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    <title>NISCAIR Online Periodicals Repository Collection: IJCT Vol.17(5) [September 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10447</link>
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      <title>Voltammetric ultra trace level determination of gallium</title>
      <link>http://nopr.niscair.res.in/handle/123456789/10457</link>
      <description>Title: Voltammetric ultra trace level determination of gallium
&lt;br/&gt;
&lt;br/&gt;Authors: Sharma, P; Dubey, S
&lt;br/&gt;
&lt;br/&gt;Abstract: The optimum conditions for the determination&#xD;
of sub µg &#xD;
level gallium have been developed employing differential pulse polarography. A detection&#xD;
limit of 0.01 &lt;img src='/image/spc_char/micro.gif' border=0&gt; g/mL has been achieved. Zinc and indium did not interfere.
&lt;br/&gt;
&lt;br/&gt;Page(s): 396-399</description>
      <pubDate>Sun, 29 Aug 2010 22:58:59 GMT</pubDate>
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    <item>
      <title>Visible light-driven photocatalytic degradation and mineralization of neutral red dye in a slurry photoreacter</title>
      <link>http://nopr.niscair.res.in/handle/123456789/10456</link>
      <description>Title: Visible light-driven photocatalytic degradation and mineralization of neutral red dye in a slurry photoreacter
&lt;br/&gt;
&lt;br/&gt;Authors: Pare, Brijesh; Singh, Pardeep; Jonnalagadda, S B
&lt;br/&gt;
&lt;br/&gt;Abstract: Hydroxyl radicals (OH&lt;sup&gt;.&lt;/sup&gt;) induced photocatalytic degradation&#xD;
of neutral red was investigated in a batch slurry reactor, in the&#xD;
presence of visible light illuminated ZnO. The effects of process parameters&#xD;
such as catalyst loading, initial substrate&#xD;
concentration, Fenton reagent, temperature, solar light and&#xD;
oxidant, and anion concentration were investigated. In the&#xD;
presence of visible light, ZnO/Fenton process was found to be most efficient&#xD;
for the decolorization of dye. Both artificial visible radiation and solar&#xD;
light degraded dye efficiently in the presence of ZnO. The destruction of&#xD;
chromophoric part and aromatic&#xD;
skelton of dye were ascertained by the disappearance of&#xD;
absorption bands in UV/Vis spectra of dye with respect to&#xD;
irradiation time. Complete COD reduction was observed in 8 h of irradiation&#xD;
time. CO&lt;sub&gt;2&lt;/sub&gt; and NO&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;-&lt;/sup&gt; ions&lt;sup&gt; &lt;/sup&gt;were&#xD;
identified as final&#xD;
mineralization products.
&lt;br/&gt;
&lt;br/&gt;Page(s): 391-395</description>
      <pubDate>Sun, 29 Aug 2010 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>A new method for the spectrophotometric determination of fexofenadine hydrochloride</title>
      <link>http://nopr.niscair.res.in/handle/123456789/10455</link>
      <description>Title: A new method for the spectrophotometric determination of fexofenadine hydrochloride
&lt;br/&gt;
&lt;br/&gt;Authors: Narayana, B; Veena, K
&lt;br/&gt;
&lt;br/&gt;Abstract: A novel, sensitive and selective reaction&#xD;
has been proposed for the assay of fexofenadine hydrochloride (FFH) in bulk and&#xD;
dosage forms using chloramine-T (CAT) and two dyes malachite green (MAG) and&#xD;
xylene cyanol FF (XFF). Spectrophotometric method entail the addition of a&#xD;
known excess of chloramine-T to fexofenadine hydrochloride in hydrochloric acid&#xD;
medium followed by the determination of residual oxidant by reacting it with a&#xD;
fixed amount of malachite green, measuring the absorbance at 615 nm (method A),&#xD;
or xylene cyanol FF, measuring the absorbance at 612 nm (method B). The&#xD;
apparent molar absorptivities are calculated to be 4.09×10&lt;sup&gt;4&lt;/sup&gt; L mol&lt;sup&gt;-1&lt;/sup&gt;&#xD;
cm&lt;sup&gt;-1&lt;/sup&gt;, 3.07×10&lt;sup&gt;4&lt;/sup&gt; L mol&lt;sup&gt;-1&lt;/sup&gt; cm&lt;sup&gt;-1 &lt;/sup&gt;for&#xD;
method A and B respectively. Both methods are of comparable accuracy and&#xD;
precision. There is no interference from common additives and excipients. The&#xD;
method has been applied to the determination of fexofenadine hydrochloride in&#xD;
pharmaceutical samples and the results are statistically compared with those of&#xD;
literature UV-spectrophotometric method by applying student’s &lt;i style=""&gt;t&lt;/i&gt;-test and &lt;i style=""&gt;F&lt;/i&gt;-test.
&lt;br/&gt;
&lt;br/&gt;Page(s): 386-390</description>
      <pubDate>Sun, 29 Aug 2010 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Electrolytic deposition of Zn-Mn-Mo alloys from a citrate bath</title>
      <link>http://nopr.niscair.res.in/handle/123456789/10454</link>
      <description>Title: Electrolytic deposition of Zn-Mn-Mo alloys from a citrate bath
&lt;br/&gt;
&lt;br/&gt;Authors: Rastogi, Renu; Pandey, Archana
&lt;br/&gt;
&lt;br/&gt;Abstract: Zn-Mn-Mo alloys were electrodeposited from a citrate bath and the&#xD;
influence of various parameters such as current density, 2.0-6.0 Adm&lt;sup&gt;-2&lt;/sup&gt;;&#xD;
temperature, 20-35ºC; pH, 2.0-2.15; duration of deposition 20-50 min and&#xD;
concentration of the constituent metals were studied. The electrolytic bath&#xD;
consists of zinc sulphate (20-35 gL&lt;sup&gt;-1&lt;/sup&gt;), manganese sulphate&#xD;
(50-80 gL&lt;sup&gt;-1&lt;/sup&gt;), ammonium molybdate (3-6 gL&lt;sup&gt;-1&lt;/sup&gt;), citric acid&#xD;
(5 gL&lt;sup&gt;-1&lt;/sup&gt;) and starch (1 gL&lt;sup&gt;-1&lt;/sup&gt;). Semi bright, light gray&#xD;
adherent deposits were generally obtained containing 88.98-99.82% Zn, 0.06-8.70%&#xD;
Mn and 0.10-2.32% Mo. The variation of cathode polarization with current&#xD;
density or the pH under the conditions was studied. Morphological studies have&#xD;
also been done.
&lt;br/&gt;
&lt;br/&gt;Page(s): 381-385</description>
      <pubDate>Sun, 29 Aug 2010 22:58:59 GMT</pubDate>
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