Page 350 - Elements of Chemical Reaction Engineering Ebook
P. 350

Chap. 6   Questions and Problems                               32 1
                                   In1  each  of  the  questions and  problems below,  rather  than  just  drawing  a box
                               around :your answer, write a sentence or two describing how  you solved the problem,
                               the assumptions you  made, the reasonableness of  your answer, what you learned, and
                               any other facts that you want to include.
                               P6-1   (a)  Make up and solve an original problem to illustrate the principles of this
                                          chapter. See Problem P4-1 for guidelines.
                                      (b) Write a question based on teh material in this chapter that q-tical   thinking.
                                          Explain why your question quim critical thinking. IHint: See prehce p. n.1
                                      (c)  choose a FAQ from Chapter 6 to be eliminated and say why it should be elimin&ed.
                                      (a)  Listen to the audios   on the CD and pick one and say why it was the
                                          most helpful.
                                      (e)  Which example on the CD ROM Lecture notes for Chapter 6 was least helpful?
                               P6-2   (a)  What if you could vary the temperature in Example 6-_1? What tempera-
                                          ture and CSTR space-time would you use to maximize YD for an entering
                                          concentration of A of  1 mol/dm3? What temperature would you choose?
                                      (b)  What if the reactions in Example 6-3 were carried out in a CSTR instead
                                          of  a PBR? What would be the corresponding optimum conversion and
                                          space-time, tLpt ?
                                      (c)  What if you  varied the catalyst particle size in Example 6-6? Would  it
                                          increase or decrease  SXT ?  [Hint: Use  a  form of  Equation (S6-18) and
                                          make a plot of  SXT versus a.]
                                      (d)  What feed conditions and reactors or combination of  reactors shown in
                                          Figure 6-3 would you use to
                                          (1)  maximize the overall selectivity   in Example 6-8? Start by  plot-
                                              ting SCF as a function of OB in a  10-dm3 PFR;
                                          (2)  maximize the yield of  YFA with and the overall selectivity of  & ?
                                      (e)  What if you could vary the ratio of  hydrogen to mesitylene in the feed
                                          (0.2 < OH < 5) in Example 6-6. What is the effect of  OH on  topt ? Plot
                                          the optimum yield of xylene as a function of  QH.  Plot the selectivity 5,
                                          as a function of  BH. Suppose that the reactions could be run at different
                                          temperatures. What would be the effect of the ratio of k, to k2 on topt and
                                          on the selectivity SXT and the yield?
                                       (f)  Repeat part (d) for Example 6-7.
                                       (8)  How  would pressure drop affect the results shown in Figure E6-8.1;'
                               P6-3B   The  hydrogenation of  0-cresol  2-methylphenol (MP)  is  carried  out  over  a
                                       Ni-catalyst [Znd.  Eng. Chem. Res., 28, 693 (1989)l to form 2-methylcyclo~hex-
                                       anone (ON), which then reacts  to form two  stereoisomers, cis- (cs-OL) and
                                       trans  (tr-OL)-2-methylcyclohexanol. The  equilibrium  compositions  (on  a
                                       hydrogen-free basis) are shown in Figure P6-3.
                                       (a)  Plot (sketch) the selectivities of ON to cs-OL and of tr-OL to cs-OL as a
                                          function of temperature in the range 100 to 300°C.
                                       (b) Estimate the heat of reaction for the isomerization
                                                            tr-OL       cs-OL
                                       (c)  Plot (sketch) the yields of MP to tr-OL and of MP to ON as functions of
                                          temperature assuming a stoichiometric feed.
                                P6-4,   (a)  What  reaction schemes and conditions would you  use to maximize the '
                                          selectivity parameters S for the following parallel reactions:
                                                  A + c ._j D      r,, = 800e(-2~=T)C~CC
                                                  A+C ---+ U,  ru = 10e(-3002T)CACc

                                          where D is the desired product and U, is the undesired product?
   345   346   347   348   349   350   351   352   353   354   355