Faculty Publications

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    A Computer Aided Cooling Curve Analysis method to study phase change materials for thermal energy storage applications
    (Elsevier Ltd, 2016) Sudheer, R.; Prabhu, K.N.
    The suitability of a simple Computer Aided Cooling Curve Analysis (CACCA) technique for characterizing thermal energy storage phase change materials (PCM) was proposed in the present work. Two modes of CACCA, namely, Newtonian and Fourier techniques were used to predict the phase transition temperatures, the latent heat of fusion and thermal diffusivities of PCMs. Solidification of potassium nitrate and zinc-8% aluminium alloy (ZA8) was studied using CACCA method. These PCMs were chosen to demonstrate the ability of the proposed technique to characterize PCMs freezing at a single temperature as well as over a range of temperatures. CACCA method showed that potassium nitrate and ZA8 are suitable candidate materials for TES applications operating at 300-350 °C and 350-450 °C respectively. © 2015 Elsevier Ltd.
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    Cooling Curve Analysis of Micro- and Nanographite Particle-Embedded Salt-PCMs for Thermal Energy Storage Applications
    (Springer New York LLC barbara.b.bertram@gsk.com, 2017) Sudheer, R.; Prabhu, K.N.
    In recent years, the focus of phase change materials (PCM) research was on the development of salt mixtures with particle additives to improve their thermal energy storage (TES) functionalities. The effect of addition of microsized (50 ?m) and nanosized (400 nm) graphite particles on TES parameters of potassium nitrate was analyzed in this work. A novel technique of computer-aided cooling curve analysis was employed here to study the suitability of large inhomogeneous PCM samples. The addition of graphite micro- and nanoparticles reduced the solidification time of the PCM significantly enhancing the heat removal rates, in the first thermal cycle. The benefits of dispersing nanoparticles diminished in successive 10 thermal cycles, and its performance was comparable to the microparticle-embedded PCM thereafter. The decay of TES functionalities on thermal cycling is attributed to the agglomeration of nanoparticles which was observed in SEM images. The thermal diffusivity property of the PCM decreased with addition of graphite particles. With no considerable change in the cooling rates and a simultaneous decrease in thermal diffusivity, it is concluded that the addition of graphite particles increased the specific heat capacity of the PCM. It is also suggested that the additive concentration should not be greater than 0.1% by weight of the PCM sample. © 2017, ASM International.
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    Porous cobalt chalcogenide nanostructures as high performance pseudo-capacitor electrodes
    (Elsevier Ltd, 2017) Bhat, K.S.; Shenoy, S.; Nagaraja, H.S.; Sridharan, K.
    Electrochemical supercapacitor is an essential technology that is pivotal for the development of reliable energy storage devices. Herein, we report the fabrication of supercapacitor electrodes using nanostructured porous cobalt chalcogenide (CoTe2 and CoSe2) electrodes, anticipating an enhanced performance owing to their higher contact area with electrolyte and large pore volume enabling shorter diffusion paths for ion exchange. In this regard, we synthesized CoTe2 and CoSe2 nanostructures via an anion-exchange-reaction between pre-synthesized Co(OH)2 hexagonal nanosheets and chalcogen (tellurium and selenium) ions under hydrothermal conditions. Structural, morphological and compositional properties of the as-synthesized materials are examined using X-ray diffraction, Raman spectroscopy, scanning electron microscopy, high resolution transmission electron microscopy and energy dispersive X-ray spectroscopy. Pseudo-capacitive properties of CoTe2 and CoSe2 nanostructures as working electrodes are studied through cyclic voltammetry and galvanostatic charge-discharge methods using an electrochemical workstation. CoSe2 electrode delivered a specific capacitance of 951 F g?1 at a scan rate of 5 mV s?1, which surprisingly is almost three times higher in comparison to CoTe2 electrode (360 F g?1). Both CoTe2 and CoSe2 electrodes exhibited good capacitance retention capability for 2500 CV cycles. The superior electrochemical performance of the nanoporous CoSe2 electrode indicate their applicability for high-performance energy storage device applications. © 2017 Elsevier Ltd
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    Characterization of linear low-density polyethylene with graphene as thermal energy storage material
    (Institute of Physics Publishing helen.craven@iop.org, 2019) Chavan, S.; Gumtapure, V.; Arumuga Perumal, D.A.
    In this work authors reported the preparation and characterization of composite phase change material (CPCM) using the direct-synthesis method by blending the Linear low-density polyethylene (LLDPE) with Carboxyl Functionalized Graphene (f-Gr). LLDPE is selected as base material and f-Gr is dispersed into three different concentrations 1.0, 3.0, and 5.0 wt% and referred as CPCM-1, CPCM-2 and CPCM-3 respectively. Experimental analysis is carried out through Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM) and Differential scanning calorimeter (DSC). The preset study assesses the influences of nanoparticle concentration on thermophysical properties, thermal performance and thermal storage characteristics of CPCMs. Results show that addition of f-Gr improves the thermal conductivity and latent heat of fusion of LLDPE. However, f-Gr slightly reduces the melting temperature and decreased the crystallization temperature. Therefore, this study reveals that f-Gr, addition to LLDPE has substantial potential for improving the thermal energy storage performance. © 2019 IOP Publishing Ltd.
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    Characterization of metals and salts-based thermal energy storage materials using energy balance method
    (John Wiley and Sons Inc. P.O.Box 18667 Newark NJ 07191-8667, 2019) Agarwala, S.; Prabhu, N.K.
    Thermal energy storage technologies minimize the imbalance between energy production and demand. In this context, latent heat storage materials are of great importance as they have a higher density of energy storage as compared with the sensible heat storage materials. The present study involves the characterization of energy storage materials using an energy balance cooling curve analysis method. The method estimates the convective heat transfer coefficient in the solidification range to characterize the phase change materials for applications in energy storage. The method is more beneficial than the Computer Aided Cooling Curve analysis methods as it eliminates baseline calculations and the associated fitting errors. Metals (Sn) and salts (KNO3 and NaNO 3) were used in the present work. Phase change characteristics like the rate of cooling, liquidus and solidus temperatures, time for solidification, and enthalpy of phase change were estimated for both metals and salts. It was observed that the energy balance cooling curve analysis method worked very well for metals but not well suited for low conductivity salts. Salts could not be characterized since the thermal gradient existing within the salt sample was not considered in this method. © 2019 Wiley Periodicals, Inc.
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    Thermal property study of fatty acid mixture as bio-phase change material for solar thermal energy storage usage in domestic hot water application
    (Elsevier Ltd, 2019) B.V., R.M.; Gumtapure, V.
    For the correct design, simulation and specific application of the latent heat thermal energy storage (LHTES) system, detailed evaluation of phase change material (PCM) properties are essential. Present study aims to analyze the thermal and volume dependent behavior of available organic Bio-PCM OM55, using conventional thermal gravimetric analyzer (TGA), thermal constant analyzer (TCA), differential scanning calorimeter (DSC) and in-house T-history method (THM). Execution of the mentioned thermal analysis outcome with significant information of OM55. TGA shows that OM55 is thermally stable within the operating temperature 45–60 °C, because the maximum permissible degradation temperature 154.6 °C is much higher than operating temperature range. The OM55 has considerable thermal conductivity compared to the existing PCM, which is already used in domestic solar water heating (DSWH) applications. The evaluation of transition temperature, isothermal enthalpy, and specific heat by THM are well compared with the DSC analysis. Comparison of DSC and THM analysis showed that the behavior of OM55 is volume independent. The overall study concluded that OM55 is a potential Bio-PCM. However, for the optimum amount of energy storage and discharge in OM55, it is recommended to operate the LHTES unit over a temperature range between 46–59 °C for domestic hot water application. © 2019 Elsevier Ltd
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    PMMA-LZO Composite Dielectric Film with an Improved Energy Storage Density
    (Springer New York LLC barbara.b.bertram@gsk.com, 2019) Kishor Kumar, M.J.; Kalathi, J.T.
    Energy storage materials in modern electronic devices and renewable energy systems are inevitable. The incorporation of inorganic fillers into the polymer matrix is a promising option for the advancement of storage materials with high energy density. The agglomeration of inorganic fillers in the polymer matrix and phase separation remain the main obstacles to efficient applications of the composites for energy storage. Here, the primary attention was given to achieve a uniform distribution of high-k LZO (Lanthanum Zirconium Oxide) filler into a PMMA (Polymethylmethacrylate) matrix to enhance the dielectric constant and energy storage density of PMMA while keeping dielectric loss at minimum. We prepared PMMA-LZO composite films with variable LZO content by ultrasound-assisted mixing followed by spin coating the solution on ITO (Indium tin oxide) coated glass. The effect of LZO content on dielectric properties of the LZO-PMMA films was studied. Dielectric constant (k) of PMMA was found to be increased from 3.1 to 15.3 at 15 vol.% LZO loading with a dielectric loss of 0.0582. However, 10 vol.% LZO loaded PMMA showed an improved dielectric constant of 13.4 while the dielectric loss remained the same as that of the neat PMMA. The LZO-PMMA films with 10 vol.% and 15 vol.% of LZO loading exhibited maximum energy density of 5.94 J cm?3 and 6.53 J cm?3, respectively. Overall, the 10 vol.% LZO loading was found to be optimum to achieve a stable film with improved dielectric properties. This work provides a viable approach for the development of flexible, high-energy density materials with a minimum dielectric loss. © 2019, The Minerals, Metals & Materials Society.
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    Effect of dopants on the energy storage performance of reduced graphene oxide/polyaniline nanocomposite
    (Elsevier Ltd, 2019) Viswanathan, A.; Nityananda Shetty, A.N.
    The nanocomposites comprising of reduced graphene oxide (rGO) and polyaniline (PANI) were synthesized by facile insitu single step chemical methods, with glacial acetic acid (AA) and methane sulphonic acid (MSA) as dopants for PANI. The rGO/PANI nanocomposites synthesized with the similar weight percentages of constituents exhibited better electrochemical performance in the presence of MSA than in the presence of AA, in the real two-electrode supercapacitor cell system. The nanocomposite of weight percentages of rGO-6.7%, and PANI-93.33% (GP93MSA), with MSA as dopant exhibited a remarkable feature of increase in energy storage when the number of cycles was increased. It exhibited a maximum enhancement of 237.44% in its energy storage performance, after 13600 cycles as compared to the performance before the onset of cyclic test. The high performances obtained with GP93MSA include high specific capacitance of 512.82 F g?1, specific capacity of 615.38 C g?1, energy density of 102.56 W h kg?1 and a power density of 1.8954 kW kg?1 at 1 A g?1. The energy density of the supercapacitor with GP93MSA as the electrode material, is of the same order as that of Li-ion batteries. Also, GP93MSA showcased good cyclic stability up to 23000 cycles. © 2019 Elsevier Ltd
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    Numerical and experimental analysis on thermal energy storage of polyethylene/functionalized graphene composite phase change materials
    (Elsevier Ltd, 2020) Chavan, S.; Gumtapure, V.; Arumuga Perumal, A.P.
    The main driving force behind the present work is environmental issues caused due to the usage of plastics, and energy issues. Current work attempts to address these problems by converting recycled plastics into thermal storage materials (TSM). Unfavorable thermophysical properties of plastic make it impractical but these inadequacies can be amended by blending with additives of superior thermophysical properties like, functionalized graphene. Numerical and experimental analysis are carried out to assess the thermal performance of TSMs (LLDPE, CPCM-1, CPCM-2 and CPCM-3) and check the compatibility of the materials. The phase change temperature of TSM is 123 to 125 °C and heat of fusion is 71.95 to 97 kJ/kg. Several thermal characteristics are analyzed to assess thermal performance and the amount of heat energy supplied, rate of heat transfer, and heat storage efficiency are deliberated. Results shown energy level enhancement of 43.17, 50.42, 54 and 50.61% for LLDPE, CPCM-1, CPCM-2 and CPCM-3 respectively. Among the TSM CPCM-2 shows relatively better storage capability (54% enhancement) due to incorporation of optimum concentration of enhancing material. The solidification process takes place through convection and radiation mode of heat transfer, at the completion of solidification process the TSM energy content reduces to 97.5, 96, 96 and 96% for LLDPE, CPCM-1,CPCM-2 and CPCM-3 respectively. This work concludes that, recycled plastics can be blended and it can be converted into efficient thermal storage material. © 2019 Elsevier Ltd
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    Influence of glutaraldehyde on dynamic properties of poly(vinyl alcohol) polymer
    (ICE Publishing, 2020) Mohan Kumar, G.C.M.; Jeyaraj, J.; Nagamadhu, M.
    This study investigated the dynamic mechanical properties of poly(vinyl alcohol) (PVA; (CH2CH(OH)) n ) cross-linked with glutaraldehyde (GA; OHC(CH2)3CHO).*The cross-linked polymer was prepared by using a conventional casting technique and then treated with sulfuric acid (H2SO4) for 24 h.*The flexural properties during static and dynamic modes were studied using a three-point bending condition.*The static flexural properties are improved with the addition of 30% GA in PVA, with higher value of strain.*It was observed that the dynamic mechanical properties of PVA improved significantly with an increase in cross-linking percentage.*The storage and loss moduli increased drastically with the addition of the cross-linker up to 20%, and marginal changes occurred with further addition of the cross-linker.*The fracture behavior was transformed from ductile to brittle for more than 20% cross-linker.*Shifting of the rubber region and liquid region with higher temperatures was observed in storage and loss modulus plots.*Improvement in the adhesion factor, cross-linking density and effectiveness was observed for GA up to 25%.*The test duration was estimated using the Williams-Landel-Ferry model for different temperatures.*The major changes were in the modulus in the rubbery plateau region.*The cross-linked polymer had much greater storage and loss moduli, indicating a closer network structure and higher stiffness.* © 2020 ICE Publishing: All rights reserved.