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    <title>NISCAIR Online Periodicals Repository Community: IJC-A Vol.51A [2012]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/13334</link>
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      <url>http://nopr.niscair.res.in/retrieve/59046</url>
      <link>http://nopr.niscair.res.in/handle/123456789/13334</link>
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      <title>Alkaline hydrolysis of isatin in the  presence of mixed CTAB and Triton X-100 micellar systems: Micellisation and  kinetic investigations</title>
      <link>http://nopr.niscair.res.in/handle/123456789/15207</link>
      <description>Title: Alkaline hydrolysis of isatin in the  presence of mixed CTAB and Triton X-100 micellar systems: Micellisation and  kinetic investigations
&lt;br/&gt;
&lt;br/&gt;Authors: Srikanth, V; Shyamala, P; Satyanarayana, A; Rao, P V Subba
&lt;br/&gt;
&lt;br/&gt;Abstract: Micellisation behaviour of mixed surfactants&#xD;
of CTAB and Triton X-100 in the presence of isatin has been studied by surface&#xD;
tension measurements over a wide range of Triton X-100 mole fractions and total&#xD;
surfactant concentrations. The average &#xD;
interaction parameter has been evaluated using Rubingh theory and found to be&#xD;
-0.396 indicating synergistic behaviour in the mixed micelles. Kinetic studies&#xD;
showed that the pseudo first &#xD;
order rate constant increases with increase in mole fraction &#xD;
of Triton X-100 at constant total surfactant concentration &#xD;
and decreases with increase in total surfactant concentration at &#xD;
constant mole fraction of Triton X-100. Kinetic analysis has been carried out&#xD;
using a Berezin pseudophase model and binding &#xD;
constants determined to explain the micellar effect.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1701-1705</description>
      <pubDate>Wed, 28 Nov 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Effect on thermal behaviour of polyamide 66/clay nanocomposites with inorganic flame retardant additives</title>
      <link>http://nopr.niscair.res.in/handle/123456789/15206</link>
      <description>Title: Effect on thermal behaviour of polyamide 66/clay nanocomposites with inorganic flame retardant additives
&lt;br/&gt;
&lt;br/&gt;Authors: Rathi, Sudesh; Dahiya, J B
&lt;br/&gt;
&lt;br/&gt;Abstract: Polyamide 66&#xD;
(PA66)/clay nanocomposites have been prepared with inorganic additives by melt&#xD;
blending method using an extruder. Inorganic additives such as potassium&#xD;
nitrate, zinc borate and magnesium hydroxide along with organic phosphinate&#xD;
have been used to study their effect on thermal behaviour of PA66/clay&#xD;
nanocomposites. The nanocomposites have been characterized by XRD which&#xD;
confirms the formation of intercalated and/or exfoliated nanocomposites. The&#xD;
thermal degradation behaviour of nanocomposites has been studied by TG, DTA,&#xD;
DSC and FTIR. PA66/30B nanocomposite is thermally stable in the higher&#xD;
temperature range beyond 450 °C with increase in char yield due to formation of&#xD;
nanocomposite and hindered diffusion of volatile products. DSC curve of&#xD;
PA66/30B shows an endothermic peak at 452 °C with higher heat of absorption&#xD;
(378 J/g) during the decomposition stage due to intercalation of PA66 between&#xD;
the 30B interlayers. The presence of a band in the FTIR spectrum in the range&#xD;
2224−2245 cm&lt;sup&gt;&lt;span style="font-family:Symbol;mso-ascii-font-family:&#xD;
" times="" new="" roman";mso-hansi-font-family:"times="" roman";mso-char-type:symbol;="" mso-symbol-font-family:symbol"="" lang="EN-GB"&gt;-1&lt;/span&gt;&lt;/sup&gt; in all&#xD;
PA66 nanocomposites char residue samples at 400 °C indicates the presence of&#xD;
nitrile group in the degradation products of PA66. The addition of zinc borate&#xD;
along with organic phosphinate induces a change in path of decomposition of&#xD;
polymer, leading to higher char formation which may protect the polymer from&#xD;
burning.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1677-1685</description>
      <pubDate>Wed, 28 Nov 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Accelerated polymorphous transformations of alumina induced by  copper ions impede spinel formation</title>
      <link>http://nopr.niscair.res.in/handle/123456789/15205</link>
      <description>Title: Accelerated polymorphous transformations of alumina induced by  copper ions impede spinel formation
&lt;br/&gt;
&lt;br/&gt;Authors: Kiss, E; Ratković, S; Vujičić, Dj; Boskovic, G
&lt;br/&gt;
&lt;br/&gt;Abstract: Slower copper spinel formation on alumina&#xD;
type supports relative to zinc and magnesium spinel formation has been&#xD;
investigated. Spinel formation occurs at high temperatures and is usually&#xD;
accompanied by polymorphous transformations of alumina support and sintering.&#xD;
In samples containing zinc and magnesium ions, decelerated polymorphous&#xD;
transformations of alumina occur relative to the transformation of pure aluminum&#xD;
sample. The impeded phase transformation of alumina coincides&#xD;
with decreased degree of sintering. In contrast, copper ions accelerate&#xD;
polymorphous transformations of alumina, and consequently the corresponding&#xD;
copper-alumina&lt;sub&gt;&lt;span style="mso-bidi-font-weight:bold"&gt; &lt;/span&gt;&lt;/sub&gt;spinel&#xD;
formation is slower. Accelerated sintering may be explained by accelerated&#xD;
phase transformation of alumina, which itself is caused by copper ions slowing&#xD;
down spinel formation.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1669-1676</description>
      <pubDate>Wed, 28 Nov 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>&lt;span style="font-size:11.0pt;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";mso-bidi-font-family:Mangal; mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language:HI" lang="EN-GB"&gt;Catalytic activity of liquid phase prepared Cu-Zn-Al catalyst for CO hydrogenation in a fixed be&lt;span style="font-size:11.0pt;mso-bidi-font-size:14.0pt;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";mso-bidi-font-family:Mangal; mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language:HI" lang="EN-GB"&gt;d reactor&lt;/span&gt;&lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/15204</link>
      <description>Title: &lt;span style="font-size:11.0pt;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";mso-bidi-font-family:Mangal; mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language:HI" lang="EN-GB"&gt;Catalytic activity of liquid phase prepared Cu-Zn-Al catalyst for CO hydrogenation in a fixed be&lt;span style="font-size:11.0pt;mso-bidi-font-size:14.0pt;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";mso-bidi-font-family:Mangal; mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language:HI" lang="EN-GB"&gt;d reactor&lt;/span&gt;&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Luan, Chunhui; Zhang, Anrong; Wang, Xiaodong; Huang, Wei; Yin, Lihua
&lt;br/&gt;
&lt;br/&gt;Abstract: Cu-Zn-Al catalyst prepared by a complete&#xD;
liquid phase technology for CO hydrogenation has been investigated in a fixed&#xD;
bed reactor in terms of catalytic performance and&#xD;
compared with catalysts prepared by a traditional method such as &#xD;
co-precipitation. The catalysts are characterized by XRD, NH&lt;sub&gt;3&lt;/sub&gt;-TPD, H&lt;sub&gt;2&lt;/sub&gt;-TPR&#xD;
and XPS. Results show that the activity of the liquid phase prepared&#xD;
catalyst is much lower in fixed bed reactor than in a slurry reactor. It was&#xD;
also much lower than that of the catalyst prepared by co-precipitation,&#xD;
although its stability is higher. XPS and XRD characterization&#xD;
reveal that there are obvious differences in the structure, morphology and&#xD;
surface state of the catalysts prepared by the two methods. In the catalyst&#xD;
prepared by liquid phase technology, Cu exists in the form of metallic Cu even&#xD;
though the catalyst is unreduced and there are more acid&#xD;
sites and more carbon on its surface than on the surface of the&#xD;
co-precipitation catalyst. It is concluded that there is a surface carbon film&#xD;
covering the liquid phase catalyst, and the carbon film is an important reason for&#xD;
the low activity when the catalyst is applied to fixed bed reactor. Coke&#xD;
burning off, an effective way for removing the surface carbon, improves the&#xD;
catalyst activity in a fixed reactor.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1663-1668</description>
      <pubDate>Sat, 08 Dec 2012 16:04:59 GMT</pubDate>
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