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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/20576</link>
    <description />
    <pubDate>Thu, 08 Oct 2026 17:59:54 GMT</pubDate>
    <dc:date>2026-10-08T17:59:54Z</dc:date>
    <item>
      <title>Synthesis of a new cesium selective calix[4]arene based chromoionophore</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20820</link>
      <description>Title: Synthesis of a new cesium selective calix[4]arene based chromoionophore
Authors: Arora, V; Chawla, H M; Francis, T; Nanda, M; Singh, S P
Abstract: A novel azo-pyridyl calix[4]arene, (5,11,&#xD;
17,23-tetrakis(4'-azopyridyl)-25,26,27,28-tetrahydroxycalix[4]arene), has been synthesized&#xD;
in the 1,3-alternate conformation by coupling debutylated calix[4]arene with a diazotized&#xD;
solution of 4-aminopyridine. The synthesized chromoionophore gives a large bathochromic&#xD;
shift (119 nm) with an increase in the intensity of absorption on addition of a&#xD;
methanolic solution of CS&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt;. The selectivity&#xD;
coefficients for Cr&lt;sup&gt;3+&lt;/sup&gt; and Ni&lt;sup&gt;2+&lt;/sup&gt; has been determined to be &lt;i&gt;K&lt;/i&gt;&lt;sub&gt;cr&lt;/sub&gt;&lt;sup&gt;3+&lt;/sup&gt;&lt;i&gt;,&#xD;
&lt;/i&gt;&lt;sub&gt;C&lt;/sub&gt;&lt;sub&gt;s&lt;/sub&gt;&lt;sup&gt;+&lt;/sup&gt; = 6.6 and &lt;i&gt;K&lt;/i&gt;&lt;sub&gt;Ni&lt;/sub&gt;&lt;sup&gt;2+&lt;/sup&gt;&#xD;
, &lt;sub&gt;C&lt;/sub&gt;&lt;sub&gt;s&lt;/sub&gt;&lt;sup&gt;+&lt;/sup&gt;  = 66, while other alkali and alkaline earth metal&#xD;
ions do not interfere. The synthesized calixarene derivative has the potential to&#xD;
be used for development of ionic filters.
Page(s): 3041-3043</description>
      <pubDate>Mon, 01 Dec 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20820</guid>
      <dc:date>2003-12-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Microdetermination of anti-hypertensive drug Captopril using 2,6-dichlorophenol indophenol</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20819</link>
      <description>Title: Microdetermination of anti-hypertensive drug Captopril using 2,6-dichlorophenol indophenol
Authors: Srivastava, Ashutosh; Khare, Bindu; Argal, Rupali; Patel, Sandeep
Abstract: A method has been developed for quantitative&#xD;
microdetermination of antihypertensive drug Captopril &lt;i&gt;in vitro &lt;/i&gt;as well as&#xD;
&lt;i&gt;in vivo &lt;/i&gt;samples, spectrophotometrically using 2,6-dichlorophenol&#xD;
indophenol [2 ,6-DCPIP). The sulphydryl moiety, of the Captopril is quantitatively&#xD;
oxidized to its corresponding [1,1'-dithiobis'(2-methyl-1-oxopropane-3,1 diyl)bis-L-proline]disulphide&#xD;
by 2,6-DCPIP exhibiting stoichiometry of 2:1. The reaction product has been characterized&#xD;
by FTIR and NMR spectral studies. The method is rapid, accurate with high&#xD;
precision and can be applied for determining drugs in pharmaceutical preparations&#xD;
as well as &lt;i&gt;in-vivo &lt;/i&gt;samples.
Page(s): 3036-3040</description>
      <pubDate>Mon, 01 Dec 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20819</guid>
      <dc:date>2003-12-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>&lt;i&gt;Ortho-substituted &lt;/i&gt;aniline-N-salicylidenes as corrosion inhibitors for zinc in sulphuric acid</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20818</link>
      <description>Title: &lt;i&gt;Ortho-substituted &lt;/i&gt;aniline-N-salicylidenes as corrosion inhibitors for zinc in sulphuric acid
Authors: Desai, M N; Talati, J D; Shah, Neesha K
Abstract: The corrosion of zinc in sulphuric acid&#xD;
containing different &lt;i&gt;o&lt;/i&gt;-substituted aniline-N-salicylidenes has been studied&#xD;
with respect to inhibitor and acid concentration, period of exposure and temperature.&#xD;
All the five compounds studies show high (95-97%) inhibitive efficiency. At 0.5%&#xD;
inhibitor concentration in 0.5 &lt;i&gt;M &lt;/i&gt;acid, the order of efficiency is: &lt;i&gt;o-&lt;/i&gt;HNS&lt;i&gt;&#xD;
&lt;/i&gt;(95.5%) &lt; &lt;i&gt;o-&lt;/i&gt; CNS (96.8%) &lt; &lt;i&gt;o-&lt;/i&gt;AnNS&lt;i&gt; &lt;/i&gt;(99.7%) ≤&lt;i&gt; o&lt;/i&gt;-TNS&#xD;
(99.8%) ≤ ANS (99.9%). The activation energies are higher in inhibited than in uninhibited&#xD;
acid. It appears that an efficient inhibitor is characterized by a relatively&#xD;
greater decrease in the free energy of adsorption. Galvanostatic polarization studies&#xD;
indicate that these are mixed type inhibitors with predominant action on the local&#xD;
cathodes. Cathodic protection in the presence of these inhibitors has been studied.&#xD;
The inhibitors appear to function through adsorption due to the presence of the&#xD;
imine (-C=N-) group and conjugated double bonds.
Page(s): 3027-3035</description>
      <pubDate>Mon, 01 Dec 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20818</guid>
      <dc:date>2003-12-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Determination of cadmium, lead, copper, antimony and bismuth in high purity arsenic and arsenous oxide by differential pulse anodic stripping voltammetry</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/20817</link>
      <description>Title: Determination of cadmium, lead, copper, antimony and bismuth in high purity arsenic and arsenous oxide by differential pulse anodic stripping voltammetry
Authors: Sounderajan, Suvarna; Palrecha, M M
Abstract: A simple and rapid differential pulse anodic&#xD;
stripping method for simultaneous determination of cadmium, lead, copper, antimony&#xD;
and bismuth in high purity arsenic and arsenous oxides is described. The most suitable&#xD;
supporting electrolyte is found to be 2&lt;i&gt;M&lt;/i&gt; HCl. This method is suitable for&#xD;
the determination of Cd, Sb, Bi (0.1μg g&lt;sup&gt;-1&lt;/sup&gt;) , Cu(0.3μg g&lt;sup&gt;-1&lt;/sup&gt;)&#xD;
and Pb(0.5 μg g&lt;sup&gt;-1&lt;/sup&gt;) (with about 100mg as sample) with a relative standard&#xD;
deviation of 15-20%.
Page(s): 3025-3026</description>
      <pubDate>Mon, 01 Dec 2003 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/20817</guid>
      <dc:date>2003-12-01T00:00:00Z</dc:date>
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