Elif Ozden-Yenigun

MWCNTs/P(St-co-GMA) Composite Nanofibers of Engineered Interface Chemistry for Epoxy Matrix Nanocomposites

Strengthened nanofiber-reinforced epoxy matrix composites are demonstrated by engineering composite electrospun fibers of multi-walled carbon nanotubes (MWCNTs) and reactive P(St-co-GMA). MWCNTs are incorporated into surface-modified, reactive P(St-co-GMA) nanofibers by electrospinning; functionalization of these MWCNT/P(St-co-GMA) composite nanofibers with epoxide moieties facilitates bonding at the interface of the cross-linked fibers and the epoxy matrix, effectively reinforcing and toughening the epoxy resin. Rheological properties are determined and thermodynamic stabilization is demonstrated for MWCNTs in the P(St-co-GMA)-DMF polymer solution. Homogeneity and uniformity of the fiber formation within the electrospun mats are achieved at polymer concentration of 30 wt %. Results show that the MWCNT fraction decreases the polymer solution viscosity, yielding a narrower fiber diameter. The fiber diameter drops from an average of 630 nm to 460 nm, as the MWCNTs wt fraction (1, 1.5, and 2%) is increased. The electrospun nanofibers of the MWCNTs/P(St-co-GMA) composite are also embedded into an epoxy resin to investigate their reinforcing abilities. A significant increase in the mechanical response is observed, up to >20% in flexural modulus, when compared to neat epoxy, despite a very low composite fiber weight fraction (at about 0.2% by a single-layer fibrous mat). The increase is attributed to the combined effect of the two factors the inherent strength of the well-dispersed MWCNTs and the surface chemistry of the electrospun fibers that have been modified with epoxide to enable cross-linking between the polymer matrix and the nanofibers.

Polyacrylonitrile (PAN)/crown ether composite nanofibers for the selective adsorption of cations

In this study, we prepared electrospun polyacrylonitrile (PAN) nanofibers functionalized with dibenzo-18-crown-6 (DB18C6) crown ether and showed the potential of these fibers for the selective recovery of K+ from other both mono- and divalent ions in aqueous solutions. Nanofibers were characterized by SEM, FTIR and TGA. SEM results showed that the crown ether addition resulted in thicker nanofibers and higher mean fiber diameters, in a range of 138 to 270 nm. Batch adsorption experiments were conducted in order to evaluate the potential of the crown ether modified nanofibers as an adsorbent for ion removal. The maximum adsorption capacity of the crown ether modified nanofibers for K+ was 0.37 mmol g−1 and the nanofibers followed the selectivity sequence of K+ > Ba2+ > Na+ ∼ Li+ for single ion experiments. Adsorption of Ba2+ ions onto crown ether-modified nanofiber was examined by XPS and the results confirmed the adsorption of the ion. Mixed ion adsorption experiments revealed competitive adsorption between K+ and Ba2+ ions for the available binding sites. This effect was not observed for the other monovalent ions present in the solution and exceptionally high selectivities for K+ over Li+ and Na+ were obtained. Also the crown ether modified nanofibers exhibited good regeneration properties and a good reusability over multiple consecutive adsorption–desorption cycles. Electrospinning is thus shown to be a very versatile tool to prepare crown ether functional polymer adsorbents for the selective recovery of ions.

Nanofiber-enhanced lightweight composite textiles for acoustic applications

This paper proposes lightweight textile acoustic structure, wherein electrospun polyacrylonitrile-based nanofibers enhance sound absorption properties with no weight and thickness penalty. Polyacrylonitrile nanofibers with diameter of 110 ± 7 nm were electrospun on spacer-knitted fabrics by varying deposition amount and surface coating arrangement. Proposed novel approach eliminated additional processing steps such as handling and post-lamination and provided easy scalability of nanofibers at macro-scale. The results showed that the sound absorption of nano-enhanced specimens was improved drastically when deposited amount of nanofibers or its effective surface area increased. Sound propagation paths in different configurations were interpreted from sound absorption and air permeability measurements. The sound absorption coefficient values up to 0.7 are achieved in the low and medium frequency ranges with no weight and thickness penalty by tuning deposition amount and surface coating arrangement.

The stability and dispersion of carbon nanotube-polymer solutions: A molecular dynamics study:

Carbon nanotubes have been explored to increase the mechanical properties and electrical conductivity of polymeric fibers through compounding with polymer to be extruded into fibers. However, this route creates major challenges because carbon nanotubes have strong cohesion and tend to aggregate and precipitate due to their poor interfacial interaction with polymers. In this study, classical molecular dynamics simulations are used to predict and characterize carbon nanotubes-polymer interface mechanism in two different polymer matrices: polyvinyl butyral and polystyrene-co-glycidyl methacrylate. The dominated interface mechanisms are discovered to shed light on carbon nanotubes dispersion in solvent based systems and to explore the prerequisites for stabilized nanofluids. Our results showed that π-stacking interactions between aromatic groups and graphene surfaces of carbon nanotubes as in polystyrene-co-glycidyl methacrylate systems, play an important role in dispersion of carbon nanotubes, whereas slight repulsions between carbon nanotubes and polyvinyl butyral chains lead to large morphological differences and carbon nanotubes bundles in many chain systems. Altogether, the results indicated that polymers with structures having strong interactions with the surfaces of carbon nanotubes through π–π interactions are more effective in dispersing carbon nanotubes and caused stabilized solutions in wet fiber processing.

Macroscopic assembly of flexible and strong green graphene fibres

Graphene fibres have great potential in future wearable electronics due to their promising thermal and electrical properties. However, fibre brittleness limits their implementation and researchers are still seeking easily scalable and eco-friendly production methods. Here we propose a green and continuous wet-spinning assembly approach to continuously spin flexible graphene oxide (GO) fibres. Highly stable aqueous GO suspensions up to 40 mg mL−1 are achieved and GO fibres are spun from highly oriented liquid crystals through a customized continuous fibre production line. As-spun GO fibres with specific ultimate tensile strength of 7 N/tex show strain to failure (%) of 10%; subsequent NaBH4 chemical reduction gives graphene fibres with electrical conductivity of 214 S cm−1. The scalable production presented here facilitates flexible, strong and electrically conductive graphene fibres, which have emerged as promising graphene based electronic textiles and sensors.