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The difference between antisymmetric COO− stretching vibration band and symmetric COO− stretching vibration band is 160 cm−160
The bending vibration band at 584 cm−1 and stretching vibration band at 1627 cm−1 are induced by structure Fe–O vibration.
The vibration band between 1000 and 1100 cm−1 suggested the presence of saccharide derivatives.
Another vibration band was detected in the range of 1000 1200 cm−1 (Fig. 5a,b).
The bending vibration band of O H is observed at wave numbers 875cm−11.
A weak C H asymmetric stretching vibration band was observed at 2920 cm−1.
When the Tg was higher, the intensity of the Si-O bending vibration band increased and shift at the same time that the peak at 870 cm-1 decreased, and the Si-O bending vibration band became more apparent.
The occurrence of intramolecular hydrogen bonding interactions was confirmed by the broad OH stretching vibration band in the IR spectra.
The stretching vibration band at 3434 cm−1 can be correlated with hydroxyl groups (OH) adsorbed on the surface.
Thus, the vibration band at 900 and 1,000 can1 can be attributed to Si-O-Pr asymmetric mode.
In addition, the weak peak at 1,165 cm−1 is related to the C-O vibration band.
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