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when the CO 2 partial pressure is in the range 30–90 psi. The following
            reactions occur in this case:

                 K 2 CO 3 þ CO 2 þ H 2 O , 2KHCO 3                       ð12Þ
                 K 2 CO 3 þ H 2 S , KHS þ KHCO 3                         ð13Þ
            It can be seen from reaction (12) that a high partial pressure of CO 2 is
            required to keep KHCO 3 in solution, and in Eq. (13), H 2 S will not react if
            the CO 2 pressure is not high. For this reason, this process cannot achieve a
            low concentration of acid gases in the exit stream and a polishing process
            is needed (molecular sieve). An elevated temperature is also necessary to
            ensure that potassium carbonate and reaction products (KHCO 3 and
            KHS) remain in solution. Thus, this process cannot be used for gases
            containing H 2 S only.
                 The hot carbonate process which is given in Figure 7 is referred to as
            the ‘‘hot’’ process because both the absorber and the regenerator operate

            at elevated temperatures, usually in the range (230–240 F). In Figure 7, the
            sour gas enters at the bottom of the absorber and flows countercurrently
            to the carbonate liquid stream. The sweet gas exits at the top of the

            absorber. The absorber is operated at 230 F and 90 psia. The rich






























            Figure 7  Hot carbonate process.






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