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344   Industrial Wastewater Treatment, Recycling, and Reuse



             0.0035                          0.007
             0.0030                          0.005
            Pore volume (cm 3 /g A°)  0.0020  Pore Volume (cm 3 /g A°) 0.006
             0.0025
                                             0.004
                                             0.003
             0.0015
             0.0010
             0.0005                          0.002
                                             0.001
             0.0000                          0.000
                  0   500  1000  1500  2000      0  200  400  600  800  1000  1200
           (a)           Pore diameter (A°)  (b)         Pore diameter (A°)
          Figure 8.11 Pore size distribution of BMO. (a) BJH adsorption pore volume and (b) BJH
          desorption pore volume.


                Banana Peel < Tea Waste < NeemLeaf < ActivatedEgg Shell
                           < ActivatedNeem Leaf < ActivatedTea Waste

             Considerable differences in surface area are observed for the natural and
          chemically activated forms of adsorbents.


          8.3.4 X-ray Diffraction
          XRD patterns provide information on the particle size and defects, while the
          peak relative intensities provide insight into the atomic distribution in
          the unit cell. For the correct interpretation of powder diffractograms, a good
          peak-to-background ratio is an important issue. The background in powder
          diffraction can originate from many sources, which can be related to instru-
          ments or the sample itself. The analysis of XRD patterns and diffraction
          peaks will characterize the crystalline phase of the adsorbent. This is partic-
          ularly important in the case of synthesized metal oxides.
             Powder XRD patterns were obtained with PAN analytical, X’pert PRO
                                                       ˚
          using 40 kV, 30 mA, Cu Ka radiation (l¼1.5405 A) with a scan speed of

          2y¼5 min   1  in the scan range from 10 to 130 2y. Qualitative analysis was

          performed by the Powder Diffraction File database. The XRD method
          appears to be a reliable method for studying surface area, which requires
          the use of crystal size measurement. The peak broadening is a suitable
          XRD parameter (Schwertmann and Latham, 1986) used for determining
          the mean crystallite dimension.
             The Debye-Scherrer equation is often used to calculate the mean
          crystallite size.
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