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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33641</link>
    <description />
    <items>
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        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/33697" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/33696" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/33695" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/33694" />
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    <dc:date>2026-10-11T06:42:24Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/33697">
    <title>Influence of organic solvents, head-groups and temperature on the  micellization behavior of some cationic surfactants</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33697</link>
    <description>Title: Influence of organic solvents, head-groups and temperature on the  micellization behavior of some cationic surfactants
Authors: Sood, A K; Kaur, Rupinderjit; Banipal, T S
Abstract: The effect of organic solvents, viz.,&#xD;
dioxane, dimethylformamide and ethylene glycol on the micellization behavior of&#xD;
cationic surfactants, i.e., tetradecyltrimethyl ammonium bromide (TTAB),&#xD;
tetradecyldimethylbenzyl ammonium chloride (C14BCl) and their dimeric&#xD;
homologue, dimethylene-1,2-bis(tetradecyldimethyl ammonium bromide) (14-2-14)&#xD;
is studied in aqueous solutions using conductometric and viscometric techniques&#xD;
at different temperatures (288.15–318.15 K). &#xD;
It is observed that the critical micelle concentration and degree of counterion&#xD;
dissociation values increase with the increase in volume percentage and the&#xD;
temperature. Studies on the the temperature dependence of the CMC values show&#xD;
that the standard Gibbs free energy of micellization values increase with the&#xD;
concentration of organic solvents and temperature whereas the opposite trend is&#xD;
observed for&lt;sub&gt; &lt;/sub&gt;enthalpy. The randomness of the system decreases in&#xD;
presence of solvents. &#xD;
The relative viscosity of the surfactants was found to be more in presence of&#xD;
ethylene glycol among the studied systems. &#xD;
The effect of temperature on relative viscosity for these systems has also been&#xD;
discussed.
Page(s): 34-43</description>
    <dc:date>2016-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/33696">
    <title>&lt;span style="font-size:15.0pt;mso-bidi-font-size: 13.0pt;font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-bidi-font-family:"Times New Roman";mso-ansi-language:EN-US;mso-fareast-language: EN-US;mso-bidi-language:AR-SA;mso-bidi-font-weight:bold" lang="EN-US"&gt;Internal pressure, free volume and excess thermodynamic properties of methyl acrylate+1-alkanols (C&lt;sub&gt;4&lt;/sub&gt;&lt;span style="font-size:15.0pt;mso-bidi-font-size: 13.0pt;font-family:Symbol;mso-ascii-font-family:"Times New Roman";mso-fareast-font-family: "Times New Roman";mso-hansi-font-family:"Times New Roman";mso-bidi-font-family: "Times New Roman";mso-ansi-language:EN-US;mso-fareast-language:EN-US; mso-bidi-language:AR-SA;mso-char-type:symbol;mso-symbol-font-family:Symbol; mso-bidi-font-weight:bold" lang="EN-US"&gt;-&lt;span style="font-size:15.0pt;mso-bidi-font-size: 13.0pt;font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-bidi-font-family:"Times New Roman";mso-ansi-language:EN-US;mso-fareast-language: EN-US;mso-bidi-language:AR-SA;mso-bidi-font-weight:bold" lang="EN-US"&gt;C&lt;sub&gt;10&lt;/sub&gt;) binary mixtures from ultrasonic speed and density&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33696</link>
    <description>Title: &lt;span style="font-size:15.0pt;mso-bidi-font-size: 13.0pt;font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-bidi-font-family:"Times New Roman";mso-ansi-language:EN-US;mso-fareast-language: EN-US;mso-bidi-language:AR-SA;mso-bidi-font-weight:bold" lang="EN-US"&gt;Internal pressure, free volume and excess thermodynamic properties of methyl acrylate+1-alkanols (C&lt;sub&gt;4&lt;/sub&gt;&lt;span style="font-size:15.0pt;mso-bidi-font-size: 13.0pt;font-family:Symbol;mso-ascii-font-family:"Times New Roman";mso-fareast-font-family: "Times New Roman";mso-hansi-font-family:"Times New Roman";mso-bidi-font-family: "Times New Roman";mso-ansi-language:EN-US;mso-fareast-language:EN-US; mso-bidi-language:AR-SA;mso-char-type:symbol;mso-symbol-font-family:Symbol; mso-bidi-font-weight:bold" lang="EN-US"&gt;-&lt;span style="font-size:15.0pt;mso-bidi-font-size: 13.0pt;font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-bidi-font-family:"Times New Roman";mso-ansi-language:EN-US;mso-fareast-language: EN-US;mso-bidi-language:AR-SA;mso-bidi-font-weight:bold" lang="EN-US"&gt;C&lt;sub&gt;10&lt;/sub&gt;) binary mixtures from ultrasonic speed and density&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Authors: Nain, A K; Droliya, P
Abstract: The experimental values of ultrasonic speeds&#xD;
and densities, of binary mixtures of methyl acrylate with 1-butanol, &#xD;
1-hexanol, 1-octanol and 1-decanol have been used to calculate the internal&#xD;
pressures, free volumes, excess internal pressures, excess free volumes, excess&#xD;
free energy, excess enthalpy and excess entropy of mixing over the entire&#xD;
composition range at 298.15 K using regular solution theory. The results have&#xD;
been interpreted in terms of intermolecular interactions between the component&#xD;
molecules in the mixture. The variations of these excess properties with&#xD;
composition indicate that the methyl acrylate-alkanol interaction in these mixtures&#xD;
follows the order: 1-butanol &gt; 1-hexanol &gt; 1-octanol &gt; 1-decanol. It&#xD;
is observed that the order of interactions in these mixtures depends upon the&#xD;
length of alkyl chain in the studied 1-alkanol molecules. In addition, the&#xD;
values of ultrasonic speeds have also been calculated theoretically for these&#xD;
mixtures using scaled particle theory and found to be in good agreement with&#xD;
experimental findings.
Page(s): 23-33</description>
    <dc:date>2016-01-14T11:34:37Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/33695">
    <title>Photocatalytic degradation of ciprofloxacin·HCl using Aeroxide&lt;sup&gt;®&lt;/sup&gt; P-25 TiO&lt;sub&gt;2&lt;/sub&gt; photocatalyst: Comparative evaluation of solar and artificial radiation</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33695</link>
    <description>Title: Photocatalytic degradation of ciprofloxacin·HCl using Aeroxide&lt;sup&gt;®&lt;/sup&gt; P-25 TiO&lt;sub&gt;2&lt;/sub&gt; photocatalyst: Comparative evaluation of solar and artificial radiation
Authors: Shetty, Rohit; Kothari, Gaurav; Tambe, Amruta S; Kulkarni, Bhaskar D; Kamble, Sanjay P
Abstract: The&#xD;
photocatalytic degradation of ciprofloxacin (CFX) has been investigated using Aeroxide&lt;sup&gt;®&lt;/sup&gt;&#xD;
P-25 TiO&lt;sub&gt;2&lt;/sub&gt; photocatalyst in the presence of solar as well as&#xD;
artificial radiation. The effects of different operating parameters like&#xD;
initial concentration of CFX, catalyst loading, &lt;i&gt;p&lt;/i&gt;H of solution and&#xD;
effect of co-existing ions on photocatalytic degradation of CFX have been&#xD;
investigated with a view to establish the optimum operating conditions. It is&#xD;
observed that as the initial concentration of CFX increases, the rate of&#xD;
photocatalytic degradation decreases. Optimum catalyst loading is observed at 1&#xD;
g L&lt;sup&gt;-1&lt;/sup&gt; for CFX concentration of 100 mg L&lt;sup&gt;-1&lt;/sup&gt;. Over the &lt;i&gt;p&lt;/i&gt;H&#xD;
range 3-11, maximum degradation rate occurs at &lt;i&gt;p&lt;/i&gt;H 9. The mechanism and&#xD;
intermediates formed during the photocatalytic degradation of CFX are discussed&#xD;
based on UPLC-MS/MS analysis. From kinetic studies, it is found that the&#xD;
photocatalytic degradation obeys pseudo-first order kinetics. The degradation&#xD;
rate constant using solar radiation is about 1.7 times higher than that under&#xD;
artificial radiation.
Page(s): 16-22</description>
    <dc:date>2016-01-14T11:31:14Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/33694">
    <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;Photocatalytic degradation of methylene blue and methyl violet using cation doped (Sn&lt;sup&gt;2+&lt;/sup&gt; and Ag&lt;sup&gt;+&lt;/sup&gt;) barium tellurite phosphate, Ba&lt;sub&gt;2&lt;/sub&gt;TeO(PO&lt;sub&gt;4&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/33694</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;Photocatalytic degradation of methylene blue and methyl violet using cation doped (Sn&lt;sup&gt;2+&lt;/sup&gt; and Ag&lt;sup&gt;+&lt;/sup&gt;) barium tellurite phosphate, Ba&lt;sub&gt;2&lt;/sub&gt;TeO(PO&lt;sub&gt;4&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;&lt;/span&gt;
Authors: Reddy, CH Sudhakar; Sreenu, K; Reddy, J R; Ravi, G; Guje, Ravinder; Malathi, M; Vithal, M
Abstract: One-dimensional barium tellurite phosphate&#xD;
of composition, Ba&lt;sub&gt;2&lt;/sub&gt;TeO(PO&lt;sub&gt;4&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;, is prepared by&#xD;
solid state method. Tin (Sn&lt;sup&gt;2+&lt;/sup&gt;) and silver (Ag&lt;sup&gt;+&lt;/sup&gt;) doped Ba&lt;sub&gt;2&lt;/sub&gt;TeO(PO&lt;sub&gt;4&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;&#xD;
materials are prepared via a facile room temperature ion-exchange method.&#xD;
Structural, morphological, and optical properties of all the materials are&#xD;
characterized by powder X-ray diffraction, FT-IR, SEM-EDS, and UV-visible&#xD;
diffuse reflectance spectroscopy techniques. The band gap energy (E&lt;sub&gt;g&lt;/sub&gt;)&#xD;
of all the phosphates is deduced from their Kubelka–Munk (KM) plot. The&#xD;
synthesized phosphates are used as photocatalyst for the degradation of&#xD;
methylene blue and methyl violet dyes under the visible light irradiation. The&#xD;
systematic degradation pathways of the dyes are studied in the presence of all&#xD;
the photocatalysts and scavengers. The stability and reusability of all the&#xD;
photocatalyst are assessed by the cycling runs in the photodegradation&#xD;
experiment.
Page(s): 9-15</description>
    <dc:date>2016-01-01T00:00:00Z</dc:date>
  </item>
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