Browsing by Author "Shanmugharaj, A.M."

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Interparticle interactions and lacunarity of mechano-chemically activated fly ash
(2015) Patil, A.G.; Shanmugharaj, A.M.; Anandhan, S.
A class F fly ash was subjected to high-energy ball milling-induced mechano-chemical activation aided by a surfactant. The resultant nanostructured fly ash was characterized by various techniques. X-ray fluorescence results showed that the amount of iron oxide was reduced from 4.39% to 2.75% after pre-treatment of fly ash by magnetic separation. Ethyl acetate as the milling medium, a ball to powder ratio of 12:1 and 2wt% of surfactant reduced the average particle size of fly ash to 329nm and led to a specific surface area of 8.73m2/g. The decrease in crystallite size of mechano-chemically activated fly ash was confirmed from a reduction in peak intensity with a broadened amorphous phase by X-ray diffraction studies. X-ray photoelectron spectroscopic characterization illustrated that peak area of major elements (O, Si and Al) increased after milling. Morphological and FTIR studies revealed that the smooth and inert surface of the fly ash was converted to a rough and more reactive one after mechano-chemical activation. The surface modification of fly ash with the surfactant was determined from FTIR spectroscopy. Also, a fractal approach was used to characterize the lacunarity of the agglomerates in the nanostructured fly ash. 2014 Elsevier B.V.
Interparticle interactions and lacunarity of mechano-chemically activated fly ash
(Elsevier, 2015) Patil, A.G.; Shanmugharaj, A.M.; Anandhan, S.
A class F fly ash was subjected to high-energy ball milling-induced mechano-chemical activation aided by a surfactant. The resultant nanostructured fly ash was characterized by various techniques. X-ray fluorescence results showed that the amount of iron oxide was reduced from 4.39% to 2.75% after pre-treatment of fly ash by magnetic separation. Ethyl acetate as the milling medium, a ball to powder ratio of 12:1 and 2wt% of surfactant reduced the average particle size of fly ash to 329nm and led to a specific surface area of 8.73m2/g. The decrease in crystallite size of mechano-chemically activated fly ash was confirmed from a reduction in peak intensity with a broadened amorphous phase by X-ray diffraction studies. X-ray photoelectron spectroscopic characterization illustrated that peak area of major elements (O, Si and Al) increased after milling. Morphological and FTIR studies revealed that the smooth and inert surface of the fly ash was converted to a rough and more reactive one after mechano-chemical activation. The surface modification of fly ash with the surfactant was determined from FTIR spectroscopy. Also, a fractal approach was used to characterize the lacunarity of the agglomerates in the nanostructured fly ash. © 2014 Elsevier B.V.
Physico-chemical and piezoelectric characterization of electroactive nanofabrics based on functionalized graphene/talc nanolayers/PVDF for energy harvesting
(Springer Science and Business Media B.V., 2021) Shetty, S.; Shanmugharaj, A.M.; Anandhan, S.
Poly(vinylidene fluoride) (PVDF) is a versatile polymer, whose dielectric, piezoelectric and ferroelectric properties can be augmented by a range of processing routes and/or additives. We developed a flexible nanogenerator using electrospun PVDF/COOH-functionalized graphene nanosheet (FGNS)/talc nanosheet (TNS) hybrid nanocomposites. TNS loading was fixed at 0.50 wt% while FGNS loading was varied (0.05, 0.10, 0.15, and 0.20 wt %) in these nanofabrics and their structure–property relationship was explored. Incorporation of FGNS led to formation of an electrically conductive network in the polymer matrix aided by TNS and electrospinning. The uniform dispersion of the filler nanosheets led to effective enhancement of the electroactive ?-phase of the PVDF matrix. Crystallinity and polymorphism in these systems were explored by FTIR spectroscopy, X-ray diffraction and differential scanning calorimetry. A nanogenerator made of the nanofabric containing 0.5 wt% of TNS and 0.10 wt% of FGNS was mechanically impacted by pneumatic actuator (operating pressure 0.4 MPa), resulting in an output voltage of 12.9 V and a power density of 1.72 µW/cm2, respectively. The piezoelectric coefficient (d33) of this nanofiber system was 61 pm/V as revealed by piezoelectric force microscopy. These novel nanocomposites could be used in flexible energy-harvesting devices. © 2021, The Polymer Society, Taipei.
Some new observations on the structural and phase evolution of nickel titanate nanofibers
(2017) Kumar, B.S.; Shanmugharaj, A.M.; Kalpathy, S.K.; Anandhan, S.
In this study, we report for the first time the synthesis of nickel titanate (NTO) nanofibers containing a mixture of ilmenite and spinel phases of NTO, at an atypical low temperature. Precursor nanofibers produced by sol-gel electrospinning were calcined at three different temperatures to produce the NTO nanofibers. Thermal analysis along with X-ray photoelectron spectroscopy confirmed the formation of non-crystalline stable phases of TiN and Ti-O-N that restrained the formation of ilmenite NTO, and the Ni-rich environment pushed the Ti atoms to tetrahedral sites to form a defective spinel structure. The crystallite size of spinel NTO was observed to increase as a function of the calcination temperature above 700 C, as the activation energy for coalescence and growth of spinel NTO was favorable. NTO nanofibers obtained above the calcination temperature of 700 C exhibited new band gap energy around 2.5 eV in Tauc plot. Oxygen vacancies in these ceramic nanofibers decreased as the calcination temperature was increased. A hypsochromic shift of 20 nm in the photoluminescence spectra suggested that the material had a Ni2+ rich NTO (spinel). 2017 Elsevier Ltd and Techna Group S.r.l.
Some new observations on the structural and phase evolution of nickel titanate nanofibers
(Elsevier Ltd, 2017) Kumar, B.S.; Shanmugharaj, A.M.; Kalpathy, S.K.; Anandhan, S.
In this study, we report for the first time the synthesis of nickel titanate (NTO) nanofibers containing a mixture of ilmenite and spinel phases of NTO, at an atypical low temperature. Precursor nanofibers produced by sol-gel electrospinning were calcined at three different temperatures to produce the NTO nanofibers. Thermal analysis along with X-ray photoelectron spectroscopy confirmed the formation of non-crystalline stable phases of TiN and Ti-O-N that restrained the formation of ilmenite NTO, and the Ni-rich environment pushed the Ti atoms to tetrahedral sites to form a defective spinel structure. The crystallite size of spinel NTO was observed to increase as a function of the calcination temperature above 700 °C, as the activation energy for coalescence and growth of spinel NTO was favorable. NTO nanofibers obtained above the calcination temperature of 700 °C exhibited new band gap energy around 2.5 eV in Tauc plot. Oxygen vacancies in these ceramic nanofibers decreased as the calcination temperature was increased. A hypsochromic shift of 20 nm in the photoluminescence spectra suggested that the material had a Ni2+ rich NTO (spinel). © 2017 Elsevier Ltd and Techna Group S.r.l.