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    <title>NOPR Community:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/16298</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 00:10:36 GMT</pubDate>
    <dc:date>2026-10-10T00:10:36Z</dc:date>
    <item>
      <title>&lt;span style="font-size:12.0pt;line-height: 115%;font-family:"Times New Roman","serif";mso-fareast-font-family:"Times New Roman"; mso-ansi-language:EN-IN;mso-fareast-language:EN-IN;mso-bidi-language:HI" lang="EN-IN"&gt;Effect of Fe&lt;sup&gt;3+&lt;/sup&gt; substitution on structural and macro-magnetic properties of yttrium iron garnet&lt;/span&gt;</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/24318</link>
      <description>Title: &lt;span style="font-size:12.0pt;line-height: 115%;font-family:"Times New Roman","serif";mso-fareast-font-family:"Times New Roman"; mso-ansi-language:EN-IN;mso-fareast-language:EN-IN;mso-bidi-language:HI" lang="EN-IN"&gt;Effect of Fe&lt;sup&gt;3+&lt;/sup&gt; substitution on structural and macro-magnetic properties of yttrium iron garnet&lt;/span&gt;
Authors: Modi, Kunal B; Shah, H J; Trivedi, U N; Vara, R P; Chhantbar, M C; Joshi, H H
Abstract: The structural and&#xD;
bulk magnetic properties of Fe&lt;sup&gt;3+&lt;/sup&gt; substituted yttrium iron garnet with&#xD;
general formulaY&lt;sub&gt;3-x&lt;/sub&gt;Fe&lt;sub&gt;5+x&lt;/sub&gt;O&lt;sub&gt;12&lt;/sub&gt; (&lt;i&gt;x &lt;/i&gt;= 0.0, 0.05,&#xD;
0.15,0.30 and 0.50) have been investigated by means of X-ray diffraction, EDAX,&#xD;
high field magnetization and low field a.c. susceptibility measurements. It is found&#xD;
that substituted Fe&lt;sup&gt;3+&lt;/sup&gt; ions occupy &lt;i&gt;c&lt;/i&gt;-sites and increase in lattice&#xD;
&#xD;
constant for &lt;i&gt;x&amp;gt;&#xD;
&lt;/i&gt;0.30 is due to presence of Fe&lt;sup&gt;2+&lt;/sup&gt; ions, determined through EDAX, on&#xD;
&lt;i&gt;a&lt;/i&gt;-sites. Variation of magneton number with &lt;i&gt;x &lt;/i&gt;can be explained satisfactorily&#xD;
assuming the collinear spin ordering model and Neel temperature values deduced experimentally&#xD;
from a.c. suscepti bility measurements are in good agreement to those calculated&#xD;
theoretically.
Page(s): 502-506</description>
      <pubDate>Mon, 01 Dec 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/24318</guid>
      <dc:date>2003-12-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Glass forming ability of Te-Bi-Se based alloys</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/24317</link>
      <description>Title: Glass forming ability of Te-Bi-Se based alloys
Authors: Saxena, Manish; Agarwal, Animesh; Bhatnagar, P K
Abstract: In the present work,&#xD;
the relationships for the glass transition temperature &lt;i&gt;T&lt;sub&gt;g&lt;/sub&gt;, &lt;/i&gt;the&#xD;
peak temperature &lt;i&gt;T&lt;sub&gt;p&lt;/sub&gt;, &lt;/i&gt;and the difference of crystallization temperature&#xD;
and glass transition temperature, (&lt;i&gt;T&lt;sub&gt;c&lt;/sub&gt;&lt;/i&gt; -&lt;i&gt; T&lt;sub&gt;g&lt;/sub&gt;&lt;/i&gt;), for different heating&#xD;
rates have been studied with the increase&#xD;
in Bi content. With the increase in heating rates &lt;i&gt;T&lt;sub&gt;g&lt;/sub&gt;, T&lt;sub&gt;c &lt;/sub&gt; &lt;/i&gt;and &lt;i&gt;T&lt;sub&gt;p&lt;/sub&gt; &lt;/i&gt;are found to increase.&#xD;
The glass transition temperature represents the strength or rigidity of the glass&#xD;
structure. This analysis helps in finding the suitability of an alloy to be used&#xD;
in phase transition optical memories/ switches.
Page(s): 498-501</description>
      <pubDate>Mon, 01 Dec 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/24317</guid>
      <dc:date>2003-12-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Dielectric properties and a.c. electrical conductivity of aqueous solution grown pure and iodine doped poly (vinyl alcohol) films</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/24316</link>
      <description>Title: Dielectric properties and a.c. electrical conductivity of aqueous solution grown pure and iodine doped poly (vinyl alcohol) films
Authors: Sengwa, R J; Kaur, Kulvinder
Abstract: Poly vinyl alcohol&#xD;
(PVA) films of uniform thicknesses 280, 120, 80, 50 and 25 microns, and also 50&#xD;
micron PVA films doped with 4, 3, 2 and 1 wt% iodine of PVA weight in aqueous solution&#xD;
have been prepared by solution grown technique. Ag-PVA-Ag sandwich structures&#xD;
of film capacitors have been fabricated for their dielectric characterization. The&#xD;
capacitance and dissipation factor of these capacitors are measured in the frequency&#xD;
range 100Hz-100 kHz at 25°C. The dielectric permittivity ɛ&lt;i&gt;'&lt;/i&gt;, loss ɛ&lt;i&gt;"&lt;/i&gt;,&#xD;
and a.c. conductivity σ, have been determined using the measured values of&#xD;
capacitance and dissipation factor. It is found that the value of ɛ&lt;i&gt;'&lt;/i&gt; decreases&#xD;
with increase in frequency and increases with the film thickness while&#xD;
dielectric loss ɛ&lt;i&gt;"&lt;/i&gt; shows marked variation with frequency. For iodine&#xD;
doped films, values of ɛ&lt;i&gt;'&lt;/i&gt; and ɛ&lt;i&gt;"&lt;/i&gt; vary anomalously with the&#xD;
increase in concentration of iodine. From the a.c. conduction studies, it is observed&#xD;
that the a.c. conductivity of pure PVA films increases with the film thickness&#xD;
and vary almost linearly with frequency in the range of 10-&lt;sup&gt;11&lt;/sup&gt; -10&lt;sup&gt;-8&lt;/sup&gt;&#xD;
S cm&lt;sup&gt;-1&lt;/sup&gt;. Further it is found that there is anomalous variation in conductivity&#xD;
of iodine doped PVA film with increase in iodine concentration. From these dielectric&#xD;
studies, it seems that an increase in ɛ&lt;i&gt;'&lt;/i&gt; and ɛ&lt;i&gt;"&lt;/i&gt; with the increase&#xD;
in PVA film thickness is due to the residual water or variation in degree of syndiotacticity&#xD;
of PVA chain. In case of iodine doped PVA films, the variations in crystalline&#xD;
and complex formation of PVA molecules with iodine are responsible to change the&#xD;
dielectric parameters.
Page(s): 492-497</description>
      <pubDate>Mon, 01 Dec 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/24316</guid>
      <dc:date>2003-12-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Biofilm formation on structural materials in deep sea environments</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/24315</link>
      <description>Title: Biofilm formation on structural materials in deep sea environments
Authors: Venkatesan, R; Dwarakadasa, E S; Ravindran, M
Abstract: Biofilm&#xD;
formation on structural materials in deep-sea environment after long duration&#xD;
of exposure is reported here for the first time. Some structural material specimens&#xD;
such as steel, steel with zinc and aluminum anodes and carbon fibre-reinforced composite&#xD;
were exposed at depths of 500, 1200, 3500 and 5100 m for 174 days. The bacterial&#xD;
colony formation&#xD;
&#xD;
on these specimens&#xD;
was studied after their retrieval from the ocean. Macrofouling was not found in&#xD;
any of these materials. Carbon fibre-reinforced composite did not support bacterial&#xD;
colony formation at all the tested depths. Steel supported bacterial colonies&#xD;
at all depths. Aluminium and zinc anodes did not support bacterial colonies at 3500&#xD;
and 5100 m depths.&#xD;
&#xD;
This could be&#xD;
related to lower temperatures prevailing at these depths. Also, all the&#xD;
identified bacterial colonies were aerobic as dissolved oxygen was present even&#xD;
at 5100 m depth. Hence, anaerobic conditions did not exist during exposure under&#xD;
these structural conditions. Dissolved oxygen data at the experimental site is also&#xD;
presented and discussed.
Page(s): 486-491</description>
      <pubDate>Mon, 01 Dec 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/24315</guid>
      <dc:date>2003-12-01T00:00:00Z</dc:date>
    </item>
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