RESUMEN
Three bilayer muscles [polypyrrole-paraphenolsulfonic acid/polypyrrole-dodecylbenzensulfonic acid (PPy-HpPS/PPy-DBS) asymmetric bilayer, PPy-HpPS/tape, and PPy-DBS/tape] were characterized during potential cycling in NaPF6 aqueous solutions. In parallel, the angular displacement of the muscle was video-recorded. The dynamo-voltammetric (angle-potential) and coulo-dynamic (charge-potential) results give the reaction-driven ionic exchanges in each PPy film. Electrochemical reactions drive the exchange of anions from the PPy-HpPS layer and cations from the PPy-DBS layer. This means that both layers from the asymmetric bilayer follow complementary volume changes (swelling/shrinking or shrinking/swelling), owing to complementary ionic exchanges (entrance/expulsion) driven by the bilayer oxidation or reduction. The result is a cooperative actuation; the bending amplitude described by the asymmetric bilayer muscle is one order of magnitude larger than those attained from each of the conducting polymer/tape muscles. The cooperative actuation almost eliminates creeping effects. A large dynamical hysteresis persists, which can be attributed to an irreversible reaction of the organic acid components at high overpotentials.
RESUMEN
Thick films of the polypyrrole-para-phenolsulfonic acid (PPy-HpPS) blend were electrogenerated on stainless steel plates. The self-supported films, once peeled off from the metal, were electrochemically characterized in aqueous solutions of NaCl and NaPF6. The Na, Cl, P, S and F content of films, after attaining a different oxidation state, were determined by EDX. The bending movements of the bilayer (PPy-HpPS)/tape artificial muscle were video recorded during potential sweeps in both solutions allowing the translation of the prevalent ionic exchanges driven by the biomimetic reactions into macroscopic movements. Ionic exchanges between the film and the solution, biomimetic structural processes in the film, driving prevalent electrochemical reactions and film compositions related to each of the different structural potential domains defined by coulovoltammetric results were clarified. In NaPF6 solutions a prevalent exchange of anions exists: the film swells by oxidation and shrinks by reduction. In NaCl solutions prevailing exchange of cations or anions occurs in different potential ranges. Reactions related to the HpPS content play important roles at the more cathodic and more anodic overpotentials. The described methodology could be translated to biological reactions including reactive biopolymers.
RESUMEN
The streaklines of unsteady separation on two kinds of pitching airfoils, the NACA65-0910 and a blunt trailing edge airfoil, were studied by dye flow visualization and by the Schlieren method. The latter visualized the discrete vortices shed from the leading edge. The results of these visualization studies allow a comparison between the dynamic behavior of the streakline of unsteady separation and that of the discrete vortices shed from the leading edge. The influence of the airfoil configuration on the flow characteristics was also examined. Furthermore, the scale of a discrete vortex forming the recirculation region was investigated. The non-dimensional pitching rate was k = 0.377, the angle of attack alpha(m) = 16 degrees and the pitching amplitude was fixed to A = +/-6 degrees for Re = 4.0 x 10(3) in this experiment.