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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/30778</link>
    <description />
    <pubDate>Mon, 12 Oct 2026 12:06:02 GMT</pubDate>
    <dc:date>2026-10-12T12:06:02Z</dc:date>
    <item>
      <title>Solvent extraction and separation studies of osmium (VIII) with Bis-2 ethylhexyl phosphoric acid</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/30896</link>
      <description>Title: Solvent extraction and separation studies of osmium (VIII) with Bis-2 ethylhexyl phosphoric acid
Authors: Sherikar, A V; Phalke, P N; Dhadke, P M
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:"times="" roman";mso-ansi-language:en-us;="" mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;A new method is proposed&#xD;
for the extraction of Os (VIII) from its acidic solution with 0.01M Bis-2 ethylhexyl&#xD;
phosphoric acid (HDEHP). The metal ion from the loaded organic phase is&#xD;
stripped with mixture of thiourea and HCl and then determined by the thioerea&#xD;
method. The method is simple and can be used for the selective extraction and&#xD;
separation of osmium from other metal ions.&lt;/span&gt;
Page(s): 59-60</description>
      <pubDate>Wed, 01 Jan 1997 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/30896</guid>
      <dc:date>1997-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Liquid-liquid extraction of trivalent lanthanides from nitric acid by 2-mercapto- 4, 4, 6-trimethyl-( 1H, 4H)-pyrimidine-1-acetic acid</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/30895</link>
      <description>Title: Liquid-liquid extraction of trivalent lanthanides from nitric acid by 2-mercapto- 4, 4, 6-trimethyl-( 1H, 4H)-pyrimidine-1-acetic acid
Authors: Kumar, Ashok
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:"times="" roman";mso-ansi-language:en-us;="" mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;A new method for the&#xD;
extraction and spectrophotometric determination of La (III), Pr(III), Nd(III),&#xD;
Sm(III), Gd(III) and Tb(III) from dilute aqueous nitrate media by 2-mercapto-4,&#xD;
4, 6-trimethyl-(1H, 4H)-pyrimidine-1-acetic acid (MTPAcH) has been developed.&#xD;
Various polar organic solvents have been examined. Maximum enhancement is&#xD;
observed in the presence of 40% acetonitrile. Very poor extractability&#xD;
necessitated the use of calcium nitrate as the salting out agent.&lt;/span&gt;
Page(s): 57-58</description>
      <pubDate>Wed, 01 Jan 1997 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/30895</guid>
      <dc:date>1997-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Synthesis of 8-aminoceramidone derivatives by modified two step process</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/30894</link>
      <description>Title: Synthesis of 8-aminoceramidone derivatives by modified two step process
Authors: Raval, D A; Chauhan, Y B
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:"times="" roman";mso-ansi-language:en-us;="" mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;Disperse dyes of the type&#xD;
8-aminoceramidone derivatives have been synthesized by condensation of&#xD;
bromamine acid (1-amino-4-bromoanthraquinone-2-sulfonic acid) with various&#xD;
arylamines followed by simultaneous desulphonation and cyclization with a&#xD;
mixture of concentrated sulphuric and orthophosphoric acids which saves the&#xD;
time and reduces the cost. Addition of optimum quantity of urea minimizes&#xD;
charring of the dyes by concentrated acids. The dyeing properties of these&#xD;
fifteen dyes have been assessed on polyesters.&lt;/span&gt;
Page(s): 53-56</description>
      <pubDate>Wed, 01 Jan 1997 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/30894</guid>
      <dc:date>1997-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Mercury spillage through smoke-stakes of an integrated steel plant: Effects on soil and ground water</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/30893</link>
      <description>Title: Mercury spillage through smoke-stakes of an integrated steel plant: Effects on soil and ground water
Authors: Pervez, Shamsh; Pandey, G S
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:"times="" roman";mso-ansi-language:en-us;="" mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;Massive coal consumption&#xD;
has been shown by steel industries. Mercury emission from the stacks of steel&#xD;
industries was reported earlier. The respective samples of soil, ground water&#xD;
and pond water were collected from the susceptible and non-susceptible sites&#xD;
around the steel plant within a distance of 10 km. Samples were analyzed for&#xD;
the presence of mercury by mercury analyzer. Mercury concentration more than&#xD;
1:0 ppm was observed in soils of high susceptible Sites. Mercury concentration&#xD;
in the range of 0.5-1.0 ppm was observed in the east and west direction of the&#xD;
plant upto a distance of 7 km. In case of ground water and pond water&#xD;
contamination, mercury concentration was found to be more than 10.0 ppb upto a&#xD;
distance of 10 km at high susceptible sites. Concentration range of 10.0&#xD;
ppb-1.0 ppb was observed within the distance of 7 km at less susceptible sites.&#xD;
Concentration below the permissible limits for drinking water (1.0 ppb) was&#xD;
observed beyond the distance of 7 km at less susceptible sites.&lt;/span&gt;
Page(s): 49-52</description>
      <pubDate>Wed, 01 Jan 1997 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/30893</guid>
      <dc:date>1997-01-01T00:00:00Z</dc:date>
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