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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/19940</link>
    <description />
    <pubDate>Fri, 09 Oct 2026 18:42:53 GMT</pubDate>
    <dc:date>2026-10-09T18:42:53Z</dc:date>
    <item>
      <title>Synthesis and characterization of a Hg(II) selective II-butyl acetate cerium(IV) phosphate as a new intercalated fibrous ion exchanger: Effect of surfactants on the adsorption behaviour</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20033</link>
      <description>Title: Synthesis and characterization of a Hg(II) selective II-butyl acetate cerium(IV) phosphate as a new intercalated fibrous ion exchanger: Effect of surfactants on the adsorption behaviour
Authors: Varshney, K G; Rafiquee, M Z A; Somya, Amita; Drabik, Milan
Abstract: &lt;i&gt;n&lt;/i&gt;-butyl acetate Ce(IV) phosphate,&#xD;
a new Hg(II) selective, intercalated fibrous ion exchanger, has been synthesized&#xD;
and characterized by its ion exchange properties, thermal stability and adsorption&#xD;
behaviour for metal ions, X-ray, IR, TGA/DTA and SEM studies. Effect of surfactants&#xD;
on the adsorption behaviour of the material has also been studied. The exchanger&#xD;
has been found to be selective for Hg(II), hence, it can be utilized for the separation&#xD;
of this metal ion from other heavy metals from aqueous media. Studies on the effect&#xD;
of surfactants on the adsorption behaviour of this material show that&#xD;
for heavy metals ion, the adsorption increases with the concentration of anionic&#xD;
surfactants up to the CMC value and then decreases. But, for cationic, surfactants,&#xD;
the reverse is true. For non-ionic surfactant,&#xD;
&#xD;
adsorption remains constant up to the CMC&#xD;
value and then increases. For alkaline earths, the exchanger shows the same&#xD;
trend as above for cationic and non-ionic surfactants. However, for anionic surfactants,&#xD;
it is constant throughout the whole concentration range.
Page(s): 1856-1860</description>
      <pubDate>Tue, 01 Aug 2006 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20033</guid>
      <dc:date>2006-08-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Solid phase extraction and spectrophotometric determination of platinum(IV) with N-(3,5-dihydroxyphenyl)N'-(4-aminobenzenesulfonate)-thiourea</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20032</link>
      <description>Title: Solid phase extraction and spectrophotometric determination of platinum(IV) with N-(3,5-dihydroxyphenyl)N'-(4-aminobenzenesulfonate)-thiourea
Authors: Li, Zhigang; Li, Xuemei; Zhu, Liya; Hu, Qiufen; Chen, Jing; Yang, Guangyu
Abstract: A highly sensitive, selective and rapid method&#xD;
for the determination of platinum(IV) based on its rapid reaction with N-(3,5-dihydroxyphenyl)-Nʹ&#xD;
-(4-aminobenzenesulfonate)-thiourea&#xD;
&#xD;
(DHPABT) and the solid phase extraction of&#xD;
the Pt(IV)-DHPABT complex with a polymer-based C&lt;sub&gt;18&lt;/sub&gt; cartridge has&#xD;
been developed. In 0.05 - 0.5 mol L&lt;sup&gt;-1&lt;/sup&gt; HCl medium, DHPABT reacts with&#xD;
platinum(IV) to form a violet complex of a molar ratio 1:3 (platinum: DHPABT). This&#xD;
complex is enriched by the solid phase extraction with polymer-based C&lt;sub&gt;18&lt;/sub&gt;&#xD;
cartridge and an&#xD;
&#xD;
enrichment factor of 200 has been obtained.&#xD;
The molar absorptivity of the complex is 1.01 × 10&lt;sup&gt;5&lt;/sup&gt;L mol&lt;sup&gt;-1&lt;/sup&gt;&#xD;
cm&lt;sup&gt;-1&lt;/sup&gt; &amp;nbsp;at 760 nm, and Beer's law&#xD;
is obeyed in the range of 0.01-3.0 μg mL&lt;sup&gt;-1&lt;/sup&gt;. The&#xD;
&#xD;
relative standard deviation for eleven&#xD;
replicate analysis of 0.01μg mL&lt;sup&gt;-1&lt;/sup&gt; &amp;nbsp;solution is 1.86 %. The detection limit reaches&#xD;
0.02 μg/L in the original samples.&#xD;
This method has been applied to the determination of platinum&#xD;
(IV) in water and soil samples. The relative standard deviation&#xD;
is 3.0- 3.3%&lt;i&gt; &lt;/i&gt;and the standard recoveries are in the range&#xD;
88 -107%. The determined values agree with those obtained by ICP-MS&#xD;
method.
Page(s): 1852-1855</description>
      <pubDate>Tue, 01 Aug 2006 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20032</guid>
      <dc:date>2006-08-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Voltammetric response of 2,4-D-molecularly imprinted film modified glassy carbon electrodes</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20031</link>
      <description>Title: Voltammetric response of 2,4-D-molecularly imprinted film modified glassy carbon electrodes
Authors: Wang, Zhihua; Kang, Jingwan; Liu, Xiaoyu; Ma, Yongjun
Abstract: A novel voltammetric sensor has been developed&#xD;
by changing medium based on the molecular recognition of the template by imprinted&#xD;
technology. The sensitive layer has been prepared by electropolymerization of &lt;i&gt;ortho&lt;/i&gt;-phenylenediamine&#xD;
and resorcinol on glassy carbon electrode in the presence of the template molecule.&#xD;
Cyclic voltammetry and a.c. impedance studies have been carried out to&#xD;
investigate the properties of the polymeric&#xD;
&#xD;
film. After the template extraction from the&#xD;
resultant solution, rebinding of 2,4-D has been done from 0.1 mol/L H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;&#xD;
containing the analyte. The amount of bonded 2,4-D has been determined by differential&#xD;
pulse voltammetry. The sensor exhibits good sensitivity and reproducibility for&#xD;
2,4-D by virtue of the interaction between molecularly imprinted binding sites and&#xD;
template.
Page(s): 1848-1851</description>
      <pubDate>Tue, 01 Aug 2006 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20031</guid>
      <dc:date>2006-08-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>LSER and LFER in the reaction of benzimidazole with benzyl bromide</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20030</link>
      <description>Title: LSER and LFER in the reaction of benzimidazole with benzyl bromide
Authors: Reddy, S Ranga; Manikyamba, P
Abstract: The second order rate constants of the nucleophilic&#xD;
substitution reaction of benzyl bromide with benzimidazole have been obtained&#xD;
conductometrically in 11 different solvents in the&#xD;
&#xD;
temperature range 303-318 K. The rate constants&#xD;
are correlated with the polarisability (&lt;i&gt;P&lt;/i&gt;)&lt;i&gt; &lt;/i&gt;of the solvent and hydrogen&#xD;
bond acceptor basicity (&lt;i&gt;β&lt;/i&gt;) of tile solvent leading to a biparametric equation,&#xD;
log &lt;i&gt;k&lt;/i&gt; = -7.86+20.23&lt;i&gt;P&lt;/i&gt; + 1.45β (n = 11, &lt;i&gt;R &lt;/i&gt;= 0.93,&#xD;
SE =0.08). Substituent effect on rate of the reaction suggests that both electron&#xD;
donating group (&lt;i&gt;p&lt;/i&gt;-CH&lt;sub&gt;3&lt;/sub&gt;) and electron withdrawing groups (&lt;i&gt;p&lt;/i&gt; -NO&lt;sub&gt;2&lt;/sub&gt;, &lt;i&gt;p&lt;/i&gt;-Br) enhance the rate of the reaction compared to&#xD;
the unsubstituted compound. The substituted (&lt;i&gt;p&lt;/i&gt; -NO&lt;sub&gt;2&lt;/sub&gt;, &lt;i&gt;p&lt;/i&gt;-Br) and the unsubstituted compound form a linear&#xD;
free energy relationship.
Page(s): 1844-1847</description>
      <pubDate>Tue, 01 Aug 2006 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20030</guid>
      <dc:date>2006-08-01T00:00:00Z</dc:date>
    </item>
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