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    <title>NOPR Community:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/31723</link>
    <description />
    <pubDate>Fri, 09 Oct 2026 10:44:05 GMT</pubDate>
    <dc:date>2026-10-09T10:44:05Z</dc:date>
    <item>
      <title>Electrical behaviour of sisal fibre</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/32553</link>
      <description>Title: Electrical behaviour of sisal fibre
Authors: Chand, Navin
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;Electrical&#xD;
properties such as dielectric. constant, dissipation factor and resistivity of&#xD;
sisal fibre have been determined. Resistivity increases from 5.5 x 10&lt;sup&gt;10&lt;/sup&gt;&#xD;
to 8.09  x  10&lt;sup&gt;10&lt;/sup&gt; ohm cm with the increase in&#xD;
voltage from 22 to 145 V. A mechanism of conduction in this fibre is proposed.&lt;/span&gt;
Page(s): 287-288</description>
      <pubDate>Sun, 01 Dec 1991 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/32553</guid>
      <dc:date>1991-12-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Configuration of thick places in rotor-spun polyester yarn</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/32552</link>
      <description>Title: Configuration of thick places in rotor-spun polyester yarn
Authors: Ishtiaque, S M; Saxena, Ajay Kumar
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" color:black;mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:="" ar-sa"=""&gt;A new technique for classifying thick places by their configuration is&#xD;
proposed. Using this technique the thick places in a 24 tex polyester yarn have&#xD;
been classified into four categories. The technique has been found to be very&#xD;
useful in determining the stage at which thick places increase and in&#xD;
correcting the situation&lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" color:#333333;mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:="" ar-sa"=""&gt;.&lt;/span&gt;&lt;/span&gt;
Page(s): 285-286</description>
      <pubDate>Sun, 01 Dec 1991 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/32552</guid>
      <dc:date>1991-12-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Synthesis of 2-(aryl/hetaryl)azo-3,4-dihydroxy-5-( 4-nitrophenyl)- thiophene-1, 1-dioxide derivatives and their dyeing properties</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/32551</link>
      <description>Title: Synthesis of 2-(aryl/hetaryl)azo-3,4-dihydroxy-5-( 4-nitrophenyl)- thiophene-1, 1-dioxide derivatives and their dyeing properties
Authors: Mavlankar, S V; Rangnekar, D W
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;Preparation&#xD;
of 2-(aryl/hetaryl)azothiophene derivatives (&lt;b&gt;VIa-g&lt;/b&gt;) was achieved by&#xD;
coupling 3,4-dihydroxy-5-(4-nitrophenyl)-thiophene-1, 1-dioxide-2-carboxylic&#xD;
acid (&lt;b&gt;III&lt;/b&gt;) with diazonium salts (&lt;b&gt;Va-g&lt;/b&gt;) derived from aryl and&#xD;
hetaryl amines (&lt;b&gt;IVa-g&lt;/b&gt;).The intermediate &lt;b&gt;III&lt;/b&gt; was obtained in&#xD;
excellent yield by the condensation of diethyl oxalate and 4-nitrobenzylsulphonyl&#xD;
acetic acid in a single step. These compounds when applied on polyester fibres&#xD;
as disperse dyes gave yellow to red-violet shades with good pick-up, moderate&#xD;
light fastness and good sublimation fastness.&lt;/span&gt;
Page(s): 282-284</description>
      <pubDate>Sun, 01 Dec 1991 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/32551</guid>
      <dc:date>1991-12-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>&lt;span style="font-size:11.0pt;line-height:115%; font-family:"Calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family: "Times New Roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font: minor-latin;mso-bidi-font-family:Calibri;mso-bidi-theme-font:minor-latin; mso-ansi-language:EN-US;mso-fareast-language:EN-US;mso-bidi-language:AR-SA"&gt;Synthesis and dyeing characteristics of 2-(aryl/hetaryl)- styryl-8-dicyanomethyleneindeno[1,2-&lt;i&gt;d&lt;/i&gt;]thiazoles&lt;/span&gt;</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/32550</link>
      <description>Title: &lt;span style="font-size:11.0pt;line-height:115%; font-family:"Calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family: "Times New Roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font: minor-latin;mso-bidi-font-family:Calibri;mso-bidi-theme-font:minor-latin; mso-ansi-language:EN-US;mso-fareast-language:EN-US;mso-bidi-language:AR-SA"&gt;Synthesis and dyeing characteristics of 2-(aryl/hetaryl)- styryl-8-dicyanomethyleneindeno[1,2-&lt;i&gt;d&lt;/i&gt;]thiazoles&lt;/span&gt;
Authors: Rangnekar, D W; Mavlankar, S V
Abstract: &lt;span style="font-size:11.0pt;line-height:115%;&#xD;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:calibri;mso-bidi-theme-font:minor-latin;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;2-Methyl-8-dicyanomethyleneindeno[1,2-&lt;i&gt;d&lt;/i&gt;]thiazole(&lt;b&gt;III&lt;/b&gt;)&#xD;
obtained by the condensation of 3-dicyanomethyleneindan-1-one(&lt;b&gt;II&lt;/b&gt;) with&#xD;
thioacetamide in presence of idodine and dimethylsulphoxide was reacted with&#xD;
different aryl and hetaryl aldehydes (&lt;b&gt;IVa-e&lt;/b&gt;) to give&#xD;
2-(aryl/hetaryl)-styryl-8-dicyanomethyleneindeno[1,2-&lt;i&gt;d&lt;/i&gt;]thiazoles (&lt;b&gt;Va-e&lt;/b&gt;).&#xD;
These compounds when applied as disperse dyes on polyester fibres showed good&#xD;
pick up, moderate light fastness and excellent sublimation fastness.&lt;/span&gt;
Page(s): 279-281</description>
      <pubDate>Sun, 01 Dec 1991 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/32550</guid>
      <dc:date>1991-12-01T00:00:00Z</dc:date>
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