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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18286" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/18286</id>
  <updated>2026-10-09T10:53:11Z</updated>
  <dc:date>2026-10-09T10:53:11Z</dc:date>
  <entry>
    <title>Sodium anthraquinone-2-sulphonate sensitized photoreduction of methylene violet</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18344" />
    <author>
      <name>Bansal, W R</name>
    </author>
    <author>
      <name>Singh, Kulvir</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18344</id>
    <updated>2016-07-20T04:43:11Z</updated>
    <published>2002-08-01T00:00:00Z</published>
    <summary type="text">Title: Sodium anthraquinone-2-sulphonate sensitized photoreduction of methylene violet
Authors: Bansal, W R; Singh, Kulvir
Abstract: Sodium&#xD;
anthraquinone-2-sulphonate sensitizes the photoreduction of methylene violet in&#xD;
aqueous medium in the presence of hydrogen donors, isopropyl alcohol and benzhydrol,&#xD;
to give leuco methylene violet. Reduction takes place by reducing sodium&#xD;
anthraquinone-2-sulphonate produced through hydrogen&#xD;
&#xD;
abstraction by&#xD;
excited triplet state of sodium anthraquinone-2- sulphonate from the hydrogen&#xD;
donors. Effect of viscosity and role of electron transfer have been examined by&#xD;
adding ethylene glycol and triethylamine respectively. ϕ&lt;sub&gt;LMV&lt;/sub&gt; reaches&#xD;
a plateau at 4.0 and 1.7×10&lt;sup&gt;-2&lt;/sup&gt; mol dm&lt;sup&gt;-3&lt;/sup&gt; of IPA and BPH&lt;sub&gt;2&lt;/sub&gt;&#xD;
concentrations where ϕ&lt;sub&gt;LMV&lt;/sub&gt; =&#xD;
1.7 and 1.0 respectively. Difference in maximum quantum&#xD;
&#xD;
yields in the&#xD;
case of IPA and BPH&lt;sub&gt;2&lt;/sub&gt; has been explained. ϕ&lt;sub&gt;LMV&lt;/sub&gt;&#xD;
is not afected by viscosity change.
Page(s): 1652-1656</summary>
    <dc:date>2002-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Differential pulse polarographic determination of lead (II) in complex materials after adsorption of its trifluoroethylxanthate-cetyl-trimethylammonium ion-associated complex on microcrystalline naphthalene or on trifluoroethylxanthate cetyltrimethylammonium- naphthalene adsorbent</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18343" />
    <author>
      <name>Puri, B K</name>
    </author>
    <author>
      <name>Atamjyot</name>
    </author>
    <author>
      <name>Lal, Keemti</name>
    </author>
    <author>
      <name>Bansal, Himanshu</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18343</id>
    <updated>2016-07-20T04:42:17Z</updated>
    <published>2002-08-01T00:00:00Z</published>
    <summary type="text">Title: Differential pulse polarographic determination of lead (II) in complex materials after adsorption of its trifluoroethylxanthate-cetyl-trimethylammonium ion-associated complex on microcrystalline naphthalene or on trifluoroethylxanthate cetyltrimethylammonium- naphthalene adsorbent
Authors: Puri, B K; Atamjyot; Lal, Keemti; Bansal, Himanshu
Abstract: Lead(II) is&#xD;
adsorbed as lead trifluoroethylxanthate (TFEX) cetyltrimethylammonium (CTMA) ion&#xD;
pair complex on microcrystalline naphthalene quantitatively in the &lt;i&gt;p&lt;/i&gt;H range&#xD;
4.50- 10.50. In the absence of cetyltrimethylammonium as the counter ion, the adsorption&#xD;
is only 80%. Lead(II) is desorbed with HCl and determined with a differential&#xD;
pulse polarograph. Dissolved oxygen is removed by adding 3 ml of 4% NaBH&lt;sub&gt;4&lt;/sub&gt;&#xD;
solution. Alternatively, lead (II) can be quantitatively adsorbed on TFEXCTMA- naphthalene&#xD;
adsorbent packed in a column at a flow rate&#xD;
&#xD;
of 1-2 ml&#xD;
min&lt;sup&gt;-1&lt;/sup&gt;.Well defined peak has been obtained in this medium at -0.40 V&#xD;
versus S.C. E. Cyclic voltammetric, differential polarographic and D.C. polarographic&#xD;
studies indicate that lead(II) has been reduced reversibly in a two-electron reduction&#xD;
under these conditions. The detection limit is 0.20 μg ml&lt;sup&gt;-1&lt;/sup&gt; at the minimum&#xD;
instrumental settings (signal-to-noise ratio =2). Linearity is maintained in the&#xD;
concentration range 0.5 -16.40μg ml&lt;sup&gt;-1&lt;/sup&gt; with correlation factor of 0.9997&#xD;
and a relative standard deviation of ±l.07%. Various parameters such as the effect&#xD;
of &lt;i&gt;p&lt;/i&gt;H, volume of aqueous phase, flow rate and the interference of a large&#xD;
number of metal ions and anions on the determination of lead(II) have been&#xD;
studied in detail to optimize the conditions for its trace determination in various&#xD;
standard alloys, standard biological materials and environmental samples.
Page(s): 1646-1651</summary>
    <dc:date>2002-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Simultaneous second derivative spectrophotometric determination of nickel(II) and copper(II) using diacetylmonoxime isonicotinoyl hydrazone</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18342" />
    <author>
      <name>Chandrasekhar, K B</name>
    </author>
    <author>
      <name>Reddy, K Hussain</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18342</id>
    <updated>2016-07-20T04:30:32Z</updated>
    <published>2002-08-01T00:00:00Z</published>
    <summary type="text">Title: Simultaneous second derivative spectrophotometric determination of nickel(II) and copper(II) using diacetylmonoxime isonicotinoyl hydrazone
Authors: Chandrasekhar, K B; Reddy, K Hussain
Abstract: A derivative&#xD;
spectrophotometric method, based on the use of second-derivative absorption spectra,&#xD;
has been developed for the simultaneous determination of nickel (II) and&#xD;
copper(II) in aqueous medium using diacetylmonoxime isonicotionyl hydrazone (DMIH).&#xD;
The reagent gives intense colour reaction&#xD;
&#xD;
with nickel(II)&#xD;
and copper(II) in basic medium. The zero-order&#xD;
&#xD;
spectrophotometric&#xD;
method for the determination of these metal ions has been developed in aqueous medium.&#xD;
The molar absorptivity and Sandell's sensitivity for nickel(II) and copper(II) are&#xD;
1.75×10&lt;sup&gt;4&lt;/sup&gt;; 1.12×10&lt;sup&gt;4&lt;/sup&gt; lit. Mol&lt;sup&gt;-1&lt;/sup&gt; cm&lt;sup&gt;-1&lt;/sup&gt;&#xD;
and 0.00335, 0.00565 μg of metal/cm&lt;sup&gt;2&lt;/sup&gt; respectively. Beer's law is&#xD;
obeyed in the range 0.235-2.35 and 0.25-2.54 μg/ml&lt;i&gt; &lt;/i&gt;for Ni(II) and Cu(II)&#xD;
respectively. The proposed simultaneous method involves the use of peak-to-base&#xD;
line measurement techniques.
Page(s): 1643-1645</summary>
    <dc:date>2002-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and characterization of some phthalanilic and maleanilic acid derivatives of arsenic(III)</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/18341" />
    <author>
      <name>Chauhan, H P S</name>
    </author>
    <author>
      <name>Singh, R K</name>
    </author>
    <author>
      <name>Porwal, B</name>
    </author>
    <author>
      <name>Kori, Kavita</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/18341</id>
    <updated>2016-07-20T04:41:30Z</updated>
    <published>2002-08-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and characterization of some phthalanilic and maleanilic acid derivatives of arsenic(III)
Authors: Chauhan, H P S; Singh, R K; Porwal, B; Kori, Kavita
Abstract: Replacement&#xD;
reaction of arsenic trichloride and 2-chloro- 1,3- dithia-2 -arsacyclopentane with&#xD;
sodium salts of phthalanilic and maleanilic acids (prepared &lt;i&gt;in situ &lt;/i&gt;by&#xD;
the reaction of corresponding anilic acids with sodium isopropoxide in the&#xD;
mixture benzene and isopropanol) in the 1:3 and 1:1 molar ratios respectively,&#xD;
in benzene and isopropanol mixture, yield the arsenic derivatives of the type [L]&lt;sub&gt;3&lt;/sub&gt;&#xD;
As and [L] AsSCH&lt;sub&gt;2&lt;/sub&gt;CH&lt;sub&gt;2&lt;/sub&gt;S (where L = phthalanilate&#xD;
&#xD;
and maleanilate&#xD;
anions). These derivatives have been characterized by elemental analysis as well&#xD;
as IR and &lt;sup&gt;1&lt;/sup&gt;H NMR spectral studies.
Page(s): 1639-1642</summary>
    <dc:date>2002-08-01T00:00:00Z</dc:date>
  </entry>
</feed>

