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    <title>NISCAIR Online Periodicals Repository Collection: IJCT Vol.17(2) [March 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7625</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7638" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7637" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7636" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7635" />
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    <title>The Collection's search engine</title>
    <description>Search the Channel</description>
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    <link>http://nopr.niscair.res.in/simple-search</link>
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7638">
    <title>Extraction chromatographic separation of molybdenum(VI) with high molecular weight liquid anion exchanger</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7638</link>
    <description>Title: Extraction chromatographic separation of molybdenum(VI) with high molecular weight liquid anion exchanger
&lt;br/&gt;
&lt;br/&gt;Authors: Kokate, Sudarshan J; Gavande, Amol A; Vikhe, Vittal K; Aher, Haribhau R; Kuchekar, Shashikant R
&lt;br/&gt;
&lt;br/&gt;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.
&lt;br/&gt;
&lt;br/&gt;Page(s): 154-157</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7637">
    <title>Spectrophotometric determination of frusemide by its oxidation with ceric ammonium sulphate</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7637</link>
    <description>Title: Spectrophotometric determination of frusemide by its oxidation with ceric ammonium sulphate
&lt;br/&gt;
&lt;br/&gt;Authors: Narayana, B; Ashwini, K
&lt;br/&gt;
&lt;br/&gt;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.
&lt;br/&gt;
&lt;br/&gt;Page(s): 150-153</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7636">
    <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>http://nopr.niscair.res.in/handle/123456789/7636</link>
    <description>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
&lt;br/&gt;
&lt;br/&gt;Authors: Gülfen, Mustafa; Aydın, Ali Osman
&lt;br/&gt;
&lt;br/&gt;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;
&lt;br/&gt;
&lt;br/&gt;Page(s): 145-149</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7635">
    <title>Synthesis of a biodegradable polyacrylonitrile/sodium silicate nanocomposite fire retardant</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7635</link>
    <description>Title: Synthesis of a biodegradable polyacrylonitrile/sodium silicate nanocomposite fire retardant
&lt;br/&gt;
&lt;br/&gt;Authors: Samal, Ramakanta; Sahoo, Prafulla K
&lt;br/&gt;
&lt;br/&gt;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).
&lt;br/&gt;
&lt;br/&gt;Page(s): 139-144</description>
  </item>
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