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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10063" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/10063</id>
  <updated>2026-10-09T23:28:03Z</updated>
  <dc:date>2026-10-09T23:28:03Z</dc:date>
  <entry>
    <title>Synthesis, characterization and thermal decomposition of  di-(2,4,6-trimethylanilinium) sulphate</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10073" />
    <author>
      <name>Kapoor, Inder Pal Singh</name>
    </author>
    <author>
      <name>Kapoor, Manisha</name>
    </author>
    <author>
      <name>Singh, Gurdip</name>
    </author>
    <author>
      <name>Fröhlich, Roland</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10073</id>
    <updated>2010-08-21T16:30:52Z</updated>
    <published>2010-08-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis, characterization and thermal decomposition of  di-(2,4,6-trimethylanilinium) sulphate
Authors: Kapoor, Inder Pal Singh; Kapoor, Manisha; Singh, Gurdip; Fröhlich, Roland
Abstract: Di-(2,4,6-trimethylanilinium)&#xD;
sulphate [2,4,6-TMAS] was synthesized by reaction of 2,4,6-trimethylaniline&#xD;
with concentrated sulphuric acid at room temperature. The crystal structure of&#xD;
this salt was determined using single crystal X-ray diffraction. It&#xD;
crystallizes in orthorhombic space group Pna2&lt;sub&gt;1&lt;/sub&gt;, &lt;i style=""&gt;a&lt;/i&gt;= 7.7115(1) Å, &lt;i style=""&gt;b&lt;/i&gt;= 30.3746 (6)&#xD;
Å, &lt;i style=""&gt;c&lt;/i&gt;=16.9251 (3)Å , &lt;img src='/image/spc_char/alpha.gif' border=0&gt;=&lt;img src='/image/spc_char/beta.gif' border=0&gt;=&lt;img src='/image/spc_char/gamma.gif' border=0&gt;[°]=90°, &lt;i style=""&gt;V&lt;/i&gt;=3964.43 (12)A and &lt;i style=""&gt;Z&lt;/i&gt;=8.&#xD;
The structure contains 2,4,6-trimethylanilinium ions that share vertices&#xD;
through intermolecular H- bonds with sulphate ions and a water molecule.&#xD;
Notably thermal and microwave heatings of di-(2,4,6-TMA)S have afforded&#xD;
3-amino-2,4,6-trimethylbenzenesulphonic acid (3-A-2,4,6-TMBSA) with release of&#xD;
a molecule of amine and water. It has been suggested that the proton transfer&#xD;
from anilinium to SO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2- &lt;/sup&gt;ion is a primary and rate&#xD;
controlling step. Further di-(2,4,6-TMA)S and 3-A-2,4,6-TMBSA were&#xD;
characterized by infrared, mass spectrometry, elemental and thermogravimetric-&#xD;
differential scanning calorimetric (TG-DSC) analyses. The mean value for the&#xD;
energy of activation (83.0 kJ mol&lt;sup&gt;-1&lt;/sup&gt;) for the conversion of&#xD;
di-(2,4,6-TMA)S to 3-A-2,4,6-TMBSA has been determined from isothermal&#xD;
thermogravimetry data.
Page(s): 305-310</summary>
    <dc:date>2010-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Characterization, dielectric and optical studies of nano-cerium phospho iodate synthesized by chemical co-precipitation method</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10072" />
    <author>
      <name>Indulal, C R</name>
    </author>
    <author>
      <name>Vaidyan, A V</name>
    </author>
    <author>
      <name>Kumar, G Sajeev</name>
    </author>
    <author>
      <name>Raveendran, R</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10072</id>
    <updated>2010-08-24T16:30:13Z</updated>
    <published>2010-08-01T00:00:00Z</published>
    <summary type="text">Title: Characterization, dielectric and optical studies of nano-cerium phospho iodate synthesized by chemical co-precipitation method
Authors: Indulal, C R; Vaidyan, A V; Kumar, G Sajeev; Raveendran, R
Abstract: Nanoparticles of cerium phospho iodate belong to the class of tetravalent&#xD;
metal acid (TMA) salt are synthesized by chemical co-precipitation method. The&#xD;
particle size obtained from X-ray diffraction spectrum is found to be in the&#xD;
range of 30 nm. Surface morphology is studied from SEM images. The chemical&#xD;
composition of the sample has been verified using EDAX. The optical studies are&#xD;
carried out using FTIR and UV techniques. The stretching and bending&#xD;
frequencies of the sample are studied using the FTIR spectrum. The optical&#xD;
direct band gap of the material calculated using the Tauc’s relation is found&#xD;
to be 3.4 eV. The dielectric behaviour of the samples is studied at various&#xD;
temperatures and frequencies and ac electrical conductivity is also calculated.&#xD;
It is found that dielectric constant decreases with increase in frequency.
Page(s): 299-304</summary>
    <dc:date>2010-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Preparation and studies of chemically deposited Cu&lt;sub&gt;4&lt;/sub&gt;SnS&lt;sub&gt;4 &lt;/sub&gt;thin films in the presence of complexing agent Na&lt;sub&gt;2&lt;/sub&gt;EDTA</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10071" />
    <author>
      <name>Kassim, Anuar</name>
    </author>
    <author>
      <name>Kuang, Zulkefly</name>
    </author>
    <author>
      <name>Sharif, Atan</name>
    </author>
    <author>
      <name>Tee, Tan Wee</name>
    </author>
    <author>
      <name>Min, Ho Soon</name>
    </author>
    <author>
      <name>Nagalingam, Saravanan</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10071</id>
    <updated>2010-08-17T16:30:38Z</updated>
    <published>2010-08-01T00:00:00Z</published>
    <summary type="text">Title: Preparation and studies of chemically deposited Cu&lt;sub&gt;4&lt;/sub&gt;SnS&lt;sub&gt;4 &lt;/sub&gt;thin films in the presence of complexing agent Na&lt;sub&gt;2&lt;/sub&gt;EDTA
Authors: Kassim, Anuar; Kuang, Zulkefly; Sharif, Atan; Tee, Tan Wee; Min, Ho Soon; Nagalingam, Saravanan
Abstract: The Cu&lt;sub&gt;4&lt;/sub&gt;SnS&lt;sub&gt;4&lt;/sub&gt; thin films are&#xD;
deposited onto indium tin oxide glass substrate by chemical bath deposition&#xD;
method. The disodium ethylenediaminetetraacetic acid is used as a complexing&#xD;
agent during deposition process. The structural, morphological and optical&#xD;
properties of the deposited films have been studied using X-ray diffraction,&#xD;
atomic force microscopy and UV-Vis spectrophotometer, respectively. The&#xD;
presence of Na&lt;sub&gt;2&lt;/sub&gt;EDTA promotes the deposition of better quality films.&#xD;
The XRD analysis shows that these films have a high crystallinity with&#xD;
orthorhombic structure. The AFM images indicated that these films are uniform,&#xD;
compact with larger grains. The absorption spectra confirmed that the thicker&#xD;
film has higher absorption properties. The band gap of 1.6 eV with direct transition&#xD;
is observed.
Page(s): 295-298</summary>
    <dc:date>2010-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Microstructure of 2 and 28-day cured Portland limestone cement pastes</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10070" />
    <author>
      <name>Sezer, Gözde İnan</name>
    </author>
    <author>
      <name>Çopuroğlu, Oğuzhan</name>
    </author>
    <author>
      <name>Ramyar, Kambiz</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10070</id>
    <updated>2010-08-19T16:30:13Z</updated>
    <published>2010-08-01T00:00:00Z</published>
    <summary type="text">Title: Microstructure of 2 and 28-day cured Portland limestone cement pastes
Authors: Sezer, Gözde İnan; Çopuroğlu, Oğuzhan; Ramyar, Kambiz
Abstract: In&#xD;
this study, microstructures of limestone cement pastes cured for 2 and 28 days&#xD;
are investigated. For this purpose, limestone and clinker are separately ground in a&#xD;
ball-mill until obtained a given constant 32 µm sieve residue. The gypsum is&#xD;
kept constant as 5% by weight of cement. Cement pastes with 0.5 water/binder&#xD;
ratios and 0, 6, 35% limestone/clinker ratios are prepared. After 2 and 28 days&#xD;
standard curing, ESEM&#xD;
investigations are carried out on these specimens. It is found that hydration products are accumulated around limestone&#xD;
particles. In 2 days, compared to the control specimen, pore percentages of cements&#xD;
containing 6% limestone are decreased whereas pore percentages of cement pastes&#xD;
containing &#xD;
35% limestone are increased. The difference between porosities of the control&#xD;
paste and limestone cement paste is decreased at 28 days.
Page(s): 289-294</summary>
    <dc:date>2010-08-01T00:00:00Z</dc:date>
  </entry>
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