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Highly porous-cellulose-acetate (CA) nanofibers were prepared by an electrospinning process based on a nonsolvent-induced phase separation (NIPS) mechanism, and their PM2.5 capture efficiencies were evaluated. The NIPS condition during the electrospinning process was achieved by selecting appropriate good and poor solvents based on the Hansen solubility parameters of CA. N,N-dimethylacetamide (DMAc) was used as the good solvent, while dichloromethane (DCM), tetrahydrofuran (THF), and acetone were used as poor solvents. Porous-CA nanofibers were observed upon using the binary solvent systems of DCM:DMAc = 1:9, DCM:DMAc = 2:8, and THF:DMAc = 1:9, and the CA nanofibers formed using the DCM/DMAc system with DCM:DMAc = 1:9 were found to have the highest specific surface area of 1839 m2/g. Based on the optimized binary solvent system with DCM:DMAc = 1:9, porous-CA nanofibers were prepared and characterized according to the CA content in the electrospinning mixture. The results confirmed that a porous structure was formed well from the surface to the core of the nanofibers. The composition range of the ternary mixture of CA and two solvents capable of producing porous-CA nanofibers was mapped on a ternary phase diagram, and highly efficient PM2.5 capture with 98.2% efficiency was realized using porous-CA nanofibers obtained using a 10 wt.% CA solution. This work provides a new strategy for improving the efficiency of porous-nanofiber filters for PM2.5 capture.

Multifunctional nanofibers for particulate matter (PM) and volatile organic compounds (VOCs) removal from the indoor atmospheric environment were manufactured from eco-friendly natural cellulose materials via electrospinning using an optimized solvent system containing 1-ethyl-3-methylimidazolium acetate (EmimAC) and dimethylformide (DMF) in a 3:7 volume ratio. EmimAC improved the cellulose stability, whereas DMF improved the electrospinnability of the material. Various cellulose nanofibers were manufactured using this mixed solvent system and characterized according to the cellulose type, such as hardwood pulp, softwood pulp, and cellulose powder, and cellulose content ranging from 6.0–6.5 wt%. The correlation between the precursor solution alignment and electrospinning properties indicated an optimal cellulose content of 6.3 wt% for all cellulose types. The hardwood pulp-based nanofibers possessed the highest specific surface area and exhibited high efficiency for eliminating both PM and VOCs, with a PM2.5 adsorption efficiency of 97.38%, PM2.5 quality factor of 0.28, and toluene adsorption of 18.4 mg/g. This study will contribute to the development of next-generation eco-friendly multifunctional air filters for indoor clean-air environments.

A 3YSZ (3 mol% yttria-stabilized zirconia) ceramic green body with 50 vol% of ceramic content was 3D-printed by supportless stereolithography under optimal drying, debinding, and sintering conditions in order to achieve high strength and density. The viscosity and flowability of the ceramic nanocomposite resins were optimized by adjusting the amounts of non-reactive diluents. The ceramic 3D-printed objects have a high polymer content compared to ceramics samples manufactured by conventional manufacturing processes, and the attraction between layers is weak because of the layer-by-layer additive method. This causes problems such as layer separation and cracking due to internal stress generated when materials such as solvents and polymers are separated from the objects during the drying and debinding processes; therefore, the drying and debinding conditions of 3YSZ ceramic 3D-printed objects were optimized based on thermogravimetry–differential thermal analysis. The sintering conditions at various temperatures and times were analyzed using X-ray diffraction, SEM, and flexural strength analysis, and the body of the 3YSZ ceramic 3D-printed object that sintered at 1450 °C for 150 min had a relative density of 99.95% and flexural strength of 1008.5 MPa. This study widens the possibility of manufacturing ceramic 3D-printed objects with complex shapes, remarkable strength, and unique functionality, enabling their application in various industrial fields.

In an effort to fabricate a wearable piezoelectric energy harvester based on core-shell piezoelectric yarns with external electrodes, flexible piezoelectric nanofibers of BNT-ST (0.78Bi0.5Na0.5TiO3-0.22SrTiO3) and polyvinylidene fluoride-trifluoroethylene (PVDF-TrFE) were initially electrospun. Subsequently, core-shell piezoelectric nanofiber yarns were prepared by twining the yarns around a conductive thread. To create the outer electrode layers, the core-shell piezoelectric nanofiber yarns were braided with conductive thread. Core-shell piezoelectric nanofiber yarns with external electrodes were then directly stitched onto the fabric. In bending tests, the output voltages were investigated according to the total length, effective area, and stitching interval of the piezoelectric yarns. Stitching patterns of the piezoelectric yarns on the fabric were optimized based on these results. The output voltages of the stitched piezoelectric yarns on the fabric were improved with an increase in the pressure, and the output voltage characteristics were investigated according to various body movements of bending and pressing conditions.

Flexible lead-free piezoelectric nanofibers, based on BNT-ST (0.78Bi0.5Na0.5TiO3-0.22SrTiO3) ceramic and poly(vinylidene fluoride-trifluoroethylene) (PVDF-TrFE) copolymers, were fabricated by an electrospinning method and the effects of the degree of alignment in the nanofibers on the piezoelectric characteristics were investigated. The microstructure of the lead-free piezoelectric nanofibers was observed by field emission scanning electron microscope (FE-SEM) and the orientation was analyzed by fast Fourier transform (FFT) images. X-ray diffraction (XRD) analysis confirmed that the phase was not changed by the electrospinning process and maintained a perovskite phase. Polarization-electric field (P-E) loops and piezoresponse force microscopy (PFM) were used to investigate the piezoelectric properties of the piezoelectric nanofibers, according to the degree of alignment—the well aligned piezoelectric nanofibers had higher piezoelectric properties. Furthermore, the output voltage of the aligned lead-free piezoelectric nanofibers was measured according to the vibration frequency and the bending motion and the aligned piezoelectric nanofibers with a collector rotation speed of 1500 rpm performed the best.