Page 124 - Adsorbents fundamentals and applications
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CARBON MOLECULAR SIEVES  109

              Monolithic composites of activated carbon fibers with phenolic resin as the
            binder have been prepared for a variety of possible applications, including gas
            separation (Burchell, 1999; Kimber et al., 1996). The low-density composites
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            with densities <0.25 g/cm are particularly promising for gas separation as well
            as energy storage (CH 4 and H 2 ) applications. A detailed discussion on these
            types of materials has been given by Burchell (1999). Methane storage will be
            discussed in Chapter 10.


            5.6.1. Adsorption Isotherms
            A large body of experimental data on the adsorption isotherms exists in the liter-
            ature (both journal publications and commercial brochures). With the exception
            of methane storage, most of the data are related to purification, particularly for
            environmental applications. Comparing different ACFs, the amounts adsorbed
            are, in general, directly dependent on the BET surface area and the micropore
            volume of the ACF. However, the heats of adsorption on ACF are higher than
            those on the granulated activated carbon. This is shown in Table 5.9 for hydro-
            carbons and CO 2 . The data in Table 5.9 are taken from Kuro-Oka et al. (1984),
            Meredith and Plank (1967), Laukhuf and Plank (1969), and Reich et al., (1980).
              Adsorption of SO 2 , NO, and various VOCs on ACF has been studied. Fig-
            ure 5.19 shows the adsorption capacities of benzene, toluene, and phenol for a
            number of ACFs. The corresponding capacities for commercial activated carbons
            (GACs) are 0.33 g/g (benzene), 0.35 g/g (toluene), and 0.30 g/g (phenol). These
            are near the lowest values of the various ACFs. The adsorption of NO by ACFs
            has been studied extensively by Kaneko (1998). Comparing a number of GACs
            and ACFs, the amounts adsorbed of NO were higher on the ACFs. For example,
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            for two samples with the same BET surface area (860 m /g), the amounts were
            17 mg/g (at 13 kPa and 303 K) for the GAC compared with 65 mg/g for a PAN-
            based ACF; and at 80 kPa and 303 K, these values were 47 mg/g for GAC and
            115 mg/g for the ACF. The adsorption of SO 2 by ACF was studied extensively
            by Mochida and co-workers (e.g., Mochida et al., 1997a; 1997b). However, the
            focus of their studies was on the catalytic activity for oxidation of SO 2 to SO 3
            in the presence of both O 2 and liquid water (to form sulfuric acid). Moderate
            activities at room temperature were reported. The mechanism of the reaction is
            not understood, although molecular orbital studies have indicated the importance
            of surface oxides on carbon for the catalytic activity (Yang and Yang, 2002).
              Enhanced adsorption capacities by the small pores of ACF have also been
            observed for adsorption from aqueous solutions. Sakoda et al. (1987) reported
            the adsorption isotherms of trichloroethylene and tetrachloroethylene on a number
            of ACFs derived from phenolic resin, as shown in Figure 5.21. These data are
            compared with that on GAC, and the enhancement is clearly seen.


            5.7. CARBON MOLECULAR SIEVES
            Because they are less hydrophilic than zeolites but have molecular sieving prop-
            erties, carbon molecular sieves (CMS’s or MSC’s) can be used more efficiently
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