TY - JOUR
T1 - Synthesis, structure, and properties of N-2-hydroxylpropyl-3-trimethylammonium-O-carboxymethyl chitosan derivatives
AU - Liu, Qun
AU - Chen, Jialiang
AU - Yang, Xiaodeng
AU - Qiao, Congde
AU - Li, Zhi
AU - Xu, Chunlin
AU - Li, Yan
AU - Chai, Jinling
N1 - 3pk
post-print, 12 months, CC BY-NC-ND
mail till Xu 15.2.2021 /LN
PY - 2020/2/1
Y1 - 2020/2/1
N2 - N-2-hydroxylpropyl-3-trimethylammonium-O-carboxymethyl chitosan (HTCMCh) was synthesized through homogeneous reaction. The effects of different reaction condition on the properties of HTCMCh were characterized by FTIR, NMR, SEM, TEM, DLS, XRD, TGA, and DSC. The results of FTIR spectra, 1H NMR, and 13C NMR proved the successful synthesis of HTCMCh. The DS was dependent upon reaction time and pretreated pH of the starting material, independent of temperature and nepoxy/n-NH2. With increasing reaction time, the crystallinity of HTCMCh decreased, and the intermolecular interactions transformed from hydrogen bonding to strong electrostatic interactions, which enhanced HTCMCh thermal stability. SEM observations showed smooth cross section morphologies of HTCMCh films. With the increase in reaction time, the tensile strength significantly increased. The viscoelasticity transformed from viscous to elastic with aging time, confirming the formation of polyelectrolyte complexes. The optimum reaction conditions: reaction time of 2 h, an initial material pH of 9.47, nepoxy/n-NH2 of 2/1.
AB - N-2-hydroxylpropyl-3-trimethylammonium-O-carboxymethyl chitosan (HTCMCh) was synthesized through homogeneous reaction. The effects of different reaction condition on the properties of HTCMCh were characterized by FTIR, NMR, SEM, TEM, DLS, XRD, TGA, and DSC. The results of FTIR spectra, 1H NMR, and 13C NMR proved the successful synthesis of HTCMCh. The DS was dependent upon reaction time and pretreated pH of the starting material, independent of temperature and nepoxy/n-NH2. With increasing reaction time, the crystallinity of HTCMCh decreased, and the intermolecular interactions transformed from hydrogen bonding to strong electrostatic interactions, which enhanced HTCMCh thermal stability. SEM observations showed smooth cross section morphologies of HTCMCh films. With the increase in reaction time, the tensile strength significantly increased. The viscoelasticity transformed from viscous to elastic with aging time, confirming the formation of polyelectrolyte complexes. The optimum reaction conditions: reaction time of 2 h, an initial material pH of 9.47, nepoxy/n-NH2 of 2/1.
KW - N-2-hydroxylpropyl-3-trimethylammonium--carboxymethyl chitosan
KW - Synthesis
KW - Physicochemical properties
U2 - 10.1016/j.ijbiomac.2019.12.125
DO - 10.1016/j.ijbiomac.2019.12.125
M3 - Article
SN - 0141-8130
VL - 144
SP - 568
EP - 577
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
ER -