Experimental verification of theoretical prediction of fiber to fiber contacts in electrospun multilayer nano-microfibrous assemblies: effect of fiber diameter and network porosity

Average number of fiber-to-fiber contacts in a fibrous structure is a prerequisite to investigate the mechanical, optical and transport properties of stochastic nanomicrofibrous networks. In this research work, based on theoretical analysis presented for the estimation of the number of contacts between fibers in electrospun random multilayer nanofibrous assembles, experimental verification for theoretical dependence of fiber diameter and network porosity on the fiber to fiber contacts has been provided. The analytical model formulated is compared with the existing theories to predict the average number of fiber contacts of nanofiber structures. The effect of fiber diameters and network porosities on average number of fiber contacts of nano-microfiber mats has been investigated. A comparison is also made between the experimental and theoretical number of inter-fiber contacts of multilayer electrospun random nanomicrofibrous networks. It has been found that both the fiber diameter and the network porosity have significant effects on the properties of fiber-to-fiber contacts.

Overcoming interfacial affinity issues in natural fiber reinforced polylactide biocomposites by surface adsorption of amphiphilic block copolymers

This work demonstrates that the interfacial properties in a natural fiber reinforced polylactide biocomposite can be tailored through surface adsorption of amphiphilic and biodegradable poly (ethylene glycol)-b-poly-(L-lactide) (PEG-PLLA) block copolymers. The deposition from solvent solution of PEG-PLLA copolymers onto the fibrous substrate induced distinct mechanisms of molecular organization at the cellulosic interface, which are correlated to the hydrophobic/hydrophilic ratios and the type of solvent used. The findings of the study evidenced that the performance of the corresponding biocomposites with polylactide were effectively enhanced by using these copolymers as interfacial coupling agents. During the fabrication stage, diffusion of the polylactide in the melt induced a change in the environment surrounding block copolymers which became hydrophobic. It is proposed that molecular reorganization of the block copolymers at the interface occurred, which favored the interactions with both the hydrophilic fibers and hydrophobic polylactide matrix. The strong interactions such as intra- and intermolecular hydrogen bonds formed across the fiber−matrix interface can be accounted for the enhancement in properties displayed by the biocomposites. Although the results reported here are confined, this concept is unique as it shows that by tuning the amphiphilicity and the type of building blocks, it is possible to control the surface properties of the substrate by self-assembly and disassembly of the amphiphiles for functional materials.