        c x dc x ¼   c  ð2:58Þ
                                       2pkT          2kT        2
                       0            0
              Thus, the collision per unit time per unit area along x direction in terms of
            average molecular speed is

                                             1
                                        J x ¼ C N   c                    ð2:59Þ
                                             4
   62   63   64   65   66   67   68   69   70   71   72