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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22608" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/22608</id>
  <updated>2026-10-09T08:20:23Z</updated>
  <dc:date>2026-10-09T08:20:23Z</dc:date>
  <entry>
    <title>Sodium carbonate—From natural resources to Leblanc and back</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22707" />
    <author>
      <name>Wisniak, Jaime</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22707</id>
    <updated>2013-10-29T16:35:46Z</updated>
    <published>2003-01-01T00:00:00Z</published>
    <summary type="text">Title: Sodium carbonate—From natural resources to Leblanc and back
Authors: Wisniak, Jaime
Abstract: The development of sodium carbonate as a&#xD;
major commodity is intimately attached to the chemical revolution that took&#xD;
place in the eighteenth and nineteenth century. Strong political and economical&#xD;
reasons led to the search of synthetic procedures to replace the natural sources&#xD;
of soda that were available by the seventeenth century. Eventually Nicolas&#xD;
Leblanc developed a synthetic process that used common salt as raw material.&#xD;
Implementation of&#xD;
&#xD;
Leblanc’s procedure led to such serious environmental&#xD;
problems, e.g., acid rain, that the first laws for environmental protection&#xD;
were enacted in England.&#xD;
Treatment of the obnoxious gaseous, liquid, and solid wastes of the process resulted&#xD;
in new processes for the manufacture of chlorine and sulphur. Leblanc's process&#xD;
came to an end with the development of the Solvay process. Eventually, the&#xD;
discovery of huge fields of natural sodium carbonate in the U.S. led to the&#xD;
decline of the Solvay process.
Page(s): 99-112</summary>
    <dc:date>2003-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>A simple sensitive spectrophotometric method for determination of dichlorvos in environmental samples</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22706" />
    <author>
      <name>Asthana, Anupama</name>
    </author>
    <author>
      <name>Pillaia, Ajai</name>
    </author>
    <author>
      <name>Gupta, V K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22706</id>
    <updated>2013-10-28T16:37:11Z</updated>
    <published>2003-01-01T00:00:00Z</published>
    <summary type="text">Title: A simple sensitive spectrophotometric method for determination of dichlorvos in environmental samples
Authors: Asthana, Anupama; Pillaia, Ajai; Gupta, V K
Abstract: A sensitive method has been developed for&#xD;
spectrophotometric determination of an organophosphorous pesticide dichlorvos,&#xD;
also known as 2,2 dichlorovinyl methyl phosphate or dichlorophos. The method is&#xD;
based on hydrolysis of dichlorvos by sodium hydroxide to produce&#xD;
dichloroacetaldehyde, which on coupling with phloroglucinol in alkaline medium,&#xD;
gives orange colour. The orange dye shows absorption maxima at 475 nm and obeys&#xD;
Beer's&#xD;
&#xD;
law in the range of 10-100μg/25 mL&#xD;
(0.4 to 4 ppm) of solution. The molar absorptivity and Sandell's sensitivity&#xD;
were found to be 4.53×10&lt;sup&gt;4 &lt;/sup&gt;l mol&lt;sup&gt;-1&lt;/sup&gt;cm&lt;sup&gt;-1&lt;/sup&gt; and&#xD;
0.0048 μg cm&lt;sup&gt;-2&lt;/sup&gt; respectively. The method has been&#xD;
successfully applied for the determination of dichlorvos in water, agricultural&#xD;
soil and vegetables.
Page(s): 96-98</summary>
    <dc:date>2003-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Removal of arsenic from water by coagulation treatment using iron and magnesium salt</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22705" />
    <author>
      <name>Ghosh, B</name>
    </author>
    <author>
      <name>Das, M C</name>
    </author>
    <author>
      <name>Gangopadhyay, A K</name>
    </author>
    <author>
      <name>Das, T B</name>
    </author>
    <author>
      <name>Singh, K</name>
    </author>
    <author>
      <name>Lal, S</name>
    </author>
    <author>
      <name>Mitra, S</name>
    </author>
    <author>
      <name>Ansari, S H</name>
    </author>
    <author>
      <name>Goswami, T K</name>
    </author>
    <author>
      <name>Chakraborty, S K</name>
    </author>
    <author>
      <name>Banerjee, N N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22705</id>
    <updated>2016-07-20T04:52:23Z</updated>
    <published>2003-01-01T00:00:00Z</published>
    <summary type="text">Title: Removal of arsenic from water by coagulation treatment using iron and magnesium salt
Authors: Ghosh, B; Das, M C; Gangopadhyay, A K; Das, T B; Singh, K; Lal, S; Mitra, S; Ansari, S H; Goswami, T K; Chakraborty, S K; Banerjee, N N
Abstract: Arsenic in ground water assumes a&#xD;
predicament of global dimension. Among the various methods of removal of arsenic&#xD;
from contaminated water, coagulation-filtration route has been examined in&#xD;
details covering effect of &lt;i&gt;p&lt;/i&gt;H,&#xD;
coagulant type and its dose, and initial arsenic load in water. A set of batch&#xD;
experiments were conducted in the laboratory to investigate arsenic removal&#xD;
efficiency from spiked aqueous solution as well as a few ground water samples&#xD;
collected from the affected zone of West Bengal (India). The removal kinetics&#xD;
of aqueous arsenic spiked samples with iron/magnesium salt as coagulants were&#xD;
studied to assess&#xD;
the&#xD;
feasibility for the use in the arsenic removal&#xD;
in water treatment plant, and a plausible kinetic behaviour in their removal&#xD;
process has been discussed. A comparative performance efficiency for iron salt&#xD;
in contrast to magnesium salt as coagulant has&#xD;
been&#xD;
examined to&#xD;
&#xD;
establish the superiority of iron system.&#xD;
Increase in background ionic species such as Cl&lt;sup&gt;ˉ&lt;/sup&gt;,&#xD;
NO&lt;sub&gt;3&lt;/sub&gt;ˉ and&#xD;
SO&lt;sup&gt;2-&lt;/sup&gt;&lt;sub&gt;4&lt;/sub&gt; in&#xD;
test solution with iron system have been performed in which Cl&lt;sup&gt;ˉ&lt;/sup&gt; and NO&lt;sub&gt;3&lt;/sub&gt;ˉ&#xD;
ions showed&#xD;
no effect on the efficiency of arsenic removal, while pronounced lowering&#xD;
effect has been observed in case of SO&lt;sup&gt;2-&lt;/sup&gt;&lt;sub&gt;4&lt;/sub&gt; ion.&#xD;
This investigation suggests that for community supply of arsenic free water,&#xD;
the proposed protocol-coagulation with iron salt and subsequent filtration hold&#xD;
promise.
Page(s): 87-95</summary>
    <dc:date>2003-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>TLC studies and separation of heavy metal cations on soil amended silica gel layers developed with surfactant-mediated solvent systems</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22704" />
    <author>
      <name>Mohammad, Ali</name>
    </author>
    <author>
      <name>Jabeen, Nahed</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22704</id>
    <updated>2016-07-20T05:02:47Z</updated>
    <published>2003-01-01T00:00:00Z</published>
    <summary type="text">Title: TLC studies and separation of heavy metal cations on soil amended silica gel layers developed with surfactant-mediated solvent systems
Authors: Mohammad, Ali; Jabeen, Nahed
Abstract: Thin-layer chromatography (TLC) of ten heavy&#xD;
metal cations was performed on soil, silica gel and soil mixed with silica gel&#xD;
sorbent phases using aqueous solutions of cetyl trimethyl ammonium bromide&#xD;
(CTAB), sodium dodecyl sulphate (SDS), polyoxyethylene dodecyl ether (Brij-35)&#xD;
and &lt;i&gt;iso&lt;/i&gt;-octylphenoxypolyethoxy ethanol (TX-100) surfactants with or&#xD;
without added urea, nitrate or chloride of ammonium and sodium phosphate as&#xD;
mobile phases. In&#xD;
&#xD;
all, twenty-nine stationary and&#xD;
twenty-five mobile phases were used in order to examine the mobility pattern&#xD;
and to find out the best TLC system for metal cations separation from their&#xD;
multicomponent mixtures on soil mixed with silica gel layers. The mobility of all cations was insignificant on pure soil layers irrespective&#xD;
of the nature of mobile phase used. Addition of silica gel into soil bed leads&#xD;
to the increase of mobility and facilitates the separation of metal&#xD;
&#xD;
cations. Amongst surfactant solutions, CTAB&#xD;
at concentration level of 0.5 M was found to be most effective, the analytical&#xD;
potentiality of which was further improved in the presence of urea. The TLC&#xD;
system comprising of silica gel plus 0.6 M urea (1:1,&lt;i&gt;v/v&lt;/i&gt;)&#xD;
as mobile&#xD;
phase was found most favourable for achieving separations of metal ions from their&#xD;
multicomponent mixtures. A few such separations worth mentioning include, Fe&lt;sup&gt;3+&lt;/sup&gt;-Cu&lt;sup&gt;2+&lt;/sup&gt;-Ni&lt;sup&gt;2+&lt;/sup&gt;-Hg&lt;sup&gt;2+&lt;/sup&gt;,&#xD;
Zn&lt;sup&gt;2+&lt;/sup&gt;-Cd&lt;sup&gt;2+&lt;/sup&gt;-Hg&lt;sup&gt;2+&lt;/sup&gt;, Ni&lt;sup&gt;2+&lt;/sup&gt;-Cu&lt;sup&gt;2+&lt;/sup&gt;-Fe&lt;sup&gt;3+&lt;/sup&gt;,&#xD;
Zn&lt;sup&gt;2+&lt;/sup&gt;-Fe&lt;sup&gt;3+&lt;/sup&gt;-Ni&lt;sup&gt;2+&lt;/sup&gt;-Hg&lt;sup&gt;2+&lt;/sup&gt;, Pb&lt;sup&gt;2+&lt;/sup&gt;-Cd&lt;sup&gt;2+&lt;/sup&gt;-Hg&lt;sup&gt;2+&lt;/sup&gt;&#xD;
and Ni&lt;sup&gt;2+&lt;/sup&gt;-Cu&lt;sup&gt;2+&lt;/sup&gt;-Pb&lt;sup&gt;2+&lt;/sup&gt;. &lt;i&gt;R&lt;/i&gt;&lt;sub&gt;F&lt;/sub&gt; values&#xD;
of metal ions on soil amended with alumina, kieselguhr, cellulose and fly ash&#xD;
layers have also been determined. Salting - in effect exhibited by certain&#xD;
metal ions like Cd&lt;sup&gt;2+&lt;/sup&gt;, Ni&lt;sup&gt;2+&lt;/sup&gt; or Co&lt;sup&gt;2+&lt;/sup&gt;, Ag&lt;sup&gt;+&lt;/sup&gt;,&#xD;
Hg&lt;sup&gt;2+&lt;/sup&gt; has been reported. Effect on mobility of metal ions, by&#xD;
replacing urea with different fertilizers in the CTAB containing mobile phase&#xD;
has also been examined.
Page(s): 79-86</summary>
    <dc:date>2003-01-01T00:00:00Z</dc:date>
  </entry>
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