Faculty Publications
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Item An Insight into the Gelatinization Properties Influencing the Modified Starches Used in Food Industry: A review(Springer, 2022) Chakraborty, I.; N, P.; Mal, S.S.; Paul, U.C.; Rahman, M.H.; Mazumder, N.Native starch is subjected to various forms of modification to improve its structural, mechanical, and thermal properties for wider applications in the food industry. Physical, chemical, and dual modifications have a substantial effect on the gelatinization properties of starch. Consequently, this review explores and compares the different methods of starch modification applicable in the food industry and their effect on the gelatinization properties such as onset temperature (To), peak gelatinization temperature (Tp), end set temperature (Tc), and gelatinization enthalpy (ΔH), studied using differential scanning calorimetry (DSC). Chemical modifications including acetylation and acid hydrolysis decrease the gelatinization temperature of starch whereas cross-linking and oxidation result in increased gelatinization temperatures. Common physical modifications such as heat moisture treatment and annealing also increase the gelatinization temperature. The gelatinization properties of modified starch can be applied for the improvement of food products such as ready-to-eat, easily heated or frozen food, or food products with longer shelf life. © 2022, The Author(s).Item Crystallinity, conductivity, and magnetic properties of PVDF-Fe 3O4 composite films(2011) Bhatt, A.S.; Bhat, D.K.; Santosh, M.S.The formation of Fe3O4 nanoparticles by hydrothermal process has been studied. X-ray Diffraction measurements were carried out to distinguish between the phases formed during the synthesis. Using the synthesized Fe3O4 nanoparticles, poly(vinyledene fluoride)-Fe3O4 composite films were prepared by spin coating method. Scanning electron microscopy of the composite films showed the presence of Fe3O4 nanoparticles in the form of aggregates on the surface and inside of the porous polymer matrix. Differential Scanning calorimetry revealed that the crystallinity of PVDF decreased with the addition of Fe3O4. The conductitivity of the composite films was strongly influenced by the Fe3O4 content; conductivity increased with increase in Fe3O4 content. Vibration sample magnetometry results revealed the ferromagnetic behavior of the synthesized iron oxide nanoparticles with a Ms value of 74.50 emu/g. Also the presence of Fe3O4 nanoparticles rendered the composite films magnetic. © 2010 Wiley Periodicals, Inc.Item Crystallinity, magnetic and electrochemical studies of PVDF/Co 3O4 polymer electrolyte(Elsevier Ltd, 2012) Bhatt, A.S.; Bhat, D.K.Organic-inorganic nanocomposites are gaining importance in the recent times as polymer electrolyte membranes. In the present work, composites were prepared by combining nano sized Co3O4 and poly(vinyledene fluoride) (PVDF), using spin coating technique. The surface of the PVDF/Co 3O4 system characterized through field emission scanning electron microscopy (FESEM) revealed a porous structure of the films. The nanoparticles tend to aggregate on the surface and inside the pores, leading to a decrease in the porosity with an increase in Co3O4 content. Co3O4 nanoparticles prohibit crystallization of the polymer. Differential scanning calorimetry (DSC) studies revealed a decrease in crystallinity of PVDF/Co3O4 system with an increase in the oxide content. Magnetic property studies of the composite films revealed that with an increase in Co3O4 content, the saturation magnetization values of the nanocomposites increased linearly, showing successful incorporation of the nanoparticles in the polymer matrix. Further, ionic conductivity of the composite films was evaluated from electrochemical impedance spectroscopy. Addition of Co3O4 nanoparticles enhanced the conductivity of PVDF/Co3O4 system. © 2011 Elsevier B.V. All rights reserved.Item Effect of Mn on cooling behaviour and microstructure of chill cast Zn-Al (ZA8) alloy(2012) Ramesh, G.; Vishwanatha, H.M.; Prabhu, K.N.In the present work, the effect of manganese addition to ZA8 alloy on thermal analysis parameters, heat transfer and microstructure was investigated. The thermal analysis parameters were found to be significantly affected by chemical modification of ZA8 alloy. Cooling curve and differential scanning calorimetry analyses of modified alloy showed nucleation of new phase other than b dendrites. Chilling of modified alloy resulted in decreased liquidus temperature and enhanced eutectoid transformation. Further, chilling avoids the formation of intermetallic compounds in modified alloy. The heat flux transients were estimated using inverse modelling during solidification of unmodified and modified alloys against different chills. The peak heat flux decreased on addition of Mn to ZA8 alloy. Differential scanning calorimetry analysis indicated that the addition of Mn to ZA8 alloy decreases the heat of solidification. The addition of Mn to ZA8 alloy increased the contact angle, indicating decreased wettability of the modified alloy on the chill surface. The microstructure of ZA8 with Mn showed an increased amount of b phase and a decreased amount of eutectic. X-ray diffraction analysis confirmed the formation of MnAl6 intermetallics in Mn added ZA8 alloy. Chilling with chemical modification resulted in enhanced decomposition of b phase. © 2012 Institute of Materials, Minerals and Mining.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 Miscibility, water uptake, ion exchange capacity, conductivity and dielectric studies of poly(methyl methacrylate) and cellulose acetate blends(2013) Jois, H.S.S.; Bhat, D.K.In the last few decades, polymer blends with good miscibility and conductivity have been the focus of study for material scientists. Here, polymer blends of Poly(methyl methacrylate) (PMMA) and Cellulose acetate (CA) of varying blend compositions have been prepared by solution casting method and their miscibility, water uptake, ion exchange capacity (IEC) proton conductivity, and dielectric properties have been studied. Dimethyl formamide (DMF) was used as solvent. Fourier transform infrared spectra (FTIR) and Differential scanning calorimetry (DSC) measurements have been used to analyze the miscibility of the blends. Up to 50/50 PMMA/CA, water uptake showed an increasing trend and for other compositions the value decreased. Ion exchange capacity and conductivity of the blends decreased with increase in PMMA content of the blends. The variations in the blend properties have been attributed to the presence of specific interactions and exchangeable groups in the blend system. The proton conductivity of the blends is in the order of 10-3 S cm-1. Impedance analysis of the blends indicated the absence of any relaxation phenomenon in the blend system. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3074-3081, 2013 Copyright © 2013 Wiley Periodicals, Inc.Item Use of nano-ATH as a multi-functional additive for poly(ethylene-co-vinyl acetate-co-carbon monoxide)(Springer Verlag service@springer.de, 2014) George, G.; Mahendran, A.; Anandhan, S.Flame retardant aluminum hydroxide (ATH) nanoparticles of size ?10-20 nm were dispersed in ethylene-vinyl acetate-carbon monoxide terpolymer (EVACO) via solution casting. The effect of filler loading on the crystallizability, thermal, mechanical, flammability, optical and electrical properties of EVACO was evaluated. At 1 % filler loading nano-ATH particles exhibited very good dispersibility in the EVACO matrix and the % crystallinity of EVACO is the highest at this filler loading. The changes in crystallinity were studied by X-ray diffractometry and differential scanning calorimetry. The highest tensile strength was observed for the composite with 1 % nano-ATH loading, which has the best filler dispersion, and the decay in the tensile properties at higher filler loading is due to agglomerations of ATH nanoparticles and polymer-filler interface debonding. The UV absorption of these composites is augmented irrespective of the nano-ATH loading and ATH emerges as a good absorber of UV light. The DC electrical conductivity study of the composites proves that the addition nano-ATH is an efficient way to improve the dielectric properties of EVACO. The presence of nano-ATH improves the flame retardance of these composites. © 2014 Springer-Verlag Berlin Heidelberg.Item Role of N-vinyl-2-pyrrolidinone on the thermoresponsive behavior of PNIPAm hydrogel and its release kinetics using dye and vitamin-B12 as model drug(2014) Maheswari, B.; JagadeeshBabu, P.E.; Agarwal, M.Temperature-sensitive hydrogels hold great promise in biological applications as they can respond to changes in physiological temperature to produce a desired effect like controlled drug delivery. In this study, a series of poly(N-isopropylacrylamide-co-N-vinyl-2-pyrrolidinone) thermosensitive hydrogels were synthesized by radical copolymerization of NIPAm with 1-vinyl-2-pyrrolidinone (NVP). By altering the initial NIPAm/NVP mole ratios, copolymers were synthesized to have their own distinctive lower critical solution temperature which was established using differential scanning calorimetry. The swelling behavior of the hydrogel was analyzed gravimetrically and it was observed that reswelling rate increases with increasing NVP mole ratio. Further characterizations of the hydrogels were performed using Fourier transform infrared spectroscopy and scanning electron microscopy. Release kinetics with respect to temperature was studied using methylene blue dye solution and vitamin B12. Kinetic modeling of the release profile revealed that the release mechanism is a non-Fickian diffusion mechanism. These results suggested that this material has potential application as intelligent drug carriers. The quantities of residual monomers in the PIV4 hydrogel were determined by HPLC method, and the results show almost complete conversion. © 2013 Taylor & Francis.Item Influence of organically modified clay mineral on domain structure and properties of segmented thermoplastic polyurethane elastomer(2014) Anandhan, S.; Lee, H.S.Segmented polyether-urethane/organically modified montmorillonite (O-MMT) nanocomposites were synthesized with poly(tetramethylene glycol) (PTMG), 4,4?-diphenylmethane diisocyanate (MDI), butane diol (BD), and a commercially available clay Cloisite-30B® (O-MMT). The state of dispersion of the clay crystals in the thermoplastic polyurethane elastomer (TPU) matrix was studied by X-ray diffraction and transmission electron microscopy (TEM). The phase-separated morphology of the TPU was revealed by high-resolution TEM (HRTEM) and atomic force microscopy (AFM). O-MMT caused a marginal increase in the glass transition temperature of the soft segments of the TPU and this increase is proportional to the amount of O-MMT in the nanocomposites. Differential scanning calorimetry (DSC) was employed to study the effect of O-MMT on the extent of phase separation in the TPU in these nanocomposites. Thermogravimetric analysis (TGA) results indicate a substantial improvement in the thermal stability of TPU by the addition of O-MMT. Tensile strength and elastic modulus are dramatically decreased by the incorporation of O-MMT into TPU, which is due to the hindrance of the phase-separation process by the exfoliated clay-layered crystals. © The Author(s) 2012 Reprints and permissions:sagepub.co.uk/journalsPermissions.nav.Item Identification of robust synthon in the molecular salts of 2-aminothiazole with substituted benzoic acids: A case study(Springer India sanjiv.goswami@springer.co.in, 2014) Oruganti, M.; Pallepogu, R.; Trivedi, D.R.Six new salts of an API intermediate 2-aminothiazole with different carboxylic acid coformers were synthesized and characterized by IR (Infrared spectroscopy), 1H-NMR, DSC (Differential scanning calorimetry), XRPD (X-ray powder diffraction) and single crystal XRD. The crystal structure of the salts with benzoic acid, 2,3-, 2,4-, 2,5-, 2,6- dihydroxybenzoic acids and 2,4-dinitrobenzoic acid were determined. The thiazole moiety exhibited solvent (polarity) assisted tautomerism in all reported salts and proton transfer was noticed to the ring N of thiazole due to which two point supramolecular synthon N+-H(thiazole)?O-(acid), N-H(amine)?O-(acid) was observed. The crystal structures were studied with respect to the positional effect of the competing functional groups like hydroxyl (-OH) and nitro (-NO2) as well as their donor and acceptor abilities for hydrogen bonding. The presence of the non-conventional hydrogen bond (C-H?O) has been found to play a critical role in the formation of secondary supramolecular architectures. © 2014 Indian Academy of Sciences.