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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/7625" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/7625</id>
  <updated>2026-10-11T16:51:17Z</updated>
  <dc:date>2026-10-11T16:51:17Z</dc:date>
  <entry>
    <title>Extraction chromatographic separation of molybdenum(VI) with high molecular weight liquid anion exchanger</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/7638" />
    <author>
      <name>Kokate, Sudarshan J</name>
    </author>
    <author>
      <name>Gavande, Amol A</name>
    </author>
    <author>
      <name>Vikhe, Vittal K</name>
    </author>
    <author>
      <name>Aher, Haribhau R</name>
    </author>
    <author>
      <name>Kuchekar, Shashikant R</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/7638</id>
    <updated>2010-03-26T16:30:22Z</updated>
    <published>2010-03-01T00:00:00Z</published>
    <summary type="text">Title: Extraction chromatographic separation of molybdenum(VI) with high molecular weight liquid anion exchanger
Authors: Kokate, Sudarshan J; Gavande, Amol A; Vikhe, Vittal K; Aher, Haribhau R; Kuchekar, Shashikant R
Abstract: New and innovative separation method was developed for extraction of&#xD;
molybdenum(VI) from aqueous chloride media with &lt;i style=""&gt;N&lt;/i&gt;-&lt;i style=""&gt;n&lt;/i&gt;-octylaniline (liquid&#xD;
anion exchanger) coated on silica gel. Molybdenum(VI) was quantitatively&#xD;
extracted from 1.25 M HCl, eluted with distilled water and determined by&#xD;
spectrophotometric method. Different parameters &lt;i style=""&gt;viz&lt;/i&gt;. effect of HCl concentration, &lt;i style=""&gt;N&lt;/i&gt;-&lt;i style=""&gt;n&lt;/i&gt;-octylaniline&#xD;
concentration and flow rate of mobile phase were studied. The method was&#xD;
applied for separation of molybdenum(VI) from binary mixtures and synthetic&#xD;
mixtures corresponding to alloys and fertilizer samples.
Page(s): 154-157</summary>
    <dc:date>2010-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Spectrophotometric determination of frusemide by its oxidation with ceric ammonium sulphate</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/7637" />
    <author>
      <name>Narayana, B</name>
    </author>
    <author>
      <name>Ashwini, K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/7637</id>
    <updated>2010-03-26T16:30:25Z</updated>
    <published>2010-03-01T00:00:00Z</published>
    <summary type="text">Title: Spectrophotometric determination of frusemide by its oxidation with ceric ammonium sulphate
Authors: Narayana, B; Ashwini, K
Abstract: A simple and sensitive spectrophotometric&#xD;
method is described for the determination of frusemide (FRU). The method is&#xD;
based on the reaction of FRU with measured excess of ceric ammonium sulphate&#xD;
(CAS) followed by the determination of unreacted oxidant using xylene cyanol FF&#xD;
(XC) (Method A) and safranin O (SAF) (Method B). The reaction mixture exhibited&#xD;
maximum absorbance at 612 nm (Method A) and 526 nm (Method B). The calibration&#xD;
graph was linear from 20.00 to 30.00 µg mL&lt;sup&gt;-1 &lt;/sup&gt;and 6.00 to 16.00 µg mL&lt;sup&gt;-1&#xD;
&lt;/sup&gt;for methods A and B respectively. The apparent molar absorptivity and&#xD;
Sandell’s sensitivity for method A and B were calculated to be 1.160×10&lt;sup&gt;4&lt;/sup&gt;&#xD;
L mol&lt;sup&gt;-1&lt;/sup&gt;cm&lt;sup&gt;-1&lt;/sup&gt;, 2.025&lt;img src='/image/spc_char/cross.gif' border=0&gt;10&lt;sup&gt;4 &lt;/sup&gt;L mol&lt;sup&gt;-1&lt;/sup&gt; cm&lt;sup&gt;-1&lt;/sup&gt; and &#xD;
2.82×10&lt;sup&gt;-3 &lt;/sup&gt;µg cm&lt;sup&gt;-2&lt;/sup&gt;, 0.0163 µg cm&lt;sup&gt;-2&lt;/sup&gt;&#xD;
respectively. The method has been applied for the determination of frusemide in&#xD;
pure and dosage forms.
Page(s): 150-153</summary>
    <dc:date>2010-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Dissolution of copper from a primary chalcopyrite ore calcined with and without Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; in sulphuric acid solution</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/7636" />
    <author>
      <name>Gülfen, Mustafa</name>
    </author>
    <author>
      <name>Aydın, Ali Osman</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/7636</id>
    <updated>2010-03-22T16:30:25Z</updated>
    <published>2010-03-01T00:00:00Z</published>
    <summary type="text">Title: Dissolution of copper from a primary chalcopyrite ore calcined with and without Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; in sulphuric acid solution
Authors: Gülfen, Mustafa; Aydın, Ali Osman
Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="country-region"&gt;&lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="place"&gt;&lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="City"&gt;&#xD;
&#xD;
&#xD;
&#xD;
Dissolution of copper from a primary chalcopyrite ore supplied from Damar mine area in Murgul-Artvin, Turkey, has been investigated in&#xD;
sulphuric acid solution after the calcination with and without Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;.&#xD;
The chalcopyrite with and without Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; were performed by&#xD;
thermogravimetric (TG) analysis, and the calcined chalcopyrite samples were&#xD;
characterized by &#xD;
X-ray diffraction (XRD). In the leaching experiments, the effects of calcination&#xD;
temperature, sulphuric acid concentration, solid/liquid ratio, agitation rate,&#xD;
particle size and dissolution temperature and time on copper dissolution were&#xD;
examined. It was found that Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; addition contributed to&#xD;
sulphation during the calcination and then copper dissolution. &#xD;
&#xD;
&lt;/smarttagtype&gt;&lt;/smarttagtype&gt;&lt;/smarttagtype&gt;
Page(s): 145-149</summary>
    <dc:date>2010-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis of a biodegradable polyacrylonitrile/sodium silicate nanocomposite fire retardant</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/7635" />
    <author>
      <name>Samal, Ramakanta</name>
    </author>
    <author>
      <name>Sahoo, Prafulla K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/7635</id>
    <updated>2010-03-23T16:30:30Z</updated>
    <published>2010-03-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis of a biodegradable polyacrylonitrile/sodium silicate nanocomposite fire retardant
Authors: Samal, Ramakanta; Sahoo, Prafulla K
Abstract: Polyacrylonitrile (PAN)/Sodium silicate (SS) nanocomposite was&#xD;
synthesized via non-conventional emulsifier free emulsion method using an &lt;i style=""&gt;in situ&lt;/i&gt; developed transition metal complex&#xD;
Cu(II)/EDTA taking potassium monopersulfate (KMPS) as initiator, with a novel&#xD;
motive of converting hydrophobic homopolymer PAN into hydrophilic nanocomposite&#xD;
by the inclusion of SS to the homopolymer. The formation of the PAN/SS&#xD;
nanocomposite was confirmed by infrared spectra (IR). Furthermore, as&#xD;
evidenced by transmission electron microscopy (TEM), the composite so obtained&#xD;
was found to have nano scale structure. X-ray diffraction (XRD) was carried out&#xD;
suggesting that the silicate layers were exfoliated or intercalated during the&#xD;
polymerization process. An increase in the thermal stability for the developed&#xD;
nanocomposite was recorded by thermogravimetric analysis (TGA). The combustion&#xD;
behaviour has been evaluated using oxygen consumption cone calorimeter and the&#xD;
nanocomposite exhibited good fire retardancy. The PAN/SS nanocomposite was&#xD;
found to be biodegradable as tested by sludge water and further confirmed by&#xD;
scanning electron microscopy (SEM).
Page(s): 139-144</summary>
    <dc:date>2010-03-01T00:00:00Z</dc:date>
  </entry>
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