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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/46581</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 20:47:05 GMT</pubDate>
    <dc:date>2026-10-10T20:47:05Z</dc:date>
    <item>
      <title>Thermodynamic view of hydrophobic association of side chains of aromatic amino acids</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46736</link>
      <description>Title: Thermodynamic view of hydrophobic association of side chains of aromatic amino acids
Authors: Iyengar, RR; Bhattacharya, P K
Abstract: The hydrophobic association constants, K. for the side chains of phenylalanine, tyrosin and tryptophan betains have been evaluated employing the difference in the mode of self-association of the optically pure -betains and their -mixtures and using the equation of Rose and Drago. The corresponding association free energy, &lt;img src='http://www.niscair.res.in/jinfo/delta.gif' border=0&gt;&lt;em&gt;G&lt;/em&gt;, values for benzyl-, &lt;em&gt;p&lt;/em&gt;-hydroxybenzyl- and (3-indolyl)methyl groups have been determined as - 15.90, - 19.92 and - 20.21 kJmol&lt;sup&gt;-1&lt;/sup&gt; respectively, after correcting for partial overlap of aromatic ring in &lt;img src='http://www.niscair.res.in/jinfo/small.gif' border=0&gt;-&lt;img src='http://www.niscair.res.in/jinfo/small.gif' border=0&gt;/&lt;img src='http://www.niscair.res.in/jinfo/smaller.gif' border=0&gt; - &lt;img src='http://www.niscair.res.in/jinfo/smaller.gif' border=0&gt; dimers.
Page(s): 445-451</description>
      <pubDate>Thu, 01 Jun 1989 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46736</guid>
      <dc:date>1989-06-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Pressure dependence of catalysed and inhibited burning rate of composite solid propellants</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46735</link>
      <description>Title: Pressure dependence of catalysed and inhibited burning rate of composite solid propellants
Authors: Rastogi, R P; Syal, V; Singh, Haridwar; Nerlekar, K A
Abstract: Data on ambient temperature burning rates for an aluminized HTPB composite propellant family with bimodal AP and a total solids loading of roughly 80% over the pressure range from 35 to 105 kg/cm&lt;sup&gt;2&lt;/sup&gt; have been reported. Data are also reported for the additive free base line formulation and formulations with individual rate modifying additives (Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;, copper oxide, CaCO&lt;sub&gt;3&lt;/sub&gt;, SrCO&lt;sub&gt;3&lt;/sub&gt;) at 2% level. Results have been correlated with rate expressions of Summerfield, Rice, Rastogi and several other empirical relations and relative merits of different equations have been assessed. Further, the experimental data of Blair on pressure and temperature dependence and of Singh on formulation dependence of burning rate have also been analysed. The results show that burning rate is directly proportional to (T&lt;sub&gt;i&lt;/sub&gt;)&lt;sup&gt;1/4&lt;/sup&gt;&lt;em&gt;, &lt;/em&gt;in agreement with the prediction based on burning rate expression of Rastogi &lt;em&gt;et al. &lt;/em&gt;(T&lt;sub&gt;i&lt;/sub&gt;, is the initial temperature in kelvin).
Page(s): 452-457</description>
      <pubDate>Thu, 01 Jun 1989 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46735</guid>
      <dc:date>1989-06-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Catalytic redox reaction of nitric oxide and carbon monoxide on perovskites</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46734</link>
      <description>Title: Catalytic redox reaction of nitric oxide and carbon monoxide on perovskites
Authors: Salker, A V; Chakrabarty, D K; Keer, H V
Abstract: Kinetics of oxidation-reduction reaction between CO and NO over perovskite catalysts LaMnO&lt;sub&gt;3&lt;/sub&gt;) and LaCoO&lt;sub&gt;3&lt;/sub&gt;), prepared by ceramic and wet methods, has been studied in the temperature range of 473-1000 K. Results have been discussed in the light of X-ray powder diffraction, atomic absorption spectrometry, gas chromatography, electrical conductivity and surface area measurements. The rate-controlling step in the catalytic reduction of NO by CO is presumably the active site reduction process.
Page(s): 458-462</description>
      <pubDate>Thu, 01 Jun 1989 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46734</guid>
      <dc:date>1989-06-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Physicochemical studies on thermal analysis of magnesium tris(malonato) ferrate(III) decahydrate</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/46733</link>
      <description>Title: Physicochemical studies on thermal analysis of magnesium tris(malonato) ferrate(III) decahydrate
Authors: Randhawa, B S; Kaur, Sandeep; Bassi, P S
Abstract: Thermal decomposition of magnesium tris(malonato)ferrate(III) decahydrate, i.e. Mg&lt;sub&gt;3&lt;/sub&gt;[Fe(CH&lt;sub&gt;2&lt;/sub&gt;C&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt;)&lt;sub&gt;3&lt;/sub&gt;]&lt;sub&gt;2&lt;/sub&gt;.10H&lt;sub&gt;2&lt;/sub&gt;O has been studied in the temperature range of 300-1073 K in static air atmosphere using Mossbauer, IR, TGDTA- DTG and XRD techniques. Thermolysis of the above salt proceeds without the salt undergoing reduction to Fe(II) intermediate, The particle size of ɑ-Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;, formed as an intermediate increases with increase in decomposition temperature from 473 K to 773 K, At higher temperature, fine particles of magnesium ferrite, MgFe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; are formed as a result of solid state reaction between ɑ-Fe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; and magnesium oxide.
Page(s): 463-466</description>
      <pubDate>Thu, 01 Jun 1989 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/46733</guid>
      <dc:date>1989-06-01T00:00:00Z</dc:date>
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