It is difficult to produce rubbery polymer nanofibers, that is, polybutadiene, by the method of electrospinning, since during electrospinning rubbery polymer fibers join and entangles due to their low Tg. For this reason, it is not easy to achieve the fiber form out of these polymers. Homogeneously electrospun carbon nanotubes (CNT)‐filled polybutadiene (PBu) and poly(ethylene oxide) (PEO) composite elastomeric fibers exhibit distinctive physical features such as uniform fiber diameter and distribution with significant improvements in thermomechanical properties. Controlled hydrophilicity/hydrophobicity with the components allows to generate homogenous, thermally stable and stretchable bio‐composite scaffold, and fibrous antibacterial membrane scaffolds out of PBu/PEO/CNT composite. We have combined the exciting properties of PEO with high pore density with the rubber elasticity of PBu via dissolving them in a dichloromethane/ethyl acetate organic solvent, and subsequently producing electrospun woven fibers with different PBu/PEO ratios. Frequency‐dependent thermomechanical characterization via dynamic mechanical analysis reveals pronounced changes in the onset and extent of melting, as well as the storage and loss modulus values at the onset of melting, in particular when small amounts (1.25% by wt%) of CNTs are present. The characteristic bands were detected for the PBu/PEO and PBu/PEO/CNT samples by means of Raman and Fourier‐transform infrared spectroscopy. CNT addition increases the hydrophobicity via the increase in roughness as attained by atomic force microscopy. 相似文献
Two series of functional polymers, α,ω‐bi[2,4‐dinitrophenyl][poly(ethylene oxide)‐b‐poly(2‐methoxystyrene)‐b‐poly(ethylene oxide)] (DNP‐PEO‐P2MS‐PEO‐DNP) and α,ω‐bi[2,4‐dinitrophenyl caproic][poly(ethylene oxide)‐b‐poly(2‐methoxystyrene)‐b‐poly(ethylene oxide)] (CDNP‐PEO‐P2MS‐PEO‐CDNP), were synthesized by anionic living polymerization. The polymers were characterized by FT‐IR, 1H‐NMR and Gel Permeation Chromatography (GPC). The molecular weight distributions for the lower molecular weight functional polymers were slightly broad (1.3–1.5). However, the molecular weight distributions for higher molecular weight polymers were narrower (1.1–1.2). Differential scanning calorimetry (DSC) studies showed thermal transitions indicative of the presence of microphases in the polymer solid state. The polymers were white powders and soluble in tetrahydrofuran. The binding affinity of DNP‐PEO‐P2MS‐PEO‐DNP ligands towards anti DNP IgE was determined by titrations with fluorescently labeled FITC‐IgE. A water soluble CDNP‐PEO‐P2MS‐PEO‐CDNP/DMEG (dimethoxyethylene glycol) complex binds and achieves steady state binding with solution IgE within a few seconds. This strongly suggests that CDNP functional polymers with improved water solubility have potential in therapeutics. Higher molecular weight (water insoluble) CDNP‐PEO‐P2MS‐PEO‐CDNP polymers were electrosprayed as fibers (500 nm) on silicon surface. Fluorescence spectroscopy clearly showed that RBL mast cells were interacting with the fibers suggesting that the cell‐surface receptors were clustered along the fiber surface. These observations suggest that the functional polymers hold promise for developing an antibody detection device. 相似文献
Summary: Electrically conducting polypyrrole‐poly(ethylene oxide) (PPy‐PEO) composite nanofibers are fabricated via a two‐step process. First, FeCl3‐containing PEO nanofibers are produced by electrospinning. Second, the PEO‐FeCl3 electrospun fibers are exposed to pyrrole vapor for the synthesis of polypyrrole. The vapor phase polymerization occurs through the diffusion of pyrrole monomer into the nanofibers. The collected non‐woven fiber mat is composed of 96 ± 30 nm diameter PPy‐PEO nanofibers. FT‐IR, XPS, and conductivity measurements confirm polypyrrole synthesis in the nanofiber.
An SEM image of the PPy‐PEO composite nanofibers. The scale bar in the image is 500 nm. 相似文献
Fairly uniform chitosan (CS)/poly(ethylene oxide) (PEO) ultrafine fibers containing silver nanoparticles (AgNPs) were successfully
prepared by electrospinning of CS/PEO solutions containing Ag/CS colloids by means of in situ chemical reduction of Ag ions.
The presence of AgNPs in the electrospun ultrafine fibers was confirmed by X-ray diffraction patterns. The AgNPs were evenly
distributed in CS/PEO ultrafine fibers with the size less than 5 nm observed under a transmission electron microscope. X-ray
photoelectron spectroscopy suggested that the existence of Ag―O bond in the composite ultrafine fibers led to the tight combination
between Ag and CS. Evaluation of antimicrobial activities of the electrospun Ag/CS/PEO fibrous membranes against Escherichia coli showed that the AgNPs in the ultrafine fibers significantly enhanced the inactivation of bacteria. 相似文献
Biopolymer chitosan was used to modify the mechanical properties of soluble eggshell membrane protein(SEP) films.The SEP/chitosan blend films were prepared by solution casting from 10%aqueous acetic acid.Tensile strength and elongation at break of the blend films increased with increasing amount of chitosan.Microphase separation was observed by field emission scanning electron microscopy,although interaction between the two components was revealed by FTIR.The biocompatibility of SEP/chitosan blend films ... 相似文献
Summary: Uniform core‐sheath nanofibers are prepared by electrospinning a water‐in‐oil emulsion in which the aqueous phase consists of a poly(ethylene oxide) (PEO) solution in water and the oily phase is a chloroform solution of an amphiphilic poly(ethylene glycol)‐poly(L ‐lactic acid) (PEG‐PLA) diblock copolymer. The obtained fibers are composed of a PEO core and a PEG‐PLA sheath with a sharp boundary in between. By adjusting the emulsion composition and the emulsification parameters, the overall fiber size and the relative diameters of the core and the sheath can be changed. A mechanism is proposed to explain the process of transformation from the emulsion to the core‐sheath fibers, i.e., the stretching and evaporation induced de‐emulsification. In principle, this process can be applied to other systems to prepare core‐sheath fibers in place of concentric electrospinning and it is especially suitable for fabricating composite nanofibers that contain water‐soluble drugs.
Schematic mechanism for the formation of core‐sheath composite fibers during emulsion electrospinning. 相似文献
The present study describes the harnessing of revalued cow milk (denoted as waste milk) for fabricating casein fibers (CAS) with enhanced mechanical performance and antibacterial properties by the electrospinning method. For this purpose, polyethylene oxide (PEO) was employed (10 and 20 wt%) as a binder for the appropriate electrospun CAS fibers. Different amount of tannic acid (TA) was incorporated into casein/polyethylene oxide fibers (CAS/PEO) as a crosslinker agent, bringing filaments with a diameter of ca. 2 µm. The incorporation of 4 wt% of TA promotes the fibers' reticulation, forming a stable three-dimensional network. Also, the mechanical performance of CAS/PEO fibers was improved, where the tensile strength was increased from 0.91 MPa to 1.88 MPa with 4 % of TA, while the breaking elongation was increased from 93.74 % to 274.56 %. This behavior benefits the processing of fibers by electrospinning. Furthermore, the TA addition during the electrospun of CAS/PEO fibers enhances fibers' wettability properties and thermal stability induced by the crosslinker agent. Additionally, the antibacterial activity (AA) test demonstrates that CAS fibers can inhibit the growth of Gram-positive S. aureus and Gram-negative E. coli after 0.5 h, 1.5 h, 3 h, and 24 h of contact, which is generated by the TA addition. Our results suggest that the electrospun fabrication of CAS/PEO fibers with TA as a crosslinker agent represents an innovative harnessing of waste milk to produce functional textiles with potential biological application. 相似文献
The electrospinning technique was used to spin ultra-thin fibers from several polymer/solvent systems. The diameter of the electrospun fibers ranged from 16 nm to 2 μm. The morphology of these fibers was investigated with an atomic force microscope (AFM) and an optical microscope. Polyethylene oxide) (PEO) dissolved in water or chloroform was studied in greater detail. PEO fibers spun from aqueous solution show a “beads on a string” morphology. An AFM study showed that the surface of these fibers is highly ordered. The “beads on a string” morphology can be avoided if PEO is spun from solution in chloroform; the resulting fibers show a lamellar morphology. Polyvinylalcohol (PVA) dissolved in water and cellulose acetate dissolved in acetone were additional polymer/solvent systems which were investigated. Furthermore, the electrospinning process was studied: different experimental lay-outs were tested, electrostatic fields were simulated, and voltage - current characteristics of the electrospinning process were recorded. 相似文献
Centrifugal force spinning (CFS), also known as centrifugal spinning, forcespinning, or rotary jet spinning, provides considerably higher production rates than electrospinning (ES), but the more widespread use of CFS as an alternative depends on the ability to produce fibers with robust thermal and mechanical properties. Here, we report the CFS of poly(ethylene oxide) (PEO) fibers made using a spinning dope formulated with acetonitrile (AcN) as the volatile solvent, and we describe the thermal and mechanical properties of the centrifugally-spun fibers. Even though the formation, diameter, and morphology of electrospun and centrifugally-spun PEO fibers are relatively well-studied, the article presents three crucial contributions: the pioneering use of PEO solutions in AcN as spinning dope, characterization of crystallinity and mechanical properties of the centrifugally-spun PEO fibers, and a comparison with the corresponding properties of electrospun fibers. We find that fiber formation occurrs for the chosen CFS conditions if polymer concentration exceeds the entanglement concentration, determined from the measured specific viscosity. Most significantly, the centrifugally spun PEO fibers display crystallinity, modulus, elongation-at-break, and fiber diameter that rival the properties of electrospun PEO fibers reported in the literature. 相似文献
Polydiacetylenes (PDAs), a family of conjugated polymers, are very intriguing materials in several aspects. Especially, the stimulus‐induced apparent blue‐to‐red transition of the PDAs has led to the development of a variety of PDA‐based chemosensors. In the current work, we synthesized PDA monomers bearing trimethyl amine (PCDA‐DMEDA) and incorporated them with Poly(ethylene oxide) (PEO) into electrospun fibers. For the first time, we successfully demonstrated that PDA‐based electrospun fibers can be used for the naked‐eye detection of HCl gas by simple color change (blue to red). 相似文献
Composites of electrospun poly(ethylene oxide) (PEO) fibers and silver nanoparticles (Ag NPs) were used as a soft template for coating with TiO2 by atomic layer deposition (ALD). Whereas the as‐deposited TiO2 layers on PEO fibers and Ag NPs were completely amorphous, the TiO2 layers were transformed into polycrystalline TiO2 nanotubes (NTs) with embedded Ag NPs after calcination. Their plasmonic effect can be controlled by varying the thickness of the dielectric Al2O3 spacer between Ag NPs and dye molecules by means of the ALD process. Electronic and spectroscopic analyses demonstrated enhanced photocurrent generation and solar‐cell performance due to the intense electromagnetic field of the dye resulting from the surface plasmon effect of the Ag NPs. 相似文献