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  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/24323">
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/24323</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/24444" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/24441" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/24440" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/24439" />
      </rdf:Seq>
    </items>
    <dc:date>2026-10-09T20:49:29Z</dc:date>
  </channel>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/24444">
    <title>Low temperature synthesis of MoO&lt;sub&gt;3&lt;/sub&gt; through the use of NH&lt;sub&gt;2&lt;/sub&gt;OH.HC1&lt;b&gt; &lt;/b&gt;as reducing agent</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/24444</link>
    <description>Title: Low temperature synthesis of MoO&lt;sub&gt;3&lt;/sub&gt; through the use of NH&lt;sub&gt;2&lt;/sub&gt;OH.HC1&lt;b&gt; &lt;/b&gt;as reducing agent
Authors: Mallikarjuna, N N; Venkataraman, A
Abstract: This paper reports a novel technique for&#xD;
the synthesis of MoO&lt;sub&gt;3&lt;/sub&gt; through the reduction of ammonium molybdate&#xD;
using hydroxylamine hydrochloride as a reductant. MoO&lt;sub&gt;3&lt;/sub&gt; is formed&#xD;
upon thermal decomposition of the reduced ammonium molybdate. The progress of&#xD;
the formation of the oxide is understood on the basis of structure and thermal&#xD;
studies.
Page(s): 303-306</description>
    <dc:date>2001-10-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/24441">
    <title>Synthesis and characterization of IPP-g-glycidylmethacrylate copolymer</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/24441</link>
    <description>Title: Synthesis and characterization of IPP-g-glycidylmethacrylate copolymer
Authors: Brahmbhatt, Ragesh B; Patel, Alpesh C; Devi, Surekha
Abstract: Isotactic polypropylene (IPP) was grafted&#xD;
with glycidylmethacrylate (GMA) using benzoylperoxide as free radical initiator&#xD;
in an inert atmosphere and toluene as solvent at 110°C temperature. Various&#xD;
reaction conditions such as monomer and initiator concentration, time,&#xD;
temperature, medium and atmosphere were optimized for achieving higher % of&#xD;
grafting. Maximum 2.8% grafting was observed. The graft copolymers were characterized&#xD;
by thermal and spectral methods.
Page(s): 297-302</description>
    <dc:date>2001-10-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/24440">
    <title>Hydration of C&lt;sub&gt;4&lt;/sub&gt;AF in the presence of artificial CaSO&lt;sub&gt;4&lt;/sub&gt; and lime</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/24440</link>
    <description>Title: Hydration of C&lt;sub&gt;4&lt;/sub&gt;AF in the presence of artificial CaSO&lt;sub&gt;4&lt;/sub&gt; and lime
Authors: El-Alfi, S; Abd-Aleem, S; El-Didamony, H
Abstract: The ferrite phase consists of about 8-13&#xD;
wt% portland cement. This phase has received little attention with regard to&#xD;
its hydration. The aim of present investigation is to synthesize the ferrite&#xD;
phase and study the rate of hydration in the presence of CaSO&lt;sub&gt;4&lt;/sub&gt; and&#xD;
CaO up to 28-days in suspension. This study is followed by the determination of&#xD;
the free lime as well as&#xD;
&#xD;
combined water con tents and the&#xD;
hydration products by the XRD analysis. The results revealed that whatever the&#xD;
amount of CaSO&lt;sub&gt;4&lt;/sub&gt; the monosulphate AF&lt;sub&gt;m&lt;/sub&gt; was the only phase&#xD;
formed from 6 h up to 28-days and the ettringite AF&lt;sub&gt;t&lt;/sub&gt; was not formed.&#xD;
In the presence of 1 mol CaSO&lt;sub&gt;4&lt;/sub&gt; and 2 mol CaO, the monosulphate AF&lt;sub&gt;m&lt;/sub&gt;&#xD;
with carboaluminate was the dominant phase at 28-days. When the amount of CaSO&lt;sub&gt;4&lt;/sub&gt;&#xD;
was increased to 3 mol with the same amount of lime the hydration was retarded&#xD;
in comparison with that containing 1 mol of CaSO&lt;sub&gt;4&lt;/sub&gt;. Very small amount&#xD;
of sulphoaluminate ferrite hydrate was formed with residual reactants such as C&lt;sub&gt;4&lt;/sub&gt;AF,CaSO&lt;sub&gt;4&lt;/sub&gt;&#xD;
and Ca(OH)&lt;sub&gt;2&lt;/sub&gt;.
Page(s): 292-296</description>
    <dc:date>2001-10-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/24439">
    <title>Structural and dielectric properties of KTiOPO&lt;sub&gt;4&lt;/sub&gt; ceramic</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/24439</link>
    <description>Title: Structural and dielectric properties of KTiOPO&lt;sub&gt;4&lt;/sub&gt; ceramic
Authors: Choudhary, S N; Prasad, K; Choudhary, R N P
Abstract: Ceramic samples of KTiOPO&lt;sub&gt;4 &lt;/sub&gt;are&#xD;
prepared using chemical method. X-ray diffraction (XRD) technique has been used&#xD;
to check the formation of single phase KTiOPO&lt;sub&gt;4&lt;/sub&gt; compound. The cell&#xD;
parameters obtained by XRD analyses are &lt;i&gt;a = &lt;/i&gt;20.125(8) Å, &lt;i&gt;b = &lt;/i&gt;8.433(1)&#xD;
Å and &lt;i&gt;c = &lt;/i&gt;11.492(4) Å in orthorhombic crystal system. The ceramic&#xD;
samples of KTiOPO&lt;sub&gt;4&lt;/sub&gt; have&lt;i&gt; &lt;/i&gt;been characterized by dielectric&#xD;
studies. The room temperature values of dielectric constant and dielectric loss&#xD;
are found to be 10.32 and 0.12 respectively at 1 kHz.
Page(s): 289-291</description>
    <dc:date>2001-10-01T00:00:00Z</dc:date>
  </item>
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