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    <title>DSpace Collection:</title>
    <link>http://localhost:8081/jspui/handle/123456789/4969</link>
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        <rdf:li rdf:resource="http://localhost:8081/jspui/handle/123456789/17949" />
        <rdf:li rdf:resource="http://localhost:8081/jspui/handle/123456789/17832" />
        <rdf:li rdf:resource="http://localhost:8081/jspui/handle/123456789/17830" />
        <rdf:li rdf:resource="http://localhost:8081/jspui/handle/123456789/17829" />
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    <dc:date>2025-07-26T23:57:29Z</dc:date>
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  <item rdf:about="http://localhost:8081/jspui/handle/123456789/17949">
    <title>SYNTHESIS OF NiO NANOPARTICLES AND STUDY THEIR PROPERTIES</title>
    <link>http://localhost:8081/jspui/handle/123456789/17949</link>
    <description>Title: SYNTHESIS OF NiO NANOPARTICLES AND STUDY THEIR PROPERTIES
Authors: Sanger, Amit
Abstract: NiO nanoparticles were synthesized using simple wet chemical method. These nanoparticles&#xD;
were calcinated at different temperatures 300°C-1000°C (S1-S5) and their structural properties&#xD;
were studied using X-ray diffraction (XRD), Field Emission Scanning Electron Microscopy&#xD;
(FESEM) and Transmission Electron Microscopy (TEM). X-ray diffraction observations and&#xD;
FESEM images of the calcinated NiO samples indicate that the crystallinity and the particles&#xD;
size both were increasing with increase in calcination temperatures. The XRD results confirm&#xD;
the decrease in strain with respect to calcinated temperature. This may be due to the surface&#xD;
effects and defects existed in the samples. TEM results confirm the polycrystalline nature of&#xD;
samples by SAED pattern. The electrical properties of the NiO pellets were examined by four&#xD;
probe method by measuring direct current (DC) conductivities at different temperatures. The&#xD;
activation energy (Ea) decreases from 0.57eV to 0.33eV when pellets annealed from 300°C to&#xD;
800°C. The conductivity of samples increased with increase in particle size. It is because that&#xD;
electrons felt low resistance during travel due to large grain size. The optical properties were&#xD;
examined by Photoluminescence (PL) spectroscopy. The emission band came out in the visible&#xD;
range. The surface effects dominated the optical characteristics. The magnetic properties were&#xD;
examined by SQUID. The magnetic moment values come out 3.081.tB to 8.07lB from the&#xD;
measurement. The Weiss constant increased with the particle size and overcome the Ned&#xD;
temperature which may be due to the superexchange properties of NiO samples. The samples&#xD;
did not show any superparamagnetic effect at room temperature which may be due to the&#xD;
multidomain nature of particles.</description>
    <dc:date>2013-06-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8081/jspui/handle/123456789/17832">
    <title>SYNTHESIS AND CHARACTERIZATION OF T102@NiO NANOSTRUCTURES</title>
    <link>http://localhost:8081/jspui/handle/123456789/17832</link>
    <description>Title: SYNTHESIS AND CHARACTERIZATION OF T102@NiO NANOSTRUCTURES
Authors: Kumar, Vijayesh
Abstract: A method to synthesize Ti02@NiO core shell nanostructures was developed for a number of&#xD;
applications such as photocatalysis, DSSC, biotechnogical fields etc. The square faced NiO&#xD;
nanorods were synthesized by thermal decomposition of nickel oxalate dihydrate nanorods,&#xD;
which was prepared by reverse micellar route. The two microemulsions contains oil phase (iso&#xD;
octane as non polar solvent, n-butanol as co-surfactant and CTAB surfactant) and 0.1 M salt&#xD;
solution as water phase reacts to form nickel oxalate dihydrate nanorods. TiO2 nanoparticles&#xD;
were synthesized by hydrolysis of titanium tetra isopropoxide (TT'IP). TiO2 nanoparticles were&#xD;
- coated on the surface of NiO nanorods by electrostatic interaction and then product was annealed&#xD;
at suitable temperature to get Ti02@NiO core shell nanorods. These nanorods were&#xD;
characterized by PXRD, FESEM, TEM, UV-Vis spectroscopy, SQUID. In another study, NiO&#xD;
nanoparticles were fabricated through the chemical precipitation method by using nickel nitrate,&#xD;
sodium hydroxide as precursor materials and CTAB as surfactant. PXRD data gives the primary&#xD;
characterization about the crystalline NiO nanostructures. TiO2 coating on these nanostructures&#xD;
was done by using titanium tetra isopropoxide as precursor and NH40H as capping agent. The&#xD;
shell of T102 can be analyzed by FESEM and PXRD, and so there is pre calculated amount of&#xD;
precursor has been used. Core shell structure reduces the surface charge recombination as TiO2&#xD;
coating acts as a blocking layer for electron to reduce back recombination. Using these&#xD;
nanostructures, a good the photocatalytic performance is expected.</description>
    <dc:date>2013-06-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8081/jspui/handle/123456789/17830">
    <title>SYNTHESIS OF VARIOUS NANOCOMPOSITES AND STUDY OF THEIR BIOMEDICAL APPLICATIONS</title>
    <link>http://localhost:8081/jspui/handle/123456789/17830</link>
    <description>Title: SYNTHESIS OF VARIOUS NANOCOMPOSITES AND STUDY OF THEIR BIOMEDICAL APPLICATIONS
Authors: Matai, Ishita
Abstract: Emergence of multi-resistant organisms (MROs) leads to ineffective treatment with&#xD;
the currently available medications which pose a great threat to public health and food&#xD;
technology sectors. In this regard, there is an urgent need to strengthen the present&#xD;
therapies or to look over for other potential alternatives such as use of "metal&#xD;
nanocomposites" and "herbal drug loaded polymeric nanofibers". Thus, the present&#xD;
study focuses on synthesis of silver-zinc oxide (Ag-ZnO) nanocomposites which will&#xD;
have a broad-spectrum antibacterial activity against Gram-positive and Gram-negative&#xD;
bacteria. Ag-ZnO nanocomposites of varied molar ratios were synthesized by simple&#xD;
microwave assisted reactions in the absence of surfactants. The crystalline behavior,&#xD;
composition and morphological analysis of the prepared powders were evaluated by&#xD;
X-ray diffraction, infrared spectroscopy, field emission scanning electron microscopy&#xD;
(FE-SEM) and energy dispersive X-ray (EDX) analysis. Particle size measurements&#xD;
were carried out by transmission electron microscopy (TEM). Staphylococcus aureus&#xD;
(S. aureus) and recombinant green fluorescent protein (GFP) expressing antibiotic&#xD;
resistant Escherichia coil (E. coil) were selected as Gram-positive and Gram-negative&#xD;
11&#xD;
model systems respectively and the bactericidal activity of Ag-ZnO nanocomposite&#xD;
were studied. The minimum inhibitory concentration (MIC) and minimum killing&#xD;
concentration (MKC) of the nanocomposite against the model systems were&#xD;
determined by visual turbidity analysis and optical density analysis. Qualitative and&#xD;
quantitative assessments of its antibacterial effects were performed by fluorescent&#xD;
microscopy, fluorescent spectroscopy and Gram staining measurements. Excellent&#xD;
bactericidal activity at low concentrations of nanocomposites was observed in both&#xD;
A&#xD;
the bacterial model systems suggesting its potential application as a broad-spectrum&#xD;
antibacterial agent. Changes in cellular morphology were examined by atomic force&#xD;
microscopy (AFM), FE-SEM and TEM. Finally, on the basis of the present&#xD;
investigation and previously published reports, a plausible antibacterial mechanism of&#xD;
Ag-ZnO nanocomposites was proposed. Also, electrospinning technique was utilized&#xD;
to fabricate chitosan-PEO (Polyethylene oxide) nanofibers loaded with herbal drug.&#xD;
The morphology, homogeneity and diameter of the synthesized nanofibers were&#xD;
determined by FE-SEM analysis. Visual turbidity analysis and fluorescence&#xD;
microscopy were done to determine the MIC and MKC values of herbal drug. Further,&#xD;
the antibacterial activity of drug loaded nanofibers was determined by fluorescence&#xD;
microscopy against GFP E.coii. The fabricated nanofibers exhibited good&#xD;
antibacterial activity at low concentrations of herbal drug suggesting its implications&#xD;
in wound dressings.</description>
    <dc:date>2013-06-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8081/jspui/handle/123456789/17829">
    <title>SYNTHESIS OF PVP STABILIZED SILVER NANOSTRUCTURES AND STUDY OF THEIR PHYSICAL AND BIOLOGICAL PROPERTIES</title>
    <link>http://localhost:8081/jspui/handle/123456789/17829</link>
    <description>Title: SYNTHESIS OF PVP STABILIZED SILVER NANOSTRUCTURES AND STUDY OF THEIR PHYSICAL AND BIOLOGICAL PROPERTIES
Authors: Kumar, Harsh
Abstract: 1'he present work reports synthesis of l'VP coated silver nanostructures in a self assembled&#xD;
bottom-Lip approach. Their characterization carried out by XRD, FTIR, AFM, FESEM and&#xD;
'l'FM. 'their optical, electrical and antibacterial activities have also been analysed. The size of&#xD;
Ag —PVP nanoparticles also found to be the function of concentration of seed Ag particles&#xD;
used for their preparation. For different seed concentration (106 rnol/dm3) at: 1.73, 2.88 and&#xD;
5. 19. the particle size (nm) decreases as: 15, 7 and 2 respectively. 'Fhese particles undergo&#xD;
aoZ~ tol rc-1o1 a tioii to form chain like structure upon ageing.&#xD;
l:i.cshly prepared optimized silver nanoparticles show an absorption peak around 399 1101&#xD;
which red shifted upon ageing to 409 nm along with the appearance of a new peak at 263 nm,&#xD;
indicating a change in there morphology as arrived by electron microscopic studies. These&#xD;
nanosiructures exhibit interesting fluorescing behaviour, depending upon the excitation&#xD;
energy. Under 450 nm excitation, emission was observed to have various characteristic bands&#xD;
at 468. 494, 511, 530 and 563 nm respectively.&#xD;
Ag-PVP nanochains were tested for antibacterial activity against E.coli and S. aureus.&#xD;
l'hesc particles were found to inhibit the growth of' S. aureus at 6 ig/gL. As synthesized,&#xD;
silver nanostructures may find applications in the field of optoelectronics, biosensing and&#xD;
b iotec hn o logy</description>
    <dc:date>2013-06-01T00:00:00Z</dc:date>
  </item>
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