• Textile Coloration and Finishing
• /
• v.7 no.3
• /
• pp.53-59
• /
• 1995

In foam dyebath assisted with and without solvent (iso-propylacohol) for polyester and polyester(30%)/nylon(70%) (P3/N7) nonwoven fabrics, adsorption behavior of polyester and P3/N7 nonwovens dyed with C.I. Disperse Red 4 (Red 4), C.I. Acid Violet 54(Violet 54) and Red 4/Violet 54 were investigated by determining the K/S value. The K/S values of polyester and P3/N7 nonwovens in the foam dyeing was greatly enchanced by adding the iso-propylalcohol, but these values were not higher than the carrier dyeing. Dyeabilities of polyester/nylon blended nonwoven fabrics to Red 4, Violet 54 and Red 4/Violet 54 in the foam dyeing were influenced by the affinity of dye to fiber.

• 한국전산유체공학회:학술대회논문집
• /
• 2008.03b
• /
• pp.92-95
• /
• 2008

We performed the theoretical calculation of CN Violet radiation using the code SPRADIAN07 to predict the Lee et al.'s experimental measurements and to reinvestigate $C_2$ dissociation rate. CN Violet radiations are calculated under the Boltzmann and non-Boltzmann distribution using two chemical reaction sets: Park-Losev-G\"{o}kcen-Tsang and Park-Losev-G\"{o}kcen-Tsang-Lee models. Our SPRADIAN07 calculations show improvement in prediction of absolute radiation intensity of CN Violet and its decay rate by Park-Losev-G\"{o}kcen-Tsang reaction set with $C_2$ dissociation rate coefficient of $k_f$ = 1.5${\times}$10$^{16}$ exp(-71,600/$T_x$) cm$^3$ mole$^{-1}$ s$^{-1}$.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
• /
• v.20 no.4
• /
• pp.318-324
• /
• 2007

We report on a strong violet luminescence emitted from the ZnO:Al films grown on glass substrate by radio-frequency magnetron sputtering. The growth of high-quality thin films and their optical properties are controlled by adjusting the mixture ratio of Ar and $O_2$, which is used as the sputtering gas. The crystallinity of the films is improved as the oxygen flow ratio is decreased, as evidenced in both x-ray diffractometer and atomic force microscope measurements. As for the violet luminescence measured by photoluminescence (PL) spectroscopy, the peak energy and intensity of the PL signal are decreased with increasing the oxygen flow ratio. The peak energy of the violet PL spectrum for the thin film with an oxygen flow ratio of 50 % is almost constant, regardless of the increase of laser Power and temperature. These results indicate that the violet PL signal is probably due to defects related to interstitial Zn atoms.

• Bulletin of the Korean Chemical Society
• /
• v.22 no.1
• /
• pp.84-86
• /
• 2001

• Journal of Life Science
• /
• v.10 no.4
• /
• pp.333-339
• /
• 2000

To identify genes involved in the decolorization of crystal violet, we isolated random mutants generated by transponson insertion in crystal violet-declorizing bacterium, Citrobacter sp. The resulting mutant bank yielded mutants with six distinct phenotypes, and Southern hybridization with a Tn5 fragment as a probe showed a single hybridized with six distinct phenotypes, and Southern hybridization with a Tn5 fragment as a probe showed a single hybridized band in the mutants Ctg 2, 5 an 6, whereas two and three bands were detected in Ctg1, 4 and 3, respectively. Tn5-inserted genes were isolated and the DNA sequence flanking Tn5 was determined. From comparison with a sequence database, putative protein product encoded by ctg 5 was identified as E. coli maltose transproter(Mal G) homolog, whereas the deduced amino acid sequence of the other ctg genes did not show any significant similarity with any DNA or protein sequency. Therefore, these results indicate that the other ctg genes except ctg 5 encode new proteins responsible for decolorization of crystal violet.

• Journal of the Korean Electrochemical Society
• /
• v.7 no.1
• /
• pp.9-15
• /
• 2004

Cyclic voltammetry and chronocoulometry have been used for characterization of catechol violet (CV) at the hanging mercury drop electrode in acetic acid-sodium acetate buffer solution. At pH 2.94 a nearly symmetric cyclic voltammetric wave due to an irreversible weak adsorption of CV on mercury was obtained at concentration of $0.53{\mu}mol\;dm ^{-3}$. Under these conditions, CV adsorbes in a monolayer. Upon increasing the concentration, the symmetry of the wave decreases; it can be attributed to a mixed diffusion adsorption process. The amount of the adsorbed catechol violet on the HMDE expressed as surface concentration as well as the surface areaf occupied by one molecule$(\sigma)$ were calculated. It was found that the values obtained for f and o utilizing cyclic voltammetric and chrono-coulometry are almost identical. A 1:1 and 1:2 Th (IV)-CV complexes are formed on addition of thorium (IV) to catechol violet. These complexes are adsorbed and reduced on the HMDE at more negative potentials than the peak potential of free CV, Using the square-wave (SW) technique, the adsorptive cathodic stripping voltammetry, ACSV, of these complexes was studied. It was found that the SW-ACSV of Th(IV)-CV can be applied to the determination of thorium at the nanomole level. Optimum conditions and the analytical method of determination were presented and discussed.

• Bulletin of the Korean Chemical Society
• /
• v.10 no.4
• /
• pp.357-359
• /
• 1989

The ion aggregates formed between cationic triphenylmethane dyes and tetraphenylborate(TPB) or tetrakis(4-fluorophenyl) borate (TFB) anions have been investigated spectroscopically. The photometric sensitivities of the dyes are found to be increasing in the order pararosaniline < malachite green < methyl violet 2B < crystal violet < ethyl violet. Cetyltrimethylammonium bromide(CTAB) and Triton X-100(TX-100) destroy the ion aggregates. By comparing the concentration of surfactant beyond which dye-borate mixed solutions behave identically with the dye blank, the order of hydrophobicity appears to be parallel with that of photometric sensitivity.

• The Korean Journal of Ecology
• /
• v.16 no.1
• /
• pp.51-61
• /
• 1993

Crystal violet, a typical triphenylmenthane dye (N, N, N', N', N", N"-hexa methylparaosaniline), extensively used in textile dye, industry and research, has been suggested to cause tumor growth in botton-feeding fishes. For the isolation of crystal violet degrading bacteria, wastewaters were sampled from plants' wastewater treatment facility, textile treatment facility, textile wastewater treatment plant and etc.. The most efficient strain in crystal violet degrading bacteria was identified as Klebsiella oxytoca. Added sole carbon source in PAS minimal media was 10mg/l crystal violet, which incubated at 30。C, the degrading efficiency was maximum 12.3%. When fructose, glucose, sucrose and yeast-extract were added 0.01% in PAS media respectively, the degrading efficiency were all 96% within 24 hours.

• Korean Journal of Materials Research
• /
• v.16 no.3
• /
• pp.145-150
• /
• 2006

Various colors of light emitting diodes(LED) and four-band white light sources are obtained using a violet LED and various phosphor films. $BaMg_2Al_{16}O_{27}:Eu\;(blue),\;SrGa_2S_4:Eu\;(green),\;and\;Eu(TTA)_3(PTA)$ (red) phosphors are dispersed in poly-vinyl-alcohol aqueous solutions, and phosphor films are prepared by coating the suspensions to PET film. The narrow band emission of $Eu(TTA)_3(PTA)$ phosphor has excellent red luminescent property for four-band white light excited by the violet LED.

• The Korean Journal of Ceramics
• /
• v.4 no.1
• /
• pp.28-32
• /
• 1998

This paper reports on photoluminescence (PL), luminescence decay curves, and compositional analysis of porous silicon(PS) which is aged under air ambient by Fourier transform infrared vibrational spectroscopy (FTIR) and by Auger electron spectroscopy (AES). Porous silicos which has been aged under air ambient yields two PL band structures, i.e. blue/violet PL and red PL. The evolution of a blue/violet band is pronounced, especially for thin PS film which is prepared in dilute HF solution. The blue/violet PL band has been observed initially to increrase rapidly with aging, then saturated with further atmospheric aging. The ambient air aged PS exhibits a fast decay time of sub-nanosecond at room temperature and shows appreciably faster decay time than that at 20K. Atmospheric aging of this thin blue/violet luminescing PS yield non-stoichiometric oxide judging from the vibrational spectra of Si-O and AES analysis.