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Solar water evaporators (SWE) have shown growing interest due to their capacity to transform sunlight to thermal energy. In this work, SWE were prepared based on microwave-expanded graphite as light absorber deposited onto an ecological porous substrate obtained by casting a mixture of coconut fibers and recycled polystyrene. The materials were characterized by SEM, FTIR and UV/Vis-NIR spectroscopies, and thermogravimetric analyses. It was observed that the light absorber film presented high and wide light absorption in the solar electromagnetic spectrum and increased superficial area when compared to the unexpanded graphite film counterpart. Nanopores between 400 and 900 nm and microcavities in the 200 to 500 μm range were formed at the surface of the SWE after 6 seconds of microwave exposure, which are destroyed at higher exposure times. SWE of laboratory scale diameter were tested for water evaporation at different light intensities, microwave expanding time, and thicknesses to determine their effects on evaporation rate and efficiency. It was observed that SWE rates increased from 1.09 ± 0.006 to 1.73 ± 0.007 kg h −1 m −2 for unexpanded and expanded graphite through 6 seconds, respectively; being the latter the best SWE reaching 91.5% of efficiency at 1200 W m −2 of illumination. This efficiency was stable after reaching the maximum stable efficiency in only 15 minutes. The scaling-up of the process was studied in a SWE of 6.1 cm in diameter using a bigger glass cell in the presence of pure water or simulated seawater (3.5% NaCl), achieving efficiencies of 89.8% and 86.1%, respectively.

The demand for the development of new therapies and devices for controlled drug release has been continuously increasing, especially those based on materials sensitives to external stimuli, such as electricity. Therefore, in this work, acrylamide was polymerized in the presence of chitosan (CS), using N,N 0methylenebisacrylamide as cross-linking, followed by immersion in pyrrole aqueous solution and chemical polymerization to obtain an electroactive hydrogel of polyacrylamide/CS/polypyrrole (PA/CS/PPy) (67.5/7.5/25% wt.); this electroactive hydrogel was later used in drug delivery controlled by electricity studies. The synthesized PA/CS/PPy hydrogel was characterized by scanning electron microscopy, FTIR spectroscopy, and thermogravimetric analysis. It was observed that the hydrogel presented pores in the range of 50-200 μm with CS and PPy well incorporated to the cross-linked PA. The hydrogel swelling percentage (S) was determined at different pHs. It was observed that S was independent of pH, with S = 700% and a swelling kinetics described by the Fickian diffusion mechanism at alkaline pH. PA/CS/PPy hydrogel was used to absorb captopril (a drug for hypertension control), and its kinetics release at different applied potentials and pH was studied. Release kinetics were described by the Korsmeyer-Peppas model, while release mechanism was a Case-II transport without current at alkaline pH; under electrical stimuli, the mechanism presented an anomalous transport with ON-OFF profile, increasing the release rate with the applied voltage showing its electroactivity in the captopril release.