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    <title>NISCAIR Online Periodicals Repository Collection: IJCT Vol.17(6) [November 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10710</link>
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      <title>Determination of boron in zirconium-niobium alloys by spectrophotometry</title>
      <link>http://nopr.niscair.res.in/handle/123456789/10721</link>
      <description>Title: Determination of boron in zirconium-niobium alloys by spectrophotometry
&lt;br/&gt;
&lt;br/&gt;Authors: Ramanjaneyulu, P S; Sayi, Y S; Ramakumar, K L
&lt;br/&gt;
&lt;br/&gt;Abstract: Boron doped zirconium-niobium&#xD;
alloy rods are used as neutron reactivity control rods in advanced nuclear&#xD;
reactors. Accurate knowledge about the boron content in this alloy is an&#xD;
essential requirement prior to its usage in nuclear reactors. In view of the&#xD;
refractory nature of the alloy, boron determination in these type of matrices&#xD;
is a challenging task. Also due to non-availability of matrix matched reference&#xD;
materials, direct solid analysis cannot be resorted to. Quantitative&#xD;
dissolution of the matrix without losing any boron followed by its&#xD;
determination is the only alternative. In the present work, Zr-Nb sample was&#xD;
dissolved in (NH&lt;sub&gt;4&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; and H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;&#xD;
taking care to prevent the loss of boron. Boron was selectively separated&#xD;
employing batch extraction with 10% 2-ethyl hexane 1,3 diol in chloroform and&#xD;
determined spectrophotometrically as B-Curcumin complex. Absorbance was&#xD;
measured at 550 nm. The precision and accuracy of the method is 3%. The absolute&#xD;
detection limit of the method is 12 ng. The method has been evaluated by&#xD;
standard addition method and validated by ICP-AES technique.
&lt;br/&gt;
&lt;br/&gt;Page(s): 468-470</description>
      <pubDate>Fri, 29 Oct 2010 22:58:59 GMT</pubDate>
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      <title>Conductometric studies on solvation behaviour of citric acid in water + methanol and water + ethanol mixtures at different temperatures</title>
      <link>http://nopr.niscair.res.in/handle/123456789/10720</link>
      <description>Title: Conductometric studies on solvation behaviour of citric acid in water + methanol and water + ethanol mixtures at different temperatures
&lt;br/&gt;
&lt;br/&gt;Authors: Bhat, J Ishwara; Manjunatha, M N
&lt;br/&gt;
&lt;br/&gt;Abstract: The paper reports the study on the effect of&#xD;
solvation of the species of citric acid in water + methanol and water + ethanol&#xD;
mixtures (&lt;i style=""&gt;v/v&lt;/i&gt;) on its conductivity&#xD;
behaviour as a function of temperature. The specific conductance was measured&#xD;
in the temperature range 283-313 K and the evaluated equivalent conductance was&#xD;
analyzed by Kraus-Bray and Shedlovsky models of conductivity. Limiting molar&#xD;
conductance (λ&lt;sup&gt;0&lt;/sup&gt;&lt;sub&gt;m&lt;/sub&gt;), dissociation constant (&lt;i style=""&gt;K&lt;/i&gt;&lt;sub&gt;C&lt;/sub&gt;) and association constant&#xD;
(&lt;i style=""&gt;K&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt;) were evaluated for&#xD;
all solvent compositions. The limiting molar conductance was found to decrease&#xD;
with the increase in amount of co-solvent to water. &lt;i style=""&gt;K&lt;/i&gt;&lt;sub&gt;c&lt;/sub&gt; increased with increase in temperature till 60%&#xD;
methanol and 40% ethanol with a later decrease. Fuoss Accascina equation was&#xD;
applied and it was proved that the formation of ion pairs and scanty amount of&#xD;
ion triplets takes place in the system. Walden product, corrected Stokes radius&#xD;
(r&lt;sub&gt;i&lt;/sub&gt;), thermodynamic parameters and solvation number also have been&#xD;
evaluated. Born relation of solvation was verified. These data were used to&#xD;
study the nature of ion-solvent and solvent-solvent interactions existing in&#xD;
the system under prevailing conditions.
&lt;br/&gt;
&lt;br/&gt;Page(s): 462-467</description>
      <pubDate>Fri, 29 Oct 2010 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Comminution behaviour of microwave heated two sulphide copper ores</title>
      <link>http://nopr.niscair.res.in/handle/123456789/10719</link>
      <description>Title: Comminution behaviour of microwave heated two sulphide copper ores
&lt;br/&gt;
&lt;br/&gt;Authors: Kaya, Erol
&lt;br/&gt;
&lt;br/&gt;Abstract: The effect&#xD;
of microwave irradiation on the comminution of two sulphide copper ores with&#xD;
different mineralogy were investigated to enhance the milling processes. Each&#xD;
ore was subjected to microwave radiation for varying time periods to determine&#xD;
their heating profiles. Changes in breakage characteristics with the microwave&#xD;
exposure time were quantified by sieving breakage, standard Bond work index&#xD;
grindability and single particle drop weight comminution tests. The results of&#xD;
the sieving breakage tests with the untreated and microwaved samples indicated&#xD;
significant improvements in the size reduction due to microwave energy induced&#xD;
macro fracturing. Differing ore mineralogy has been shown to affect the&#xD;
effectiveness of microwave assisted size reduction. The results of the standard&#xD;
Bond work index grindability tests performed with both the microwave treated&#xD;
copper ores, on the other hand, suggested no significant improvements in&#xD;
grindability. The single particle fracture experiments performed with an&#xD;
Ultrafast Load Cell (UFLC) indicated similar results of no significant&#xD;
improvements in the fracture energies of the microwave treated ore samples.
&lt;br/&gt;
&lt;br/&gt;Page(s): 455-461</description>
      <pubDate>Fri, 29 Oct 2010 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Oxidation of phenol using LaMnO&lt;sub&gt;3&lt;/sub&gt; perovskite, TiO&lt;sub&gt;2&lt;/sub&gt;, H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2 &lt;/sub&gt;and UV radiation</title>
      <link>http://nopr.niscair.res.in/handle/123456789/10718</link>
      <description>Title: Oxidation of phenol using LaMnO&lt;sub&gt;3&lt;/sub&gt; perovskite, TiO&lt;sub&gt;2&lt;/sub&gt;, H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2 &lt;/sub&gt;and UV radiation
&lt;br/&gt;
&lt;br/&gt;Authors: Singh, Chandrakant; Rakesh, Meeta
&lt;br/&gt;
&lt;br/&gt;Abstract: LaMnO&lt;sub&gt;3&lt;/sub&gt; perovskite has been used for the&#xD;
treatment of aqueous solution of phenol using stoichiometric amount of H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;&#xD;
and combination of TiO&lt;sub&gt;2&lt;/sub&gt; and UV radiation. The oxidation of phenol&#xD;
was studied with [UV radiation]; &#xD;
[H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; and UV]; [TiO&lt;sub&gt;2&lt;/sub&gt; and UV]; [LaMnO&lt;sub&gt;3&lt;/sub&gt;&#xD;
and UV]; [TiO&lt;sub&gt;2&lt;/sub&gt;, H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; and UV]; [LaMnO&lt;sub&gt;3&lt;/sub&gt;,&#xD;
H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; and UV]; to establish the effectiveness of different&#xD;
systems when compared with perovskite catalyst. Results show that the phenol&#xD;
degradation efficiencies decreased in the following order [LaMnO&lt;sub&gt;3&lt;/sub&gt;, H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;&#xD;
and UV] &amp;gt; [TiO&lt;sub&gt;2&lt;/sub&gt;, H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2 &lt;/sub&gt;and UV] &amp;gt; [LaMnO&lt;sub&gt;3&lt;/sub&gt;&#xD;
and UV] &amp;gt; [TiO&lt;sub&gt;2&lt;/sub&gt; and UV]&amp;gt; [H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; and UV ]&#xD;
&amp;gt; [UV]. UV-VIS spectra result of phenol degradation shows that as the&#xD;
concentration of catalyst increases, its activity increases. The optimum&#xD;
concentration of catalyst was 0.60 g/L for 100 ppm phenol solution. Perovskite&#xD;
catalyst after reaction is completely regenerated by calcinations at 800°C for 2 h and retains a&#xD;
similar catalytic performance
&lt;br/&gt;
&lt;br/&gt;Page(s): 451-454</description>
      <pubDate>Fri, 29 Oct 2010 22:58:59 GMT</pubDate>
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