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                                                                          s
                            s
                       where c  are the mass fractions, V s   are the partial molar volumes, M  are the molar masses, and the index
                       0 refers to the initial value of a variable. Complete mathematical description of the polymer actuator
                       requires the solution of mass transport (diffusion) equation, momentum balance, and Poisson equation
                       for potential distribution, the discussion of which is beyond the scope of this book.  An interesting
                       consequence of the addition of the chemical strain in (8.46) is the explicit appearance of the pressure
                       term in the electrochemical potential driving the diffusion. The total mass diffusion flux will have a
                       component proportional to the negative gradient of the pressure, which for the case of water, will result
                       in a relaxation phenomena observed experimentally. The total flux of component s is then given by
                                                  s  s
                                                                 s
                                                --------------∇ m () +(
                                          J =  – rc W   os  T  pV +  RT ln ( fc ) +  z Φ)        (8.53)
                                                                           s
                                                                               s
                                           s
                                                 M s
                              s
                                                         s
                                                                                                 s
                       where W  is the mobility of component s, z  is the valence of component s, p is the pressure, f  is the
                       activity coefficient, and Φ is the electric potential. We have omitted the cross-coupling terms that would
                       appear in a fully coupled Onsager-type formulation. Interested readers are referred to [Enikov 2000b] and
                       the references therein for further details.
                       8.6 Future Trends
                       The future MEMS are likely to be more heterogeneous in terms of materials and structures. Bio-MEMS
                       for example, require use of nontoxic, noncorrosive materials, which is not a severe concern in standard
                       IC components. Already departure from the traditional Si-based MEMS can be seen in the areas of optical
                       MEMS using wide band-gap materials, nonlinear electro-optical polymers, and ceramics. As pointed
                       earlier, the submicron size of the cantilever-based sensors brings the thermal noise issues in mechanical
                       structures. Further reduction in size will require molecular statistic description of the interaction forces.
                       For example, carbon nanotubes placed on highly oriented pyrolytic graphite (HOPG) experience
                       increased adhesion force when aligned with the underlying graphite lattice [Falvo et al. 2000]. The future
                       mechatronic systems are likely to become an interface between the macro and nano domains.

                       References

                       Butt, H., Jaschke, M., “Calculation of thermal noise in atomic force microscopy,” Nanotechnology, 6,
                           pp. 1–7, 1995.
                       Eikerling, M., Kharkats, Y.I., Kornyshev, A.A., Volfkovich, Y.M., “Phenomenological theory of electro-
                           osmotic effect and water management in polymer proton-conducting membranes,” Journal of the
                           Electrochemical Society, 145(8), pp. 2684–2698, 1998.
                       Evans, T.H., Journal of Applied Mechanics, 6, p. A-7, 1939.
                       Enikov, E.T., Nelson, B., “Three dimensional microfabrication for multi-degree of freedom capacitive
                           force sensor using fiber chip coupling,” J. Micromech. Microeng., 10, pp. 492–497, 2000.
                       Enikov, E.T., Nelson, B.J., “Electrotransport and deformation model of ion exhcange membrane based
                           actuators,” in Smart Structures and Materials 2000, Newport Beach, CA, SPIE vol. 3987, March,
                           2000.
                       Falvo, M.R., Steele, J., Taylor, R.M., Superfine, R., “Gearlike rolling motion mediated by commensurate
                           contact: carbon nanotubes on HOPG,” Physical Review B, 62(6), pp. 665–667, 2000.
                       Faupel, J.H., Fisher, F.E., Engineering Design: A Synthesis of Stress Analysis and Materials Engineering, 2nd
                           Ed., Wiley & Sons, New York, 1981.
                       Liu, R., Her, W.H., Fedkiw, P.S., “In situ electrode formation on a nafion membrane by chemical plati-
                           nization,” Journal of the Electrochemical Society, 139(1), pp. 15–23, 1990.
                       Gierke, T.D., Hsu,  W.S., “The cluster-network model of ion clusturing in perfluorosulfonated mem-
                           branes,” in Perfluorinated Ionomer Membranes, A. Eisenberg and H.L. Yeager, Eds., vol. 180, American
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