• Title/Summary/Keyword: azo dye

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Studies on the Transfer Printing of Cotton Fabrics (면직물의 건식전사날염에 관한 연구)

  • Hwang, Jong-Ho;Lee, Seok-Young;Cho, Hwan
    • Textile Coloration and Finishing
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    • v.7 no.3
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    • pp.31-37
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    • 1995
  • Effects of glycol pretreatment conditions such as concentration and molecular weight of glycols and dye types of different constitutions on the degree of transfer were investigated when transfer printed onto the cotton fabric with disperse dyestuffs. Obtained results are as follows ; 1. Although the degree of transfer increases linearly with temperature a time, above a certain critical point, they show decremental aspects for both of C.I. Disperse Orange 3 and C.I. Diperse Violet 1. 2. Degree of transfer increases with molecular weight of glycols, but PEG 200 which has a moleular weight 200 and boiling point of 300$^{\circ}C$ is more effcient than that of lower molecular weight. 3. Degree of tansfer for the C.I. Disperse Orange 3 having constitution of azo benzene type is somewhat higher than that of C.I. Disperse Violet 1 of amino anthraquinone.

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Development of Metal Complex Dyestuffs with High Fastness and High Adsorption (고견뢰도 및 고흡진율 특성의 금속 착염 염료의 개발)

  • Kim, Woon-Tai;Nam, Won-Woo;Sohn, Byoung-Chung
    • Journal of the Korean Applied Science and Technology
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    • v.12 no.2
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    • pp.115-120
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    • 1995
  • Diazotization of 2-Amino-5-nitrophenol was Synthesized by the direct diazotization method. The diazonium salts are usually stabilized in the from of double salts. The double salts of zinc chloride are the Commonest, and the double salt method is Specially applicable to the yield-up of coupling. The azo dye(2-naphthol-1-(2'-diazo-5'-nitrophenol)) is Converted into a chromium Complex by heating($100^{\circ}C$) with chromic formate, and DMF. The removal of inorganic salts from dyestuffs was performed in DMF solvent. This effect was more pronounced. From these results, It was obtained to liquid dyestuffs of metal complex with High fastness and high adsorption.

Effect of Molecular weight of Atactic Poly(vinyl alcohol) (PVA) on the Polarizing Efficiency of PVA/Azo Dye Polarizer (PVA/아조염료계 편광필름의 편광효율에 따른 혼성배열 폴리비닐알코올의 분자량 효과)

  • Park, Joo-Min;Kim, Sam-Soo;Lyoo, Won-Seok
    • Proceedings of the Korean Fiber Society Conference
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    • 2003.10b
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    • pp.104-107
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    • 2003
  • Poly(vinyl alcohol) (PVA) obtained by the saponification of poly(vinyl ester) like poly(vinyl acetate) o. poly(vinyl pivalate) is a linear semicrystalline polymer, which has been widely used as fibers for clothes and industries, films, membranes, medicines for drug delivery system, and cancer cell-killing embolic materials[1-3]. PVA fibers and films have high tensile and compressive strengths, high tensile modulus, and good abrasion resistance due to its highest crystalline lattice modulus. (omitted)

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Neodymium doped mixed metal oxide derived from CoAl-layered double hydroxide: Considerable enhancement in visible light photocatalytic activity

  • Khodam, Fatemeh;Amani-Ghadim, Hamid Reza;Aber, Soheil;Amani-Ghadim, Ali Reza;Ahadzadeh, Iraj
    • Journal of Industrial and Engineering Chemistry
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    • v.68
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    • pp.311-324
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    • 2018
  • Herein,the Neodymium ion ($Nd^{3+}$) doped CoAl-LDH have been successfully prepared via co-precipitation method and was used as a precursor of Nd-doped CoAl-mixed metal oxides (MMO). The photocatalytic activity of doped LDH and MMO was investigated in the degradation of an azo dye, C.I. Acid Red 14, under visible light irradiation. DRS and PL analysis demonstrated decreasing in the band gap energy and recombination of photo-induced charge carriers of Nd-doped LDH and MMO compared with the pristine CoAL-LDH. Due to significant difference in photocatalytic performance. A power law empirical kinetic model was obtained for predicting the photocatalytic degradation efficiency.

Decolorization of Acid Orange II from Aqueous Solutions using Loess (황토를 이용한 Acid Orange II의 색도제거)

  • Park, Jae Hong
    • Journal of Korean Society on Water Environment
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    • v.27 no.2
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    • pp.141-146
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    • 2011
  • Loess, a natural clay, was evaluated as an adsorbent for the decolorization of Acid Orange II, an azo and reactive dye, from aqueous solution. Adsorption studies were performed at $30^{\circ}C$ and the effect of reaction time, loess dosage, initial concentration, loess particle size, pH, agitation rate were investigated to determine the optimum operation conditions. The removal efficiencies of color were measured to evaluate the effectiveness of loess. From this study, it was found that optimal reaction time was 10 min. Color removal efficiencies of Acid Orange II were increased as higher loess dosage, initial concentration and agitation rate. However, color removal efficiencies decreased when pH is high and loess particle becomes large. Adsorption of Acid Orange II fitted to the pseudo-second-order rate kinetics more than first-order rate kinetics. Langmuir and Freundlich adsorption isotherm constants and correlation coefficients were calculated and compared. It was concluded that the adsorption data of Acid Orange II onto loess fitted to the Freundlich model more than Langmuir model.

A Study on the Determination of$N(NO_2^-),\;N(NO_3^-)$and$N(NH_4^+)$in Environmental Samples by Flow Injection Analysis (흐름주입분석법에 의한 환경시료 중$N(NO_2^-),\;N(NO_3^-)$$N(NH_4^+)$의 정량분석에 관한 연구)

  • Rhee, Jae Seong;Kim, Young Sang;Jung, Yun Hee;Rhee, Hee Jung
    • Journal of the Korean Chemical Society
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    • v.41 no.5
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    • pp.256-265
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    • 1997
  • A rapid and sequential method was studied, which can determine nitrite, nitrate and ammonium ion in soil or water samples with flow injection analysis. Geometric factors including injection volume, length of the reaction coil and flow rate of carrier solution were investigated prior to sample measurement. Nitrite was determined at 540 nm by Griess reaction producing azo dye between N-(1-naphthylethylenediamine dihydrochloride) and sulfanilamide. Nitrate was also measured under the help of reduction mechanism toward nitrite with hydrazine. Ammonium was analyzed at 440 nm with Nessler's reagent. At the optimum condition, the detection limit(S/N=3) has been shown 0.1 ㎍/mL N(NO2-), 0.4 ㎍/mL N(NO3-) and 0.3 ㎍/mL N(NH4+) respectively. The results measured by colorimetry, ion chromatography and FIA were compared showing 80%-125% reasonable match each other. Injection throughput rate could be performed better than 30 times per hour.

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Electrochemical Treatment of Dye Wastewater Using Fe, RuO2/Ti, PtO2/Ti, IrO2/Ti and Graphite Electrodes (RuO2/Ti, PtO2/Ti, IrO2/Ti 및 흑연전극을 이용한 염료폐수의 전기화학적 처리)

  • Kim, A Ram;Park, Hyun Jung;Won, Yong Sun;Lee, Tae Yoon;Lee, Jae Keun;Lim, Jun Heok
    • Clean Technology
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    • v.22 no.1
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    • pp.16-28
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    • 2016
  • Textile industry is considered as one of the most polluting sectors in terms of effluent composition and volume of discharge. It is well known that the effluents from textile dying industry contain not only chromatic substances but also large amounts of organic compounds and insolubles. The azo dyes generate huge amount of pollutions among many types of pigments. In general, the electrochemical treatments, separating colors and organic materials by oxidation and reduction on electrode surfaces, are regarded as simpler and faster processes for removal of pollutants compared to other wastewater treatments. In this paper the electrochemical degradation characteristics of dye wastewater containing CI Direct Blue 15 were analyzed. The experiments were performed with various anode materials, such as RuO2/Ti, PtO2/Ti, IrO2/Ti and graphite, with stainless steel for cathode. The optimal anode material was located by changing operating conditions like electrolyte concentration, current density, reaction temperature and initial pH. The degradation efficiency of dye wastewater increased in proportion to the electrolyte concentration and the current density for all anode materials, while the temperature effect was dependent on the kind. The performance orders of anode materials were RuO2/Ti > PtO2/Ti > IrO2/Ti > graphite in acid condition and RuO2/Ti > IrO2/Ti > PtO2/Ti > graphite in neutral and basic conditions. As a result, RuO2/Ti demonstrated the best performance as an anode material for the electrochemical treatment of dye wastewater.

Synthesis of magnetite iron pumice composite for heterogeneous Fenton-like oxidation of dyes

  • Cifci, Deniz Izlen;Meric, Sureyya
    • Advances in environmental research
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    • v.9 no.3
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    • pp.161-173
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    • 2020
  • The removal of two dyes, namely Methylene Blue (MB) and Reactive Brillant Red (RR) from aqueous solution was investigated using magnetite iron coated pumice (MIP) composite in the Fenton-like oxidation process. A weight ratio of 2.5 g (with the molar ratio of Fe3+ to Fe2+ to be 2) (5%) of iron to the total pumice (50 g) was enabled during synthesis of catalyst. Surface composition and characteristics of the catalyst were assessed by SEM-EDX, FT-IR, Raman spectral analysis. The effect of the amount of pumice solely used or MIP, H2O2 concentration, pH and initial concentration of MB or RR dyes on Fenton-like process efficiency was investigated. EDAX spectrums of pumice and MIP showed that oxygen and silisium are the major elements. The Fe content of MIP increased to 2.24%. SEM, FT-IR and Raman spectrums confirmed the impregnation of Fe on pumice surface. The experimental results revealed that high removal rates of dyes could be obtained using MIP that demonstrated a higher stability for removal of MB dye. pH affected the removal efficiency of both dyes and the degradation of both dyes was sharply dropped when pH was increased above 4. The removal of dyes did not significantly change with increasing H2O2 concentration. Degradation rates of both MB and RR dyes increased 3.3 and 2.8 times with the use of MIP compared to pumice alone, respectively. Furthermore, MIP enabled a good removal efficiency at higher dye concentrations. It can be emphasized that MIP composite can be used in the heterogeneous Fenton-like systems considering the economic and easily separation aspects.

Degradation of Chlorinated Phenolic Compounds by Soil Actinomycetes Isolated from the Contami-nated Soil Nearby the Kyung-An River (경안천 유역 오염토양에서 분리한 방선균의 염화 페놀계 화합물 분해)

  • 김성민;김창영;김응수
    • Microbiology and Biotechnology Letters
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    • v.30 no.3
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    • pp.287-292
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    • 2002
  • Lignin-peroxidase (LiP) has been considered as one of the most important industrial enzymes for biodegradation of various recalcitrant toxic compounds such as chlorinated aromatic hydrocarbons and azo-dyes. Recently, several soil actinomycetes have been reported to secrete a functionally-similar lignin-peroxidase called actinomycetes lig-nin-peroxidase (ALiP). In this manuscript, we isolated over 100 morphologically distinct actinomycetes from the contaminated soils around 10 different gas stations located nearby the Kyung-An river. Among these actinomycetes screened based on the congo-red dye-decolorization activities, one newly-isolated actinomycetes named SMA-2 showed the most significant dye-decoloring activity on the congo-red plate as well as a significant ALiP activity in a yeast-extract-malt-extract liquid media supplemented with starch. The optimum SMA-2 culture condition fur ALiP production was determined and the kinetic parameters fur the SMA-2 AkIP activity were characterized. The optimally-cultured SMA-2 also exhibited the oxidation activities toward various recalcitrant aromatic compounds including phenol, 2- chlorophenol, 4- chlorophenol, 2,4- dichlorophenol ,2,6- dichlorophenol, and 2,4, f-trichlorophe - not, suggesting a potential application of SMA-2 for contaminated soil bioremediation.