Characterization and antibacterial properties of Ag NPs doped nylon 6 tree-like nanofiber membrane prepared by one-step electrospinning

A hierarchically Ag/nylon 6 tree-like nanofiber membrane (Ag/PA6 TLNM) was fabricated by adding tetrabutylammonium chloride (TBAC) and silver nitrate (AgNO3) into spinning solution via one-step electrospinning. TBAC presented in PA6/formic acid (HCOOH) spinning solution was able to cause the formation of a tree-like structure due to its space steric structure and the increasing of solution conductivity. Electrospinning solvent acted as a reducing agent for in situ conversion of AgNO₃ into silver nanoparticles (Ag NPs) during the solution preparation. SEM, TEM, FT-IR XPS and XRD confirmed that Ag NPs were doped in the prepared nanofiber membrane successfully and the mechanical properties, pore size distribution and hydrophilicity of the membranes were investigated. The results showed that the tree-like structure improved the mechanical properties and hydrophilicity of the membrane while ensuring high specific surface area and small pore size. And the Ag/PA6 TLNM showed superior antibacterial properties against both E. coli and S. aureus compared with common Ag/PA6 nanofiber membranes (Ag/PA6 NMs). All of the results show that the Ag/PA6 TLNM would have potential applications in water purification.     

Functionalization of graphene nanosheets and its dispersion in PMMA/PEO blend: Thermal,electrical, morphological and rheological analyses

Graphene nanoplatelet (GnP) was chemically functionalized by amine groups for improvement of compatibility in poly(methyl methacrylate) (PMMA)/poly(ethylene oxide) (PEO) blend. PMMA/PEO (90/10) nanocomposites with non-functionalized GnP and functionalized GnP (FGnP) were prepared by solution casting method. Successful grafting of amine groups on the GnP surface was confirmed by Fourier transform infrared (FT-IR) and X-ray diffraction (XRD) analysis. The Transmission electron microscopy (TEM) images showed that the dispersion state of FGnP was better than that of GnP in PMMA/PEO nanocomposites. The effects of FGnP and GnP on rheological, thermal and electrical properties of PMMA/PEO nanocomposites were investigated by various methods. The results indicated that the FGnP-based nanocomposites had higher storage modulus, glass transition temperature and thermal stability as compared to the GnP-based nanocomposites. The electrical conductivity of the nanocomposites with FGnP was better than that of GnP-based nanocomposites. The higher conductivity was attributed to homogeneous and well dispersion state of FGnP in PMMA/PEO nanocomposites.     

Metal oxide/polymer hybrid nanofiber as flexible moisture absorbent

In order to realize flexible organic light emitting diode (OLED), it is critically important to protect moisture and oxygen penetration into the flexible device through the polymer substrates because of intrinsically poor stability of organic materials of OLED to moisture. Since complete protection of the moisture penetration is almost impossible, moisture absorbents are used inside OLED. In this study, metal oxide/polymer hybrid nanofiber with mechanical flexibility and efficient moisture absorption capability was fabricated by electrospinning. Hydrophilic poly(vinyl pyrrolidone) (PVP) or hydrophobic poly(vinylidenefluoride) (PVDF) and calcium oxide (CaO) were used as the fiber forming polymers and as the moisture absorbing particle, respectively. Polymers were first dissolved in appropriate solvents and CaO was then dispersed in the prepared polymer solutions. The hybrid solution was then electrospun, producing the hybrid nanofiber web looking like paper with thickness of about 100 µm. It was observed that all CaO particles were uniformly held by the nanofiber. It was also observed that only a small portion of the surface of CaO particles was covered by fiber since the fiber diameter was much smaller than the CaO particle size. This implied effective moisture absorption through the free surface of CaO. The hybrid nanofiber absorbed moisture very efficiently upto about 70 % of the nanofiber mass. Once moisture was absorbed by the nanofiber, it was never released even at 150 °C in vacuum for 2 hours. It is, therefore, expected that the nanofiber may be applied as the flexible thin moisture absorbent to improve stability of the flexible OLED.     

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.     

Highly hydrophobic nanofibrous surfaces genearated by poly(vinylidene fluoride)

Lotus-leaf-like nanofibrous surfaces were prepared by electrospinning hydrophobic poly(vinylidene fluoride) (PVDF) from a mixed solvent of N,N-dimethylformamide (DMF) and acetone. PVDF fibrous mats with a bead-on-string morphology were generated because the nonpolar acetone decresed the viscosity of the PVDF solution and promoted the evaporation of the solution during electrospinning process. The morphology of the nanofibirous surface was examined by scanning electron microscopy. Micron-sized beads were introduced to the electrospun PVDF mats, resulting in enhanced hydrophobicity of the electrospun mats. The addition of a small amount (0.05 vol%) of acetic acid to the polymer solution effectively improved the bead-on-string morphology of the electrospun mats, and led to a higher water contact angle (WCA). The electrospun PVDF fibrous mat showed a maximum WCA of 148.5° due to the appropriate surface roughness.     

Functionalized graphene nanoplatelets/poly(ethylene oxide) nanocomposites: Correlation between crystallization behavior and mechanical performance

Poly(ethylene oxide) (PEO) nanocomposites containing pristine or functionalized graphene nanoplatelets (FGnP) prepared via solution blending and thermal and mechanical properties of nanocomposites were investigated. Chemical functionalization of graphene nanoplatelets was conducted through an amidation reaction between carboxylic acid groups of acidified graphene and hydroxyl groups of polyethylene glycol (PEG). An interfacial linkage and a good dispersion of FGnP was observed via scanning electron microscope (SEM). Differential scanning calorimetry (DSC) analysis revealed that the degree of crystallinity of samples decreased by addition of graphene nanoplatelets, while the size of spherulites increased as indicated by polarized optical microscope (POM). A lower degree of crystallinity and larger spherulites were detected in the case of FGnP. Filler/matrix interfacial adhesion was also remarkably influenced the mechanical properties of PEO as an effective reinforcement of matrix obtained upon the addition of FGnP nanosheets compared to untreated graphene.     

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.     

Metal ion adsorbability of electrospun wool keratose/silk fibroin blend nanofiber mats

In this study, electrospun wool keratose (WK)/silk fibroin (SF) blend nanofiber was prepared and evaluated as a heavy metal ion adsorbent which can be used in water purification field. The WK, which was a soluble fraction of oxidized wool keratin fiber, was blended with SF in formic acid. The electrospinnability was greatly improved with an increase of SF content. The structure and properties of WK/SF blend nanofibers were investigated by SEM, FTIR, DMTA and tensile test. Among various WK/SF blend ratios, 50/50 blend nanofiber showed an excellent mechanical property. It might be due to some physical interaction between SF and WK molecules although FTIR result did not show any evidence of molecular miscibility. As a result of metal ion adsorption test, WK/SF blend nanofiber mats exhibited high Cu²⁺ adsorption capacity compared with ordinary wool sliver at pH 8.5. It might be due to large specific surface area of nanofiber mat as well as numerous functional groups of WK. Consequently, the WK/SF blend nanofiber mats can be a promising candidate as metal ion adsorption filter.     

Highly porous three-dimensional poly(lactide-co-glycolide) (PLGA) microfibrous scaffold prepared by electrospinning method: A comparison study with other PLGA type scaffolds on its biological evaluation

In this study, a three-dimensional (3D) poly(lactide-co-glycolide) (PLGA) microfibrous scaffold with high porosity (ca. 90 % porosity) was developed for evaluating its performance in tissue engineering application. A dope solution of PLGA/polyethylene oxide (PEO) blend was electrospun into a methanol coagulation bath for fabricating highly porous 3D PLGA scaffold and a salt leaching method was used for making interconnected pores of 100?C200 ??m size inside the scaffold. The morphological structure, pore size and porosity of the microfibrous scaffold were determined, and compared with twodimensional (2D) mat-type and 3D sponge-type of PLGA scaffold. Also, swelling ratio, water uptake and compressive strength were compared in order to elucidate the structure-property relationships of different types of the scaffolds, especially in a wet condition. As a result of scanning electron microscopy (SEM) observation, normal human dermal fibroblasts (nHDF) were migrated, attached, and proliferated well inside the 3D scaffold. MTT assay confirmed that the highly porous 3D PLGA microfibrous scaffold had superior cell adhesion and proliferation abilities due to fibrous structure of large specific surface area, and interconnected pore structure. Therefore, this high performance 3D PLGA scaffold can have a high potentiality for application in tissue engineering in comparison with conventional PLGA scaffolds.     

Mechanical properties and in vitro degradation of PLGA suture manufactured via electrospinning

The current research discusses the efforts to achieve a Poly(lactide-co-glycolide)(PLGA) nanofiber yarn using two differently charged nozzles with potential application as surgery suture. First, electrospinning parameters such as solution concentration, applied voltage, feed rate were optimized to produce yarn with smooth nanofibers. In order to improve the properties of produced suture, heat setting setup was developed. Two heat setting techniques, including hot water and dry heat were applied, and the influence of the heat setting process on the mechanical properties of yarn was studied. The results showed that heat setting with boiling water was the best method. At first strength, E-modulus and extension of prepared suture were 36.6 MPa, 0.9 GPa and 68.8 % respectively. After improvement with heat setting, strength and E-modulus increased to 63.7 MPa, 2.7 GPa respectively and extension decreased to 29.7 %. Finally, in order to analyze knot performance, two types of surgical knot (square and surgeon) were used, and mechanical properties were investigated. The presence of knot lessens mechanical properties for each two type. Square knot showed better mechanical properties than surgeon’s knot. With square knot strength, E-modulus and extension were 62.1 MPa, 2.1 GPa, 28.6 %, respectively. In vitro study of nanofiber yarn degradation behavior showed that the mechanical properties were decreased. This could be due to greater surface area of nanofibers exposed to surrounding environment.     

PEG6000胁迫对大麦幼苗叶片表皮蜡质组分及其透性的影响

为了探究干旱胁迫条件下大麦幼苗叶片表皮蜡质组分和含量与品种保水能力的关系,采用PEG6000模拟干旱胁迫,研究干旱胁迫对大麦幼苗叶片表皮蜡质组分、含量及叶片表皮透性的影响。结果发现,胁迫6d后,大麦幼苗叶片的表皮蜡质总量和各组分含量均呈极显著增加。气相色谱-质谱联用分析表明,大麦幼苗叶片表皮蜡质的主要组分为醇类、酸类、醛类、酮类、烷烃类、酚类、酯类及一些未知物质,其中含量较多的组分为醇类和酸类,其次为醛类,且这三种蜡质组成成分的增加量也相对较多,说明在大麦幼苗叶片蜡质组分中,醇类、酸类和醛类物质的合成是大麦幼苗叶片表皮蜡质对干旱胁迫响应的关键。表皮蜡质的合成受植物体内水分状况的调控,尤其是蜡质组分中的醛类、酮类、醇类和酯类物质的合成受胁迫影响较大,是构成表皮蜡质应激反应的主要成分。蜡质含量高的品种的失水率相对较低,在逆境胁迫下可以保持相对较高的含水量,但除品种垦啤6号外,其他品种的叶绿素浸出率均增加,这可能是由不完整的表皮或蜡质组分中大量的醇类物质造成的。     

Investigation of Parameters for Preparing Nanofiber Yarn via a Stepped Airflow-assisted Electrospinning

Electrospinning is a simple and cost-effective method to prepare fiber with nanometer scale. More importantly, 3D flexible nanofiber yarns that fabricated by electrospinning have shown excellent application prospects in smart textiles, wearable sensors, energy storage devices, tissue engineering, and so on. However, current methods for preparing electrospinning nanofiber yarns had some limitations, including low yarn yield and poor yarn structure. In this paper, a stepped airflow-assisted electrospinning method was designed to prepare continuously twisted nanofiber yarn through introducing stepped airflow into traditional electrospinning system. The stepped airflow could not only help to improve nanofiber yield, but also good for controlling the formed nanofibers to be deposited in a small area. In addition, the experimental methods of single factor variables were used to study the effects of stepped airflow pressure, applied voltage, spinning distance, solution flow rate, air pumping volume and friction roller speed on nanofiber yarn yield, nanofiber diameter, yarn twist and mechanical property. The results showed that prepared nanofiber yarns exhibited perfect morphologies and the yield of nanofiber yarn could reach to a maximum of 4.207 g/h. The breaking strength and elongation at break of the prepared yarn could reach to 23.52 MPa and 30.61 %, respectively.     

Electrospun curcumin loaded poly(lactic acid) nanofiber mat on the flexible crosslinked PVA/PEG membrane film: Characterization and <Emphasis Type="Italic">in vitro</Emphasis> release kinetic study

Herein, a biodegradable and biocompatible composite comprising of support membrane based on crosslinked PVA/PEG film and curcumin loaded electrospun poly(lactic acid) (PLA) nanofiber mat is introduced. The membrane film was prepared from PVA/PEG blend followed by crosslinking with an optimum amount of citric acid, 15 wt.%. After then, PLA solutions with different curcumin content, 0-11 wt.%, were electrospinned on the prepared membrane substrate. The prepared film showed high water absorption, water vapor transmission rate and superior mechanical properties with improved elastic modulus, tensile strength and with an elongation of around 320 % with respect to the non-crosslinked one. Also, the scanning electron microscopy was revealed uniformly dispersed pores throughout the membrane film with a nearly narrow in size distribution centered at 36 μm. As well, a nanostructure porous morphology was found for the electrospun fibrous curcumin loaded PLA from the scanning electron microscopy micrographs and the average fiber diameter was decreased with curcumin content. In vitro drug release from the prepared flexible composite into the vertical diffusion cell was recorded by the measuring curcuminoids content using high performance liquid chromatography and drug release kinetic evaluations were revealed that the release pattern of all prepared samples, containing different content of curcumin, well fitted to the Higuchi’s model signifying diffusion-controlled release mechanism. As well, the determined release rate at the second release stages, i.e. steady state flux (J), was varied from 0.31 to 43.53 μg·cm^-2·h^-1 with increasing drug content from 1 to 11 wt.%. Regarding this results, this flexible composite by providing the moist environment along with miraculous healing properties of curcumin, can be potential candidate for transdermal drug delivery.     

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.     

Preparation of aminated polyacrylonitrile porous fiber mat and its Application for Cr(VI) ion removal

Porous polyacrylonitrile (PAN) fiber mat was prepared by electrospinning PAN in N,N-dimethylformide solution with poly(methyl methacrylate) (PMMA) as pore-forming agent. Then, the porous PAN fiber mat was chemical modified by the tetraethylenepentamine to acquire aminated porous polyacrylonitrile (APPAN) fiber mat. Common aminated PAN fiber mat was also prepared for comparison. The surface morphologies of the APPAN and PAN fiber mat were characterized by scanning electron microscopy (SEM) and the corresponding specific surface areas were also measured. FT-IR/ATR spectra of the APPAN and PAN fiber mat were recorded for analysis of the surface chemical structures. The Cr(VI) absorption results demonstrated that the porous structure in the fiber could obviously increase the absorption capacity of the fiber mat.     

纳米TiO_2/天然橡胶复合材料的抗菌性研究

采用溶胶凝胶法,以钛酸四丁酯掺杂金属Ag制备纳米二氧化钛(Ag-TiO2)水溶胶,并与天然胶乳湿法共混制备得到纳米TiO2/天然橡胶复合材料。紫外可见光谱表明,金属Ag能提高TiO2的光催化性能;透射电子显微镜观察到TiO2颗粒粒径为50nm左右,并且均匀的吸附在胶粒表面。研究此复合材料的抗菌性能结果表明,其具有良好的抗细菌和抗霉菌效果,对大肠杆菌的抗菌率达到90%以上,特别是硫化过后的纳米TiO2/天然橡胶复合材料的抗细菌率更达98.5%。     

Preparation and BSA Adsorption Behavior of Chitosan-arginine Based Nanofiber Membranes

In this work, an affinity nanofiber membrane was successfully prepared by solution blowing of arginine-modified chitosan (CS-Arg) for bovine serum albumin (BSA) adsorption. CS-Arg was firstly synthesized by coupling L-arginine onto chitosan backbone. Then, CS-Arg nanofiber membranes (CANFs) were fabricated using solution blowing process with Polylactide (PLA) as assistant polymer. The results showed that CANFs effectively adsorbed BSA, and the adsorption capacities were influenced by the degrees of substitution (DS) of arginine in CS, pH value, contact time, and initial protein concentration. The highest adsorption capacity of 445.19 mg/g was achieved uvnder the following conditions: DS of 43.7 %, pH of 7.14, and initial concentration of 3.0 mg/ml. BSA adsorbed on the CANFs membrane conformed to Langmuir model, and the adsorption rate was consistent with the second-order kinetics model. This work implies that an arginine-modified chitosan nanofiber-based novel biomaterial has a potential application in adsorption of BSA.     

Gallium arsenide (GaAs) nanofibers by electrospinning technique as future energy server materials

Gallium arsenide (GaAs) does have superior electronic properties compared with silicon. For instant, it has a higher saturated electron velocity and higher electron mobility. Weak mechanical properties and high production cost are the main drawbacks of this interesting semiconductor. In this study, we are introducing production of GaAs nanofibers by electrospinning methodology as a very low cost and yielding distinct product technique. In general, nano-fibrous shape is strongly improving the physical properties due to the high surface area to volume ratio of this nanostructure. The mechanical and environmental properties of the GaAs compound have been modified since GaAs nanofibers have been produced as a core inside a poly(vinyl alcohol) (PVA) shell. GaAs/PVA nanofibers were prepared by electrospinning of gallium nitrate/PVA solution in presence of arsenic vapor. The whole process was carried out in a closed hood equipped with nitrogen environment. FT-IR, XPS, TGA and UV-Vis spectroscopy analyses were utilized to confirm formation of GaAs compound. Transmission electron microscope (TEM) analysis has revealed that the synthesized GaAs compound is crystalline and does have nano-fibrous shape as a core inside PVA nanofibers. To precisely recommend the prepared GaAs nanofiber mats to be utilized in different applications, we have measured the electric conductivity and the band gap energies of the prepared nanofiber mats. Overall, the obtained results affirmed that the proposed strategy successfully remedied the drawbacks of the reported GaAs structures and did not affect the main physical properties of this important semiconductor.     

Tuning the properties of PVDF or PVDF-HFP fibrous materials decorated with ZnO nanoparticles by applying electrospinning alone or in conjunction with electrospraying

Novel composite nanofibrous materials of poly(vinylidene fluoride) (PVDF) or poly(vinylidene fluoride-cohexafluoropropylene) (PVDF-HFP) and ZnO nanoparticles were prepared by conjunction of electrospinning and electrospraying techniques. Simultaneous electrospinning of concentrated solution of PVDF or PVDF-HFP and electrospraying of suspension of ZnO in diluted PVDF or PVDF-HFP solution enable the preparation of materials consisting of fibers on which ZnO was deposited on the fibers’ surface (design type “on”). These fibrous materials were compared with materials consisting of PVDF or PVDF-HFP fibers in which ZnO was incorporated in the fibers (design type “in”) and which were obtained by one-pot electrospinning of a suspension of ZnO nanoparticles in concentrated PVDF or PVDF-HFP solution. The fiber morphology and the presence of ZnO “in” or “on” the fibers were observed by scanning electron microscopy (SEM) and by transmission electron microscopy (TEM). The effect of the used technique on the type, size and shape of the obtained structures was discussed. The fibrous mats were studied by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), X-ray diffraction (XRD), contact angle measurements and mechanical tests as well. It was found that the decoration of fibers with ZnO resulted in increase of their thermal stability and hydrophobicity. The microbiological tests showed that the materials of design type “on” possessed strong antibacterial activity against the pathogenic microorganism Staphylococcus aureus. The results suggest that, due to their antibacterial activity, the obtained composite materials are suitable for wound dressing applications.     

PAN-based carbon nanofiber absorbents prepared using electrospinning

This study takes polyacrylonitrile (PAN) as a raw material for PAN-based nanofiber nonwoven prepared using electrospinning. First we construct a thermal-stable process for the fabrication of oxidized nanofiber nonwovens as the precursor. A semi-open high-temperature erect furnace is then used with steam as the activator, through carbonization and activation processes to prepare carbon nanofiber absorbents continuously. The experiment varies the production rate and activator flow rate to prepare carbon nanofiber absorbents. Experimental results show that carbon nanofiber adsorbents are primarily made up of micropores and mesopores, averaging under 20 Å. Given a production rate of 10–20 cm/min with a matching activator feed rate of 120 ml/min, the specific surface area can reach about 1000 m²/g, producing an adsorption ratio of carbon tetrachloride over 200 %.