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Adsorption                                                                                       483



                                                               15.3 LABORATORY AND PILOT PLANT
            TABLE 15.5
                                                                     STUDIES
            Length and Velocity of Wave Front for Different
            Conditions by Computer Simulation                  The most important laboratory data to be generated are
                                                               isotherms. A pilot plant study can add more specific informa-
                         Conditions                 Results
                                                               tion about the behavior of a given system.
                          HLR      C 0          L wf    v wf
            Adsorbate    (m=h)   (mg=L)   Run   (m)    (m=day)
                                                               15.3.1 QUESTIONS FOR A LABORATORY=PILOT PLANT
            Effect of C 0
                                                                       STUDY
            Rhodamine-B    4.2     200   TEBV   0.20    0.037
             dye                   500   PYSO   0.28    0.090  Some of the questions for a pilot plant investigation include
                                  1000   QGUR   0.40    0.170  type of carbon, bed depth, hydraulic loading rate, hydraulic
                                  2000   QUPR   1.00    0.360  conductivity of the packed bed, backwash head needed, pre-
            Effect of HLR                                      treatment advisable, etc. The foregoing list comprises inde-
            Rhodamine-B    4.2     500   PYSO   0.28    0.090  pendent variables which may be imposed on the column, one
             dye           8.4           DFTP   0.45    0.180  at a time, to assess the effect. The dependent variables of
                          33.7           DFUH   1.30    0.68   interest include the wave front, C(Z) t and the breakthrough
                                                                             .
                                                               curve, C(t) Z ¼ Z max
            Source: Adapted from Vagliasindi, Wave front behavior in adsorption
                  reactors, MS Thesis, Department of Civil Engineering, Colorado  15.3.1.1  Isotherm Determination
                  State University, Fort Collins, CO, p. 74, 1991.
                                                               As described in Section 15.2.1.2 the experimental determin-
            Adsorbent was Dowex 50 cation exchange resin. X* ¼ 726,434; 745,060;
                                                               ation of an isotherm is the basis for the prediction of wave-
             751,483; 754,736 mg Rhodamine-b=g Dowex 50 resin for C 0 ¼ 200, 500,
                                                               front velocity, v wf , as described by Equation 15.48, Section
             1000, 2000 mg Rh-B=L, respectively.
                                                               15.2.4.1. As noted, most waters contain more than one soluble
                                                               organic compound and so the isotherm for a specific com-
                                                               pound in a particular mixture would be unique. If TOC
            some compounds by bacterial metabolism. In fact, the  reduction is an objective, then a pseudo isotherm, as measured
            presence of a metabolizing compound is likely to promote  by TOC, may be used as an estimate of adsorbent capacity.
            such colonization. While some view the bacterial coloniza-
            tion as a positive effect, the bacteria may cause higher  15.3.1.2  Determine v(wave front)
            impedance to the diffusion of adsorbate molecules to  The velocity of the wave front, v wf , may be determined by
            adsorption sites.                                  (1) successive direct measurement from sample taps along a




                     2.0                                          12

                                                                  10      1,4-Dioxane
                     1.5
                                               p-Chlorophenol      8                Nitromethane


                    C/C 0  1.0                                   Concentration (mol/L)×10 –5  6


                                               p-Nitrophenol       4
                     0.5
                                                                   2
                                                                                        Methyl ethyl ketone
                                                                                 n-Butanol
                     0.0                                           0
                        0     100    200    300     400    500      0        5        10       15       20
                  (a)                  Time (h)                 (b)                 Time (h)
            FIGURE 15.18  Examples of breakthrough curves that illustrate chromatographic effect for multi-solute adsorbate systems (data points not
            shown). (a) Bi-solute adsorbate system. (From Fritz, W. et al., Competitive adsorption of dissolved organics on activated carbon, Chap. 9, in:
            Suffet, I.H. and McGuire, M.J. (Eds.), Activated Carbon Adsorption of Organics from the Aqueous Phase, Vol. 1, Ann Arbor Science
            Publishers, Ann Arbor, MI, p. 205, 1980.) (b) Four-solute adsorbate system. (From McGuire, M.J. and Suffet, I.H., The calculated net
            adsorption energy concept, Chap. 4, in: Suffet, I.H. and McGuire, M.J. (Eds.), Activated Carbon Adsorption of Organics from the Aqueous
            Phase, Vol. 1, Ann Arbor Science Publishers, Ann Arbor, MI, p. 625, 1980.)
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