Effects of ferric chloride on structure, surface morphology and combustion property of electrospun polyacrylonitrile composite nanofibers

In this work, the pure polyacrylonitrile (PAN) nanofibers and PAN/FeCl₃ composite nanofibers were prepared by an electrospinning process. Electrospinning solution properties including viscosity, surface tension and conductivity, had been measured and combined with the results of Scanning electron microscopy (SEM), Atomic force microscope (AFM) and Micro Combustion Calorimeter (MCC) to investigate the effects of FeCl₃ on the structure, surface morphology and combustion property of electrospun PAN nanofibers, respectively. It was found from SEM images that the diameters of composite nanofibers were decreased with the addition of FeCl₃, which was attributed predominantly to the increased conductivity of the polymer solutions compared to viscosity and surface tension. The AFM analyses revealed that the surface morphology of electrospun nanofibers changed from smooth and wrinkle-like structure (without FeCl₃) to rough and ridge-like structure (with FeCl₃). The results characterized by MCC showed that the loading of FeCl₃ decreased the heat release rate (HRR) and improved the combustion property of composite nanofibers.     

Shape memory properties of electrospun nafion nanofibers

Nanoscaled non-woven fibers with shape memory effect are successfully fabricated via electrospinning method from Nafion solutions consisting of a little poly(ethylene oxide) (PEO). Scanning electron microscopy (SEM) investigation shows the electrospun nanofibers with average diameters in the range 170–410 nm. The electrospun nanofibers exhibit excellent shape memory properties. When deformed Nafion nanofibers are stimulated upon heat, the temporary shape responds rapidly, and then recovers to the permanent shape in less than one minute. The shape recovery ratios and shape fixity ratios of Nafion nanofibers with 0.3 wt%, 0.5 wt% and 0.7 wt% PEO are all above 90 %. In shape memory cycle, fibrous structure is stable after the stretching recovery. Shape memory Nafion nanofibers have various potential applications in smart structures and materials in the future.     

Fabrication of electrospun antimicrobial nanofibers containing metronidazole using nanospider technology

Nanospider technology as a modified electrospinning technique was used for the fabrication of electrospun nanofibers based on poly(vinyl alcohol) (PVA)/poly(ethylene oxide) (PEO) blend as drug delivery system (DDS) for metronidazole (MTZ) as an antimicrobial drug. Electrospun PVA/PEO/MTZ composite nanofibers were stabilized against disintegration in water by heating in oven at 110°C, or by soaking in isopropyl alcohol for 6 hrs. Incorporation of MTZ into electrospun nanofibers was confirmed by SEM, FT-IR spectra and TGA. The drug release results showed that the burst release was suppressed with stabilized electrospun nanofibers compared with non-stabilized ones. Electrospun PVA/PEO/MTZ composite nanofibers exhibited remarkable antimicrobial activity against Escherichia coli, Pseudomonas aeruginosa, Aspergillus niger, Penicillium notatum and Aspergillus flavus which varies with the species of the tested organisms.     

Electrospinning of cellulose nanofibers mat for laminated epoxy composite production

In this study, a new approach consisting of chemical treatment steps followed by electrospinning process was applied to produce cellulose nanofibers from wheat straws. Wheat straws were initially pretreated by NaOH solution to open the complex structure of raw materials and remove non-cellulosic materials. Then, acid and alkali hydrolysis was separately performed to eliminate hemicellulose and soluble lignin. Also, bleaching processes were implemented to remove the insoluble lignin. Cellulose nanofibers were produced by electrospinning of various concentrations of cellulose in different solvents including sodium hydroxide/urea/thiourea, pure trifluoroacetic acid (TFA), and TFA/methylene chloride. Images obtained by Scanning Electron Microscope (SEM) showed long and uniform nanofibers produced from electrospinning of cellulose/TFA/methylene chloride solution. An epoxy based laminated composite was prepared by a lamina of cellulose microfiber and electrospun nanofiber mat using hand lay-up composite manufacturing method. The fracture surface of the epoxy nanocomposite was analyzed by SEM images. In addition, the mechanical properties of laminated epoxy composites were compared with pure epoxy by conducting tensile and impact tests. Tensile test results showed that the ultimate tensile strength, elongation, and modulus of laminated epoxy nanocomposites were significantly increased. Moreover, it was found that by adding a nanofiber lamina in the epoxy composite, the impact resistance was significantly improved as a result of crack growth prevention.     

Facile fabrication of carbon nanotubes/polystyrene composite nanofibers for high-performance electromagnetic interference shielding

Polystyrene (PS) composites with nanofibrous structure consisting of multi-walled carbon nanotubes (MWCNTs) with 0-10 wt.% of nanofiller have been fabricated via electrospinning technique. The surface morphology and thermal properties of the composites were evaluated by scanning electron microscopy (SEM) and thermo-gravimetric analysis (TGA). The SEM analysis of the composite nanofibers samples revealed that the average diameter of the nanofibers increases with increasing MWCNTs content. The resultant MWCNTs/PS composite nanofibers diameters were in the range of 391±63 to 586±132 nm. The thermal stability of composites was increased after addition of MWCNTs to PS matrix. The electrical conductivity of the composites with different weight percentage of MWCNTs was investigated at room temperature. Electrical conductivity of MWCNTs/PS composite nanofiber followed percolation theory having a percolation threshold V _c= 0.45 vol% (~0.75 wt. %) and critical exponent q=1.21. The electrical conductivity and thermal properties confirmed the presence of good dispersion and alignment MWCNTs encapsulated within the electrospun nanofibers. The electromagnetic interference (EMI) shielding effectiveness of the MWCNTs/PS composites was examined in the measurement frequency range of 8.2-12.4 GHz (X-band). The total EMI shielding efficiency of MWCNTs/PS composite nanofibers increased up to 32 dB. The EMI shielding results for MWCNTs/PS composite nanofibers showed that absorption loss was the major shielding mechanism and reflection was the secondary mechanism. The present study has shown the possibility of utilizing MWCNTs/PS composite nanofibers as EMI shielding/absorption materials.     

Preparation and characterization of (polyurethane/nylon-6) nanofiber/ (silicone) film composites <Emphasis Type="Italic">via</Emphasis> electrospinning and dip-coating

This paper reports on the preparation and characterization of nanofibers and nanofiber/film composites fabricated by electrospinning and dip-coating. The polymers in this study consist of polyurethane, nylon-6, and silicone. Scanning electron microscopy (SEM), fiber distribution, X-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR) and tensile tests were conducted. The electrospun nylon-6 nanofiber/dip-coated silicone film (dried for 5 min) showed the optimum tensile strength and strain results, showing an increase in tensile strength of 63 % compared to pure nylon-6 nanofiber alone. XRD and FTIR verified the presence of individual polymers in the composite matrix. The electrospun PU nanofiber produced the biggest fiber diameter, while electrospun nylon-6, and PU/nylon-6 produced uniform fiber diameters, with PU/nylon-6 obtaining very random and curved fiber morphology.     

Preparation of luminescing nanocrystal and its application to electrospinning

In this study, quantum dots (QDs) having the photophysical properties of brightness, photostability and narrow emission were synthesized. The electrospinning has been introduced to be a simple technique for generating ultrathin fibers. Herein, we have synthesized QDs and electrospun polyvinylacetate (PVAc) nanofibers having these strongly luminescing QDs particles. The size and morphology of QDs were recorded with transmission electron microscopy (TEM). The structural nanofiber webs have been discussed by scanning electron microscopy (SEM). And fluorescence properties of strongly luminescing QDs nanofibers were also discussed.     

Electrospun nanostructures based on polyurethane/MWCNTs for strain sensing applications

Electrically conductive nanofibers were fabricated from elastic polyurethane (PU) and PU/multiwalled carbon nanotubes (MWCNTs) nanocomposite by electrospinning method. The nanocomposites were electrospun at various MWCNTs loading. Electron microscopy was used to investigate nanofibers morphology and dispersion of MWCNTs in the electrospun nanofibers. The results showed that the presence of the MWCNTs promoted the creation of fibrous structures in comparison with the PU without MWCNTs. On the other hand, increasing the MWCNTs content resulted in a slight increase in the average fiber diameter. TEM micrographs and mechanical properties of the electrospun mats indicated that the homogeneous dispersion of MWCNTs throughout PU matrix is responsible for the considerable enhancement of mechanical properties of the nanofiber mats. Electrical behavior of the conductive mats was also studied, in view of possible sensor applications. Cyclic experiments were conducted to establish whether the electrical properties were reversible, which is an important requirement for sensor materials.     

Fabrication and characterization of polyamide6-room temperature ionic liquid (PA6-RTIL) composite nanofibers by electrospinning

In the present work, polyamide6-room temperature ionic liquid (PA6-RTIL) composite nanofibers and membranes were successfully prepared for the first time by an electrospinning technique. The surface morphology, component analysis, mechanical properties, thermal properties and conductivity of the PA6-RTIL composite membranes were investigated by field-emission scanning electron microscope (FE-SEM), fourier transform infrared spectrometer (FT-IR), tensile testing, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and digit multimeter, respectively. The morphology, fiber diameter, mechanical strength of the obtained fibers can be controlled by changing experimental parameters for electrospinning, especially the content of RTIL in original electrospun mixture solution. The composite fibrous membranes showed ideal mechanical properties and significantly enhanced conductivity, which may be attributed to intrinsic high mechanical strength of PA6 and conductivity of RTIL.     

Measuring tensile strength of nanofibers using conductive substrates and dynamic mechanical analyzer

Though the tensile strength of nanofibers is essential to determine their application fields, few studies have been conducted on this topic, due to the difficulties involved in the preparation of single nanofiber tensile specimens, the manipulation of the clamping device, and the sensing of the nano- force and strain. A bundle testing method was employed in this work to measure the tensile strength of nanofibers. For this purpose, a conductive substrate was designed to hold several thousand nanofibers extruded from a spinning nozzle and align them uniaxially during the electrospinning process. This substrate was designed for a dynamic mechanical analyzer (DMA), because most DMAs are equipped with fine sensors sensitive enough to measure a very small force and strain. Nylon 6 nanofibers were electrospun and collected on the substrate. Then, they were elongated simultaneously in the DMA until they were fractured, showing that the aligned nanofibers have superior tensile strength and modulus compared to their counterpart microfibers and thus suggesting that polymeric nanofibers have the potential to be used as reinforcement fibers for composite materials.     

Studies of electrospinning process of zirconia nanofibers

Eletriospinning process was used to fabricate Zirconia nanofibers and polyvinyl pyrrolidone (PVP) was employed in this procedure. SEM, TGA, FT-IR and XRD were used to investigate the electrospinning process. Pure PVP was electrospun at the same conditions as comparisons. The results indicated that the fibers had an average diameter about 80 nm with smooth surface. FT-IR spectrum and TGA curve proved that PVP was removed from the fibers after a thermal treatment. It was found that the crystal structure of Zirconia changed at different calcination temperature. The use of PVP, bicomponent solvent of water and ethanol and inorganic salt had positive effects on the morphology of the fibers.     

Crystallization of PVDF in graphene-filled electrospun PVDF/PMMA nanofibers processed at three different conditions

In this study, the morphology and crystal polymorphism of electrospun blend nanocomposite of graphene filled-polyvinylidene fluoride (PVDF)/poly(methyl methacrylate) (PMMA) nanofibers were investigated. The preparation of the nanofibers was carried out by synthesis of PMMA/graphene as a masterbatch through in-situ polymerization, and then followed by compounding with PVDF solution in the different ratios. The process of electrospinning was done at three selective conditions of temperature, moist and ordinary environment. Crystallinity, morphology and thermal properties of nanofibers were characterized by X-ray diffraction spectroscopy (XRD), differential scanning calorimetric (DSC), Transmittance Electron Microscopy (TEM), Thermogravimetric Analyses (TGA), and Field Emission Scanning Electron Microscopic (FE-SEM). The enhancement of β crystal formation in the electrospun graphene-filled blend nanofibers was confirmed by XRD and DSC results. This can be ascribed by the benefits of solution casting, mechanical stretching, high electric field, PMMA interactions and graphene restrictions, altogether in one simple process. Also, presence of water molecules during the electrospinning causes the orientation of fluorine atoms in PVDF due to polar-polar interactions which enhance the polar conformation even in the pure PVDF nanofibers.     

Synthesis of Ag-Loaded TiO<Subscript>2</Subscript> Electrospun Nanofibers for Photocatalytic Decolorization of Methylene Blue

Titanium dioxide (TiO₂) is one of the excellent photocatalysts used for degradation of environmetal pollutants. In this work, 2.5, 5.0 and 7.5 wt.% of silver (Ag)-loaded TiO₂ nanofibers of mean size 52–134 nm were synthesized by electrospinning method. These electrospun nanofibers were calcined at 500 °C to enable the transformation of Rutile (R) phase to Anatase (A), elimination of reaction moieties from the TiO₂ matrix and subsequently formation of Ag clusters. The effect of Ag loading on the morphology, crystal structure, phase transformation, and band gap of these electrospun nanofibers have been characterized by scannining electron microscopy (SEM), X-ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR), raman spectroscopy and UV-visible spectroscopy. These nanofibers exhibited a red-shift in the absorbance edge and a significant enhancement of light absorption in the wavelength range of 250–550 nm. These electrospun nanofibers were investigated for photodecomposition of methylene blue (MB), and photocatalytic decolorization rates were determined by pseudo-first-order equation. The rate constants for the pure and those of 2.5, 5.0, and 7.5 wt% Agloaded TiO₂ nanofibers were computed to be 0.1439 min^-1, 0.1608 min^-1, 0.1876 min^-1, and 0.2251 min^-1 respectively.     

Electrospun poly(tetrafluoroethylene) nanofiber membranes from PTFE-PVA-BA-H<Subscript>2</Subscript>O gel-spinning solutions

As a kind of high-performance fibers, PTFE fiber has been widely used in many fields because of its unique characteristics. In this study, the poly(tetrafloroethylene) (PTFE) nanofibers manufactured by electrospinning method was reported. The gel-spinning solution of poly(tetrafluoroethylene)/poly(vinyl alcohol)/boric acid (PTFE/PVA/BA), which was prepared by the gel process of the mixture of PTFE, PVA, BA and redistilled water, was electrospun to form PTFE/PVA/BA composite nanofibers. After calcinating, the PTFE nanofibers with diameters of 200 nm to 1000 nm were obtained. The fibers before and after calcinating were characterized by scanning electron microscopy (SEM), thermogravimetric analysis (TGA), X-ray diffraction (XRD), FT-IR spectrum analysis and X-ray photoelectron spectroscopy (XPS), respectively, and the mechanical and hydrophobic properties of the fibers were also investigated. The results showed that the PTFE nanofiber membranes could be electrospun effectively used the gel-spinning solution of PTFE/PVA/BA, and may realize the applications in the fields of high-temperature filtration, catalyst supports, battery separator and so on.     

Fabrication of poly(vinyl alcohol) nanofibers by wire electrode-incorporated electrospinning

Wire electrodes for needleless electrospinning consist of stainless steel wires in place of cylinder electrodes. The effects of different numbers of constituent stainless steel wires on the morphology and diameter of polyvinyl alcohol (PVA) fibers are examined. With 1, 2, 3, or 4 stainless steel wires being twisted as wire electrodes, an 8, 10, or 12 wt.% polyvinyl alcohol (PVA) solution is electrospun into PVA nanofibers by using a needleless electrospinning machine. The morphology and diameter of PVA nanofibers is observed by scanning electron microscopy. The combination of the number of stainless steel wires (two), PVA solution (10 wt.%), and the collecting distance (10 cm) results in the finest diameter and an evenly formed fiber morphology. In addition, the nanofibers exhibit a wide range of diameters when electrospun with an electrode consisting of more than two stainless steel wires. Compared with the cylinder electrode, the use of a wire electrode can form nanofibers, which results in a more even morphology.     

Enhanced electrical properties of electrospun nylon66 nanofibers containing carbon nanotube fillers and Ag nanoparticles

In this study, we describe the preparation and characterization of electrospun Nylon66 composite nanofibers incorporated with carbon nanotubes (CNT) fillers and silver nanoparticles. We have incorporated the composites in to Nylon66 nanofibers to enhance the characteristics of the resultant composite nanofibers. The resultant composite nanofibers were characterized by using field-emission scanning electron microscopy, energy dispersive X-ray analysis, high-resolution transmission electron microscopy, X-ray diffraction, and current-voltage (I–V) measurement analysis. The morphology of the composite nanofibers exhibited densely arranged mesh-like ultrafine nanofibers which were strongly bound in between the main fibers. From I–V characteristics, it was observed that the incorporation of CNT fillers and Ag nanoparticles in to electrospun Nylon66 composite nanofibers can be significantly enhanced the electrical properties.     

Electrospun nanofibers of poly(NPEMA-co.-CMPMA): Used as Heavy metal ion remover and water sanitizer

Homo and copolymers of monomers 2-(N-phthalimido) ethylmethacrylate (NPEMA) and 4-Chloro-3-methyl phenyl methacrylate (CMPMA) were prepared in N,N-dimethyl formamide (DMF) solution at 70 °C using 2,2-azobisisobutyronitrile (AIBN) as initiator. The solution of poly(NPEMA-co.-CMPMA) in 20 % DMF was used to fabrication electrospun nanofiber by electrospinning technique. IR data were primarily employed to characterize polymers. The formation of nanofibers was identified by SEM study. The metal ion uptake capacity of copolymers and nanofibers were obtain by batch equilibrium method using different metal ion solution. The antimicrobial activity of the copolymers, Polymer nanocomposites and their nanofibers were tested against different microbial organisms by using quantitative method. The main objective of this investigation was to find whether nanofiber are better remover of metal ions compared to copolymers. It was also aimed to study the efficacy of nanofibers of copolymers and copolymer composite with nano Ag as water sanitizer.     

Functional electrospun cellulosic nanofiber mats for antibacterial bandages

Functionalization of cellulosic nanofibers was established to develop antibacterial bandages. The functionalization was conducted through preparation of carboxymethyl cellulose (CMC) containing different metal nanoparticles (MNPs) such as copper nanoparticles (CuNPs), iron nanoparticles (FeNPs) and zinc nanoparticles (ZnNPs). Fourier Transform Infrared spectroscopy was used to characterize CMC containing MNPs and scanning electron microscopy coupled with high energy dispersive X-ray (SEM-EDX) to study the surface morphology of CMC with and without MNPs. Furthermore, back scattering electron detector was used to show the position of metal nanoparticles on the microcrystalline CMC. In addition, UV-visible spectroscopy was used to confirm MNPs formation. Nanofiber mats of CMC containing MNPs were synthesized using electrospinning technique. Surface morphology of electrospun CMC containing MNPs was characterized using SEM. The obtained data revealed that elctrospun CMC nanofibers containing MNPs were smooth and uniformly distributed without bead formation. The average fiber diameters were in the range of 150 to 200 nm and the presence of MNPs in the nanofiber did not affect the size of the electrospun nanofiber diameter. Transmission electron microscopy (TEM) images displayed that MNPs were existed inside and over the surface of the electrospun nanofibers without any agglomeration. The average particle diameters of MNPs were 29-39 nm for ZnNPs, 23-27 nm for CuNPs and 22-26 nm for FeNPs. Moreover, Water uptake of electrospun nanofiber mats and the release of MNPs from nanofibers were evaluated. Nevertheless, electrospun CMC nanofibers containing MNPs had an excellent antibacterial activity against Gram-negative bacteria Escherichia coli and Gram-positive bacteria Staphylococcus aureus.     

Antibacterial effect of carbon nanofibers containing Ag nanoparticles

Silver nanoparticles imbedded in polyacrylonitrile (PAN) nanofibers and converted into carbon nanofibers by calcination was obtained in a simple three-step process. The first step involves conversion of silver ions to metallic silver nanoparticles, through reduction of silver nitrate with dilute solution of PAN. The second step involves electrospinning of viscous PAN solution containing silver nanoparticles, thus obtaining PAN nanofibers containing silver nanoparticles. The third step was converting PAN/Ag composites into carbon nanofibers containing silver nanoparticles. Scanning electron microscopy (SEM) revealed that the diameter of the nanofibers ranged between 200 and 800 nm. Transmission electron microscopy (TEM) and energy dispersive spectroscopy (EDS) showed silver nanoparticles dispersed on the surface of the carbon nanofibers. The obtained fiber was fully characterized by measuring and comparing the FTIR spectra and thermogravimetric analysis (TGA) diagrams of PAN nanofiber with and without imbedded silver nanoparticles, in order to show the effect of silver nanoparticles on the electrospun fiber properties. The obtained carbon/Ag composites were tested as gram-class-independent antibacterial agent. The electrosorption of different salt solutions with the fabricated carbon/Ag composite film electrodes was studied.     

Microstructure of heat-treated PAN nanofibers

A simple and modified electrospinning technique was utilized to prepare aligned and heat treated Polyacrylonitrile nanofibers by using a rotating drum fixed on top of syringe needles and applying upward hot air flow which can facilitate to heat nanofibers in electrospinning zone. Polyacrylonitrile nanofibers were electrospun from its 14 wt% solution in dimethylformamide under practical conditions. Angular power spectrum analysis showed better fiber alignment with increasing take up speed, although SEM studies demonstrated wider diameters of nanofibers being produced by modified method. The glass transition temperature of all prepared samples were determined between 70 °C and 90 °C using DSC technique. The Quantitative analysis of WAXD patterns has revealed the positive effect of modified method on the degree of crystallization of nanofibers heat treated at higher take up speed. The maximum chain orientation factor of 0.27 was determined for nanofibers collected at linear velocity of 114.5 m/min in the modified set up using Raman Spectroscopy technique.