<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15962" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/15962</id>
  <updated>2026-10-10T21:41:50Z</updated>
  <dc:date>2026-10-10T21:41:50Z</dc:date>
  <entry>
    <title>Role of triethanolamine and furfuraldehyde on the electrochemical deposition and  dissolution- behaviour of zinc</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16790" />
    <author>
      <name>Rethinam, A John</name>
    </author>
    <author>
      <name>Bapu, G N K Ramesh</name>
    </author>
    <author>
      <name>Muralidharan, V S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16790</id>
    <updated>2016-07-20T04:28:03Z</updated>
    <published>2004-03-01T00:00:00Z</published>
    <summary type="text">Title: Role of triethanolamine and furfuraldehyde on the electrochemical deposition and  dissolution- behaviour of zinc
Authors: Rethinam, A John; Bapu, G N K Ramesh; Muralidharan, V S
Abstract: The search&#xD;
for the development of non-cyanide zinc plating baths resulted in identification of newer&#xD;
complexing ligands. The deposition and&#xD;
dissolution of zinc was studied by cyclic voltammetric studies using a&#xD;
bath composition consisted of 0.12M Zinc oxide, 2.75M sodium hydroxide and&#xD;
required quantity of triethanolamine&#xD;
and furfuraldehyde. Glassy&#xD;
carbon (GC), Platinum and SCE were used as working electrode, counter&#xD;
electrode and reference&#xD;
electrode respectively. The studies were made at different concentrations of the&#xD;
above additives at various&#xD;
scan rates at 30°C,&#xD;
&#xD;
The pH&#xD;
of the bath was maintained at 11.5 to 12.0. The deposition of zinc from zincate&#xD;
solutions undergoes successive reduction to zinc. The chemical step followed by&#xD;
first electron transfer is the slow step. Triethanolamine and furfuraldehyde&#xD;
were found to participate in the electron transfer process. Detailed mechanism&#xD;
of deposition and dissolution in presence of triethanolamine and furfuraldehyde&#xD;
are discussed.
Page(s): 207-212</summary>
    <dc:date>2004-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Study on the fluoride removal characteristics of mineral (fluorapatite)</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16786" />
    <author>
      <name>Singh, I B</name>
    </author>
    <author>
      <name>Prasad, M</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16786</id>
    <updated>2016-07-20T04:18:59Z</updated>
    <published>2004-03-01T00:00:00Z</published>
    <summary type="text">Title: Study on the fluoride removal characteristics of mineral (fluorapatite)
Authors: Singh, I B; Prasad, M
Abstract: The effectiveness&#xD;
of low grade fluorapatite bearing mineral on fluoride removal has not been examined&#xD;
earlier. For identification of such mineral, a preliminary assessment of&#xD;
performance of mineral is essential in order to know which aspect is necessary&#xD;
to carry out further research for development of mineral based defluoridation&#xD;
technology. In this study batch adsorption study was performed to evaluate the fluoride&#xD;
removal potential of low cost rock phosphate (fluroapatite) mineral at pH 4, 5&#xD;
and 6. The optimum dose was determined to be 1.5, 2.5 and 3.5 g mineral at pH&#xD;
4, 5 and 6, respectively. The first order adsorption rate constants derived by&#xD;
Lagergren equation at different pH, clearly indicates the fast removal kinetics&#xD;
at pH 4. The comparatively high solubility of mineral and an increase of&#xD;
calcium concentration at pH 4 appears to be the main reason for fast removal&#xD;
reaction. There was no effect of mineral quantity on fluoride removal after&#xD;
solution pH became alkaline. The various aspects of the study including recyclability&#xD;
of mineral are discussed.
Page(s): 185-189</summary>
    <dc:date>2004-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Role of matrix material in the characterization of  high-purity copper by flame and graphite furnace AAS</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16785" />
    <author>
      <name>Kumar, Sanjukta A</name>
    </author>
    <author>
      <name>Sanglikar, Manisha B</name>
    </author>
    <author>
      <name>Shaikh, Mahzebin S</name>
    </author>
    <author>
      <name>Sudersanan, M</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16785</id>
    <updated>2016-07-20T04:19:36Z</updated>
    <published>2004-03-01T00:00:00Z</published>
    <summary type="text">Title: Role of matrix material in the characterization of  high-purity copper by flame and graphite furnace AAS
Authors: Kumar, Sanjukta A; Sanglikar, Manisha B; Shaikh, Mahzebin S; Sudersanan, M
Abstract: Matrix&#xD;
effect in the determination of trace metallics in high-purity copper has been&#xD;
evaluated for estimation of Ag, Cr, Fe, Ni, Pb, Sb, and Zn by FAAS and GFAAS.&#xD;
Matrix effects were less significant for FAAS while it was quite important for&#xD;
GFAAS. Methods have been standardized for determination of various trace elements&#xD;
after separation of matrix element and pre-concentration of the analytes. For&#xD;
separation of matrix two different procedures were standardized: (i) co-precipitation&#xD;
of metal hydroxides using La as carrier and (ii) electro deposition. To&#xD;
validate&#xD;
&#xD;
the method,&#xD;
the recovery of metal ions were tested and were found to be satisfactory. The&#xD;
methods have been applied to the determination of these impurities in&#xD;
high-purity copper samples. For the determination of silver, a selective deposition&#xD;
method was adopted in order to avoid co-deposition of copper. These three different&#xD;
modes of matrix separation were found to be complementary to each other for&#xD;
determination of various critical trace elements in high purity electrolytic&#xD;
copper.
Page(s): 170-177</summary>
    <dc:date>2004-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and characterization of  SAPO-35 from non-aqueous systems with different silicon content</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16784" />
    <author>
      <name>Venkatathri, N</name>
    </author>
    <author>
      <name>Sivasanker, S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16784</id>
    <updated>2016-07-20T05:04:10Z</updated>
    <published>2004-03-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and characterization of  SAPO-35 from non-aqueous systems with different silicon content
Authors: Venkatathri, N; Sivasanker, S
Abstract: The molecular&#xD;
sieve SAPO-35 with different silicon content has been synthesized in a non-aqueous&#xD;
medium using haxamethyleimine template. It has been characterized by XRD, SEM,&#xD;
Carbon and Nitrogen analysis, MASNMR, FT-IR techniques and Methanol to olefin&#xD;
reaction. The study indicates that XRD, FT-IR and &lt;sup&gt;29&lt;/sup&gt;Si MASNMR&#xD;
properties did not change on increase in silicon incorporation. No silicon&#xD;
ilands were found on increase in silicon concentration. However, SEM photograph&#xD;
reveals that the particle size increased on increase in silicon content in the&#xD;
framework. The morphology also changes from bundles of platlets to cuboid, on&#xD;
more silicon incorporation. The catalytic activity of methanol to olefin&#xD;
conversion increases with silicon content and the selectivity is higher than ZSM-5&#xD;
catalyst. Butene is formed as a main product.
Page(s): 260-265</summary>
    <dc:date>2004-03-01T00:00:00Z</dc:date>
  </entry>
</feed>

