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    Biodegradability of PMMA blends with some cellulose derivatives
    (2006) Bhat, D.K.; Muthu, M.S.
    High polymer blends of Polymethyl methacrylate (PMMA) with cellulose acetate (CA) and Cellulose acetate phthalate (CAP) of varying blend compositions have been prepared to study their biodegradation behavior and blend miscibility. Films of PMMA-CA, and PMMA-CAP blends have been prepared by solution casting using Acetone and Dimethyl formamide(DMF) as solvents respectively. Biodegradability of these blends has been studied by four different methods namely, soil burial test, enzymatic degradation, and degradation in phosphate buffer and activated sludge degradation followed by water absorption tests to support the degradation studies. Degradation analysis was done by weight loss method. The results of all the tests showed sufficient biodegradability of these blends. Degradability increased with the increase in CA and CAP content in the blend compositions. The miscibility of PMMA-CA and PMMA-CAP blends have been studied by solution viscometric and ultrasonic methods. The results obtained reveal that PMMA forms miscible blends with either CA or CAP in the entire composition range. Miscibility of the blends may be due to the formation of hydrogen bond between the carbonyl group of PMMA and the free hydroxyl group of CA and CAP. © Springer Science+Business Media, Inc. 2006.
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    Miscibility of poly(methylmethacrelate) and cellulose acetate butyrate blends in dimethyl formamide
    (2008) Muthu, M.S.; Bhat, D.K.
    The miscibility of poly(methylmethacrelate) (PMMA) and cellulose acetate butyrate (CAB) blends in dimethyl formamide (DMF) have been investigated by viscosity, density, refractive index and ultrasonic velocity studies. The polymer-solvent and blend-solvent interaction parameters and heat of mixing have been calculated using the viscosity, density and ultrasonic velocity data. The results indicated the existence of positive interactions in the blend polymer solutions and that they are miscible in dimethyl formamide in the entire composition range between 303-323 K. The study also revealed that variation in the temperature does not affect the miscibility of PMMA and CAB blends in DMF significantly. The presence of hydrogen bonding in the blends in the solid state has also been indicated by FTIR studies. SEM images also supported the miscibility of blends.
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    Thermal degradation and swelling of thermoplastic vulcanizates from NBR/SAN and NBR/Scrap computer plastics blends
    (Huthig GmbH, 2009) Anandhan, S.; Rajeev, R.S.; De, S.K.; Bhowmick, A.K.
    Thermoplastic elastomeric blends of nitrile rubber (NBR)/poly(styrene- coacrylonitrile) (SAN) and NBR/scrap computer plastics (SCP) based on acrylonitrile-butadiene-styrene terpolymer (ABS) were prepared. Thermoplastic elastomeric blends of NBR/SAN containing various amounts of a model waste nitrile rubber powder (w-NBR) were also prepared. Thermogravimetric analysis of the above blends was performed in a nitrogen atmosphere. Both Friedman and Flynn-Wall-Ozawa methods were used for the evaluation of activation energies of thermal degradation of these blends. The dynamically vulcanised blends exhibit higher amount of activation energies for thermal degradation than the unvulcanised ones. Swelling studies were performed in various solvents having different solubility parameter values and maximum swelling was found to occur in a solvent having a solubility parameter that was closer to that of the blend components, i.e., around 20MPa1/2. Dynamically vulcan-ised blends show excellent resistance to IRM #903 oil as well as four chosen solvents possessing different solubility parameters (E).
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    Miscibility of polymethylmethacrylate and polyethyleneglycol blends in tetrahydrofuran
    (2009) Muthu, M.S.; Bhat, D.K.; Renganathan, N.G.
    The miscibility of polymethylmethacrylate (PMMA) and polyethyleneglycol (PEG) blends in tetrahydrofuran. (THF) has been investigated by viscosity, density, refractive index, and ultrasonic velocity studies. Various interaction parameters such as polymer-solvent and blend-solvent interaction parameters and heat of mixing have been calculated using the viscosity, density, and ultrasonic velocity data. The results indicated the existence of positive interactions in the blend polymer solutions and that they are miscible in THF in the entire composition range. The study also revealed that variation in the temperature does not affect the miscibility of PMMA and PEG blends in THF significantly. The presence of hydrogen bonding in the blends in the solid state has also been indicated by FTIR studies. © 2008 Wiley Periodicals, Inc.
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    Polyvinyl alcohol-polystyrene sulphonic acid blend electrolyte for supercapacitor application
    (2009) Muthu, M.S.; Bhat, D.K.
    A new polymer blend electrolyte based on poly vinyl alcohol and poly styrene sulphonic acid has been studied as an electrolyte for supercapcitors. A carbon-carbon supercapacitor has been fabricated using this electrolyte and its electrochemical characteristics and performance have been studied. The conductivity has been calculated using the bulk impedance obtained through impedance spectroscopy. The real and imaginary parts of the electrical modulus of samples show a long tail feature, which can be attributed to high capacitance of the material. The super capacitor showed a fairly good specific capacitance of 40 F g- 1 and a time constant of 5 s. © 2008 Elsevier B.V. All rights reserved.
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    Miscibility of poly(vinylidene fluoride) and cellulose acetate blends in dimethyl formamide
    (Chemical Publishing Co., 2011) Muthu, M.S.; Bhat, D.K.
    The miscibility of poly(vinylidene fluoride) (PVDF) and cellulose acetate blends in dimethyl formamide has been investigated by viscosity, density, refractive index and ultrasonic velocity studies. The polymer-solvent and blend-solvent interaction parameters and heat of mixing have been calculated using the viscosity, density and ultrasonic velocity data. The results indicated the existence of positive interactions in the blend polymer solutions and that they are miscible in dimethyl formamide in the entire composition range between 303-323 K. The study also revealed that the variation in the temperature does not affect the miscibility of poly(vinylidene fluoride) and cellulose acetate blends in DMF significantly. The presence of hydrogen bonding in the blends in the solid state has also been indicated by FTIR studies. SEM images also supported the miscibility of blends.
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    Electrochemical properties of chitosan-Co3O4 nanocomposite films
    (Elsevier B.V., 2011) Bhatt, A.S.; Bhat, D.K.; Santosh, M.S.
    Chitosan-Co3O4 composite films have been prepared by solution casting method. The obtained films have been characterised by XRD and FESEM. The electrical properties of the films are examined by impedance spectroscopy in the temperature range 303-343 K. The impedance plot of the films pronounces the role of temperature in charge-transfer resistance of the composite. Frequency as well as temperature dependencies of dielectric constant and dielectric loss exhibit the general trend followed by carrier dominated dielectrics. Electric modulus parameters give an insight on the ionic conductivity and relaxation phenomena of the composite films. The dielectric parameters along with modulus data have been exploited to discuss the conduction mechanism in the material. The minimum activation energy of 3.9 kJ mol -1 and maximum room temperature conductivity of 1.94 × 10 -2 S cm-1 were found for composite film with 8% Co 3O4 content. © 2011 Elsevier B.V. All rights reserved.
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    Miscibility studies of chitosan and starch blends in buffer solution
    (2012) Sudhakar, Y.N.; Holla, S.R.; Muthu, M.; Bhat, D.K.
    The miscibility of chitosan (CS) and starch in buffer solution (CH 3COOH and CH 3COONa) has been investigated by viscosity, density and refractive index methods at 303K, 313K, and 323K. Various interaction parameters such as polymer-polymer and blend-solvent interaction parameters and heat of mixing have been calculated using viscosity and density data. The results indicated the existence of positive interactions in the blend polymer solutions and that they are miscible below 40% of starch compositions. The study also revealed that variation of temperature does have significant effect on the miscibility of chitosan and starch blends. © 2012 Copyright Taylor and Francis Group, LLC.
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    Extruded poly(ethylene-co-octene)/fly ash composites - Value added products from an environmental pollutant
    (Kluwer Academic Publishers, 2012) Anandhan, S.; Sundar, S.M.; Senthil, T.; Mahendran, A.R.; Shibulal, G.S.
    Fly ash (FA) is a by-product generated during combustion of coal and has caused serious environmental concerns. In an effort to utilize FA beneficially, we developed composites from an ethylene-octene random copolymer (EOC) and unmodified as well as surfacemodified class-F fly ash (MFA) by twin screw extrusion. Addition of 20 wt% of MFA to EOC improves its tensile strength by 150%; also, MFA improves stress at 100% and 300% strains (M100 and M300) of EOC. Thermal stability of EOC matrix is appreciably improved by the addition of either FA or MFA, while the melting behavior is not appreciably influenced by either. Fractography study reveals an improved adhesion between the EOC and MFA particles up to a filler loading of 20%, beyond which the adhesion between EOC and MFA is weakened causing a reduction in mechanical properties. The 'flammable' nature of EOC changes to 'self extinguishing' on addition of even 10 wt% of FA or MFA, as found out from LOI study. © Springer Science+Business Media B.V. 2012.
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    LiClO4-doped plasticized chitosan and poly(ethylene glycol) blend as biodegradable polymer electrolyte for supercapacitors
    (Institute for Ionics, 2013) Sudhakar, Y.N.; Muthu, M.; Bhat, D.K.
    Biodegradable polymer electrolyte comprising the blend of chitosan (CS) and poly(ethylene glycol) (PEG) plasticized with ethylene carbonate and propylene carbonate, as host polymer, and lithium perchlorate (LiClO4), as a dopant, was prepared by solution casting technique. The ionic conductivity has been calculated using the bulk impedance obtained through impedance spectroscopy. The variation of conductivity and dielectric properties has been investigated as a function of polymer blend ratio, plasticizer content and LiClO4 concentration at temperature range of 298-343 K. The DSC thermograms show two broad peaks for CS/PEG blend and increased with increase in the LiClO4 content. The maximum conductivity has been found to be 1. 1 × 10-4 S cm-1 at room temperature for 70:30 (CS/PEG) concentration. The electric modulus of the electrolyte film exhibits a long tail feature indicative of good capacitance. The activation energy of all samples was calculated using the Arrhenius plot, and it has been found to be 0. 12 to 0. 38 eV. A carbon-carbon supercapacitor has been fabricated using this electrolyte, and its electrochemical characteristics and performance have been studied. The supercapacitor showed a fairly good specific capacitance of 47 F g-1. © 2012 Springer-Verlag.