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Physisorbents like zeolites, activated carbons, silica, and alumina gels have been traditionally used for separation of bulk or trace carbon dioxide from a gas mixture using a pressure or a thermal swing adsorption process. These processes are generally operated at near ambient or at moderate temperatures (say <100 °C) because the equilibrium sorption capacity and selectivity of sorption of CO 2 on the physi-sorbents rapidly decrease at higher temperatures. Recently, a variety of reversible CO 2 chemisorbents have been developed which offer decent sorption capacity and high selectivity for CO 2 at relatively higher temperatures (∼150 to 500 °C). Some of these chemisorbents even exhibit high selectivity of CO 2 sorption in the presence of H 2 O which is mechanistically impossible for a physisorbent. Consequently, these chemisorbents can be used in (a) sorption enhanced reaction (SER) concepts for production of fuel-cell grade H 2 from natural gas by low temperature steam-methane reformation reaction at ca. 400−500 °C or from synthesis gas by water−gas shift reaction at ca. 200−400 °C, and (b) removal and recovery of CO 2 from a flue gas at a temperature of 150−200 °C without precooling, predrying, and precompression. A comprehensive review of this subject is presented.
Lee et al. (Tue,) studied this question.