The high-throughput atomization of polymer solutions for fiber synthesis in a single step aided with corona ionizers

• Published in: Scientific reports 2023-08, Vol.13 (1), p.12639-12639, Article 12639
• Main Authors: Modesto-López, Luis B., Gañán-Calvo, Alfonso M.
• Format: Article
• Language: English
• Subjects: 639/166; 639/766/189; Air flow; Electric fields; Fabrication; Fibers; Filter media; Flow rates; Humanities and Social Sciences; multidisciplinary; Nanotechnology; Nanotubes; Polymers; Polyvinylpyrrolidone; Science; Science (multidisciplinary); Wound healing
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-39801-3

Polymer microfibers are ubiquitous structures across virtually all technological fields. Their applications include, for instance, filter media, tissue regeneration, wound healing and dressing, and reinforcement materials. The most effective methods for fabrication of fibrous micro and nanomaterials rely on electric fields to spin a liquid jet into an ultrafine thread that rapidly dries up forming a fiber. Continuous spinning and collection leads to formation of fiber mats. Here we report a robust yet simple approach for the massive production of liquid threads, which upon acquiring electrical charges in-flight are collected downstream in the form of fibers. The entire process takes place on-line in a single step. The liquid threads are produced through the fragmentation of a polymer solution bulk due to a turbulent interaction of a gas–liquid interface in the interior of an engineered device, a so-called Flow Blurring atomizer. The particularity of this approach consists precisely in such vigorous interaction, at the micrometer scale, which triggers a bubbly motion in the interior of the device, that is a “micro-mixing”. Subsequently, the threads are passed through ionized air currents, at ambient conditions, and then stretched to sub-micrometer dimensions by electric fields. Polyvinylpyrrolidone (PVP) as well as carbon nanotubes (CNTs) or graphene oxide sheets (GOSs)-containing PVP fibers, with diameters in the range 100–900 nm, were synthesized via this approach. In the cases studied herein the method was operated at liquid flow rates (i.e. production rates) of 0.2 mL/min but it could be readily increased up to a few tens of mL/min. The method requires further improvement and optimization, nevertheless it is a promising alternative for mass production of polymer fibers.