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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22614" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/22614</id>
  <updated>2026-10-10T12:21:25Z</updated>
  <dc:date>2026-10-10T12:21:25Z</dc:date>
  <entry>
    <title>The Dead Sea—A live pool of chemicals</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22829" />
    <author>
      <name>Wisniak, Jaime</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22829</id>
    <updated>2013-10-31T16:45:30Z</updated>
    <published>2002-01-01T00:00:00Z</published>
    <summary type="text">Title: The Dead Sea—A live pool of chemicals
Authors: Wisniak, Jaime
Abstract: The Dead Sea&#xD;
has been a source of chemicals since ancient times. Large scale production of potash&#xD;
by solar evaporation started in 1931 and today the Dead Sea is intensively exploited&#xD;
by Israel and Jordan as a major&#xD;
source of potash, bromine, and magnesium, for agriculture and the chemical and automotive&#xD;
industries. A smart coupling of solar evaporation and&#xD;
&#xD;
knowledge of the complex phase diagram allows&#xD;
a one-to-one easy separation of the principal salts present in the brine. A description&#xD;
of the properties of the Dead Sea is provided&#xD;
together with a chemical engineering analysis of the processes used to realize&#xD;
its commercial potential.
Page(s): 79-87</summary>
    <dc:date>2002-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Mild steel deterioration with time in various aqueous salt solutions</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22828" />
    <author>
      <name>Mehra, Rita</name>
    </author>
    <author>
      <name>Soni, Aditi</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22828</id>
    <updated>2013-10-31T16:42:57Z</updated>
    <published>2002-01-01T00:00:00Z</published>
    <summary type="text">Title: Mild steel deterioration with time in various aqueous salt solutions
Authors: Mehra, Rita; Soni, Aditi
Abstract: The corrosivity of water supplies need to&#xD;
be evaluated in view of the aesthetic problems in water and also because of the&#xD;
potential public health importance. As such, some recent work on mild steel&#xD;
deterioration has been carried out. The results assessed from weight loss measurements&#xD;
for different chemical mediums support the chloride aggressiveness&#xD;
&#xD;
reported in literature. But the relative&#xD;
behaviour of other ions vary with time being lesser in concentration as per potable&#xD;
water quality standards. Potentiostatic polarisation results have also been carried&#xD;
out to determine the effect of different anions and time on corrosion rate through&#xD;
changes in potential. The corrosion potential (&lt;i&gt;E&lt;/i&gt;&lt;sub&gt;corr·&lt;/sub&gt;), corrosion&#xD;
current (&lt;i&gt;I&lt;/i&gt;&lt;sub&gt;corr&lt;/sub&gt;·),&#xD;
&#xD;
Tafel slopes, corrosion rate have been obtained&#xD;
from polarisation experiments using a three electrode set-up. For reliability of&#xD;
results, the data has been statistically analysed.
Page(s): 74-78</summary>
    <dc:date>2002-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Influence of anions on corrosion inhibition and hydrogen permeation through mild steel in acidic solutions in the presence of &lt;i&gt;p&lt;/i&gt;-tolyl thiourea</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22827" />
    <author>
      <name>Muralidharan, S</name>
    </author>
    <author>
      <name>Madhavan, K</name>
    </author>
    <author>
      <name>Karthikeyan, S</name>
    </author>
    <author>
      <name>Iyer, S Venkatakrishna</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22827</id>
    <updated>2013-11-01T16:44:34Z</updated>
    <published>2002-01-01T00:00:00Z</published>
    <summary type="text">Title: Influence of anions on corrosion inhibition and hydrogen permeation through mild steel in acidic solutions in the presence of &lt;i&gt;p&lt;/i&gt;-tolyl thiourea
Authors: Muralidharan, S; Madhavan, K; Karthikeyan, S; Iyer, S Venkatakrishna
Abstract: The influence of anions such as chloride&#xD;
and sulphate on the inhibition of corrosion of mild steel by &lt;i&gt;p&lt;/i&gt;-tolyl&#xD;
thiourea (PTTU) in 1N HCl and 1N H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; has been studied&#xD;
using weight loss and gasometric measurements, Galvanostatic polarisation studies&#xD;
and ac impedance measurements. The compound is found to be less inhibitive in 1N&#xD;
HCl than in 1 N H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;. The influence of &lt;i&gt;p&lt;/i&gt;-tolyl thiourea&#xD;
on the extent of hydrogen permeated through mild steel in acidic solutions has been&#xD;
studied using electro-permeation technique. The compound is found to enhance&#xD;
the permeation of hydrogen through mild steel in both the acids. The adsorption&#xD;
of &lt;i&gt;p&lt;/i&gt;-tolyl thiourea on the mild steel surface from both the acids obeys Temkin's&#xD;
adsorption isotherm. The increase of charge transfer resistance (&lt;i&gt;R&lt;/i&gt;&lt;sub&gt;t&lt;/sub&gt;)&lt;i&gt;&#xD;
&lt;/i&gt;and decrease in double layer capacitance (&lt;i&gt;C&lt;/i&gt;&lt;sub&gt;d1&lt;/sub&gt;) values of the&#xD;
metal electrode in the presence of the test compound (PTTU) show the adsorption&#xD;
of the compound on the metal surface.
Page(s): 68-73</summary>
    <dc:date>2002-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and dissolution of chromium substituted magnetites in V(II)-EDTA formulation</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22826" />
    <author>
      <name>Manjanna, J</name>
    </author>
    <author>
      <name>Venkateswaran, G</name>
    </author>
    <author>
      <name>Sherigara, B S</name>
    </author>
    <author>
      <name>Nayak, P V</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22826</id>
    <updated>2013-11-10T16:41:50Z</updated>
    <published>2002-01-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and dissolution of chromium substituted magnetites in V(II)-EDTA formulation
Authors: Manjanna, J; Venkateswaran, G; Sherigara, B S; Nayak, P V
Abstract: Chemical cleaning or scale removal of boilers,&#xD;
heat exchangers etc., involves the dissolution of metal oxides, which are corrosion&#xD;
products from the base metal. Iron oxides mainly hematites and magnetites are&#xD;
commonly found in the case of Fe based alloys due to corrosion. The decontamination&#xD;
of primary system surface of water-cooled nuclear reactors, in particular Pressurized&#xD;
Light Water Reactor (PWR)/ Pressurized Heavy Water Reactor (PHWR) involves the dissolution&#xD;
of iron oxides formed under reducing coolant chemistry environment ca. magnetite&#xD;
type of oxide matrix. Thus in the present study, the dissolution characteristics&#xD;
of Cr-substituted (0-20 at% Cr) magnetites (c.s.m) in V(II)-EDTA formulation at&#xD;
353±5 K are reported. The oxides employed were prepared synthetically by co-precipitation&#xD;
method, moderately sintered and physic-chemically characterized. The dissolution&#xD;
rate coefficient, &lt;i&gt;k&lt;/i&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;i&gt; &lt;/i&gt;and the percentage of dissolution&#xD;
were determined. The oxidative pre-treatment of these oxides employing viz., AP,&#xD;
NP and HMnO&lt;sub&gt;4&lt;/sub&gt; had resulted in improved dissolution.
Page(s): 60-67</summary>
    <dc:date>2002-01-01T00:00:00Z</dc:date>
  </entry>
</feed>

