Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-02T23:32:51.748Z Has data issue: false hasContentIssue false

Electrospinning and Characterization of the Stable and “Metastable” Self-Assembled Poly(ethylene oxide)-Urea Complexes

Published online by Cambridge University Press:  01 February 2011

Yang Liu
Affiliation:
[email protected]@yahoo.com, University of Montreal, Chemistry, Montreal, Canada
Hélène Antaya
Affiliation:
[email protected]@yahoo.com, University of Montreal, Chemistry, Montreal, Canada
Christian Pellerin
Affiliation:
[email protected]@yahoo.com, University of Montreal, Chemistry, Montreal, Canada
Get access

Abstract

Solution electrospinning was used to prepare fibers of both the stable – trigonal α and “metastable” – orthorhombic β complexes between poly(ethylene oxide) (PEO) and urea. The 300-800 nm fibers were highly crystalline and both types presented a relatively large level of molecular orientation. Characterization of the poorly-studied β complex was performed using wide-angle X-ray diffraction, infrared spectroscopy, optical microscopy and differential scanning calorimetry. It was shown that β complex possesses a 3:2 PEO:urea stoichiometry, in contrast with a previously suggested 1:1 molar ratio, and that the α inclusion complex keeps the 4:9 molar ratio as when prepared by the conventional co-crystallization method. A new structural model was suggested for the β complex, in which the unit cell would contain 12 PEO repeat units (4 chains in the ab plane with 3 repeat units along the c axis) and 8 urea molecules arranged in a ribbon-like structure and intercalated between the two PEO layers. This layer-structured β complex is quite different from the usual channel-like α inclusion complex and results in different phase transitional properties.

Type
Research Article
Copyright
Copyright © Materials Research Society 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Liu, Y., Pellerin, C., Macromolecules 39, 8886 (2006).Google Scholar
2. Liu, Y., Pellerin, C., PMSE Preprints 97, 630 (2007).Google Scholar
3. Liu, Y., Cui, L., Guan, F., Hedin, N. E., Zhu, L., Fong, H., Macromolecules 40, 6283 (2007).Google Scholar
4. Stephens, J. S., Chase, D. B., Rabolt, J. F., Macromolecules 37, 877 (2004).Google Scholar
5. Lee, K. H., Snively, C. M., Givens, S., Chase, D. B., Rabolt, J. F., Macromolecules 40, 2590 (2007).Google Scholar
6. Liu, Y., Antaya, H., Pellerin, C., J. Polym. Sci. Part B Polym. Phys. 46, 1903 (2008).Google Scholar
7. Ye, H. M., Peng, M., Xu, J., Guo, B. H., Chen, Q., Yun, T. L., Ma, H., Polymer 48, 7364 (2007).Google Scholar
8. Chenite, A., Brisse, F., Macromolecules 24, 2221 (1991).Google Scholar
9. Bogdanov, B., Mikhailov, M., Uzov, K., Gavrailova, G., J. Polym. Sci. B: Polym. Phys. 32, 387 (1994).Google Scholar
10. Eaton, D. F., Anderson, A. G., Tam, W., Wang, Y., J. Am. Chem. Soc. 109, 1886 (1987).Google Scholar
11. Shang, Q.-Y., Dou, X., Hudson, B. S., Nature 352, 703 (1991).Google Scholar