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Recently, polyacetylene (PA) has been receiving renewed scientific attention due to its electrical properties, potentially useful for energy applications (e.g., fabrication of electrodes for rechargeable batteries and supercapacitors), and unique functional characteristics (e.g., gas trap, oxygen scavenger, EMI shielding, etc.). This chemical compound can be obtained in the form of polyacetylene–PVOH copolymers simply through the chemical dehydration of poly(vinyl alcohol) (PVOH), which is a very common type of polymer, widely used in packaging and other technological areas. This very inexpensive chemical reaction for the large-scale synthesis of PA/polyvinylenes is investigated by reacting PVOH with sulfuric acid at room temperature. In this process, PVOH, shaped in the form of a film, is dipped in sulfuric acid (i.e., H2SO4 at 95%–97%) and, after complete chemical dehydration, it is mechanically removed from the liquid phase by using a nylon sieve. The reduction process leads to a substantial PVOH film conversion into PA, as demonstrated by infrared spectroscopy (ATR mode). Indeed, the ATR spectrum of the reaction product includes all the characteristic absorption bands of PA. The reaction product is also characterized through the use of UV–Vis spectroscopy in order to evidence the presence in the structure of conjugated carbon–carbon double bonds of various lengths. Differential scanning calorimetry (DSC) and thermogravimetric analysis are used to investigate the PA solid-state cis–trans isomerization and thermal stability in air and nitrogen, respectively. XRD is used to verify the polymer amorphous nature. [ABSTRACT FROM AUTHOR]

Chronic skin wounds affect more than 40 million patients worldwide, representing a huge problem for healthcare systems. This study elucidates the optimization of an in situ gelling polymer blend powder for biomedical applications through the use of co-solvents and functional excipients, underlining the possibility of tailoring microparticulate powder properties to generate, in situ, hydrogels with advanced properties that are able to improve wound management and patient well-being. The blend was composed of alginate, pectin, and chitosan (APC). Various co-solvents (ethanol, isopropanol, and acetone), and salt excipients (sodium bicarbonate and ammonium carbonate) were used to modulate the gelation kinetics, rheology, adhesiveness, and water vapor transmission rate of the gels. The use of co-solvents significantly influenced particle size (mean diameter ranging from 2.91 to 5.05 µm), depending on the solvent removal rate. Hydrogels obtained using ethanol were able to absorb over 15 times their weight in simulated wound fluid within just 5 min, whereas when sodium bicarbonate was used, complete gelation was achieved in less than 30 s. Such improvement was related to the internal microporous network typical of the particle matrix obtained with the use of co-solvents, whereas sodium bicarbonate was able to promote the formation of allowed particles. Specific formulations demonstrated an optimal water vapor transmission rate, enhanced viscoelastic properties, gel stiffness, and adhesiveness (7.7 to 9.9 kPa), facilitating an atraumatic removal post-use with minimized risk of unintended removal. Microscopic analysis unveiled that porous inner structures were influencing fluid uptake, gel formation, and transpiration. In summary, this study provided valuable insights for optimizing tailored APC hydrogels as advanced wound dressings for chronic wounds, including vascular ulcers, pressure ulcers, and partial and full-thickness wounds, characterized by a high production of exudate. [ABSTRACT FROM AUTHOR]

Surface acoustic waves (SAW) 433 and 315 MHz, two-port resonator-based oscillators coated with a Langmuir-Blodgett (LB) thin layer of chemosensitive cadmium arachidate (CdA) offer highly sensitive chemical acoustic sensors for detection and monitoring of organic vapors at room temperature, and LB CdA film-coated silica optical fibers (SOF) are successfully fabricated and studied. Results reveal that six molecular species such as ethanol, methanol, isopropanol, ethylacetate, acetone and toluene are identified and recognized by a specific index.

Designing the foam structures in terms of density and morphology gives the chance to tune their mechanical and functional properties to the specific application. Nowadays, this design has been leveled up by the introduction of graded foams which are characterized by spatially nonuniform densities and/or morphologies. Graded foams have proved superior compared to uniform one in numerous examples and loading conditions but in pure compressive loading, where properties such as the Young's modulus of graded foams are always inferior to uniform ones. When using sintered beads foams, macroscopic pure compression may induce local bending on the single bead, which can be exploited to induce stiffening. This thesis was investigated on both polystyrene and thermoplastic polyurethane samples made by foamed beads sintered in a cylindrical mold. The response to compressive tests of graded foams made by sintering beads having nonuniform cells structures was compared to the uniform counterparts. The results evidenced that, at same average density, foams had up to a 30% ca. of increase of the Young's modulus when the beads are characterized by a denser outer layer. [ABSTRACT FROM AUTHOR]