Novel gigahertz frequency dielectric relaxations in chitosan films
Molecular relaxations of chitosan films have been investigated in the wide frequency range of 0.1 to 3 × 10 9 Hz from −10 °C to 110 °C using dielectric spectroscopy. For the first time, two high-frequency relaxation processes (in the range 10 8 to 3 × 10 9 Hz) are reported in addition to the low fre...
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Veröffentlicht in: | Soft matter 2014-11, Vol.1 (43), p.8673-8684 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Molecular relaxations of chitosan films have been investigated in the wide frequency range of 0.1 to 3 × 10
9
Hz from −10 °C to 110 °C using dielectric spectroscopy. For the first time, two high-frequency relaxation processes (in the range 10
8
to 3 × 10
9
Hz) are reported in addition to the low frequency relaxations α and β. These two relaxation processes are related to the vibrations of OH and NH
2
/NH
3
+
, respectively. The high-frequency relaxations exhibit Arrhenius-type dependencies in the temperature range 10 °C to 54 °C with negative activation energy; this observation is traceable to hydrogen bonding reorientation. At temperatures above the glass transition temperature (54 °C), the activation energy changes from negative to positive values due to breaking of hydrogen bonding and water loss. Upon cooling in a sealed environment, the activation energies of two relaxation processes are nearly zero. FTIR and XRD analyses reveal associated structural changes upon heating and cooling. These two new high-frequency relaxation processes can be attributed to the interaction of bound water with OH and NH
2
/NH
3
+
, respectively. A plausible scenario for these high-frequency relaxations is discussed in light of impedance spectroscopy, TGA, FTIR and XRD measurements.
Temperature-dependence relaxation time of OH side groups
versus
1/
T
for chitosan films in the heating and cooling process. The solid lines represent Arrhenius-type dependence fitting. Schematic of proposed molecular interactions. |
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ISSN: | 1744-683X 1744-6848 |
DOI: | 10.1039/c4sm01804d |