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The electrospinning technique was used to prepare nanofibers samples consisting of three groups, each group has a different polystyrene concentration (12, 14, 16 wt.%). Multiwalled carbon nanotubes were added to each group with four ratios to yield four samples comprising (polystyrene/MWCNT) constituents. The UV-Visible test was carried out to know how uniformly nanofibers and Mutli-walled carbon nanotubes were distributed in the polymeric nanofibers and their effect on the final nanofiber's properties through the absorption peaks. The morphological test used "Field Emission Scanning Electron Microscope". The results showed that; MWCNTS has a dominant effect on prepared nanofibers in the (12 wt.% Polystyrene) group, and both (PS, MWCNT) have a shared effect, highest steady absorption curves, and uniformly scattered radiation at (14 wt.% PS) group, and random results at (16 wt.% PS) group. From FESEM results we notice that increasing polymer concentration causes an increase in the nanofiber's diameter and beads formation chance increases at (12,16 wt.% PS) groups. In the group of (14 wt.% Polystyrene), it produces nanofibers with free beads and uniform distribution, the addition of MWCNT lowers the diameter of nanofibers much more and enhances the orientation, and improves their UV absorption, strength, and mechanical properties. [ABSTRACT FROM AUTHOR]

In this study, conductive and transparent polycaprolactone (PCL)/carbon black (CB) nanofibers are produced by electrospinning. In order to investigate the effect of solvent system on the optoelectrical properties of PCL/CB nanofibers, the fibers are produced from two different solvent systems; namely, chloroform (CHL) and dimetyl formamid (DMF). For optoelectrical characterization, nanofibers are produced with different deposition times in the range of 1–10 minutes. Surface, optical, electrical and optoelectrical properties of the PCL/CB nanofibers are evaluated. Nanofibers produced from CHL solvent system results in non-uniform nanofibers with higher diameters. They also give a larger diameter distribution. On the other hand, nanofibers with uniform and smaller diameters are obtained from DMF system. UV-spectrophotometer analysis show that nanofiber mats produced from both solvent systems have similar optical transparencies. Lower sheet resistance values are obtained with the nanofiber mats produced from DMF system according to electrical characterizations. Higher Figure of Merit values are calculated for the nanofiber mats produced in DMF solvent system. Considering all the results, it can be concluded that PCL/CB nanofibers produced from DMF solvent system are better candidates compared to the nanofibers produced from CHL solvent system for optoelectrical applications. [ABSTRACT FROM AUTHOR]

Electrospun polyacrylonitrile (PAN) nanofibers were pre-oxidized under 1, 2, and 3 wt% of KMnO4aqueous solutions. Scanning electron microscopy, Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, X-ray diffraction and Raman spectroscopy were used to study the effect of KMnO4concentration on the structures and properties of PAN-based heat stabilized and carbonized electrospun nanofiber mats. In FT-IR spectra of the preoxidized samples a new peak at 2340 cm−1designated to MnO4–C=N conjugation was revealed. Chemical modification by KMnO4was used to decrease the average diameter, increase the Bragg spacing, and decrease the preferred orientation and the crystal size. According to the Raman spectra, the bandwidths of the G mode became wider in the cases of preoxidized samples, while the G mode intensities belonging to the crystalline regions were decreased. According to the TGA studies, the weight losses in the preoxidized samples were severe due to the permanganate attack. [ABSTRACT FROM PUBLISHER]