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366                                        12  Carbon Capture and Storage

            12.6 CO 2 Separation by Absorption

            CO 2 absorption can also be classified into physical and chemical absorptions.
            Physical absorption requires much lower energy to regenerate the solvent than
            chemical absorption. A conceptual comparison between chemical and physical
            absorption capacity at different absorbate partial pressures is shown in Fig. 12.6.
            Physical absorption is not economical for absorption of gases with a low partial
            pressure, say from the combustion flue gas. It aims at compressed gases.



            12.6.1 Physical Absorption


            Physical absorption processes use organic or inorganic solvents to absorb CO 2 from
            the carrier gases. The process capacity is governed by Henry’s law described in
            Eq. (2.76); the equilibrium solubility of CO 2 in a solvent is


                                              P CO 2
                                            ¼                           ð12:25Þ
                                        c CO 2
                                               H
            where c CO 2  is the equilibrium CO 2 concentration in the solvent, P CO 2  is the CO 2
            partial pressure in the gas phase, and H is the corresponding Henry’s constant.
            Practically speaking, solvent with a great CO 2 solubility is preferred at a reasonable
            cost for physical CO 2 absorption.
              Physical absorption is primarily used for high pressure CO 2 separation to
            increase the solubility in the solvent. Refrigerated methanol (CH 3 OH) was con-
            sidered an effective CO 2 solvent for CO 2 sequestration at low temperature. The
                                                    ¼ 1 atm is 10 L of CO 2 per liter
            solubility of CO 2 in methanol at −10 °C and P CO 2
            of methanol, which is 4 times that of water.





















            Fig. 12.6 Relative solvent loading versus partial pressure of the absorbate gas
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