361 resultados para needleless electrospinning


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Copper/poly(vinyl alcohol) (PVA) nanocables have been successfully obtained by electrospinning a PVA-protected copper nanoparticle solution. The molar ratio of copper ions to PVA (in terms of VA repeating units) plays an important role in the formation of copper/PVA nanocables. The average diameter of the copper cores and PVA shells is about 100 and 400 nm, respectively. The structures of the copper/PVA nanocables are characterized by transmission electron microscopy (TEM) and their formation is confirmed by scanning electron microscopy (SEM).

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A polyacrylonitrile (PAN) nanofiber containing Ag nanoparticles was prepared by an electrospinning technology. To prevent the nanoparticles from coagulating in polymer solutions, an approach of in-situ preparing nanoparticles in PAN solution was used. Diameters of the nanoparticles and nanofiber as well as distribution of the former in the latter were characterized by Transmission electron microscopy. Crystal structure of the nanoparticles was given by X-ray diffraction. Absorption spectrum of the nanocomposites was measured by UV-Vis. Conductivity of the nanocomposites was compared with the pure PAN nanofiber.

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The present article describes a new titanium oxide‐based (TiO2) photocatalyst that shows promise for acceleration of dye degradation. A hierarchical TiO2 nanostructure comprising nanorods on‐nanofibres has been prepared using a sol–gel route and electrospinning. Calcination of electrospun nanobre mats was performed in air at 500 °C. The TiO2 nanofibre surface was then exploited as a ‘seeding ground’ to grow TiO2 nanorods by a solvothermal process in NaOH. The nanofibres had a diameter of approximately 100 nm while the nanorods were evenly distributed on the nanofibre surface with a mean diameter of around 50–80 nm. The hierarchical nanostructure showed enhanced photocatalytic activity when compared to pure TiO2 nanofibres. This improved efficiency in degrading methylene blue through the photocatalytic process was attributed to the larger specific surface area of the TiO2 nanostructures, as well as high surface‐to‐volume ratio and higher reactive surface resulting in enhanced surface adsorption and interfacial redox reaction.

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In this study, two power supplies having positive/ground and negative/ground electrode output ends were used separately for electrospinning of polyacrylonitrile nanofibers. Depending on type of power supply and electrode connection, electrospinning led to different fiber diameters and deposition areas. The nozzle was connected to a high voltage end while the collector was grounded. Regardless of power supply used, finer fibers with a larger deposition area were obtained, compared to that using the same setup but with a reverse electrode connection. With an increase in the applied voltage, fiber deposition area, and productivity increased for all electrode connections. Grounded nozzles provide much better control over fiber deposition than the reverse electrode connections. Finite element modeling was used to analyze the electric field profile in the electrospinning zone. It was revealed that high electric intensity was mainly located in the part that was charged with a high voltage electrode, which could explain the differences in fiber diameter and deposition area.

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This paper investigates the preparation and electrospinning of acidified-oxidized potato starch. In this article, acidified-oxidized potato starch was prepared by adding ammonium persulfate as an oxidizing agent and hydrochloric acid as a catalyst. The effect of reaction time, temperature, the concentration of hydrochloric acid and the content of ammonium persulfate on the viscosity and content of carboxyl were discussed. The optimum reaction conditions were as follows: 1.5 hours ,50℃, 0.5mol/l HCl, 2.5% (NH4)2S2O8. And then, the acidified-oxidized potato starch prepared at the optimum condition was dissolved in dimethyl sulfoxide (DMSO) to be electrospinned by contrast to native starch. Electrospinning of 5wt%-21wt% of modified starch in DMSO produced beads, beaded fibers, and smooth fibers, depending on the concentration range. Smooth fibers were observed until the concentration reached 19wt%, while native starch was 5wt%.

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A special Micro-Nano fiberous composite structure composed of nano- and micro-scale fiber of Polycaprolactone (PCL) and Gelatin produced by using single nozzle electrospinning instrument. By controlling the solution (polymer concentration and polymer composition percent) and processing parameters of electrospinning (feed rate and electrostatic field), different portion of nano and micro fibers in the structure is achieved. This method can result a one-stage method of fabrication of Micro-Nano fiberous composite structure instead of previously used twostage process or using additional facility to produce structure near-similar to this composite structure. The resulting materials finely mingle nano- and micro fibers together, rather than simply juxtaposing them, as is commonly found in the literature. The results obtained from SEM, Flow Porosimetry, and DMA led the authors to confirm that the structure has very versatile and improved properties for many applications like cell culture scaffolds. These favourable mechanical and structural properties can provide easier opening of spaces for cell penetration to deeper levels of the scaffold and withstand to tensions during to clinical handling.

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In this study, the formation of polystyrene (PS) nanofibers during electrospinning process was investigated using a simple coagulation method. The fiber diameter, bead size and bead density of the PS nanofibers electrospun from the solutions with three different PS concentrations were studied. It revealed that the initial stage of electrospinning was responsible for fiber thinning, while the later stage is responsible for improving the fiber uniformity.

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In this work, a spinning metal wire collector was employed to continuously collect polyacrylonitrile (PAN) nanofibers produced by a disc fiber generator and coil them around a polyethylene terephthalate (PET) yarn. The obtained composite yarns exhibited a core/shell structure (PET yarn/PAN nanofibers) with nanofibers orderly arranged on the surface of the PET yarn. The electric field analysis showed that the position of metal wire had insignificant effect on the formed electric field and high intensity electric field was formed at the disc circumferential area, which provided a constant electric field for the production of uniform nanofibers. The spinning solution, spinning speed of metal wire, and winding speed were found to play an important role in producing good quality nanofiber yarns, in terms of morphology, strength, and productivity. Pure nanofiber yarns were obtained after dissolving the core yarns in a proper solvent. This method has shown potential for the mass production of nanofiber yarns for industrial applications.