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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/26150</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 07:34:31 GMT</pubDate>
    <dc:date>2026-10-10T07:34:31Z</dc:date>
    <item>
      <title>Reaction kinetics of Parachlorophenol and Sodiumhydroxide</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/26483</link>
      <description>Title: Reaction kinetics of Parachlorophenol and Sodiumhydroxide
Authors: Natarajan, M; Nalini, P; Dawn, S S; Mary, D; Balu, K
Abstract: &lt;span style="font-size:&#xD;
12.0pt;font-family:" times="" new="" roman";mso-bidi-language:ar-sa"=""&gt;Sodium phenoxide&#xD;
is one of the important raw materials used in the manufacture of clofibrate, a&#xD;
product of medicinal value. Reaction between p-chlorophenol and sodium hydroxide&#xD;
is carried out at atmospheric conditions to yield sodium phenoxide. It &lt;span style="font-size:12.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" hiddenhorzocr;mso-bidi-language:ar-sa"=""&gt;is &lt;span style="font-size:12.0pt;&#xD;
font-family:" times="" new="" roman";mso-bidi-language:ar-sa"=""&gt;observed experimentally that&#xD;
the reaction is second order and the rate constant is estimated as 12.51 x 10&lt;sup&gt;-3&lt;/sup&gt;&#xD;
L/mol/min. &#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 348</description>
      <pubDate>Sun, 01 Apr 2001 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/26483</guid>
      <dc:date>2001-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Biokinetic Studies of Tannery Effluent Under Aerobic Oxidation Process</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/26482</link>
      <description>Title: Biokinetic Studies of Tannery Effluent Under Aerobic Oxidation Process
Authors: Prakash, N B
Abstract: A laboratory scale experiment was conducted&#xD;
on aerobic digestion of tannery effluent using cowdung as the seed material. The&#xD;
BOD removal of 95.8 per cent was obtained at an optimum organic load of 0.6 kg BOD/m&lt;sup&gt;3&lt;/sup&gt;/d&lt;i&gt;.&#xD;
&lt;/i&gt;Biokinetic coefficients were calculated for the data obtained to study the&#xD;
metabolic performance of the microorganisms.
Page(s): 344-347</description>
      <pubDate>Sun, 01 Apr 2001 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/26482</guid>
      <dc:date>2001-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Microemulsion and Conventional Emulsion Copolymerizations of Styrene with n-Butyl Methacrylate, and Characterization of the Copolymers</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/26481</link>
      <description>Title: Microemulsion and Conventional Emulsion Copolymerizations of Styrene with n-Butyl Methacrylate, and Characterization of the Copolymers
Authors: Reddy, G V Ramana; Balaji, T S; Kannan, P
Abstract: Microemulsion (ME) and conventional emulsion&#xD;
(CE) copolymerization of styrene (STY) with n-butyl methacrylate (BMA) were carried&#xD;
out at 70&lt;sup&gt;o&lt;/sup&gt;C under inert atmosphere with sodiumlauryl sulphate (SLS)&#xD;
as surfactant, n-hexanol (HA) as cosurfactant and potassium persulphate (KPS)&#xD;
as the free radical initiator. Five monomer mixtures in the initial reaction mixtures&#xD;
were used and the reactions were arrested at lower conversions. The copolymers thus&#xD;
obtained were characterized by FTIR, NMR, TG/DTA, GC and GPC. The monomer&#xD;
composition of the copolymers were evaluated from the &lt;sup&gt;1&lt;/sup&gt;HNMR spectral&#xD;
data. The reactivity&#xD;
&#xD;
ratios for the ME and CE copolymerization&#xD;
of styrene (STY) (r&lt;sub&gt;STY&lt;/sub&gt;) with n-butyl methacrylate (BMA) (r&lt;sub&gt;BMA&lt;/sub&gt;)&#xD;
as determined by Fineman-Ross (F-R), Kelen-Tudos (K-T) and Mayo-Lewis (M-L) methods&#xD;
were 0.74±0.02 and 0.64±0.02, and 0.58±0.02 and 0.39 ±0.02, respectively.
Page(s): 336-343</description>
      <pubDate>Sun, 01 Apr 2001 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/26481</guid>
      <dc:date>2001-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Synthesis and Antimicrobial Activity of Some New N-Methylpiperazinylthiadiazoles and Their Azetidinones</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/26480</link>
      <description>Title: Synthesis and Antimicrobial Activity of Some New N-Methylpiperazinylthiadiazoles and Their Azetidinones
Authors: Jaish, L; Srivastava, S K
Abstract: A series of 2-arylidenimino-5-( N&lt;sup&gt;4&lt;/sup&gt;-methyl-N&lt;sup&gt;l&lt;/sup&gt;-piperazinylmethyl)-1 ,3,4-thiadiazole,&#xD;
&lt;b&gt;4&lt;/b&gt;, have been synthesized via condensation of 2-amino -5-(N&lt;sup&gt;4&lt;/sup&gt;-methyl-N&lt;sup&gt;1&lt;/sup&gt;-piperazinylmethyl)-1,3,4-thiadiazole&#xD;
with various carbonyl compounds. Cycloaddition of chloroacetyl chlorride to &lt;b&gt;4&lt;/b&gt;&#xD;
gives 1-[5'-(N&lt;sup&gt;4&lt;/sup&gt;- methyl-N&lt;sup&gt;1&lt;/sup&gt;-piperazinylmethyl)-1', 3',&#xD;
4'-thiadiazole-2'-yl]-4-substituted-3-chloro-2-azetidinones, &lt;b&gt;5&lt;/b&gt;. Compounds&#xD;
&lt;b&gt;4&lt;/b&gt; and &lt;b&gt;5&lt;/b&gt; have been screened for their antibacterial and antifungal&#xD;
activities.
Page(s): 331-335</description>
      <pubDate>Sun, 01 Apr 2001 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/26480</guid>
      <dc:date>2001-04-01T00:00:00Z</dc:date>
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