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    <title>NISCAIR Online Periodicals Repository Collection: IJCT Vol.12(5) [September 2005]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/8567</link>
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      <title>Removal and recovery of nitrate from water by ZnCl&lt;sub&gt;2&lt;/sub&gt; activated carbon from coconut coir pith, an agricultural solid waste</title>
      <link>http://nopr.niscair.res.in/handle/123456789/8683</link>
      <description>Title: Removal and recovery of nitrate from water by ZnCl&lt;sub&gt;2&lt;/sub&gt; activated carbon from coconut coir pith, an agricultural solid waste
&lt;br/&gt;
&lt;br/&gt;Authors: Namasivayam, C; Sangeetha, D
&lt;br/&gt;
&lt;br/&gt;Abstract: Nitrate removal from&#xD;
aqueous solution was investigated using ZnCl&lt;sub&gt;2 &lt;/sub&gt;activated carbon&#xD;
developed from coir pith. Influence of contact time, adsorbent dose, nitrate&#xD;
concentration, pH and temperature were investigated. Two theoretical adsorption&#xD;
isotherms namely Langmuir and Freundlich were used to describe the experimental&#xD;
results. The Langmuir adsorption capacity (&lt;i style=""&gt;Q&lt;/i&gt;&lt;sub&gt;o&lt;/sub&gt;)&#xD;
was found to be 10.3 mg nitrate per g of the adsorbent. Adsorption followed&#xD;
second order kinetics. Adsorption was maximum in the pH range 3-10. pH effect&#xD;
and desorption studies showed that ion exchange mechanism might be involved in&#xD;
the adsorption process. Effects of foreign ions such as chloride, sulphate,&#xD;
phosphate and perchlorate on the removal of nitrate have also been&#xD;
investigated. Removal of nitrate from ground water was also tested. Results&#xD;
show that ZnCl&lt;sub&gt;2&lt;/sub&gt; activated coir pith carbon is effective for the&#xD;
removal of nitrate from water.
&lt;br/&gt;
&lt;br/&gt;Page(s): 513-521</description>
      <pubDate>Mon, 29 Aug 2005 22:58:59 GMT</pubDate>
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    <item>
      <title>Platinum—From exotic to commodity</title>
      <link>http://nopr.niscair.res.in/handle/123456789/8682</link>
      <description>Title: Platinum—From exotic to commodity
&lt;br/&gt;
&lt;br/&gt;Authors: Wisniak, Jaime
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="place"&gt;&#xD;
&#xD;
&#xD;
&#xD;
Platinum was brought to Europe&#xD;
in the middle of the sixteenth century and was soon recognized a true metal, which&#xD;
could not be fused. It remained an expensive curiosity for almost 200 years,&#xD;
until scientists learned its properties, how to melt it in large quantity, and&#xD;
discovered that four new elements, rhodium, iridium, osmium, and palladium,&#xD;
accompanied it (the platinum group metals). The early uses of platinum were in&#xD;
jewelry, laboratory ware, and coin manufacture. By the end of the nineteenth&#xD;
century a platinum-rhodium alloy was adopted for constructing the standard&#xD;
meter and kilogram. Production of platinum grew very slowly; it was only about&#xD;
one ton per year by 1911. The breakthrough came with the discovery of the&#xD;
extraordinary the catalytic properties of the platinum metal group. Today these&#xD;
metals stand at the heart of the petrochemical industry and are the basis of&#xD;
all the means for controlling the emission of obnoxious gases of motor&#xD;
vehicles. Annual production has now reached near 190 tons.&#xD;
&#xD;
&lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 601-614</description>
      <pubDate>Mon, 29 Aug 2005 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Study of water vapour adsorption on nickel-chromia H-D exchange catalyst</title>
      <link>http://nopr.niscair.res.in/handle/123456789/8681</link>
      <description>Title: Study of water vapour adsorption on nickel-chromia H-D exchange catalyst
&lt;br/&gt;
&lt;br/&gt;Authors: Gill, J S; Ramakrishnan, P; Singh, H
&lt;br/&gt;
&lt;br/&gt;Abstract: Adsorption of water&#xD;
vapour on a series of nickel-chromia samples has been studied. Nickel-chromia,&#xD;
with 15% chromium is an active catalyst for H-D (hydrogen-deuterium) exchange&#xD;
in hydrogen-water system, where water is in vapour phase. Water vapour&#xD;
adsorption/desorption indicate that it is adsorbed on the catalyst both&#xD;
physically and chemically. The 15% chromium catalyst sample has been treated&#xD;
with phenylethyl triethoxy silane to make it hydrophobic and active in liquid&#xD;
water-hydrogen system of H-D exchange. Water vapour adsorption isotherm on the&#xD;
treated sample shows the hydrophobization of the catalyst.
&lt;br/&gt;
&lt;br/&gt;Page(s): 559-562</description>
      <pubDate>Mon, 29 Aug 2005 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Four rapid and sensitive methods for the assay of amoxycillin in pharmaceuticals using bromate-bromide mixture and two dyes</title>
      <link>http://nopr.niscair.res.in/handle/123456789/8680</link>
      <description>Title: Four rapid and sensitive methods for the assay of amoxycillin in pharmaceuticals using bromate-bromide mixture and two dyes
&lt;br/&gt;
&lt;br/&gt;Authors: Ramakrishna, V; Basavaiah, K
&lt;br/&gt;
&lt;br/&gt;Abstract: Four new methods using titrimetry and&#xD;
spectrophotometry are described for the rapid determination of amoxycillin in&#xD;
bulk drug and dosage forms. In direct titrimetry (Method A), the drug is&#xD;
titrated with bromate–bromide mixture in acid medium using methyl orange&#xD;
indicator. Back titrimetry (Method B) entails adding a known excess amount of&#xD;
bromate-bromide mixture to the drug solution in acid medium, followed by&#xD;
determination of residual bromine iodometrically. Both spectrophotometric&#xD;
methods are based on the oxidation–bromination of amoxyciillin by &lt;i style=""&gt;in situ&lt;/i&gt; generated bromine followed by&#xD;
estimation of unreacted bromine with methyl orange (Method C) or indigo carmine&#xD;
(Method D) and measuring the change in absorbance at 520 or 610 nm. In all the&#xD;
methods, qunatitation is based on the amount of bromate that has reacted with&#xD;
amoxycillin. The experimental conditions have been optimized. Calculations are&#xD;
based on 1:1 and 1:2 (amoxycillin: bromate) stoichiometry for method A and&#xD;
Method B, respectively. Method A is applicable over 2-16 mg range, and 1-9 mg&#xD;
of amoxycillin could be determined by method B. In spectrophotometric methods,&#xD;
the absorbance is found to increase linearly with increasing concentration of&#xD;
amoxycillin which is corroborated by the calculated correlation coefficient (&lt;i style=""&gt;r&lt;/i&gt;) of 0.9964 (Method C) and 0.9959&#xD;
(Method D). The calibration graphs are found to be linear over 0.1–1.2 and 0.5 –&#xD;
4.0 &lt;img src='/image/spc_char/micro.gif' border=0&gt; g mL&lt;sup&gt;-1 &lt;/sup&gt;for method C and&#xD;
method D, respectively. Method C with a molar absorptivity of 1.60 &lt;img src='/image/spc_char/cross.gif' border=0&gt; 10&lt;sup&gt;5&lt;/sup&gt; L mol&lt;sup&gt;-1 &lt;/sup&gt;cm&lt;sup&gt;-1 &lt;/sup&gt;is found to be&#xD;
more sensitive than method D (ε = 5.83 &lt;img src='/image/spc_char/cross.gif' border=0&gt; 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;). The limits of&#xD;
detection and quantification for both spectrophotometric methods are reported.&#xD;
Statistical evaluation of the methods was examined by determining intra-day and&#xD;
inter-day precisions. The methods were applied to the determination of&#xD;
amoxycillin pharmaceutical formulations. No interference was observed from&#xD;
excipients and the validity of the methods was tested against a reference&#xD;
method.
&lt;br/&gt;
&lt;br/&gt;Page(s): 543-549</description>
      <pubDate>Mon, 29 Aug 2005 22:58:59 GMT</pubDate>
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