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Phenolic Wastewater Treatment: Development and Applications of New Adsorbent Materials  335


























              Figure 8.1 FTIR spectrum of untreated banana peel powder.

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              with a resolution of 2 cm . For mixed metal oxides, IR spectra were
              collected in Far-IR region below 400 cm  1  because a majority of the peaks
              lie in this region.
                 The FTIR spectrum of untreated BP (Figure 8.1) depicts a sharp peak at
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              3427.27 cm , which is indicative of H-bonded OH group stretching.
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              Another intense band at 1633.59 cm  is ascribed to hydrated hydroxyl
              groups (dOH). The band centered at 1045.35 cm  1  corresponds to the
                                                                     1
              stretching vibration of the SidO bond. The band at 1244 cm  indicates
              the presence of a carboxyl group.
                 The FTIR spectrum of unmodified TW is shown in Figure 8.2.The
              intense, nearly sharp adsorption band at 3425 cm  1  can be assigned to OH
              stretching of a hydroxyl group. These vibrations are often associated with H
              bonds; thus the surface dOH groups interact with water molecules adsorbed
              (Zawadzki, 1980). The sharp and intense bands at 2925 and 2363 cm  1  belong
                                                                             1
              to HdCdH stretching, while the broad and intense peak at 1638 cm
              belongs to C]O stretching of amides. The peak position at 1053 cm  1  is
                                                                             1
              compatible with a silicate ion, while the broad band centered at 668 cm
              maybelinkedtothe CdH group frequencies of acetylenic linkage.
                 The FTIR spectrum of AES (Figure 8.3) also indicates the presence
                                                                            1
              of hydrogen bonded OdH stretching at 3444.63 and 2925.81 cm .
              The CdO functional group can be envisaged from the presence of intense
                                                                    1
              to minor peaks at 1257.50, 1205.43, 1118.64, and 1062.70 cm . The pres-
                                                                    1
              ence of a silicate ion is revealed by the sharp peak at 939.27 cm , while the
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