<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>DSpace Collection:</title>
  <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/1761" />
  <subtitle />
  <id>http://localhost:8080/xmlui/handle/123456789/1761</id>
  <updated>2026-05-08T08:57:48Z</updated>
  <dc:date>2026-05-08T08:57:48Z</dc:date>
  <entry>
    <title>Angiogenic Profiling of Synthesized Carbon Quantum Dots</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/5142" />
    <author>
      <name>Shereema, R M</name>
    </author>
    <author>
      <name>Sruthi, T V</name>
    </author>
    <author>
      <name>Kumar, V B S</name>
    </author>
    <author>
      <name>Rao, T P</name>
    </author>
    <author>
      <name>Shankar, S S</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/5142</id>
    <updated>2026-04-20T04:21:15Z</updated>
    <published>2015-10-20T00:00:00Z</published>
    <summary type="text">Title: Angiogenic Profiling of Synthesized Carbon Quantum Dots
Authors: Shereema, R M; Sruthi, T V; Kumar, V B S; Rao, T P; Shankar, S S
Abstract: A simple method was employed for the synthesis of green&#xD;
luminescent carbon quantum dots (CQDs) from styrene soot. The CQDs&#xD;
were characterized by transmission electron microscopy, X-ray photoelectron&#xD;
spectroscopy, Fourier transform infrared, and Raman spectroscopy. The&#xD;
prepared carbon quantum dots did not show cellular toxicity and could&#xD;
successfully be used for labeling cells. We also evaluated the effects of carbon&#xD;
quantum dots on the process of angiogenesis. Results of a chorioallantoic&#xD;
membrane (CAM) assay revealed the significant decrease in the density of&#xD;
branched vessels after their treatment with CQDs. Further application of&#xD;
CQDs significantly downregulated the expression levels of pro-angiogenic&#xD;
growth factors like VEGF and FGF. Expression of VEGFR2 and levels of&#xD;
hemoglobin were also significantly lower in CAMs treated with CQDs,&#xD;
indicating that the CQDs inhibit angiogenesis. Data presented here also show&#xD;
that CQDs can selectively target cancer cells and therefore hold potential in&#xD;
the field of cancer therapy.</summary>
    <dc:date>2015-10-20T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>MAX Phase Ternary Carbide Derived 2-D Ceramic Nanostructures [CDCN] as Chemically Interactive Functional Fillers for Damage Tolerant Epoxy Polymer Nanocomposites</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/4843" />
    <author>
      <name>Vaisakh, S S</name>
    </author>
    <author>
      <name>Mahesh, K V</name>
    </author>
    <author>
      <name>Balanand, S</name>
    </author>
    <author>
      <name>Metz, R</name>
    </author>
    <author>
      <name>Hassanzadeh, M</name>
    </author>
    <author>
      <name>Ananthakumar, S</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/4843</id>
    <updated>2024-04-05T10:16:35Z</updated>
    <published>2015-01-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Microwave Accelerated Synthesis of Zinc Oxide Nanoplates and their Enhanced Photocatalytic Activity Under UV and Solar Illuminations</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/4842" />
    <author>
      <name>Anas, S</name>
    </author>
    <author>
      <name>Rahul, S</name>
    </author>
    <author>
      <name>Babitha, K B</name>
    </author>
    <author>
      <name>Mangalaraja, R V</name>
    </author>
    <author>
      <name>Ananthakumar, S</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/4842</id>
    <updated>2024-04-05T10:15:57Z</updated>
    <published>2015-11-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2015-11-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Microwave Assisted Aqueous Synthesis of Organosilane Treated Mesoporous Si@ZnO Nano Architectures as Dual-functional, Photocatalysts</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/4841" />
    <author>
      <name>Babitha, K B</name>
    </author>
    <author>
      <name>Linsha, V</name>
    </author>
    <author>
      <name>Anas, S</name>
    </author>
    <author>
      <name>Mohamed, A P</name>
    </author>
    <author>
      <name>Kiran, M</name>
    </author>
    <author>
      <name>Ananthakumar, S</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/4841</id>
    <updated>2024-04-05T10:10:50Z</updated>
    <published>2015-06-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2015-06-01T00:00:00Z</dc:date>
  </entry>
</feed>

