This study investigates the use of low molecular weight poly(ethylene glycol) (PEG) as a plasticizer for poly(lactic acid) (PLA). PLA/PEG blend films were prepared using the solvent casting method with varying mixing ratios. The films were analyzed using differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and dynamic rheological analysis. The results indicate that the addition of PEG as a plasticizer affects the thermal and mechanical properties of the PLA/PEG blend films. The study found that the glass transition and cold crystallization temperatures decreased with increasing PEG content up to 20 wt%, while the crystallinity and crystallization rate increased. The blends with up to 20 wt% PEG were miscible, but phase separation occurred when the plasticizer content was increased to 30 wt%. Subsequently, amorphous samples of neat PLA and PLA plasticized with 10 wt% of PEG underwent annealing at various temperatures (T_a = 80–120 °C) for durations t_a of 1 and 24 h. The samples were then analyzed using DSC and DMA. The addition of PEG to PLA altered the content of α′ and α crystalline forms compared to neat PLA at a given (T_a; t_a) and favored the formation of a mixture of α′ and α crystals. The crystallinity achieved upon annealing increased with increasing T_a or t_a and with the incorporation of PEG.

In the present work, the dielectric properties of recycled liquid crystals (LCs) (non-purified, purified, and doped with diamond nanoparticles at 0.05, 0.1, and 0.2 wt%) were investigated. The studied LC mixtures were obtained from industrial recycling of end-of-life LC displays presenting mainly nematic phases. Dielectric measurements were carried out at room temperature on a frequency range from 0.1 to 10⁶ Hz using an impedance analyzer. The amplitude of the oscillating voltage was fixed at 1 V using cells with homogeneous and homeotropic alignments. Results show that the dielectric anisotropy of all purified samples presents positive values and decreases after the addition of diamond nanoparticles to the LC mixtures. DC conductivity values were obtained by applying the universal law of dielectric response proposed by Jonscher. In addition, conductivity of the doped LC mixtures is lower than that of the undoped and non-purified LC.

Polylactic acid (PLA) is a promising biodegradable polymer whose widespread application is hindered by inherent brittleness. Polyethylene glycol (PEG) is a common plasticizer, but the effects of intermediate molecular weights, such as 4000 g/mol, on the coupled thermal, mechanical, and rheological properties of PLA remain insufficiently understood. This study presents a comprehensive analysis of PLA plasticized with 0–20 wt% PEG 4000, employing differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and rheology. DSC confirmed excellent miscibility and a significant glass transition temperature (T_g) depression exceeding 19 °C for the highest concentration. A complex, non-monotonic evolution of crystallinity was observed, associated with the formation of different crystalline forms (α′ and α). Critically, DMA revealed that the material’s thermo-mechanical response is dominated by its thermal history: while the plasticizing effect is masked in highly crystalline, as-cast films, it is unequivocally demonstrated in quenched amorphous samples. The core finding emerges from a targeted rheological investigation. An anomalous increase in melt viscosity and elasticity at intermediate PEG concentrations (5–15 wt%), observed at 180 °C, was systematically shown to vanish at 190 °C and in amorphous samples. This proves that the anomaly stems from residual crystalline domains (α′ precursors) persisting near the melting point, not from a transient molecular network. These results establish that PEG 4000 is a highly effective PLA plasticizer whose impact is profoundly mediated by processing-induced crystallinity. This work provides essential guidelines for tailoring PLA properties by controlling thermal history to optimize flexibility and processability for advanced applications, specifically in melt-processing for flexible packaging.

Electron Beam (EB) irradiation was utilized to decontaminate model systems of industrial polymers that contain a brominated flame retardant (BFR). Acrylonitrile-butadiene-styrene (ABS) and Polycarbonate (PC) are two types of polymers commonly found in Waste Electrical and Electronic Equipment (WEEE). In this study, these polymers were exposed to EB irradiation to degrade DecaBromoDiphenylEther (DBDE), one of the most toxic BFRs. Fourier-transform infrared spectroscopy analysis demonstrated an 87% degradation rate of DBDE for the ABS-DBDE system and 91% for the PC-DBDE system following an 1800 kGy irradiation dose. Thermal analysis using Differential Scanning Calorimetry revealed the presence of crosslinking in ABS and a minor reduction in the glass transition temperature of PC after EB processing. Polymers exhibited thermal stability after photolysis, as indicated by thermogravimetric analysis. In summary, EB irradiation had no impact on the overall thermal properties of both polymers. High-resolution mass spectrometry analysis has confirmed the debromination of both ABS-DBDE and PC-DBDE systems. Therefore, the results obtained are promising and could offer an alternative approach for removing bromine and other additives from plastic E-waste.

Chemical, structural, and thermal properties of recovered nematic Liquid Crystal (LC) mixtures were investigated by applying several analytical techniques. A large quantity (65,700) of End-Of-Life (EOL) Liquid Crystal Display (LCD) screens were used to extract these LC blends. The studied EOL-LCD screens were heterogeneous in nature, particularly due to their different brands, production years, and dimensions. The collected TV and computer screens, as well as tablets, presented an average diagonal size of 24 inches. Chemical characterization revealed that the recovered compounds present typical chemical structures of LC molecules by the simultaneous presence of aliphatic chains and aromatic and polar groups. POM observations of these samples exhibited Schlieren and marble-like textures at room temperature, which are typical of nematic LCs. Moreover, thermal characterization and thermo-optical analysis showed that these LC mixtures displayed a broad nematic phase between −90 °C and +70 °C.

The thermal degradation behavior of Poly(2-ethyl hexyl hcrylate) (Poly(2-EHA)), blended with a commercially available nematic liquid crystal (LC) mixture, was investigated by thermal gravimetric analysis (TGA). Different heating rates, ranging from 5 to 200 °C/min, were applied under an inert atmosphere. Based on the TGA results, activation energies (E_α) at different conversion rates (α) were determined using three integral isoconversion methods: Flynn-Wall-Ozawa (FWO), Tang, and Kissinger-Akahira-Sunose (KAS). It can be noticed that the global evolution of these activation energies was the same for the three models. The coefficient of determination R² presented values generally higher than 0.97. Using these models, the E_α value for the LC remains constant at 64 kJ/mol for all conversions rates. For the polymer Poly(2-EHA), applying the Tang and FWO models, the activation energy presents a variation ranging from 80 kJ/mol, for conversion α = 0.1, to 170 kJ/mol, for α = 0.9. For the third model (KAS), this energy varies between 80 and 220 kJ/mol in the same range of α.