Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-26T15:46:11.833Z Has data issue: false hasContentIssue false

Small Angle X-Ray Scattering, FTIR and SEM Characterization of Nanostructured PVA/TEOS Hybrids by Chemical Crosslinking

Published online by Cambridge University Press:  01 February 2011

Herman S. Mansur
Affiliation:
Department of Metallurgical and Materials Engineering, Federal University of Minas Gerais, Rua Espírito Santo, 35/2° andar, 30160.030, Centro, Belo Horizonte, MG, [email protected]
Alexandra A.P. Mansur
Affiliation:
Department of Metallurgical and Materials Engineering, Federal University of Minas Gerais, Rua Espírito Santo, 35/2° andar, 30160.030, Centro, Belo Horizonte, MG, [email protected]
Get access

Abstract

In the present work, novel hybrid nanostructured composites were produced to be used in many potential applications such as biomedical, drug delivery systems, tri-dimensional scaffolds for biomaterials and tissue engineering, biomembranes and optical devices among others. Hybrids were synthesized by reacting poly (vinyl alcohol) (PVA) in aqueous acid solution with silicon alcoxide tetraethoxysilane (TEOS). PVA/TEOS hybrids were also modified in the nanometer-scale by crosslinking with glutaraldehyde (GA) during the synthesis involving hydrolysis and policondensation of PVA/TEOS. The hybrids were characterized by Fourier Transform Infrared Spectroscopy (FTIR), Small Angle X-ray Scattering (SAXS) and Scanning Electron Microscopy (SEM). FTIR spectra have shown major vibration bands associated with organic-inorganic chemical groups present in the hybrid composite PVA/TEOS. Also, typical absorption bands related to glutaraldehyde alkyl chain have indicated the crosslinking reaction of the hybrid network with glutaraldehyde (PVA/TEOS/GA). SAXS results have indicated different nano-ordered disperse phases for PVA, PVA/TEOS hybrid and PVA/TEOS/GA chemically crosslinked hybrid. SEM micrographs have shown morphology difference between PVA and PVA hybrid samples.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

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

[1] (a) Yano, S., Kurita, K. and Iwata, K., Materials Science and Eng. C, 6, 75 (1998).Google Scholar
(b) Yano, S., Kurita, K., Iwata, K., Furukawa, T., and Kodomari, M., Polymer, 44, 3515 (2003).Google Scholar
[2] Kickelbick, G., Prog. Polym. Sci., 28, 83 (2003).Google Scholar
[3] Matejka, L., Dukh, O. and Hlavata, D., Macromolecules, 36, 7977 (2004).Google Scholar
[4] Mansur, H., Vasconcelos, W., Orefice, R., Journal of Non-crystalline Solids, 273, 109 (2000).Google Scholar
[5] Chiavacci, L.A, Dahmouche, K, Santilli, C.V, Bermudez, V de Zea, Carlos, L.D, Briois, V and Craievich, A.F, J. Appl. Cryst., 36, 405 (2003).Google Scholar
[6] Orthaber, D., Bergmann, A. and Glatter, O., J. Appl. Cryst., 33, 218 (2000).Google Scholar
[7] Habsuda, J., Simon, G.P., Cheng, Y. B., Hewitt, D.G. and Toh, H., Polymer, 43, 4123 (2002).Google Scholar
[8] Christova, D., Ivanova, S., Ivanova, G., Polymer Bulletin, 50, 367 (2003).Google Scholar
[9] Kim, J. H., Min, B. R., Won, J., Kang, Y. S., Chem. Commun., 22, 2732, (2002).Google Scholar
[10] Mansur, H. S., Orefice, R. L., A. Mansur, A.P., Polymer 45, 7193, (2004).Google Scholar