Poly(ethylene 2,5-furandicarboxylate) (PEF) is regarded as a bio-based alternative or complementary polyester for the widely used fossil resource-based polyester, poly(ethylene terephthalate) (PET). High-speed melt spinning of PEF of low and high molecular weight (L-PEF, H-PEF) was conducted, and the structure and properties of the resultant as-spun fibers were investigated. The occurrence of orientation-induced crystallization was confirmed for the H-PEF at the take-up velocity of 6.0 km/min, the highest speed for producing PET fibers in the industry. Molecular orientation and crystallinity of the as-spun fibers increased with the increase of take-up velocity, where the H-PEF fibers always showed a higher degree of structural development than the L-PEF fibers. The tensile modulus of the high-speed spun H-PEF fibers was relatively low at 5 GPa, whereas a sufficiently high tensile strength of approximately 500 MPa was measured. These values are adequately high for the application in the general semi-engineering fiber field.

Although several studies have reported that the addition of bamboo charcoal (BC) to polylactide (PLA) enhances the properties of PLA, to date, no study has been reported on the fabrication of ultrafine BC/poly(L-lactide) (PLLA) webs via electrospinning. Therefore, ultrafine fiber webs of PLLA and BC/PLLA were prepared using PLLA and BC/PLLA raw fibers via a novel laser electrospinning method. Ultrafine PLLA and BC/PLLA fibers with average diameters of approximately 1 μm and coefficients of variation of 13–23 and 20–46% were obtained. Via wide-angle X-ray diffraction (WAXD) analysis, highly oriented crystals were detected in the raw fibers; however, WAXD patterns of both PLLA and BC/PLLA webs implied an amorphous structure of PLLA. Polarizing microscopy images revealed that the webs comprised ultrafine fibers with uniform diameters and wide variations in birefringence. Temperature-modulated differential scanning calorimetry measurements indicated that the degree of order of the crystals in the fibers was lower and the molecules in the fibers had higher mobilities than those in the raw fibers. Transmittance of BC/PLLA webs with an area density of 2.6 mg/cm² suggested that the addition of BC improved UV-shielding efficiencies.

High-speed melt spinning of polylactide (PLA) was conducted and the structure and multiple melting behavior of the as-spun fibers were investigated. In the analysis of temperature modulated differential scanning calorimetry (TMDSC) thermograms for the as-spun PLA fibers taken-up at 1 and 6 km/min, the peaks around the melting temperature region in the reversing heat flow (RHF) and nonreversing heat flow (NRHF) curves were mainly separated into (1) a pair of an endothermic peak (Peak L) in RHF and an exothermic peak (Peak R) in NRHF in a low temperature region, (2) an endothermic peak (Peak M) both in RHF and NRHF (only in RHF for PLA fiber spun at the low-speed) in an intermediate temperature region, and (3) an endothermic peak (Peak H) both in RHF and NRHF in a higher temperature region. Wide-angle X-ray diffraction (WAXD) measurements were conducted during the heating process of the as-spun fibers cut into powders. In the case of fibers obtained at 1 km/min, disordered crystals, i.e. α′-form crystals, were formed through cold crystallization followed by a disorder-to-order phase transition, i.e. α′ to α crystalline modification, with partial melting of the α′ crystals around 148.5°C in the temperature range of Peaks R and L. Finally, the α form crystals melted above 169.4°C, in the temperature range of Peak H. On the other hand, the PLA crystals generated by the orientation-induced crystallization during the spinning process at a spinning velocity of 6 km/min did not show a WAXD profile of perfect α form crystals but showed an intermediate structure having lattice spacings between the α′ and α forms. Such intermediate crystals did not transformed into α form crystals during the heating process.