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    <title>NISCAIR Online Periodicals Repository Collection: IJCT Vol.12(1) [January 2005]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/8563</link>
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      <title>PET waste based polyurethane adhesive for rubber joints</title>
      <link>http://nopr.niscair.res.in/handle/123456789/8599</link>
      <description>Title: PET waste based polyurethane adhesive for rubber joints
&lt;br/&gt;
&lt;br/&gt;Authors: Desai, S D; Patel, J V; Patel, M R; Sinha, V K
&lt;br/&gt;
&lt;br/&gt;Abstract: Biomaterial&#xD;
based polyhydric compounds were synthesized and utilized for the&#xD;
depolymerization of PET. Three different oligomers were synthesized by using 5,&#xD;
15 and 25% PET. Depolymerized oligomers were esterified with dehydrated castor&#xD;
oil (DCO) fatty acids to give polyester polyols. Polyurethane adhesives were&#xD;
synthesized using these polyols for joining rubber-rubber assembly. Bond&#xD;
strength was measured by 180° peel&#xD;
test. Mode of failure was studied by scanning electron microscopy (SEM)&#xD;
analysis. Depolymerised PET oligomers, polyols and polyurethane were&#xD;
characterized by FTIR spectroscopy. Also, polyurethane adhesives were evaluated&#xD;
for their performance and chemical resistance.
&lt;br/&gt;
&lt;br/&gt;Page(s): 82-87</description>
      <pubDate>Wed, 29 Dec 2004 22:58:59 GMT</pubDate>
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      <title>Photocatalytic degradation of 3,4-dichlorophenol using TiO&lt;sub&gt;2&lt;/sub&gt; in a shallow pond slurry reactor</title>
      <link>http://nopr.niscair.res.in/handle/123456789/8598</link>
      <description>Title: Photocatalytic degradation of 3,4-dichlorophenol using TiO&lt;sub&gt;2&lt;/sub&gt; in a shallow pond slurry reactor
&lt;br/&gt;
&lt;br/&gt;Authors: Toor, Amrit Pal; Verma, Anoop; Jotshi, Chand K; Bajpai, Pramod K; Singh, Vasundhara
&lt;br/&gt;
&lt;br/&gt;Abstract: In&#xD;
the present study, the TiO&lt;sub&gt;2 &lt;/sub&gt;mediated photocatalytic degradation of&#xD;
3,4-dichlorophenol, as a model compound, has been investigated using a low cost&#xD;
non-concentrating shallow pond slurry reactor at laboratory scale under a&#xD;
variety of conditions. The degradation was studied by monitoring the change in&#xD;
substrate concentration employing UV-spectroscopic analysis, decrease in COD&#xD;
values and increase in chloride formation as a function of irradiation time.&#xD;
The effect of&lt;i style=""&gt; &lt;/i&gt;pH, catalyst loading,&#xD;
substrate concentration, UV intensity, aperture to volume ratio of the reactor&#xD;
and presence of electron acceptors such as hydrogen peroxide besides molecular&#xD;
oxygen, on degradation, was studied. The degradation rates were strongly&#xD;
influenced by some of these parameters. The optimum parameters for maximum&#xD;
degradation were determined. The degradation of 3,4-dichlorophenol can be&#xD;
emulated in sunlight using a similar large-scale shallow pond reactor for the&#xD;
solar detoxification in open atmosphere.
&lt;br/&gt;
&lt;br/&gt;Page(s): 75-81</description>
      <pubDate>Wed, 29 Dec 2004 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Free radical copolymerization of limonene with butyl methacrylate: Synthesis and characterization</title>
      <link>http://nopr.niscair.res.in/handle/123456789/8597</link>
      <description>Title: Free radical copolymerization of limonene with butyl methacrylate: Synthesis and characterization
&lt;br/&gt;
&lt;br/&gt;Authors: Sharma, Saroj; Srivastava, A K
&lt;br/&gt;
&lt;br/&gt;Abstract: The radical copolymerization of&#xD;
monocyclic terpene namely limonene with butyl methacrylate  in xylene at 80±0.1°C for 50 min, using benzoylperoxide (BPO) as an initiator has been carried out under the inert&#xD;
atmosphere of nitrogen. The system follows ideal kinetics &lt;i style=""&gt;i.e&lt;/i&gt;. &lt;i style=""&gt;R&lt;/i&gt;&lt;sub&gt;p&lt;/sub&gt; &lt;img src='/image/spc_char/alpha.gif' border=0&gt; [BPO]&lt;sup&gt;0.5&lt;/sup&gt;[BMA]&lt;sup&gt;1.0&lt;/sup&gt;[Lim.]&lt;sup&gt;–1.0&lt;/sup&gt;.&#xD;
The rate of polymerization (&lt;i style=""&gt;R&lt;/i&gt;&lt;sub&gt;p&lt;/sub&gt;)&#xD;
decreases as [limonene] increases, which might be due to penultimate unit&#xD;
effect. The overall energy of activation has been calculated as 34 kJ/mol. The&#xD;
formation of the copolymer is confirmed by the presence of bands at 1727 and&#xD;
2956 cm&lt;sup&gt;–1&lt;/sup&gt; due to ester carbonyl of butyl methacrylate and olefinic&#xD;
C–H stretching of limonene, respectively. Further, the peaks at 3.8–4.2 and&#xD;
5.0–5.6 &lt;img src='/image/spc_char/delta1.gif' border=0&gt;, were observed in &lt;sup&gt;1&lt;/sup&gt;H&#xD;
NMR spectra due to methylene proton adjacent to ester linkage of butyl&#xD;
methacrylate and  trisubstituted olefinic&#xD;
protons of limonene, respectively. The value of reactivity ratios &lt;i style=""&gt;r&lt;/i&gt;&lt;sub&gt;1&lt;/sub&gt;(BMA) = 0.125 and &lt;i style=""&gt;r&lt;/i&gt;&lt;sub&gt;2&lt;/sub&gt;(Lim.)= 0.026 has been&#xD;
calculated by using Kelen-Tüdos method. Alfrey-Price Q–e parameter for limonene&#xD;
has been calculated as 0.30 and –0.46. The glass transition temperature of the&#xD;
copolymer is determined as 35 &lt;sup&gt;o&lt;/sup&gt;C.
&lt;br/&gt;
&lt;br/&gt;Page(s): 62-67</description>
      <pubDate>Wed, 29 Dec 2004 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Phosphorus-From discovery to commodity</title>
      <link>http://nopr.niscair.res.in/handle/123456789/8596</link>
      <description>Title: Phosphorus-From discovery to commodity
&lt;br/&gt;
&lt;br/&gt;Authors: Wisniak, Jaime
&lt;br/&gt;
&lt;br/&gt;Abstract: Phosphorus is nearly the most widely and evenly distributed&#xD;
element on the surface of the earth, and probably the most subdivided. From a&#xD;
laboratory curiosity in the seventeeth century, it became recognized as a&#xD;
fundamental element of life and a large chemical commodity, improving&#xD;
agriculture and industry like very few other discoveries by men have done.
&lt;br/&gt;
&lt;br/&gt;Page(s): 108-122</description>
      <pubDate>Wed, 29 Dec 2004 22:58:59 GMT</pubDate>
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