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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22611</link>
    <description />
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        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22755" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22738" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22737" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22736" />
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    <dc:date>2026-10-10T23:53:10Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22755">
    <title>Preparation and characterization of lobster shell chitosan: Modification of traditional method</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22755</link>
    <description>Title: Preparation and characterization of lobster shell chitosan: Modification of traditional method
Authors: Chatterjee, S; Guha, A K; Chatterjee, B P
Abstract: Preparation of chitosan from lobster shells&#xD;
by Hackman method and modified Hackman method was compared with respect to, their&#xD;
physico-chemical properties, molecular weight, degree of deacetylation,&#xD;
polydispersity and crystallinity. In modified method maximum yield (78%) of&#xD;
chitosan with almost 91% degree of deacetylation determined by first derivative&#xD;
UV spectra was achieved. Molecular size distribution as&#xD;
well as average size of chitosan produced by Hackman method was higher (PI&#xD;
1.205, particle size 1448.6 nm) and of &lt;img src='http://www.niscair.res.in/jinfo/mbar.gif' border=0&gt;&lt;sub&gt;wt&lt;/sub&gt; 10 ×10&lt;sup&gt;5&lt;/sup&gt;&#xD;
when compared to chitosan produced by modified Hackman method (PI 0.8832,&#xD;
particle size 95.3 nm) of &lt;img src='http://www.niscair.res.in/jinfo/mbar.gif' border=0&gt;&lt;sub&gt;wt&lt;/sub&gt; 3.98×10&lt;sup&gt;5&lt;/sup&gt;. X-ray&#xD;
powdered diffraction showed that chitosan prepared by Hackman method&#xD;
was found to be more crystalline, Bragg refractions 13.3°2θ (d = 6.66Å) and&#xD;
19.7°2θ (d = 4.51Å), respectively than chitosan produced by modified method, Bragg&#xD;
refraction 13.6°2θ (d = 6.51Å). This method provides quality product in less&#xD;
time and is economical.
Page(s): 350-354</description>
    <dc:date>2003-07-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22738">
    <title>James Dewar — More than a flask</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22738</link>
    <description>Title: James Dewar — More than a flask
Authors: Wisniak, Jaime
Abstract: James Dewar (1842-1923) is widely known for his pioneering work in cryogenics, of being the first to achieve the liquefaction of hydrogen, by the flask that carries his name, and by his studies about the behaviour of living organisms and materials under conditions of extreme cold. Although he was an excellent experimentalist, he did not leave many significant theoretical contributions.
Page(s): 424-434</description>
    <dc:date>2003-07-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22737">
    <title>Kinetics of esterification of tri-ethylene glycol-methacrylic acid reaction system</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22737</link>
    <description>Title: Kinetics of esterification of tri-ethylene glycol-methacrylic acid reaction system
Authors: Notay, J S; Bhagade, S S
Abstract: Catalysis of esterification reaction of&#xD;
triethylene glycol and methacrylic acid has been reported. A kinetic empirical&#xD;
expression correlating the fractional conversion of&#xD;
methacrylic acid, with catalyst concentration, mole ratio&#xD;
(glycol to methacrylic acid) and temperature is&#xD;
presented for tri-ethylene glycol-methacrylic acid reaction system&#xD;
using methane sulphonic acid and sulphuric acid as homogenous catalyst.
Page(s): 420-423</description>
    <dc:date>2003-07-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22736">
    <title>Effect of substituents on corrosion inhibition efficiency of arylisothiocyanates and their condensation products with thiosemicarbazide for corrosion of copper in aqueous chloride solution</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22736</link>
    <description>Title: Effect of substituents on corrosion inhibition efficiency of arylisothiocyanates and their condensation products with thiosemicarbazide for corrosion of copper in aqueous chloride solution
Authors: Singh, M M; Rastogi, R B; Upadhyay, B N; Yadav, M
Abstract: The inhibition of copper corrosion in&#xD;
1.5% sodium chloride solution was studied at 25, 35 and 45°C using different concentrations&#xD;
of thiosemicarbazide, &lt;i&gt;p&lt;/i&gt;-methoxyphenyl isothiocyanate, &lt;i&gt;p&lt;/i&gt;-methylphenyl&#xD;
isothiocyanate and &lt;i&gt;p-&lt;/i&gt;chlorophenyl isothiocyanate and their corresponding&#xD;
condensation products with thiosemicarbazide. The inhibition efficiency IE of&#xD;
these compounds was evaluated by weight loss and electrochemical polarisation&#xD;
techniques.&#xD;
&#xD;
Substitution at &lt;i&gt;p&lt;/i&gt;-position in the&#xD;
phenyl group resulted in change in IE in the following order for both the aryl isothiocyanates&#xD;
and their corresponding condensation products with thiosemicarbazide-&lt;i&gt;p&lt;/i&gt;-chlorophenyl-&lt;&#xD;
phenyl- &lt; &lt;i&gt;p&lt;/i&gt;-methylphenyl- &lt;&lt;i&gt;p&lt;/i&gt;-methoxyphenyl.
Page(s): 414-419</description>
    <dc:date>2003-07-01T00:00:00Z</dc:date>
  </item>
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