“…Recently, PLLA textile fibers with tremendous application value and market potential in various fields have garnered considerable enthusiasm as an eco-friendly alternative to the most widely used nylon and poly(ethylene terephthalate) (PET) fibers in modern industry and life. − In comparison with these petrochemical-based fibers, PLLA fibers possess not only exceptional sustainability but also some advantageous physical properties, such as better elastic recovery, higher moisture regain, better weathering stability, as well as lower flammability and smoke generation. ,, Various types of commercial PLLA fibers including monofilaments, multifilaments, staple fibers, short-cut fibers, and spunbond fabrics have been fabricated using conventional melt spinning technology. , Unfortunately, the application potential of PLLA fibers has not been fully realized until now, mostly because the very slow crystallization rate of PLLA makes it hard to obtain fibers with a high crystallinity (e.g., 55–60%) even under intensive elongational flow conditions (which can notably accelerate the crystallization kinetics of semicrystalline polymers by orders of magnitude relative to the quiescent condition − ) involved in melt spinning. ,, In this case, the low crystallinity (i.e., 20–30%) cannot provide the melt-spun PLLA fibers with sufficient heat resistance for ironing and dyeing (both of them typically take place above 120 °C) due to the limitation of relatively low glass transition temperature ( T g ) of around 55–60 °C. ,, On the other hand, the insufficient heat resistance also significantly hampers their use in numerous environments where low thermal shrinkage and high dimensional stability are required. Thermal annealing provides a straightforward pathway to improve the heat resistance of PLLA fibers via enhancing crystallinity, but it is time-consuming and only limited improvement has been obtained . Actually, for semicrystalline polymers consisting of alternating crystalline and amorphous phases, their performance is also strongly dependent on crystal structure, crystal morphology, and lamellae orientation. ,− Formation of an oriented crystal structure is favorable for improving the performance of polymers. ,,,, Imposing an intensive flow field seems to be a facile method to trigger dramatically enhanced crystallization kinetics as well as highly oriented crystallization of polyolefin. ,, Nevertheless, for semirigid PLLA chains, flow conditions involved in conventional melt spinning at low speeds (usually 200–1000 m/min) cannot meet the essential requirement for h...…”