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  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/34187">
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/34187</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/34194" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/34193" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/34192" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/34191" />
      </rdf:Seq>
    </items>
    <dc:date>2026-10-11T06:30:19Z</dc:date>
  </channel>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/34194">
    <title>Utilization of sodium montmorillonite clay for enhanced electrochemical sensing  of amlodipine</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/34194</link>
    <description>Title: Utilization of sodium montmorillonite clay for enhanced electrochemical sensing  of amlodipine
Authors: Sikkander, A Mohamed; Vedhi, C; Manisankar, P
Abstract: &lt;span style="font-size:9.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-bidi-font-family:="" mangal;mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:="" hi"="" lang="EN-GB"&gt;Nanosize surface of sodium montmorillonite has been prepared via sonication&#xD;
and deposited on glassy carbon electrodes for use as working electrode in a&#xD;
highly sensitive electrochemical biosensor for the detection of trace amounts&#xD;
of the calcium channel blocking drug, amlodipine. The cyclic voltammetric&#xD;
behaviour of amlodipine is studied in the &lt;i style="mso-bidi-font-style:normal"&gt;p&lt;/i&gt;H&#xD;
range of 1.0−13.0. In alkali medium (&lt;i style="mso-bidi-font-style:normal"&gt;p&lt;/i&gt;H&#xD;
13.0) the sensor shows good response. Cyclic voltammograms show one oxidation&#xD;
peak and one broad reduction peak, which may be due to the oxidation of&#xD;
secondary amino group and reduction of chlorine and nitro groups respectively.&#xD;
Plots of log peak current and potential when correlated with &#xD;
log scan rate, indicate irreversible electron diffusion controlled redox&#xD;
reaction. The optimum conditions have been established by differential pulse&#xD;
stripping voltammetry. The anodic peak current is linear with concentration of&#xD;
the analyte at optimum conditions; the detection limit has been determined to&#xD;
be &lt;span style="mso-bidi-font-weight:bold"&gt;0.01 μ&lt;span style="font-size:9.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" "times="" roman";mso-bidi-font-family:mangal;mso-ansi-language:en-gb;="" mso-fareast-language:en-us;mso-bidi-language:hi;mso-bidi-font-weight:bold"="" lang="EN-GB"&gt;g/mL.&#xD;
&lt;span style="font-size:9.0pt;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";mso-bidi-font-family:mangal;="" mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:hi"="" lang="EN-GB"&gt;A&#xD;
simple, sensitive and time-saving differential pulse stripping voltammetric&#xD;
procedure has been developed for estimation of amlodipine in its formulations&#xD;
as tablets.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 571-575</description>
    <dc:date>2016-05-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/34193">
    <title>Synthesis of heteroatom-doped  ZnO nanoparticles as an efficient  visible light photocatalyst and its photoelectrochemical performance</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/34193</link>
    <description>Title: Synthesis of heteroatom-doped  ZnO nanoparticles as an efficient  visible light photocatalyst and its photoelectrochemical performance
Authors: Wu, Wenjie; Zhu, Xiaodan; Yin, Qiaoqiao; Tan, Linxiang; Ke, Xiaoxia; Qiao, Ru
Abstract: &lt;span style="font-size:9.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-bidi-font-family:="" "times="" roman";mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-US"&gt;Heteroatom-doped ZnO nanoparticles (Zn&lt;sub&gt;1-x&lt;/sub&gt;Ni&lt;sub&gt;x&lt;/sub&gt;O&#xD;
NPs) have been synthesized by a simple solvothermal approach. The&#xD;
photocatalytic activity of the products has been evaluated by a photoassisted&#xD;
degradation of Rhodamine B in aqueous solution under visible light irradiation.&#xD;
All the heteroatom-doped semiconductors exhibit better photocatalytic activities&#xD;
than pure ZnO, with the 1 mol% Ni&lt;sup&gt;2+&lt;/sup&gt;-doped ZnO showing the best&#xD;
photocatalytic activity. From the transient photocurrent response and&#xD;
electrochemical impedance spectroscopic experiments it is observed that the&#xD;
photogenerated charges of the Ni-doped ZnO show longer lifetime and higher&#xD;
separation than that of pure ZnO, leading to its superior visible light&#xD;
photoactivity. The active species tests indicate that the hydroxyl radical and&#xD;
active holes were primarily responsible for the enhanced photocatalytic performance&#xD;
of Rhodamine B, and the superoxide radical takes part partially in the&#xD;
oxidation process. A possible photocatalytic mechanism is proposed. Good&#xD;
photostability and reusability of the product show that the studied&#xD;
nanoparticles have potential application in dye wastewater treatment.&lt;/span&gt;
Page(s): 566-570</description>
    <dc:date>2016-05-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/34192">
    <title>Hydrolytic cleavage of paraoxon and parathion by oximate and functionalized oximate ions: A comparative study</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/34192</link>
    <description>Title: Hydrolytic cleavage of paraoxon and parathion by oximate and functionalized oximate ions: A comparative study
Authors: Dewangan, Hitesh K; Kandpal, Neha; Nagwanshi, Rekha; Satnami, Manmohan L
Abstract: &lt;span style="font-size:11.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-bidi-font-family:="" mangal;letter-spacing:-.1pt;mso-ansi-language:en-gb;mso-fareast-language:en-us;="" mso-bidi-language:hi"="" lang="EN-GB"&gt;Bimolecular reactions of O,O-diethyl-O-&lt;i&gt;p&lt;/i&gt;-nitrophenylphosphate&#xD;
(paraoxon) and O,O-diethyl-O-&lt;i&gt;p&lt;/i&gt;-nitrophenyl phosphorothioate (parathion)&#xD;
with oximate (pyridinealdoxime 2-PyOx&lt;sup&gt;-&lt;/sup&gt; and 4-PyOx&lt;sup&gt;-&lt;/sup&gt;) &lt;span style="font-size:11.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" "times="" roman";mso-bidi-font-family:mangal;mso-ansi-language:en-gb;="" mso-fareast-language:en-us;mso-bidi-language:hi"="" lang="EN-GB"&gt;and its functionalized oximate,&#xD;
4-(hydroxyimino)methyl)-1-alkylpyridinium bromide ions (alkyl = C&lt;sub&gt;10&lt;/sub&gt;H&lt;sub&gt;21&lt;/sub&gt;&#xD;
(4-C&lt;sub&gt;10&lt;/sub&gt;PyOx&lt;sup&gt;-&lt;/sup&gt;); &#xD;
alkyl = C&lt;sub&gt;12&lt;/sub&gt;H&lt;sub&gt;25&lt;/sub&gt; (4-C&lt;sub&gt;12&lt;/sub&gt;PyOx&lt;sup&gt;-&lt;/sup&gt;))&#xD;
have been investigated in aqueous and cationic micellar media of&#xD;
cetylpyridinium bromide, cetyltrimethyl-ammonium bromide and&#xD;
cetyltetradecyltrimethylammonium bromide at &lt;i&gt;p&lt;/i&gt;H 9.5 and 27 &lt;sup&gt;o&lt;/sup&gt;C.&#xD;
Under the micellized condition, &#xD;
a 1.2×10&lt;sup&gt;3&lt;/sup&gt; fold and 9.0×10&lt;sup&gt;6&lt;/sup&gt; fold rate enhancement over the&#xD;
aqueous reaction of paraoxon (&lt;i style="mso-bidi-font-style:normal"&gt;k&lt;/i&gt;&lt;sub&gt;o&lt;/sub&gt;&#xD;
= 7.5×10&lt;sup&gt;-8&lt;/sup&gt; s&lt;sup&gt;-1&lt;/sup&gt;) and parathion &#xD;
(&lt;i style="mso-bidi-font-style:normal"&gt;k&lt;/i&gt;&lt;sub&gt;o&lt;/sub&gt; = 9.5×10&lt;sup&gt;-11&lt;/sup&gt;)&#xD;
is observed.&lt;/span&gt;&lt;/span&gt;
Page(s): 560-565</description>
    <dc:date>2016-05-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/34191">
    <title>&lt;span style="font-size:13.0pt;mso-bidi-font-size: 8.0pt;font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-bidi-font-family:"Times New Roman";letter-spacing:-.1pt;mso-ansi-language: EN-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Vapour phase hydrogenation of aqueous levulinic acid to γ-valerolactone over CuZnAlO hydrotalcite&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/34191</link>
    <description>Title: &lt;span style="font-size:13.0pt;mso-bidi-font-size: 8.0pt;font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-bidi-font-family:"Times New Roman";letter-spacing:-.1pt;mso-ansi-language: EN-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Vapour phase hydrogenation of aqueous levulinic acid to γ-valerolactone over CuZnAlO hydrotalcite&lt;/span&gt;
Authors: Jaya, V Swarna; Sudhakar, Medak
Abstract: &lt;span style="font-size:11.0pt;mso-bidi-font-size:&#xD;
10.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-bidi-font-family:"times="" roman";letter-spacing:-.1pt;mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"&gt;Vapour phase&#xD;
hydrogenation of levulinic acid to &#xD;
γ-valerolactone has been accomplished in aqueous phase over&#xD;
copper-zinc-aluminum hydrotalcite, prepared by co-precipitation method using&#xD;
nitrate salts as their precursors. The hydrotalcite system exhibits superior&#xD;
activity in the hydrogenation and cyclization of 10% aqueous solution of&#xD;
levulinic acid with &gt;99% selectivity for γ-valerolactone at 275 &lt;sup&gt;o&lt;/sup&gt;C&#xD;
under atmospheric pressure of hydrogen (flow rate of H&lt;sub&gt;2&lt;/sub&gt;-30 mL/min). &lt;/span&gt;
Page(s): 554-559</description>
    <dc:date>2016-05-01T00:00:00Z</dc:date>
  </item>
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