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3
                 0.25 < d  < 0.50 mm; total flow: 350 cm /min; feed composition: 25% EtOH, 75%
                          p
                                                                                 18
                 H O; P = 1 atm. (Reproduced with permission from Ref  . Copyright 2002, Elsevier.)
                   2
                 Figure 9.2 Ethanol conversion (X      EtOH ) as a function of reaction temperature over 0.5%
                 Pt/Al O , 1% Pd/Al O , 2% Rh/Al O , and 5% Ru/Al O  catalysts. Experimental
                                        2 3
                                                                              2 3
                       2 3
                                                         2 3
                 conditions: mass of catalyst: 0.65 g; particle diameter: 0.18 < d  < 0.25 mm; TOTAL
                                                                                         p
                                 3
                                                           −1
                 Flow: 120 cm /min; GHSV = 9350 h ; feed composition: 12.5% EtOH, 37.5% H O
                                                                                                              2
                                                                                           24
                 (balance He); P = 1 atm. (Reproduced with permission from Ref  . Copyright 2008,
                 Springer.)
                 Figure 9.3 (a) Effect of the nature of the support on the catalytic performance and (b)
                 selectivity toward CO over Pt (0.5 wt%) supported on the indicated commercial oxide
                 carriers. Experimental conditions: same as in Figure 9.2. (Reproduced in part from Ref
                 37 . Copyright 2012, Elsevier.)


                 Figure 9.4 Reaction steps for the dry reforming of methane. (a) Adsorption and
                 dissociation of CH  and CO  on the metal and the metal–support interface,
                                                 2
                                      4
                 respectively. (b) CO and H  desorption are fast steps. (c) Surface hydroxyls are formed
                                                2
                 from hydrogen and oxygen spillover. (d) Surface oxygen species or hydroxyls oxidize
                 the hydrogen depleted surface methyl-like species (*CH ), forming *CH O species and
                                                                                                  x
                                                                                x
                                                                 12
                 finally CO and H . (Reproduced from Ref  . Copyright 2012, Springer.)
                                    2
                 Figure 9.5 Methane conversion for transition metal catalysts supported on either silica
                 or alumina [reacting mixture: CH :CO :He (10:10:80); total flow rate: 100 mL/min]:
                                                      4
                                                            2
                                                                                                        50
                 (a) at 723 K, TOS 45 min; (b) at 1023 K TOS 5 min. (Reproduced from Ref  .
                 Copyright 1996, Elsevier.)

                 Figure 9.6 Schematic representation of the bifunctional mechanism proposed by
                 Takanabe for the steam reforming of acetic acid over a Pt/ZrO  catalyst. (Reproduced
                                                                                       2
                 from Ref   115 . Copyright 2004, Elsevier.)

                 Figure 9.7 Comparison among thermodynamic data (lines) and experimental results
                 (symbols) of molar ratios of H  (♦), CO  (▪), CH  (●) and CO (▲), and the conversion
                                                    2
                                                              2
                                                                        4
                 of glycerine (▼) on 13 wt% Ni–6 wt% La O /Al O  catalyst at steady state, 0.4 MPa,
                                                                 2 3
                                                                         2 3
                 different temperatures, and 1:9 glycerol/water ratio. (Reproduced from Ref            135 .
                 Copyright 2012, Elsevier.)
                 Figure 9.8 (a) H  selectivity and (b) glycerol conversion at selected temperatures over
                                    2
                 Al O -supported catalysts. Reaction conditions: Water/glycerol ratio = 6:1, FFR:
                    2 3
                                                    −1
                 0.5 mL/min (GHSV = 51,000 h ), data collected after 1 h of operation. (Reproduced
                 from Ref   139 . Copyright 2004, Elsevier.)

             Chapter 10
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