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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/26149</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 05:19:40 GMT</pubDate>
    <dc:date>2026-10-10T05:19:40Z</dc:date>
    <item>
      <title>Comparative Evaluation of the Effect of Butylated and Isobutylated Derivatives of M-F Resins on Wood-finish Properties</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/26472</link>
      <description>Title: Comparative Evaluation of the Effect of Butylated and Isobutylated Derivatives of M-F Resins on Wood-finish Properties
Authors: Sarma, Biswajit; Dolui, Swapan K; Sharma, Ashok K
Abstract: The effect of butylated and isobutylated&#xD;
derivatives of melamine-formaldehyde (M-F) resins in an acid-catalysed lacquer formulation&#xD;
on wood finish properties is compared by determining the finish properties such&#xD;
as drying time, shelf-life, resistance towards different chemicals, hardness and&#xD;
impact resistance. Results are discussed in detail.
Page(s): 153-158</description>
      <pubDate>Thu, 01 Feb 2001 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/26472</guid>
      <dc:date>2001-02-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Study of Dyes Used in Fake and Adulterated Petrol Samples</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/26471</link>
      <description>Title: Study of Dyes Used in Fake and Adulterated Petrol Samples
Authors: Malve, M K; Krishnamurthy, R; Shinde, B M
Abstract: The study deals with dyes from petrol,&#xD;
fake petrol, green petrol or patrex and adulteration of these fuels with blue kerosene.&#xD;
A High Performance Thin Layer Chromatography (HPTLC) study of above fuels indicates&#xD;
the difference in dye properties compared to that of genuine petrol. Also dye from&#xD;
blue kerosene was detected in few petrol samples and patrex samples,&#xD;
&#xD;
indicating adulteration of blue kerosene in&#xD;
above fuels. In addition to dye study, other tests like density and distillation&#xD;
characteristics for petrol, Raxon, SBP and green petrol have also been studied.
Page(s): 151-152</description>
      <pubDate>Thu, 01 Feb 2001 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/26471</guid>
      <dc:date>2001-02-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Effect of NTA and pH on Lead(II) Adsorption by the Hydrous Oxides of Mn, Fe, and A1</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/26470</link>
      <description>Title: Effect of NTA and pH on Lead(II) Adsorption by the Hydrous Oxides of Mn, Fe, and A1
Authors: Abraham, Beena T; Anirudhan, T S
Abstract: The object of this work was to study the influence&#xD;
of nitrilotriacetic acid (NTA) on Pb(II) adsorption by different hydrous oxide&#xD;
gels (MnOOH, FeOOH and AlOOH) at different pH levels. The surface charge density&#xD;
as a function of pH in aqueous solution of NaNO&lt;sub&gt;3&lt;/sub&gt;, NTA and Pb-NTA has&#xD;
been determined. In the presence of NTA the values of zero point charge (pH&lt;sub&gt;zpc)&lt;/sub&gt;&#xD;
for AlOOH, FeOOH and MnOOH were shifted downwards from 9.2 to 8.5, 7.3 to 6.5 and&#xD;
3.8 to 3.6 respectively. The pH&lt;sub&gt;zpc&lt;/sub&gt; values for AlOOH, FeOOH and MnOOH&#xD;
in the presence of Pb and NTA were found to be 7.3, 6.0, and 3.2 respectively. An&#xD;
empirical&#xD;
&#xD;
relationship has been obtained to predict&#xD;
the pH&lt;sub&gt;zpc&lt;/sub&gt; at any amount of NTA adsorption on AlOOH. The adsorption characteristics&#xD;
of Pb and NTA in presence of each other has been studied. The adsorption of Pb(II)&#xD;
in presence of NTA was greater than NTA adsorption in presence of Pb(II). The maximum&#xD;
adsorption of Pb (II) in presence of NTA occur at a pH range of 3.0-4.0. The oxide&#xD;
surface carries a net positive charge at pH range 3.0-4.0 thus negatively charged&#xD;
Pb-NTA&lt;sup&gt;2-&lt;/sup&gt; complex can be readily adsorbed.
Page(s): 145-150</description>
      <pubDate>Thu, 01 Feb 2001 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/26470</guid>
      <dc:date>2001-02-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Assessment of Degree of Carbonisation of Industrial Cokes/Chars with CV:FC Ratio</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/26469</link>
      <description>Title: Assessment of Degree of Carbonisation of Industrial Cokes/Chars with CV:FC Ratio
Authors: Rao, K S; Kamavisdar, A; Jalgaonkar, R D; Sirociya, R S; Khanwalkar, S R; Meshram, R M; Sahay, R K
Abstract: The degree of coking or completeness of carbonisation&#xD;
in the production of industrial cokes/ chars is assessed with the help of appropriately&#xD;
corrected percentage value of residual volatile matter. Although coke reflectance&#xD;
has good correlation with final carbonisation temperature, its determination is&#xD;
time consuming. As CV:FC ratio has been shown to ascertain the degree of devolatilisation&#xD;
in heat altered coals, as well as in laboratory prepared cokes/chars it is worthwhile&#xD;
to consider its utility for assessing the degree of carbonisation in industrial&#xD;
coking practice too. Studies conducted on a range of industrial cokes/chars reveal&#xD;
that CV:FC ratio :(i) is directly related to residual volatile matter percentage,&#xD;
(ii) can differentiate between iso-volatile cokes/chars by assessing respective&#xD;
degree of coking and (iii) can indicate the order of final coking temperature reached&#xD;
even in cokes/chars having widely varying residual volatile matter percentages.It&#xD;
may, therefore, be inferred that CV: FC ratios provide a simple alternative route&#xD;
for assessing final coking temperature of industrial cokes/chars.
Page(s): 141-144</description>
      <pubDate>Thu, 01 Feb 2001 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/26469</guid>
      <dc:date>2001-02-01T00:00:00Z</dc:date>
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