• Title/Summary/Keyword: Azo disperse dyes

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Dyeability of Nylon Fabrics with Dyestuff for Supercritical Fluid Dyeing (1) : C.I. Disperse Red 167, C.I. Disperse Violet 93 (초임계 유체 염색용 염료에 따른 Nylon 섬유의 염색 특성 (1) : C.I. Disperse Red 167, C.I. Disperse Violet 93 Azo계 염료)

  • Choi, Hyunseuk;Park, Shin;Kim, Taeyoung
    • Textile Coloration and Finishing
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    • v.32 no.4
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    • pp.217-225
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    • 2020
  • In this study, the dyeing characteristics of nylon fabric which is dyed with supercritical fluid were investigated. There were two dyes used in the dyeing experiment: C.I. Disperse Red 167 and C.I. Disperse Violet 93. Dyeing temperature, pressure, and leveling time were fixed at 110℃, 250bar, 60minutes, and the experiment was conducted with dyeing concentration of 0.1, 0.3, 0.5, and 0.85% o.w.f. The analysis of the experimental results was found out through the measurement of washing fastness and color coordinate. In addition, the calibration curve of each dye was drawn up and the amount of remaining dye was checked by measuring the absorbance of the residual dye. As a result of color difference measurement, as the concentration increased, the L⁎ value decreased and the K/S value increased. However, the increase in K/S value compared to the amount of input decreased as the concentration increased. The comparative experiment on the amount of residual dye(C.I. Disperse Red 167) in the pot showed that 99.14% of the amount was dyed at the concentration of 0.1% o.w.f, while it rapidly decreased to 77% at 0.85% o.w.f. C.I. Disperse Violet 93 dye also decreased from 0.5% o.w.f to 93.91%. In the washing fastness experiment of both dyes, the level of washing fastness began to decrease from samples dyed at 0.5% o.w.f. It may be because the simply absorbed dye was produced instead of completely being fixed in the amorphous region of the nylon fiber.

Synthesis, Tautomeric Structure, Dyeing Characteristics, and Antimicrobial Activity of Novel 4-(2-Arylazophenyl)-3-(2-hydroxyphenyl)-1-phenyl-2-pyrazolin-5-ones

  • Metwally, M.A.;Bondock, S.A.;El-Desouky, S.I.;Abdou, M.M.
    • Journal of the Korean Chemical Society
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    • v.56 no.1
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    • pp.82-91
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    • 2012
  • Novel azopyrazolin-5-one dyes 4a-f were synthesized by the regioselective reaction of phenylhydrazine with 2,3,4-chromantrione-3-arylhydrazones 2a-f. The acid dissociation constants $pK_a$ for the series prepared were determined and correlated by the Hammett equation. The results of such correlation together with the spectral data indicated that the studied compounds exist predominantly in the hydrazone keto structure, (D) as the Z-configuration. The dyes were applied to polyester fabrics, affording orange-yellow shades and assessments of their dyeing performance are considered. Further, the compounds 4a-f were screened for their antimicrobial activity against various microorganisms.

Dispersant-free dyeing of polyester with temporarily solubilised azo disperse dyes from pyridone derivatives (피리돈계 일시적 수용성 아조 분산염료를 이용한 폴리에스테르 섬유의 염색)

  • 이정진;한남근;이원재;최재홍;김재필
    • Proceedings of the Korean Fiber Society Conference
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    • 2002.04a
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    • pp.143-146
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    • 2002
  • 폴리에스테르를 염색할 수 있는 분산염료는 비수용성이기 때문에 염색시 염욕 내에서 응집, 결정화되는 현상을 방지하기 위하여 반드시 분산제를 첨가하여야 한다. 그러나 분산제를 사용하더라도 분산염료를 염욕 내에서 완전한 분산상태로 만들 수 없으며, 염색시 여러 원인에 의해 염료의 재응집 현상이 발생될 수 있을 뿐만 아니라 최근 거론되고 있는 환경문제로 인하여 분산제의 사용이 제한될 가능성도 있다. (중략)

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Characterization of Diester functional-based Alkali-clearable Azo Disperse dyes (Diester계 치환기를 이용한 분산염료의 알칼리 영향성에 관한 연구)

  • Choe, Jong-Yun;Choe, Jae-Hong;Lee, Hyeon-Yeong;Gwon, O-Tak
    • Proceedings of the Korean Society of Dyers and Finishers Conference
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    • 2008.10a
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    • pp.25-26
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    • 2008
  • 일반적인 분산염료, Phthalimide계 중간체로 사용한 분삼염료, Diester계 커플러만 이용한 분산염료와 비교한 Diester계 치환기를 이용한 분산 염료들은 R/C조건과 EtOAc와 증류수로 층분리하여 증류수층의 UV-Vis absorbance은 떨어지고 용해성은 증가한다. 그리고 Thiopene ring만 가진 염료와 비교한 염료들은 같은 파장에서의 UV-Vis absorbance은 떨어져 용해도는 증가하고 Thiopene ring과 Azo group의 분해에 의한 화합물 때문에 단파장에서의 UV-Vis absorbance가 크게 증가하여 염색 폐수의 색도를 감소시킬 수 있다.

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Carrier Dyeing of Polyester Fabrics in Alkaline Dyebath (폴리에스테르직물의 알칼리욕에서의 Carrier염색)

  • 조은자;남성우;김인회
    • Textile Coloration and Finishing
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    • v.13 no.6
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    • pp.381-390
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    • 2001
  • The optimum carrier concentrations were obtained by the maxmium exhaustion ratios of polyester fabrics at 8$0^{\circ}C$ . The optimum concentrations of methylsalicylate, acetophenone, anisole, propiophenone, 2-ethyl hexyl alcohol, ethylene glycol and propylene glycol were $3g/\ell,\;12g/\ell,\;7g/\ell,\;5g/\ell,\;3g/\ell,\;35g/\ell,\;and\;40g/\ell$, respectively Azo, anthraquinone, and quinoline disperse dyes were quite stable up to PH 10.3, but nitro disperse dye were severely hydrolyzed in alkaline dyeing. The tensile strength decreased with increasing dyebath pH because the polyester fabrics were easily decomposed by alkali. The reduction cleaning could be canceled in alkaline dyeing because the carriers were solved by alkali during dyeing.

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Carrier Dyeing of Polyester Fabrics in Alkaline Dyebath (폴리에스테르직물의 알칼리욕에서의 Carrier염색)

  • Jo, Eun Ja;Nam, Seong U;Kim, In Hoe
    • Textile Coloration and Finishing
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    • v.13 no.6
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    • pp.23-23
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    • 2001
  • The optimum carrier concentrations were obtained by the maxmium exhaustion ratios of polyester fabrics at 80℃. The optimum concentrations of methylsalicylate, acetophenone, anisole, propiophenone, 2-ethyl hexyl alcohol, ethylene glycol and propylene glycol were 3g/ℓ, 12g/ℓ, 7g/ℓ, 5g/ℓ, 3g/ℓ, 35g/ℓ, and 40g/ℓ, respectively. Azo, anthraquinone, and quinoline disperse dyes were quite stable up to pH 10.3, but nitro disperse dye were severely hydrolyzed in alkaline dyeing. The tensile strength decreased with increasing dyebath pH because the polyester fabrics were easily decomposed by alkali. The reduction cleaning could be canceled in alkaline dyeing because the carriers were solved by alkali during dyeing.

Synthesis, Fastness and Spectral Properties of Some New Azo Pyrazole and Pyrazolotriazole Derivatives (Pyrazole과 Pyrazolotriazole 유도체의 합성 및 특성 연구)

  • Rizk, Hala F.;El-Badawi, Mahmoud A.;Ibrahim, Seham A.;El-Borai, Mohamed A.
    • Journal of the Korean Chemical Society
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    • v.54 no.6
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    • pp.737-743
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    • 2010
  • Coupling of 5-amino-1,3-diaryl-pyrazoles 1a-c with diazonium salts of different aryl amines gave a series of novel 1,3-diaryl-5-amino-4-arylazopyrazoles 3a-l. Such compounds could be also obtained by reaction of 5-amino-1,3-diaryl-4-nitroso- 1H-pyrazoles 2a-c with different aryl amines in alkaline medium. Oxidation of azo derivatives 3a-l with cupric acetate, in dimethyl formamide and stream of air, gave 2,4,6-triaryl-2,4-dihydropyrazolo [4,3-d]-1,2,3-triazoles 4a-l. and the fluorescence properties of the cyclic triazoles were studied. Diazotization of 5-amino-1,3-diaryl-1H-pyrazoles 1a-c by sodium nitrite in ortho-phosphoric acid followed by coupling with some aryl amines gave o-aminoazo compounds 5a-f. Cyclisation of compounds 5a-f in pyridine and cupric acetate gave the corresponding triazoles 6a-f. The coupling of compounds 6a-f with different aryl diazonium salts gave compounds 7a-j. The synthesized dyes were applied to polyesters as disperse dyes and the fastness properties were evaluated.

A Study on the Properties of Azo Disperse Dyes Containing Ethyleneimine Derivatives (III) - Application to Microfibre Polyester and Nylon 6.6 Fabrics - (에틸렌이민 유도체를 갖는 아조계 분산염료의 염색성에 관한 연구(III) - 폴리에스테르 및 나일론 6.6 극세사 섬유에의 응용 -)

  • Sunwoo, Kong Hyun;Burkinshaw, S M
    • Textile Coloration and Finishing
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    • v.8 no.6
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    • pp.9-26
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    • 1996
  • 이 연구의 목적은 에틸렌이민 유도체를 갖는 아조계 분산 염료의 나일론 6.6 섬유에의 응용과 최적화된 폴리에스테르 및 나이론 극세사 섬유 염색 조건의 확립이다. 세가지 아지리디닐 모노 아조 염료와 이들 염료의 가수분해 된 형태 그리고 디메틸아닐린계 아조 염료의 폴리에스테르 및 나일론 6.6 극세사 섬유에 대한 염색 및 견뢰도 성질이 조사되었다. 염색 조건 중 pH의 변화에 따른 섬유상의 염착량 변화 조사에서 뚜렷한 경향을 얻을 수 없었으며, 이는 극세사 섬유의 물리적 성질이 두드러지게 착용한 이유라 여겨진다. 염색된 폴리에스테르 극세사 섬유상에서, 아지리디닐 염료는 이들의 가수 분해된 형태 그리고 디메틸아닐린계 아조 염료의 비교하여 개선된 견뢰도 성질을 나타내었다. 아지리디닐 아조 염료의 나일론 극세사 섬유 염색 시 pH 증가에 따라 세탁 및 광견뢰도가 개선되었고, pH8의 염색 조건에서 최적 견뢰도 개선을 나타내었다. 아지리디닐 아조 염료가 이들 염료의 가수분해 된 형태 그리고 디메틸아닐린계 아조 염료와 비교하여 폴리에스테르 및 나일론 섬유상에서 보다 개선된 견뢰도 성질을 나타내었고 이는 섬유와 염료간의 공유 결합으로 기인한 것으로 여겨진다.

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