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The effect of epoxy dilution with acetone on the mechanical performance of epoxy-coated alkali-resistant glass (ARG) fabric embedded in a lime-based mortar is studied experimentally. The mechanical behaviour of the composite system is assessed in uni-axial tensile tests, according to the ICC guidelines. Epoxy is diluted in acetone and several concentrations, namely 10%, 25%, 50%, 75% and 90%, are considered in an attempt to define a decay law for strength, ductility and dissipated energy at failure. Although epoxy-coating promotes a striking improvement of the mechanical performance with respect to the uncoated specimens, epoxy dilution appears to little affect the global response, even at very low epoxy-to-solvent ratios. Actually, a notable increase in the ultimate strength and strain as well as dissipation capacity are evidenced for 75% dilution. Indeed, epoxy resin is able to uniformly impregnate the bundles of the yarns in a very thin layer, still preserving its contribution to the mechanical performance. In fact, wettability of the yarns plays a fundamental role in the mechanical performance of the laminate for it limitates telescopic failure. A threshold of viscosity is identified. Above this limit, the high quality of impregnation overcomes the issue of the reduction of the amount of epoxy resin in the coating. Besides, dilution strongly promotes the ease of application, as a result of the resin viscosity being sharply reduced. Most remarkably and contrarily to common expectation, the specific energy dissipated at failure exhibits a maximum point, whence an optimal dilution ratio exists which best balances interphase strength and ductility.

Polymeric nanocomposites containing Fe3O4 nanoparticles were prepared through a chemical route under different precursor-to-solvent ratios and were submitted to structural and morphologic characterization. The embedded nanoparticles, containing pure magnetite and characterized by considerable polydispersity, are rather homogeneously dispersed in the matrix. The magnetic properties of two representative samples were analyzed in detail between T = 5 K and room temperature. Magnetic effects clearly associated with the Verwey monoclinic to cubic transition with transition temperatures distributed in the interval 95–120 K were put in evidence. On heating through this region, the coercive field and the maximum susceptibility of hysteresis loops display marked downward/upward steps, respectively, while the high-field magnetization is not affected at all; a comparable upward step is measured in the FC/ZFC curves. Reporting the maximum susceptibility as a function of the reciprocal of the coercive field in the interval from T = 95 to T = 120 K, and using the predictions for single-domain nanoparticles with randomly distributed axes of uniaxial and cubic anisotropy (the former/latter case being applicable below/above the Verwey transition, respectively), the evolution of the transformed cubic-anisotropy fraction upon heating has been studied, and the distribution of Verwey transition temperatures related to the sample polydispersity has been accurately determined. The low-temperature value of the uniaxial anisotropy constant is obtained from coercive field measurements and found to be comparable to, albeit slightly higher than the corresponding quantity measured in bulk crystalline magnetite.

This paper investigates the shape memory capabilities of semicrystalline networks, focusing the attention on poly(e-caprolactone) (PCL) systems, a class of materials that allows to satisfy important requirements for their applications as biomedical devices, such as the good biocompatibility, the fast recovery of large “temporary” shape configurations, and the easy tailoring of the transformation temperatures. The materials were prepared with various crosslink densities and crosslinking methodologies; in particular, beside a thermal crosslinking based on reactive methacrylic end groups, a novel type of covalently crosslinked semicrystalline systems was prepared by a sol-gel approach from alkoxysilane-terminated PCL precursors, so as to avoid potentially toxic additives typically used for free-radical thermal curing. The materials were subjected to biological tests, to study their ability in sustaining cell adhesion and proliferation, and to thermal characterizations, to evaluate the possibility to tailor their melting and crystallization temperatures. The one-way shape memory (i.e., the possibility to set the material in a given configuration and to recover its pristine shape) and the two-way shape memory response (i.e., the triggered change between two distinguished shapes on the application of an on-off stimulus) were studied by applying optimized thermo-mechanical cyclic histories. The ability to fix the applied shape and to recover the original one on the application of heating (i.e., the one-way effect) was evaluated on tensile bars; further, to investigate a potential application as self-expandable stents, isothermal shape memory experiments were carried out also on tubular specimens, previously folded in a temporary compact configuration. The two-way response was studied through the application of a constant load and of a heating/cooling cycle from above melting to below the crystallization temperature, leading to a reversible elongation/contraction effect, involving maximum strain changes up to about 80%, whose extent may be controlled through the crosslink density.