Hostname: page-component-586b7cd67f-tf8b9 Total loading time: 0 Render date: 2024-11-24T11:10:22.142Z Has data issue: false hasContentIssue false

Thermal, Mechanical and Magneto-Mechanical Characterization of Liquid Crystalline Elastomers Loaded with Iron Oxide Nanoparticles

Published online by Cambridge University Press:  06 February 2015

Stephany Herrera-Posada
Affiliation:
Department of Chemical Engineering, University of Puerto Rico, Mayagüez 00681, Puerto Rico
Barbara O. Calcagno
Affiliation:
Department of General Engineering, University of Puerto Rico, Mayagüez 00681, Puerto Rico
Aldo Acevedo
Affiliation:
Department of Chemical Engineering, University of Puerto Rico, Mayagüez 00681, Puerto Rico
Get access

Abstract

Liquid crystalline elastomers (LCEs) are materials that reveal unusual mechanical, optical and thermal properties due to their molecular orientability characteristic of low molar mass liquid crystals while maintaining the mechanical elasticity distinctive of rubbers. As such, they are considered smart shape-changing responsive systems. In this work, we report on the preparation of magnetic sensitized nematic LCEs using iron oxide nanoparticles with loadings of up to 0.7 wt%. The resultant thermal and mechanical properties were characterized by differential scanning calorimetry, expansion/contraction experiments and extensional tests. The magnetic actuation ability was also evaluated for the neat elastomer and the composite with 0.5 wt% magnetic content, finding reversible contractions of up to 23% with the application of alternating magnetic fields (AMFs) of up to 48 kA/m at 300 kHz. Thus, we were able to demonstrate that the inclusion of magnetic nanoparticles yields LCEs with adjustable properties that can be tailored by changing the amount of particles embedded in the elastomeric matrix, which can be suitable for applications in actuation, sensing, or as smart substrates.

Type
Articles
Copyright
Copyright © Materials Research Society 2015 

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

Zentel, R., Angew. Chem. Int. Ed. Engl. Adv. Mater., 28, 1407 (1989).CrossRefGoogle Scholar
Davis, F. J., J. Mater. Chem., 3, 551, (1993).CrossRefGoogle Scholar
Ohm, C., Brehmer, M., and Zentel, R., Adv. Mater., 22, 3366 (2010).CrossRefGoogle Scholar
Li, C., Liu, Y., Lo, C., and Jiang, H., Soft Matter, 7, 7511 (2011).CrossRefGoogle Scholar
Yang, L., Setyowati, K., Li, A., Gong, S., and Chen, J., Adv. Mater., 20 2271 (2008).CrossRefGoogle Scholar
Courty, S., Mine, J., Tajbakhsh, A. R., and Terentjev, E. M., Europhys. Lett., 64, 654 (2003).CrossRefGoogle Scholar
Haberl, J. M., Sánchez-Ferrer, A., Mihut, A. M., Dietsch, H., Hirt, A. M., and Mezzenga, R., Adv. Mater., 25, 1787 (2013); Nanoscale, 5, 5539(2013).CrossRefGoogle Scholar
Riou, O., Zadoina, L., Lonetti, B., Soulantica, K., Mingotaud, A.-F., Respaud, M., Chaudret, B., and Mauzac, M., Polymers, 4, 448 (2012).CrossRefGoogle Scholar
Kaiser, A., Winkler, M., Krause, S., Finkelmann, H., and Schmidt, A. M., J. Mater. Chem., 19, 538 (2009).CrossRefGoogle Scholar
Küpfer, J. and Finkelmann, H., Makromol. Chem. Rapid Commun., 12, 717 (1991).CrossRefGoogle Scholar
Ali, S. A., Al-Muallem, H. A., Rahman, S. U., and Saeed, M. T., Corros. Sci., 50, 3070 (2008).CrossRefGoogle Scholar
Domenici, V., Laguta, V. V, and Belous, A. G., J. Phys. Chem. C, 114, 10782 (2010).CrossRefGoogle Scholar
Chen, F., Clough, A., Reinhard, B. M., Grinsta, M. W., Jiang, N., Koga, T., and Tsui, O. K. C., Macromolecules, 46, 4663, (2013).CrossRefGoogle Scholar
Hanemann, T. and Szabó, D. V., Materials, 3, 3468 (2010).CrossRefGoogle Scholar
Ji, Y., Marshall, J. E., and Terentjev, E. M., Polymers, 4, 316 (2012).CrossRefGoogle Scholar
Fu, S.Y., Feng, X.Q., Lauke, B., and Mai, Y.W., Compos. Part B Eng., 39, 933 (2008).CrossRefGoogle Scholar