<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns="http://purl.org/rss/1.0/" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/8394">
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/8394</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/30405" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/30404" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/8427" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/8426" />
      </rdf:Seq>
    </items>
    <dc:date>2026-10-10T08:20:02Z</dc:date>
  </channel>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/30405">
    <title>Solar photocatalytic oxidation and removal of arsenic from ground water</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/30405</link>
    <description>Title: Solar photocatalytic oxidation and removal of arsenic from ground water
Authors: Majumder, Ayan; Chaudhuri, Malay
Abstract: &lt;span style="mso-bidi-language:HI"&gt;In a laboratory study, the effectiveness of&#xD;
combined tartrate and citrate as photocatalyst in solar photocatalytic oxidation&#xD;
and removal of arsenic from ground water was studied and a method, using a&#xD;
naturally occurring tartrate-citrate&#xD;
&#xD;
&lt;span style="mso-bidi-language:HI"&gt;photocatalyst that can be used at the household&#xD;
level to treat small quantities of drinking water was developed. Kinetic tests performed&#xD;
with 250 µg/L, As(III)-spiked ground water in presence of 5 mg/L Fe(II) and 50 µM&#xD;
photocatalyst, showed equal&#xD;
&#xD;
&lt;span style="mso-bidi-language:HI"&gt;efficiency of tartrate and citrate in combination&#xD;
for oxidation and removal of arsenic from ground water in 6 h solar illumination.&#xD;
Presence of silicate moderately decreased the removal of arsenic, while&#xD;
phosphate had more drastic effect on arsenic removal. With the increase in&#xD;
initial As(III) concentration above 250 µg/L, 5 mg/L Fe(II) did not achieved&#xD;
the removal to below 50 µg/L, although the maximum removal efficiency was 80%.&#xD;
Extract of tamarind (fruit of the tree &lt;i&gt;Tamarindus indica), &lt;/i&gt;a natural&#xD;
source of tartrate-citrate (equivalent to 50 IlM tartrate and citrate) achieved&#xD;
the arsenic oxidation and removal from 250-260 µg/L arsenic-bearing water to&#xD;
below 50 µg/L. The method performed within a l-L closed PET bottle showed&#xD;
similar removal and can be applied at the household level to treat small&#xD;
quantities of drinking water.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 122-128</description>
    <dc:date>2005-04-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/30404">
    <title>Burr size minimization in drilling using Taguchi technique</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/30404</link>
    <description>Title: Burr size minimization in drilling using Taguchi technique
Authors: Gaitonde, V N; Achyutha, B T; Siddeswarappa, B
Abstract: &lt;span style="mso-bidi-language:HI"&gt;Burr formation in drilling is one of the serious&#xD;
problems in precision engineering and mass production. The exit burr degrades&#xD;
the precision of products and causes additional cost of deburring. Since&#xD;
deburring processes are not yet well automated, the productivity of advanced&#xD;
manufacturing systems is often reduced. However, these processes are labour intensive&#xD;
and add to the total cost of components. Therefore, understanding the drilling&#xD;
burr formation and its dominant parameters is essential for controlling the&#xD;
burr size. This paper describes the Taguchi method based robust design philosophy&#xD;
for minimization of burr size- in drilling. Four parameters, namely, cutting&#xD;
speed, feed rate, point angle and clearance angle were identified and the&#xD;
ranges of the parameters for the present investigation was determined from&#xD;
&#xD;
&lt;span style="mso-bidi-language:HI"&gt;preliminary experiments. Each parameter was&#xD;
investigated at three levels to study the non-linearity effect of the&#xD;
parameters. Taguchi method based L&lt;sub&gt;9&lt;/sub&gt; orthogonal array was selected&#xD;
and experiments were conducted as per experimental layout plan. Based on signal&#xD;
to noise ratio analysis, the optimal settings of the process parameters have&#xD;
been determined. Confirmation tests have also been performed to predict and&#xD;
verify the &#xD;
&#xD;
&lt;span style="mso-bidi-language:HI"&gt;adequacy of the additive models for determining&#xD;
the optimal burr size.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 91-96</description>
    <dc:date>2005-04-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/8427">
    <title>Correlations for predicting detonation temperature of pure and mixed CNO and CHNO explosives</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/8427</link>
    <description>Title: Correlations for predicting detonation temperature of pure and mixed CNO and CHNO explosives
Authors: Keshavarz, M H
Abstract: In this paper, detonation temperature of CNO and CHNO&#xD;
explosives is evaluated by the base of atomic composition and heat of&#xD;
formation. It is shown here how only atomic composition and condensed phase&#xD;
heat of formation of CNO and CHNO explosives are sufficient for reliable&#xD;
prediction of detonation temperature as compared to complicated computer codes.&#xD;
New correlations are introduced so that they can easily be applied for&#xD;
determining detonation temperature via specified different pathways of&#xD;
decomposition of explosives. Calculated detonation temperatures by this&#xD;
procedure for both pure and explosive formulations show good agreement with&#xD;
respect to measured and the BKWS-EOS predictions of detonation temperatures.
Page(s): 158-164</description>
    <dc:date>2005-04-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/8426">
    <title>Preparation of ferrites from the combustion of metal nitrate-oxalyl dihydrazide solutions</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/8426</link>
    <description>Title: Preparation of ferrites from the combustion of metal nitrate-oxalyl dihydrazide solutions
Authors: Randhawa, B S; Dosanjh, H S; Kaur, Manpreet
Abstract: Spinel ferrites, MFe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; (M= Co, Ni, Cu, Zn) have&#xD;
been prepared by a redox chemical reaction between aqueous solutions of metal&#xD;
nitrates, ferric nitrate and oxalyl dihydrazide (ODH). On rapid heating the&#xD;
reaction mixture undergoes an abrupt exothermic redox chemical reaction that&#xD;
facilitates atomic scale mixing of the cations. This leads to the formation of&#xD;
stoichiometrically pure and single-phase nanoparticle ferrites at comparatively&#xD;
reduced temperature (400&lt;sup&gt;o&lt;/sup&gt;C) and in less time than possible by the&#xD;
conventional ceramic method. The final thermolysis products (ferrites) have&#xD;
been characterized by various physico-chemical techniques, i.e., XRD, IR, SEM&#xD;
and magnetic studies (saturation magnetization and Curie temperature).
Page(s): 151-154</description>
    <dc:date>2005-04-01T00:00:00Z</dc:date>
  </item>
</rdf:RDF>

