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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/20825</link>
    <description />
    <items>
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        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/20929" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/20854" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/20853" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/20852" />
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    <dc:date>2026-10-05T10:48:56Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/20929">
    <title>Thermodynamics of interaction between &lt;img src='http://www.niscair.res.in/jinfo/small.gif' border=0&gt;-cystine and sodium/magnesium chloride in aqueous solution</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/20929</link>
    <description>Title: Thermodynamics of interaction between &lt;img src='http://www.niscair.res.in/jinfo/small.gif' border=0&gt;-cystine and sodium/magnesium chloride in aqueous solution
Authors: Li, Dacheng; Yu, Qingjiang; Wang, Yong; Sun, Dezhi
Abstract: Interactions of &lt;img src='http://www.niscair.res.in/jinfo/small.gif' border=0&gt;-cystine&#xD;
with sodium chloride and magnesium chloride have been studied by determining&#xD;
the solubility of cystine in aqueous salt solutions of different concentration&#xD;
at varying temperatures. The interaction thermodynamic parameters have been&#xD;
estimated with the solubility data. The results show that both NaCl and MgCl&lt;sub&gt;2&lt;/sub&gt;&#xD;
in water is beneficial to dissolution of &lt;img src='http://www.niscair.res.in/jinfo/small.gif' border=0&gt;-cystine.&#xD;
Enthalpy or entropy of interaction between &lt;img src='http://www.niscair.res.in/jinfo/small.gif' border=0&gt;-cystine and NaCl is negative while that between &lt;img src='http://www.niscair.res.in/jinfo/small.gif' border=0&gt;-cystine&#xD;
and MgCl&lt;sub&gt;2&lt;/sub&gt; is positive. These interesting results are discussed in&#xD;
the light of static electricity theory as well as hydration of ions.
Page(s): 1126-1130</description>
    <dc:date>2002-06-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/20854">
    <title>Silica enriched faujasitic zeolite-Y from flyash</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/20854</link>
    <description>Title: Silica enriched faujasitic zeolite-Y from flyash
Authors: Meshram, S U; Rayalu, S S; Munshi, K N; Hasan, M Z
Abstract: Various process modifications to enrich silica&#xD;
in zeolite-Y have been carried out by increasing substantially the SiO&lt;sub&gt;2&lt;/sub&gt;&#xD;
&lt;i&gt;/&lt;/i&gt;Al&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; ratio from 1.8-2.0 to 2.5-3.0 with&#xD;
consequent increase in thermal stability. Some new phases of zeolites have been&#xD;
observed with improved silica alumina ratio up to 3.0 to 3.5. Crystallinity has&#xD;
been monitored by XRD analysis, ranging from 70-99% for different samples.
Page(s): 1212-1216</description>
    <dc:date>2002-06-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/20853">
    <title>A study of the underpotential deposited hydrogen on the nickel deposited electrode in alkaline media</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/20853</link>
    <description>Title: A study of the underpotential deposited hydrogen on the nickel deposited electrode in alkaline media
Authors: Jafarian, M; Mahjani, M G; Hoseni, M; Gohal, F
Abstract: Hydrogen evolution reaction has been studied&#xD;
on the nickel deposited electrode. Two reduction peaks at -1 V/Ag-AgCl and -1.3V/Ag-AgCl&#xD;
and one oxidation peak at - 1.3V/Ag-AgCl have been observed. Shift due to oxidation&#xD;
peak arises from change of cathodic limit, attributed to the two competitive reactions&#xD;
on the surface. The peak located on the more anodic side is due to the oxidation&#xD;
of H&lt;sub&gt;UPD&lt;/sub&gt; and the second peak due to the oxidation of H&lt;sub&gt;OPD&lt;/sub&gt; The&#xD;
sodium ion has no effect on the hydrogen evolution reaction. The diffusion coefficient&#xD;
of hydrogen is calculated to be D=2.88×10&lt;sup&gt;-10&lt;/sup&gt; cm&lt;sup&gt;2&lt;/sup&gt; s&lt;sup&gt;-1&lt;/sup&gt; using impedance technique.
Page(s): 1208-1211</description>
    <dc:date>2002-06-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/20852">
    <title>Spectral and thermal studies of homodinuclear and heterodinuclear glutathione complexes</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/20852</link>
    <description>Title: Spectral and thermal studies of homodinuclear and heterodinuclear glutathione complexes
Authors: Garg, Bhagwan S; Kumar, Deo Nandan; Singh, B K
Abstract: The complexes of the types [M&lt;sub&gt;2&lt;/sub&gt;LSO&lt;sub&gt;4&lt;/sub&gt;.2H&lt;sub&gt;2&lt;/sub&gt;O]&#xD;
where L=GSH, M = Co(II), Cu(II), Zn(II), Cd(II) and [MM'LSO&lt;sub&gt;4&lt;/sub&gt;.2H&lt;sub&gt;2&lt;/sub&gt;O]&#xD;
where L = GSH, M = Cu(II), M' = Zn(II) and M = Co(II), M' = Cd(II)] have been prepared&#xD;
and characterized by elemental analysis, magnetic susceptibility measurements, JR,&#xD;
EPR, electronic spectral studies and thermal analysis. Deprotonation and&#xD;
coordination of thiol group occurs and glycine residue binds with the metal ions&#xD;
in all the complexes. Copper(II) and cobalt(II) complexes show low magnetic&#xD;
moment. EPR spectral data show that complexes have planar geometry. Ligand to metal&#xD;
charge transfer are observed in all the complexes and d-d transition are also&#xD;
observed in copper(II) and cobalt(II) complexes. Thermal decomposition of all the&#xD;
complexes proceeds via first order kinetics.
Page(s): 1205-1207</description>
    <dc:date>2002-06-01T00:00:00Z</dc:date>
  </item>
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