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OPPORTUNITIES




























                              Figure 4 -  Simplifi ed block scheme integrating unit operations of E-RWGS, electrolytic hydrogen production with Solid
                              Oxide Electrolysis Cell – SOEC, Alkaline Electrolyzer – AE, Polymer Electrolyte Membrane Electrolyzer – PEME amd
                              methanol synthesis.
                            catalyst and iii) avoiding the use of a reforming furnaces.  to other metal species with increased catalytic properties
                            However, other electrifi ed reactor solutions could include  such as it would occur in Nickel-Cobalt catalyst particles.
                                              33
                            induction-heated reactors  in which reactions occur on  These solutions under development for electrifi ed SR ap-
                            catalysts constituted by magnetic particles having a high  plication, can be exploited, possibly with a greater advan-
                            Curie temperature that inside a magnetic fi eld could be  tage, also for E-RWGS reactors in which the reaction heat
                            selectively heated and possibly transfer the reaction heat  would be ca. 1/5 of the heat required by SR.
                                                                     We have hence examined the possibility of utilising the as-
                     TABLE 6             Case A  Case B              sociated CO2 emissions of a biomethane production plant
                                                                     developing H&M balances for a process solution fed with
       Purge                              0%      10%                300 Nm3/h of carbon dioxide as a reference case. Brief-
       Hydrogen consumption               875     895   Nm3/h        ly it is mentioned that we have considered to compress
                                                                     either, the carbon dioxide and the hydrogen fl ows at 50
                                     [A]  2623,3  2683,3  KWth
                                                                     MPa and subsequently to divide the hydrogen fl ow in two
       Carbon dioxide consumption         300     300   Nm3/h        streams. One stream is mixed with the carbon dioxide and
                                     [B]  13,38  13,38  kmol/h       the mixture is pre-heated at 650°C before entering in the
                                                                     E-RWGS reactor that is assumed to operate at 950°C.
       Methanol productionm (1)                                   [J]  405,6  334,4  kg/h
                                                                     The syngas at the exit of the reactor is cooled at 20°C for
                                          9,73    8,03  TPD          removing the water content from the reaction mixture and
                                     [C]  12,66  10,44  kmol/h       then mixed with a hydrogen fl ow for allowing the achieve-
                                                                     ment of a methanol module M equal to 2 v/v. This adjusted
                                     [D]  2243,2  1849,4  KWth
                                                                     synthesis gas is then pre-heated to 250°C before entering
       Carbon dioxide emission (2)                                 [F]  13,56  116,73  kg/h  into the methanol synthesis reactor operating at 50 MPa.
       Gross power consumption                                   [E]  468,5  384,6  kWel  The obtained stream is cooled at 25°C for separating the
                                                                     liquid and the gaseous phase and that is partially purged
       Power production                   105,7  181,6  kWel
                                                                     for avoiding the build-up of inert molecules (e.g. methane)
       Net power consumption                                     [G]  362,8  203  kWel  and recycled to the methanol synthesis reactor. More in
       PEME electrolyzer consumption (4)         4025  4117  kWel    detail it is reported that for what it concerns the E-RWGS
                                                                     reactor it has been assumed that it could operate at the
       Overall gross power consumption                      [H]  4493,5  4501,6  kWel
                                                                     adiabatic equilibrium at 950°C e 5.0 MPa.
       Overall net power consumption                           [I]  4387,8  4320  kWel  For what concerns the methanol synthesis reactor, it has
       LHV  effi ciency                                                                   [D/A]  85,50%  68,90%     been assumed that it could be operated at 5.0 MPa at
                                                                     an isothermal temperature of 250°C and that it could be
       1st principle effi ciency                         [(D-G)/A]  71,70%  61,40%     simulated as an isothermal equilibrium reactor with an ap-
       1st principle effi ciency (3)               [(D-E)/A]         67,70%  54,60%     proach temperature of 10°C. Noteworthy, the results ob-
       Overall effi ciency                            [D/H]   51,10%  42,80%     tained in the simulation, have been compared with those
                                                                     of an industrial reactor utilising a Cu/ZnO/Al O  based cat-
       Overall  effi ciency  (3)                                                [D/I]   49,90%  41,10%     alyst and operating at a GHSV of 8,000 h . 2  3
                                                                                                  -1
       Carbon  conversion                                                    [C/B]  94,60%  78,00%     Table 6 compares consumption features in two cases in
                                                                     which:
       Carbon specifi c emission                             [F/J]  33,43  349,08  g CO /kg_Methanol
                                                          2          •   Case (A) consider a process scheme in which the
       (1) referred to pure methanol                                     gas of the methanol loop cycle is not purged and
       (2) atmospheric emissions withou energy recovery                  contains 7.5% v/v of methane entering inside the re-
       (3) excluding thermal recovery                                    actor and the 9.5% v/v of methane at the exit of the
       (4) assuming a 4.6 kWh/Nm3 of H  consumption                      reactor,
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