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  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/31725">
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/31725</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/32542" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/32541" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/32540" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/32539" />
      </rdf:Seq>
    </items>
    <dc:date>2026-10-10T23:54:03Z</dc:date>
  </channel>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/32542">
    <title>Dyeing behaviour of open-end and ring-spun cotton yarns</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/32542</link>
    <description>Title: Dyeing behaviour of open-end and ring-spun cotton yarns
Authors: Iyer, V; Shenai, V A
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;The&#xD;
differences in the dyeing behaviour of open-end and ring-spun yarns have been&#xD;
studied using a number of direct, vat and reactive dyes, and the absorbance&#xD;
values for the percentage exhaustion and dye uptake for a fixed period are&#xD;
reported. The percentage exhaustion does not show any significant difference&#xD;
between rotor-spun and ring-spun yarns whether dyed separately or in the same&#xD;
dye-bath. The dye uptake values, however, are generally higher for rotor-spun&#xD;
yarns when dyed with ring-spun yarns in one dye-bath.&lt;/span&gt;
Page(s): 236-238</description>
    <dc:date>1991-09-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/32541">
    <title>Effect of sliver preparation on fibre disorder at rotor groove</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/32541</link>
    <description>Title: Effect of sliver preparation on fibre disorder at rotor groove
Authors: Ishtiaque, S M; Saxena, Ajay
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;The&#xD;
fibre disorder at rotor groove was measured by using Lindsley's technique. The&#xD;
effect of draw frame passages on fibre disorder at rotor groove and in feed&#xD;
sliver was studied. Fibre orientation at rotor groove has been found to be&#xD;
inferior to that in feed sliver. Better fibre straightening with no significant&#xD;
improvement in fibre parallelization is achieved with the second drawing&#xD;
passage.&lt;/span&gt;
Page(s): 233-235</description>
    <dc:date>1991-09-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/32540">
    <title>Synthesis of azo disperse dyes containing thiadiazole ring for dyeing acetate and/or other fibres</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/32540</link>
    <description>Title: Synthesis of azo disperse dyes containing thiadiazole ring for dyeing acetate and/or other fibres
Authors: Fadda, A A; Amer, F A; El-Said, A M; Elagizy, S A
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;Twenty&#xD;
arylazo derivatives of 5-(2-hydroxyphenyl)-2-phenylamino-1,3,4-thiadiazole and&#xD;
its 3-ethyl derivative have been prepared for use as dyestuffs. The effect of&#xD;
the nature and orientation of substituents in the diazonium component on the&#xD;
colour of azo dyes is discussed. The dyeing performance of the dyes on&#xD;
different fibres has also been assessed.&lt;/span&gt;
Page(s): 226-232</description>
    <dc:date>1991-09-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/32539">
    <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 of 3-aryl- and hetaryl-azo- 2-carbethoxy-4,6-dimethylthieno- [2,3-&lt;i&gt;b&lt;/i&gt;]pyridines and their application on polyester fibres as disperse dyes&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/32539</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 of 3-aryl- and hetaryl-azo- 2-carbethoxy-4,6-dimethylthieno- [2,3-&lt;i&gt;b&lt;/i&gt;]pyridines and their application on polyester fibres as disperse dyes&lt;/span&gt;
Authors: Rangnekar, D W; Kamat, P Y
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-chloro-3-cyano-4,6-dimethylpyridine&#xD;
obtained from 3-cyano-4,6-dimethyl-2-pyridone by treatment with phosphorus&#xD;
pentachloride in refluxing phosphorus oxychloride was reacted with ethyl&#xD;
thioglyocollate in refluxing methanol containing anhydrous sodium carbonate to&#xD;
get 3-amino-2-carbethoxy- 4,6-dimethylthieno[2,3-&lt;i&gt;b&lt;/i&gt;]pyridine.&#xD;
3-Amino-2-carbethoxy thieno[2,3-&lt;i&gt;b&lt;/i&gt;]pyridine derivative thus obtained was&#xD;
di.azotized and coupled with N,N-dialkylanilines and heterocyclic hydroxy&#xD;
couplers to result 3-aryl- and hetaryl-aw-2-carbethoxy-4,6-dimethylthieno[2,3-&lt;i&gt;b&lt;/i&gt;]pyridines.&#xD;
These azo dyes when applied on polyester fibres as disperse dyes gave yellow to&#xD;
red violet shades with excellent pick up, moderate light fastness and good to&#xD;
very good sublimation fastness.&lt;/span&gt;
Page(s): 223-225</description>
    <dc:date>1991-09-01T00:00:00Z</dc:date>
  </item>
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