<?xml version="1.0" encoding="UTF-8"?>
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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31707" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/31707</id>
  <updated>2026-10-11T10:12:22Z</updated>
  <dc:date>2026-10-11T10:12:22Z</dc:date>
  <entry>
    <title>Syntheses and dyeing characteristics of arylene bisazo 3-aminophenols and their polycondensates with formaldehyde</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/32310" />
    <author>
      <name>Patel, H S</name>
    </author>
    <author>
      <name>Prajapati, M D</name>
    </author>
    <author>
      <name>Shah, S N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/32310</id>
    <updated>2016-07-20T05:31:36Z</updated>
    <published>1995-06-01T00:00:00Z</published>
    <summary type="text">Title: Syntheses and dyeing characteristics of arylene bisazo 3-aminophenols and their polycondensates with formaldehyde
Authors: Patel, H S; Prajapati, M D; Shah, S N
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;Five&#xD;
arylene bisazo 3-aminophenols &lt;b&gt;(IVa-e)&lt;/b&gt; and their corresponding&#xD;
polycondensates with formaldehyde &lt;b&gt;(Va-e)&lt;/b&gt; were prepared and their dyeing&#xD;
performance on nylon and polyester was assessed. The compounds &lt;b&gt;IVa-e&lt;/b&gt; and&#xD;
&lt;b&gt;Va-e&lt;/b&gt; gave yellow, orange, red and brown shades with moderate to good&#xD;
light and wash fastness on nylon and polyester. The polymerization of &lt;b&gt;IVa-e&lt;/b&gt;&#xD;
with formaldehyde on dyed nylon and polyester was also carried out and the&#xD;
dyeing properties of polymerized compounds compared with those of the polymeric&#xD;
compounds &lt;b&gt;Va-e&lt;/b&gt;.&lt;/span&gt;
Page(s): 112-114</summary>
    <dc:date>1995-06-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <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;Syntheses of 3-aryl-5-[2'-(&lt;i&gt;α&lt;/i&gt;-pyridophthalonyl)]rhodanines and their dyeing performance on acetate and/or other fibres&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/32309" />
    <author>
      <name>Fadda, A A</name>
    </author>
    <author>
      <name>Aly, M M</name>
    </author>
    <author>
      <name>Etman, H A</name>
    </author>
    <author>
      <name>Fouda, A</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/32309</id>
    <updated>2016-07-20T05:29:29Z</updated>
    <published>1995-06-01T00:00:00Z</published>
    <summary type="text">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;Syntheses of 3-aryl-5-[2'-(&lt;i&gt;α&lt;/i&gt;-pyridophthalonyl)]rhodanines and their dyeing performance on acetate and/or other fibres&lt;/span&gt;
Authors: Fadda, A A; Aly, M M; Etman, H A; Fouda, 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;="" color:black;mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:="" ar-sa"=""&gt;3-Aryl-5-[2'-(&lt;i&gt;α&lt;/i&gt;-pyridophthalonyl)]rhodanines &lt;b&gt;&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;color:#080808;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;(&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;color:black;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;IVa-e)&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&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;color:black;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;&#xD;
were prepared by the treatment of 2-(2'-pyridyl N-oxide)indan-1,3-dione &lt;b&gt;(II)&lt;/b&gt;&#xD;
with different arylrhodanines &lt;b&gt;(IIIa-e)&lt;/b&gt; at 90°C in presence of acetic&#xD;
anhydride and their dyeing performance on polyester, polyacrylic and wool&#xD;
fibres was assessed. The effect of nature and orientation of substituents on&#xD;
the colour of these compounds was also studied. All the compounds showed good&#xD;
affinity towards wool fibres and have no affinity towards polyester and poly&#xD;
acrylic fibre&lt;span style="font-size:11.0pt;line-height:115%;font-family:&#xD;
" 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:#080808;mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:="" ar-sa"=""&gt;s&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;color:black;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 108-111</summary>
    <dc:date>1995-06-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Ambient temperature bleaching of jute fibre using hydrogen peroxide</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/32308" />
    <author>
      <name>Pandey, S N</name>
    </author>
    <author>
      <name>Chattopadhyay, S N</name>
    </author>
    <author>
      <name>Basu, G</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/32308</id>
    <updated>2016-07-20T05:27:55Z</updated>
    <published>1995-06-01T00:00:00Z</published>
    <summary type="text">Title: Ambient temperature bleaching of jute fibre using hydrogen peroxide
Authors: Pandey, S N; Chattopadhyay, S N; Basu, G
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;
possibility of bleaching jute fibre at ambient temperature has been explored&#xD;
using sodium persulphate as peroxygen booster. Different combinations of the&#xD;
concentrations of hydrogen peroxide, sodium hydroxide, sodium silicate and&#xD;
sodium persulphate were used by utilizing the technique of central composite&#xD;
rotatable plan (CCRP). Analysis of regression coefficients and contour diagrams&#xD;
revealed that the whiteness increases with the increase in concentration of&#xD;
hydrogen peroxide up to a certain limit and then decreases. Individual effect&#xD;
of sodium silicate and sodium persulphate on whiteness is marginal but their&#xD;
interaction with sodium hydroxide has considerable positive effect The process&#xD;
needs minimum concentration of sodium hydroxide as its individual effect on&#xD;
whiteness is negative. The overall effect of the variables on bundle strength&#xD;
is not much significant A recipe using 90 gpl of hydrogen peroxide, 25 gpl of&#xD;
sodium hydroxide, 20 gpl of sodium silicate and 7.5 gpl of sodium persulphate&#xD;
is suggested to obtain an acceptable level of whiteness without affecting the&#xD;
bundle strength of the fibre.&lt;/span&gt;
Page(s): 102-107</summary>
    <dc:date>1995-06-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Utilization of carboxymethyl guaran derivatives in printing cotton fabrics with reactive dyes</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/32307" />
    <author>
      <name>Ragheb, A A</name>
    </author>
    <author>
      <name>Kamel, M</name>
    </author>
    <author>
      <name>El-Thalouth, I Abd</name>
    </author>
    <author>
      <name>Nassar, S H</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/32307</id>
    <updated>2016-07-20T05:25:30Z</updated>
    <published>1995-06-01T00:00:00Z</published>
    <summary type="text">Title: Utilization of carboxymethyl guaran derivatives in printing cotton fabrics with reactive dyes
Authors: Ragheb, A A; Kamel, M; El-Thalouth, I Abd; Nassar, S H
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;
suitability of carboxymethyl guaran derivatives as thickeners in printing of&#xD;
cotton fabrics with reactive dyes has been studied. It is observed that the&#xD;
colour strength of the printed fabrics depends upon the nature of the thickener&#xD;
used, time allowed before printing, means of colour fixation and the nature of&#xD;
the reactive dye used. Cotton fabrics printed using carboxymethyl guaran of DS&#xD;
1.27 or more have soft handle and exhibit overall fastness properties nearly&#xD;
identical to those of the fabrics printed using sodium alginate. Cotton fabrics&#xD;
printed using Carboxymethyl guaran of low DS (0.77) acquire higher &lt;i&gt;K/&lt;/i&gt;S&#xD;
but their handle is harsh. The stability of the printing pastes on storing has&#xD;
also been investigated.&lt;/span&gt;
Page(s): 97-101</summary>
    <dc:date>1995-06-01T00:00:00Z</dc:date>
  </entry>
</feed>

