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1.
Polyethylene terephthalate (PET)/biomedical polyurethane (BPU) composite nanofibers with modulated mechanical properties are electrospun by varying the weight ratios of PET and BPU polymers in the mixture. The effect of BPU content on the morphology, porosity, thermal properties, and crystalline structures are systematically investigated. It is shown that uniform PET/BPU nanofibers can be formed through optimization. When the content of BPU is low (0?C7 %), better elongation of the nanofibrous mats is obtained with the increase of BPU content, whereas further increasing the BPU polymer (up to 15 %) results in a decreased breaking elongation as well as the mechanical strength of composites. The formed nanofibrous mats may find potential applications in tissue engineering and vascular graft.  相似文献   

2.
The four binary fatty acid eutectics of capric-lauric acid (CA-LA), capric-myristic acid (CA-MA), capric-palmitic acid (CA-PA), and capric-stearic acid (CA-SA) were firstly prepared as solid-liquid phase change materials (PCMs); then, the composite phase change nanofibers consisting of CA-based binary fatty acid eutectic and polyethylene terephthalate (PET) were fabricated by electrospinning for thermal energy storage. The maximum mass ratios of fatty acid eutectics versus PET in the nanofibers could reach up to 2/1. The FE-SEM images revealed that the composite nanofibers possessed smooth and cylindrical morphological structure having diameters of about 100–300 nm. The fatty acid eutectic could be uniformly distributed in the three-dimension network structure of the PET nanofibers. The FT-IR results indicated that the fatty acid eutectic and PET had no chemical reaction and exhibited good compatibility with each other. The DSC measurements showed that the prepared composite nanofibers had appropriate phase transition temperatures (about 5–38 °C) based upon climatic requirement, whilst the phase change temperatures and the enthalpy values of the composite nanofibers could be adjusted by changing the contents and the types of binary fatty acid eutectics in the nanofibers. The TGA results suggested that the onset thermal degradation temperatures and charred residues at 700 °C of the composite nanofibers were lower than those of pure PET nanofibers, but higher than those of fatty acid eutectic, which were caused by the fact that the PET had better thermal stability than fatty acid eutectic.  相似文献   

3.
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.  相似文献   

4.
In this study, various concentrations of polyethylene terephthalate (PET) polymeric solution were investigated to produce hollow nanofiber yarn. First, the electrospining apparatus was designed in a way that to put PVA multifilament in the core and to twist PET nanofibers onto multifilament yarn as a sheath simultaneously, followed by dissolving PVA yarn in hot water, PET hollow nanofiber yarn was produced. In this survey, it has been observed that the average thickness of sheath increased by increasing concentrations of PET polymeric solution. Results showed that maximum efficiency of extracting the PVA multifilament from the hollow yarn under certain conditions (concentration of 18 % (w/v) of PET, applied voltage of 10 kV, and flow rate of 0.0526 ml/h) was more than 85 %. The mechanical and physical properties of PET hollow yarns were investigated and indicated that the hollow nanofiber yarns at concentration of 30 % and 18 % polymeric solution had the lowest strength and the highest regain moisture, respectively.  相似文献   

5.
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.  相似文献   

6.
Synthesis of biocompatible polymer nanofibers is valuable, due to their use as a cover for burns and as a replacement for bandage because of their antimicrobial properties. In this study, electrospinning of chitosan(Ch) and nanofibers synthesis with antibacterial properties was investigated. Nanofibers with antibacterial properties were synthesized by electrospun of Ch/poly(L-lactide)(PLA)/Imipenem(Imi) polymer solution. The results showed that the optimized ratio of Ch/PLA polymer solution was ratio of 50:50 and Ch 2 wt% and PLA 10 wt% polymer solution was the best weight percentage for nanofiber preparation. Also, the average diameter of Ch/PLA/Imi nanofibers was 143 nm and measured with ImageJ software. Afterwards, the antibacterial properties of Imi as additives (with different percentages) was studied in the polymer solution. The scanning electron microscopy (SEM) images and antibacterial tests were showed that the electrospun of Ch/PLA/Imi polymeric nanofibers were effective against Gram negative bacteria Escherichia coli (E. coli) and inhibited growth of E. coli. The growth and viability percentage of fibroblast cells with nanofibers in αMEM culture are at desirable levels after 6 days.  相似文献   

7.
In this paper, the structure and optical properties of poly(methyl methacrylate) (PMMA) nanofibers and films were investigated. Differential scanning calorimetery (DSC) and Wide-Angle X-ray scattering (WAXS) results confirmed the amorphous structure of both nanofibers and films. Low angle X-ray diffraction (LA-XRD) revealed the presence of voids and/or particles with the spacing of 128.4 Å within the nanofibers. From the Porod plots, a three-dimensional surface fractal for the nanofibers and a mass fractal structure for the films were derived. By the interpretation of Small Angle X-ray scattering (SAXS), the shape and size of the particles in the samples were assessed. It was concluded that the particles shape within the nanofibers and the films were globular, with the radius of gyration of 8.5 nm for the nanofibers and 16.5 nm for the films. The nanofiber mat showed less light transparency when compared with the film. This phenomenon could be attributed to the difference in the physical shape, as well as scattering of the light by the voids or particles within the nanofibers.  相似文献   

8.
Cellulose nanowhisker (CNW) reinforced electrospun Bombyx mori silk fibroin (SF) nanofibers were fabricated. The morphology, structure, and mechanical properties of nanofibers were investigated by FE-SEM, TEM, FTIR, and tensile testing. It was found that the nanofiber size decreased obviously from 250 nm in the unreinforced mat to 77–160 nm in the CNW reinforced mats depending on the CNW content due to the increased conductivity of spinning dope. In the reinforced mats, the CNWs were embedded in the SF matrix separated from each other, and aligned along the fiber axis. There was a positive correlation between the CNW content and the tensile strength and Young’s modulus of reinforced mats. However the strain at break dropped gradually with the increase of CNW. When the CNW content was 2 w/w%, the tensile strength and Young’s modulus of reinforced SF nanofiber mats were about 2 times higher than those of unreinforced mat.  相似文献   

9.
The electrospinnability of aloe vera gel and the release mechanism as well as the kinetic of its release from poly vinyl alcohol (PVA) nanofibrous matrix is reported. Addition of PVA by an amount of only 1 % (w/w) to aloe vera solution made its electrospinning possible leading, to the fabrication of aloe vera nanofiber (99 %) with an average diameter of around 80 nm. Electrospinning of aloe vera-PVA solutions (25-75, 50-50, 75-25) led to the fabrication of nanofibers with average diameter of around 55, 105 and 110 nm, respectively. FTIR analysis showed no reaction between aloe vera and PVA. X-ray diffraction patterns showed no considerable effect from aloe vera on the amorphous structure of PVA. The release mechanism of aloe vera from PVA matrix in phosphate buffer solution was of Ficki type and the kinetic of the release followed Higuchi model. Aloe vera or aloe vera-PVA electrospun nanofibers may be used as an aloe vera release system in wound care. In a phosphate buffer solution, at least 60 percent of aloe vera is released in the first hour and about 90 % of aloe vera is released in 2-4 hours depending on the diameter of the nanofibers.  相似文献   

10.
The aim of the present study was to prepare nanofibers loaded with montelukast, a cysteinyl leukotrienes (CysLTs) inhibitor, with anti-inflammatory properties effective on wound healing. Polymeric nanofibers containing montelukast were spun by electrospinning method using different ratios of the blend of two biodegradable polymers of poly(methyl vinyl etherco-maleic acid) (PMVEMA) and poly(lactic-co-glycolic acid) (PLGA) at the total polymer concentration of 37 %, the distance of the needle to rotating screen of 19 cm, the voltage of 12 Kv and the rate of injection of 0.2 ml/h. The ratio of two polymers in the blend and the concentration of montelukast were optimized based on the diameter of the nanofibers, drug loading percent and release efficiency by a full factorial design. The morphology, diameter and diameter distribution of the nanofibers were studied by scanning electron microscopy (SEM). Drug loading percent in the nanofibers was determined by extracting the loaded drug from a specific surface of the nanofibers which was subsequently analyzed spectrophotometrically. The drug release rate from the nanofibers was studied in phosphate buffer solution (pH 7.4) containing 0.5 % Tween 20 at predetermined time intervals until 10 days. The cytotoxicity of the designed nanofibers was evaluated on mouse fibroblast cells using trypan blue method, their platelet adherence property was quantified by measuring the lactate dehydrogenase (LDH) activity and confirmed by SEM micrographs. The optimized ratio of PLGA/PMVEMA was 3:1 with the total concentration of polymers as 37 % loaded with 30 % of montelukast produced nanofibers with a diameter of 157.6 nm, drug loading percent of 43.7 % and release efficiency of 75 % after 10 days. The cell viability was similar in nanofibers and the negative control group. The platelets adhesion to the nanofibers was more than the negative control group (p<0.05).  相似文献   

11.
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.  相似文献   

12.
We report on the preparation and electrical characterization of nylon-6 nanofibers via electrospinning technique. During electrospinning, the polymer solution became highly ionized and emerging out of the micro-tip syringe by forming mesh-like ultrafine nanofibers structure in between the main fibers. The resultant nylon-6 nanofibers were well-oriented with uniform structure. The diameter of the ultrafine nanofibers (7 to 40 nm) is one order less than those of main fibers (100 to 200 nm). The current-voltage (I-V) measurements revealed a linear curve with an occurrence of negative differential resistance (NDR) behavior. The existence of NDR region in the nylon-6 nanofibers can be attributed to the tunneling current through the ultrafine structures. The fabrication of nanofibers, in the form of ultrafine mesh-like form, is relatively fast and inexpensive, and it paves the way to build up of new dimension for nano device applications.  相似文献   

13.
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.  相似文献   

14.
The effect of impact force when using inclined water jets on splittable bicomponents hydroentangled fabrics are investigated focusing on changes in tensile properties and fiber splitting. The results indicated that with increase of impact force, the tensile strength was increased in both machine direction (MD) and crosswise direction (CD). On changing of water jet inclination angle, the tensile strength was the highest at 10 degree followed by 20 degree and the last 0 degree. The highest fiber splitting were observed in pie segment (PA6/PET) followed by island in sea (PA6/COPET) fiber but no fiber splitting was observed for island in sea (PET/COPET) fiber. The impact force in inclined mode of impact, played a great role in improving fiber splitting and tensile properties of hydroentangled nonwoven fabrics. The Scanning Electron Microscope (SEM) photos were used for investigation of fiber splitting by comparing fiber diameter before and after hydroentanglement.  相似文献   

15.
Nanofibrous poly(vinylidene fluoride) (PVDF) sheets were produced by electrospinning and grafted with oxirane groups using radiation induced grafting of glycidyl methacrylate (GMA) followed by treatment with N-methyl-D-glucamine (NMDG). The NMDG density in the nanofibers was tuned by optimization of the immobilisation reaction variables using response surface methodology (RSM). The various properties of NMDG-containing nanofibers were evaluated using Fourier-transform infrared (FT-IR) spectroscopy, field emission scanning electron microscopy (FESEM), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The NMDG-containing nanofibers were tested for boron selective removal from solutions. A maximum glucamine density yield of 2.2 mmol/g was obtained at 15 wt%, 87 oC, 64.7 min and 150 % for NMDG concentration, temperature, time and degree of grafting (DG), respectively. The applied procedure incorporating RSM was found to be highly effective in the optimization of covalently immobilised glucamine on the oxirane modified PVDF based-nanofibrous structure and in imparting an excellent combination of physico-chemical and boron retention properties. A complete boron removal was achieved in 100 mg/l boron solution adsorbent with a dosage of 0.6 g at pH 7 in 2 h time. This was accompanied by a promising reusability suitable for boron removal from solutions.  相似文献   

16.
GSP/gelatin composite nanofiber membranes containing silver nanoparticles were successfully fabricated as a novel biomaterial by electrospinning. The silver nanoparticles (AgNPs) were synthesized with the grape seed polyphenols (GSP) as reducing agent in aqueous solution of gelatin, and then the GSP/gelatin/AgNPs mixed solution was electrospun into nanofibers at 55 °C. The scanning electron microscopy (SEM) confirmed that the composite fibers were uniform and the average fiber diameter ranged between 150 nm and 230 nm with an increase in applied potentials from 14 kV to 22 kV. And the transmission electron microscopy (TEM) showed that silver nanoparticles distributed individually in the fibers with the average particle size of about 11 nm. Furthermore, the ultraviolet visible spectrophotometer (UV-vis spectroscopy) test demonstrated that all of Ag+ converted to Ag0 when the concentration of gelatin was 24 wt% and the mass ratio of GSP to AgNO3 was about 5:2. The antibacterial activities of the fiber membranes against E.coli and S.aureus were measured via a shake flank test and demonstrated good performance after the importation of silver nanopaticles. Cytotoxicity testing also revealed that fiber membranes contained silver nanoparticles had no cyto-toxic. All the results indicated that the GSP was effective for the formation and stabilization of silver nanoparticles in composite nanofibers mats which had the potential for applications in antimicrobial tissue engineering and wound dressing.  相似文献   

17.
Building proton transfer channel is an important strategy to optimize the proton transfer process of the proton exchange membrane (PEM). In this work, sulfonated pre-oxidized nanofibers were prepared by solution blowing of polyacrylonitrile (PAN) nanofibers followed by pre-oxidization and sulfonating, and the nanofibers were composited with SPEEK to enhance its performance as PEM. The results of the proton conductivity verified that the employment of sulfonated pre-oxidized nanofibers improved the proton conductivity. Meanwhile, the introduction of the sulfonated pre-oxidized nanofibers realized the upgrades of the thermostability and water absorbency of the membrane, and led to the decrease of the swelling property and methyl alcohol’s permeability of the material. It is indicated that the composite membrane is promising materials for PEM fuel cells.  相似文献   

18.
This study evaluated the potential application of an atmospheric plasma (AP) treatment as a pre-treatment for digital textile printing (DTP) of polyester (PET) fabrics and cotton, in order to determine its viability as an alternative to the usual chemical treatment. The surface properties of the AP-treated fabrics were examined through scanning electron microscopy (SEM) and contact angle, and the physical properties, such as electrostatic voltage and water absorbance, were tested. The properties of cotton and PET with the AP treatment were found to be dependent on number of repetitions and electric voltage. Although no remarkable surface differences were observed by SEM in the fabrics before and after treatment, the static contact angle of the PET after AP treatment was decreased from 85 ° to 24 ° at wave. In addition, the charge decay time decreased as the voltage and number of treatments increased. The absorption height of PET changed after exposure to 7 mm with increasing measurement time. The K/S with and without the AP pre-treated and DTP finished cotton was better than that with the usual chemical modification. In PET, the 0.5 kW and 1 time AP-treated specimen showed the highest K/S values.  相似文献   

19.
Biocompatible polyvinyl alcohol (PVA)-styrylpyridinium (SbQ)/β-cyclodextrin (β-CD) composite nanofibers were obtained by electrospinning in this study. PVA-SbQ was used as the foundation polymer as well as crosslinking agent, β-CD was incorporated to achieve expected properties such as improved mechanical properties and thermal stability. The Fourier transform infrared spectroscopy (FTIR) spectra confirmed the existence of β-CD, and the morphologies and average fiber diameters of the electrospun composite nanofibers were also analyzed by SEM. X-ray diffraction patterns (XRD) of PVA-SbQ/β-CD composite nanofibers revealed that the inclusion of β-CD in the nanofibers affected the ordered phase of PVA. Besides, the thermal analyses revealed the improvement in the thermal properties for PVA-SbQ/β-CD composite nanofibers. It was found that the crosslinked composite nanofibers showed a clear higher tensile strength (TS) as well as a greater elongation at break (EB). Eventually, antifungal drug griseofulvin (GSV) has been loaded into the composite nanofibers by formation of its inclusion complex with β-CD in aqueous solution, ultraviolet light (UV-Vis) spectral analysis showed that the drug-loading nanofibers had certain sustained release effect.  相似文献   

20.
β-chitin was isolated from marine waste, giant Humboldt squid Dosidicus gigas, and further converted to nanofibers by use of a collider machine under acidic conditions (pH 3). The FTIR, TGA, and NMR analysis confirmed the efficient extraction of β-chitin. The SEM, TEM, and XRD characterization results verified that β-chitin crystalline structure were maintained after mechanical treatment. The mean particle size of β-chitin nanofibers was in the range between 10 and 15 nm, according to the TEM analysis. In addition, the β-chitin nanofibers were converted into films by the simple solvent-casting and drying process at 60 °C. The obtained films had high lightness, which was evidenced by the CIELAB color test. Moreover, the films showed the medium swelling degree (250–290%) in aqueous solutions of different pH and good mechanical resistance in the range between 4 and 17 MPa, depending on film thickness. The results obtained in this work show that marine waste can be efficiently converted to biomaterial by use of mild extractive conditions and simple mechanical treatment, offering great potential for the future development of sustainable multifunctional materials for various industrial applications such as food packaging, agriculture, and/or wound dressing.  相似文献   

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