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Controlling the Physical Properties of Random Network Based Shape Memory Polymer Foams

Published online by Cambridge University Press:  01 February 2011

Pooja Singhal
Affiliation:
[email protected] Texas A&M University Biomedical Engineering, College Station, Texas, United States
Thomas S Wilson
Affiliation:
[email protected] Lawrence Livermore National Laboratory Livermore, United States
Duncan J Maitland
Affiliation:
[email protected] Texas A&M University Biomedical Engineering, 3120 TAMU College Station, Texas, 77843, United States
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Abstract

Shape memory polymers (SMPs) are increasingly being considered for use in minimally invasive medical devices. For safe deployment of implanted devices it is important to be able to precisely control the actuation temperature of the device. In this study we report the effect of varying monomer composition on the glass transitions/actuation temperatures (Tg) of novel low density shape memory foams. The foams were based on hexamethylenediisocyanate (HDI), triethanolamine (TEA) and tetrakis (2-hydroxyl propyl) ethylenediamine (HPED), and were produced via a combination of chemical and physical blowing process. The process for post-foaming cleaning was also varied. Foams were characterized by DSC, DMA, and for shape memory. No clear trends were observed for foam samples without cleaning, and this was attributed to process chemicals acting as plasticizers. In foams cleaned via washing and/or sonication, the Tg was observed to decrease for compositions that were higher in the TEA content. Also, no change in shape memory behavior was observed for varying compositions. This work demonstrates the ability to tailor actuation transition temperature while maintaining shape memory behavior for low density foams suitable for aneurysm treatment.

Type
Research Article
Copyright
Copyright © Materials Research Society 2010

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References

1 Lendlein, A. Jiang, H. Y. Junger, O. and Langer, R. Nature 434, 879882 (2005).Google Scholar
2 Sahoo, N. G. Jung, Y. C. and Cho, J. W. Materials and Manufacturing Processes 22, 419423 (2007).Google Scholar
3 Sahoo, N. G. Jung, Y. C. Goo, N. S. and Cho, J. W. Macromolecular Materials and Engineering 290, 10491055 (2005).Google Scholar
4 Liu, C. Qin, H. and Mather, P. T. Journal of Materials Chemistry 17 (16), 15431558 (2007).Google Scholar
5 Leng, J. S. Lv, H. B. Liu, Y. J. and Du, S. Y. Applied Physics Letters 91, 14410 (2007).Google Scholar
6 Buckley, P. R. McKinley, G. H. Wilson, T. S. Small, W. Benett, W. J. Bearinger, J. P. McElfresh, M. W. and Maitland, D. J. IEEE Transactions on Biomedical Engineering 53, 20752083 (2006).Google Scholar
7 Razzaq, M. Y. Anhalt, M. L. Frormann and Weidenfeller, B. Materials Science and Engineering: A 444, 227235 (2007).Google Scholar
8 Small, W. IV , Singhal, P. Wilson, T. S. and Maitland, D. J. Journal of Materials Chemistry, DOI: 10.1039/b923717h (2010).Google Scholar
9 Wilson, T. S. Bearinger, J. P. Herberg, J. L. Marion, J. E. III , Wright, W. J. Evans, C. L. and Maitland, D. J. Journal of Applied Polymer Science 106 (1), 540551 (2007).Google Scholar
10 Sperling, L.H. Introduction to Physical Polymer Science, 4th Ed. (John Wiley & Sons, New Jersey, 2006).Google Scholar
11 Seyler, R. J. Assignment of the Glass Transition, Volume 1294 of STP/ASTM (ASTM International, 1994) p. 90.Google Scholar
12 Seyler, R. J. Assignment of the Glass Transition, Volume 1294 of STP/ASTM (ASTM International, 1994) p. 107.Google Scholar