Page 191 - Principles of Catalyst Development
P. 191

CATALYST  CHARACTERIZATION                                       179


                              CO  METHANATION  ON  NICKEL  CATAYLST
                      1.0
                  'I                                        340"C
                   a:                  _-0---0 -----0-
                   J:
                  ~
                   I
                   CI
                   rn
                   w
                   ....I   0.5
                   0
                   ~
                   u.i
                   .....
                   e(                                       250"C
                   a:               __ ----cr--~~-------,-o-
                        0
                       1000          1500         2000          2500

                                         IMPELLER  RPM
             Figure 7.34.  Typical  results  with  a  well·mixed  reactor, showing the effect of mixing speed.

            however, difficult to design for many small applications,  especially at high
            temperatures.

            7.5.2.3.  Batch  Reactors

                Batch  reactors  are  not  common  in  experimental  catalysis  since  flow
            systems are so simple. They are most often found with liquid phase reactors
            using  slurried  catalysts.  Good  mixing  is  essential  and  c:hecks  should  be
            made to eliminate external diffusion problems. Also it is  necessary to vary
            catalyst loading during the experiment as a means of detecting vapor-liquid
            interfacial  effects. (21)
                Gradientless and recirculation gas phase reactors may also be operated
            in  a  batch  mode by eliminating  flow,  but there  is  usually  little  advantage
            to this in catalyst development.


            7.5.2.4.  Pulse  Reactors
                These are rapid, simple reactors that offer economy of feed and provide
            protection  against  process  deactivation.  A  typical  scheml~ is  given  in  Fig.
            7.26.  The  operation  is  transient  so  that  concentrations  change  over  the
            surface.  Kinetic  interpretations  are  difficult  for  any  but  first-order  rate
            equations.(255)  Pulse  reactors  do  have  utility  in  poison  titration  measure-
            ments,  in  determining  activities  of the  "fresh"  surface,  and  for  following
            surface conditioning.
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