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    <title>NISCAIR Online Periodicals Repository Community: Indian Journal of Chemical Technology (IJCT)</title>
    <link>http://nopr.niscair.res.in/handle/123456789/55</link>
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      <url>http://nopr.niscair.res.in/retrieve/132</url>
      <link>http://nopr.niscair.res.in/handle/123456789/55</link>
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      <title>The Community's search engine</title>
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      <title>Electrodeposition mechanism of aluminium from aluminium chloride-N-(n-butyl)pyridinium chloride room temperature molten salt</title>
      <link>http://nopr.niscair.res.in/handle/123456789/16969</link>
      <description>Title: Electrodeposition mechanism of aluminium from aluminium chloride-N-(n-butyl)pyridinium chloride room temperature molten salt
&lt;br/&gt;
&lt;br/&gt;Authors: Ali, M R; Nishikata, A; Tsuru, T
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:12.0pt;line-height:&#xD;
115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN"&gt;Electrodeposition&#xD;
of aluminium has been carried out by controlled-current and controlled-potential&#xD;
methods from acidic aluminum(III) chloride-N-(&lt;i&gt;n&lt;/i&gt;-butyl)pyridinium&#xD;
chloride (BPC) molten bath at room temperature. The electrodeposition of&#xD;
aluminium from acidic AlCl&lt;sub&gt;3&lt;/sub&gt;-BPC melt occurs via instantaneous&#xD;
nucleation mechanism in the very initial stage of the crystal growth. The&#xD;
deposition reaction mechanisms of aluminium in the acidic AlCl&lt;sub&gt;3&lt;/sub&gt;-BPC&#xD;
molten bath are revealed by electrochemical analysis. The experimental Tafel&#xD;
slope of 20 mV dec&lt;sup&gt;-1&lt;/sup&gt; and the calculated transfer coefficient (α&lt;sub&gt;c&lt;/sub&gt;)&#xD;
of 3 suggest that the rate determining step is a chemical reaction involving&#xD;
the release of the complexing agents via three consecutive single electron&#xD;
transfer steps. The influence of various conditions on electrodeposition and&#xD;
the morphology of the electrodeposited layers have been investigated by X-ray&#xD;
diffractometry and scanning electron microscopy. On increasing the current&#xD;
density smaller particle size and better adhesiveness of the electrodeposited&#xD;
layers have been obtained. The cathodic current efficiency for the deposition&#xD;
of Aluminium is about 99.8%.&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 317-324</description>
      <pubDate>Fri, 29 Oct 1999 22:58:59 GMT</pubDate>
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    <item>
      <title>Synthesis and characterization of epoxy resins containing zinc chloride</title>
      <link>http://nopr.niscair.res.in/handle/123456789/16967</link>
      <description>Title: Synthesis and characterization of epoxy resins containing zinc chloride
&lt;br/&gt;
&lt;br/&gt;Authors: Pandey, Saurabh; Srivastava, A K
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:12.0pt;line-height:&#xD;
115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN"&gt;As&#xD;
evidenced from IR spectroscopy, ZnCl&lt;sub&gt;2&lt;/sub&gt;-forms a complex with oxygen&#xD;
atom of epichlorohydrin and thus cures the epoxy resins simultanteusly. Differential&#xD;
Scanning Calorimetry (DSC) studies show that the properties, like degree of&#xD;
cure, percent crystallinity, glass transition temperature of the epoxy resin&#xD;
improved significantly. The Scanning Electron Microscopy (SEM) studies confirms&#xD;
the presence of zinc metal in the epoxy resin. The activation energy is 95 KJ/mol&#xD;
and order of reaction is first.&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 313-316</description>
      <pubDate>Fri, 29 Oct 1999 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Hydrazine and substituted hydrazines as corrosion inhibitors for mild steel in simulated seawater</title>
      <link>http://nopr.niscair.res.in/handle/123456789/16965</link>
      <description>Title: Hydrazine and substituted hydrazines as corrosion inhibitors for mild steel in simulated seawater
&lt;br/&gt;
&lt;br/&gt;Authors: Suresh, G S; Aravinda, C L; Ahamed, M F; Mayanna, S M
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:12.0pt;line-height:&#xD;
115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN"&gt;The&#xD;
corrosion of mild steel in simulated seawater containing various concentrations&#xD;
of hydrazine, phenylhydrazine and 2, 4-dinitrophenylhydrazine has been studied&#xD;
by polarization technique. These compounds inhibit corrosion effectively even&#xD;
in trace concentration. The degree of corrosion inhibition is a function of temperature,&#xD;
concentration and nature of the inhibitor. The corrosion current density,&#xD;
percentage inhibitor efficiency and thermodynamic parameters for the surface&#xD;
adsorption of inhibitors were calculated for the inhibition process. The IR&#xD;
spectra of the film formed on the corroding surface indicated the formation of complex&#xD;
between the inhibitor molecule and the mild steel. The inhibitors appeared to&#xD;
function through a general adsorption mode following the Frumkin adsorption&#xD;
isotherm. The thermodynamic parameters of adsorption showed a strong&#xD;
interaction of these inhibitor molecules with the mild steel surface. The&#xD;
results revealed that these compounds act as mixed inhibitors for mild steel in&#xD;
simulated seawater.&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 301-304</description>
      <pubDate>Fri, 29 Oct 1999 22:58:59 GMT</pubDate>
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    <item>
      <title>Photo-oxidative degradation of Direct Yellow 12 using hydrogen peroxide</title>
      <link>http://nopr.niscair.res.in/handle/123456789/16963</link>
      <description>Title: Photo-oxidative degradation of Direct Yellow 12 using hydrogen peroxide
&lt;br/&gt;
&lt;br/&gt;Authors: Rathi, Aparna; Pandit, M; Sharma, R K
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:12.0pt;line-height:&#xD;
115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN"&gt;The&#xD;
photo-oxidation process by combination of UV light and H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;&#xD;
generates hydroxyl radicals which are capable of oxidising many organic compounds&#xD;
which are refractory type and difficult to oxidize by conventional chemical&#xD;
treatment. In the present study, photo-oxidation of Direct Yellow 12 (DY 12)&#xD;
dye has been carried out in an annular type photoreactor using 8 Watt low&#xD;
pressure mercury lamp along with H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; as oxidant.&#xD;
Synthetic dye solutions of 50 mg/L concentration were used to carry out the&#xD;
experiments. Complete dye degradation and colour removal took place within 30&#xD;
min with 85-95 % reduction in COD (Chemical Oxygen Demand) value. The process&#xD;
of degradation is dependent upon the &lt;i&gt;p&lt;/i&gt;H of the solution.&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 297-300</description>
      <pubDate>Fri, 29 Oct 1999 22:58:59 GMT</pubDate>
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