<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>NOPR Community:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/30962" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/30962</id>
  <updated>2026-10-09T12:21:06Z</updated>
  <dc:date>2026-10-09T12:21:06Z</dc:date>
  <entry>
    <title>&lt;span style="font-size:11.0pt;line-height:115%; font-family:Calibri;mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: "Times New Roman";mso-ansi-language:EN-IN;mso-fareast-language:EN-US; mso-bidi-language:HI"&gt;Liquid-liquid extraction of thorium(IV) with binary mixture of PC88A and TOPO from aqueous HCIO&lt;sub&gt;4&lt;/sub&gt; media&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31074" />
    <author>
      <name>Mishra, Sujata</name>
    </author>
    <author>
      <name>Chakravortty, Y</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31074</id>
    <updated>2016-07-20T05:58:39Z</updated>
    <published>1996-11-01T00:00:00Z</published>
    <summary type="text">Title: &lt;span style="font-size:11.0pt;line-height:115%; font-family:Calibri;mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: "Times New Roman";mso-ansi-language:EN-IN;mso-fareast-language:EN-US; mso-bidi-language:HI"&gt;Liquid-liquid extraction of thorium(IV) with binary mixture of PC88A and TOPO from aqueous HCIO&lt;sub&gt;4&lt;/sub&gt; media&lt;/span&gt;
Authors: Mishra, Sujata; Chakravortty, Y
Abstract: &lt;span style="font-size:11.0pt;line-height:&#xD;
115%;font-family:Calibri;mso-fareast-font-family:" dejavu="" sans";mso-bidi-font-family:="" mangal;color:#00000a;mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-US"&gt;The extraction of thorium(IV) with PC88A is very high&#xD;
from low HCIO&lt;sub&gt;4&lt;/sub&gt; concentration. It gradually decreases with increase&#xD;
in acidity. The addition of synergist TOPO to PC88A in kerosene improves the&#xD;
extraction of thorium(IV) from 0.2-1.6 M HCIO&lt;sub&gt;4&lt;/sub&gt; solution. The study&#xD;
with different diluents shows maximum distribution ratios obtained in case of&#xD;
kerosene.&lt;/span&gt;
Page(s): 373-374</summary>
    <dc:date>1996-11-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>A comparative evaluation of cephalosporin -C production in stirred tank reactor and air lift reactor</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31071" />
    <author>
      <name>Srivastava, Pradeep</name>
    </author>
    <author>
      <name>Nigam, V K</name>
    </author>
    <author>
      <name>Kundu, Subir</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31071</id>
    <updated>2016-07-20T05:57:36Z</updated>
    <published>1996-11-01T00:00:00Z</published>
    <summary type="text">Title: A comparative evaluation of cephalosporin -C production in stirred tank reactor and air lift reactor
Authors: Srivastava, Pradeep; Nigam, V K; Kundu, Subir
Abstract: &lt;span style="font-size:11.0pt;line-height:&#xD;
115%;font-family:Calibri;mso-fareast-font-family:" dejavu="" sans";mso-bidi-font-family:="" mangal;color:#00000a;mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-US"&gt;Cephalosporins group of antibiotics are more resistant&#xD;
to β lactamases than penicillins and are produced from cephalosporin - C (CPC),&#xD;
which is exclusively produced by fermentations. Many strains are used for the&#xD;
production of CPC. However, &lt;i&gt;Cephalosporium acremonium&lt;/i&gt; is widely used&#xD;
because of its high yield The CPC production is a highly aerobic process.&#xD;
Sucrose was found to be the most suitable substrate at 30 g/L. The CPC&#xD;
production has been studied in 2.0 L stirred tank reactor (STR) and 1.4 L air&#xD;
lift reactor (ALR), and performance compared, using a working volume 1.0 L. The&#xD;
maximum specific growth rate was 0.045 and 0.037 h&lt;sup&gt;-1&lt;/sup&gt; in STR and ALR&#xD;
respectively. The maximum cell mass concentrations were 685 mg L&lt;sup&gt;-1&lt;/sup&gt;&#xD;
in ALBR and 780 mg L&lt;sup&gt;-1&lt;/sup&gt; in STR. The specific antibiotic productivity&#xD;
based on power input (CPC/(P/ V) is higher by a factor of 2.4 in ALR than in STR.&lt;/span&gt;
Page(s): 371-372</summary>
    <dc:date>1996-11-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Solvent extraction separation of Cu(II) and Ni(II) with bis(2,4,4-trimethylpentyl) dithiophosphinic acid (Cyanex 301)</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31070" />
    <author>
      <name>Shinde, Priyadarshini S</name>
    </author>
    <author>
      <name>Dhadke, P M</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31070</id>
    <updated>2016-07-20T05:56:41Z</updated>
    <published>1996-11-01T00:00:00Z</published>
    <summary type="text">Title: Solvent extraction separation of Cu(II) and Ni(II) with bis(2,4,4-trimethylpentyl) dithiophosphinic acid (Cyanex 301)
Authors: Shinde, Priyadarshini S; Dhadke, P M
Abstract: &lt;span style="font-size:11.0pt;line-height:&#xD;
115%;font-family:Calibri;mso-fareast-font-family:" dejavu="" sans";mso-bidi-font-family:="" mangal;color:#00000a;mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-US"&gt;The extraction behaviour of copper(II) and nickel(lI)&#xD;
with bis(2,4,4-trimethyl pentyl)dithiophosphinic acid has been studied at&#xD;
various parameters such as, &lt;i&gt;p&lt;/i&gt;H, acidity, reagent concentration,&#xD;
equilibration period, solvent effect and effect of diverse ions. The copper(II)&#xD;
was quantitatively extracted from 0.5 MHCI with 5 x 10&lt;sup&gt;-3&lt;/sup&gt; M Cyanex&#xD;
301 and nickel(II) was extracted at &lt;i&gt;p&lt;/i&gt;H 8.00 with 5 x 10&lt;sup&gt;-3&lt;/sup&gt;&#xD;
MCyanex 301. The brownish yellow copper complex absorbed at 440 nm while&#xD;
coloured complex of nickel showed maximum absorption at 340 nm. Both metals&#xD;
were separated from multicomponent mixtures. The proposed method was&#xD;
successfully employed for the determination of copper and nickel in real samples.&lt;/span&gt;
Page(s): 367-370</summary>
    <dc:date>1996-11-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Solvent extraction separation of molybdenum(VI) with dibenzo 18-Crown-6 from chloride solutions</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31069" />
    <author>
      <name>Rane, Sneha S</name>
    </author>
    <author>
      <name>Khopkar, S M</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31069</id>
    <updated>2016-07-20T05:55:28Z</updated>
    <published>1996-11-01T00:00:00Z</published>
    <summary type="text">Title: Solvent extraction separation of molybdenum(VI) with dibenzo 18-Crown-6 from chloride solutions
Authors: Rane, Sneha S; Khopkar, S M
Abstract: &lt;span style="font-size:11.0pt;line-height:&#xD;
115%;font-family:Calibri;mso-fareast-font-family:" dejavu="" sans";mso-bidi-font-family:="" mangal;color:#00000a;mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-US"&gt;Molybdenum(Vl) was quantitatively extracted with 0.01&#xD;
M dibenzo 18-Crown-6 (DB18C6) in dichloroethane from 3-8 M hydrochloric acid,&#xD;
and was stripped with 0.05 M hydrochloric acid. After dryashing it was&#xD;
determined spectrophotometrically as its complex with Tiron at 390 nm. Other&#xD;
crown ethers such as 15C5, DC18C6 and DB24C8 were ineffective for extraction&#xD;
but with DB18C6 the extraction was quantitative. Amongst diluents only&#xD;
dichloroethane was effective. The stripping was complete with dilute solutions&#xD;
(0.05 M) of hydrochloric acid. Molybdenum(Vl) was separated from large number&#xD;
of elements with which it is generally associated in minerals. The method was&#xD;
extended for analysis of molybdenum in real samples. The relative standard&#xD;
deviation was ± 1.2%.&lt;/span&gt;
Page(s): 363-366</summary>
    <dc:date>1996-11-01T00:00:00Z</dc:date>
  </entry>
</feed>

