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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/21081</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 12:30:39 GMT</pubDate>
    <dc:date>2026-10-10T12:30:39Z</dc:date>
    <item>
      <title>Liquid-liquid extraction and separation of gallium(III) with Cyanex 921</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/21201</link>
      <description>Title: Liquid-liquid extraction and separation of gallium(III) with Cyanex 921
Authors: Mishra, B Y; Rokade, M D; Dhadke, P M
Abstract: A simple and rapid&#xD;
method for the separation of gallium(III) from aqueous chloride media with tri-&lt;i&gt;n&lt;/i&gt;-octylphosphine&#xD;
oxide (Cyanex 921) is described. Gallium(III) has been extracted with Cyanex&#xD;
921 in toluene in the &lt;i&gt;p&lt;/i&gt;H range 4.5-6.0 and stripped back with 2.0 &lt;i&gt;M &lt;/i&gt;HNO&lt;sub&gt;3&lt;/sub&gt;.&#xD;
The effects of &lt;i&gt;p&lt;/i&gt;H, equilibration period, diluents, diverse ion and stripping&#xD;
agents on the extraction of gallium(III) have been studied. The equilibrium&#xD;
constant and the thermodynamic parameters,Δ&lt;i&gt;H, &lt;/i&gt;Δ&lt;i&gt;S &lt;/i&gt;and Δ&lt;i&gt;G&lt;/i&gt; have&#xD;
been evaluated. The method has been extended for binary and multicomponent separation&#xD;
of gallium(III).
Page(s): 1114-1116</description>
      <pubDate>Sun, 01 Oct 2000 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/21201</guid>
      <dc:date>2000-10-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Ion-exchange properties of 8-hydroxyquinoline-biuret-formaldehyde tercopolymers</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/21200</link>
      <description>Title: Ion-exchange properties of 8-hydroxyquinoline-biuret-formaldehyde tercopolymers
Authors: Gurnule, Wasudeo B; Juneja, H D; Paliwal, L J
Abstract: Tercopolymer (8-HQBF)&#xD;
prepared by condensation of 8-hydroxyquinoline (8-HQ) and biuret (B) with formaldehyde&#xD;
(F) in the presence of 2&lt;i&gt;M &lt;/i&gt;HCl as catalyst was proved to be a selective&#xD;
&#xD;
chelating ion-exchange&#xD;
tercopolymer for certain metals. Chelating ion-exchange properties of this tercopolymers&#xD;
are studied for Fe&lt;sup&gt;3+&lt;/sup&gt;, Cu&lt;sup&gt;2+&lt;/sup&gt;, Ni&lt;sup&gt;2+&lt;/sup&gt;, Co&lt;sup&gt;2+&lt;/sup&gt;,&#xD;
Zn&lt;sup&gt;2+&lt;/sup&gt;,&lt;i&gt; &lt;/i&gt;Cd&lt;sup&gt;2+&lt;/sup&gt; and Pb&lt;sup&gt;2+&lt;/sup&gt; ions. A batch equilibrium&#xD;
method has been employed in the study of the selectivity of metal ion uptake involving&#xD;
the measurements of the distribution of a given metal ion between the polymer&#xD;
sample and a solution containing the metal ion. The study has been carried out over a wide&#xD;
&lt;i&gt;p&lt;/i&gt;H range and in media of various ionic strengths. The polymer shows a&#xD;
higher selectivity for Fe&lt;sup&gt;3+&lt;/sup&gt;, Cu&lt;sup&gt;2+&lt;/sup&gt; and Ni&lt;sup&gt;2+&lt;/sup&gt; ions&#xD;
than for Co&lt;sup&gt;2+&lt;/sup&gt;, Zn&lt;sup&gt;2+&lt;/sup&gt;,&lt;i&gt; &lt;/i&gt;Cd&lt;sup&gt;2+&lt;/sup&gt; and Pb&lt;sup&gt;2+&lt;/sup&gt;&#xD;
ions.
Page(s): 1110-1113</description>
      <pubDate>Sun, 01 Oct 2000 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/21200</guid>
      <dc:date>2000-10-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Spectrophotometric determination of vanadium(V) using methdilazine hydrochloride in minerals and steel samples</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/21199</link>
      <description>Title: Spectrophotometric determination of vanadium(V) using methdilazine hydrochloride in minerals and steel samples
Authors: Melwanki, M B; Seetharamappa, J
Abstract: Methdilazine&#xD;
hydrochloride has been used as a sensitive and selective reagent for the rapid spectrophotometric&#xD;
determination of vanadium(V). The reagent gives instantaneously a red coloured species&#xD;
on reaction with vanadium(V) in phosphoric acid medium and exhibits maximum&#xD;
absorbance at 512 nm with Sandell's sensitivity of 6.72 ng cm&lt;sup&gt;-2&lt;/sup&gt;. Beer's&#xD;
law is obeyed over the concentration range 0.2-5.4 ppm; the optimum&#xD;
concentration range is 0.5-5.0 ppm. The method has been successfully applied to the analysis of&#xD;
vanadium steels and minerals.
Page(s): 1107-1109</description>
      <pubDate>Sun, 01 Oct 2000 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/21199</guid>
      <dc:date>2000-10-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Solvent extraction and spectrophotometric determination of Fe(II) with 1,3-diphenyl-4- carboethoxy pyrazole-5-one</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/21198</link>
      <description>Title: Solvent extraction and spectrophotometric determination of Fe(II) with 1,3-diphenyl-4- carboethoxy pyrazole-5-one
Authors: Patil, R K; Dhuley, D G
Abstract: A quick and selective&#xD;
method is developed for extractive spectrophotometric determination of Fe(II) using&#xD;
1,3-diphenyl-4- carboethoxy pyrazole-5-one as the reagent. The wine-red coloured&#xD;
1:3 (metal:ligand) complex in chloroform medium absorbs maximally at 525 nm. Beer's&#xD;
law is obeyed in the concentration range 0.5-10 μg/ml of Fe(II). The molar absorptivity&#xD;
and Sandell's sensitivity are found to be 1.156×10&lt;sup&gt;3&lt;/sup&gt;1 mol&lt;sup&gt;-1&lt;/sup&gt;&#xD;
cm&lt;sup&gt;-1&lt;/sup&gt; and 0.0483 μgcm&lt;sup&gt;-2&lt;/sup&gt; respectively. The effect of &lt;i&gt;p&lt;/i&gt;H,&#xD;
equilibration time, reagent concentration and foreign ions have also been studied.&#xD;
The application of the method has been applied for the&#xD;
&#xD;
determination of&#xD;
Fe(II) in pharmaceutical samples.
Page(s): 1105-1106</description>
      <pubDate>Sun, 01 Oct 2000 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/21198</guid>
      <dc:date>2000-10-01T00:00:00Z</dc:date>
    </item>
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