Faculty Publications

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    Thermodynamic miscibility and thermal and mechanical properties of poly(ethylene-co-vinyl acetate-co-carbon monoxide)/poly(vinyl chloride) blends
    (John Wiley and Sons Inc, 2015) SelvaKumar, M.; Mahendran, A.; Bhagabati, P.; Anandhan, S.
    This paper reports the miscibility and thermal and mechanical properties of solution cast binary blends of poly(ethylene-co-vinyl acetate-co-carbon monoxide) (EVACO) and poly(vinyl chloride) (PVC). The composition of these blends was varied from 10:90 to 90:10 of PVC/EVACO (w/w %). Fourier transform infrared spectroscopy revealed an extensive intermolecular attraction between the blend components, which accounts for their mutual solubility. The differential scanning calorimetry study revealed that the blend components are miscible with each other in all proportions as they exhibited a single glass transition temperature. Tensile strength, moduli, and thermal stabilities of these blends significantly improved with increasing proportion of PVC. © 2014 Wiley Periodicals, Inc.
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    Characterization of composites based on biodegradable poly(vinyl alcohol) and nanostructured fly ash with an emphasis on polymer-filler interaction
    (SAGE Publications Ltd info@sagepub.co.uk, 2016) Patil, A.G.; SelvaKumar, M.; Anandhan, S.
    A thermal power station fly ash (FA) was mechanochemically activated by high-energy ball milling that yielded nanostructured FA. This nanostructured FA was incorporated into biodegradable poly(vinyl alcohol) (PVA) matrix by solution mixing and ultrasonication. Transmission electron micrographs revealed that the smooth spherical particles of FA were changed into irregular and rough ones; in addition, the particle size of FA was reduced to a few hundred nanometers, and its specific surface area value increased after the high-energy milling process. All these factors, in turn, led to a thermodynamically favorable interaction between the mechanochemically activated FA and PVA as evidenced by Fourier transform infrared spectroscopy. The incorporation of a very small amount of the nanostructured FA led to an increase in crystallinity of the polymer matrix. The glass transition temperature of the PVA matrix increased by about 18°C when 5 wt% of the nanostructured FA was used as the reinforcement. © The Author(s) 2014.
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    Physicochemical characteristics of bio-based thermoplastic polyurethane/graphene nanocomposite for piezoresistive strain sensor
    (John Wiley and Sons Inc. P.O.Box 18667 Newark NJ 07191-8667, 2020) Khalifa, M.; Ekbote, G.S.; Anandhan, S.; Wuzella, G.; Lammer, H.; Mahendran, A.R.
    Herein, we report the physicochemical characteristics and piezoresistive strain sensing performance of flexible thin film comprising graphene and bio-based thermoplastic polyurethane (TPU) prepared by solution cast method. A detailed analysis was carried to study the influence of graphene nanoplatelets on the morphological, thermal, mechanical, and electrical properties of TPU nanocomposite. Upon increasing the graphene nanoplatelets loading, the thermal stability and tensile properties improved remarkably, while glass transition temperature decreased slightly. Owing to better dispersion of graphene, the electrical conductivity was significantly increased, which broaden the utilization of the nanocomposite for various applications. The piezoresistive sensor was able to respond to various stress modes such as tapping, bending, and finger touch. The piezoresistive sensor was sensitive and achieved a gauge factor of 11. Sensor attached to finger, showed distinctive response upon bending at different angles and showed high stability and reproducibility even after >10,000 cycles under repetitive constant load. Also, the nanocomposite was able to detect any breakage or fracture in the form of change in electrical resistance. A combination of bio-based TPU and graphene offered improved physical properties and high sensing performance, which could be a potential material in flexible electronics and structural health monitoring systems. © 2020 Wiley Periodicals, Inc.