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360   Industrial Wastewater Treatment, Recycling, and Reuse


          Table 8.8 Binary component equilibrium results and total adsorption yield in the solute
          mixture of 4-CP+phenol a
          C e(4-CP)  C e(P)    q e(4-CP)  q e(P)    Ad (4-CP)  Ad (P)  Ad (total)
                1
                          1
                                               1
                                     1
          (mg L )   (mg L )    (mg g )   (mg g )    %        %       %
          464.87    621.66     53.11     37.55      53.51    37.83   45.67
          402.49    531.56     39.81     31.21      59.75    46.84   53.29
          314.63    444.1      34.21     27.75      68.53    55.59   62.06
          257.3     365.88     29.68     25.34      74.27    63.41   68.84
          204.86    307.51     29.39     22.99      79.51    69.25   74.38
          117.94    169.12     22.02     20.74      88.21    83.09   85.65
           86.28    126.67     20.3      19.42      91.37    87.43   89.4
          a                                    1
           Conditions: C 0,4-CP : C 0,P ¼1:1 ratio, C 0,i ¼1000 mg L

          obtained from single-solute data. Besides, the surface characteristic of an ANL
          adsorbent and the presence of the electron-withdrawing dCl group impli-
          cates their role in the higher uptake. For the experimental study of this com-
          bination, 4-CP had a similar concentration to phenol. Among the various
          binary solute investigations, the minimum adsorption yield occurred in the
          combined of 4-CP+phenol system. Table 8.8 shows a decrease in the
          adsorbed phase concentration. A total adsorption yield of 89.40% was
          achieved at a high adsorbent dose. It is again evident from this table that
          the adsorption yield of 4-CP is higher than for phenol in all the doses of adsor-
          bent. Overall, an antagonistic effect is observed in this binary combination
          because both capacities decreased drastically.



          8.8 DESORPTION STUDIES

          Desorption and regeneration studies are important in adsorption. Desorp-
          tion may occur either by thermal treatment or through suitable desorbing
          agents. More acidic groups such as carboxyls and lactones can be desorbed
          as CO 2 at 200–650 C, while the less acidic (phenol and carbonyl) basic

          groups may be desorbed as CO or a mixture of CO and CO 2 in the range

          of 500–1000 C(Brennan et al., 2001). In the present study, however, for
          phosphoric acid-activated adsorbents, a chemical method of regeneration
          was employed.
             Figures 8.18 and 8.19 show desorption of 4-NP, 4-CP, and phenol for
          ATW and AES adsorbents, respectively. The study shows maximum
          desorption efficiency using NaOH for 4-CP and phenol while HNO 3 also
          served as a good eluent for desorption of 4-NP-loaded adsorbents. In the
          case of ATW, maximum desorption of 27.02%, 28.66%, and 52.44% was
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