Faculty Publications
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Item Parametric study of manufacturing ultrafine polybenzimidazole fibers by electrospinning(Springer, 2012) Anandhan, S.; Ponprapakaran, K.; Senthil, T.; George, G.Polybenzimidazole (PBI), a high performance polymer, was synthesized from 3,3?-diaminobenzidine (DAB) and isophthalic acid (IPA) through polycondensation. The chemical structure of PBI was confirmed by Fourier transform infrared spectroscopy. Thermal characterization of PBI was done by thermogravimetry and differential scanning calorimetry. PBI nanofibers were fabricated by electrospinning of N, N-dimethyl acetamide solutions of PBI of different solution concentrations, at different voltages. The effects of solution and process parameters (namely, solution concentration and DC voltage) on morphology and average diameter of electrospun PBI fibers were investigated. The electrospun ultrafine fibers' diameter and morphology were characterized by using scanning electron microscopy. Nanofibers were obtained only from PBI solutions of concentrations 12 and 14 % (w/v). At concentrations of 8, 10, and 16 %, fibers could not be obtained. The process parameters were optimized by using the statistical tool, factorial or two-way ANOVA (analysis of variance), DOE (design of experiments) and the results indicate that the applied voltage and the interaction of voltage and solution concentration are influential in determining the diameter and morphology of the electrospun ultrathin PBI fibers. Electrospun PBI fibers, as small as 56 nm, could be successfully produced by using the right combination of solution concentration and spinning voltage. © 2012 Central Institute of Plastics Engineering & Technology.Item Chemical-resistant Ultrafine Poly(styrene-co-acrylonitrile) Fibers by Electrospinning: Process Optimization by Design of Experiment(2013) Senthil, T.; George, G.; Anandhan, S.The effects of solution and processing parameters on the morphology and diameter of electrospun poly(styrene-co-acrylonitrile) fibers were investigated by design of experiment. Morphology of the electrospun fiber mats were investigated by scanning electron microscopy. With increasing solution concentration, fiber morphology changed from that of a spindle-like beaded one to smooth, and the average fiber diameter increased from 96 to 876 nm. Average fiber diameter gradually increased with applied voltage; however, fiber morphology was only slightly influenced by flow rate. Regression analysis results reveal that solution concentration has the most significant impact on the average and standard deviation of fiber diameter. © 2013 Copyright Taylor and Francis Group, LLC.Item Structural characterization of nano-crystalline Co3O4 ultra-fine fibers obtained by sol-gel electrospinning(2013) George, G.; Anandhan, S.In this paper, we report the obtention of ultrafine fibers of cobalt oxide (Co3O4) by combining electrospinning method with high-temperature calcinations from the precursor sol of poly(2-ethyl-2- oxazoline) (PEtOx)/cobalt acetate tetrahydrate [Co(CH3COO) 2·4H2O] in water. The optimum electrospinning conditions for obtaining precursor composite nanofibers from PEtOx/Co(CH 3COO)2·4H2O solution in water, to produce ceramic nanofibers, were studied. The average fiber diameter of the precursor composite fibers measured by scanning electron microscopy (SEM) was approximately 200 nm. Thermogravimetric analysis of PEtOx was performed to estimate the suitable calcination temperature of the precursor fibers. SEM images of the ceramic fibers obtained after calcination revealed the shrinkage in diameter due to complete degradation of the polymer and Co(CH 3COO)2·4H2O. Fourier transform infrared spectroscopy was used to ensure the complete pyrolysis of polymer during calcinations of the composite fibers. Crystalline properties of the ceramic fibers were studied by X-ray diffraction and high resolution transmission electron microscopy. The ceramic fibers are polycrystalline with an average grain size of ?40 nm obtained at a calcination temperature of 773 K. It was observed that the grain sizes increased as the calcination temperature was increased, due to self assembly mechanism. © 2013 Springer Science+Business Media New York.Item Synthesis and characterisation of nickel oxide nanofibre webs with alcohol sensing characteristics(Royal Society of Chemistry, 2014) George, G.; Anandhan, S.In this study, nickel oxide (NiO) nanofibres were obtained by a sol-gel electrospinning process followed by calcination from an aqueous sol of poly(2-ethyl-2-oxazoline)/nickel acetate tetrahydrate. Thermogravimetric analysis was used to determine the degradation temperature of the composite fibres, so as to get nickel oxide nanofibres. X-ray photoelectron spectroscopy and X-ray diffraction studies revealed the complete elimination of the organic phase from NiO fibres during calcination. The change in grain size with calcination temperature was determined by X-ray diffraction. The defects in fibres resulted in the modification of their Raman spectra as compared with that of a single crystal. The magnetic properties of the fibres were reduced as the calcination temperature was increased; this is due to the presence of non-stoichiometric defects. As the calcination temperature was increased, the amount of defects was reduced, which induced a difference in the band gap energy of the fibres. Sensitivity of the NiO fibres towards five different alcohols was studied, and the sensitivity towards ethanol was the highest. © The Royal Society of Chemistry 2014.Item Comparison of structural, spectral and magnetic properties of NiO nanofibers obtained by sol-gel electrospinning from two different polymeric binders(Elsevier Ltd, 2015) George, G.; Anandhan, S.NiO is a p-type semiconductor with wide band gap energy. In this study, nickel oxide nanofibers were fabricated by sol-gel electrospinning followed by high temperature calcination, using two sacrificial polymeric binders. Poly(2-ethyl-2-oxazoline) (PEtOx) in water and styrene-acrylonitrile random copolymer (SAN) in N,N- dimethylformamide (DMF) along with nickel (II) acetate tetrahydrate (NATH), as metal oxide precursor, were the two distinct polymeric systems used in this study. The morphological and structural properties of NiO fibers obtained from the aforementioned systems were compared with each other. The degradation behavior of the sacrificial polymeric binder imparted a significant effect on the properties of the obtained NiO fibers. The grain sizes and the activation energies for grain growth of NiO fibers from two systems were different. The non-stoichiometric NiO fibers obtained from the SAN/NATH system had a better ferromagnetic behavior as compared with that produced from the PEtOx/NATH system. This non-stoichiometry made a difference also in the optical band gap energies of the NiO nanofibers. © 2015 Elsevier Ltd.