Page 114 - Adsorbents fundamentals and applications
P. 114

ADSORPTION FROM SOLUTION AND EFFECTS OF SURFACE FUNCTIONALITIES  99

                         Table 5.4. Freundlich isotherm constants for adsorp-
                         tion on activated carbon from aqueous solution at
                           ◦
                         25 C
                         Compound               K[(mg/g)       1/n
                                                (L/mg) 1/n ]
                         Benzene                    1.0       1.60
                         Toluene                  100         0.45
                         p-Xylene                 200         0.42
                         Ethylbenzene             175         0.53
                         o-Xylene                 174         0.47
                         Chlorobenzene             28         0.40
                         1,2-Dichlorobenzene       54         0.41
                         1,2,4-Trichlorobenzene   129         0.44
                         Nitrobenzene              68         0.43
                         Phenol                    21         0.54
                         2-Nitrophenol             99         0.34
                         4-Nitrophenol             76         0.25
                         Chloroform                 2.6       0.73
                         Benzoic acid               0.76      1.80
                         Styrene                  327         0.48
                         PCB                      14100       1.03
                         From Dobbs and Cohen, 1980; Weber and DiGiano, 1996.


              The interactions outlined in Chapter 2 are operative in the adsorption of organ-
            ics. In addition to these interactions, hydrogen bonds as well as chemical bonds
            may also form. The solubility is also a factor, that is, the solute–solvent interac-
            tions, as discussed above. In general, adsorption depends on molecular weight,
            functional groups, polarizability (which scales roughly with molecular weight),
            polarity, and hydrophobicity (or lack of solubility). Numerous studies have been
            made in attempting to correlate adsorption with these molecular properties (Al-
            Bahrani and Martin, 1976; Abe et al., 1980; Jankowska et al., 1991).


            5.5.2. Effects of Surface Functionalities on Adsorption
            Aqueous solution of phenol is the most studied solution on the effects of func-
            tionalities on adsorption. As mentioned above, in light of the results of Grant
            and King (1990), the effects of functionalities on adsorption of phenols should
            be studied separately for reversible and irreversible adsorption. The results sum-
            marized below are for the total adsorption at equilibrium.
              Dramatic effects of oxidation and reduction of the carbon surface on the
            adsorption of phenol and nitrobenzene were first shown by Coughlin and Ezra
            (1968). Surface oxygen functionalities were increased by oxidation with ammo-
            nium thiosulfate solution, and reduction was performed with zinc amalgam in
            HCl solution. The isotherms of phenol on three carbon samples are shown in
   109   110   111   112   113   114   115   116   117   118   119