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12.6  CO 2 Separation by Absorption                             371

                     0
            Table 12.7 k for different amines [9]
                     g
                                               7
            Amine                         k   10 mole= m   Pað  2  Þ  Capacity (mole/kg)
                                           0
                                           g
            Piperazine (PZ)               8.5                   0.79
            PZ/bis-aminoethylether        7.3                   0.67
            2-Methyl PZ/PZ                7.1                   0.84
            2-Methyl PZ                   5.9                   0.93
            2-Amino-2-methyl propanol (AMP)  2.4                0.96
            PZ/aminoethyl PZ              8.1                   0.67
            PZ/AMP                        7.5                   0.70
            Hydroxyethyl PZ               5.3                   0.68
            PZ/AMP                        8.6                   0.78
            2-Piperidine ethanol          3.5                   1.23
            Monoethanolamine (MEA)        3.6                   0.66
            MEA                           4.3                   0.47
            Methydiethanolamine (MDEA)/PZ)  8.3                 0.99
            MDEA/PZ                       6.9                   0.80
            Kglycinate                    3.2                   0.35
            Ksarconinate                  5                     0.35
            MEA/PZ                        7.2                   0.62


                           0
              The measured k for different amines and amine alternatives are summarized in
                           g
            Table 12.7. There is no obvious correlation between the mass transfer coefficients
            and the capacities of different amines.


            12.6.2.3 Amine-Based CO 2 Capture Process

            MEA is considered the baseline solvent for CO 2 capture. The design of a MEA
            based CO 2 absorption tower follows the principles introduced in Sect. 5.2.Ina
            typical CO 2 scrubber, the flue gas at 40–60 °C enters the tower from the bottom
            while a 20–30 wt% MEA solution flows downward continuously from the top.
            Because MEA is corrosive, diluted instead of concentrated MEA is used. After
            selective absorption of CO 2 from the flue gas, the CO 2 -rich amine solution is
            drained off from the bottom of the absorber.
              The rich solvent is regenerated in a stripper that operates at 100–140 °C. The
            energy required for solvent regeneration can be from waste heat recovery from a
            steam and/or a reboiler. A high-efficiency heat exchanger can also be employed to
            recycle the heat from the rich solvent from the absorber tower. The recovered gas
            phase contains steam and CO 2 , which are separated from each other by conden-
            sation. The final concentrated CO 2 stream is ready for CO 2 transport and storage.
              As the most widely used solvent for CO 2 capture, MEA is still not an ideal
            solvent yet. Throughout the process, solvent degradation may take place in the
            presence of oxygen. Furthermore, secondary air emission is produced due to the
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