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    <title>NISCAIR Online Periodicals Repository Collection: IJC-A Vol.49A(07) [July 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9916</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/9924" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/9923" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/9922" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/9921" />
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    <title>The Collection's search engine</title>
    <description>Search the Channel</description>
    <name>search</name>
    <link>http://nopr.niscair.res.in/simple-search</link>
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/9924">
    <title>Photo-oxidative degradation of an azo dye direct red 31 in the presence of ZnS catalyst</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9924</link>
    <description>Title: Photo-oxidative degradation of an azo dye direct red 31 in the presence of ZnS catalyst
&lt;br/&gt;
&lt;br/&gt;Authors: Rao, A Nageswara; Sivasankar, B; Sadasivam, V
&lt;br/&gt;
&lt;br/&gt;Abstract: The photocatalytic degradation of&#xD;
direct red 31 on irradiation with UV light in the presence of ZnS photocatalyst&#xD;
has been reported. Effect of &lt;i style=""&gt;p&lt;/i&gt;H, weight of catalyst and&#xD;
concentration of dye on the degradation has been studied. A higher removal of&#xD;
dye is observed under mildly acidic conditions. The optimum weight of catalyst&#xD;
loading is found to be 3.0 g/L. The dye degradation obeys first order kinetics&#xD;
and is explained on the basis of Langmuir-Hinshelwood mechanism.
&lt;br/&gt;
&lt;br/&gt;Page(s): 901-905</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/9923">
    <title>Fluorescence resonance energy transfer from proflavin hemisulphate to rose bengal in aqueous micellar solution</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9923</link>
    <description>Title: Fluorescence resonance energy transfer from proflavin hemisulphate to rose bengal in aqueous micellar solution
&lt;br/&gt;
&lt;br/&gt;Authors: Bhattar, S L; Kolekar, G B; Patil, S R
&lt;br/&gt;
&lt;br/&gt;Abstract: The fluorescence&#xD;
resonance energy transfer from proflavine hemisulphate to rose bengal in&#xD;
aqueous sodium dodecyl sulfate has been investigated at room temperature using&#xD;
steady-state&#xD;
fluorescence spectroscopy technique. The fluorescence of&#xD;
proflavine hemisulphate is quenched by rose bengal and the quenching is in&#xD;
accordance with Stern-Volmer relationship. The efficiency of energy transfer is&#xD;
found to depend upon&#xD;
concentration of rose bengal. The value of critical energy transfer distance&#xD;
calculated by using Foster relationship (27.2 Å) is less than 50 Å, indicating&#xD;
efficient energy transfer occurs in this&#xD;
donor-acceptor pair.
&lt;br/&gt;
&lt;br/&gt;Page(s): 896-900</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/9922">
    <title>Synthesis and characterization of a mixed cationic tetrasulfidotungstate monohydrate</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9922</link>
    <description>Title: Synthesis and characterization of a mixed cationic tetrasulfidotungstate monohydrate
&lt;br/&gt;
&lt;br/&gt;Authors: Srinivasan, Bikshandarkoil R; Mhalsikar, Rathan G; Näther, Christian; Bensch, Wolfgang
&lt;br/&gt;
&lt;br/&gt;Abstract: Synthesis and structural characterization of a mixed cationic&#xD;
tetrasulfidotungstate monohydrate (dabcoH)&lt;sub&gt;3&lt;/sub&gt;(NMe&lt;sub&gt;4&lt;/sub&gt;)[WS&lt;sub&gt;4&lt;/sub&gt;]&lt;sub&gt;2&lt;/sub&gt;.&#xD;
H&lt;sub&gt;2&lt;/sub&gt;O (dabco = 1,4-diazabicyclo[2.2.2]octane; NMe&lt;sub&gt;4&lt;/sub&gt; =&#xD;
tetramethylammo-nium) is described. The compound crystallizes in the&#xD;
centrosymmetric monoclinic space group &lt;i style=""&gt;P2&lt;sub&gt;1&lt;/sub&gt;/c&lt;/i&gt;&#xD;
and its structure consists of three crystallographically independent&#xD;
monoprotonated (dabcoH)&lt;sup&gt;+&lt;/sup&gt; cations, a tetramethylammonium cation, two&#xD;
unique tetrasulfidotungstate anions, and a lattice water. The organic cations,&#xD;
[WS&lt;sub&gt;4&lt;/sub&gt;]&lt;sup&gt;2-&lt;/sup&gt; anion and lattice water are linked by several&#xD;
weak H-bonding interactions.
&lt;br/&gt;
&lt;br/&gt;Page(s): 891-895</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/9921">
    <title>Speciation of chromium in aqueous samples by solid phase extraction using multiwall carbon nanotubes impregnated with D2EHPA</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9921</link>
    <description>Title: Speciation of chromium in aqueous samples by solid phase extraction using multiwall carbon nanotubes impregnated with D2EHPA
&lt;br/&gt;
&lt;br/&gt;Authors: Vellaichamy, S; Palanivelu, K
&lt;br/&gt;
&lt;br/&gt;Abstract: A&#xD;
solid phase extraction system has been developed for the speciation of&#xD;
chromium(III) and chromium(VI). This method is based on the adsorption of&#xD;
chromium(III) on D2EHPA impregnated with multiwall carbon nanotubes and has&#xD;
been compared with commercially available activated carbon impregnated with&#xD;
D2EHPA. The chromium concentration has been determined by inductively coupled&#xD;
plasma atomic emission spectroscopy. The effect of parameters such as &lt;i&gt;p&lt;/i&gt;H&#xD;
of the aqueous solution, amount of adsorbent, contact time, initial ion&#xD;
concentration, sample volume, eluent type and D2EHPA concentration have been&#xD;
investigated. The results indicate that the maximum adsorption of chromium(III)&#xD;
is at &lt;i&gt;p&lt;/i&gt;H 4.5 ± 0.1 on the multiwall carbon nanotubes. Desorption studies&#xD;
have been carried out with 0.25 &lt;i style=""&gt;M&lt;/i&gt; Br&lt;sub&gt;2&lt;/sub&gt;&#xD;
in 1.0 &lt;i style=""&gt;M&lt;/i&gt; NaOH wherein quantitative&#xD;
recovery of the chromium(III) has been observed. The adsorption capacity of&#xD;
MWCNTs- D2EHPA is found to be 0.96 mg g &lt;sup&gt;-1&lt;/sup&gt; for chromium with&#xD;
detection limit of chromium 0.05 mg mL&lt;sup&gt;-1&lt;/sup&gt;.  The highest pre-concentration factor of 60&#xD;
could be obtained for 300 mL of sample volume. &#xD;
The developed method has been applied for the speciation of chromium in&#xD;
natural water sample and the pre-concentration method is satisfactory&#xD;
(recoveries &gt; 98 %, rsd &lt; 10 %, &lt;i&gt;n &lt;/i&gt;= 5) for chromium species&#xD;
determination.
&lt;br/&gt;
&lt;br/&gt;Page(s): 882-890</description>
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