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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/41758</link>
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    <pubDate>Thu, 08 Oct 2026 14:20:42 GMT</pubDate>
    <dc:date>2026-10-08T14:20:42Z</dc:date>
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      <title>Thermodynamic analysis of critical limits in Belousov-Zhabotinskii reaction system</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/41851</link>
      <description>Title: Thermodynamic analysis of critical limits in Belousov-Zhabotinskii reaction system
Authors: Rastogi, R P; Syal, V; Misra, G P
Abstract: Stability of the Belousov-Zhabotinskii (B-Z) reaction system containing bromate, ceric ammonium sulphate, sulphuric acid and mixed organic substrates (oxalic acid + acetone) has been examined using the thermodynamic theory of Glansdorff and Prigogine at the two critical limits of [acetone] and also in the oscillatory domain. The sign of excess entropy production due to perturbation in [HBrO&lt;sub&gt;2&lt;/sub&gt;] has been estimated by taking into account the subset of reactions involving HBrO&lt;sub&gt;2&lt;/sub&gt;. Numerical estimates of sign of relative excess entropy production for different reactions have been made using the latest accepted values of the rate constants (Field and Forsterling) as well as values of Field and Boyd. The thermodynamic analysis suggests that the reaction system is stabilized either when (i) the contribution to the excess entropy production due to destruction of HBrO&lt;sub&gt;2&lt;/sub&gt; by Br&lt;sup&gt;-&lt;/sup&gt; exceeds the negative contribution due to autocatalytic reaction step or when (ii) the contribution of disproportionation of HBrO&lt;sub&gt;2&lt;/sub&gt; to the excess entropy production exceeds or becomes comparable to the negative contribution due to autocatalytic reaction step. Situation (i) corresponds to lower limit of [acetone] while (ii) corresponds to upper limit of [acetone]. Instability can occur when the negative contribution due to the autocatalytic reaction exceeds the sum of contributions of disproportionation of HBrO&lt;sub&gt;2&lt;/sub&gt; and its destruction by Br&lt;sup&gt;-&lt;/sup&gt;.
Page(s): 203-208</description>
      <pubDate>Fri, 01 Mar 1991 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/41851</guid>
      <dc:date>1991-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Dimensional response of engineering polymeric elastomers in the presence of halo-substituted benzenes</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/41850</link>
      <description>Title: Dimensional response of engineering polymeric elastomers in the presence of halo-substituted benzenes
Authors: Harogoppad, S B; Aminabhavi, T M
Abstract: Dimensional response of several engineering polymers in the presence of halo-substituted benzenes has been studied by weight-gain and swelling measurements. The experimental data have been used to estimate the diffusion coefficients, kinetic rate constants, activation parameters and molar mass between crosslinks for all the polymer-solvent systems.
Page(s): 209-214</description>
      <pubDate>Fri, 01 Mar 1991 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/41850</guid>
      <dc:date>1991-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Template copolymerization of methyl methacrylate and styrene on poly(methyl methacrylate)</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/41849</link>
      <description>Title: Template copolymerization of methyl methacrylate and styrene on poly(methyl methacrylate)
Authors: Awasthi, Sanjay K; Srivastava, A K
Abstract: The radical copolymerization of methyl methacrylate and styrene using syn-poly(methyl methacrylate) (M͞&lt;sub&gt;V&lt;/sub&gt; = 98,890) as template in dimethylformamide (DMF), at 60° for 150 minutes results in an alternate copolymer, as evidenced from NMR spectroscopy. Yiscometric measurements have shown that complexation between template and oligomer of syn-PMMA is maximum at template/copolymer ratio of 1:1 and the time of complexation is about 9 min. The average molecular weight (M͞&lt;sub&gt;V&lt;/sub&gt;) of $ughter copolymer is not identical to that of template because of chain transfer reaction to template. The template effect and average molecular weight' (M͞&lt;sub&gt;V&lt;/sub&gt;) of daughter copolymer are direct functions of concentration as well as M͞&lt;sub&gt;V&lt;/sub&gt; of template. The energies of activation for template and blank polymerization are 46.0 and 64.0 kJ mol&lt;sup&gt;-1&lt;/sup&gt; respectively. The system follows Mechanism II, as evidenced from effect of an analogue and dioxane.
Page(s): 215-218</description>
      <pubDate>Fri, 01 Mar 1991 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/41849</guid>
      <dc:date>1991-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Studies on NO&lt;sub&gt;X&lt;/sub&gt; conversion over transition metal ion (TMI) dopeq alumina-boria system</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/41848</link>
      <description>Title: Studies on NO&lt;sub&gt;X&lt;/sub&gt; conversion over transition metal ion (TMI) dopeq alumina-boria system
Authors: Bose, J M; Banerjee, D; Guha, D
Abstract: Catalytic decomposition of NO&lt;sub&gt;X&lt;/sub&gt; has been studied using a fixed bed tubular flow reactor in the temperature range 573-773K, over six aluminium-borate catalysts (containing 2Al&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3.&lt;/sub&gt;B&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; as the major phase and 9Al&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3.&lt;/sub&gt;2B&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; as the minor phase) doped with different transition metals. The catalyst phases have been characterised by XRD, IR, ESR and ESCA studies on fresh and used catalyst samples. The results indicate structural stability of the catalyst phase over the experimental temperature range and oxidation of Co&lt;sup&gt;2+&lt;/sup&gt; to CO&lt;sup&gt;3+&lt;/sup&gt; accompanied by surface migration of CO&lt;sup&gt;3+ &lt;/sup&gt; species. No valence change in the other transition metal ions and surface oxygen enrichment in, the used catalyst .is observed. Kinetic studies show a first order dependence, on NO&lt;sub&gt;X&lt;/sub&gt; partial pressure in the lower temperature: region, except in the case of the mixed doped catalyst. Breaks in the Arrhenius plots at about 673K are noted for all the catalysts.
Page(s): 219-224</description>
      <pubDate>Fri, 01 Mar 1991 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/41848</guid>
      <dc:date>1991-03-01T00:00:00Z</dc:date>
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