Structure of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) fibers prepared by drawing and annealing processes has been analyzed through wide-angle X-ray diffraction (WAXD), density, infrared dichroism, and birefringence measurements. There are three different types of crystalline structure in these f
Thermal and spectroscopic characterization of microbial poly(3-hydroxybutyrate) submicrometer fibers prepared by electrospinning
✍ Scribed by G.-M. Kim; G. H. Michler; S. Henning; H.-J. Radusch; A. Wutzler
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 597 KB
- Volume
- 103
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
Abstract
Submicrometer fibers based on the microbially synthesized ultra‐high‐molecular‐weight poly(3‐hydroxybutyrate) (PHB) were generated by an electrospinning (ES) process with chloroform as the solvent. To characterize the resulting electrospun fibers in comparison with the pure PHB before ES, differential scanning calorimetry, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy were performed. The diameters of the electrospun fibers characterized by SEM were in the range 400–1000 nm. Thermal analysis showed that the electrospun fibers contained both helical (α form) and trans‐zigzag (β form) crystals, whereas the solution‐cast PHB films mostly possessed the common helical structure. In addition, the crystallinity of the electrospun PHB fibers increased compared to that of the solution‐cast PHB films. Conformational changes occurred with the high extensional flow in the ES jets. Furthermore, the results from polarized FTIR measurements demonstrate that PHB molecules were oriented parallel to the fiber axis. As a result, the electrospun fibers exhibited strong birefringence under the polarized light. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1860–1867, 2007
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