The role of organic solvents in governing the crystallization and morphology of semi-crystalline poly-l-lactide (PLLA) sheets was systematically investigated. Three different organic solvents; ethyl acetate (EA), o-dichlorobenzene (ODCB), and nitrobenzene (NB), with a solubility parameter analogous to PLLA and with a high capability of swelling, were chosen. It has been witnessed that the degree of crystallization and crystal morphology depends highly on the degree of swelling and evaporation rate of the solvent. Besides, the temperature and time of treatment played a significant role in the crystallization of polymers. The effect of different solvents and curing times are reflected by the measured X-ray diffraction (XRD) peaks and the differences are best shown by the unit cell size. The largest variation is observed along the c-axis, indicating shorter bonds, thus, showing better conformation after NB and ODCB treatment. The percentage of crystallinity calculated using the classical relative crystallinity index of XRD shows closer values to those calculated with differential scanning calorimetry (DSC) data, but a huge variation is observed while using the LeBail deconvolution method. The strong birefringence of polarised optical micrograph (POM) and the crystal morphology of scanning electron micrograph (SEM) also evidenced the orientation of polymer crystallites and increased crystallinity after solvent-supported heat treatment.

The paper deals with the study of seven selected natural plant oils. Differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA) and thermally stimulated discharge (TSD) methods were used. It has been found that most of the oils tested are in a glassy state at low temperature and have multiple transitions in the low temperature range. DSC shows complex melting-like processes or glass transition. For both DMA and TSD, the scaffold supportive method was used and found as a suitable one. DMA and TSD proved more sensitive than DSC and revealed at least two transitions between − 120 and − 40 °C. In the case of three oils (argan, avocado and sunflower), current reversal was observed by TSD; this symptom cannot be fully explained at the moment.

Poly-L-lactic acid (PLLA) has been produced by ring-opening polymerization method. During the polymerization processes different temperatures and process times have been applied to reach an optimum setup that was used to produce sample. The sample was measured by Fourier-transform infrared spectroscopy (FTIR), gel permeation chromatography (GPC) and differential scanning calorimetry (DSC) methods to identify the structure, molar mass and define the glass transition temperatures of product and obtain general information about the physical and chemical properties of material. Based on the results of measures, the material’s crystallinity was also investigated. The plasticization of PLLA has been also investigated. During the experiments, previously produced material (PLLA synthesized by polycondensation) was plasticised by adding of glycerol-dioleate. The plasticized material was also measured by FTIR, GPC and DSC methods to check the basic physical and chemical parameters of the material. According to the results of the measurements that were found, by this approach, the glass transition temperature of PLLA was reduced by 7 °C that indicated the glycerol-dioleate might act as a plasticizer for PLLA material without any deviation in the chemical structure of material.

The development of sustainable and mechanically versatile polymeric materials is essential to meet the growing demand for eco-friendly, high-performance products. This study investigates the mechanical properties of blends comprising polyvinyl chloride (PVC), thermoplastic polyurethane (TPU), and glycerol diacetate monolaurate, a bio-based plasticizer derived from waste cooking oil, addressing the underexplored combined effects of these components. By varying the proportions, the blends’ tensile strength, elasticity, elongation at break, and hardness were tailored for diverse applications. Incorporating the bio-plasticizer significantly enhanced the PVC’s flexibility and elongation at break, while reducing its tensile strength and rigidity. The addition of TPU further enhanced the elasticity, toughness, and resilience, with the final properties governed by synergistic interactions between PVC’s rigidity, TPU’s elasticity, and the plasticizer’s softening effects. Dynamic mechanical analysis (DMA) confirmed that the bio-plasticizer enhanced the compatibility between the PVC and TPU, leading to ternary PVC/TPU/bio-plasticizer blends with an improved elasticity and elongation at break, without a significant loss in tensile strength. These blends exhibited a broad range of tunable properties, enabling applications from flexible films to impact-resistant components. Overall, these findings highlight the potential of PVC/TPU/bio-plasticizer systems to deliver high-performance materials with enhanced sustainability. This work offers valuable insights for developing greener polymer systems and advancing the creation of tailored materials for diverse industrial applications in alignment with global sustainability goals.

Polymer blending enhances material properties by combining different polymers, which requires careful consideration of both thermodynamic and technological compatibility. This study investigates the compatibility of polyvinyl chloride (PVC), thermoplastic polyurethane (TPU), and a bio-plasticizer in blends produced via roll milling at various mixing ratios. Compatibility and morphology were analyzed using thermally stimulated discharge (TSD), dynamic mechanical analysis (DMA), and scanning electron microscopy (SEM), while mechanical and thermal properties were assessed by mechanical testing and thermogravimetric analysis (TGA). The PVC/TPU (100/30) blend exhibited superior phase compatibility over PVC/TPU (100/50), as indicated by a single relaxation peak in TSD and DMA, along with a more homogeneous morphology and enhanced tensile properties. The PVC/TPU/bio-plasticizer (100/20/50) blend showed a well-balanced mechanical performance and improved phase homogeneity. The TSD peak maxima trends for the TPU/bio-plasticizer blend highlighted the bio-plasticizer’s dual role in enhancing flexibility at low concentrations while restricting molecular mobility at higher concentrations. TGA revealed TPU’s positive effect on PVC’s degradation profile, while the bio-plasticizer reduced thermal stability. These findings demonstrate that blending PVC, TPU, and bio-plasticizer creates compatible materials with enhanced and diverse properties, making them suitable for industrial applications.