The present research reports the investigation of the role of an oligomeric polyadipate plasticizer (206 3NL), and a nucleating agent aromatic sulfonate derivative (LAK301) on thermal behaviours of poly-lactic acid (PLA) evaluated through differential scanning calorimetry (DSC) measurements in order to investigate the separated effect due to the addition of plasticizer and nucleating agent on the thermal behavior of PLA respectively. Binary and ternary systems containing PLA/206 3NL/LAK301 have been developed. All samples have been prepared by melt-blending. The results of the present study show that LAK301 acts as a very efficient nucleating agent by increasing crystallinity percentage from 5.6% in pure PLA to 12% in PLA/LAK301 5%wt/206 3NL, and that (206 3NL) is a compatible plasticizer for PLA as the glass temperature drops down from 59.4 °C in pure PLA to 38.9 °C in blends of PLA-NL 15 wt%. Also the approach of investigating the compatibility in ternary system where the plasticizer and nucleating agent have a synergic effect on thermal properties as well on crystallinity and glass transition temperature of PLA were addressed. In fact in ternary blends of PLA/LAK301/206 3NL with 5 wt% of LAK301 the glass transition temperature was reduced to 30.3 °C and PLA crystallinity increased to 39 wt%

Polyurethanes (PUs) are one of the most versatile polymeric materials, making them suitable for a wide range of applications. Currently, petroleum is still the main source of polyols and isocyanates, the two primary feedstocks used in the PU industry. However, due to future petroleum price uncertainties and the need for eco-friendly alternatives, recent efforts have focused on replacing petrol-based polyols and isocyanates with counterparts derived from renewable resources. In this study, waste cooking oil was used as feedstock to obtain polyols (POs) for new sustainable polyurethane foams (PUFs). POs with various hydroxyl numbers were synthesized through epoxidation followed by oxirane ring opening with diethylene glycol. By adjusting reagent amounts (acetic acid and H₂O₂), epoxidized oils (EOs) with different epoxidation degrees (50–90%) and, consequently, POs with different OH numbers (200–300 mg KOH/g) were obtained. Sustainable PUFs with high bio-based content were produced by mixing the bio-based POs with a commercial partially bio-based aliphatic isocyanate and using water as the blowing agent in the presence of a gelling catalyst and additives. Various water (4, 8, 15 php) and gelling catalyst (0, 1, 2 php) amounts were tested to assess their effect on foam properties. PUFs were also prepared using EOs instead of POs to investigate the potential use of EOs directly in PUF production. Characterization included morphological, chemical, physical, thermal, and mechanical analyses. The rigid PUFs exhibited high density (150–300 kg/m³) and stability up to 200 °C. The combined use of bio-based polyols with partially bio-based isocyanate and water enabled PUFs with a bio-based content of up to 77 wt.%. EOs demonstrated potential in PUF production by bypassing the second synthesis step, enhancing sustainability, and significantly reducing energy and costs; however, PUF formulations with EOs require optimization due to lower epoxy ring reactivity.

The development of collagen-based composite materials for bone tissue engineering requires a comprehensive understanding of their rheological and structural behavior to ensure processability and functional stability. This study investigates the viscoelastic and morphological properties of nanocomposite slurries composed of hydroxyapatite (HA) nanoparticles dispersed in acetic acid solutions of bovine or fish-derived collagen peptides. Frequency and strain sweep tests revealed solid-like behavior and shear-thinning characteristics consistent with printable bioinks. Both formulations yield stresses between 0.7 and 1.5 kPa, values comparable to those reported for 3D-printable HA composites. Over ten days of aging, fish-based formulations retained higher viscosity and modulus, indicating improved temporal stability relative to bovine-based ones. Drop-casting tests confirmed the formation of homogeneous, highly opalescent films, with surface profilometry showing lower waviness for the fish-derived blend, suggesting enhanced microstructural uniformity. These results demonstrate that acetic acid-mediated collagen–HA interactions generate stable, high-fidelity slurries suitable for additive manufacturing applications. The superior rheological properties of fish collagen formulations highlight the influence of peptide source on network evolution, offering valuable insight for optimizing collagen–ceramic composites in regenerative and biomedical applications.

This study investigates the industrial potential of red gypsum (RG), a major by-product of titanium dioxide (TiO₂) production, for the development of thermoplastic polypropylene (PP)-based composites via melt extrusion, targeting agricultural applications. Prior to compounding, RG was thermally treated at approximately 200 °C to remove residual moisture and chemically bound water, resulting in its anhydrous form (CaSO₄). PP/RG composites were then formulated with RG loadings up to 20 wt.%, employing stearic acid (SA) as a compatibilizer. The resulting materials were thoroughly characterized and successfully processed through industrial-scale injection molding up to 250 °C. Morphological and FTIR analyses confirmed the role of SA in enhancing both filler dispersion and interfacial adhesion between RG and the PP matrix. SEM images revealed finer and more uniformly distributed RG particles, resulting in a reduced loss of ductility and elongation at break typically associated with filler addition. Specifically, the Young’s Modulus increased from 1.62 GPa (neat PP) up to 3.21 GPa with 20 wt.% RG and 0.6 wt.% SA. The addition of 0.6 wt.% SA also helped limit the reduction in stress at break from 46.68 MPa (neat PP) to 34.05 MPa and similarly mitigated the decrease in Charpy impact energy, which declined slightly from 2.66 kJ/m² (neat PP) to 2.24 kJ/m² for composites containing 20 wt.% RG. Preliminary phytotoxicity was assessed using germination tests on Lepidium sativum L. seeds. Eluates from both untreated and SA-treated RG powders resulted in germination indices below 80%, indicating phytotoxicity likely due to high sulfate ion concentrations. In contrast, eluates from composite pellets exhibited germination indices equal to or exceeding 100%, demonstrating the absence of phytotoxic effects. These results highlight the suitability of the developed composites for applications in floriculture and horticulture. The optimized composite pellets were successfully processed via injection molding to manufacture plant pots, which exhibited a dark brown coloration, confirming the effective pigmenting function of RG. These results demonstrate the potential of red gypsum to serve both as a functional filler and pigment in PP composites, providing a sustainable alternative to iron oxide pigments and promoting the valorization of industrial waste through resource recovery.

This study investigates the use of bio-based polyurethane foams (PUFs) containing phase change material (PCM) microparticles as a sustainable alternative for the automotive sector. These foams are synthesized using polyols derived from waste cooking oil (WCO), aligning with circular economy principles. To evaluate the thermophysical properties of these materials and, more in general, their thermal behavior, the use of non-destructive thermographic techniques has been proposed. This technique enables a rapid, full-field thermal analysis without physical contact, making it especially suitable for porous and heterogeneous structures like foams. As a reference, both virgin and foams with PCM were characterized in terms of density and thermal conductivity using well-established methods. Then, Lock-in thermography has been used as the first attempt technique to investigate variations in thermal behavior due to different thermophysical material properties based on the thermal response in transmission configuration. The thermographic approach proves to be an effective tool not only for assessing thermal behavior but also for supporting quality control and process optimization of sustainable polymeric materials.