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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19936" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/19936</id>
  <updated>2026-10-09T03:20:45Z</updated>
  <dc:date>2026-10-09T03:20:45Z</dc:date>
  <entry>
    <title>Atomic absorption spectrometric determination of copper after adsorption of its sodiumdiethyldithiocarbamate complex on a new polymeric adsorbent</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19980" />
    <author>
      <name>Atamjyot</name>
    </author>
    <author>
      <name>Jain, Preeti</name>
    </author>
    <author>
      <name>Puri, B K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19980</id>
    <updated>2013-07-23T16:34:08Z</updated>
    <published>2006-02-01T00:00:00Z</published>
    <summary type="text">Title: Atomic absorption spectrometric determination of copper after adsorption of its sodiumdiethyldithiocarbamate complex on a new polymeric adsorbent
Authors: Atamjyot; Jain, Preeti; Puri, B K
Abstract: An atomic absorption spectrometric method&#xD;
for the determination of trace amounts of copper in various synthetic samples after&#xD;
adsorption of its sodiumdiethyldithiocarbamate complex on a new polymeric adsorbent&#xD;
has been developed. The copper complex is quantitatively adsorbed on the polymeric&#xD;
adsorbent in the &lt;i&gt;p&lt;/i&gt;H range of 2.9-9.0. After filtration, the copper&#xD;
&#xD;
complex is eluted with 10 mL of dimethyl formamide&#xD;
and the metal is determined by atomic absorption spectroscopy. Beer's law is obeyed&#xD;
in the concentration range 0.15-2.0 ppm of copper in the final DMF solution&#xD;
with a correlation factor of 0.9989. Ten replicates of 2 ppm of Cu give a mean absorbance&#xD;
of 0.209 with a relative standard deviation of 1.6%. Various experimental conditions&#xD;
such as effect of &lt;i&gt;p&lt;/i&gt;H on complexation/adsorption retention, volume of&#xD;
buffer solution, amount of reagent, amount of adsorbent, standing time, flow rate,&#xD;
volume of aqueous phase, choice of organic solvent have been optimized.
Page(s): 409-411</summary>
    <dc:date>2006-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Solvent extraction separation of thorium(IV) from nitric acid with Cyanex 272</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19979" />
    <author>
      <name>Karve, Manjusha</name>
    </author>
    <author>
      <name>Belwalkar, Smruti</name>
    </author>
    <author>
      <name>Rajgor, Reeta</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19979</id>
    <updated>2013-07-22T16:37:27Z</updated>
    <published>2006-02-01T00:00:00Z</published>
    <summary type="text">Title: Solvent extraction separation of thorium(IV) from nitric acid with Cyanex 272
Authors: Karve, Manjusha; Belwalkar, Smruti; Rajgor, Reeta
Abstract: Thorium(IV) has been quantitatively extracted&#xD;
from 1×10&lt;sup&gt;-3&lt;/sup&gt; &lt;i&gt;M &lt;/i&gt;nitric acid with 1×10&lt;sup&gt;-3&lt;/sup&gt; &lt;i&gt;M &lt;/i&gt;Cyan&#xD;
ex 272 in xylene. It has been&lt;i&gt; &lt;/i&gt;stripped from the organic phase with 4 &lt;i&gt;M&#xD;
&lt;/i&gt;hydrochloric acid and&lt;i&gt; &lt;/i&gt;determined spectrophotometrically as its complex&#xD;
with Arsenazo(III) at 655 nm. The method developed has been applied for&lt;i&gt; &lt;/i&gt;the&#xD;
separation of thorium(IV) from chromium(VI), vanadium(V), hafnium(IV), zirconium(IV),&#xD;
titanium(IV), iron(III), cobalt (II),&lt;i&gt; &lt;/i&gt;calcium(II) and some rare earth elements.&#xD;
The applicability of the method has been checked for separation of thorium(IV) from&lt;i&gt;&#xD;
&lt;/i&gt;associated elements in the synthetic mixtures and monazite sand.The method is&#xD;
simple, rapid and selective for thorium(IV) with a relative standard deviation&#xD;
of 0.27%.
Page(s): 406-408</summary>
    <dc:date>2006-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Differential pulse polarographic determination of tetramethylthiuram disulphide</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19978" />
    <author>
      <name>Verma, B C</name>
    </author>
    <author>
      <name>Kumar, Satish</name>
    </author>
    <author>
      <name>Chauhan, Chetan</name>
    </author>
    <author>
      <name>Sharma, D K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19978</id>
    <updated>2013-07-30T16:37:38Z</updated>
    <published>2006-02-01T00:00:00Z</published>
    <summary type="text">Title: Differential pulse polarographic determination of tetramethylthiuram disulphide
Authors: Verma, B C; Kumar, Satish; Chauhan, Chetan; Sharma, D K
Abstract: A differential pulse polarographic method&#xD;
for the determination of tetramethylthiuram disulphide (TMTD) by making use of its&#xD;
reaction with copper(I) perchlorate in&#xD;
&#xD;
acetonitrile has been developed. TMTD reacts&#xD;
with copper(I)&#xD;
&#xD;
perchlorate (1:1 molar ratio) and&#xD;
exhibits a well-defined, diffusion-controlled peak at - 120 mV showing five times&#xD;
more sensitivity than the one obtained due to TMTD alone. The linear relationship&#xD;
between concentration of TMTD and current intensity of peak at - 120 m V can be&#xD;
successfully adapted to the analysis of some fungicide and rubber accelerator formulations&#xD;
based on TMTD.
Page(s): 402-405</summary>
    <dc:date>2006-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Kinetics and mechanism of oxidation of arsenous acid by Waugh-type enneamolybdomanganate(IV)</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19977" />
    <author>
      <name>Bhosale, B D</name>
    </author>
    <author>
      <name>Gokavi, G S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19977</id>
    <updated>2013-07-23T16:34:58Z</updated>
    <published>2006-02-01T00:00:00Z</published>
    <summary type="text">Title: Kinetics and mechanism of oxidation of arsenous acid by Waugh-type enneamolybdomanganate(IV)
Authors: Bhosale, B D; Gokavi, G S
Abstract: The reaction between As(III) and Waugh-type&#xD;
enneamolybdomanganate(IV) has been studied in perchloric acid medium. The reaction&#xD;
follows a second order kinetics with an order of unity each on both the&#xD;
reactants and proceeds with a complimentary two-electron outer-sphere path. The&#xD;
reaction is accelerated by [H&lt;sup&gt;+&lt;/sup&gt;] ions due to protonation equilibria of&#xD;
the oxidant. The first two protonation constants of the enneamolybdomanganate(IV)&#xD;
anion have been determined by &lt;i&gt;p&lt;/i&gt;H metric titration and found to be 2.0 × 10&lt;sup&gt;3&lt;/sup&gt;&#xD;
and 316 dm3 Mol&lt;sup&gt;-1&lt;/sup&gt;. The product of reaction, enneamolybdomanganous(II)&#xD;
has been synthesized to study the effect of the added product. Both ammonium salts&#xD;
of enneamolybdomanganate(IV) and enneamolybdomanganous(II) have been characterized&#xD;
by FTIR and AAS. The reaction is&#xD;
&#xD;
unaffected by change in ionic strength and&#xD;
the free radical test is negative which suggests direct two-electron transfer from&#xD;
As(III) to oxidant. Di-protonated form of enneamolybdomanganate(IV) has been&#xD;
found to be active oxidant species. The solvent polarity and the thermodynamic parameters&#xD;
suggest the outer sphere mechanism.
Page(s): 398-401</summary>
    <dc:date>2006-02-01T00:00:00Z</dc:date>
  </entry>
</feed>

