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Nanoporous thermosets via Reactive Encapsulation of a Chemically Inert Solvent versus Free Radically Polymerized and Phase Separating Systems

Published online by Cambridge University Press:  01 February 2011

Vijay I. Raman
Affiliation:
Department of Chemical Engineering, Drexel University, Philadelphia, PA-19104.
Giuseppe R. Palmese
Affiliation:
Department of Chemical Engineering, Drexel University, Philadelphia, PA-19104.
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Abstract

Nanoporous thermosets are used as polyelectrolytes in fuel cells, separation membranes, and sensors and actuators, etc. Design of nanoporous thermosets for such applications entails controlling permeability by tailoring the pore size and pore chemistry. Usually free radically polymerizing and simultaneously phase separating systems are used to synthesize porous thermosets. A novel method of synthesizing nanoporous polymeric materials is employed in this work. This technique involves the synthesis of nanoporous thermosets by reactive encapsulation of an inert solvent using step-growth crosslinking polymerization reaction carried out until completion without phase separation into macroscopic phases. Key structural features of the porous materials synthesized by the reactive encapsulation technique were investigated by Scanning Electron Microscopy (SEM) after extraction and supercritical drying using carbon dioxide. Micrographs of the materials synthesized using the reactive encapsulation technique showed that the porous materials of pore size less than 100nm are obtained. Micrographs also showed that the reactive encapsulation technique can be employed to synthesize nanoporous polymeric materials of desired porosity and pore size by changing the solvent content. In addition, porous thermosets were also synthesized using free radical chemistry and phase separating system. The differences in the porous morphology of both these systems were enunciated using SEM micrographs.

Type
Research Article
Copyright
Copyright © Materials Research Society 2004

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References

REFERENCES

1) Peled, E., Livshits, V., Duvdevani, T.. Journal of Power Sources. 106 (2002) 245248.Google Scholar
2) Liu, Yu, Lee, J. Y., Kang, E. T., Wang, Peng and Tan, K. L.. Reactive and Functional Polymers. 47 (2001) 201213.Google Scholar
3) Krause, B., van der Vegt, N. F. A. and Wessling, M.. Desalination. 144 (2002) 57.Google Scholar
4) Drzal, P. L., Halasa, A. F. and Kofinas, P.. Polymer. 41 (2000) 46714677.Google Scholar
5) Saleh, Omar A. and Sohn, Lydia L.. Nano Letters. 3 (2003) 3738.Google Scholar
6) Chung, Young-Min and Rhee, Hyun-Ku. Catalysis Letters. 85 (2003) 159164.Google Scholar
7) Toimil Molares, M. E., Brotz, J.; Buschmann, V.; Dobrev, D.; Neumann, R.; Scholz, R.; Schuchert, I. U.; Trautmann, C.; Vetter, , J. Nuclear Instruments & Methods in Physics Research, Section B: Beam Interactions with Materials and Atoms. 185 (2001) 192197.Google Scholar
8) Wang, Q.C; Svec, F; Frechet, , J.M. Journal of chromatography A. 669 (1994) 230235.Google Scholar
9) Chieng, T.H., Gan, L.M., Chew, C.H., Ng, S.C., Pey, K.L.. Langmuir. 12 (1996) 319324.Google Scholar