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Effects of hydrogen bonding on starch granule dissolution, spinnability of starch solution, and properties of electrospun starch fibers.

Authors :
Wang, Wenyu
Wang, He
Jin, Xin
Wang, Hongjie
Lin, Tong
Zhu, Zhengtao
Source :
Polymer. Sep2018, Vol. 153, p643-652. 10p.
Publication Year :
2018

Abstract

Abstract This paper reports the effects of hydrogen bonding on the starch granule dissolution, spinnability of the starch solution, and the properties of the electrospun starch fibers. Dissolution behaviors of the starch granules in dimethyl sulfoxide (DMSO) and water mixed solvents are characterized by confocal laser microscope, differential scanning calorimetry (DSC), and rheologic measurement. The starch granules are dissolved in the 100%DMSO or 6%H 2 O/94%DMSO solvent, resulting in good electrospinnability. On the other hand, the gelatinization behavior is observed for the starch granules in the 22%H 2 O/78%DMSO solvent, resulting in poor fiber formation during electrospinning. Infrared spectroscopy, DSC, x-ray diffraction, and mechanical property characterizations of the electrospun starch nanofibers suggest that the water content in the solvent plays an important role in the properties of the nanofibers. The dissolution behavior, electrospinnability, and the properties of the electrospun nanofibers are explained by the effects of the DMSO and H 2 O molecules on the ubiquitous hydrogen bonds in starch. Highlights • Ratio of dimethyl sulfoxide and water in the mixed solvent affects dissolution of starch. • High water content results in gelatinization and poor electrospinnability of the starch solution. • Aprotic dimethyl sulfoxide dissociates hydrogen bonds of starch, resulting in uniform nanofiber. • Water in solvent affects formation of hydrogen bonds and properties of the electrospun nanofibers. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00323861
Volume :
153
Database :
Academic Search Index
Journal :
Polymer
Publication Type :
Academic Journal
Accession number :
131946714
Full Text :
https://doi.org/10.1016/j.polymer.2018.08.067