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    <title>DSpace Collection:</title>
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        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/4843" />
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/4842" />
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/4841" />
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    <dc:date>2026-04-08T10:27:16Z</dc:date>
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  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/4843">
    <title>MAX Phase Ternary Carbide Derived 2-D Ceramic Nanostructures [CDCN] as Chemically Interactive Functional Fillers for Damage Tolerant Epoxy Polymer Nanocomposites</title>
    <link>http://localhost:8080/xmlui/handle/123456789/4843</link>
    <description>Title: MAX Phase Ternary Carbide Derived 2-D Ceramic Nanostructures [CDCN] as Chemically Interactive Functional Fillers for Damage Tolerant Epoxy Polymer Nanocomposites
Authors: Vaisakh, S S; Mahesh, K V; Balanand, S; Metz, R; Hassanzadeh, M; Ananthakumar, S
Abstract: A 2-dimensional ceramic nanostructure was successfully processed out of nanolamellar 312 MAX phase&#xD;
ternary carbide, titanium silicon carbide, Ti3SiC2 (TSC), via a simple shear-induced delamination&#xD;
technique. It has been explored as a functional nanofiller for obtaining chemically homogeneous, lowfriction, self-lubricating epoxy nanocomposites. The structural characterization of the MAX phase&#xD;
Carbide Derived Ceramic Nanostructure (CDCN) was carried out using Dynamic Light Scattering (DLS),&#xD;
Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) analysis.&#xD;
Subsequently, CDCN was mixed with Araldite CY 225 (DGEBA) at different percentages and thermally&#xD;
cured using Aradur HY 925 hardener at 130  C to make epoxy–Ti3SiC2 nanocomposites. The effect of&#xD;
CDCN-nanofiller was studied on epoxy rheology, glass transition temperature (Tg), thermal stability,&#xD;
flexural and compressive strengths, microhardness, dry sliding wear and friction properties. It was found&#xD;
that, unlike other ceramic fillers, CDCN chemically interacts with epoxy and readily dispersed in a&#xD;
polymer matrix without any deleterious structural defects. It resulted in the formation of physicochemically homogeneous microstructures. Epoxy composites prepared with CDCN filler attained 50%&#xD;
more mechanical strength and hardness. Wear analysis trends indicate Ti3SiC2 nano reinforcement&#xD;
possibly formed a lubricating tribo-chemical film that decreases the wear rate and coefficient of friction.&#xD;
This work is significant in such a way that a novel nanofiller has been identified from MAX phase carbide&#xD;
family which offers a self-lubricating interface and produces mechanically reliable, damage tolerant&#xD;
epoxy composite for state-of-the-art engineering applications.</description>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/4842">
    <title>Microwave Accelerated Synthesis of Zinc Oxide Nanoplates and their Enhanced Photocatalytic Activity Under UV and Solar Illuminations</title>
    <link>http://localhost:8080/xmlui/handle/123456789/4842</link>
    <description>Title: Microwave Accelerated Synthesis of Zinc Oxide Nanoplates and their Enhanced Photocatalytic Activity Under UV and Solar Illuminations
Authors: Anas, S; Rahul, S; Babitha, K B; Mangalaraja, R V; Ananthakumar, S
Abstract: Photoactive zinc based nanoplates were developed through a rapid microwave synthesis. A low temperature thermolysis reaction in a surfactant medium was initially performed for producing microwave&#xD;
active zinc based polar precursors. Using these precursors, the zinc oxide nanopowder having platelet&#xD;
morphologies were prepared. The nanoplatelets exhibited random growth with non-polar (1 0 1) surface&#xD;
as the major growth plane. The structural and functional features ofthe resultant zinc oxide samples were&#xD;
monitored using XRD, FTIR, TEM and PL. The photocatalytic activities of the samples were investigated&#xD;
through the standard photoreduction kinetics using the methylene blue dye. The catalytic efficiencies of&#xD;
the samples were checked both under UV and sunlight. A comparative study was also performed with&#xD;
the standard TiO2 sample. The analyses revealed that the microwave derived zinc oxide have higher&#xD;
catalytic efficiency, than the standard titania samples, both under UV and sunlight illuminations. The&#xD;
unique nature of the zinc oxide non-polar surfaces can be attributed due to the presence of more active&#xD;
two dimensional open surfaces and the higher content of oxygen defect concentrations.</description>
    <dc:date>2015-11-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/4841">
    <title>Microwave Assisted Aqueous Synthesis of Organosilane Treated Mesoporous Si@ZnO Nano Architectures as Dual-functional, Photocatalysts</title>
    <link>http://localhost:8080/xmlui/handle/123456789/4841</link>
    <description>Title: Microwave Assisted Aqueous Synthesis of Organosilane Treated Mesoporous Si@ZnO Nano Architectures as Dual-functional, Photocatalysts
Authors: Babitha, K B; Linsha, V; Anas, S; Mohamed, A P; Kiran, M; Ananthakumar, S
Abstract: A facile aqueous synthesis has been reported for the preparation of organosilane treated ZnO nano&#xD;
architectures (Si@ZnO) via microwave strategy. An in-situ addition of 3-aminopropyl trimethoxy silane&#xD;
(APTMS) resulted in the formation of polysiloxane network that effectively controlled the exaggerated&#xD;
growth of ZnO finally produced high surface area, mesoporous Si@ZnO nano clusters. The formation of a&#xD;
polysiloxane network was confirmed from the FTIR analysis. Reduction in the crystallite size was verified&#xD;
from the powder X-ray diffraction and TEM analyses. Silane treated ZnO shows highly stable dispersion,&#xD;
in aqueous medium. The quantum confinement effect of size controlled Si@ZnO was confirmed from the&#xD;
blue shift in UV–vis absorption spectra. As a function of APTMS concentration both surface charge and&#xD;
surface area was found to enhance from ( 12) to (+35.5) mV and 18 to 80 m2 g 1&#xD;
, respectively. Such&#xD;
positively charged Si@ZnO nano architectures showed property highly receptive to anionic dyes for the&#xD;
adsorption as well as photodegradation. In this study, size controlled, surface engineered, dual-functional&#xD;
photoactive adsorbent is successfully designed which is potentially useful for the recovery and recycling&#xD;
of dye contaminated water.</description>
    <dc:date>2015-06-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/4840">
    <title>Monoclinic LaGa1-xMnxGe2O7: a New Blue Chromophore based on Mn3+ in the Trigonal Bipyramidal Coordination with Longer Apical Bond Lengths</title>
    <link>http://localhost:8080/xmlui/handle/123456789/4840</link>
    <description>Title: Monoclinic LaGa1-xMnxGe2O7: a New Blue Chromophore based on Mn3+ in the Trigonal Bipyramidal Coordination with Longer Apical Bond Lengths
Authors: Saraswathy, D; Rao, P P; Sameera, S; James, V; Raj, A K V
Abstract: New blue inorganic oxide materials LaGa1−xMnxGe2O7 are developed by a solid state reaction method. Substitution of Mn3+ in LaGaGe2O7 changes the color from white (x = 0) to blue (x = 0.1–0.4). The blue color is due to the absorption in the energy region of 1.7–2.5 eV.</description>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </item>
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