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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/20127</link>
    <description />
    <pubDate>Fri, 16 Oct 2026 02:19:05 GMT</pubDate>
    <dc:date>2026-10-16T02:19:05Z</dc:date>
    <item>
      <title>Catalytic kinetic spectrophotometric determination of palladium(II) and its application to the determination of traces of propylthiouracil</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20145</link>
      <description>Title: Catalytic kinetic spectrophotometric determination of palladium(II) and its application to the determination of traces of propylthiouracil
Authors: Jabbari, A; Barzegar, M; Mohammadi, M
Abstract: The catalytic-kinetic method has been proposed&#xD;
for the determination of palladium(II) based on its catalytic effect on the reaction&#xD;
of crystal violet with hypophosphite. The reaction has&#xD;
&#xD;
been monitored spectrophotometrically at 590&#xD;
nm over the range 0.071-2.850 ppm of Pd(II). The influence of reaction&#xD;
variables and the effect of interfering ions have been studied. The limit of detection&#xD;
and relative standard deviation are 0.071 ppm and 2.76%, respectively. The&#xD;
developed method has been applied to the determination of Pd(II) in river water&#xD;
and Pd-C catalyst. The proposed method has also been applied for the&#xD;
determination of propylthiouracil in pharmaceutical samples based on its&#xD;
inhibitory effect on the palladium(II)-catalyzed reaction between crystal violet&#xD;
and hypophosphite ions. The decrease in absorbance of crystal violet at 590 nm&#xD;
is proportional to 1.7-248.0 ppb of PTU. The limit of detection and RSD are 1.7&#xD;
ppb and 2.53%, respectively.
Page(s): 1215-1218</description>
      <pubDate>Wed, 01 Jun 2005 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20145</guid>
      <dc:date>2005-06-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Determination of cadmium(II), copper(II) and zinc(II) in water samples by flame atomic absorption spectrometry after cloud point extraction</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20144</link>
      <description>Title: Determination of cadmium(II), copper(II) and zinc(II) in water samples by flame atomic absorption spectrometry after cloud point extraction
Authors: Shemirani, Farzaneh; Abkenar, Shiva Dehghan; Jamali, Mohammad Reza
Abstract: A preconcentration method for determination&#xD;
of low concentrations of Cd(II), Cu(II), and Zn(II) in water, using cloud point&#xD;
extraction is proposed. The analytes in the initial aqueous&#xD;
&#xD;
solution have been complexed with 8-hydroxyquinoline,&#xD;
with 0.06% (&lt;i&gt;w/v&lt;/i&gt;)&lt;i&gt; &lt;/i&gt;Triton X-114 added as surfactant. The complexation&#xD;
allows the separation of the analytes from other elements, which are not complexed.&#xD;
After phase separation, based on the c loud point of the mixture and dilution of&#xD;
the surfactant-rich phase with acidified methanolic solution, the enriched analytes&#xD;
have been determined by flame atomic absorption spectrometry. After&#xD;
&#xD;
optimization of complexation and&#xD;
extraction conditions, good enrichment factors have been obtained. The detection&#xD;
limits are 0.15 ng ml&lt;sup&gt;-1&lt;/sup&gt; for Cd(II), 0.72 ng ml&lt;sup&gt;-1&lt;/sup&gt;, for Cu(II)&#xD;
and 0.03 ng ml&lt;sup&gt;-1&lt;/sup&gt; &amp;nbsp;, for Zn(II)&#xD;
in the initial solution. The relative standard deviations are lower than 3.1 %.&#xD;
The method has been applied for analysis of the studied ions in tap water and&#xD;
river water samples. The method has been validated by the analysis of standard reference&#xD;
material.
Page(s): 1211-1214</description>
      <pubDate>Wed, 01 Jun 2005 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20144</guid>
      <dc:date>2005-06-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Chelation ion-exchange properties of 2, 2'-dihydroxybiphenyl-urea-formaldehyde (2:1:3) resin</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20143</link>
      <description>Title: Chelation ion-exchange properties of 2, 2'-dihydroxybiphenyl-urea-formaldehyde (2:1:3) resin
Authors: Jadhao, Manjusha M; Paliwal, L J; Bhave, N S
Abstract: The resin 2,2'-dihydroxybiphenyl-urea-formaldehyde&#xD;
[BPhUF], has been synthesized by the condensation of 2,2'dihydroxybiphenyl [BPh]&#xD;
and urea [U] with formaldehyde [F] in&#xD;
&#xD;
2: 1:3 molar ratio in presence of 2&lt;i&gt;M &lt;/i&gt;HCl&#xD;
as a catalyst. UV-Vis, IR and NMR spectral studies have been carried out to elucidate&#xD;
the structure of resin. Ion exchange properties of this resin have been studied&#xD;
by batch equilibrium method for Fe&lt;sup&gt;3+&lt;/sup&gt;, Cu&lt;sup&gt;2+&lt;/sup&gt;, Ni&lt;sup&gt;2+&lt;/sup&gt;,&#xD;
Co&lt;sup&gt;2+&lt;/sup&gt;,Zn&lt;sup&gt;2+&lt;/sup&gt;, Cd&lt;sup&gt;2+&lt;/sup&gt; and Pb&lt;sup&gt;2+&lt;/sup&gt; ions over the&#xD;
&lt;i&gt;p&lt;/i&gt;H range, 1.5 to 6.5 and in media of various ionic strengths. In presence&#xD;
of chloride and nitrate ions, the uptake of Fe&lt;sup&gt;3+&lt;/sup&gt;, Cu&lt;sup&gt;2+&lt;/sup&gt; and&#xD;
Ni&lt;sup&gt;2+&lt;/sup&gt; ions increases with increasing concentration of electrolyte&#xD;
while for Co&lt;sup&gt;2+&lt;/sup&gt;,Zn&lt;sup&gt;2+&lt;/sup&gt;, Cd&lt;sup&gt;2+&lt;/sup&gt; and Pb&lt;sup&gt;2+&lt;/sup&gt;&#xD;
ions, it decreases with increasing concentration of chloride, nitrate and sulphate&#xD;
ions. The resin shows a higher selectivity for Fe&lt;sup&gt;3+&lt;/sup&gt; ion over any other&#xD;
ion. Study of distribution ratio as a function of &lt;i&gt;p&lt;/i&gt;H indicates that the amount&#xD;
of metal ion taken up by resin increases with the increasing &lt;i&gt;p&lt;/i&gt;H of the medium.
Page(s): 1206-1210</description>
      <pubDate>Wed, 01 Jun 2005 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20143</guid>
      <dc:date>2005-06-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Ultrasonic studies of substituted isoxazoles and pyrazolines in dioxane and dioxane-water mixtures at different temperatures</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20142</link>
      <description>Title: Ultrasonic studies of substituted isoxazoles and pyrazolines in dioxane and dioxane-water mixtures at different temperatures
Authors: Ikhe, Shashikant A; Narwade, M L
Abstract: Ultrasonic velocities and densities of 3-(2-hydroxy-3-bromo-5-methylphenyl)-5-phenyl isoxazole (L&lt;sub&gt;1&lt;/sub&gt;), l-phenyl-3-(2-hydroxy-3-bromo-5-methylphenyl)-5-(4-methoxyphenyl) pyrazoline (L&lt;sub&gt;2&lt;/sub&gt;), in dioxane and different percentages of dioxane-water mixtures at different temperatures (303, 308, 313, 318, 323 K ± 0.1 K) have been evaluated at 0.01 &lt;i&gt;M &lt;/i&gt;concentration. Different acoustic properties like partial molal volume (ϕ&lt;sub&gt;v&lt;/sub&gt;), adiabatic compressibility (β&lt;sub&gt;s&lt;/sub&gt;), apparent molal compressibility (ϕ&lt;sub&gt;k(s)&lt;/sub&gt;) intermolecular free length (&lt;i&gt;L&lt;/i&gt;&lt;sub&gt;f&lt;/sub&gt;), relative association (&lt;i&gt;R&lt;/i&gt;&lt;sub&gt;A&lt;/sub&gt;)&lt;i&gt; &lt;/i&gt;and specific acoustic impedance (Z) have been determined by using single crystal interferometer at 1MHz frequency. The obtained results have been interpreted in terms of solute solvent interactions.
Page(s): 1203-1205</description>
      <pubDate>Wed, 01 Jun 2005 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20142</guid>
      <dc:date>2005-06-01T00:00:00Z</dc:date>
    </item>
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