H. Albetran

Characterization and optimization of electrospun TiO2/PVP nanofibers using Taguchi design of experiment method

Abstract TiO2 nanofibers were prepared within polyvinylpyrrolidone (PVP) polymer using a combination of sol–gel and electrospinning techniques. Based on a Taguchi design of experiment (DoE) method, the effects of sol–gel and electrospinning on the TiO2/PVP nanofibers’ diameter, including titanium isopropoxide (TiP) concentration, flow rate, needle tip-to-collector distance, and applied voltage were evaluated. The analysis of DoE experiments for nanofiber diameters demonstrated that TiP concentration was the most significant factor. An optimum combination to obtain smallest diameters was also determined with a minimum variation for electrospun TiO2/PVP nanofibers. The optimum combination was determined to be a 60% TiP concentration, at a flow rate of 1 ml/h, with the needle tip-to-collector distance at 11 cm (position a), and the applied voltage of 18 kV. This combination was further validated by conducting a confirmation experiment that used two different needles to study the effect of needle size. The average nanofiber diameter was approximately the same for both needle sizes in good accordance with the optimum condition estimated by the Taguchi DoE method.

Characteristics of X-ray attenuation in electrospun bismuth oxide/polylactic acid nanofibre mats.

The characteristics of the X-ray attenuation in electrospun nano(n)- and micro(m)-Bi2O3/polylactic acid (PLA) nanofibre mats with different Bi2O3 loadings were compared as a function of energy using mammography (i.e. tube voltages of 22-49 kV) and X-ray absorption spectroscopy (XAS) (7-20 keV). Results indicate that X-ray attenuation by electrospun n-Bi2O3/PLA nanofibre mats is distinctly higher than that of m-Bi2O3/PLA nanofibre mats at all energies investigated. In addition, with increasing filler loading (n-Bi2O3 or m-Bi2O3), the porosity of the nanofibre mats decreased, thus increasing the X-ray attenuation, except for the sample containing 38 wt% Bi2O3 (the highest loading in the present study). The latter showed higher porosity, with some beads formed, thus resulting in a sudden decrease in the X-ray attenuation.

Dynamic Diffraction Studies on the Crystallization, Phase Transformation, and Activation Energies in Anodized Titania Nanotubes

The influence of calcination time on the phase transformation and crystallization kinetics of anodized titania nanotube arrays was studied using in-situ isothermal and non-isothermal synchrotron radiation diffraction from room temperature to 900 °C. Anatase first crystallized at 400 °C, while rutile crystallized at 550 °C. Isothermal heating of the anodized titania nanotubes by an increase in the calcination time at 400, 450, 500, 550, 600, and 650 °C resulted in a slight reduction in anatase abundance, but an increase in the abundance of rutile because of an anatase-to-rutile transformation. The Avrami equation was used to model the titania crystallization mechanism and the Arrhenius equation was used to estimate the activation energies of the titania phase transformation. Activation energies of 22 (10) kJ/mol for the titanium-to-anatase transformation, and 207 (17) kJ/mol for the anatase-to-rutile transformation were estimated.