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Fig. 3 (b) presented the Fourier Transform Infrared Spectra (FTIR) of BC@TNS, BC and TNS. For BC, the peak at 1120 cm -1 was assigned to (C=O) of carbonyl groups, and bands at 2916, 1581 and 1456 cm -1 corresponded to the stretching vibration of -CHX bonds, C-C/C=C bonds and C-H bonds, respectively [45, 46]. For TNS, bands at 3400, 1630, 900 and 500 cm -1 were attributed to the -O-H stretching, H-O-H binding, four-coordinated Ti-O stretching and [TiO6] octahedron vibration, respectively [47, 48]. The FTIR spectrum of BC@TNS exhibited the representative characteristic bands from both TNS (3400, 1630, 900, 500 cm -1) and BC (2927, 1581 cm -1), confirming the successful fabrication of the composites.
Fig. 3 (b) presented the Fourier Transform Infrared Spectra (FTIR) of BC@TNS, BC and TNS. For BC, the peak at 1120 cm -1 was assigned to (C=O) of carbonyl groups, and bands at 2916, 1581 and 1456 cm -1 corresponded to the stretching vibration of -CHX bonds, C-C/C=C bonds and C-H bonds, respectively [45, 46]. For TNS, bands at 3400, 1630, 900 and 500 cm -1 were attributed to the -O-H stretching, H-O-H binding, four-coordinated Ti-O stretching and [TiO6] octahedron vibration, respectively [47, 48]. The FTIR spectrum of BC@TNS exhibited the representative characteristic bands from both TNS (3400, 1630, 900, 500 cm -1) and BC (2927, 1581 cm -1), confirming the successful fabrication of the composites.