A fundamental study of chitosan/PEO electrospinning

A highly deacetylated (97.5%) chitosan in 50% acetic acid was electrospun at moderate temperatures (25-70 °C) in the presence of a low content of polyethylene oxide (10 wt% PEO) to beadless nanofibers of 60-80 nm in diameter. A systematic quantitative analysis of the solution properties such as surface tension, conductivity, viscosity and acid concentration was conducted in order to shed light on the electrospinnability of this polysaccharide. Rheological properties of chitosan and PEO solutions were studied in order to explain how PEO improves the electrospinnability of chitosan. Positive charges on the chitosan molecule and its chain stiffness were considered as the main limiting factors for electrospinability of neat chitosan as compared to PEO, since surface tension and viscosity of the respective solutions were similar. Various blends of chitosan and PEO solutions with different component ratios were prepared (for 4 wt% total polymer content). A significant positive deviation from the additivity rule in the zero shear viscosity of chitosan/PEO blends was observed and believed to be a proof for strong hydrogen bonding between chitosan and PEO chains, making their blends electrospinnable. The impact of temperature and blend composition on the morphology and diameter of electrospun fibers was also investigated. Electrospinning at moderate temperatures (40-70 °C) helped to obtain beadless nanofibers with higher chitosan content. Additionally, it was found that higher chitosan content in the precursor blends led to thinner nanofibers. Increasing chitosan/PEO ratio from 50/50 to 90/10 led to a diameter reduction from 123 to 63 nm. Producing defect free nanofibrous mats from the electrospinning process and with high chitosan content is particularly promising for antibacterial film packaging and filtration applications.     

High Photoluminescence Polyindole/CuInS Quantum Dots for Pb Ions Sensor

Polyindole is considered an excellent conducting polymer with interested properties for different applications. A novel polyindole (PIn)/CuInS (CIS)/ZnS quantum dots (QDs) nanocomposite was synthesized via in situ polymerization of PIn in presence of CIS/ZnS QDs. By investigating the effect of CIS/ZnS QDs on optical properties of PIn, it was found that the optical band gaps of PIn, CIS/ZnS QDs, and PIn/CIS/ZnS QDs nanocomposite were 3.24 eV, 4.68 eV and 3.44 eV, respectively. From the luminance spectra, it was observed that emission peaks of PIn at 442 and 468 nm are independent of the excitation wavelength with the highest intensity at excitation wavelength of 380 nm. However, the luminance spectrum of PIn/CIS/ZnS QDs nanocomposite exhibited a quenching peak for CIS/ZnS QDs while the intensity of PIn peak was enhanced. High resolution of transmission electron microscope image of CIS/ZnS QDs revealed nanocrystals with a size of 3–4.5 nm and lattice space of 0.2 nm. PIn/CIS/ZnS QDs nanocomposite as the fluorescent probe was employed for sensing different concentrations of Pb²⁺ from 5 to 50 ppb. The reaction between PIn/CIS/ZnS QDs and Pb²⁺ was slightly quenched and fixed after 90 min. The emission peak was reduced gradually with increasing concentration of lead via photo-induced electron transfer or ion exchange mechanism. The value of correlation coefficient (R²) was 0.99, the sensitivity was 0.0041 ppb^?1 and limit of detection value was 4.48 ppb.

     

Improving toughness of ultra-high molecular weight polyethylene with ionic liquid modified carbon nanofiber

Ionic liquids (ILs) with long alkyl substituted groups, including 1-docosanyl-3-methylimidazolium bromide (IL-1) and 1-docosanyl-3-methylimidazolium hexafluorophosphate (IL-2), were synthesized and used to modify the surface of carbon nanofibers (CNF). The nanocomposite film prepared by solution-blending of ionic liquid modified CNF (i-CNF) and ultrahigh molecular weight polyethylene (UHMWPE) displayed better toughness when compared with pure UHMWPE even at very low concentrations (e.g. 0.4 wt%). The effect of ionic liquids on the elongation-to-break ratio of this nanocomposite system was investigated. The ionic liquid with hexafluorophosphate as the anion was more efficient to increase the toughness of UHMWPE due to the improved compatibility of IL with UHMWPE in the polymer matrix than that of the bromide. The rheological behavior of molten nanocomposites revealed that the storage modulus and the complex viscosity decreased with increasing ionic liquid content in the high frequency region. However, a reverse trend was observed when the frequency was less than 0.05 s⁻¹. In-situ monitoring in the change of crystallinity of the nanocomposite during tensile deformation suggested a mechanism of sliding between UHMWPE crystal regions and the surface of carbon nanofibers.     

Nanoporous poly(methyl methacrylate)-quantum dots nanocomposite fibers toward biomedical applications

In this work, poly(methyl methacrylate) (PMMA)-CdSe/ZnS quantum dots (QDs) nanocomposite fibers were fabricated via a simple electrospinning method. The parameters including concentration of PMMA, feed rate, applied voltage and working distance between the needle tip and the fiber collecting electrode were investigated and optimized to acquire large quantity, uniform and defect-free PMMA and its QD nanocomposite fibers. The surface morphology of the fibers was characterized by scanning electron microscopy (SEM), while the fluorescence emission characteristics of the polymer nanocomposite (PNC) fibers were analyzed with fluorescence microscopy. The thermal properties of the PMMA-QDs PNC fibers were explored by thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC). In comparison to the pristine PMMA fibers, the PNC fibers with only 0.1 wt% QD loading showed an improved thermal stability by 15 °C for the midpoint and onset degradation temperature. Surface chemical structure and functionalities were probed by a combination of attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS). New vibration bands were observed in the PNC fibers in the ATR-FTIR spectra, while the binding energy for both high resolution C 1s and O 1s spectra in the PNC fibers showed an apparent shift toward lower field. Rheological studies revealed a pseudoplastic behavior of both pristine PMMA and PMMA-QDs solutions. Moreover, the formed nanoporous PMMA-QDs fiber media exhibited an excellent biocompatibility as evidenced by the model Chinese hamster ovary (CHO) cell culturing test. The CHO cells demonstrated good adhesion, growth and viability in the reported testing.     

Effect of synthesis variables on the fluorescence properties of CdSe-polystyrene latexes

The development of photoluminescent materials based on the incorporation of quantum dots (QDs) into polymeric latexes has gained importance due to the multiple potential applications. Through the process of miniemulsion polymerization it is possible to encapsulate quantum particles into polymer matrix to provide both chemical stability and to maintain emission properties. The polymerization process was achieved with continuous magnetic stirring and nitrogen atmosphere. Cetyl trimethylammonium bromide (CTAB) was used as surfactant at concentration levels of 1.3 × 10^-3, 3.2 × 10^-3 and 5.4 × 10^-3 M. The initiator 2,2-azobisisobutyronitrile (AIBN) was used at 0.50 and 0.75 wt% and CdSe QDS were used at 0.075, 0.15 and 0.225 wt%, both in relation to monomer content. A STEM study on the composite latexes and later a statistical study on the measurement of polymer particle diameter let us corroborate that the increment in surfactant concentration produces a decrement in polymer particle size. The obtained composite latexes were stable and showed fluorescence by excitation with UV light. The spectrofluorometry studies indicated that in composite latexes fluorescent emission was a function of polymer particle size, showing higher intensity those formulations with smaller surfactant concentrations and bigger polymer particle size.     

Electrical conductivity and Joule heating of polyacrylonitrile/carbon nanotube composite fibers

Carbon nanotube (CNT) can exhibit electrical conductivity and introduce electric current into polymer. Using dry-jet-wet spin technology, polyacrylonitrile (PAN)/CNT composite fibers with 15 wt% and 20 wt% of CNT content were fabricated. The electrical conductivity of PAN/CNT fibers was enhanced by the annealing process at different temperatures and changed with time. These fibers could also respond to stretching, and the electrical conductivity decreased by 50% when the elongation reached 3%. In addition, electrical current can induce Joule heating effect and thermally transform PAN/CNT composite fibers. With the application of various electrical currents up to 7 mA at a fixed length, conductivity was enhanced from around 25 S/m to higher than 800 S/m, and composite fibers were stabilized in air. The temperature of composite fibers can increase from room temperature to several hundreds of degree Celsius measured by an infra-red (IR) microscope. Joule heating effect can also be estimated according to one-dimensional steady-state heat transfer equation, which reveals the temperature can be high enough to stabilize or carbonize fibers. As a result, this research provides a new idea of heating fabrics for thermal regulation, and a new approach for stabilizing and carbonizing PAN-based carbon fibers.     

Chain confinement in electrospun nanocomposites: using thermal analysis to investigate polymer-filler interactions

We investigate the interaction of the polymer matrix and filler in electrospun nanofibers using advanced thermal analysis methods. In particular, we study the ability of silicon dioxide nanoparticles to affect the phase structure of poly(ethylene terephthalate), PET. SiO₂ nanoparticles (either unmodified or modified with silane) ranging from 0 to 2.0 wt% in PET were electrospun from hexafluoro-2-propanol solutions. The morphologies of both the electrospun (ES) nanofibers and the SiO₂ powders were observed by scanning and transmission electron microscopy, while the amorphous or crystalline nature of the fibers was determined by real-time wide-angle X-ray scattering. The fractions of the crystal, mobile amorphous, and rigid amorphous phases of the non-woven, nanofibrous composite mats were quantified by using heat capacity measurements. The amount of the immobilized polymer layer, the rigid amorphous fraction, was obtained from the specific reversing heat capacity for both as-spun amorphous fibers and isothermally crystallized fibers. Existence of the rigid amorphous phase in the absence of crystallinity was verified in nanocomposite fibers, and two origins for confinement of the rigid amorphous fraction are proposed. Thermal analysis of electrospun fibers, including quasi-isothermal methods, provides new insights to quantitatively characterize the polymer matrix phase structure and thermal transitions, such as devitrification of the rigid amorphous fraction.     

A different chemical route to prepare hafnium diboride-based nanofibers: Effect of chemical composition

This study reports on the synthesis of hafnium diboride (HfB₂)-based nanofibers via electrospinning of polyhafnoxanesal (PHO)-based solution followed by pyrolyzing hafnium-boron containing polyvinylpyrrolidone precursor fibers by a moderate heat treatment at 1500°C under argon atmosphere. The influence of the molar ratios of C/Hf and B/Hf in preceramic polymer method is investigated on the final phase of HfB₂-based nanofibers. Structural, thermal, microstructural, and physical properties of the hafnium-based fibers are evaluated using Fourier transform infrared spectra (FTIR), thermogravimetry and differential scanning calorimetry (TG/DSC), X-ray diffractometer (XRD), high-temperature X-ray diffraction (HT-XRD), field-emission scanning electron microscope/energy-dispersive spectrometer (FE-SEM/EDS), and Brunauer-Emmett-Teller (BET). The results unveiled that the acidic pH was the optimal condition needed for obtaining the single phase of HfB₂ nanofibers. The precursor fibers with the stoichiometric ratio of 1:4:5 of Hf:B:C prepared under the acidic conditions converted into pure HfB₂ nanofibers having rough and porous surface after pyrolysis at 1500°C for 2 hour in argon, whereas HfB₂-HfC composite nanofibers with smooth surface were produced in the neutral conditions. The HfB₂ nanofibers with a mean diameter of ~100 nm prepared under the acidic conditions showed a higher specific surface area compared to HfB₂-HfC composite nanofibers with a diameter of ~121 nm derived in the neutral conditions.     

Electrospun composite poly(lactic acid)/polyaniline nanofibers from low concentrations in CHCl3: Making a biocompatible polyester electro-active

Nanofibers of poly(lactic acid) (PLA) blended with polyaniline (PANi) were fabricated via electrospinning at much lower PLA concentrations (∼1wt%) in CHCl₃ than reported before using a more efficient technique of preparing the solutions. The polymer nanofibers had diameters in the range 10 nm–300 nm. Nanofibers prepared with a 3 wt% PLA/PANi solution were conducting and were used to fabricate a diode which was electrically characterized and exhibited a low turn-on voltage and a rectification ratio of 500. The device characteristics were analyzed using the standard thermionic emission model of a Schottky junction and yielded an ideality factor of 1.6 and a barrier height of 0.49 eV. Using a simple circuit, the diode was able to rectify a low frequency alternating current signal with an efficiency of 10%. The ability to engineer insulating PLA into nanofibers that are electro-active extends the range of applications of this biocompatible and biodegradable polyester to include electronic devices that have reduced toxicity.     

Preparation of atactic poly(vinyl alcohol)/silver composite nanofibers by electrospinning and their characterization

Poly(vinyl alcohol) (PVA)/silver composite nanofibers were successfully prepared by the electrospinning method. Water‐based colloidal silver in a PVA solution was directly mixed without any chemical or structural modifications into PVA polymer fibers to form organic–inorganic composite nanofibers. The ratio of silver colloidal solution to PVA played an important role in the formation of the PVA/silver composite nanofibers. We prepared two different atactic PVA/silver nanocomposites with number‐average degrees of polymerization of 1700 and 4000 through electrospinning with various processing parameters, such as initial polymer concentration, amount of silver colloidal solution, applied voltage, and tip‐to‐collector distance. The PVA/silver composite nanofibers were characterized by field emission scanning electron microscopy and transmission electron microscopy (TEM). TEM images showed that silver nanoparticles with an average diameter of 30–50 nm were obtained and were well distributed in the PVA nanofibers. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Interfacial evaluation of epoxy/carbon nanofiber nanocomposite reinforced with glycidyl methacrylate treated UHMWPE fiber

Interface interactions of fiber–matrix play a crucial role in final performance of polymer composites. Herein, in situ polymerization of glycidyl methacrylate (GMA) on the ultrahigh molecular weight polyethylene (UHMWPE) fibers surface was proposed for improving the surface activity and adhesion property of UHMWPE fibers towards carbon nanofibers (CNF)‐epoxy nanocomposites. Chemical treatment of UHMWPE fibers was characterized by FTIR, XPS analysis, SEM, and microdroplet tests, confirming that the grafting of poly (GMA) chains on the surface alongside a significant synergy in the interfacial properties. SEM evaluations also exhibited cohesive type of failure for the samples when both GMA‐treated UHMWPE fiber and CNF were used to reinforce epoxy matrix. Compared with unmodified composite, a ～319% increase in interfacial shear strength was observed for the samples reinforced with both 5 wt % GMA‐grafted UHMWPE and 0.5 wt % of CNF. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43751.     

Processing and characterization of electrospun poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) nanofibrous membranes

Poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx) nanofibrous membranes were first fabricated via electrospinning from chloroform (CHCl₃) or CHCl₃/dimethylformamide (DMF) polymer solutions. The electrospinning conditions such as the polymer concentration, the solvent composition, and the applied voltage were optimized in order to get smooth and nano-sized fibers. The crystalline structure, the melting behaviors and the mechanical properties of the obtained nanofibrous membranes were characterized. With pure CHCl₃ as the solvent in the electrospinning process, the finest smooth PHBHHx fibers were about 1 μm in diameter. When DMF is added to CHCl₃ as a co-solvent, the conductivity and volatility of the solution increased and reduced, respectively, and the electrospinnability of the polymer solution increased as a result. The averaged diameters of PHBHHx fibers could be reduced down to 300-500 nm when the polymer concentration was kept at 3 wt%, the ratio of DMF/CHCl₃ was maintained at 20/80 (wt%), and the applied voltage was fixed at 15 kV during electrospinning. WAXD and DSC results indicated that the crystallization of the PHBHHx nanofibers was restricted to specific crystalline planes due to the molecular orientation along the axial direction of the fibers. The crystallization behaviors of the electrospun nanofibers were significantly different from that of the cast membranes because of the rapid solidification and the one-dimensional fiber size effect in the electrospinning process. Mechanically, the electrospun PHBHHx nanofibrous membranes were soft but tough, and their elongation at break averaged 240-300% and could be up to 450% in some cases. This study demonstrated how the size of electrospun PHBHHx fibers could be reduced by adding DMF in the solvent and gave a clue of the presence of oriented molecular chain packing in the crystalline phase of the electrospun PHBHHx fibers.     

High strength polyimide fibers with functionalized graphene

Graphene possesses unprecedented physical and chemical properties and has been thought to be ideal filler for reinforcing fibers' mechanical properties. However, graphene is difficultly dispersed in polymer which severely restrict to prepare high-strength and high-modulus composites. In this work, we report an effective method to fabricate a kind of organ-soluble polyimide (PI)/graphene composite fiber using in situ polymerization. Graphene oxide (GO) is modified by 4,4′-diaminodiphenyl ether (ODA) to obtain the GO-ODA nanosheets which exhibit excellent dispersibility and compatibility with the organ-soluble PI matrix. WAXD results show that these 2D nanosheets have a significant influence on the crystallization, aggregation or assembly behaviors of the polymer chains. The PI/graphene composite fiber containing 0.8 wt% of GO-ODA presents a tensile strength of 2.5 GPa (1.6 times higher than the pure PI fiber), and tensile modulus of 126 GPa (223% raises compared with pure PI fiber). Furthermore, the incorporation of graphene significantly improves the glass transition temperature and thermal stability of the composite fibers. Thanks to the excellent hydrophobic properties of graphene, the hydrophobic behavior of the composite fibers is greatly improved. This effective approach shows a potential application in fabricating multifunctional polymer-based composite fibers.     

Photoluminescent electrospun polymeric nanofibers incorporating germanium nanocrystals

The photoluminescent germanium nanocrystals (Ge-NCs) were successfully incorporated into electrospun polymeric nanofiber matrix in order to develop photoluminescent nanofibrous composite web. In the first step, the synthesis of Ge-NCs was achieved by nanosecond pulsed laser ablation of bulk germanium wafer immersed in organic liquid. The size, the structural and the chemical characteristics of Ge-NCs investigated by TEM, XPS, XRD and Raman spectroscopy revealed that the Ge-NCs were highly pure and highly crystalline having spherical shape within 3–20 nm particle size distribution. In the second step, Ge-NCs were mixed with polyvinyl alcohol (PVA) polymer solution, and then, Ge-NC/PVA nanofibers were obtained via electrospinning technique. The electrospinning of Ge-NCs/PVA nanoweb composite structure was successful and bead-free Ge-NCs/PVA nanofibers having average fiber diameter of 185 ± 40 nm were obtained. The STEM analysis of the electrospun Ge-NCs/PVA nanofibers elucidated that the Ge-NCs were distributed homogeneously in the polymeric nanofiber matrix. The UV–Vis absorption and photoluminescence spectroscopy studies indicated the quantum confinement effect of Ge-NCs on the optical properties of the electrospun Ge-NCs/PVA nanoweb.     

Identification of core/shell structure in Cd-Zn-Se QDs inside silicate glasses using 3D elemental distribution analysis

Core-shell structure in Cd-Zn-Se quantum dots (QDs) precipitated in the silicate glass matrix by continuous wave laser (λ = 532 nm) were demonstrated using transmission electron microscopy (TEM) and local electrode atom probe (LEAP) tomography. TEM images of the QDs in glasses after 60 min of irradiation at 9 W/cm² show two portions with different contrasts, and diameters of 5.97 and 22.49 nm, respectively; 3D elemental distribution in these glasses from LEAP tomography shows areas of high Zn concentration near the CdSe QDs. Iso-concentration images obtained using visualization software show that Cd-rich clusters were not completely covered by the Zn-rich shells in the glass after 15 min irradiation that resulted emission due to the surface defects of CdSe QDs. As the irradiation time increased to 60 min, the Zn-rich cluster gradually surrounded the Cd-rich core to form shells that eliminated the surface defects. During laser irradiation, CdSe QDs precipitated first due to the high degree of supersaturation of Cd and Se followed by the sequential incorporation of Zn on the Cd-rich QDs forming shells.     

Facile preparation and characterization of poly(vinyl alcohol)/chitosan/graphene oxide biocomposite nanofibers

Poly(vinyl alcohol) (PVA)/chitosan (CS)/graphene oxide (GO) biocomposite nanofibers have been successfully prepared using aqueous solution by electrospinning. CS colloidal gel in 1% acetic acid can be changed to homogeneous solution by using electron beam irradiation (EBI). The uniform distributions of GO sheets in the nanofibers were investigated by field emission scanning electron microscopy (FESEM) and Raman spectroscopy. FESEM images illustrated that the spread single GO sheet embedding into nanofibers was formed via self-assembly of GO sheet and PVA/CS chains. And the average diameters of the biocomposite nanofibers decreased (200, 173, 160 and 123 nm) with increasing the contents of GO (0.05, 0.2, 0.4 and 0.6 wt%). Raman spectra verified the presence of GO in the biocomposite nanofibrous mats. The mechanical properties of as-prepared materials related with GO contents. It revealed that the highest tensile strength was 2.78 MPa, which was 25% higher than that of neat PVA/CS nanofibers. Antibacterial test demonstrated that the addition of GO to PVA/CS nanofiber had great ability to increase inhibition zone till 8.6 mm. Overall, these features of PVA/CS/GO nanofibers which were prepared by eco-friendly solvent can be a promising candidate material in tissue engineering, wound healing and drug delivery system.     

A facile method to prepare ZrC nanofibers by electrospinning and pyrolysis of polymeric precursors

Zirconium carbide (ZrC) is one of the most attractive ultra-high temperature ceramics due to its excellent properties. ZrC nanofibers were fabricated via electrospinning and pyrolysis of a novel polymeric precursor, Polyzirconosaal (PZSA), with the addition of polyvinylpyrrolidone (PVP) as the spinning aid. The polymer PZSA was prepared from the chemical reaction between Polyzirconoxane (PZO) and Salicyl alcohol. The as-spun PZSA/PVP fibers were converted to ZrC nanofibers with a diameter ~200 nm after carbothermal reduction at 1300 °C in argon. The obtained ZrC nanofibers maintained its excellent fibrous morphology. The microstructures exhibited that nanoscale ZrC particles dispersed in the fibers containing free carbon. The average crystallite size of ZrC particles using Scherrer method was 42 nm. The obtained ZrC nanofibers were characterized by XRD, SEM and TEM. The current material would be particularly useful for applications such as catalyst support, filters, gas storage, supercapacitors, and phase change material support in thermal management systems.     

Effects of hard and soft components on the structure formation,crystallization behavior and mechanical properties of electrospun poly(l-lactic acid) nanofibers

The effects of multi-wall carbon nanotubes (MWCNTs) and poly(ethylene oxide) (PEO) on the structure formation, morphology, crystallization behavior and mechanical property of electrospun poly (l-lactic acid) (PLLA) nanofiber mats were investigated by field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), differential scanning calorimeter (DSC) and mechanical test. If incorporate hard filler, MWCNTs into electrospun PLLA nanofiber, the crystallinity, chain orientation, and crystallization behaviors were almost not influenced by the MWCNTs content owing to the MWCNTs mainly acted as impeding the crystal growth and chain diffusion. If incorporate small content of soft and miscible component, PEO (10 wt%) into the electrospun PLLA and PLLA/MWCNTs nanofibers, the crystallinity and crystallization rate of PLLA in nanofibers were obviously enhanced. The synergistic effect of PEO and MWCNTs in PLLA nanofibers was observed during melt-crystallization behaviors of PLLA/MWCNTs fibers. Based on those results, we found that the chain mobility is an important factor to influence the structure formation and crystallization behaviors in the electrospun nanofibers. Our results indicated that the structure and properties of electrospun nanofibers could be optimized by compounding with hard inorganic filler and soft polymer components.     

High-strength superparamagnetic composite fibers

The polymer composites of magnetic nanoparticles can be possibly used in a bulk form by preserving all the novel characteristics of magnetic nanoparticles such as superparamagnetic behavior. By introducing magnetic properties of Fe₃O₄ nanoparticles into polymer fibers, novel magnetic properties combine with the advantages of composite fibers such as light-weight and ease-of-use. Using dry-jet-wet fiber spinning technology, we have successfully fabricated iron oxide/polyacrylonitrile (Fe₃O₄/PAN) composite fibers with 10 wt% nanoparticle in the polymer matrix. Composite fiber with a diameter as small as 15 μm can achieve tensile strength and tensile modulus values as high as 630 MPa and 16 GPa, respectively. Superparamagnetic properties of Fe₃O₄ nanoparticles were preserved in the composite fibers with saturation magnetization at 80 emu/g and coercivity of 165 G.     

The morphology of electrospun polystyrene fibers

Electrospinning is a process of electrostatic fiber formation which uses electrical forces to produce polymer nanofibers from polymer solution. The electrospinning system consists of a syringe feeder system, a collector system, and a high power supplier. The important parameters in the morphology of electrospun polystyrene fibers are concentration, applied voltage, and solvent properties. Higher concentrations of the polymer solution form thicker fibers and fewer beads. When the concentration is 7 wt%, electrospun fibers have an average diameter of 340 nm, but as the concentration of PS increases to 17 wt%, the fiber diameter gradually thickens to 3,610 nm. The fiber morphology under different solvent mixture ratios and solvent mixtures has also been studied.