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    <title>NISCAIR Online Periodicals Repository Collection: IJPAP Vol.50(06) [June 2012]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14143</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/14184" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/14183" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/14182" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/14181" />
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    <title>The Collection's search engine</title>
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/14184">
    <title>Characterization of dielectric dispersion and ionic conduction behaviour of acetonitrile at low frequencies</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14184</link>
    <description>Title: Characterization of dielectric dispersion and ionic conduction behaviour of acetonitrile at low frequencies
&lt;br/&gt;
&lt;br/&gt;Authors: Choudhary, Shobhna; Sengwa, R J
&lt;br/&gt;
&lt;br/&gt;Abstract: The complex dielectric function, ionic conductivity and impedance behaviour&#xD;
of acetonitrile have been investigated over the frequency range 20 Hz-1 MHz and&#xD;
at the temperatures 15, 30 and 45°C. The real part of complex&#xD;
dielectric function increases significantly with the decrease of frequency&#xD;
below 100 kHz, confirms the contribution of electrode polarization effect in&#xD;
the dielectric properties of acetonitrile at low frequencies. The real part of&#xD;
alternating current conductivity shows the direct current ionic conductivity&#xD;
plateau in the frequency range 1 kHz-1 MHz. The complex impedance plane plots&#xD;
have been used to separate the electrode polarization effect from the bulk&#xD;
acetonitrile properties. The values of temperature dependence electrode&#xD;
polarization relaxation time have been determined from the frequency which corresponds&#xD;
to the peaks observed in the dielectric loss tangent spectra. The activation&#xD;
energies of relaxation time, conductivity and viscosity have been evaluated&#xD;
from their Arrhenius plots, and discussed in relation to the ionic conduction&#xD;
mechanism in the pure liquid state of acetonitrile.
&lt;br/&gt;
&lt;br/&gt;Page(s): 411-414</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/14183">
    <title>Effect of salinity on the dielectric properties of water</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14183</link>
    <description>Title: Effect of salinity on the dielectric properties of water
&lt;br/&gt;
&lt;br/&gt;Authors: Gadani, D H; Rana, V A; Bhatnagar, S P; Prajapati, A N; Vyas, A D
&lt;br/&gt;
&lt;br/&gt;Abstract: The complex&#xD;
permittivity &lt;img src='http://www.niscair.res.in/jinfo/belongs.gif' border=0&gt;=&lt;img src='http://www.niscair.res.in/jinfo/belongs.gif' border=0&gt;'-j&lt;img src='http://www.niscair.res.in/jinfo/belongs.gif' border=0&gt;" of distilled water and NaCl&#xD;
solutions of concentrations varying from 5000 to 35000 ppm have been measured&#xD;
in the frequency range from 200 MHz to 1.4 GHz using a Vector Network Analyzer&#xD;
(VNA). The complex permittivity of saline water collected from Kanyakumari sea&#xD;
bank has also been measured in this frequency range. It has been observed that&#xD;
the dielectric constant of water decreases slowly with increase in frequency&#xD;
from 200 MHz to 1.4 GHz for given salinity of water. At given frequency, the&#xD;
dielectric constant decreases slowly with increase in salinity from 5000 to&#xD;
35000 ppm. The dielectric loss of distilled water increases with increase in&#xD;
frequency from 200 MHz to 1.4 GHz, but for saline water it decreases with&#xD;
increase in frequency, over this frequency range. The decrease in dielectric&#xD;
loss with increase in frequency is more for higher salinity in water. The&#xD;
variation of complex permittivity of water with salinity and frequency is&#xD;
calculated using the Stogryn equations&lt;sub&gt; &lt;/sub&gt;[&lt;i style=""&gt;IEEE Trans. On Microwave Theory and Techniques&lt;/i&gt;, August 1971, pp.&#xD;
733-736] as well as with the Klein and Swift [&lt;i&gt;IEEE Transactions on Antennas and Propagation&lt;/i&gt;, Vol. AP-25, No.1, January 1977, pp. 104-111]&#xD;
equations, and the results are found to be in good agreement with corresponding&#xD;
experimental values. The variation of emissivity with variation of salinity&#xD;
calculated at fixed frequencies of 0.5, 0.9 and &#xD;
1.4 GHz have also been presented in the paper, which is very much useful for&#xD;
remote sensing applications of oceans.
&lt;br/&gt;
&lt;br/&gt;Page(s): 405-410</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/14182">
    <title>Optical and infrared properties of lithium diborate glasses doped with copper oxide: Effect of gamma irradiation</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14182</link>
    <description>Title: Optical and infrared properties of lithium diborate glasses doped with copper oxide: Effect of gamma irradiation
&lt;br/&gt;
&lt;br/&gt;Authors: El-Batal, Hatem A; El-Mandouh, Zeinab S; Zayed, Hamdia A; Marzouk, Samir Y; El-Komy, Gihan M; Hosny, Ahmed
&lt;br/&gt;
&lt;br/&gt;Abstract: A series of lithium diborate&#xD;
glasses containing successive CuO contents have been prepared by conventional&#xD;
melt annealing technique. Optical and infrared spectral properties have been&#xD;
measured before and after successive gamma irradiation to study the effect of&#xD;
gamma irradiation on the prepared glasses. Cu-doped samples show the same&#xD;
strong UV absorption as the undoped sample beside a characteristic broad&#xD;
visible band around 772 nm with marked splitting into four peaks at 614, 656,&#xD;
774 and 1064 nm in higher CuO contents. Gamma irradiation of undoped lithium&#xD;
borate glass causes the generation of induced absorption bands but the&#xD;
introduction of CuO content causes some shielding behaviour towards successive&#xD;
gamma irradiation. Infrared absorption spectra of the undoped and CuO-doped&#xD;
glasses show characteristic vibrational absorption bands related to triangular&#xD;
and tetrahedral borate units. The addition of CuO in lithium borate glasses&#xD;
causes minor changes on the intensities of the IR bands but their numbers and&#xD;
positions are retained. The same limited effect is observed with gamma&#xD;
irradiation on the measured IR bands.
&lt;br/&gt;
&lt;br/&gt;Page(s): 398-404</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/14181">
    <title>Thermoelastic properties of alkali halides at high temperatures</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14181</link>
    <description>Title: Thermoelastic properties of alkali halides at high temperatures
&lt;br/&gt;
&lt;br/&gt;Authors: Sunil, K; Sharma, B S
&lt;br/&gt;
&lt;br/&gt;Abstract: The thermoelastic&#xD;
properties of materials at high temperatures, specifically the thermal&#xD;
expansivity and the isothermal bulk modulus have been studied using the Anderson formula for&#xD;
thermal expansivity and the interatomic potential functions within the&#xD;
framework of the Born model. We have considered sixteen alkali halides with&#xD;
NaCl structure, and calculated their properties for a wide range of&#xD;
temperatures starting from room temperature up to their melting temperatures.&#xD;
Potential energy curves have been plotted and used to determine interatomic&#xD;
distances at the melting points. The results for interatomic distances, thermal&#xD;
expansivity and isothermal bulk modulus at different temperatures have been&#xD;
found to compare well with the available experimental data. The Hildebrand&#xD;
equation of state has been used to predict the pressure-volume-temperature&#xD;
relationship in case of NaCl using the Born-Mayer exponential potential&#xD;
function. The results,thus, obtained are found to present good agreement with&#xD;
the measured data.
&lt;br/&gt;
&lt;br/&gt;Page(s): 387-397</description>
  </item>
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