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    <title>NISCAIR Online Periodicals Repository Collection: IJCT Vol.15(2) [March 2008]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/852</link>
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      <title>Synthesis and photoinduced conductivity changes of polyesters with ortho-hydroxyazo groups</title>
      <link>http://nopr.niscair.res.in/handle/123456789/900</link>
      <description>Title: Synthesis and photoinduced conductivity changes of polyesters with ortho-hydroxyazo groups
&lt;br/&gt;
&lt;br/&gt;Authors: Girijan, K R; Purushothaman, E
&lt;br/&gt;
&lt;br/&gt;Abstract: The synthesis and photoinduced changes in conductivity of polyesters with ortho-hydroxyazo groups in the polymer backbone are presented. Reversible photoincrease in conductivity was observed. A reasonable explanation to this effect has been offered.
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&lt;br/&gt;Page(s): 197-200</description>
      <pubDate>Wed, 27 Feb 2008 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Spectrophotometric determination of eprosartan mesylate in raw material and experimental tablets</title>
      <link>http://nopr.niscair.res.in/handle/123456789/899</link>
      <description>Title: Spectrophotometric determination of eprosartan mesylate in raw material and experimental tablets
&lt;br/&gt;
&lt;br/&gt;Authors: Kamila, M M; Mondal, N; Ghosh, L K
&lt;br/&gt;
&lt;br/&gt;Abstract: A simple, sensitive and accurate UV spectrophotometric method has been developed for the determination of eprosartan mesylate in raw material and experimental tablets. Beer’s law was obeyed in the concentration range 2-30 μg mL⁻¹ for the drug (λ = 232 nm) with an apparent molar absorptivity and Sandell sensitivity of 2.8 × 10⁴ L.mol⁻¹cm⁻¹ and 0. 01854 µg cm⁻²/0.001A, respectively. The limits of detection and quantitation were calculated to be 0.3623 and 1.098 µg mL⁻¹, respectively. Results were validated statistically according to ICH guidelines. Validation of the method yielded good results in the concerning range (2-30 µg mL⁻¹), linearity (r² = 0.9998), precision and accuracy. The excipients present in the experimental tablets did not interfere with the method.
&lt;br/&gt;
&lt;br/&gt;Page(s): 194-196</description>
      <pubDate>Wed, 27 Feb 2008 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>o-Chlorophenol anchored tin antimonate: An ion exchanger for separation of heavy metals</title>
      <link>http://nopr.niscair.res.in/handle/123456789/898</link>
      <description>Title: o-Chlorophenol anchored tin antimonate: An ion exchanger for separation of heavy metals
&lt;br/&gt;
&lt;br/&gt;Authors: Chithra, P G; Beena, B
&lt;br/&gt;
&lt;br/&gt;Abstract: An inorgano-organic ion exchanger (SnSboCP) has been prepared by anchoring o-chlorophenol onto tin antimonate (SnSb). The ion exchanger has been characterized by elemental, spectral and thermal analysis. Chemical stability of the exchanger in acidic, basic and organic media has been assessed. Ion exchange capacity (i.e.c) has been determined and distribution behaviour towards several metal ions in different electrolyte solutions with varying concentrations has been studied and a few binary separations achieved.
&lt;br/&gt;
&lt;br/&gt;Page(s): 190-193</description>
      <pubDate>Wed, 27 Feb 2008 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Determination of palladium using 2-thiobarbituric acid as a releasing agent</title>
      <link>http://nopr.niscair.res.in/handle/123456789/897</link>
      <description>Title: Determination of palladium using 2-thiobarbituric acid as a releasing agent
&lt;br/&gt;
&lt;br/&gt;Authors: Karthikeyan, J; Parameshwara, P; Shetty, A Nityananda; Shetty, Prakash
&lt;br/&gt;
&lt;br/&gt;Abstract: A simple, rapid and accurate complexometric method for the determination of palladium(II) is proposed, based on the selective masking property of 2-thiobarbituric acid towards palladium(II). In the presence of diverse metal ions, palladium(II) is complexed with excess of EDTA and the surplus EDTA is backtitrated with standard zinc sulphate solution at pH 5-6 (acetic acid-sodium acetate buffer) using xylenol orange as indicator. An excess of a 0.3% solution of 2-TBA is then added to displace EDTA from Pd(II)-EDTA complex. The released EDTA is titrated with the same standard zinc sulphate solution as before. Reproducible and accurate results are obtained in the concentration range 1.30-20.00 mg of palladium with relative error of 0.50% and coefficient of variation not exceeding 0.45%. The effects of diverse ions are studied. The method is used for the determination of palladium in alloys, hydrogenation catalysts and complexes.
&lt;br/&gt;
&lt;br/&gt;Page(s): 186-189</description>
      <pubDate>Wed, 27 Feb 2008 22:58:59 GMT</pubDate>
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