• 한국정보디스플레이학회:학술대회논문집
• /
• 2006.08a
• /
• pp.838-841
• /
• 2006

Orientational alignment patterns proved that they are very useful for realizing diverse properties of liquid crystals. Here we tried to produce the patterns combining interfered laser light and double irradiations. A photo-isomerizable polymer doped with azo dye, which induce uniform liquid crystal alignment to the uniform laser irradiation, was used as the alignment layer. Double irradiations into two orthogonal directions brought the orientation patterns similar to the checkerboard. It indicates the possibility of bistability on those patterns.

• Proceedings of the Membrane Society of Korea Conference
• /
• 2005.11a
• /
• pp.281-284
• /
• 2005

• Proceedings of the Korean Society of Dyers and Finishers Conference
• /
• 2011.03a
• /
• pp.68-68
• /
• 2011

A new chemosensor based on rhodamine B (1) for $Hg^{2+}$ and $Cu^{2+}$ was synthesized by one-step condensation reaction of rhodamine B hydrazide and Azo dye. Studying for its fluorogenic and colorimetric behaviors towards various metal ions, extreme sensitivity and selectivity were achieved by the detection of $Hg^{2+}$ and $Cu^{2+}$ over other commonly coexistent metal ions, which were accompanied by ring opening of a rhodamine spirocycle framework. In acetonitrile, the presence of $Hg^{2+}$ and $Cu^{2+}$ induces the formation of a Dye 1-ion complex, which was deduced by spectroscopy.

• Journal of the Korean Society of Clothing and Textiles
• /
• v.13 no.4
• /
• pp.380-387
• /
• 1989

The Purpose of this study was to investigate the color changes of acid dyed wool fabrics after imparting permanent pleats with si-ro-set finish. Monoethanolamine sulfite was used as a reducing agent. Color changes were determined by measuring CIELAB values after treating the dyed fabrics with various setting temperatures, times and concentrations of MEAS. Setting temperature affected the color changes: in the order of $150^{\circ}C>130^{\circ}C>170^{\circ}C$ Setting time had a tendency to increase the color change. As the concentration of MEAS increased, $\delta$ E was increased. Azo dye was more affected than anthraquinone dye by MEAS treatment. Color changes were mainly due to $\delta$ L.

• Textile Coloration and Finishing
• /
• v.26 no.3
• /
• pp.165-172
• /
• 2014

Novel super hydrophobic orange dyes having maximum absorption band at 450-500nm were synthesized to dye polyolefin fibers such as polypropylene and ultra high molecular weight polyethylene fibers, using 4-alkylanilines and ${\beta}$-naphthol. Their absorption spectra at visible range showed almost the same, which meant that the alkyl substituents introduced to chromophore did not affect on color appearance of the dyes. Considering both color strength and wash fastness, the decyl-substituted dye was determined as the optimum one practically. From the dyeing results at various conditions, the optimum dyeing was $130^{\circ}C$ for 1 hour with 5% owf of dyes. The good fastness ratings to washing, rubbing were obtained showing 4-5 for both fibers. Light fastness was also acceptable giving rating 3-4 for polypropylene fibers and rating 3 for ultra high molecular weight polyethylene fibers.

• Textile Coloration and Finishing
• /
• v.13 no.4
• /
• pp.234-240
• /
• 2001

In order to improve the washing fastness of dyed polyester artificial suede fabric, it was dyed by using auto and anthraguinone type disperse dyes and treated with 3 different reduction clearing methods. The reduction clearing methods used in this study were normal alkaline reduction clearing, $N_2$ gas replacement method, and ultrasonic treatment during normal reduction clearing. The results were as followings ; The washing fastness property of dyed polyester artificial suede fabric was slightly improved by reduction clearing with $N_2$ gas replacement or with ultrasonic treatment comparing with normal alkaline reduction clearing. It was found that the use of $N_2$ gas replacement or ultrasonic treatment during reduction clearing eave effective removal of unfixed dyes on the fiber surface. We also obtained that the azo type disperse dye on polyester artificial fabric suede fabric showed higher wash fastness than anthraquinone type disperse dye.

• Advances in environmental research
• /
• v.5 no.3
• /
• pp.189-200
• /
• 2016

This study aimed at advanced oxidation of hetero tri-functional reactive dye Acid orange 7 using photo-Fenton conditions in a lab-scale experiment. Decolourisation of Acid Orange 7 dye by Fenton's process was dependent on concentration of Hydrogen peroxide, Ferrous sulphate, pH, and contact time. A $2^3$ factorial design was used to evaluate the effects of these key factors: pH, Fe(II), and $H_2O_2$ concentration, for a dye concentration of 50 mg/L with COD of 340 mg/L at pH 3.0. The response function was removal of colour under optimised conditions; pH 3.0, [Fe(II)] 40.83 mg/L, [$H_2O_2$] 4.97 mmol/L; 13.6 min. of treatment resulting in 100% colour removal. The final COD of treated wastewater was nil suggesting that AOP is a potentially useful process of color removal and dye degradation/mineralisation of effluent having AO7. Minimum contact time for complete decolourisation was at 5 mmol/l $H_2O_2$ concentration. Increase in $FeSO_4$ (mg/l) concentration resulted in decrease of time for complete decolourisation. Box-Behnken Design was used to optimize the process variables. Maximum and minimum levels of pH (3-5), $H_2O_2$ (4-6 mmol/l), $FeSO_4$ (30-46 mg/l) and contact time (5-15 minutes) were used. The statistical analysis revealed a value of 0.88 for coefficient of regression ($R^2$) indicating a good fit of model. Calculated F-value was found higher than the tabulated value confirming to significance of the model. Based on student's t-test, Ferrous sulphate, pH, and contact time have a positive effect on the percent decolourisation of Acid Orange 7.

• Journal of the Korean Chemical Society
• /
• v.28 no.6
• /
• pp.425-432
• /
• 1984

We obtained fast dyed polypropylene fiber, which has no functional group to be dyed, by producing a carbene on the dye molecule by the pyrolysis of lithium salt of dye molecule-tosylhydrazone, then the carbene simultaneously inserted into a C-H bond of polypropylene. To investigate the possibility of actual use in the industry, a variety of reactive azo dyes were prepared from aldehyde, acetophenone and benzophenone derivatives by changing reactive site of precursors which greatly affected properties of dyes. Reactive dyes of the benzophenone derivatives were excellent in the reaction with polypropylene, especially, a dye prepared from chloroaminobenzophenone with N,N-dimethyl aniline was found most excellent.

• Journal of the Korean Chemical Society
• /
• v.32 no.5
• /
• pp.443-451
• /
• 1988

New crown ether dye-Ⅰ and dye-Ⅱ having an azo group(-N=N-) were synthesized from monobenzo-15-crown-5 and dibenzo-18-crown-6. These dyes showed ${\lambda}_{max}$ of 377 and 383nm respectively. The complexes of alkali metal ions ($Na^+$, $K^+$, $Cs^+$) with dye ligands showed band shift (390~400nm) and intensity increased. For a given anion, the extraction constants are in the order of $K^+$ < $Cs^+$ < $Na^+$ for dye-Ⅰ and $Cs^+$ < $Na^+$ < $K^+$ for dye-Ⅱ. These results show that the selectivity of crown ethers toward the alkali metal ions is dependant on the charge density of cation and the size of crown ether cavity. For a given cation, the order of the extraction constant is $Cl^-$ < $Br^-$ < $I^-$ < picrate. This order coincides with the degree of anion solvation effect.

• YAKHAK HOEJI
• /
• v.40 no.2
• /
• pp.135-140
• /
• 1996

Ion-selective poly(vinyl chloride)(PVC) membrane electrodes for the determination of the calcium antagonist verapamil and its pharmaceutical preparations were described. Verapam il-superchrome garnet Y(SGY), lumogallion(LG), acid red 97(AR97), Dragendorff(DD) and Meyer reagent ion pairs were inverstigated as an electroactive compound for membrane electrode. Stable potentiometric response was obtained with azo dye at pH 6.5-4.0 and with DD, and Meyer reagent at pH 6.5-3.0. The best plasticizer was 49w/w% 2-nitrophenyl octyl ether for azo dye, and 65.3w/w% tri(n-butyl) citrate for DD and Meyer reagent. Potentiometric response slopes of optimized membrane electrodes based on SGY, LG, AR97, DD, and Meyer complex for verapamil were 52.49, 54.88, 50.81, 54.13 and 49.31 mV/dec., respectively. Lower limits of linear range were $1.0{\times}10^6M$ for SGY, LG, and AR97, while those for DD and Meyer reagent were $4{\times}10^{-6}M$. Detection limits for all these electrodes were $1{\times}10^{-5}M,\;4{\times}10^{-6}M,\;1.8{\times}10^{-6}M,\;8{\times}10^{-7}M,\;and\;1{\times}10^{-6}M$ with relative standard deviation of 2.56, 3.6, 3.96, 2.56, 3.20%, respectively.