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28  Chapter 2: Kinetics and Ideal Reactor Models

                                 Then equation 2.2-2 becomes, for i =  A,


                                                     (-rA)  =  -(v,lV)(dSldt)                 (2.2-6)  /



                             (3) Normalization may be by means of the system volume V . This converts nA  into
                                 a volumetric molar concentration (molarity) of A, CA, defined by






                                 If we replace  nA  in equation 2.2-2 by cAV  and  allow  V  to vary, then we have


                                                     (-).A)  = 2!2$ - ?$                      (2.2-8)




                                 Since  (-?-A)  is now related to two quantities, CA  and V, we require additional
                                 information connecting CA (or nA)  and V. This is provided by an equation of
                                 state of the general form

                                                         v =  v(nA, T, P)

                             (3a) A special case of equation 2.2-8 results if the reacting system has constant vol-
                                  ume (i.e., is of constant density). Then  dVldt  = 0, and


                                                 (-,-A) = -dc,/dt   (constant density)       (2.2-10)



                             Thus, for a constant-density reaction in a BR, r, may be interpreted as the slope of
                           the  CA-t   relation. This is illustrated in Figure 2.2, which also shows that rA  itself depends
                           on  t  , usually decreasing in magnitude as the reaction proceeds, with increasing  t  .






                                     rAl  = slope at cA1,   tl










                                                     rA2  = slope at  cA2,  tp




                            Figure  2.2 Interpretation of rA  for an isothermal,
                            constant-density batch system
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