Shape Memory Polymer Process Development

Superior two-dimensional filters can be fabricated easily via electrospinning.

This work introduces a simple technique of separately fabricating electrospun short fibers. This technique employs a paper mesh, which is placed between the needle tip and counter electrode of the electrospinning unit. Usability of this technique was examined by fabricating fine fibers consisting of different kinds of polymers.

(Left) The setup of the Electrospinning apparatus. A highly charged polymer solution or melt loaded in a syringe is spewed out from the syringe needle and travels toward the counter electrode, which serves as a fiber collector because of the high electric field. Consequently, fine fibers are formed on the counter electrode. Those fibers formed are always laid on the counter electrode horizontally, and it is a benefit for fabricating a dense nonwoven fiber mat (right).
For the electrospinning apparatus, a highly charged polymer solution or melt loaded in a syringe is spewed out from the syringe needle and travels toward the counter electrode, which serves as a fiber collector because of the high electric field. Consequently, fine fibers are formed on the counter electrode. Those fibers formed are always laid on the counter electrode horizontally, and it is a benefit for fabricating a dense, nonwoven fiber mat. On the other hand, it becomes a drawback when it comes to extracting fine fibers separately, since the fibers collected on the counter electrodes stick to one another.

It was observed in the electrospinning that partially blocking the traveling path of the highly charged polymer between the needle tip and counter electrode with a cardboard frame resulted in the formation of fibers between the cardboard frame and the counter electrode vertically to the counter electrode. This phenomenon was employed for separately fabricating electrospun short fibers.

Two kinds of polymer solutions were prepared to be electro-spun: 2.5 g of polynorobornen (PN) was dissolved into 50 g of THF in the water bath at 70 °C. Once it was fully dissolved, it was cooled down to room temperature; 11.5g of polyvinyl acetate (PVAc) was dissolved into 100g of DMF in the water bath at 70 °C. Once it was fully dissolved, it was cooled down to room temperature.

Using the setup without a paper mesh, the electrospinning of PN and PVAc was carried out, where the voltage was ~10 kV and the gap between the needle tip and counter electrode was ~10 cm. The PN fibers were formed horizontally to the counter electrode surface and stuck together. These fibers could not be extracted separately. PVAc fibers were also formed on the counter electrode surface horizontally.

The highly charged polymer solution in the syringe was spewed out toward the counter electrode under the high voltage, where the voltage was ~10 kV and the gap between the needle tip and counter electrode was ~10 cm. It passed through the paper mesh, resulting in the formation of fine fibers separately between the paper mesh and counter electrode. Compared with PN fibers, the fiber diameter was quite large. Fiber diameter heavily depends on the condition of electrospinning such as voltage, gap between the needle tip and counter electrode, and the ratio of PN and solvent. Since it was difficult to precisely control the experimental condition, it was difficult to fabricate the same-diameter fibers. It was confirmed that the paper mesh method could be used for fabricating the PN fibers separately.

The formation process of the separately formed short fibers was considered. Fiber ingredient is spewed out from the needle tip, and it travels toward the paper mesh. It is trapped with the mesh and immediately it is stretched toward the counter electrode, resulting in the short fiber formation. Using a high-speed camera, the fiber formation process was analyzed. Once the voltage was applied between the syringe needle tip and counter electrode, the fiber ingredient was continuously supplied to the paper mesh. The polymer supply continued from beginning to end in this experiment. But fiber formation between the needle tip and counter electrode was not induced for a while, even after the start of the polymer supply at t=0 ms. Fiber formation suddenly started at t=40 ms. The fiber continued to grow and was completed at t=160 ms. During the fiber-growing process, the fiber initially kept on waving but gradually subsided to stillness.

The fiber formation was not a continuous process. First, the fiber ingredient accumulated on the paper mesh. Secondly, the fiber jet was suddenly spewed out from the paper mesh to the counter electrode, resulting in a fiber. Since there were a number of holes on the paper mesh, fiber formation was induced not only at one hole, but at multiple holes. Even though the supply of fiber ingredient continued at single position of paper mesh, the accumulated fiber ingredient flew to the multiple holes of the paper mesh, eventually resulting in the fiber formation from those multiple holes. A number of short fibers were formed between the multiple holes of paper mesh and the counter electrode.

This fiber fabrication technique was applicable for the fabrication of polymer-metal composite fibers, but it is important to use a highly volatile solvent for the preparation of the polymer ingredient to be electrospun. Otherwise, the fibers are not effectively formed separately.

This work was done by Hirohisa Tamagawa of Gifu University, Japan, for the Asian Office of Aerospace Research and Development. For more information, download the Technical Support Package (free white paper) at www.defensetechbriefs.com/tsp  under the Manufacturing & Prototyping category. AFRL-0153



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Shape Memory Polymer Process Development

(reference AFRL-0153) is currently available for download from the TSP library.

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