Here, a novel melt electrospinning method to produce few‐micron and nanometer thick fibers is presented, in which a polymer‐coated wire with a sharp tip is used as the polymer source. The polymer coating is melted via Joule heating of the source wire and extracted toward the target via electrostatic forces. The high viscosity and low charge density of polymer melts lower their stretchability in melt. The method relies on confining the Taylor cone and reducing initial jet diameter via concentrated electrostatic fields as a means to reduce the diameter of fibers. As a result, the initial jet diameter and the final fiber diameter are reduced by an order of magnitude of three to ten times, respectively, using wire melt electrospinning compared to syringe‐ and edge‐based electrospinning. The fiber diameter melt electrospun via this novel method is 1.0 ± 0.9 µm, considerably thinner than conventional melt electrospinning techniques. The generation of thin fibers are explained in terms of the electrostatic field around the wire tip, as obtained from finite element analysis (FEA), which controls the size and shape of the melt electrospun jet.

In this study, both modeling and experimental approaches are used to demonstrate that downstream volumetric heating of electrospun fibers during melt electrospinning can result in markedly decreased fiber diameters. Previous melt electrospinning techniques were limited to production of micron‐sized fibers. This is because high viscosity and low electrical conductivity of the polymer melt coupled with rapid heat loss to the surroundings resulted in solidification of the jet before it had been significantly stretched by the electric field. In our study, we utilize a model for non‐isothermal melt electrospinning in the presence of a volumetric heat source. Our simulation results demonstrate that downstream heating does reduce the fiber diameter, and is therefore a feasible approach for resolving the limitations of melt electrospinning. In addition, our model has also been used to capture the effect of the surrounding temperature, which affects the thinning of the fiber through surface rather than volumetric interactions. Finally, melt electrospinning experiments are utilized to validate the model predictions for downstream heating. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017, 55, 1393–1405

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We have demonstrated noncontact heating of melt electrospun polymer fibers by using radio-frequency (RF) fields which heat carbon nanotube (CNT) receptors inside the fibers. RF radiation is attractive as it allows for noncontact heating of polymers with low concentrations of CNTs. We observed that the heating rate scales with the CNT loading even below the bulk electrical percolation threshold, suggesting that individual CNTs can serve as RF receptors/heat sources. This capability eliminates the requirement for a percolated network of CNTs inside a fiber as a means to enable heating. We also showed that a strong radial temperature gradient will develop within the fibers. For a 2 μm diameter fiber, the temperature of the core is 10−15 °C higher than the surface. Hence, the temperature of the core can surpass the melting temperature inside the fiber without altering the morphology of the fibers (i.e., without fusing between fibers). These electrospun fibers that can be stimulated through RF energy can be used for applications such as plastic electric heaters, hyperthermia treatment, and heatgenerating textiles.

Electrospinning is commonly used for fabrication of polymer fibers. Melt electrospinning, instead of the commonly used solution electrospinning, offers many advantages in generating polymer fibers without using solvents. However, polymer melts have high viscosity which poses major limitations in producing low diameter fibers. Here, melt electrospinning is investigated at elevated temperatures in inert atmosphere to reduce fiber diameters while suppressing thermal degradation. Two types of spinneret configurations, syringe and wire, with two distinct outcomes are studied. In syringe‐based electrospinning, increasing the nozzle temperature from 300 to 360 °C in nitrogen reduced fiber diameter significantly from 33 ± 5 to 10 ± 4 µm. Electrospinning in nitrogen leads to formation of fibers even at a high nozzle temperature of 360 °C, while this temperature leads to thermal degradation when spinning in air. In contrast, increasing the temperature of wire electrospinning setup do not lead to a noticeable reduction in diameter. This is attributed to the viscosity‐dependent flow rate in this method. Increasing the temperature leads to increased flow rates, promoting the formation of thicker fibers, while the increased stretchability promotes the formation of thinner fibers. The results clearly demonstrate advantages of developing polymer microfibers in inert atmosphere to avoid thermal degradation with a temperature‐independent flow control.