“…The peaks at 900–1300 cm –1 and below 650 cm –1 are assigned to the symmetrical stretching vibration of PO 3 . The peak at 970 cm –1 is assignable to the stretching modes of P–O, and that at about 750 cm –1 corresponds to nonbridging oxygen Ti–O bond vibrations. , In the spectrum of MEA-TiP, the peaks at 3550 and 3480 cm –1 corresponding to P–OH are no longer visible, replaced by a broad band at 2200–3700 cm –1 that might be due to the overlapped absorptions of ammonium, −CH 2 , −OH, and hydrogen bonds, indicating that P–OH became P–O –+ NH 3 –C 2 H 5 OH. ,,, In the spectrum of PVA, there is a broad and strong absorption at 3000–3700 cm –1 , peaking at 3377 cm –1 , which is due to the symmetrical stretching vibration of hydroxyl groups in PVA. The peaks at 2800–3000 cm –1 are due to −CH 2 , and that at 1645 cm –1 can be assumed to be the hydroxyl bending vibration.…”