Search

In this work, the behavior of carbon fiber reinforced polymer composites (CFRPs) interleaved with electrospun veils under low velocity impact (LVI) conditions and extreme environmental temperatures was investigated. 2/2 twill carbon fiber/epoxy laminates were subjected to LVI at three energy levels (10, 20, and 30 J), and three temperatures (−50°C, room temperature, and 100°C). Two interleaved configurations were explored (six veils placed symmetrically with respect to the middle plane of the laminate and with respect to the external layers of the laminate). Particularly at room temperature and up to 20 J, nanofibrous interlayers effectively reduced localized deformation (by about 13.0%) and delamination (by about 12.2%) when positioned in the outer ply interleaved configuration compared to the reference laminate. At 100°C, this effect is maintained at 10 J, preventing an increase in the delaminated area. At −50°C and 10 J, the promotion of delamination prevented back surface fiber failure. Regarding post‐impact flexural properties, the presence of nanoveils ensured superior mechanical properties compared to the corresponding reference laminate impacted at the same conditions, demonstrating their efficacy in enhancing the damage tolerance of the overall laminate. Highlights: Electrospun veils were interleaved in 20 layers of 2/2 twill carbon/epoxy laminate.Three configurations were tested under LVI at 10 J, 20 J, 30 J, and −50°C, RT, and 100°C.Observed damage modes include delamination, indentation, and back surface fiber cracks.Veils symmetrically placed in external layers limit delamination at 20 J (RT) and 10 J (100°C).Electrospun veils enhanced CFRP bending and residual post‐impact properties at RT and 100°C. [ABSTRACT FROM AUTHOR]

Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) is a highly promising biodegradable and bio-based thermoplastic recognized for its environmental benefits and potential versatility. However, its industrial adoption has been limited due to its inherent brittleness and suboptimal processability. Despite these challenges, PHBV's performance can be tailored for a wide range of applications through strategic modifications, particularly by blending it with other biodegradable polymers or reinforcing it with natural fibers and bio-based fillers. This study explores the potential of brewers' spent grain (BSG) as a sustainable source for the development of PHBV biocomposites. The biocomposites were synthesized by incorporating arabinoxylan-bound benzoate, which can be derived from BSG, as a sustainable filler at concentrations of 4% and 10% w/w. The resulting materials were characterized using tensile testing, scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The findings demonstrate that the incorporation of functionalized arabinoxylan significantly enhances the mechanical properties of PHBV, preserves its thermal stability, and increases its crystallinity (from 59.9% to 67.6%), highlighting a positive impact on both material performance and processing characteristics. [ABSTRACT FROM AUTHOR]

Cleavable bio-based epoxy resin systems are emerging, eco-friendly, and promising alternatives to the common thermoset ones, providing quite comparable thermo-mechanical properties while enabling a circular and green end-of-life scenario of the composite materials. In addition to being designed to incorporate a bio-based resin greener than the conventional fully fossil-based epoxies, these formulations involve cleaving hardeners that enable, under mild thermo-chemical conditions, the total recycling of the composite material through the recovery of the fiber and matrix as a thermoplastic. This research addressed the characterization, processability, and recyclability of a new commercial cleavable bio-resin formulation (designed by the R-Concept company) that can be used in the fabrication of fully recyclable polymer composites. The resin was first studied to investigate the influence of the different post-curing regimes (room temperature, 100 °C, and 140 °C) on its thermal stability and glass transition temperature. According to the results obtained, the non-post-cured resin displayed the highest Tg (i.e., 76.6 °C). The same post-curing treatments were also probed on the composite laminates (glass and carbon) produced via a lab-scale vacuum-assisted resin transfer molding system, evaluating flexural behavior, microstructure, and dynamic-mechanical characteristics. The post-curing at 100 °C would enhance the crosslinking of polymer chains, improving the mechanical strength of composites. With respect to the non-post-cured laminates, the flexural strength improved by 3% and 12% in carbon and glass-based composites, respectively. The post-curing at 140 °C was instead detrimental to the mechanical performance. Finally, on the laminates produced, a chemical recycling procedure was implemented, demonstrating the feasibility of recovering both thermoplastic-based resin and fibers. [ABSTRACT FROM AUTHOR]

In this work, five different dextran-based cryogels for controlled drug release are investigated. Vitamin B12 was used as a model drug for in vitro release tests. Two different drug-loading procedures were adopted, leading to very different drug release curves. Indeed, a fast Fickian release was observed when freeze-dried samples of DEX40PEG360MA and DEX40PEG500MA were infused with the drug after cryogel formation. On the contrary, a slowed highly non-Fickian behavior arises when the drug is loaded before the low-temperature crosslinking step, leading to the cryogel formation. The non-Fickian drug release, observed for all the five different dextran-based cryogels investigated, is actually due to the cryoconcentration phenomenon, modeled with a two-step release process. The proposed transport model accurately predicts experimental release curves characterized by a long lag time, confirming that dextran-based cryogels are suitable for controlled release. [ABSTRACT FROM AUTHOR]

Cryogels represent a valid strategy as scaffolds for tissue engineering. In order to adequately support adhesion and proliferation of anchorage-dependent cells, different polymers need to be combined within the same scaffold trying to mimic the complex features of a natural extracellular matrix (ECM). For this reason, in this work, gelatin (Gel) and chondroitin sulfate (CS), both functionalized with methacrylic groups to produce CSMA and GelMA derivatives, were selected to prepare cryogel networks. Both homopolymer and heteropolymer cryogels were produced, via radical crosslinking reactions carried out at −12 °C for 2 h. All the scaffolds were characterized for their mechanical, swelling and morphological properties, before and after autoclave sterilization. Moreover, they were evaluated for their biocompatibility and ability to support the adhesion of human gingival fibroblasts and tenocytes. GelMA-based homopolymer networks better withstood the autoclave sterilization process, compared to CSMA cryogels. Indeed, GelMA cryogels showed a decrease in stiffness of approximately 30%, whereas CSMA cryogels of approximately 80%. When GelMA and CSMA were blended in the same network, an intermediate outcome was observed. However, the hybrid scaffolds showed a general worsening of the biological performance. Indeed, despite their ability to withstand autoclave sterilization with limited modification of the mechanical and morphological properties, the hybrid cryogels exhibited poor cell adhesion and high LDH leakage. Therefore, not only do network components need to be properly selected, but also their combination and ability to withstand effective sterilization process should be carefully evaluated for the development of efficient scaffolds designed for tissue engineering purposes. [ABSTRACT FROM AUTHOR]