Metal-enhanced fluorescence of mixed coumarin dyes by silver and gold nanoparticles: Towards plasmonic thin-film luminescent solar concentrator

Energy Technology Data Exchange (ETDEWEB)

El-Bashir, S.M., E-mail: elbashireg@yahoo.com [Department of Physics and Astronomy, Science College, King Saud University, Riyadh, KSA (Saudi Arabia); Department of Physics Faculty of Science, Benha University (Egypt); Barakat, F.M.; AlSalhi, M.S. [Department of Physics and Astronomy, Science College, King Saud University, Riyadh, KSA (Saudi Arabia)

2013-11-15

Poly(methyl methacrylate) (PMMA) nanocomposite films doped with mixed coumarin dyestuffs and noble metal nanoparticles (60 nm silver and 100 nm gold) were prepared by spin coating technique. The effect of silver and gold nanoparticles on the film properties was studied by Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), transmission electron microscopy (TEM), scanning electron microscopy (SEM), UV–vis absorption and fluorescence spectroscopy measurements. DSC measurements indicated the increase of the glass transition temperature of the films by increasing nanogold concentration, recommending their promising thermal stability towards hot climates. It was found that the fluorescence signals of the mixed coumarin dyes were amplified by 5.4 and 7.15 folds as a result of metal enhanced fluorescence (MEF). The research outcomes offered a potential application of these films in solar energy conversion by plasmonic thin film luminescent solar concentrator (PTLSC). -- Graphical abstract: Plasmonic thin film luminescent solar concentrators. Highlights: • Metal enhanced fluorescence was achieved for mixed coumarin dyes doped in PMMA nanocomposite films. • The amplification of the fluorescence signals is dependent on the concentration of silver and gold nanoparticles. • These films is considered as potential candidates for plasmonic thin film luminescent solar concentrators (PTLSCs)

Determination of plasma albumin concentration in healthy and diseased turtles: a comparison of protein electrophoresis and the bromcresol green dye-binding method.

Science.gov (United States)

Müller, Kerstin; Brunnberg, Leo

2010-03-01

In reptile medicine, plasma chemistry analysis is widely used for the evaluation of an individual's health status. The standard method for the determination of plasma albumin concentration is protein electrophoresis combined with the determination of total protein concentration, but the bromcresol green (BCG) dye-binding method is also used. The reliability of the BCG method for the measurement of albumin concentration in reptiles is unknown. The aim of this study was to compare the plasma albumin values of turtles obtained by protein electrophoresis and the BCG method. Between March 2008 and September 2008, heparinized plasma samples from 16 clinically healthy and 10 diseased turtles of different species were collected. Plasma albumin concentrations were measured by protein electrophoresis and by the BCG method. The results of the 2 methods were compared using Passing-Bablok regression and Bland-Altman plots. Albumin concentration measured by BCG was weakly correlated with the corresponding protein electrophoretic values in all turtles (r(s)=.610, Palbumin concentration measured with the 2 different methods differed significantly in all turtles (P=.009; Wilcoxon's test) and in healthy turtles (P=.005) but not in diseased animals (P=.241). In the Bland-Altman plot a systematic error was found between the 2 methods in diseased turtles. Measurement of albumin by the BCG dye-binding method may lead to inaccurate results for plasma albumin concentration, especially in ill turtles. Therefore, for health assessment in turtles, albumin should be measured by protein electrophoresis.

''Stenungsund-77'': smoke plume measurements with a pulsed dye laser

Energy Technology Data Exchange (ETDEWEB)

Gustafsson, G; Hartmann, B; Spangstedt, G; Steinvall, O

1977-12-01

This report describes some of the results obtained in a field experiment at Stenungsund in May 1977, under the support and coordination of the Swedish Space Corporation. We made lidar measurements with a pulsed tunable dye laser working at wavelengths in the uv and visible part of the spectrum. The study concerned SO/sub 2/-absorption, NO/sub 2/-absorption, and particle scattering in the smoke plume of an oil fuel electric power plant. The SO/sub 2/-burden in the plume, near the smoke stack exit, as estimated from our lidar measurements, is compatible with in situ measurements and calculated values. The NO/sub 2/-concentration proved to be lower than the sensitivity limit of our lidar system. The particle scattering experiments led to qualitative results, and only permitted order of magnitude estimates of particle concentrations. They show, however, that a low power, eye safe uv lidar was capable of tracking plumes undiscernible to the eye, out to a distance of 2 to 3 km.

Study the effect of dye concentration on optical history using circular polarization holographic grating in thin polymeric film

International Nuclear Information System (INIS)

Mohajerani, E.; Hosain Nataj, N.

2006-01-01

By studying the effect of dye concentration, we obtained the optimal dye concentration for recording holographic gratings. The history of circular polarization grating is also investigated. We built polarization holographic grating with more than 2 weeks history. By using a mask in front of pump beam, different pictures could be built up in the film.

KINETIC BEHAVIOR OF SOME AZO DYES DECOLORIZATION BY VARIATION OF ZINC OXIDE AND TITANIUM DIOXIDE CONCENTRATIONS

Directory of Open Access Journals (Sweden)

Wallace J. C. da Silva

Full Text Available The decolorization of three monoazo dyes (acid orange 7, direct orange 34, and methyl orange, one diazo dye (direct yellow 86 and one tetraazo dye (direct red 80 were mediated by n-type semiconductors as ZnO and TiO2 under pseudo-first order conditions at 30 ºC. The decolorization rate constants of these azo dyes were determined, varying the semiconductor concentration for the majority of them from 1.0 to 10.0 g L-1. In general, the highest rate constants were displayed for ZnO. This work elucidates that the decolorization capacity depends on the charge, structure, and adsorption of the azo dye on the semiconductor surface as well as the agglomeration of the photocatalyst particles.

Modified dynamical equation for dye doped nematic liquid crystals

Energy Technology Data Exchange (ETDEWEB)

Manohar, Rajiv, E-mail: rajlu1@rediffmail.co [Liquid Crystal Research Lab, Physics Department, University of Lucknow, Lucknow 226007 (India); Misra, Abhishek Kumar; Srivastava, Abhishek Kumar [Liquid Crystal Research Lab, Physics Department, University of Lucknow, Lucknow 226007 (India)

2010-04-15

Dye doped liquid crystals show changed dielectric properties in comparison to pure liquid crystals. These changes are strongly dependent on the concentration of dye. In the present work we have measured dielectric properties of standard nematic liquid crystals E-24 and its two guest host mixtures of different concentrations with Anthraquinone dye D5. The experimental results are fitted using linear response and in the light of this we have proposed some modifications in the dynamical equation for the nematic liquid crystals by introducing two new variables as dye concentration coefficients. The limitations of the proposed equation in high temperature range have also been discussed. With the help of the proposed dynamical equation for the guest-host liquid crystals (GHLCs) it is possible to predict the various parameters like rotational viscosity, dielectric anisotropy and relaxation time for GHLCs at other concentrations of dye in liquid crystals theoretically.

Dyes assay for measuring physicochemical parameters.

Science.gov (United States)

Moczko, Ewa; Meglinski, Igor V; Bessant, Conrad; Piletsky, Sergey A

2009-03-15

A combination of selective fluorescent dyes has been developed for simultaneous quantitative measurements of several physicochemical parameters. The operating principle of the assay is similar to electronic nose and tongue systems, which combine nonspecific or semispecific elements for the determination of diverse analytes and chemometric techniques for multivariate data analysis. The analytical capability of the proposed mixture is engendered by changes in fluorescence signal in response to changes in environment such as pH, temperature, ionic strength, and presence of oxygen. The signal is detected by a three-dimensional spectrofluorimeter, and the acquired data are processed using an artificial neural network (ANN) for multivariate calibration. The fluorescence spectrum of a solution of selected dyes allows discreet reading of emission maxima of all dyes composing the mixture. The variations in peaks intensities caused by environmental changes provide distinctive fluorescence patterns which can be handled in the same way as the signals collected from nose/tongue electrochemical or piezoelectric devices. This optical system opens possibilities for rapid, inexpensive, real-time detection of a multitude of physicochemical parameters and analytes of complex samples.

Tunable Microfluidic Dye Laser

DEFF Research Database (Denmark)

Olsen, Brian Bilenberg; Helbo, Bjarne; Kutter, Jörg Peter

2003-01-01

We present a tunable microfluidic dye laser fabricated in SU-8. The tunability is enabled by integrating a microfluidic diffusion mixer with an existing microfluidic dye laser design by Helbo et al. By controlling the relative flows in the mixer between a dye solution and a solvent......, the concentration of dye in the laser cavity can be adjusted, allowing the wavelength to be tuned. Wavelength tuning controlled by the dye concentration was demonstrated with macroscopic dye lasers already in 1971, but this principle only becomes practically applicable by the use of microfluidic mixing...

White-rot fungus Ganoderma sp.En3 had a strong ability to decolorize and tolerate the anthraquinone, indigo and triphenylmethane dye with high concentrations.

Science.gov (United States)

Lu, Ruoying; Ma, Li; He, Feng; Yu, Dong; Fan, Ruozhi; Zhang, Yangming; Long, Zheping; Zhang, Xiaoyu; Yang, Yang

2016-03-01

The ability of the white-rot fungus Ganoderma sp.En3 to decolorize different kinds of dyes widely applied in the textile and dyeing industry, including the anthraquinone dye Remazol Brilliant Blue R (RBBR), indigo dye indigo carmine and triphenylmethane dye methyl green, was evaluated in this study. Ganoderma sp.En3 had a strong capability of decolorizing high concentrations of RBBR, indigo carmine and methyl green. Obvious reduction of Chemical Oxygen Demand was observed after decolorization of different dyes. Ganoderma sp.En3 had a strong ability to tolerate RBBR, indigo carmine and methyl green with high concentrations. High concentrations of RBBR, indigo carmine and methyl green could also be efficiently decolorized by the crude enzyme of Ganoderma sp.En3. Different redox mediators such as syringaldehyde, acetosyringone and acetovanillone could enhance the decolorization capability for higher concentration of indigo carmine and methyl green. Different metal ions had little effect on the ability of the crude enzyme to decolorize indigo carmine and methyl green. Our study suggested that Ganoderma sp.En3 had a strong capability for decolorizing and tolerating high concentrations of different types of dyes such as RBBR, indigo carmine and methyl green.

Long Distance Enhancement of Nonlinear Optical Properties Using Low Concentration of Plasmonic Nanostructures in Dye Doped Monolithic SolGel Materials (Postprint)

Science.gov (United States)

2016-05-31

Incorporation of effi cient nonlinear dyes into a solid matrix at high concentration is a real challenge. This has been achieved through the sol...NIR Lambda 750 spectrometer. The nonlinear absorption measurements at 532 and 600 nm were made with the same method and on the same occasion as for

Study of radon, thoron and toxic elements in some textile dyes

International Nuclear Information System (INIS)

Abel-Ghany, H.A.

2013-01-01

Elemental analysis of textile dyes may provide valuable information concerning the content and concentrations of element, especially the toxic ones. Such information monitors the safety of handling and using these dyes in textile industry. In addition to the safety of wearing of clothes stained with these dyes. In the present work, the specific activity of both radon and thoron were measured in nine textile dyes by using alpha emitters registration which are emitted from radon and thoron gases in CR-39 nuclear track detectors. Unexpectedly, the results obtained reports a high concentration of both radon and thoron gases in some samples (samples D5 and D9). Also the concentration of toxic elements (Cu, Pb, Zn, Mn, Cd and Cr) in textile dyes were determined by flame and graphite furnace atomic absorption spectrometry. (author)

Investigation of hair dye deposition, hair color loss, and hair damage during multiple oxidative dyeing and shampooing cycles.

Science.gov (United States)

Zhang, Guojin; McMullen, Roger L; Kulcsar, Lidia

2016-01-01

Color fastness is a major concern for consumers and manufacturers of oxidative hair dye products. Hair dye loss results from multiple wash cycles in which the hair dye is dissolved by water and leaches from the hair shaft. In this study, we carried out a series of measurements to help us better understand the kinetics of the leaching process and pathways associated with its escape from the fiber. Hair dye leaching kinetics was measured by suspending hair in a dissolution apparatus and monitoring the dye concentration in solution (leached dye) with an ultraviolet-visible spectrophotometer. The physical state of dye deposited in hair fibers was evaluated by a reflectance light microscopy technique, based on image stacking, allowing enhanced depth of field imaging. The dye distribution within the fiber was monitored by infrared spectroscopic imaging of hair fiber cross sections. Damage to the ultrafine structure of the hair cuticle (surface, endocuticle, and cell membrane complex) and cortex (cell membrane complex) was determined in hair cross sections and on the hair fiber surface with atomic force microscopy. Using differential scanning calorimetry, we investigated how consecutive coloring and leaching processes affect the internal proteins of hair. Further, to probe the surface properties of hair we utilized contact angle measurements. This study was conducted on both pigmented and nonpigmented hair to gain insight into the influence of melanin on the hair dye deposition and leaching processes. Both types of hair were colored utilizing a commercial oxidative hair dye product based on pyrazole chemistry.

Immune responses to hair dyes containing toluene-2,5-diamine

DEFF Research Database (Denmark)

Schmidt, J D; Johansen, J D; Nielsen, M M

2014-01-01

BACKGROUND: Toluene-2,5-diamine (PTD) is the most frequently used dye in oxidative hair dyes on the Scandinavian market. However, little is known about immune responses to PTD-containing oxidative hair dyes. OBJECTIVES: To study immune responses induced by PTD-containing hair dyes in mice. METHODS......: Immune responses against two different permanent hair dye products containing 1·60% (w/w) and 0·48% (w/w) PTD within the colour gel, and various concentrations of pure PTD were studied. The local inflammatory response was measured by ear swelling and cell infiltration, and T- and B-cell infiltration...... and proliferation was determined in the draining lymph nodes. RESULTS: Concentration-dependent immune responses were seen to PTD both in the skin and draining lymph nodes. The hair dye containing 1·60% PTD induced strong local inflammation and caused T- and B-cell infiltration and proliferation as well...

Simulation and measurement of complete dye sensitised solar cells: including the influence of trapping, electrolyte, oxidised dyes and light intensity on steady state and transient device behaviour.

Science.gov (United States)

Barnes, Piers R F; Anderson, Assaf Y; Durrant, James R; O'Regan, Brian C

2011-04-07

A numerical model of the dye sensitised solar cell (DSSC) is used to assess the importance of different loss pathways under various operational conditions. Based on our current understanding, the simulation describes the processes of injection, regeneration, recombination and transport of electrons, oxidised dye molecules and electrolyte within complete devices to give both time dependent and independent descriptions of performance. The results indicate that the flux of electrons lost from the nanocrystalline TiO(2) film is typically at least twice as large under conditions equivalent to 1 sun relative to dark conditions at matched TiO(2) charge concentration. This is in agreement with experimental observations (Barnes et al. Phys. Chem. Chem. Phys. [DOI: 10.1039/c0cp01855d]). The simulated difference in recombination flux is shown to be due to variation in the concentration profile of electron accepting species in the TiO(2) pores between light and dark conditions and to recombination to oxidised dyes in the light. The model is able to easily incorporate non-ideal behaviour of a cell such as the variation of open circuit potential with light intensity and non-first order recombination of conduction band electrons. The time dependent simulations, described by the multiple trapping model of electron transport and recombination, show good agreement with both small and large transient photocurrent and photovoltage measurements at open circuit, including photovoltage rise measurements. The simulation of photovoltage rise also suggests the possibility of assessing the interfacial resistance between the TiO(2) and substrate. When cells with a short diffusion length relative to film thickness were modelled, the simulated small perturbation photocurrent transients at short circuit (but not open circuit) yielded significantly higher effective diffusion coefficients than expected from the mean concentration of electrons and the electrolyte in the cell. This implies that

Using microencapsulated fluorescent dyes for simultaneous measurement of temperature and velocity fields

International Nuclear Information System (INIS)

Vogt, J; Stephan, P

2012-01-01

In this paper, a novel particle image thermometry method based on microcapsules filled with a fluorescent dye solution is described. The microcapsules consist of a liquid core of hexadecane in which the dye is dissolved and a solid polymer shell. The combination of a temperature-sensitive dye (Pyrromethene 597-8C9) and a dye showing a relatively smaller temperature sensitivity (Pyrromethene 567) in hexadecane makes application of the ratiometric LIF possible. This is necessary to compensate for fluctuations of the illuminating pulsed Nd:YAG laser (532 nm) as well as the different particle sizes. The applicability of this measurement technique is demonstrated for a cubic test cell (10 × 10 × 10 mm 3 ) with flow and temperature fields driven by natural convection and a capillary tube (1.16 mm inner diameter) inducing a temperature gradient and a Hagen–Poiseuille velocity profile. For the first case, a light sheet illumination is used making two optical accesses necessary. In the second case an inverted microscope is used, so only one optical access is needed and a volume illumination is applied. The technique facilitates high-resolution measurements (first case: 79 × 79 μm 2 ; second case: 8 × 8 μm 2 ). Although the measurement uncertainty is high compared to LIF measurements with dissolved dyes, temperature fields can be reproduced very well, and the experimental results are in good agreement with numerical computations. (paper)

Micro-Cavity Fluidic Dye Laser

DEFF Research Database (Denmark)

Helbo, Bjarne; Kristensen, Anders; Menon, Aric Kumaran

2003-01-01

We have successfully designed, fabricated and characterized a micro-cavity fluidic dye laser with metallic mirrors, which can be integrated with polymer based lab-on-a-chip microsystems without further processing steps. A simple rate-equation model is used to predict the average pumping power...... threshold for lasing as function of cavity-mirror reflectance, laser dye concentration and cavity length. The laser device is characterized using the laser dye Rhodamine 6G dissolved in ethanol. Lasing is observed, and the influence of dye concentration is investigated....

Photo-electrochemical solar cells with a SnO/sub 2/-liquid junction sensitized with highly concentrated dyes

Energy Technology Data Exchange (ETDEWEB)

Shimura, Michiko; Shakushiro, Kiyoaki; Shimura, Yukio

1986-09-01

The sensitization of a SnO/sub 2/-liquid junction cell with highly concentrated dyes was investigated. The dyes used were Crystal Violet, Methyl Violet B, Malachite Green, Pararosaniline, and Rhodamine B. Anomalous or positive photovoltages were obtained in the system when Fe(CN)/sub 6//sup 3 -/ was added. The performance of the photovoltaic cells showed an open-circuit photovoltage, Vsub(oc), of 175 mV, a short-circuit photocurrent, Isub(sc), of 12 ..mu..A, and a fill factor of 0.42. The action spectra resembled the absorption spectra of the aggregated dyes. A D-D mechanism is introduced to explain the anomaly of the photovoltage of the SnO/sub 2/ electrode sensitized with the dyes. This behaviour is relevant to the practical usage of such photo-electrochemical cells and merits further investigation.

Dyeing behaviour of gamma irradiated cotton fabric using Lawson dye extracted from henna leaves (Lawsonia inermis)

International Nuclear Information System (INIS)

Rehman, Fazal-ur; Adeel, Shahid; Qaiser, Summia; Ahmad Bhatti, Ijaz; Shahid, Muhammad; Zuber, Mohammad

2012-01-01

Dyeing behavior of gamma irradiated cotton fabric using Lawson dye extracted from henna leaves has been investigated. Cotton and dye powder are irradiated to different absorbed doses of 2, 4, 6, 8 and 10 kGy using Cs-137 gamma irradiator. The dyeing parameters such as dyeing time, electrolyte (salt) concentration and mordant concentrations using copper and iron as mordants are optimized. Dyeing is performed using un-irradiated and irradiated cotton with dye solutions and their color strength values are evaluated in CIE Lab system using Spectraflash –SF650. Methods suggested by International Standard Organization (ISO) have been employed to investigate the colourfastness properties such as colourfastness to light, washing and rubbing of irradiated dyed fabric. It is found that gamma ray treatment of cotton dyed with extracts of henna leaves has significantly improved the color strength as well as enhanced the rating of fastness properties. - Highlights: ► The optimum absorbed dose obtained for surface modification of cotton (RC) is 8 kGy. ► Irradiation has enhanced antioxidant, anti bacterial and hemolytic activities. ► Optimum dyeing conditions are 60 min dyeing time and 8 g/L salt concentration. ► At optimum conditions, color strength and fastness properties are enhanced.

Studies on widely tunable ultra-short laser pulses using energy transfer distributed feedback dye laser

International Nuclear Information System (INIS)

Ahamed, M.B.; Ramalingam, A.; Palanisamy, P.K.

2003-01-01

This paper presents both theoretical and experimental study of the characteristics of Nd: YAG laser pumped energy transfer distributed feedback dye laser (ETDFDL). Using theoretical model proposed, the behavior of ETDFDL such as the characteristics of donor DFDL, the acceptor DFDL, the dependence of their pulse width and output power on donor-acceptor concentrations and pump power are studied for dye mixture Rhodamine 6G and Cresyl Violet in detail. Experimentally using prism-dye cell configuration, the ETDFDL output is obtained and the output energy of DFDL is measured at the emission peaks of donor and acceptor dyes for different pump powers and donor-acceptor concentrations. In addition, the DFDL linewidth measurement has been carried out at the lasing wavelengths of the donor and acceptor dyes using Fabry-Perot etalon and the tunability of DFDL is measured to be in the wavelength range of 545-680 nm

Color measurement of methylene blue dye/clay mixtures and its application using economical methods

Science.gov (United States)

Milosevic, Maja; Kaludjerovic, Lazar; Logar, Mihovil

2016-04-01

Identifying the clay mineral components of clay materials by staining tests is rapid and simple, but their applicability is restricted because of the mutual interference of the common components of clay materials and difficulties in color determination. The change of color with concentration of the dye is related to the use of colorants as a field test for identifying clay minerals and has been improved over the years to assure the accuracy of the tests (Faust G. T., 1940). The problem of measurement and standardization of color may be solved by combination of colors observed in staining tests with prepared charts of color chips available in the Munsell Book of Color, published by Munsell Color Co. Under a particular set of illumination conditions, a human eye can achieve an approximate match between the color of the dyed clay sample and that of a standard color chip, even though they do have different spectral reflectance characteristics. Experiments were carried out with diffuse reflectance spectroscopy on selected clay samples (three montmorillonite, three kaolinite and one mix-layer clay samples) saturated with different concentration of methylene blue dye solution. Dominant wavelength and purity of the color was obtained on oriented dry samples and calculated by use of the I. C. I. (x, y) - diagram in the region of 400-700 nm (reflectance spectra) without MB and after saturation with different concentrations of MB solutions. Samples were carefully photographed in the natural light environment and processed with user friendly and easily accessible applications (Adobe color CC and ColorHexa encyclopedia) available for android phones or tablets. Obtained colors were compared with Munsell standard color chips, RGB and Hexa color standards. Changes in the color of clay samples in their interaction with different concentration of the applied dye together with application of economical methods can still be used as a rapid fieldwork test. Different types of clay

Laboratory measurements of selected optical, physical, chemical, and remote-sensing properties of five water mixtures containing Calvert clay and a nonfluorescing dye

Science.gov (United States)

Usry, J. W.; Whitlock, C. H.; Poole, L. R.; Witte, W. G., Jr.

1981-01-01

Total suspended solids concentrations ranged from 6.1 ppm to 24.3 ppm and sizes ranged between 1.5 micrometers and 10 micrometers with the most frequently occurring size less than 2 micrometers. Iron concentration was less than 1 percent of the total suspended solids. Nonfluorescing dye concentrations of the two mixtures were 20 ppm and 40 ppm. Attenuation coefficient for the five mixtures ranged from 4.8/m to 21.3/m. Variations in volume scattering function with phase angle were typical. Variations in attenuation and absorption coefficient with wavelength were similar for the mixtures without the dye. Attenuation coefficient of the mixtures with the dye increased for wavelengths less than 600 nm due to the dye's strong absorption peak near 500 nm. Reflectance increased as the concentration of Calvert clay increased and peaked near 600 nm. The nonfluorescent dye decreased the magnitude of the peak, but had practically no effect on the variation for wavelengths greater than 640 nm. At wavelengths less than 600 nm, the spectral variations of the mixtures with the dye were significantly different from those mixtures without the dye.

Radiation Degradation of some Commercial Dyes in Wastewater

International Nuclear Information System (INIS)

Dessouki, A.M.; Abdel-Aal, S.E.

1999-01-01

The degradation Kinetic due to irradiation of aqueous solutions of some commercial dyes, (Reactive Blue Brilliant, Reactive Yellow and Basic Blue 9 Dye (Methylene Blue 2 B), was studied. Factors affecting radiolysis of the dye such as dye concentration, irradiation dose, dose rate and ph of the solutions were studied. The effects of different additives such as nitrogen oxygen, hydrogen peroxide and sodium hypochlorite on the degradation process were investigated. The effect of irradiation dose on the different dye solutions at various concentrations, showed that the Reactive Yellow G. was very sensitive to gamma radiation. The effect of the ph of the dye solutions proved to very according type of the dye. Synergistic treatment of the dye solutions by irradiation and conventional method showed that saturation of the dye solutions with nitrogen did not enhance the radiation degradation of the dyes, while addition of oxygen resulted in a remarkable enhancement of the degradation of the dyes. Also, the addition of sodium hypochlorite (5%) and the oxidation by hydrogen peroxide resulted in more radiation degradation, Also, adsorption of the dyes onto Ga and some ion exchangers showed that Ga has the highest adsorption capacity. Radiation degradation of the toxic dye pollutants and their removal from wastewater down to concentrations not exceeding the maximum permissible concentration (Mpc) according to international standards, proved to be better than conventional methods of purification alone

Solubilization of Hydrophobic Dyes in Surfactant Solutions

Directory of Open Access Journals (Sweden)

Ali Reza Tehrani-Bagha

2013-02-01

Full Text Available In this paper, the use of surfactants for solubilization of hydrophobic organic dyes (mainly solvent and disperse dyes has been reviewed. The effect of parameters such as the chemical structures of the surfactant and the dye, addition of salt and of polyelectrolytes, pH, and temperature on dye solubilization has been discussed. Surfactant self-assemble into micelles in aqueous solution and below the concentration where this occurs—the critical micelle concentration (CMC—there is no solubilization. Above the CMC, the amount of solubilized dye increases linearly with the increase in surfactant concentration. It is demonstrated that different surfactants work best for different dyes. In general, nonionic surfactants have higher solubilization power than anionic and cationic surfactants. It is likely that the reason for the good performance of nonionic surfactants is that they allow dyes to be accommodated not only in the inner, hydrocarbon part of the micelle but also in the headgroup shell. It is demonstrated that the location of a dye in a surfactant micelle can be assessed from the absorption spectrum of the dye-containing micellar solution.

Extraction of dye

African Journals Online (AJOL)

Dyes of natural origins are great for color appreciation as any variation in the concentration of dye, mordant, type of water, soil and climate give variations in ... Grey scale and blue dyed silk were used for color fastness rating. ..... Down to Earth.

Pre-concentration and determination of tartrazine dye from aqueous solutions using modified cellulose nanosponges.

Science.gov (United States)

Shiralipour, Roohollah; Larki, Arash

2017-01-01

In this study, a new absorbent based on cellulose nanosponges modified with methyltrioctylammonium chloride (aliquat 336) was prepared and used for pre-concentration, removal and determination of tartrazine dye, using UV-vis spectrophotometry. This adsorbent was fully characterized using various instrumental techniques such as SEM, FTIR and XRD spectra. The pre-concentration and removal procedures were studied in column and batch modes, respectively. The effects of parameters such as pH of the aqueous medium, methyltrioctylammounium chloride dose, adsorbent amount, desorbing conditions and interfering ions on the adsorption of tartrazine were investigated and optimized. The fitting experimental data with conventional isotherm models revealed that the adsorption followed the Brunauer-Emmett-Teller (BET) model and the maximum adsorption capacity for tartrazine was 180mg/g with modified nanosponges. Under the optimized conditions, the calibration curve was linear over the range of 2-300ng/mL and the limit of detection was 0.15ng/mL. The relative standard deviation (RSD) for 20 and 100ng/mL of tartrazine were 3.1% and 1.5%, respectively. The proposed method was applied for pre-concentration and determination of tartrazine dye in different water samples. Copyright © 2016 Elsevier Inc. All rights reserved.

Computer Color Matching and Levelness of PEG-Based Reverse Micellar Decamethyl cyclopentasiloxane (D5 Solvent-Assisted Reactive Dyeing on Cotton Fiber

Directory of Open Access Journals (Sweden)

Alan Y. L. Tang

2017-07-01

Full Text Available The color matching and levelness of cotton fabrics dyed with reactive dye, in a non-aqueous environmentally-friendly medium of decamethylcyclopentasiloxane (D5, was investigated using the non-ionic surfactant reverse-micellar approach comprised of poly(ethylene glycol-based surfactant. The calibration dyeing databases for both conventional water-based dyeing and D5-assisted reverse micellar dyeing were established, along with the dyeing of standard samples with predetermined concentrations. Computer color matching (CCM was conducted by using different color difference formulae for both dyeing methods. Experimental results reveal that the measured concentrations were nearly the same as the expected concentrations for both methods. This indicates that the D5-assisted non-ionic reverse micellar dyeing approach can achieve color matching as good as the conventional dyeing system. The levelness of the dyed samples was measured according to the relative unlevelness indices (RUI, and the results reveal that the samples dyed by the D5 reverse micellar dyeing system can achieve good to excellent levelness comparable to that of the conventional dyeing system.

The molecular ordering phenomenon in dye-doped nematic liquid crystals

International Nuclear Information System (INIS)

Prakash Yadav, Satya; Pandey, Kamal Kumar; Kumar Misra, Abhishek; Kumar Tripathi, Pankaj; Manohar, Rajiv

2011-01-01

The experimental results of this work point out the role of the guest dye molecules in the molecular ordering of nematic liquid crystals. We have discussed the changes in the energies of interactions between rod-like nematic molecules and anthraquinone dye by considering the presence of steric and dipole-dipole interactions in the dye-doped system. The concentration of the dye plays an important role in the determination of molecular ordering in such dye-doped systems. Below a certain concentration of dye (known as the critical concentration), where the interaction between the dye molecules can be neglected, the addition of dye molecules introduces some disorder into the system in the form of domain formation. Above this critical concentration, this disorder is small.

The molecular ordering phenomenon in dye-doped nematic liquid crystals

Energy Technology Data Exchange (ETDEWEB)

Prakash Yadav, Satya; Pandey, Kamal Kumar; Kumar Misra, Abhishek; Kumar Tripathi, Pankaj; Manohar, Rajiv, E-mail: rajiv.manohar@gmail.com [Liquid Crystal Research Laboratory, Physics Department, University of Lucknow, Lucknow-226007 (India)

2011-03-15

The experimental results of this work point out the role of the guest dye molecules in the molecular ordering of nematic liquid crystals. We have discussed the changes in the energies of interactions between rod-like nematic molecules and anthraquinone dye by considering the presence of steric and dipole-dipole interactions in the dye-doped system. The concentration of the dye plays an important role in the determination of molecular ordering in such dye-doped systems. Below a certain concentration of dye (known as the critical concentration), where the interaction between the dye molecules can be neglected, the addition of dye molecules introduces some disorder into the system in the form of domain formation. Above this critical concentration, this disorder is small.

Effects of gamma irradiation on the degradation of dyes

International Nuclear Information System (INIS)

Piccinini, N.; Ferrero, F.

1975-01-01

To investigate the degradation kinetics of aqueous solutions of dyes of several classes, we studied the effects of gamma irradiation versus the dose (up to 80 krad), the dye concentration, the pH and the oxygen content of these solutions. To study the influence of some of the above-mentioned parameters, anthraquinonic dyes have been irradiated in a wide range of doses (up to 5 Mrad). Furthermore these dyes were acted upon in order to investigate the complex reactions of molecular alteration through chromatographic separations and spectrophotometric analyses. Experimental results agreed with a first order kinetics for dye concentrations lower than 0.04 g/1, and with a zero order one for higher concentrations. The pH was found to have a different influence according to the type of dye; for example we found that the degradation efficiency for anthraquinonic dyes has higher values for basic ranges. The dissolved oxygen supports the degradation in comparison with de-aerated solutions, though its influence varies according to the dye type and the pH. The oxygen action is particularly evident with high doses; in fact, tests on anthraquinonic dyes with doses up to 5 Mrad showed a marked decrease in the kinetic constants caused by the oxygen disappearance. Radiochemical degradation yields (Gd), never greater than a few units, show that the radical reactions responsible for the decolorization effect, are limited to a few transfer sequences. COD decrease, on the other hand, confirms the presence of oxidation phenomena which correspond to computed radiochemical yields (Gsub(ox)) markedly higher than those spectrophotometrically measured; such a difference is enhanced in the case of irradiation with aeration of solutions. The theoretical considerations are also described that were developed for outlining a general scheme involving the experimental results of both the kinetics and the radiochemical yield. (author)

Bioremediation of coractive blue dye by using Pseudomonas spp. isolated from the textile dye wastewater

Science.gov (United States)

Sunar, N. M.; Mon, Z. K.; Rahim, N. A.; Leman, A. M.; Airish, N. A. M.; Khalid, A.; Ali, R.; Zaidi, E.; Azhar, A. T. S.

2018-04-01

Wastewater released from the textile industry contains variety substances, mainly dyes that contains a high concentration of color and organic. In this study the potential for bacterial decolorization of coractive blue dye was examined that isolated from textile wastewater. The optimum conditions were determined for pH, temperature and initial concentration of the dye. The bacteria isolated was Pseudomonas spp. The selected bacterium shows high decolorization in static condition at an optimum of pH 7.0. The Pseudomonas spp. could decolorize coractive blue dye by 70% within 24 h under static condition, with the optimum of pH 7.0. Decolorization was confirmed by using UV-VIS spectrophotometer. This present study suggests the potential of Pseudomonas spp. as an approach in sustainable bioremediation that provide an efficient method for decolorizing coractive blue dye.

Development of high-power laser technology. Fabrication of a dye cell of the high power dye laser and development of the measurement technology of the fluid velocities in a dye cell

Energy Technology Data Exchange (ETDEWEB)

Jo, Jae Heung; Chang, Soo; Lim, Kwon; Kim, Jee Teak; Choi, Wan Hae [Hannam University, Taejon (Korea, Republic of)

1995-08-01

The computer simulation code for the simulation of the steady-state flow in a dye cell is developed by using the finite element method. The situation of the fluid flow is measured by the diode laser LDV system and compared with results of the computer simulation. The small size Fiber-Optic LDV with a directional coupler is designed and fabricated for the real time measurement of fluid velocities in a dye cell. (author). 13 refs.

Basic dye decomposition kinetics in a photocatalytic slurry reactor

International Nuclear Information System (INIS)

Wu, C.-H.; Chang, H.-W.; Chern, J.-M.

2006-01-01

Wastewater effluent from textile plants using various dyes is one of the major water pollutants to the environment. Traditional chemical, physical and biological processes for treating textile dye wastewaters have disadvantages such as high cost, energy waste and generating secondary pollution during the treatment process. The photocatalytic process using TiO 2 semiconductor particles under UV light illumination has been shown to be potentially advantageous and applicable in the treatment of wastewater pollutants. In this study, the dye decomposition kinetics by nano-size TiO 2 suspension at natural solution pH was experimentally studied by varying the agitation speed (50-200 rpm), TiO 2 suspension concentration (0.25-1.71 g/L), initial dye concentration (10-50 ppm), temperature (10-50 deg. C), and UV power intensity (0-96 W). The experimental results show the agitation speed, varying from 50 to 200 rpm, has a slight influence on the dye decomposition rate and the pH history; the dye decomposition rate increases with the TiO 2 suspension concentration up to 0.98 g/L, then decrease with increasing TiO 2 suspension concentration; the initial dye decomposition rate increases with the initial dye concentration up to a certain value depending upon the temperature, then decreases with increasing initial dye concentration; the dye decomposition rate increases with the UV power intensity up to 64 W to reach a plateau. Kinetic models have been developed to fit the experimental kinetic data well

Effects of incorporated straw on dye tracer infiltration

Science.gov (United States)

Kasteel, R.; Garnier, P.; Vachier, P.; Coquet, Y.

2003-04-01

Crop residue incorporation by conventional tillage increases the heterogeneity in the soil surface layer due to the soil tillage itself and to the presence of a zone with a high density of vegetal residues. The objective of this work was to quantify the effect of incorporated straw on the transport behaviour of the dye Brilliant Blue. We used an image analysis technique to calculate the Brilliant Blue concentration from the spectral signature (i.e. RGB values) using a calibration relationship. This method was already successfully applied in soils without organic matter and in this study we want to extend it to soils that contain fresh organic matter. The experiment took place in a loamy bare soil in the north of France at Mons-en-Chaussée in May, 2002. The soil was ploughed under dry conditions to 30 cm depth and straw was incorporated at the content of 10 Tonnes of C/ha. The infiltration experiment was carried out using an infiltrometer of 25 cm diameter at the head potential of -1 cm of water. First, water was infiltrated followed by the dye solution. The day after the infiltration, the soil was cut in horizontal sections of 50 times 50 cm. In total, 15 cross-section were photographed which were separated by a vertical distance of about 2 or 3 cm. Samples of soil and small pieces of straw were taken from the soil surface in order to measure the Brilliant Blue concentration for the calibration procedure. The volumetric water content and bulk density were measured with small cylindrical samples. After geometrical and illumination corrections of the images, we separated the soil from the straw and established a separate second-order polynomial calibration function for both relating the Brilliant Blue content to the spectral signature in each pixel. In this way we obtained spatially highly resolved concentration patterns of the dye tracer. The dye concentration distribution was found to be very heterogeneous in the soil at the local scale. In the plough layer, dye

Evaluation of field-collected drifter and subsurface fluorescein dye concentration data and comparisons to high frequency radar surface current mapping data for dispersed oil transport modeling

Energy Technology Data Exchange (ETDEWEB)

Payne, J.R. [Payne Environmental Consultants Inc., Encinitas, CA (United States); Terrill, E.; Carter, M.; Otero, M.; Middleton, W.; Chen, A. [Scripps Inst. of Oceanography, La Jolla, CA (United States); French McCay, D.; Mueller, C.; Jayko, K. [Applied Science Associates Inc., Narragansett, RI (United States); Nordhausen, W.; Lewis, R.; Lampinen, M.; Evans, T. [California Dept. of Fish and Game, San Diego, CA (United States). Office of Spill Prevention and Response; Ohlmann, C. [California Univ., Santa Barbara, CA (United States); Via, G.L.; Ruiz-Santana, H.; Maly, M.; Willoughby, B.; Varela, C. [United States Coast Guard Pacific Strike Team, Novato, CA (United States); Lynch, P.; Sanchez, P. [Marine Spill Response Corp., San Diego, CA (United States)

2007-07-01

Extensive coastal areas in the United States have been designated as pre-approved zones for dispersant applications in the event of an oil spill. Although the use of dispersants may reduce impacts to wildlife and shoreline habitats, it is recognized that the dispersed oil may cause impacts to organisms in the water column. The State of California Department of Fish and Game Office of Spill Prevention and Response is currently using oil spill fate and transport modeling to address this issue. The purpose is to develop the time and spatial scales, and equipment needs for a formal dispersed oil monitoring plan (DOMP) to document hydrocarbon water column concentrations, potentially exposed zooplankton, and the impact of the oil spills with and without dispersant use. A series of 7 fluorescein dye releases were completed off the coast of San Diego, California in order to test the operational framework for repeated sampling of dispersed oil plumes as outlined in the DOMP. The ability of high-frequency radar to provide surface current input data to oil spill models was also evaluated. The dye concentrations were measured over three spatial dimensions and time in order to verify the model-predicted movement of subsurface dye. Surface current fields at varying depths were also measured and the subsurface dye plume structure was mapped using a GPS coupled towed-fluorometer equipped with pressure sensors. Measurements were compared with data from traditional special monitoring of applied response technology (SMART). The database acquired through this program represents a technical resource that can help physical and chemical oceanographers, modelers, spill response and contingency planners involved in the debate of whether or not to use dispersants to mitigate near shore and open ocean marine oil spills. 14 refs., 2 tabs., 14 figs.

Measurement of liquid sheet using laser tagging method by photochromic dye

Science.gov (United States)

Rosli, Nurrina Binti; Amagai, Kenji

2014-12-01

Liquid atomization system has been extensively applied as the most significant process in many industrial fields. In the internal combustion engine, the combustion phenomenon is strongly influenced by the spray characteristics of the fuel given by the atomization process. In order to completely understand the whole atomization process, a detail investigation of relations between the liquid jet characteristics and the breakup phenomenon is required. In this study, a non-intrusive method called as laser tagging method by photochromic dye has been developed with aim to study the breakup process of liquid sheet in detail, covering from the behavior in film until disintegrated into ligament and droplets. The laser tagging method by photochromic dye is based on a shift in the absorption spectrum of photochromic dye molecules tagged by ultraviolet laser. The shift results a color change at the tagged region of liquid containing the dye. In this study, the motions of the dye traces were analyzed as the liquid surface velocity. As a result, liquid sheet was found to keep its velocity constantly in film before suddenly increase around broken point. However, it then decreased after broken into droplets. By forming a set of four points of dye traces on the liquid sheet, the change of relative position of the set enabled the measurement of deformation and rotational motion of the liquid sheet. As a result, the normal strain of the liquid sheet parallel to the flow direction depended on the flow behavior of ligament formation.

Measuring of nonlinearity of dye doped liquid crystals using of self phase modulation effect

International Nuclear Information System (INIS)

Abedi, M.; Jafari, A.; Tajalli, H.

2007-01-01

Self phase modulation in dye doped liquid crystals has investigated and the nonlinearity of dye doped liquid crystals is measured by this effect. The Self phase modulation effect can be used for producing optical micro rings that have many applications in photonics and laser industries.

Studies of Dye Sensitisation Kinetics and Sorption Isotherms of Direct Red 23 on Titania

Directory of Open Access Journals (Sweden)

Peter J. Holliman

2008-01-01

Full Text Available Sorption kinetics and isotherms have been measured for a commercial dye (Direct Red 23 on different samples of powdered Titania, and the data were analysed to better understand the dye sensitization process for dye sensitised solar cells (DSSCs. For the sorption kinetics, the data show rapid initial sorption (<1 hour followed by slower rate of increasing uptake between 1 and 24 hours. While higher initial concentrations of dye correspond to higher sorption overall, less dye is absorbed from higher initial dye concentrations when considered as percentage uptake. The correlation between the sorption data and model isotherms has been considered with time. The Langmuir model shows better correlations compared to the Freundlich isotherm. The dye uptake data has also been correlated with Titania characterization data (X-ray diffraction, scanning electron microscopy, BET and zero point charge analysis. Kinetic data show significantly better fits to second-order models compared to first order. This suggests that chemisorption is taking place and that the interaction between the dye sorbate and the Titania sorbent involves electron sharing to form an ester bond.

Ultrasonic assisted dyeing: dyeing of acrylic fabrics C.I. Astrazon Basic Red 5BL 200%.

Science.gov (United States)

Kamel, M M; Helmy, H M; Mashaly, H M; Kafafy, H H

2010-01-01

The dyeing of acrylic fabrics using C.I. Astrazon Basic Red 5BL 200% has been studied with both conventional and ultrasonic techniques. The effect of dye concentration, dye bath pH, ultrasonic power, dyeing time and temperature were studied and the resulting shades obtained by dyeing with both techniques were compared. Colour strength values obtained were found to be higher with ultrasonic than with conventional heating. The results of fastness properties of the dyed fabrics were studied. X-ray and Scanning Electron Microscope SEM were carried out on dyed samples using both methods of dyeing to find out an explanation for the better dyeability of acrylic fabrics with (US) method. Dyeing kinetics of acrylic fabrics using C.I. Astrazon Basic Red 5BL 200% using conventional and ultrasonic conditions were compared. The time/dye-uptake isotherms are revealing the enhanced dye-uptake in the second phase of dyeing. The values of dyeing rate constant, half-time of dyeing and standard affinity and ultrasonic efficiency have been calculated and discussed.

Occupational exposure to allergens in oxidative hair dyes

Directory of Open Access Journals (Sweden)

Polona Zaletel

2013-05-01

Full Text Available Oxidative hair dyes are the most important hair dying products. Hairdressers are exposed to the allergens found in oxidative hair dyes during the process of applying dyes to the hair, when cutting freshly dyed hair, or as a consequence of prior contamination of the working environment. pphenylenediamine, toluene-2,5-diamine and its sulphate are the most common ingredients in oxidative hair dyes that cause allergic contact dermatitis in hairdressers. Cross-reactivity of p-phenylenediamine with para-amino benzoic acid, sulphonamides, sulphonylurea, dapsone, azo dyes, benzocaine, procaine, and black henna temporary tattoos is possible. Allergic contact dermatitis is classified as delayed-type hypersensitivity, according to Coombs and Gell. Skin changes typically appear on the hands after previous sensitization to causative allergens. Combined with the patient’s overall medical and work history and clinical picture, epicutaneous testing is the basic diagnostic procedure for confirming the diagnosis and identifying the causative allergens. The simplest and most effective measure for preventing the occurrence of allergic contact dermatitis in hairdressers is prevention. Preventive measures should be applied as early as in the beginning stage of vocational guidance for this profession. It is important to include health education in the process of professional training and to implement general technical safety measures, in order to reduce sensitization to allergens in hairdressing. Here, special emphasis must be given to the correct use of protective gloves. Legislation must limit the concentration of allergenic substances in hair dyes, based on their potential hazards documented by scientific research.

Quantitative spatially resolved measurement of tissue chromophore concentrations using photoacoustic spectroscopy: application to the measurement of blood oxygenation and haemoglobin concentration

Science.gov (United States)

Laufer, Jan; Delpy, Dave; Elwell, Clare; Beard, Paul

2007-01-01

A new approach based on pulsed photoacoustic spectroscopy for non-invasively quantifying tissue chromophore concentrations with high spatial resolution has been developed. The technique is applicable to the quantification of tissue chromophores such as oxyhaemoglobin (HbO2) and deoxyhaemoglobin (HHb) for the measurement of physiological parameters such as blood oxygen saturation (SO2) and total haemoglobin concentration. It can also be used to quantify the local accumulation of targeted contrast agents used in photoacoustic molecular imaging. The technique employs a model-based inversion scheme to recover the chromophore concentrations from photoacoustic measurements. This comprises a numerical forward model of the detected time-dependent photoacoustic signal that incorporates a multiwavelength diffusion-based finite element light propagation model to describe the light transport and a time-domain acoustic model to describe the generation, propagation and detection of the photoacoustic wave. The forward model is then inverted by iteratively fitting it to measurements of photoacoustic signals acquired at different wavelengths to recover the chromophore concentrations. To validate this approach, photoacoustic signals were generated in a tissue phantom using nanosecond laser pulses between 740 nm and 1040 nm. The tissue phantom comprised a suspension of intralipid, blood and a near-infrared dye in which three tubes were immersed. Blood at physiological haemoglobin concentrations and oxygen saturation levels ranging from 2% to 100% was circulated through the tubes. The signal amplitude from different temporal sections of the detected photoacoustic waveforms was plotted as a function of wavelength and the forward model fitted to these data to recover the concentrations of HbO2 and HHb, total haemoglobin concentration and SO2. The performance was found to compare favourably to that of a laboratory CO-oximeter with measurement resolutions of ±3.8 g l-1 (±58 µM) and ±4

Quantitative spatially resolved measurement of tissue chromophore concentrations using photoacoustic spectroscopy: application to the measurement of blood oxygenation and haemoglobin concentration

Energy Technology Data Exchange (ETDEWEB)

Laufer, Jan; Delpy, Dave; Elwell, Clare; Beard, Paul [Department of Medical Physics and Bioengineering, University College London, Malet Place Engineering Building, London WC1E 6BT (United Kingdom)

2007-01-07

A new approach based on pulsed photoacoustic spectroscopy for non-invasively quantifying tissue chromophore concentrations with high spatial resolution has been developed. The technique is applicable to the quantification of tissue chromophores such as oxyhaemoglobin (HbO{sub 2}) and deoxyhaemoglobin (HHb) for the measurement of physiological parameters such as blood oxygen saturation (SO{sub 2}) and total haemoglobin concentration. It can also be used to quantify the local accumulation of targeted contrast agents used in photoacoustic molecular imaging. The technique employs a model-based inversion scheme to recover the chromophore concentrations from photoacoustic measurements. This comprises a numerical forward model of the detected time-dependent photoacoustic signal that incorporates a multiwavelength diffusion-based finite element light propagation model to describe the light transport and a time-domain acoustic model to describe the generation, propagation and detection of the photoacoustic wave. The forward model is then inverted by iteratively fitting it to measurements of photoacoustic signals acquired at different wavelengths to recover the chromophore concentrations. To validate this approach, photoacoustic signals were generated in a tissue phantom using nanosecond laser pulses between 740 nm and 1040 nm. The tissue phantom comprised a suspension of intralipid, blood and a near-infrared dye in which three tubes were immersed. Blood at physiological haemoglobin concentrations and oxygen saturation levels ranging from 2% to 100% was circulated through the tubes. The signal amplitude from different temporal sections of the detected photoacoustic waveforms was plotted as a function of wavelength and the forward model fitted to these data to recover the concentrations of HbO{sub 2} and HHb, total haemoglobin concentration and SO{sub 2}. The performance was found to compare favourably to that of a laboratory CO-oximeter with measurement resolutions of {+-}3

Quantitative spatially resolved measurement of tissue chromophore concentrations using photoacoustic spectroscopy: application to the measurement of blood oxygenation and haemoglobin concentration

International Nuclear Information System (INIS)

Laufer, Jan; Delpy, Dave; Elwell, Clare; Beard, Paul

2007-01-01

A new approach based on pulsed photoacoustic spectroscopy for non-invasively quantifying tissue chromophore concentrations with high spatial resolution has been developed. The technique is applicable to the quantification of tissue chromophores such as oxyhaemoglobin (HbO 2 ) and deoxyhaemoglobin (HHb) for the measurement of physiological parameters such as blood oxygen saturation (SO 2 ) and total haemoglobin concentration. It can also be used to quantify the local accumulation of targeted contrast agents used in photoacoustic molecular imaging. The technique employs a model-based inversion scheme to recover the chromophore concentrations from photoacoustic measurements. This comprises a numerical forward model of the detected time-dependent photoacoustic signal that incorporates a multiwavelength diffusion-based finite element light propagation model to describe the light transport and a time-domain acoustic model to describe the generation, propagation and detection of the photoacoustic wave. The forward model is then inverted by iteratively fitting it to measurements of photoacoustic signals acquired at different wavelengths to recover the chromophore concentrations. To validate this approach, photoacoustic signals were generated in a tissue phantom using nanosecond laser pulses between 740 nm and 1040 nm. The tissue phantom comprised a suspension of intralipid, blood and a near-infrared dye in which three tubes were immersed. Blood at physiological haemoglobin concentrations and oxygen saturation levels ranging from 2% to 100% was circulated through the tubes. The signal amplitude from different temporal sections of the detected photoacoustic waveforms was plotted as a function of wavelength and the forward model fitted to these data to recover the concentrations of HbO 2 and HHb, total haemoglobin concentration and SO 2 . The performance was found to compare favourably to that of a laboratory CO-oximeter with measurement resolutions of ±3.8 g l -1 (±58 �

Normalization of voltage-sensitive dye signal with functional activity measures.

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Kentaroh Takagaki

Full Text Available In general, signal amplitude in optical imaging is normalized using the well-established DeltaF/F method, where functional activity is divided by the total fluorescent light flux. This measure is used both directly, as a measure of population activity, and indirectly, to quantify spatial and spatiotemporal activity patterns. Despite its ubiquitous use, the stability and accuracy of this measure has not been validated for voltage-sensitive dye imaging of mammalian neocortex in vivo. In this report, we find that this normalization can introduce dynamic biases. In particular, the DeltaF/F is influenced by dye staining quality, and the ratio is also unstable over the course of experiments. As methods to record and analyze optical imaging signals become more precise, such biases can have an increasingly pernicious impact on the accuracy of findings, especially in the comparison of cytoarchitechtonic areas, in area-of-activation measurements, and in plasticity or developmental experiments. These dynamic biases of the DeltaF/F method may, to an extent, be mitigated by a novel method of normalization, DeltaF/DeltaF(epileptiform. This normalization uses as a reference the measured activity of epileptiform spikes elicited by global disinhibition with bicuculline methiodide. Since this normalization is based on a functional measure, i.e. the signal amplitude of "hypersynchronized" bursts of activity in the cortical network, it is less influenced by staining of non-functional elements. We demonstrate that such a functional measure can better represent the amplitude of population mass action, and discuss alternative functional normalizations based on the amplitude of synchronized spontaneous sleep-like activity. These findings demonstrate that the traditional DeltaF/F normalization of voltage-sensitive dye signals can introduce pernicious inaccuracies in the quantification of neural population activity. They further suggest that normalization

Characteristics of dye Rhoeo spathacea in dye sensitizer solar cell (DSSC)

Science.gov (United States)

Sumardiasih, Sri; Obina, Wilfrida M.; Cari; Supriyanto, Agus; Septiawan, Trio Y.; Khairuddin

2017-01-01

Dye-sensitized solar cell (DSSC) is a device that converts solar energy into electrical energy. The magnitude of the efficiency of DSSC is mainly based on the amount of dye absorbed by the surface of TiO2. In this work, used natural dye extracted from leaves Rhoeo spathacea. The dye partially used to immerse of TiO2 as working electrodes, and the rest are directly mixed TiO2 paste to obtain dye titanium dioxide.The paste TiO2 and dye titanium dioxide coated onto the fluorine-doped tin oxide (FTO) glass plate by spin coating method. The absorbance spectra of the dye, dye titanium dioxide and TiO2 were obtained by UV-Vis spectroscopy. The conductivity of the dye, dye titanium dioxide, and TiO2 was measured by two point probe El-Kahfi 100. The DSSC based on dye titanium dioxide that stirring for 5 hours the highest efficiency of 0,0520 % whereas those based on TiO2 immersed for 36 hours showed achieved 0,0501 % obtained from I-V characterization.

Characteristics of dye Rhoeo spathacea in dye sensitizer solar cell (DSSC)

International Nuclear Information System (INIS)

Sumardiasih, Sri; Obina, Wilfrida M.; Cari; Supriyanto, Agus; Septiawan, Trio Y.; Khairuddin

2017-01-01

Dye-sensitized solar cell (DSSC) is a device that converts solar energy into electrical energy. The magnitude of the efficiency of DSSC is mainly based on the amount of dye absorbed by the surface of TiO 2 . In this work, used natural dye extracted from leaves Rhoeo spathacea. The dye partially used to immerse of TiO 2 as working electrodes, and the rest are directly mixed TiO 2 paste to obtain dye titanium dioxide.The paste TiO 2 and dye titanium dioxide coated onto the fluorine-doped tin oxide (FTO) glass plate by spin coating method. The absorbance spectra of the dye, dye titanium dioxide and TiO 2 were obtained by UV-Vis spectroscopy. The conductivity of the dye, dye titanium dioxide, and TiO 2 was measured by two point probe El-Kahfi 100. The DSSC based on dye titanium dioxide that stirring for 5 hours the highest efficiency of 0,0520 % whereas those based on TiO 2 immersed for 36 hours showed achieved 0,0501 % obtained from I-V characterization. (paper)

High resolution measurement of light in terrestrial ecosystems using photodegrading dyes.

Directory of Open Access Journals (Sweden)

Javier Roales

Full Text Available Incoming solar radiation is the main determinant of terrestrial ecosystem processes, such as primary production, litter decomposition, or soil mineralization rates. Light in terrestrial ecosystems is spatially and temporally heterogeneous due to the interaction among sunlight angle, cloud cover and tree-canopy structure. To integrate this variability and to know light distribution over time and space, a high number of measurements are needed, but tools to do this are usually expensive and limited. An easy-to-use and inexpensive method that can be used to measure light over time and space is needed. We used two photodegrading fluorescent organic dyes, rhodamine WT (RWT and fluorescein, for the quantification of light. We measured dye photodegradation as the decrease in fluorescence across an irradiance gradient from full sunlight to deep shade. Then, we correlated it to accumulated light measured with PAR quantum sensors and obtained a model for this behavior. Rhodamine WT and fluorescein photodegradation followed an exponential decay curve with respect to accumulated light. Rhodamine WT degraded slower than fluorescein and remained unaltered after exposure to temperature changes. Under controlled conditions, fluorescence of both dyes decreased when temperatures increased, but returned to its initial values after cooling to the pre-heating temperature, indicating no degradation. RWT and fluorescein can be used to measure light under a varying range of light conditions in terrestrial ecosystems. This method is particularly useful to integrate solar radiation over time and to measure light simultaneously at different locations, and might be a better alternative to the expensive and time consuming traditional light measurement methods. The accuracy, low price and ease of this method make it a powerful tool for intensive sampling of large areas and for developing high resolution maps of light in an ecosystem.

Effects of the aspect ratio on the dye adsorption of ZnO nanorods grown by using a sonochemical method for dye-sensitized solar cells

International Nuclear Information System (INIS)

Choi, Seok Cheol; Yun, Won Suk; Sohn, Sang Ho; Oh, Sang Jin

2012-01-01

Well-aligned ZnO nanorods for the photoelectrode of dye-sensitized solar cells (DSSCs) were grown via a sonochemical method, and the effects of their aspect ratios on the dye adsorption in DSSCs were studied. The control of the aspect ratio of well-aligned ZnO nanorods was performed by tuning the mole concentration of zinc acetate dehydrate in the range of 0.04 ∼ 0.06M. The dye amounts adsorbed in the ZnO nanorods were estimated from the UV-Visible absorbance by using the Beer-Lambert law. The efficiency of DSSCs with ZnO nanorods was measured to investigate the effects of the aspect ratio of the ZnO nanorods on the dye adsorption properties. A change in the aspect ratio of the ZnO nanorods was founded to yield a change in their dye adsorption ability, resulting in a change in the efficiency of the DSSCs.

High-throughput measurement of polymer film thickness using optical dyes

Science.gov (United States)

Grunlan, Jaime C.; Mehrabi, Ali R.; Ly, Tien

2005-01-01

Optical dyes were added to polymer solutions in an effort to create a technique for high-throughput screening of dry polymer film thickness. Arrays of polystyrene films, cast from a toluene solution, containing methyl red or solvent green were used to demonstrate the feasibility of this technique. Measurements of the peak visible absorbance of each film were converted to thickness using the Beer-Lambert relationship. These absorbance-based thickness calculations agreed within 10% of thickness measured using a micrometer for polystyrene films that were 10-50 µm. At these thicknesses it is believed that the absorbance values are actually more accurate. At least for this solvent-based system, thickness was shown to be accurately measured in a high-throughput manner that could potentially be applied to other equivalent systems. Similar water-based films made with poly(sodium 4-styrenesulfonate) dyed with malachite green oxalate or congo red did not show the same level of agreement with the micrometer measurements. Extensive phase separation between polymer and dye resulted in inflated absorbance values and calculated thickness that was often more than 25% greater than that measured with the micrometer. Only at thicknesses below 15 µm could reasonable accuracy be achieved for the water-based films.

Toward real-time measurement of atmospheric mercury concentrations using cavity ring-down spectroscopy

Directory of Open Access Journals (Sweden)

X. Faïn

2010-03-01

Full Text Available Cavity ring-down spectroscopy (CRDS is a direct absorption technique that utilizes path lengths up to multiple kilometers in a compact absorption cell and has a significantly higher sensitivity than conventional absorption spectroscopy. This tool opens new prospects for study of gaseous elemental mercury (Hg⁰ because of its high temporal resolution and reduced sample volume requirements (<0.5 l of sample air. We developed a new sensor based on CRDS for measurement of (Hg⁰ mass concentration. Sensor characteristics include sub-ng m⁻³ detection limit and high temporal resolution using a frequency-doubled, tuneable dye laser emitting pulses at ~253.65 nm with a pulse repetition frequency of 50 Hz. The dye laser incorporates a unique piezo element attached to its tuning grating allowing it to tune the laser on and off the Hg⁰ absorption line on a pulse-to-pulse basis to facilitate differential absorption measurements. Hg⁰ absorption measurements with this CRDS laboratory prototype are highly linearly related to Hg⁰ concentrations determined by a Tekran 2537B analyzer over an Hg⁰ concentration range from 0.2 ng m⁻³ to 573 ng m⁻³, implying excellent linearity of both instruments. The current CRDS instrument has a sensitivity of 0.10 ng Hg⁰ m⁻³ at 10-s time resolution. Ambient-air tests showed that background Hg⁰ levels can be detected at low temporal resolution (i.e., 1 s, but also highlight a need for high-frequency (i.e., pulse-to-pulse differential on/off-line tuning of the laser wavelength to account for instabilities of the CRDS system and variable background absorption interferences. Future applications may include ambient Hg⁰ flux measurements with eddy covariance techniques, which require measurements of Hg⁰ concentrations with sub-ng m⁻³ sensitivity and sub-second time

Effect of Mixing Dyes and Solvent in Electrolyte Toward Characterization of Dye Sensitized Solar Cell Using Natural Dyes as The Sensitizer

Science.gov (United States)

Puspitasari, Nurrisma; Nurul Amalia, Silviyanti S.; Yudoyono, Gatut; Endarko

2017-07-01

Dye Sensitized Solar Cell (DSSC) using natural dyes (chlorophyll, curcumin from turmeric extract, and anthocyanin from mangosteen extract) have been successfully fabricated for determining the effect of variation natural dyes, mixing dyes and acetonitrile in electrolyte toward characterization of DSSC. DSSC consists of five parts namely ITO (Indium Tin Oxide) as a substrate; TiO2 as semiconductor materials; natural dyes as an electron donor; electrolyte as electron transfer; and carbon as a catalyst that can convert light energy into electric energy. Two types of gel electrolyte based on PEG that mixed with liquid electrolyte have utilized for analyzing the lifetime of DSSC. Type I used distilled water as a solvent whilst type II used acetonitrile as a solvent with addition of concentration of KI and iodine. The main purpose of study was to investigate influence of solvent in electrolyte, variation of natural dyes and mixing dyes toward an efficiency that resulted by DSSC. The result showed that electrolyte type II is generally better than type I with efficiency 0,0556 and 0,0456 %, respectively. An efficiency values which resulted from a variation of mixed three natural dyes showed the greatest efficiency compared to mixed two natural dyes and one dye, with an efficiency value can be achieved at 0,0194 % for chlorophyll; 0,111 % for turmeric; 0,0105 % for mangosteen; 0,0244% (mangosteen and chlorophyll); 0,0117 % (turmeric and mangosteen); 0,0158 % (turmeric and chlorophyll); and 0.0566 % (mixed three natural dyes).

A comparative study of carbocyanine dyes measured with TOF-SIMS and other mass spectrometric techniques

International Nuclear Information System (INIS)

Adriaensen, L.; Vangaever, F.; Gijbels, R.

2004-01-01

A series of cationic, zwitterionic and anionic carbocyanine dyes have been measured with TOF-SIMS under Ga + bombardment. In contrast to the cationic dyes, which give very intense molecular ion and characteristic fragment signals in the positive mode, the anionic dyes produce only a few fragment signals of low intensity. Even in the negative mode no molecular ions of the anionic dyes are seen in the recorded spectra. Actually, none of the studied molecules produces negative SIMS spectra containing molecular information. A comparative study was made between TOF-SIMS and other mass spectrometric techniques, namely, fast atom bombardment (FAB), electro spray ionization (ESI) and matrix assisted laser desorption ionization (MALDI). The measurements show that MALDI, ESI as well as FAB all give rise to spectra containing molecular ion signals, either in the positive, in the negative or in both modes. Unlike with TOF-SIMS, this observation also applies to the anionic dyes. Characteristic fragments of the dyes are present in all the recorded spectra. However, TOF-SIMS appears to induce more fragment ions in comparison with the other techniques. ESI, for instance, produces hardly any molecular fragments. Finally, the kind of fragment ions recorded depends upon the technique used, though some signals are produced by various techniques. For these carbocyanine dyes there is no clear correlation between the mass spectra obtained with TOF-SIMS and spectra obtained with the other techniques. This points to different desorption/ionization mechanisms, and makes it difficult, in practice, to make predictions on the feasibility of TOF-SIMS, starting from results of the other MS techniques

UV-Vis microspectrophotometry as a method of differentiation between cotton fibre evidence coloured with reactive dyes

Science.gov (United States)

Was-Gubala, Jolanta; Starczak, Roza

2015-05-01

The main purposes of this study was to assess the usefulness of microspectrophotometry (MSP), both in the ultraviolet (UV) and visible (Vis) range for discriminating single cotton fibres dyed with reactive dyes coming from the same manufacturer, as well as the possibility of evaluation of the concentration of dye in an examine fibre. This study utilised woven cotton fabrics dyed with different concentrations of one-compound reactive dyes with the commercial name Cibacron® (at present Novacron®) as the focus of the MSP analysis. The spectra were recorded in the UV-Vis range between 200 and 800 nm, in transmission mode. The results from this study illustrated that all of the analysed cotton samples dyed with reactive dyes were distinguishable between each other with the use of MSP, mostly in the visible, and also in ultraviolet range. The limit for applied MSP techniques was 0.18% of the concentration of a dye in the textile sample. The results indicate that based on the absorbance measurements for fibres constituting e.g. forensic traces it was not possible to estimate the concentration of the dye in the fibre because Beer's law did not obey. The intra-sample, and inter- sample variation, as well as dichroism effect in a case of a cotton fibres dyed with reactive dye were observed. On the basis of the results obtained for each analysed cotton sample, it was concluded that there was no correlation between colour uniformity in cotton fabric (changes in lightness, red/green and yellow/blue colour) and concentration of the reactive dye.

Optical study of planar waveguides based on oxidized porous silicon impregnated with laser dyes

Energy Technology Data Exchange (ETDEWEB)

Chouket, A. [Unite de recherche de Spectroscopie Raman, Departement de Physique, Faculte des Sciences de Tunis, Elmanar 2092, Tunis (Tunisia); Charrier, J. [Laboratoire d' Optronique CNRS-UMR FOTON 6082, Universite de Rennes 1, ENSSAT-6 rue de Kerampont, BP 80518, 22305 Lannion Cedex (France); Elhouichet, H. [Unite de recherche de Spectroscopie Raman, Departement de Physique, Faculte des Sciences de Tunis, Elmanar 2092, Tunis (Tunisia)], E-mail: habib.elhouichet@fst.rnu.tn; Oueslati, M. [Unite de recherche de Spectroscopie Raman, Departement de Physique, Faculte des Sciences de Tunis, Elmanar 2092, Tunis (Tunisia)

2009-05-15

Oxidized porous silicon optical planar waveguides were elaborated and impregnated with rhodamine B and rhodamine 6G. The waveguiding, absorption, and photoluminescence properties of these impregnated waveguides were studied. Successful impregnation of the structure with laser dyes is shown from photoluminescence and reflectivity measurements. Furthermore, the reflectivity spectra prove the homogenous incorporation of both dye molecules inside the pores of the matrices. The refractive indices of waveguide layers were determined before and after dye impregnation to indicate the conservation of guiding conditions. The optical losses in the visible wavelengths are studied as a function of dye concentration. The dye absorption is the main reason for these losses.

Isolation and screening of azo dye decolorizing bacterial isolates from dye-contaminated textile wastewater

Directory of Open Access Journals (Sweden)

Shahid Mahmood

2011-04-01

Full Text Available Azo dyes are released into wastewater streams without any pretreatment and pollute water and soilenvironments. To prevent contamination of our vulnerable resources, removal of these dye pollutants is of greatimportance. For this purpose, wastewater samples were collected from dye-contaminated sites of Faisalabad. About200 bacterial isolates were isolated through enrichment and then tested for their potential to remove RemazolBlack-B azo dye in liquid medium. Five bacterial isolates capable of degrading Remazol Black-B azo dye efficientlywere screened through experimentation on modified mineral salt medium. Isolate SS1 (collected from wastewater ofSupreme Textile Industry was able to completely remove the Remazol Black-B dye from the liquid medium in 18 h.Further, the isolate showed the best performance at the dye concentration of 100 mg L-1 medium (pH 7 and attemperature 35oC. Similarly, yeast extract proved to be the best carbon source for decolorization purpose. Theresults imply that the isolate SS1 could be used for the removal of the reactive dyes from textile effluents.

Gamma Radiolysis Studies of Aqueous Solution of Brilliant Green Dye

Directory of Open Access Journals (Sweden)

D. V. Parwate

2011-01-01

Full Text Available The effect of γ–radiation on colour intensity of aqueous solution of Brilliant Green has been investigated at two different concentrations. The degradation of Brilliant Green (BG has also been investigated in presence of suspended ZnO, by adding different amounts of ZnO. Simultaneously the conductance and pH of each solution system were measured before and after γ-irradiation. All the γ–irradiations were performed at a dose rate of 0.60 kGyhr-1 in GC-900. The maximum dose required for the complete degradation of the dye was found to be 0.39 kGy. G(-dye values were found to decrease with increase in gamma dose and were in the range 4.26 - 12.81. The conductance (7.6 - 25.3 μS and pH values increased marginally with dose for both the concentrations. The rate of decolouration was found to be high at lower doses and the efficiency of dye removal was higher at low concentration of the dye. This may be attributed to the presence of reaction by-products from the destruction of parent compound build up and compete for reaction intermediate species. The rate of reaction and rate constants were calculated and it was found that the degradation reaction follows first order kinetics. It was found that the decolouration percentage was more in dye systems in absence of ZnO.

Dye removal from textile wastewater using bioadsorbent

International Nuclear Information System (INIS)

Gardazi, S.M.H.

2014-01-01

Textile industries throughout the world produce huge quantities of dyes and pigments annually. Effluents from textile industries are dye wastewater, and disposal of these wastes to freshwater bodies causes damage to the environment. Among the treatment technologies, adsorption is an attractive and viable option, provided that the sorbent is inexpensive and readily available for use. In this study, a typical basic dye, methylene blue, in wastewater was treated using Melia azedarach sawdust. The effects of contact time, adsorbent amount and particle size were investigated on the removal efficiency of adsorbent for methylene blue. Complete removal of the dye were attained at higher adsorbent dose of 3 g/L with 50 mg/L initial dye concentration. The maximum adsorption was at 240 minutes, whereas more than 90% removal with 105 meu m particle size of 1 g/L adsorbent for same initial dye concentration. The experimental data best fits with 2 Langmuir adsorption isotherm (R= 0.991). (author)

The oxidative response and viable reaction mechanism of the textile dyes by fenton reagent

International Nuclear Information System (INIS)

Masooda, Q.; Hijira, T.; Sitara, M.; Sehar, M.; Sundus, A.; Mohsin, A.

2017-01-01

The mechanism of the degradation of the Reactive Red 239 and Reactive Blue 19 by Fenton reagent was studied by advanced oxidation process in aqueous medium. The spectroscopic technique was adopted for the measurements of dye concentration. Moreover they were determined at 540 nm and 590 nm, respectively. Kinetics of the reaction was studied under the effect of concentration of reactive dyes, concentration of oxidant were followed under pseudo first order condition and found to influence the catalytic mechanism. The pH of the medium, vibrant response of several cations and anions and influence of ionic strength on the reaction kinetics were also monitored. Physical evidences for the degradation and mineralization of the dyes were evaluated by Lime water test, Ring Test and TLC test also confirmed the degradation of dye. Inhibitory effects of dyes were observed by CO3-, HCO3-, HPO42-, Cl-, I- Al3+ and Na+. Thermodynamic activation parameters in the oxidation reaction were studied and mode of mechanism was suggested on the basic of these parameters. This study explored the safe and eco friendly degradation of the textile dyes under Pseudo first order rate constant. It was observed that Fenton assisted degradation of the dyes under controlled conditions was found to be favorable for the treatment of textile wastewater. Moreover compared to other chemical methods it is effective and harmless to the environment. (author)

Modeling the efficiency of Förster resonant energy transfer from energy relay dyes in dye-sensitized solar cells

KAUST Repository

Hoke, Eric T.

2010-02-11

Förster resonant energy transfer can improve the spectral breadth, absorption and energy conversion efficiency of dye sensitized solar cells. In this design, unattached relay dyes absorb the high energy photons and transfer the excitation to sensitizing dye molecules by Förster resonant energy transfer. We use an analytic theory to calculate the excitation transfer efficiency from the relay dye to the sensitizing dye accounting for dynamic quenching and relay dye diffusion. We present calculations for pores of cylindrical and spherical geometry and examine the effects of the Förster radius, the pore size, sensitizing dye surface concentration, collisional quenching rate, and relay dye lifetime. We find that the excitation transfer efficiency can easily exceed 90% for appropriately chosen dyes and propose two different strategies for selecting dyes to achieve record power conversion efficiencies. © 2010 Optical Society of America.

Industrial scale salt-free reactive dyeing of cationized cotton fabric with different reactive dye chemistry.

Science.gov (United States)

Nallathambi, Arivithamani; Venkateshwarapuram Rengaswami, Giri Dev

2017-10-15

Dyeing of knitted cotton goods in the industry has been mostly with reactive dyes. Handling of salt laden coloured effluent arising out of dyeing process is one of the prime concerns of the industry. Cationization of cotton is one of the effective alternative to overcome the above problem. But for cationization to be successful at industrial scale it has to be carried out by exhaust process and should be adoptable for the various dye chemistries currently practiced in the industry. Hence, in the present work, industrial level exhaust method of cationization process was carried out with concentration of 40g/L and 80g/L. The fabrics were dyed with dyes of three different dye chemistry and assessed for its dyeing performance without the addition of salt. Dye shades ranging from medium to extra dark shades were produced without the addition of salt. This study will provide industries the recipe that can be adopted for cationized cotton fabric for the widely used reactive dyes at industrial level. Copyright © 2017 Elsevier Ltd. All rights reserved.

Adsorption characteristics of brilliant green dye on kaolin

International Nuclear Information System (INIS)

Nandi, B.K.; Goswami, A.; Purkait, M.K.

2009-01-01

Experimental investigations were carried out to adsorb toxic brilliant green dye from aqueous medium using kaolin as an adsorbent. Characterization of kaolin is done by measuring: (i) particle size distribution using particle size analyzer, (ii) BET surface area using BET surface analyzer, and (iii) structural analysis using X-ray diffractometer. The effects of initial dye concentration, contact time, kaolin dose, stirring speed, pH and temperature were studied for the adsorption of brilliant green in batch mode. Adsorption experiments indicate that the extent of adsorption is strongly dependent on pH of solution. Free energy of adsorption (ΔG 0 ), enthalpy (ΔH 0 ) and entropy (ΔS 0 ) changes are calculated to know the nature of adsorption. The calculated values of ΔG 0 at 299 K and 323 K indicate that the adsorption process is spontaneous. The estimated values of ΔH 0 and ΔS 0 both show the negative sign, which indicate that the adsorption process is exothermic and the dye molecules are organized on the kaolin surface in less randomly fashion than in solution. The adsorption kinetic has been described by first-order, pseudo-second-order and intra-particle-diffusion models. It was observed that the rate of dye adsorption follows pseudo-second-order model for the dye concentration range studied in the present case. Standard adsorption isotherms were used to fit the experimental equilibrium data. It was found that the adsorption of brilliant green on kaolin follows the Langmuir adsorption isotherm

Mediator-assisted decolorization and detoxification of textile dyes/dye mixture by Cyathus bulleri laccase.

Science.gov (United States)

Chhabra, Meenu; Mishra, Saroj; Sreekrishnan, T R

2008-12-01

Laccase from basidiomycete fungus Cyathus bulleri was evaluated for its ability to decolorize a number of reactive and acidic dyes in the presence of natural and synthetic mediators. The extent of decolorization was monitored at different mediator/dye concentrations and incubation time. Among the synthetic mediators, 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) was effective at low mediator/dye ratios and resulted in 80-95% decolorization at rates that varied from 226 +/- 4 nmol min(-1) mg(-1) for Reactive Orange 1 to 1,333 +/- 15 nmol min(-1) mg(-1) for Reactive Red 198. Other synthetic mediators like 1-hydroxybenzotriazole and violuric acid showed both concentration- and time-dependent increases in percent decolorization. Natural mediators like vanillin, on the other hand, were found to be less effective on all the dyes except Reactive Orange 1. Computed rates of decolorization were about twofold lower than that with ABTS. The laccase-ABTS system also led to nearly 80% decolorization for the simulated dye mixture. No clear correlation between laccase activity on the mediator and its ability to decolorize dyes was found, but pH had a significant effect: Optimum pH for decolorization coincided with the optimum pH for mediator oxidation. The treated samples were also evaluated for toxicity in model microbial systems. The laccase-mediator system appears promising for treatment of textile wastewaters.

Photoactive dye-enhanced tissue ablation for endoscopic laser prostatectomy.

Science.gov (United States)

Ahn, Minwoo; Hau, Nguyen Trung; Van Phuc, Nguyen; Oh, Junghwan; Kang, Hyun Wook

2014-11-01

Laser light has been widely used as a surgical tool to treat benign prostate hyperplasia (BPH) over 20 years. Recently, application of high laser power up to 200 W was often reported to swiftly remove a large amount of prostatic tissue. The purpose of this study was to validate the feasibility of photoactive dye injection to enhance light absorption and eventually to facilitate tissue vaporization with low laser power. Chicken breast tissue was selected as a target tissue due to minimal optical absorption at the visible wavelength. Four biocompatible photoactive dyes, including amaranth (AR), black dye (BD), hemoglobin powder (HP), and endoscopic marker (EM), were selected and tested in vitro with a customized 532 nm laser system with radiant exposure ranging from 0.9 to 3.9 J/cm(2) . Light absorbance and ablation threshold were measured with UV-Vis spectrometer and Probit analysis, respectively, and compared to feature the function of the injected dyes. Ablation performance with dye-injection was evaluated in light of radiant exposure, dye concentration, and number of injection. Higher light absorption by injected dyes led to lower ablation threshold as well as more efficient tissue removal in the order of AR, BD, HP, and EM. Regardless of the injected dyes, ablation efficiency principally increased with radiant exposure, dye concentration, and number of injection. Among the dyes, AR created the highest ablation rate of 44.2 ± 0.2 µm/pulse due to higher absorbance and lower ablation threshold. High aspect ratios up to 7.1 ± 0.4 entailed saturation behavior in the tissue ablation injected with AR and BD, possibly resulting from plume shielding and increased scattering due to coagulation. Preliminary tests on canine prostate with a hydraulic injection system demonstrated that 80 W with dye injection yielded comparable ablation efficiency to 120 W with no injection, indicating 33% reduced laser power with almost equivalent performance. Due to

Influence of mass transfer and chemical reaction on ozonation of azo dyes

Energy Technology Data Exchange (ETDEWEB)

Choi, I.S.; Wiesmann, U. [Dept. of Environmental Engineering, Technical Univ. of Berlin, Berlin (Germany)

2003-07-01

Azo dyes can be only mineralised by chemical oxidation. In this paper the oxidation of reactive black 5 (RB 5) and reactive orange 96 (RO 96) with concentrations between 35 and 5700 mgL{sup -1} (RB 5) and between 20 and 2050 mgL{sup -1} (RO 96) is investigated. A lab scale bubble column was used, which was gassed by a mixture of O{sub 2} and O{sub 3}. The oxidation rate was influenced by mass transfer for all dye concentrations used. For lower dye concentrations mass transfer alone was decisive for reaction rate showing an enhancement factor of E {approx} 1. However, in the region of higher dye concentrations, the slope of the decreasing ozone concentration inside the liquid boundary layer increases more and more with increasing dye concentration as a result of a chemical oxidation. Therefore, the enhancement factor depends on the kind and concentration of the azo dyes. For RB 5 as an diazo dye an enhancement factor of E = 9 was observed for 3800 mgL{sup -1}, RO 96 as a mono azo dye with a remarkable higher chemical oxidation rate shows an E = 17 already for 2050 mgL{sup -1}. (orig.)

Crossflow Ultrafiltration for Removing Direct-15 Dye from Wastewater of Textile Industry

Directory of Open Access Journals (Sweden)

A.L. Ahmad

2017-11-01

Full Text Available Ultrafiltration membrane was used to treat the effluent from textile industries. Crossflow ultrafiltration using GN polymeric membrane was used to remove the dye from textile effluent. A synthetic textile effluent of Direct-15 dye was used. The study focused through the effect of feed concentration, transmembrane pressure and solution’s pH on the permeate flux and percentage of dye removal were investigated. Dye concentration had significant effects on flux values. Under the fixed pressures and pH, the flux decreased while the dye rejection increased with increasing feed concentration. Transmembrane pressure also had significant effect on flux values. Under the fixed feed concentration and pH, the flux increased while dye rejection decreased with increasing pressure. Experiment data showed that the highest flux was observed at pH 4 (acidic condition while the highest dye removal observed at pH 7. Data collection could be used to improve the effectiveness of dye removal from textile industry wastewater using membrane technology.

Removal of the hazardous dye-Tartrazine by photodegradation on titanium dioxide surface

International Nuclear Information System (INIS)

Gupta, Vinod K.; Jain, Rajeev; Nayak, Arunima; Agarwal, Shilpi; Shrivastava, Meenakshi

2011-01-01

The removal of the dye-tartrazine by photodegradation has been investigated using titanium dioxide surface as photocatalyst under UV light. The process was carried out at different pH, catalyst dose, dye concentration and effects of the electron acceptor H 2 O 2 . It was found that under the influence of TiO 2 as catalyst, the colored solution of the dye became colorless and the process followed a pseudo first order kinetics. The optimum conditions for the degradation of dye were 6 x 10 -5 M dye concentration, pH of 11, and 0.18 mg/L of catalyst dose. In order to evaluate the effect of electron acceptor, the effect of H 2 O 2 on the degradation process was also monitored and it was found that the hydroxyl radical formation and retardation of electron-hole recombination took place simultaneously. The adsorption studies of tartrazine at various dose of TiO 2 followed the Langmuir isotherm trend. In order to determine the quality of waste water, Chemical Oxygen Demand (COD) measurements were carried out both before and after the treatment and a significant decrease in the values was observed, implying good potential of this technique to remove tartrazine dye from aqueous solutions. Research highlights: →Degradation efficiency increases with increase in catalyst concentration. →Adsorption of tartrazine on TiO 2 followed the Langmuir isotherm. →The photocatalytic kinetics follows first order.

Removal of the hazardous dye-Tartrazine by photodegradation on titanium dioxide surface

Energy Technology Data Exchange (ETDEWEB)

Gupta, Vinod K., E-mail: vinodfcy@gmail.com [Indian Institute of Technology Roorkee, Department of Chemistry, Roorkee, 247667 (India); King Fahd University of Petroleum and Minerals, Chemistry Department, Dhahran (Saudi Arabia); Jain, Rajeev [Jiwaji University, Department of Environmental Chemistry, Gwalior-474011 (India); Nayak, Arunima [Indian Institute of Technology Roorkee, Department of Chemistry, Roorkee, 247667 (India); Agarwal, Shilpi; Shrivastava, Meenakshi [Jiwaji University, Department of Environmental Chemistry, Gwalior-474011 (India)

2011-07-20

The removal of the dye-tartrazine by photodegradation has been investigated using titanium dioxide surface as photocatalyst under UV light. The process was carried out at different pH, catalyst dose, dye concentration and effects of the electron acceptor H{sub 2}O{sub 2}. It was found that under the influence of TiO{sub 2} as catalyst, the colored solution of the dye became colorless and the process followed a pseudo first order kinetics. The optimum conditions for the degradation of dye were 6 x 10{sup -5} M dye concentration, pH of 11, and 0.18 mg/L of catalyst dose. In order to evaluate the effect of electron acceptor, the effect of H{sub 2}O{sub 2} on the degradation process was also monitored and it was found that the hydroxyl radical formation and retardation of electron-hole recombination took place simultaneously. The adsorption studies of tartrazine at various dose of TiO{sub 2} followed the Langmuir isotherm trend. In order to determine the quality of waste water, Chemical Oxygen Demand (COD) measurements were carried out both before and after the treatment and a significant decrease in the values was observed, implying good potential of this technique to remove tartrazine dye from aqueous solutions. Research highlights: {yields}Degradation efficiency increases with increase in catalyst concentration. {yields}Adsorption of tartrazine on TiO{sub 2} followed the Langmuir isotherm. {yields}The photocatalytic kinetics follows first order.

Adsorption of Reactive Red Dye from Wastewater Using Modified Citrulluscolosynthis Ash

Directory of Open Access Journals (Sweden)

Mohammadreza Rezaei Kahkha

2016-07-01

Full Text Available Dye-bearing wastes pose serious risks to and leave harmful effects on the environment. Increasing wastewater color intensity leads to reduced light reaching the aquatic environment, which adversely affects the life and growth of aquatic plants and invertebrates. Among the many methods available for dye removal from wastewater, membrane separation, oxidation, coagulation, and anaerobic treatment are more common but they are all costly and involve complex processes. Biosorption, in contrast, enjoys both ease of application and simple design so that it is widely used for removing dyes, heavy metals, and phenolic compounds from both water and wastewater. In this paper, the ability of citrulluscolosynthis ash as a bioadsorbent for the removal of reactive red dye is investigated for the first time. Sodium hydroxide is also used to modify the plant ash surface which expectedly enhances its dye removal efficiency. Measurements and removal levels are determined using a UV-vis spectrophotometer. Finally, the effects of pH, adsorbent dosage, dye concentration, and reaction time on dye removal efficiency are also explored. Results show that the optimum conditions to achieve maximum dye removal are as follows: A pH level of 2, an adsorbant dosage of 1.75 g l-1, an initial concentration equal to 90 mg L-1, and A reaction time of 70 min. Adsorption isotherm is found to obey the Ferundlich isotherm. Also, an adsorption capacity of 36 mg g‒1 is achieved under the best conditions. It may thus be concluded that modified citrulluscolosynthis ash can be used as an effective adsorbent to treat colored wastewaters.

Modelling of polyester fabric dyeing in the presence of ultrasonic waves

Directory of Open Access Journals (Sweden)

Kodrić Marija

2017-01-01

Full Text Available In this paper, modelling of dyeing, i.e. adsorptive behaviour of disperse dyes on polyester fibres (dyeing, under the influence of ultrasound has been considered with the aim of getting the data about mechanisms of binding the dyes and defining the conditions of dyeing process of this synthetic fibres along with additional energy source without the use of carriers, compounds that increase permeability of the fibres and help dyeing. Dyeing - adsorption is conducted under different conditions, and the concentration of dyes, mass of the substrate, recipes and time of dyeing were being varied. It has been established that ultrasound allows dyeing without carriers and the efficiency of dyeing depends on the time of contact, initial concentration of the dye and the amount of absorbent - material. There is the continuity of growth of the amount of bound dye to the mass of the absorbent. Characteristic graphs, obtained from Langmuir isotherm, have confirmed that this model ensures precise description of polyester dyeing by disperse dye. Kinetic of dyeing has been remarkably interpreted by pseudo second-order in regards to the high functionality.

UV-Vis microspectrophotometry as a method of differentiation between cotton fibre evidence coloured with reactive dyes.

Science.gov (United States)

Was-Gubala, Jolanta; Starczak, Roza

2015-05-05

The main purposes of this study was to assess the usefulness of microspectrophotometry (MSP), both in the ultraviolet (UV) and visible (Vis) range for discriminating single cotton fibres dyed with reactive dyes coming from the same manufacturer, as well as the possibility of evaluation of the concentration of dye in an examine fibre. This study utilised woven cotton fabrics dyed with different concentrations of one-compound reactive dyes with the commercial name Cibacron® (at present Novacron®) as the focus of the MSP analysis. The spectra were recorded in the UV-Vis range between 200 and 800nm, in transmission mode. The results from this study illustrated that all of the analysed cotton samples dyed with reactive dyes were distinguishable between each other with the use of MSP, mostly in the visible, and also in ultraviolet range. The limit for applied MSP techniques was 0.18% of the concentration of a dye in the textile sample. The results indicate that based on the absorbance measurements for fibres constituting e.g. forensic traces it was not possible to estimate the concentration of the dye in the fibre because Beer's law did not obey. The intra-sample, and inter- sample variation, as well as dichroism effect in a case of a cotton fibres dyed with reactive dye were observed. On the basis of the results obtained for each analysed cotton sample, it was concluded that there was no correlation between colour uniformity in cotton fabric (changes in lightness, red/green and yellow/blue colour) and concentration of the reactive dye. Copyright © 2015 Elsevier B.V. All rights reserved.

Dyeing Studies with Eucalyptus, Quercetin, Rutin, and Tannin: A Research on Effect of Ferrous Sulfate Mordant

OpenAIRE

Rattanaphol Mongkholrattanasit; Charoon Klaichoi; Nattadon Rungruangkitkrai; Nattaya Punrattanasin; Kamolkan Sriharuksa; Monthon Nakpathom

2013-01-01

Natural dyes from Eucalyptus leaf extract, quercetin, rutin, and tannin were applied to silk fabric by pad-batch and pad-dry techniques under different conditions. Ferrous sulfate was used as a mordant. The dyeing properties were evaluated by measuring K/S and CIELAB values. In addition, the different fastness properties were evaluated. The effect of dyes at different concentration levels with respect to their colour strength was also studied.

Application of natural dyes in textile industry and the treatment of dye solutions using electrolytic techniques

OpenAIRE

Abouamer, Karima Massaud

2008-01-01

This thesis was submitted for the degree of Doctor of Philosophy and awarded by Brunel University, 25/02/2008. Anodic oxidation of a commercial dye, methylene blue (MB), from aqueous solutions using an electrochemical cell is reported. Data are provided on the effects of eight different types of supporting electrolytes, concentration of electrolytes, initial dye concentration, current and electrolytic time on the percentage removal of methylene blue. Anodic oxidation was found to be effect...

In-situ Decolorization of Residual Dye Effluent in Textile Jet Dyeing Machine by Ozone

Directory of Open Access Journals (Sweden)

Irfan Ahmed Shaikh

2014-12-01

Full Text Available In this study, a new idea of decolourization was investigated in which residual dyeing effluent from textile dyeing process was treated using O3 in the same machine where it was generated. The novelty comes from the idea of doing dyeing and treatment simultaneously. At the completion of dyeing process, O3 gas was injected directly into the machine to remove colour and COD from the wastewater. To evaluate the effectiveness of new method, pilot-scale studies were performed, and decolourization of residual dyeing effluents containing C.I. Reactive Orange 7, C.I. Reactive Blue 19, and C.I. Reactive Black 5 was carried out in specially built textile jet dyeing machine. The results showed that almost 100% colour removal and 90% COD reduction were achieved when process conditions such as pH, dye concentration (mg/L, ozone production rate (g/hr, and temperature were optimized. The study concludes that new method has a great potential to eliminate the need of a separate end-of-the-pipe wastewater treatment system, thus offering an on-site and cost-effective solution.

Bulk velocity measurements by video analysis of dye tracer in a macro-rough channel

International Nuclear Information System (INIS)

Ghilardi, T; Franca, M J; Schleiss, A J

2014-01-01

Steep mountain rivers have hydraulic and morphodynamic characteristics that hinder velocity measurements. The high spatial variability of hydraulic parameters, such as water depth (WD), river width and flow velocity, makes the choice of a representative cross-section to measure the velocity in detail challenging. Additionally, sediment transport and rapidly changing bed morphology exclude the utilization of standard and often intrusive velocity measurement techniques. The limited technical choices are further reduced in the presence of macro-roughness elements, such as large, relatively immobile boulders. Tracer tracking techniques are among the few reliable methods that can be used under these conditions to evaluate the mean flow velocity. However, most tracer tracking techniques calculate bulk flow velocities between two or more fixed cross-sections. In the presence of intense sediment transport resulting in an important temporal variability of the bed morphology, dead water zones may appear in the few selected measurement sections. Thus a technique based on the analysis of an entire channel reach is needed in this study. A dye tracer measurement technique in which a single camcorder visualizes a long flume reach is described and developed. This allows us to overcome the problem of the presence of dead water zones. To validate this video analysis technique, velocity measurements were carried out on a laboratory flume simulating a torrent, with a relatively gentle slope of 1.97% and without sediment transport, using several commonly used velocity measurement instruments. In the absence of boulders, salt injections, WD and ultrasonic velocity profiler measurements were carried out, along with dye injection technique. When boulders were present, dye tracer technique was validated only by comparison with salt tracer. Several video analysis techniques used to infer velocities were developed and compared, showing that dye tracking is a valid technique for bulk velocity

Dye laser with distributed feedback and with pumping by copper-vapor laser

Energy Technology Data Exchange (ETDEWEB)

Mirza, S Yu; Soldatov, A N; Sukhanov, V B

1983-10-01

An experimental study was made for determining the characteristics of dye lasers with distributed feedback, not requiring intricate resonator structures, and the feasibility of their pumping with radiation from a metal-vapor laser. The experiments were performed with five different dyes lasing in the yellow-red (510.6 - 578.2 nm) range of the spectrum: rhodamine 110, 6G, S and ocazine 17,1 in ethyl alcohol solution. The optical equipment included a copper-vapor pumping laser with the gas-discharge tube inside a telescopic resonator of the unstable type. Pumping pulses of 20 ns duration were generated at 510.6 and 578.2 nm wavelengths and a 4 kHz repetition rate. The pumping power was varied by means of an interference filter smoothly adjustable through rotation. The pumping laser beam was focused by a cylindrical lens on the dye cell. At optimum dye concentrations, corresponding to a maximum attainable emission power, dye concentrate was added into the circulation system for determining the dependence of the pumping threshold power on the dye concentration. Also measured were the dependence of the emission efficiency on the pumping power and the tuning range of each dye laser. The efficiency was found to remain constant over the pumping power range from threshold level to eight times higher level. The results reveal different angles of laser beam divergence in the vertical plane and in the horizontal plane, the divergence angle being four times larger in the vertical plane. The conversion efficiency increased, without significant changes in spectral characteristics, with a single annular reflector instead of two reflectors. 9 references, 4 figures, 1 table.

Comparison of multiple DNA dyes for real-time PCR: effects of dye concentration and sequence composition on DNA amplification and melting temperature

DEFF Research Database (Denmark)

Guðnason, Haukur; Dufva, Hans Martin; Bang, Dang Duong

2007-01-01

investigate 15 different intercalating DNA dyes for their inhibitory effects on PCR, effects on DNA melting temperature and possible preferential binding to GC-rich sequences. Our results demonstrated that in contrast to the results of SYBR Green I, two intercalating dyes SYTO-13 and SYTO-82 do not inhibit......The importance of real-time polymerase chain reaction (PCR) has increased steadily in clinical applications over the last decade. Many applications utilize SYBR Green I dye to follow the accumulation of amplicons in real time. SYBR Green I has, however, a number of limitations that include...... the inhibition of PCR, preferential binding to GC-rich sequences and effects on melting curve analysis. Although a few alternative dyes without some of these limitations have been recently proposed, no large-scale investigation into the properties of intercalating dyes has been performed. In this study, we...

Electronic spectral study of interaction of electron donor – acceptor dyes in the ground and excited state with a metal ion. Effect of molecular structure of the dye

International Nuclear Information System (INIS)

Sardar, Sanjib Kr; Mandal, Prasun K.; Bagchi, Sanjib

2014-01-01

Interaction of manganese (II) ion with electron donor (D)–acceptor (A) dyes having symmetric D–A–D configuration of chromophores (ketocyanine dye) and the corresponding parent merocyanines (D–A configuration) in acetonitrile has been compared by monitoring the electronic absorption, and steady state and time resolved fluorescence characteristics of the dyes. Absorption spectral studies point to the formation of a 1:1 metal ion–dye (S 0 -state) complex. Equilibrium constant (K 0 ) and other thermodynamic parameters for complex formation have been determined for all the systems. Symmetric ketocyanine dyes (D–A–D) form stronger complex than the corresponding dye with D–A configuration. Quenching of fluorescence is caused due to complex formation with the cation. However, for very low concentration of salts, where complex formation is insignificant, an enhancement of fluorescence intensity takes place due to addition of salt. The absorption band of the dye undergoes a slight blue shift in the same concentration range of the metal ion. Fluorescence life time of the excited state also increases with an increase in salt concentration in that concentration range. Results have been explained in terms of formation of a weak association complex where one or more cations replace equivalent solvent molecules in the cybotatic region around the dye. The binding constant of the association complex involving cation and the dye (S 1 -state) has been determined. While the value of the binding constant is higher for a symmetric D–A–D dye relative to that for the corresponding dye with D–A configuration, the extent of fluorescence enhancement for the latter is larger. Values of decay constant for the different photophysical processes have been calculated. Formation of association complex in the S 1 -state is characterised by a slower nonradiative decay of S 1 -state of the dyes. -- Highlights: • A ketocyanine dye forms 1:1 complex with metal ions. • Slight

Case study of the sonochemical decolouration of textile azo dye Reactive Black 5

International Nuclear Information System (INIS)

Vajnhandl, Simona; Le Marechal, Alenka Majcen

2007-01-01

The decolouration and mineralization of reactive dye C.I. Reactive Black 5, a well-known representative of non-biodegradable azo dyes, by means of ultrasonic irradiation at 20, 279 and 817 kHz has been investigated with emphasis on the effect of various parameters on decolouration and degradation efficiency. Characterization of the used ultrasound systems was performed using calorimetric measurements and oxidative species monitoring using Fricke and iodine dosimeter. Experiments were carried out with low frequency probe type, and a high-frequency plate type transducer at 50, 100 and 150 W of acoustic power and within the 5-300 mg/L initial dye concentration range. Decolouration, as well as radical production, increased with increasing frequency, acoustic power, and irradiation time. Any increase in initial dye concentration results in decreased decolouration rates. Sonochemical decolouration was substantially depressed by the addition of 2-methyl-2-propanol as a radical scavenger, which suggests radical-induced reactions in the solution. Acute toxicity to marine bacteria Vibrio fischeri was tested before and after ultrasound irradiation. Under the conditions employed in this study, no toxic compounds were detected after 6 h of irradiation. Mineralization of the dye was followed by TOC measurements. Relatively low degradation efficiency (50% after 6 h of treatment) indicates that ultrasound is rather inefficient in overall degradation, when used alone

Photoactive dye enhanced tissue ablation for endoscopic laser prostatectomy

Science.gov (United States)

Ahn, Minwoo; Nguyen, Trung Hau; Nguyen, Van Phuc; Oh, Junghwan; Kang, Hyun Wook

2015-02-01

Laser light has been widely used as a surgical tool to treat benign prostate hyperplasia with high laser power. The purpose of this study was to validate the feasibility of photoactive dye injection to enhance light absorption and eventually to facilitate tissue ablation with low laser power. The experiment was implemented on chicken breast due to minimal optical absorption Amaranth (AR), black dye (BD), hemoglobin powder (HP), and endoscopic marker (EM), were selected and tested in vitro with a customized 532-nm laser system with radiant exposure ranging from 0.9 to 3.9 J/cm2. Light absorbance and ablation threshold were measured with UV-VIS spectrometer and Probit analysis, respectively, and compared to feature the function of the injected dyes. Ablation performance with dye-injection was evaluated in light of radiant exposure, dye concentration, and number of injection. Higher light absorption by injected dyes led to lower ablation threshold as well as more efficient tissue removal in the order of AR, BD, HP, and EM. Regardless of the injected dyes, ablation efficiency principally increased with input parameter. Among the dyes, AR created the highest ablation rate of 44.2+/-0.2 μm/pulse due to higher absorbance and lower ablation threshold. Preliminary tests on canine prostate with a hydraulic injection system demonstrated that 80 W with dye injection yielded comparable ablation efficiency to 120 W with no injection, indicating 33 % reduced laser power with almost equivalent performance. In-depth comprehension on photoactive dye-enhanced tissue ablation can help accomplish efficient and safe laser treatment for BPH with low power application.

Intermolecular energy transfer in binary systems of dye polymers

Science.gov (United States)

Liu, Lin-I.; Barashkov, Nikolay N.; Palsule, Chintamani P.; Gangopadhyay, Shubhra; Borst, Walter L.

2000-10-01

We present results and physical interpretations for the energy transfer mechanisms in two-component dye polymer systems. The data consist of fluorescence emission spectra and decays. Two dyes were embedded in an epoxypolymer base, and only they participated in the energy transfer. Following pulsed laser excitation of the donor dye, energy transfer took place to the accept dye. The possible transfer paths considered here were nonradiative and radiative transfer. The latter involves two steps, emission and absorption of a photon, and therefore is relatively slow, while nonradiative transfer is a fast single step resulting from direct Coulomb interactions. A predominantly nonradiative transfer is desirable for applications, for instance in wavelength shifters in high energy particle detection. We studied the concentration effects of the dyes on the energy transfer and obtained the relative quantum efficiencies of various wavelength shifters from the fluorescence emission spectra. For low acceptor concentrations, radiative transfer was found to dominate, while nonradiative transfer became dominant at increasing dye concentrations. The fluorescence decays were analyzed with a sum-of-exponentials method and with Förster kinetics. The sum of exponential model yielded mean decay times of the dye polymers useful for a general classification. The decay times decreased as desired with increasing acceptor concentration. The samples, in which nonradiative energy transfer dominated, were analyzed with Förster kinetics. As a result, the natural decay times of the donor and acceptor dyes and the critical radii for nonradiative energy transfer were obtained from a global best fit.

Using Eggshell in Acid Orange 2 Dye Removal from Aqueous Solution

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Ahmad Reza Yari

2015-05-01

Full Text Available Background and purpose: Generated dye wastewater by the textile industry is usually toxic, non-biodegradable and resistant in the environment. Eggshell is one of the inexpensive material and for the reason the vesicular structures can be used as a proper adsorbent for pollutants removal. The aim of this study is to investigate the efficiency of eggshell for removal of acid orange 2 dye from aqueous solution. Materials and Methods: In the experimental study was determined the efficacy of variant variables such as contact time (15, 30, 60, 90 and 120 min, pH (3, 7 and 11, adsorbent dose (10, 25, 50 and 75 g/L, and initial dye concentration (25, 50 and 100 mg/L. The concentration of dye by spectrophotometer ultraviolet/visible in the wavelength 483 nm was examined. Results: The results showed that with increasing contact time and adsorbent dose, the dye removal efficiency was increased, but with increasing pH and initial dye concentration the removal efficiency was decreased. The maximum of removal efficiency of acid orange 2 dye got in the optimum pH: 3, contact time: 90 min, adsorbent dose: 50 g/L and initial dye concentration: 25 mg/L. Adsorption of acid orange 2 dye (R2 = 0.87 follow the Freundlich isotherm. Conclusion: Eggshells can be used as an inexpensive and effective adsorbent for the removal of acid orange 2 dye.

Enzyme-mediated bacterial biodegradation of an azo dye (C.I. Acid blue 113): reuse of treated dye wastewater in post-tanning operations.

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Senthilvelan, T; Kanagaraj, J; Panda, R C

2014-11-01

"Dyeing" is a common practice used to color the hides during the post-tanning operations in leather processing generating plenty of wastewater. The waste stream containing dye as pollutant is severely harmful to living beings. An azo dye (C.I. Acid Blue 113) has been biodegraded effectively by bacterial culture mediated with azoreductase enzyme to reduce the pollution load in the present investigation. The maximum rate of dye degradation was found to be 96 ± 4 and 92 ± 4 % for the initial concentrations of 100 and 200 mg/l, respectively. The enzyme activity was measured using NADH as a substrate. Fourier transform infrared spectroscopy (FT-IR) analysis was confirmed that the transformation of azo linkage could be transformed into N2 or NH3 or incorporated into complete biomass. Breaking down of dye molecules to various metabolites (such as aniline, naphthalene-1,4-diamine, 3-aminobenzenesulfonic acid, naphthalene-1-sulfonic acid, 8-aminonaphthalene-1-sulfonic acid, 5,8-diaminonaphthalene-1-sulfonic acid) was confirmed by gas chromatography and mass spectra (GC-MS) and mass (electrospray ionization (ESI)) spectra analysis. The treated wastewater could be reused for dyeing operation in the leather processing, and the properties of produced leather were evaluated by conventional methods that revealed to have improved dye penetration into the grain layer of experimental leather sample and resulted in high levelness of dyeing, which helps to obtain the desired smoothness and soft leather properties.

Effects of carboxyl and ester anchoring groups on solar conversion efficiencies of TiO2 dye-sensitized solar cells

Energy Technology Data Exchange (ETDEWEB)

Sepehrifard, A.; Stublla, A.; Haftchenary, S.; Chen, S.; Potvin, P.; Morin, S. [York Univ., Toronto, ON (Canada). Dept. of Chemistry

2008-07-01

This paper reported on a study in which 2 new Ruthenium (Ru(2)) dyes bearing different anchoring groups were applied to sensitize TiO2 for dye-sensitized solar cells (DSSCs). The solar conversion efficiencies were measured. Results for 2 of the dyes which carried ester and carboxyl anchoring groups were presented. The extent and nature of the surface binding was studied using electrochemical, UV-visible, fluorescence and FTIR measurements. Solar cell performance was discussed in terms of surface concentration of chemisorbed dyes, electronic properties of the photoanodes and electrochemical properties of adsorbed dyes. The study showed that carboxylic acid groups offer better dye adsorption than ester groups. However, sensitization with warm solutions improved the adsorption of the esterified dye, most likely through transesterification. It was concluded that this may be a useful means of improving solar conversion efficiencies of ester-bearing dyes. 6 refs., 1 tab., 2 figs.

Product Diversification of Turmeric (Curcuma Domestica Val) for TextileDyes

International Nuclear Information System (INIS)

Kuntari-Sasas; Syafril-Nurdiansyah

2000-01-01

In order to increase the use of natural source and variation of naturalpigment for textile dyes, research activity has been carried out in productdiversification of turmeric for textile dyes however its fixation ability tocotton fibre in this dyes does not have strong fixation ability to cottonfibre in order to improve its colour fastness it was necessary to do aftertreatment with mordant. Up to present time, it has been well known thatturmeric was used as raw material for medicine and cosmetic. Considering thatturmeric contains of carbonyl as chromophore in natural pigment. it has highpossibility to serve it as textile dyes. In this study, turmeric wasextracted with water and used its yields for dyeing cotton fabrics. Theextraction was carried out by using water as medium with ratio of 1 : 4 byboiling until reaching the medium ratio of 1 : 2. The extracted turmeric wasre-extracted again with fresh water in the same condition as the previousextraction and repeating the process up to several times until no more dyeswill be extracted out. The mixture of the extracted dyes were then put intoevaporation to obtain dry pigment and was grinned to obtain powder dyes.Color measurement by means of spectrophotometry was subjected to the dyespowder from known various concentrations to obtain the linear calibrationcurve between dyes concentrations and absorbance. The linear equationobtained from this experiment was : Y = 0.0075 + 0.0435 X. From this equationit was calculated that the dyes yields from the whole turmeric extraction was2.6805 %, and from 3 times repeating extraction was 2.2648 % or 84.49 % fromthe whole extracted dyes. Dyeing experiment for cotton fabrics were carriedout at 60 o C for various times of dyeing (30 minutes to 120 minutes). Thedyed fabrics were then mordanted or after treatment with respected potassiumbichromate, aluminum potassium sulphate (Tawas), and diazonium salt (Red SaltB). The dyed fabrics and the mordanted ones were tested for color fastness

Bioaccumulation versus adsorption of reactive dye by immobilized growing Aspergillus fumigatus beads

International Nuclear Information System (INIS)

Wang, B.-E.; Hu Yongyou

2008-01-01

The removal of reactive brilliant blue KN-R using growing Aspergillus fumigatus (abbr. A. fumigatus) immobilized on carboxymethylcellulose (CMC) beads with respect to initial dye concentration was investigated. Bioaccumulation was the dominant mechanism of the dye removal. According to the UV-vis spectra and the results of three sets of experiments, it could be concluded that the bioaccumulation using immobilized growing A. fumigatus beads was achieved by metabolism-dependent accumulation and metabolism-independent adsorption (15-23% proportion of overall dye removal), which included biosorption by mycelia entrapped in them and adsorption on immobilization matrix. The transmission electron microscope (TEM) images showed the intracellular structures of mycelia and the toxicity of dye. It was found that the fungus had a considerable tolerance to reactive brilliant blue KN-R at initial dye concentrations of <114.7 mg/l. Though at high initial dye concentrations the growth of mycelia was inhibited significantly by the dye molecules in the growth medium, the bioaccumulation capacity was not markedly affected and the maximum bioaccumulation capacity was 190.5 ± 2.0 mg/g at an initial dye concentration of 374.4 mg/l. The bioaccumulation rates were not constant over the contact time

Reuse of Textile Dyeing Effluents Treated with Coupled Nanofiltration and Electrochemical Processes

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Valentina Buscio

2016-06-01

Full Text Available The reactive dye Cibacron Yellow S-3R was selected to evaluate the feasibility of combining nanofiltration membranes with electrochemical processes to treat textile wastewater. Synthetic dyeing effluents were treated by means of two nanofiltration membranes, Hydracore10 and Hydracore50. Up to 98% of dye removal was achieved. The influence of salt concentration and pH on membrane treatment was studied. The best dye removal yield was achieved at pH 3 in the presence of 60 g/L of NaCl. After the membrane filtration, the concentrate containing high dye concentration was treated by means of an electrochemical process at three different current densities: 33, 83, and 166 mA/cm2. Results showed a lineal relationship between treatment time and applied current density. Both permeates and electrochemically-decoloured effluents were reused in new dyeing processes (100% of permeate and 70% of decoloured concentrates. Dyed fabrics were evaluated with respect to original dyeing. Colour differences were found to be into the acceptance range.

Specific interactions within micelle microenvironment in different charged dye/surfa

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Adina Roxana Petcu

2016-01-01

Full Text Available The interactions of two ionic dyes, Crystal Violet and Methyl Orange, with different charged surfactants and also with a nonionic surfactant were investigated using surface tension measurements and visible spectroscopy in pre-micellar and post-micellar regions. It was found that for the water dominant phase systems the dye was localized between the polar heads, at the exterior of the direct micelle shells for all the systems. For the oil dominant phase systems, in case of the same charged dye/surfactant couples, the dye was localized in the micelle shell between the hydrocarbon chain of the surfactant nearby the hydrophilic head groups while for nonionic surfactant and oppositely charged dye/surfactant, localization of dye was between the oxyethylenic head groups towards the interior of the micelle core. Mixed aggregates of the dye and surfactant (below the critical micellar concentration of cationic surfactant, dye-surfactant ion pair and surfactant-micelles were present. The values of equilibrium constants (for TX-114/MO and TX-114/CV systems were 0.97 and 0.98, respectively, partition coefficients between the micellar and bulk water phases and standard free energy (for the nonionic systems were −12.59 kJ/mol for MO and −10.97 kJ/mol for CV were calculated for all the studied systems. The partition processes were exothermic and occurred spontaneously.

A Note on the Dyeing of Wool Fabrics Using Natural Dyes Extracted from Rotten Wood-Inhabiting Fungi

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Vicente A. Hernández

2018-02-01

Full Text Available Fungal isolates obtained from rotten wood samples were identified and selected by their ability to produce fungal dyes in liquid media. Fungal isolates produced natural extracellular dyes with colors ranging from red to orange, yellow and purple. Dyes from two of these fungi, Talaromyces australis (red and Penicillium murcianum (yellow, were extracted and used to dye wool samples in a Data Color Ahiba IR Pro-Trade (model Top Speed II machine. The protein nature of wool interacted well with the fungal dyes producing colors suitable for textile applications when used to a concentration of 0.1 g·L−1. Results on color fastness when washing confirmed the affinity of the dyes with wool as the dyed samples kept their color in acceptable ranges after washing, without the implementation of mordanting pretreatments or the use of fixing agents.

Current distribution evaluation of dye-sensitized solar cell using HTS-SQUID-based magnetic measurement system

Energy Technology Data Exchange (ETDEWEB)

Sakai, Kenji, E-mail: Sakai-k@okayama-u.ac.jp; Tanaka, Kohei; Kiwa, Toshihiko; Tsukada, Keiji

2016-11-15

Highlights: • Current distribution and direction of dye-sensitized solar cell (DSSC) was measured. • Electrical current flowing in the indium tin oxide (ITO) glass substrate was uniform. • The distribution of electrical current depended on I–V characteristic. • Current direction changed when the performance of DSSC is low. - Abstract: The current flowing inside a dye-sensitized solar cell (DSSC) was measured using a high-temperature superconductor superconducting quantum interference device (HTS-SQUID)-based magnetic measurement system. Further, a new evaluation method of the DSSC, which is difficult to measure using the conventional method, was investigated to improve the characteristics of the DSSC. The tangential components of the magnetic field generated from the DSSC were measured using two HTS-SQUIDs, and the intensity and direction related to the electrical current were obtained by the measured magnetic field. The DSSCs prepared with different dyes and catalytic substances showed different current-intensity mapping. The current direction was different for the DSSC with low performance. In addition, the current flowing in the ITO layer of the ITO glass substrate was also measured and the results confirmed that it had uniform distribution. These results show that the current mapping and the direction of the electrical current depend on the internal factors of the DSSC, and the detection of the magnetic field distribution generated from it is expected to lead to its new evaluation method.

Biosorption and biodegradation of a sulfur dye in high-strength dyeing wastewater by Acidithiobacillus thiooxidans.

Science.gov (United States)

Nguyen, Thai Anh; Fu, Chun-Chieh; Juang, Ruey-Shin

2016-11-01

The ability of the bacterial strain Acidithiobacillus thiooxidans to remove sulfur blue 15 (SB15) dye from water samples was examined. This bacterium could not only oxidize sulfur compounds to sulfuric acid but also promote the attachment of the cells to the surface of sulfidic particles, therefore serving as an efficient biosorbent. The biosorption isotherms were better described by the Langmuir equation than by the Freundlich or Dubinin-Radushkevich equation. Also, the biosorption process followed the pseudo-second-order kinetics. At pH 8.3 and SB15 concentrations up to 2000 mg L(-1) in the biomass/mineral salt solution, the dye removal and decolorization were 87.5% and 91.4%, respectively, following the biosorption process. Biodegradation was proposed as a subsequent process for the remaining dye (250-350 mg L(-1)). A central composite design was used to analyze independent variables in the response surface methodology study. Under the optimal conditions (i.e., initial dye concentration of 300 mg L(-1), initial biomass concentration of 1.0 g L(-1), initial pH of 11.7, and yeast extract dose of 60 mg L(-1)), up to 50% of SB15 was removed after 4 days of biodegradation. Copyright © 2016 Elsevier Ltd. All rights reserved.

Chemical vapor deposition of three aminosilanes on silicon dioxide: surface characterization, stability, effects of silane concentration, and cyanine dye adsorption.

Science.gov (United States)

Zhang, Feng; Sautter, Ken; Larsen, Adam M; Findley, Daniel A; Davis, Robert C; Samha, Hussein; Linford, Matthew R

2010-09-21

Covalently bonded monolayers of two monofunctional aminosilanes (3-aminopropyldimethylethoxysilane, APDMES, and 3-aminopropyldiisopropylethoxysilane, APDIPES) and one trifunctional aminosilane (3-aminopropyltriethoxysilane, APTES) have been deposited on dehydrated silicon substrates by chemical vapor deposition (CVD) at 150 °C and low pressure (a few Torr) using reproducible equipment. Standard surface analytical techniques such as x-ray photoelectron spectroscopy (XPS), contact angle goniometry, spectroscopic ellipsometry, atomic force microscopy, and time-of-flight secondary ion mass spectroscopy (ToF-SIMS) have been employed to characterize the resulting films. These methods indicate that essentially constant surface coverages are obtained over a wide range of gas phase concentrations of the aminosilanes. XPS data further indicate that the N1s/Si2p ratio is higher after CVD with the trifunctional silane (APTES) compared to the monofunctional ones, with a higher N1s/Si2p ratio for APDMES compared to that for APDIPES. AFM images show an average surface roughness of 0.12- 0.15 nm among all three aminosilane films. Stability tests indicate that APDIPES films retain most of their integrity at pH 10 for several hours and are more stable than APTES or APDMES layers. The films also showed good stability against storage in the laboratory. ToF-SIMS of these samples showed expected peaks, such as CN(-), as well as CNO(-), which may arise from an interaction between monolayer amine groups and silanols. Optical absorption measurements on adsorbed cyanine dye at the surface of the aminosilane films show the formation of dimer aggregates on the surface. This is further supported by ellipsometry measurements. The concentration of dye on each surface appears to be consistent with the density of the amines.

Post-treatment of anaerobically degraded azo dye Acid Red 18 using aerobic moving bed biofilm process: Enhanced removal of aromatic amines

International Nuclear Information System (INIS)

Hosseini Koupaie, E.; Alavi Moghaddam, M.R.; Hashemi, S.H.

2011-01-01

Highlights: → Biofilm process was applied as post-treatment of anaerobically degraded an azo dye. → More than 65% of the dye total metabolites was completely mineralized. → Based on HPLC analysis, more than 80% of 1-naphthylamine-4-sulfonate was removed. → Inhibition of biofilm growth was increased with increasing the initial dye concentration. → Considerable porous morphology was observed in the SEM photographs of the biofilm. - Abstract: The application of aerobic moving bed biofilm process as post-treatment of anaerobically degraded azo dye Acid Red 18 was investigated in this study. The main objective of this work was to enhance removal of anaerobically formed the dye aromatic metabolites. Three separate sequential treatment systems were operated with different initial dye concentrations of 100, 500 and 1000 mg/L. Each treatment system consisted of an anaerobic sequencing batch reactor (An-SBR) followed by an aerobic moving bed sequencing batch biofilm reactor (MB-SBBR). Up to 98% of the dye decolorization and more than 80% of the COD removal occurred anaerobically. The obtained results suggested no significant difference in COD removal as well as the dye decolorization efficiency using three An-SBRs receiving different initial dye concentrations. Monitoring the dye metabolites through HPLC suggested that more than 80% of anaerobically formed 1-naphthylamine-4-sulfonate was completely removed in the aerobic biofilm reactors. Based on COD analysis results, at least 65-72% of the dye total metabolites were mineralized during the applied treatment systems. According to the measured biofilm mass and also based on respiration-inhibition test results, increasing the initial dye concentration inhibited the growth and final mass of the attached-growth biofilm in MB-SBBRs.

Effect of Tannic Acid on the zeta Potential, Sorption, and Surface Free Energy in the Process of Dyeing of Leacril with a Cationic Dye.

Science.gov (United States)

Espinosa-Jiménez; Giménez-Martín; Ontiveros-Ortega

1998-11-01

The behavior of the surface free energy in the process of dyeing Leacril pretreated with tannic acid and subsequently dyeing with the cationic dye Rhodamine B has been studied. Also the electrokinetic behavior of these systems has been analyzed by studying the zeta potential, which has been obtained by means of the streaming potential technique. Values more significative of the zeta potential of these systems have been obtained using the three models of capillaries existing in the literature. The qualitative behavior of the zeta potential is the same for the three models of capillaries tested in this paper. These models are those of Goring and Mason, Biefer and Mason, and Chang and Robertson. The zeta potential of the systems analyzed is negative in the range of concentration of the dye in the liquid phase from 10(-6) to ca. 10(-4) M of dye. In the range of low concentrations (from 10(-6) to ca. 10(-5) M of dye) the zeta potential of the system untreated Leacril/Rhodamine B increases in absolute value due to increasing hydrophobic attractions between both the hydrophobic chains of the dye and the Leacril fibers in aqueous media. In the system Leacril treated with tannic acid/Rhodamine B, this increase is also due to the presence of hydrogen bonding between the phenolic hydroxyl groups of the tannic acid and the sulfonate and sulfate end groups of Leacril fibers. For concentrations of dye between 10(-5) and 10(-4) M of dye in solution, the zeta potential decreases in absolute value due to the electrostatic attractions between the groups negatively charged in the fiber and the cation of the dye. The zeta potential changes its sign at the highest concentrations of dye used in this work. The adsorption of Rhodamine B onto both untreated Leacril and Leacril treated with tannic acid is favored by the increasing temperature of adsorption. The behavior of the components of the surface free energy obtained by the thin-layer wicking technique led us to consider that the

Modified Multiwalled Carbon Nanotubes for Treatment of Some Organic Dyes in Wastewater

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M. I. Mohammed

2014-01-01

Full Text Available In Iraq, a large quantity of basic orange and methyl violet dyes contaminated wastewater from textile industries is discharged into Tigris River. So the aim of this work is to found an efficient and fast technique that can be applied directly for removal of such dyes from the wastewater before discharging into river. Accordingly, CNTs as a new approach prepared by CCVD technique were purified, functionalized, and used as adsorption material to remove dyes from wastewater. The effect of pH, contact time, CNTs dosage, and dyes concentration on removal of pollutants was studied. The removal percentage of both dyes was proportional to the contact time, CNTs dosage, and pH and inversely proportional to the dyes concentration. The results show that the equilibrium time was 20 and 30 min for basic orange and methyl violet dyes, respectively, and the maximum removal percentage for all dyes concentrations was at pH = 8.5 and CNTs dosage of 0.25 g/L and 0.3 g/L for methyl violet and basic orange dye, respectively. The adsorption isotherm shows that the correlation coefficient of Freundlich model was higher than Langmuir model for both dyes, indicating that the Freundlich model is more appropriate to describe the adsorption characteristics of organic pollutants.

Chemometric analysis of frequency-domain photon migration data: quantitative measurements of optical properties and chromophore concentrations in multicomponent turbid media

International Nuclear Information System (INIS)

Berger, Andrew J.; Venugopalan, Vasan; Durkin, Anthony J.; Pham, Tuan; Tromberg, Bruce J.

2000-01-01

Frequency-domain photon migration (FDPM) is a widely used technique for measuring the optical properties (i.e., absorption, μ a , and reduced scattering, μ s ' , coefficients) of turbid samples. Typically, FDPM data analysis is performed with models based on a photon diffusion equation; however, analytical solutions are difficult to obtain for many realistic geometries. Here, we describe the use of models based instead on representative samples and multivariate calibration (chemometrics). FDPM data at seven wavelengths (ranging from 674 to 956 nm) and multiple modulation frequencies (ranging from 50 to 600 MHz) were gathered from turbid samples containing mixtures of three absorbing dyes. Values for μ a and μ s ' were extracted from the FDPM data in different ways, first with the diffusion theory and then with the chemometric technique of partial least squares. Dye concentrations were determined from the FDPM data by three methods, first by least-squares fits to the diffusion results and then by two chemometric approaches. The accuracy of the chemometric predictions was comparable or superior for all three dyes. Our results indicate that chemometrics can recover optical properties and dye concentrations from the frequency-dependent behavior of photon density waves, without the need for diffusion-based models. Future applications to more complicated geometries, lower-scattering samples, and simpler FDPM instrumentation are discussed. (c) 2000 Optical Society of America

Decolorization of Anthraquinonic Dyes from Textile Effluent Using Horseradish Peroxidase: Optimization and Kinetic Study

Science.gov (United States)

Šekuljica, Nataša Ž.; Prlainović, Nevena Ž.; Stefanović, Andrea B.; Žuža, Milena G.; Čičkarić, Dragana Z.; Mijin, Dušan Ž.; Knežević-Jugović, Zorica D.

2015-01-01

Two anthraquinonic dyes, C.I. Acid Blue 225 and C.I. Acid Violet 109, were used as models to explore the feasibility of using the horseradish peroxidase enzyme (HRP) in the practical decolorization of anthraquinonic dyes in wastewater. The influence of process parameters such as enzyme concentration, hydrogen peroxide concentration, temperature, dye concentration, and pH was examined. The pH and temperature activity profiles were similar for decolorization of both dyes. Under the optimal conditions, 94.7% of C.I. Acid Violet 109 from aqueous solution was decolorized (treatment time 15 min, enzyme concentration 0.15 IU/mL, hydrogen peroxide concentration 0.4 mM, dye concentration 30 mg/L, pH 4, and temperature 24°C) and 89.36% of C.I. Acid Blue 225 (32 min, enzyme concentration 0.15 IU/mL, hydrogen peroxide concentration 0.04 mM, dye concentration 30 mg/L, pH 5, and temperature 24°C). The mechanism of both reactions has been proven to follow the two substrate ping-pong mechanism with substrate inhibition, revealing the formation of a nonproductive or dead-end complex between dye and HRP or between H2O2 and the oxidized form of the enzyme. Both chemical oxygen demand and total organic carbon values showed that there was a reduction in toxicity after the enzymatic treatment. This study verifies the viability of use of horseradish peroxidase for the wastewaters treatment of similar anthraquinonic dyes. PMID:25685837

Decolorization of Anthraquinonic Dyes from Textile Effluent Using Horseradish Peroxidase: Optimization and Kinetic Study

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Nataša Ž. Šekuljica

2015-01-01

Full Text Available Two anthraquinonic dyes, C.I. Acid Blue 225 and C.I. Acid Violet 109, were used as models to explore the feasibility of using the horseradish peroxidase enzyme (HRP in the practical decolorization of anthraquinonic dyes in wastewater. The influence of process parameters such as enzyme concentration, hydrogen peroxide concentration, temperature, dye concentration, and pH was examined. The pH and temperature activity profiles were similar for decolorization of both dyes. Under the optimal conditions, 94.7% of C.I. Acid Violet 109 from aqueous solution was decolorized (treatment time 15 min, enzyme concentration 0.15 IU/mL, hydrogen peroxide concentration 0.4 mM, dye concentration 30 mg/L, pH 4, and temperature 24°C and 89.36% of C.I. Acid Blue 225 (32 min, enzyme concentration 0.15 IU/mL, hydrogen peroxide concentration 0.04 mM, dye concentration 30 mg/L, pH 5, and temperature 24°C. The mechanism of both reactions has been proven to follow the two substrate ping-pong mechanism with substrate inhibition, revealing the formation of a nonproductive or dead-end complex between dye and HRP or between H2O2 and the oxidized form of the enzyme. Both chemical oxygen demand and total organic carbon values showed that there was a reduction in toxicity after the enzymatic treatment. This study verifies the viability of use of horseradish peroxidase for the wastewaters treatment of similar anthraquinonic dyes.

Effects of reduction products of ortho-hydroxyl substituted azo dyes on biodecolorization of azo dyes

International Nuclear Information System (INIS)

Liu Guangfei; Wang Jing; Lu Hong; Jin Ruofei; Zhou Jiti; Zhang Long

2009-01-01

The mediated effects of reduction products of some ortho-hydroxyl substituted azo dyes on biodecolorization were investigated. The results indicated that the addition of reduction products could effectively accelerate dye decolorization by Shigella sp. QRZ-1. The best accelerating effect was obtained with the addition of reduction products of Acid Red 14 (AR14), resulting in an over 3-fold increase in decolorization efficiency of many azo dyes. In sequencing batch reactor experiments, the accelerating effect of reduction products of AR14 was more obvious (1.5-fold) during the startup of the system. When the dye concentration was increased to 500 mg L -1 , the accelerated decolorization efficiency was still maintained around 95%. The presence of AR14 in the feed enhanced the decolorization performance of anaerobic sludge, indicating that the strategy may be beneficial for practical application. 1-Naphthol-2-amino-4-sulfonic acid, which is one of the reduction products of AR14, may function as redox mediator to speed up azo dye biodecolorization.

Data on final calcium concentration in native gel reagents determined accurately through inductively coupled plasma measurements

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Jeffrey Viviano

2016-03-01

Full Text Available In this article we present data on the concentration of calcium as determined by Inductively Coupled Plasma (ICP measurements. Calcium was estimated in the reagents used for native gel electrophoresis of Neuronal Calcium Sensor (NCS proteins. NCS proteins exhibit calcium-dependent mobility shift in native gels. The sensitivity of this shift to calcium necessitated a precise determination of calcium concentrations in all reagents used. We determined the calcium concentrations in different components used along with the samples in the native gel experiments. These were: 20 mM Tris pH 7.5, loading dye and running buffer, with distilled water as reference. Calcium determinations were through ICP measurements. It was found that the running buffer contained calcium (244 nM over the blank. Keywords: Neuronal calcium sensor proteins, Electrophoresis, Mobility shift, Calcium, Magnesium

Photo-oxidative degradation of Chicago Sky Blue azo dye on transition metal oxide electrodes

Energy Technology Data Exchange (ETDEWEB)

Slote, J.; Luo, J.; Hepel, M. [State Univ. of New York at Potsdam, NY (United States). Dept. of Chemistry; Zhong, C.-J. [State Univ. of New York at Binghamton, NY (United States). Dept. of Chemistry

2003-07-01

Every day, an average of 128 tons of dye staffs are discharged into waste water, causing environmental harm. The authors discussed the photo-electrical method for separating the semiconductor catalyst particles from the solution and direct control of the interfacial potential as an efficient and convenient method for degrading organic dyes. Photocurrent-potential measurements were made using a standard photoelectrochemical setup. It involved a microcomputer-controlled potentiostat and a 500 watts (W) quartz halogen lamp as the illumination source. The measurement of the photocurrent represented the difference between the current under illumination and current in the dark. Three-electrode electrochemical cells were used for all experiments. The best results concerning the degradation of dyes were obtained with tungsten oxides (WO3) and molybdenum oxides (MoO3) electrodes. Confirmation that the dyes had been fully degraded was obtained by performing absorbance measurements and a high performance liquid chromatography (HPLC) analysis of the samples after degradation. The effect on the rate of decolorisation process of Chicago Sky Blue, a diazo dye, and other dyes, of pH, potential, concentration, and type of supporting electrolyte was examined. The supporting electrolyte was found to have a strong influence on the degradation of diazo dye. Illumination with visible light yielded lower degradation rates than that with ultraviolet-visible light. It appears that Chicago Sky Blue dye sensitizes the semiconductor to expand the absorption of light energy well into visible range, despite the photoelectrochemical degradation of the dye being mainly induced by the ultraviolet light. The authors proposed the mechanisms of the reactions occurring during the photodegradation process. 6 refs., 1 fig.

A home-made system for IPCE measurement of standard and dye-sensitized solar cells

Energy Technology Data Exchange (ETDEWEB)

Palma, Giuseppina; Cozzarini, Luca; Capria, Ennio [Organic OptoElectronics Laboratory, Sincrotrone Trieste SCpA—SS 14.5, km 163.5, 34149 Basovizza (TS) (Italy); Fraleoni-Morgera, Alessandro, E-mail: alessandro.fraleoni@elettra.trieste.it, E-mail: afraleoni@units.it [Organic OptoElectronics Laboratory, Sincrotrone Trieste SCpA—SS 14.5, km 163.5, 34149 Basovizza (TS) (Italy); Flextronics Laboratory, Department of Engineering and Architecture, University of Trieste. V. Valerio 10, 34100 Trieste (TS) (Italy)

2015-01-15

A home-made system for incident photon-to-electron conversion efficiency (IPCE) characterization, based on a double-beam UV-Vis spectrophotometer, has been set up. In addition to its low cost (compared to the commercially available apparatuses), the double-beam configuration gives the advantage to measure, autonomously and with no need for supplementary equipment, the lamp power in real time, compensating possible variations of the spectral emission intensity and quality, thus reducing measurement times. To manage the optical and electronic components of the system, a custom software has been developed. Validations carried out on a common silicon-based photodiode and on a dye-sensitized solar cell confirm the possibility to adopt this system for determining the IPCE of solar cells, including dye-sensitized ones.

A home-made system for IPCE measurement of standard and dye-sensitized solar cells.

Science.gov (United States)

Palma, Giuseppina; Cozzarini, Luca; Capria, Ennio; Fraleoni-Morgera, Alessandro

2015-01-01

A home-made system for incident photon-to-electron conversion efficiency (IPCE) characterization, based on a double-beam UV-Vis spectrophotometer, has been set up. In addition to its low cost (compared to the commercially available apparatuses), the double-beam configuration gives the advantage to measure, autonomously and with no need for supplementary equipment, the lamp power in real time, compensating possible variations of the spectral emission intensity and quality, thus reducing measurement times. To manage the optical and electronic components of the system, a custom software has been developed. Validations carried out on a common silicon-based photodiode and on a dye-sensitized solar cell confirm the possibility to adopt this system for determining the IPCE of solar cells, including dye-sensitized ones.

Removal of some basic dyes by poly (Vinyl Alcohol/ acrylic acid)Hydrogel

International Nuclear Information System (INIS)

Hegazy, S.A.; Abdel-AAl, S.E.; Abdel-Rehim, H.A.; Khalifa, N.A.; El-Hosseiny, E.M.

2000-01-01

A study has made on the preparation and properties of poly (vinyl alcohol/ acrylic acid) hydrogel for the purpose of removal of cationic dyes from aqueous solutions. The effect of dose and monomer concentration on the uptake property of the hydrogel toward dye was studied. The uptake of basic methylene blue-9 dye with PVA/AAc was studied by the batch adsorption technique. The effect of pH on the dye uptake was demonstrated to find out that the suitable pH for maximum uptake occurred at pH 5. It was observed that as the concentration of dye is increased the dye uptake decreased. Furthermore, the uptake of dye by hydrogels increased as the temperature was elevated. The recovery of dye adsorbed is possible by treating the hydrogel with 5% HCl. The results obtained suggested this hydrogel possessed good removal properties towards basic methylene blue-9 dye, and this suggests that such hydrogels could be acceptable for practical uses

Decolorization and Degradation of Batik Dye Effluent using Ganoderma lucidum

Science.gov (United States)

Pratiwi, Diah; Indrianingsih, A. W.; Darsih, Cici; Hernawan

2017-12-01

Batik is product of traditional Indonesia culture that developed into a large textile industry. Synthetic dyes which widely used in textile industries including batik. Colour can be removed from wastewater effluent by chemical, physical, and biology methods. Bioremediation is one of the methods that used for processing colored effluent. Isolated White-rot fungi Ganoderma lucidum was used for bioremediation process for batik effluent. G. lucidum was developed by G. lucidum cultivation on centers of mushroom farmer Media Agro Merapi Kaliurang, Yogyakarta. The batik effluent was collected from a private small and medium Batik enterprises located at Petir, Rongkop, Gunungkidul Regency. The aim of the study were to optimize decolorization of Naphtol Black (NB) using G. lucidum. The effect of process parameters like incubation time and dye concentration on dye decolorization and COD degradation was studied. G. lucidum were growth at pH 5-6 and temperature 25°C at various Naphtol Black dye with concentration 20 ppm, 50 ppm, and 100 ppm for 30 day incubation time. The result from this study increased decolorization in line with the increasing of COD degradation. Increasing percentage of decolorization and COD degradation gradually increased with incubation time and dye concentration. The maximum decolorization and COD reduction were found to be 60,53% and 81,03%. G. lucidum had potential to decolorized and degraded COD for NB dye effluent on higher concentration.

A Critical Comparison of Methods for the Analysis of Indigo in Dyeing Liquors and Effluents

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Valentina Buscio

2014-08-01

Full Text Available Indigo is one of the most important dyes in the textile industry. The control of the indigo concentration in dyeing liquors and effluents is an important tool to ensure the reproducibility of the dyed fabrics and also to establish the efficiency of the wastewater treatment. In this work, three analytical methods were studied and validated with the aim to select a reliable, fast and automated method for the indigo dye determination. The first method is based on the extraction of the dye, with chloroform, in its oxidized form. The organic solution is measured by Ultraviolet (UV-visible spectrophotometry at 604 nm. The second method determines the concentration of indigo in its leuco form in aqueous medium by UV-visible spectrophotometry at 407 nm. Finally, in the last method, the concentration of indigo is determined by redox titration with potassium hexacyanoferrate (K3(Fe(CN6. The results indicated that the three methods that we studied met the established acceptance criteria regarding accuracy and precision. However, the third method was considered the most adequate for application on an industrial scale due to its wider work range, which provides a significant advantage over the others.

Photoactive curcumin-derived dyes with surface anchoring moieties used in ZnO nanoparticle-based dye-sensitized solar cells

International Nuclear Information System (INIS)

Ganesh, T.; Kim, Jong Hoon; Yoon, Seog Joon; Kil, Byung-Ho; Maldar, N.N.; Han, Jin Wook; Han, Sung-Hwan

2010-01-01

Photoactive, eco-friendly and high molar extinction coefficient, curcumin-derived dyes (BCMoxo and BCtCM) have been explored in ZnO nanoparticles (NPs)-based dye-sensitized solar cells (DSSCs). The boron complex curcumin dyes modified with di-carboxylic anchor groups (BCtCM) provided surface attachment with a strong UV-vis region absorption than the dye molecule without anchor groups (BCMoxo). Photoanodes primed with poly-dispersive ZnO NPs (∼80-50 nm) specifically devised for these dyes and optimized for the critical thickness, sensitization time and concentration using a solvent-free ionic electrolyte so as to get current density as high as 1.66 mA/cm 2 under 80 mW/cm 2 irradiation. Therefore, a successful conversion of visible light into electricity by using these curcumin-derived dyes (natural derived photoactive molecules) as photosensitizer in DSSCs would be a great interest in future studies for enhancing further conversion efficiencies.

Decolorization of reactive dyes under batch anaerobic condition by ...

African Journals Online (AJOL)

However, decolorization was lower for the dye of RB 49 than other two dyes in all concentrations despite 72 h incubation period by mixed anaerobic culture. All of the three dyes correlated with 1st order reaction kinetic with respect to decolorization kinetics. The results of the study demonstrated that high decolorization was ...

Perylene Derivative Dyes Luminescence in Polysiloxane Matrix in Presence of Gold Nanoparticles.

Science.gov (United States)

Mantel, Artur; Shautenbaeva, Nazerke; Irgibaeva, Irina; Aldongarov, Anuar; Lang, Albina; Barashkov, Nikolay; Mukatayev, Iskander

2016-11-01

Four perylene derivatives, including commercially available dyes Lumogen Red and Lumogen Orange, as well as 1,6,7,12-tetrachlоrоperylene-3,4,9,10-tetradicarboxydianhydride (Dye I) and 3,4:9,10-bis(1,2-benzimidazole)- 1,6,7,12-tetra(4-tert-octylphenoxy) perylene (syn/ anti-isomers) (Dye III, which was prepared from dye I through intermediate 3,4:9,10-bis(1,2-benzimidazole)-1,6,7,12-tetrachloro perylene (Dye II)) were used for preparation of polysiloxane samples (PSi) containing different concentrations of gold nanoparticles (GN). Dyes I and III demonstrate significant fluorescence intensity increase upon addition of GN independent on excitation energy. For Lumogen Red composition in PSi some increase of fluorescence intensity was observed upon addition of small concentrations of GN, while further increase of GN concentration quenches fluorescence. The increase of Lumogen Red emission intensity, which depends on energy of excitation, is probably due to the increase of radiation decay rate since excitation rate decreases. Effect of GN on Lumogen Orange provided quenching of fluorescence even at small concentrations of GN. Calculations at DFT level of approximation for dye III suggest location of GN in plane of perylene core for increase of fluorescence intensity.

Comparison of two voltage-sensitive dyes and their suitability for long-term imaging of neuronal activity.

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Stephanie Preuss

Full Text Available One of the key approaches for studying neural network function is the simultaneous measurement of the activity of many neurons. Voltage-sensitive dyes (VSDs simultaneously report the membrane potential of multiple neurons, but often have pharmacological and phototoxic effects on neuronal cells. Yet, to study the homeostatic processes that regulate neural network function long-term recordings of neuronal activities are required. This study aims to test the suitability of the VSDs RH795 and Di-4-ANEPPS for optically recording pattern generating neurons in the stomatogastric nervous system of crustaceans with an emphasis on long-term recordings of the pyloric central pattern generator. We demonstrate that both dyes stain pyloric neurons and determined an optimal concentration and light intensity for optical imaging. Although both dyes provided sufficient signal-to-noise ratio for measuring membrane potentials, Di-4-ANEPPS displayed a higher signal quality indicating an advantage of this dye over RH795 when small neuronal signals need to be recorded. For Di-4-ANEPPS, higher dye concentrations resulted in faster and brighter staining. Signal quality, however, only depended on excitation light strength, but not on dye concentration. RH795 showed weak and slowly developing phototoxic effects on the pyloric motor pattern as well as slow bleaching of the staining and is thus the better choice for long-term experiments. Low concentrations and low excitation intensities can be used as, in contrast to Di-4-ANEPPS, the signal-to-noise ratio was independent of excitation light strength. In summary, RH795 and Di-4-ANEPPS are suitable for optical imaging in the stomatogastric nervous system of crustaceans. They allow simultaneous recording of the membrane potential of multiple neurons with high signal quality. While Di-4-ANEPPS is better suited for short-term experiments that require high signal quality, RH795 is a better candidate for long-term experiments

Photoactive curcumin-derived dyes with surface anchoring moieties used in ZnO nanoparticle-based dye-sensitized solar cells

Energy Technology Data Exchange (ETDEWEB)

Ganesh, T.; Kim, Jong Hoon; Yoon, Seog Joon; Kil, Byung-Ho; Maldar, N.N. [Inorganic Nano-Materials Laboratory, Department of Chemistry, Hanyang University, Sung-Dong-Ku, Haengdang-dong 17, Seoul (Korea, Republic of); Han, Jin Wook, E-mail: jwhan@hanyang.ac.kr [Inorganic Nano-Materials Laboratory, Department of Chemistry, Hanyang University, Sung-Dong-Ku, Haengdang-dong 17, Seoul (Korea, Republic of); Han, Sung-Hwan, E-mail: shhan@hanyang.ac.kr [Inorganic Nano-Materials Laboratory, Department of Chemistry, Hanyang University, Sung-Dong-Ku, Haengdang-dong 17, Seoul (Korea, Republic of)

2010-09-01

Photoactive, eco-friendly and high molar extinction coefficient, curcumin-derived dyes (BCMoxo and BCtCM) have been explored in ZnO nanoparticles (NPs)-based dye-sensitized solar cells (DSSCs). The boron complex curcumin dyes modified with di-carboxylic anchor groups (BCtCM) provided surface attachment with a strong UV-vis region absorption than the dye molecule without anchor groups (BCMoxo). Photoanodes primed with poly-dispersive ZnO NPs ({approx}80-50 nm) specifically devised for these dyes and optimized for the critical thickness, sensitization time and concentration using a solvent-free ionic electrolyte so as to get current density as high as 1.66 mA/cm{sup 2} under 80 mW/cm{sup 2} irradiation. Therefore, a successful conversion of visible light into electricity by using these curcumin-derived dyes (natural derived photoactive molecules) as photosensitizer in DSSCs would be a great interest in future studies for enhancing further conversion efficiencies.

Photocatalytic decolorization of basic dye by TiO2 nanoparticle in photoreactor

Directory of Open Access Journals (Sweden)

Jutaporn Chanathaworn1

2012-04-01

Full Text Available Photocatalytic decolorization of rhodamine B (RB and malachite green (MG basic dyes in aqueous solution wasevaluated using TiO2 powder as a semiconductor photocatalyst under UV black light irradiation. A 0.5 L batch photoreactorcontaining dyeing solution was installed in a stainless steel chamber with air cooling under irradiation. The TiO2 powder wascharacterized by XRD observation and it was shown that the nanoparticles could be identified as 73 nm anatase crystals. Theeffects of operational parameters such as light intensity (0-114 W/m2, initial dye concentration (10-30 mg/L, and TiO2 powderloading (0.5-1.5 g/L on the decolorization of dye samples were examined. The photocatalytic decolorization rate depended onthe pollutant’s structure, such that the MG dye could be removed faster than the RB dye. Decolorization efficiency (% of thephotocatalytic system increased with increasing TiO2 loading and light intensity; however, it decreased with increasing initialdye concentration. A loading of 1.5 g TiO2/L, initial dye concentration of 20 mg/L, and light intensity of 114 W/m2 were foundto yield the highest removal efficiency of dye solution based on time requirement. The kinetics are of first order and dependon the TiO2 powder loading and dye structure. The research had a perfect application foreground.

Effect of gamma-irradiation on basic dye maxilon blue in aqueous solution

International Nuclear Information System (INIS)

Andayani, Winarti; Bagyo, Agustin S.M.; Winarno, Ermin K.; Winarno, Hendig

1998-01-01

The effects of radiation of basic dye maxilon blue have been studied. Irradiation was done at various pH (3, 5, 7, 9, and 12) with doses of 0 - 4 kGy/h. at pH 5 irradiation of dye solution with variation of concentration i.e. 10; 25; 50.8; 78.2 and 106 ppm were done. Bubbling of air were done during irradiation of dye solution. Parameters examined were the change of the spectrum by spectrophotometer, the decrease of pH by pH meter and degradation products such as organic acids by HPLC. The results showed that the percentage of degradation at acid pH is higher than that basic and neutral pH. G value (degradation) of the dye at pH 5 was 0.876 with a dose rate of 5 kGy/h. Percentage of decoloration of dye solution at initial concentration 10 and 25 ppm were higher than 90% at dose of 0.5 kGy, dye solution at initial concentration between 50 to 106 ppm were higher than 90% at 2 kGy. The equation of degradation rate of the dye was V=-d(dye)/dt = 1.4 x 10 -2 [dye] 1,1107 ppm/min. Degradation of the dye has first order pseudo with the rate constant of 1.4 x 10 -2 min -1 . Degradation products that could be detected was oxalic acid. (authors)

Application of AzollaFiliculoides Biomass in Acid Black 1 Dye Adsorption from Aqueous Solution

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Mohammad Ali Zazouli

2014-09-01

Full Text Available Background and purpose: The textile dyes are considered as important pollutants due to the toxicity on human and environment. Therefore, the dye removal from industrial effluents is necessary. This study evaluates the ability of Azolla for the adsorption of acid black 1 (AB1 dye from aqueous solution. Materials and Methods: This was an experimental-laboratory study. The Azolla biomass was sun dried, crushed and sieved to particle sizes in the range of 1-2 mm. Then, it treated with 0.1 M HCl for 5 h, followed by washing with distilled water, and it used as an adsorbent. The effect of study parameter was investigated, and the residues AB1 concentration was measured by DR2800 spectrophotometer at in λmax = 622 nm. Results: The results indicated that the efficiency of AB1 adsorption decreased with increased initial dye concentration. It increased with increased contact time and adsorbent. The highest adsorption efficiency was occurred at pH = 2. The equilibrium data were the best fitted on Langmuir isotherm and pseudo-second-order kinetic model. Conclusion: The Azolla could present high ability in dye removal. Therefore, it can be used as inexpensive and effective adsorbent in textile effluent treatment.

Green dyeing process of modified cotton fibres using natural dyes extracted from Tamarix aphylla (L.) Karst. leaves.

Science.gov (United States)

Baaka, Noureddine; Mahfoudhi, Adel; Haddar, Wafa; Mhenni, Mohamed Farouk; Mighri, Zine

2017-01-01

This research work involves an eco-friendly dyeing process of modified cotton with the aqueous extract of Tamarix aphylla leaves. During this process, the dyeing step was carried out on modified cotton by several cationising agents in order to improve its dyeability. The influence of the main dyeing conditions (dye bath pH, dyeing time, dyeing temperature, salt addition) on the performances of this dyeing process were studied. The dyeing performances of this process were appreciated by measuring the colour yield (K/S) and the fastness properties of the dyed samples. The effect of mordant type with different mordanting methods on dyeing quality was also studied. The results showed that mordanting gave deeper shades and enhanced fastness properties. In addition, environmental indicators (BOD 5 , COD and COD/BOD 5 ) were used to describe potential improvements in the biodegradability of the dyebath wastewater. Further, HPLC was used to identify the major phenolic compounds in the extracted dye.

Optical properties of natural dyes on the dye-sensitized solar cells (DSSC) performance

International Nuclear Information System (INIS)

Pratiwi, D. D.; Nurosyid, F.; Supriyanto, A.; Suryana, R.

2016-01-01

This study reported several natural dyes for application in dye-sensitized solar cells (DSSC). This study aims was to determine the effect of optical absorption properties of natural dyes on efficiency of DSSC. The sandwich structure of DSSC consist of TiO 2 as working electrode, carbon layer as counter electrode, natural dyes as photosensitizer, and electrolyte as electron transfer media. The natural dyes used in this experiment were extracted from dragon fruit anthocyanin, mangosteen peels anthocyanin, and red cabbage anthocyanin. The absorbance of dyes solutions and the adsorption of the dye on the surface of TiO 2 were characterized using UV-Vis spectrophotometer, the quantum efficiency versus wavelength was characterized using incident photon-to-current efficiency (IPCE) measurement system, and the efficiency of DSSC was calculated using I-V meter. UV-Vis characteristic curves showed that wavelength absorption of anthocyanin dye of red cabbage was 450 - 580 nm, anthocyanin of mangosteen peels was 400 - 480 nm, and anthocyanin of dragon fruit was 400 - 650 nm. Absorption spectra of the dye adsorption on the surface of TiO 2 which was resulted in the highest absorbance of red cabbage anthocyanin. IPCE characteristic curves with anthocyanin dye of red cabbage, mangosteen peels anthocyanin, and dragon fruit anthocyanin resulted quantum efficiency of 0.058%; 0.047%; and 0.043%, respectively at wavelength maximum about 430 nm. I-V characteristic curves with anthocyanin dye of red cabbage, mangosteen peels anthocyanin, and dragon fruit anthocyanin resulted efficiency of 0.054%; 0.042%; and 0.024%, respectively. (paper)

Effects of reduction products of ortho-hydroxyl substituted azo dyes on biodecolorization of azo dyes

Energy Technology Data Exchange (ETDEWEB)

Liu Guangfei [Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental and Biological Science and Technology, Dalian University of Technology, Linggong Road No. 2, Dalian 116024 (China); Wang Jing, E-mail: wangjingbio@yahoo.cn [Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental and Biological Science and Technology, Dalian University of Technology, Linggong Road No. 2, Dalian 116024 (China); Lu Hong; Jin Ruofei; Zhou Jiti; Zhang Long [Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental and Biological Science and Technology, Dalian University of Technology, Linggong Road No. 2, Dalian 116024 (China)

2009-11-15

The mediated effects of reduction products of some ortho-hydroxyl substituted azo dyes on biodecolorization were investigated. The results indicated that the addition of reduction products could effectively accelerate dye decolorization by Shigella sp. QRZ-1. The best accelerating effect was obtained with the addition of reduction products of Acid Red 14 (AR14), resulting in an over 3-fold increase in decolorization efficiency of many azo dyes. In sequencing batch reactor experiments, the accelerating effect of reduction products of AR14 was more obvious (1.5-fold) during the startup of the system. When the dye concentration was increased to 500 mg L{sup -1}, the accelerated decolorization efficiency was still maintained around 95%. The presence of AR14 in the feed enhanced the decolorization performance of anaerobic sludge, indicating that the strategy may be beneficial for practical application. 1-Naphthol-2-amino-4-sulfonic acid, which is one of the reduction products of AR14, may function as redox mediator to speed up azo dye biodecolorization.

An LED Approach for Measuring the Photocatalytic Breakdown of Crystal Violet Dye

Science.gov (United States)

Ryan, Robert E.; Underwood, Lauren W.; ONeal, Duane; Pagnutti, Mary; Davis, Bruce A.

2009-01-01

dye degradation on the slides over time, a temperature-stabilized white light LED was used to illuminate the opposite side of the slides. As the dye degraded, the amount of light from the white light LED transmitted through the slide was monitored with a spectrometer and subsequently analyzed to determine and compare the rate of dye degradation for photocatalytically coated versus uncoated slide surfaces. The long-term stability of the spectrometer/white light LED combination, which required only a single reference spectra to be taken for a time series sequence of several hours, enabled accurate measurements of transmitted light over time. Time series transmission curves were generated and results demonstrated that over time the transmission increased much more rapidly on the coated slides than on the control slides. This experimental configuration and methodology for photocatalytic activity measurement minimizes many external variable effects and allows low light level studies to be performed. This study also compares the advantages of this novel LED light source design to traditional mercury lamp systems and non-LED lamp approaches that have conventionally been used. The methodology and experimental design research summarized in this abstract is partly funded by the Department of Homeland Security, Science and Technology Directorate, and by the NASA Stennis Space Center Innovative Partnerships Program.

Bioremoval of the azo dye Congo Red by the microalga Chlorella vulgaris.

Science.gov (United States)

Hernández-Zamora, Miriam; Cristiani-Urbina, Eliseo; Martínez-Jerónimo, Fernando; Perales-Vela, Hugo Virgilio; Ponce-Noyola, Teresa; Montes-Horcasitas, María del Carmen; Cañizares-Villanueva, Rosa Olivia

2015-07-01

Discharge of dye-containing wastewater by the textile industry can adversely affect aquatic ecosystems and human health. Bioremoval is an alternative to industrial processes for detoxifying water contaminated with dyes. In this work, active and inactive biomass of the microalga Chlorella vulgaris was assayed for the ability to remove Congo Red (CR) dye from aqueous solutions. Through biosorption and biodegradation processes, Chlorella vulgaris was able to remove 83 and 58 % of dye at concentrations of 5 and 25 mg L(-1), respectively. The maximum adsorption capacity at equilibrium was 200 mg g(-1). The Langmuir model best described the experimental equilibrium data. The acute toxicity test (48 h) with two species of cladocerans indicated that the toxicity of the dye in the effluent was significantly decreased compared to the initial concentrations in the influent. Daphnia magna was the species less sensitive to dye (EC50 = 17.0 mg L(-1)), followed by Ceriodaphnia dubia (EC50 = 3.32 mg L(-1)). These results show that Chlorella vulgaris significantly reduced the dye concentration and toxicity. Therefore, this method may be a viable option for the treatment of this type of effluent.

Decomposition and decoloration of a direct dye by electron beam radiation

International Nuclear Information System (INIS)

Vahdat, Ali; Bahrami, S.H.; Arami, M.; Motahari, A.

2010-01-01

The wastewaters released by textile industries to the environment contain hazardous compounds like toxic refractory dye stuff at high concentration. In this study, electron beam irradiation-induced decoloration and decomposition of C.I. Direct Black 22 aqueous solutions were investigated. The influences of absorbed doses and initial dye concentration on the percent of decoloration, COD and pH of the solutions are described. The results show that the direct dye solutions can be effectively degraded by electron beam irradiation.

Application of Electrocoagulation Process for Reactive Red 198 Dye Removal from the Aqueous Solution

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Mansooreh Dehghani

2014-04-01

Full Text Available Abstract Background and purpose:The main objectives of this research were to evaluating the application of electrocoagulation process for 198 dye from the aqueous phase and determining the optimum operating conditions to the dye removal using aluminum and iron electrodes. Materials and Methods:The present study was conducted in bench-scale. The spectrophotometer DR 5000 was used to determine the dye concentration. The effects of pH, retention time, voltage, dye concentration on the efficiency of electrocoagulation process were investigated. Data were analyzed in SPSS for Windows 16.0 using Pearson’scorrelation coefficient to analyze the relationship between these parameters. Results:The results showed that the optimal conditions for reactive red 198 (RR-198 dye removal from the aqueous solution are pH of 11, the voltage of 32 V, the initial dye concentration of 10 ppm, and the reaction time of 40 min. Pearson correlation analysis showed that there is a significant relationship between voltage and the reaction time with the removal efficiencies (P< 0.01. Conclusion:It was revealed that the removal efficiency of dye was directly proportional to the voltage and reaction time, but inversely proportional to the initial dye concentration. In conclusion, electrocoagulation process using two-fold iron and aluminum electrodes is an appropriate method for reducing the RR-198 dye in the aqueous phase.

Fluorescence spectroscopy of Rhodamine 6G: concentration and solvent effects.

Science.gov (United States)

Zehentbauer, Florian M; Moretto, Claudia; Stephen, Ryan; Thevar, Thangavel; Gilchrist, John R; Pokrajac, Dubravka; Richard, Katherine L; Kiefer, Johannes

2014-01-01

Rhodamine 6G (R6G), also known as Rhodamine 590, is one of the most frequently used dyes for application in dye lasers and as a fluorescence tracer, e.g., in the area of environmental hydraulics. Knowing the spectroscopic characteristics of the optical emission is key to obtaining high conversion efficiency and measurement accuracy, respectively. In this work, solvent and concentration effects are studied. A series of eight different organic solvents (methanol, ethanol, n-propanol, iso-propanol, n-butanol, n-pentanol, acetone, and dimethyl sulfoxide (DMSO)) are investigated at constant dye concentration. Relatively small changes of the fluorescence spectrum are observed for the different solvents; the highest fluorescence intensity is observed for methanol and lowest for DMSO. The shortest peak wavelength is found in methanol (568 nm) and the longest in DMSO (579 nm). Concentration effects in aqueous R6G solutions are studied over the full concentration range from the solubility limit to highly dilute states. Changing the dye concentration provides tunability between ∼550 nm in the dilute case and ∼620 nm at high concentration, at which point the fluorescence spectrum indicates the formation of R6G aggregates. Copyright © 2013 Elsevier B.V. All rights reserved.

Polymerization of novel methacrylated anthraquinone dyes

Directory of Open Access Journals (Sweden)

Christian Dollendorf

2013-02-01

Full Text Available A new series of polymerizable methacrylated anthraquinone dyes has been synthesized by nucleophilic aromatic substitution reactions and subsequent methacrylation. Thereby, green 5,8-bis(4-(2-methacryloxyethylphenylamino-1,4-dihydroxyanthraquinone (2, blue 1,4-bis(4-((2-methacryloxyethyloxyphenylaminoanthraquinone (6 and red 1-((2-methacryloxy-1,1-dimethylethylaminoanthraquinone (12, as well as 1-((1,3-dimethacryloxy-2-methylpropan-2-ylaminoanthraquinone (15 were obtained. By mixing of these brilliant dyes in different ratios and concentrations, a broad color spectrum can be generated. After methacrylation, the monomeric dyes can be covalently emplaced into several copolymers. Due to two polymerizable functionalities, they can act as cross-linking agents. Thus, diffusion out of the polymer can be avoided, which increases the physiological compatibility and makes the dyes promising compounds for medical applications, such as iris implants.

Effect of dye extracting solvents and sensitization time on photovoltaic performance of natural dye sensitized solar cells

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Md. Khalid Hossain

Full Text Available In this study, natural dye sensitizer based solar cells were successfully fabricated and photovoltaic performance was measured. Sensitizer (turmeric sources, dye extraction process, and photoanode sensitization time of the fabricated cells were analyzed and optimized. Dry turmeric, verdant turmeric, and powder turmeric were used as dye sources. Five distinct types of solvents were used for extraction of natural dye from turmeric. Dyes were characterized by UV–Vis spectrophotometric analysis. The extracted turmeric dye was used as a sensitizer in the dye sensitized solar cell’s (DSSC photoanode assembly. Nano-crystalline TiO2 was used as a film coating semiconductor material of the photoanode. TiO2 films on ITO glass substrate were prepared by simple doctor blade technique. The influence of the different parameters VOC, JSC, power density, FF, and η% on the photovoltaic characteristics of DSSCs was analyzed. The best energy conversion performance was obtained for 2 h adsorption time of dye on TiO2 nano-porous surface with ethanol extracted dye from dry turmeric. Keywords: DSSC, Natural dye, TiO2 photoanode, Dye extracting solvent, Dye-adsorption time

Effect of dye extracting solvents and sensitization time on photovoltaic performance of natural dye sensitized solar cells

Science.gov (United States)

Hossain, Md. Khalid; Pervez, M. Firoz; Mia, M. N. H.; Mortuza, A. A.; Rahaman, M. S.; Karim, M. R.; Islam, Jahid M. M.; Ahmed, Farid; Khan, Mubarak A.

In this study, natural dye sensitizer based solar cells were successfully fabricated and photovoltaic performance was measured. Sensitizer (turmeric) sources, dye extraction process, and photoanode sensitization time of the fabricated cells were analyzed and optimized. Dry turmeric, verdant turmeric, and powder turmeric were used as dye sources. Five distinct types of solvents were used for extraction of natural dye from turmeric. Dyes were characterized by UV-Vis spectrophotometric analysis. The extracted turmeric dye was used as a sensitizer in the dye sensitized solar cell's (DSSC) photoanode assembly. Nano-crystalline TiO2 was used as a film coating semiconductor material of the photoanode. TiO2 films on ITO glass substrate were prepared by simple doctor blade technique. The influence of the different parameters VOC, JSC, power density, FF, and η% on the photovoltaic characteristics of DSSCs was analyzed. The best energy conversion performance was obtained for 2 h adsorption time of dye on TiO2 nano-porous surface with ethanol extracted dye from dry turmeric.

Calibration procedures for the quantitative determination of membrane potential in human cells using anionic dyes.

Science.gov (United States)

Klapperstück, Thomas; Glanz, Dagobert; Hanitsch, Stefan; Klapperstück, Manuela; Markwardt, Fritz; Wohlrab, Johannes

2013-07-01

Quantitative determinations of the cell membrane potential of lymphocytes (Wilson et al., J Cell Physiol 1985;125:72-81) and thymocytes (Krasznai et al., J Photochem Photobiol B 1995;28:93-99) using the anionic dye DiBAC4 (3) proved that dye depletion in the extracellular medium as a result of cellular uptake can be negligible over a wide range of cell densities. In contrast, most flow cytometric studies have not verified this condition but rather assumed it from the start. Consequently, the initially prepared extracellular dye concentration has usually been used for the calculation of the Nernst potential of the dye. In this study, however, external dye depletion could be observed in both large IGR-1 and small LCL-HO cells under experimental conditions, which have often been applied routinely in spectrofluorimetry and flow cytometry. The maximum cell density at which dye depletion could be virtually avoided was dependent on cell size and membrane potential and definitely needed to be taken into account to ensure reliable results. In addition, accepted calibration procedures based on the partition of sodium and potassium (Goldman-Hodgkin-Katz equation) or potassium alone (Nernst equation) were performed by flow cytometry on cell suspensions with an appropriately low cell density. The observed extensive lack of concordance between the correspondingly calculated membrane potential and the equilibrium potential of DiBAC4 (3) revealed that these methods require the additional measurement of cation parameters (membrane permeability and/or intracellular concentration). In contrast, due to the linear relation between fluorescence and low DiBAC4 (3) concentrations, the Nernst potential of the dye for totally depolarized cells can be reliably used for calibration with an essentially lower effort and expense. Copyright © 2013 International Society for Advancement of Cytometry.

Recent Advances in Heterogeneous Photocatalytic Decolorization of Synthetic Dyes

Science.gov (United States)

Muhd Julkapli, Nurhidayatullaili; Bagheri, Samira; Bee Abd Hamid, Sharifah

2014-01-01

During the process and operation of the dyes, the wastes produced were commonly found to contain organic and inorganic impurities leading to risks in the ecosystem and biodiversity with the resultant impact on the environment. Improper effluent disposal in aqueous ecosystems leads to reduction of sunlight penetration which in turn diminishes photosynthetic activity, resulting in acute toxic effects on the aquatic flora/fauna and dissolved oxygen concentration. Recently, photodegradation of various synthetic dyes has been studied in terms of their absorbance and the reduction of oxygen content by changes in the concentration of the dye. The advantages that make photocatalytic techniques superior to traditional methods are the ability to remove contaminates in the range of ppb, no generation of polycyclic compounds, higher speed, and lower cost. Semiconductor metal oxides, typically TiO2, ZnO, SnO, NiO, Cu2O, Fe3O4, and also CdS have been utilized as photocatalyst for their nontoxic nature, high photosensitivity, wide band gap and high stability. Various process parameters like photocatalyst dose, pH and initial dye concentrations have been varied and highlighted. Research focused on surface modification of semiconductors and mixed oxide semiconductors by doping them with noble metals (Pt, Pd, Au, and Ag) and organic matter (C, N, Cl, and F) showed enhanced dye degradation compared to corresponding native semiconductors. This paper reviews recent advances in heterogeneous photocatalytic decolorization for the removal of synthetic dyes from water and wastewater. Thus, the main core highlighted in this paper is the critical selection of semiconductors for photocatalysis based on the chemical, physical, and selective nature of the poisoning dyes. PMID:25054183

Recent Advances in Heterogeneous Photocatalytic Decolorization of Synthetic Dyes

Directory of Open Access Journals (Sweden)

Nurhidayatullaili Muhd Julkapli

2014-01-01

Full Text Available During the process and operation of the dyes, the wastes produced were commonly found to contain organic and inorganic impurities leading to risks in the ecosystem and biodiversity with the resultant impact on the environment. Improper effluent disposal in aqueous ecosystems leads to reduction of sunlight penetration which in turn diminishes photosynthetic activity, resulting in acute toxic effects on the aquatic flora/fauna and dissolved oxygen concentration. Recently, photodegradation of various synthetic dyes has been studied in terms of their absorbance and the reduction of oxygen content by changes in the concentration of the dye. The advantages that make photocatalytic techniques superior to traditional methods are the ability to remove contaminates in the range of ppb, no generation of polycyclic compounds, higher speed, and lower cost. Semiconductor metal oxides, typically TiO2, ZnO, SnO, NiO, Cu2O, Fe3O4, and also CdS have been utilized as photocatalyst for their nontoxic nature, high photosensitivity, wide band gap and high stability. Various process parameters like photocatalyst dose, pH and initial dye concentrations have been varied and highlighted. Research focused on surface modification of semiconductors and mixed oxide semiconductors by doping them with noble metals (Pt, Pd, Au, and Ag and organic matter (C, N, Cl, and F showed enhanced dye degradation compared to corresponding native semiconductors. This paper reviews recent advances in heterogeneous photocatalytic decolorization for the removal of synthetic dyes from water and wastewater. Thus, the main core highlighted in this paper is the critical selection of semiconductors for photocatalysis based on the chemical, physical, and selective nature of the poisoning dyes.

Kinetics of the decoloration of reactive dyes over visible light-irradiated TiO2 semiconductor photocatalyst

International Nuclear Information System (INIS)

Chatterjee, Debabrata; Patnam, Vidya Rupini; Sikdar, Anindita; Joshi, Priyanka; Misra, Rohit; Rao, Nageswara N.

2008-01-01

Photocatalytic decoloration kinetics of triazine (Reactive Red 11, Reactive Red 2, and Reactive Orange 84) and vinylsulfone type (Reactive Orange 16 and Reactive Black 5) of reactive dyes have been studied spectrophotometrically by following the decrease in dye concentration with time. At ambient conditions, over 90-95% decoloration of above dyes have been observed upon prolonged illumination (15 h) of the reacting system with a 150 W xenon lamp. It was found that the decoloration reaction followed first-order kinetics. The values of observed rate constants were found to be dependent of the structure of dyes at low dye concentration, but independent at higher concentration. It also reports for the first time the decoloration of two different dyes together in a binary dye mixture using visible light-irradiated TiO 2 photocatalyst. Rate of decoloration of two different dyes together in a binary dye mixture using visible light-irradiated TiO 2 photocatalyst is governed by the adsorptivity of the particular dye onto the surface of the TiO 2 photocatalyst

Laser-induced removal of a dye C.I. Acid Red 87 using n-type WO{sub 3} semiconductor catalyst

Energy Technology Data Exchange (ETDEWEB)

Qamar, M. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Gondal, M.A., E-mail: magondal@kfupm.edu.sa [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Laser Research Laboratory, Physics Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Hayat, K. [Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Yamani, Z.H. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Laser Research Laboratory, Physics Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Al-Hooshani, K. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)

2009-10-30

Water contamination by organic substances such as dyes is of great concern worldwide due to their utilization in many industrial processes and environmental concerns. To cater the needs for waste water treatment polluted with organic dyes, laser-induced photocatalytic process was investigated for removal of a dye derivative namely Acid Red 87 using n-type WO{sub 3} semiconductor catalyst. The degradation was investigated in aqueous suspensions of tungsten oxide under different experimental conditions using laser instead of conventional UV lamp as an irradiation source. The degradation process was monitored by measuring the change in dye concentration as a function of laser irradiation time by employing UV spectroscopic analysis. The degradation of dye was studied by varying different parameters such as laser energy, reaction pH, substrate concentration, catalyst concentration, and in the presence of electron acceptors such as hydrogen peroxide (H{sub 2}O{sub 2}), and potassium bromate (KBrO{sub 3}). The degradation rates were found to be strongly dependent on all the above-mentioned parameters. Our experimental results revealed that the dye degradation process was very fast (within few minutes) under laser irradiation as compared to conventional setups using broad spectral lamps (hours or days) and this laser-induced photocatalytic degradation method could be an effective means to eliminate the pollutants present in liquid phase. The experience gained through this study could be beneficial for treatment of waste water contaminated with organic dyes and other organic pollutants.

Estimating pollination success with novel artificial flowers: Effects of nectar concentration

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James D. Thomson

2012-10-01

Full Text Available We developed novel artificial flowers that dispense and receive powdered food dyes as pollen analogues while their nectar is replenished by capillary action. Dye receipt, which can be measured colourimetrically, is a direct surrogate for pollen receipt or female reproductive success, but can also serve to compare pollen donation (male reproductive success from flowers with different colours of dye. By allowing captive bumble bee colonies to visit large arrays of such flowers, we investigated whether total dye receipt depended on the sugar concentration of a flower’s nectar. Estimating pollen transfer, rather than simply visitation rate, is appropriate for this question because flowers with more concentrated nectar might accrue more pollen not only through higher visitation rates but also through longer visits that transfer more pollen per visit. Flowers with richer nectar did receive more dye regardless of their spatial arrangement, but the effect was greatest when rich and poor flowers were segregated in large blocks, as opposed to being intermingled.

By-product identification and phytotoxicity of biodegraded Direct Yellow 4 dye.

Science.gov (United States)

Nouren, Shazia; Bhatti, Haq Nawaz; Iqbal, Munawar; Bibi, Ismat; Kamal, Shagufta; Sadaf, Sana; Sultan, Misbah; Kausar, Abida; Safa, Yusra

2017-02-01

Citrus limon peroxidase mediated decolourization of Direct Yellow 4 (DY4) was investigated. The process variables (pH, temperature, incubation time, enzyme dose, H 2 O 2 amount, dye concentration, co-metal ions and surfactants) were optimized for maximum degradation of dye. Maximum dye decolourization of 89.47% was achieved at pH 5.0, temperature 50 °C, enzyme dose 24 U/mL, H 2 O 2 concentration 0.25 mM and DY4 concentration 18.75 mg/L and incubation time 10 min. The co-metal ions and surfactants did not affect the dye decolourization significantly. Response surface analysis revealed that predicted values were in agreement with experimentally determined responses. The degradation products were identified by UPLC/MS analysis and degradation pathway was proposed. Besides, phytotoxicity assay revealed a considerable detoxification in response of biodegradation of DY4 dye. C. limon showed promising efficiency for DY4 degradation and could possibly be used for the remediation of textile effluents. Copyright © 2016 Elsevier Ltd. All rights reserved.

Unconsumed precursors and couplers after formation of oxidative hair dyes

DEFF Research Database (Denmark)

Rastogi, Suresh Chandra; Søsted, Heidi; Johansen, Jeanne Duus

2006-01-01

Contact allergy to hair dye ingredients, especially precursors and couplers, is a well-known entity among consumers having hair colouring done at home or at a hairdresser. The aim of the present investigation was to estimate consumer exposure to some selected precursors (p-phenylenediamine, toluene......-2,5-diamine) and couplers (3-aminophenol, 4-aminophenol, resorcinol) of oxidative hair dyes during and after hair dyeing. Concentrations of unconsumed precursors and couplers in 8 hair dye formulations for non-professional use were investigated, under the conditions reflecting hair dyeing. Oxidative...... hair dye formation in the absence of hair was investigated using 6 products, and 2 products were used for experimental hair dyeing. In both presence and absence of hair, significant amounts of unconsumed precursors and couplers remained in the hair dye formulations after final colour development. Thus...

The destructive degradation of some organic textile dye compounds using gamma ray irradiation

International Nuclear Information System (INIS)

Abdel-Gawad Emara, A.S.; Abdel-Fattah, A.A.; Ebraheem, S.E.; Ali, Z.I.; Gad, H.

2001-01-01

The destructive degradation of 8 coloured reactive and direct dye compounds currently used in the textile industry has been investigated. These dyes are: Levafix Blue ERA (LB), Levafix Brilliant Red E4BA (LBR), Levafix Brilliant Yellow EGA (LBY), Drimarene Scarlet F3G (DS), Drimarene Brilliant Green X3G (DBG), Fast Yellow RL (FY), Fast Violet 2RL (FV) and Fast Orange 3R (FO). The process of degradation of the respective dye has been followed spectrophotometrically at the characteristic lmax. The variation of the colour intensity of aerated aqueous solution of the investigated dyes has been measured as a function of gamma irradiation dose. In all cases, the amplitude of the absorption bands of the dye compound was found to decrease with the increase of the gamma dose. Irradiation was carried out for actual waste and distilled water. By comparing the heights of the absorption maxima in both the visible and ultraviolet ranges, it was found that complete decolouration is attained at lower doses than that needed for the process of degradation of the dye. The kinetics of the degradation process has been traced and the kinetic constant, k 1 , was calculated and found to be concentration dependent indicating a first order reaction in all cases. The radiation-chemical yield (G-value) as a measure of the efficiency of gamma ray to degrade the respective dye was calculated for all dye compounds and it was found that the G-value in all cases increases exponentially for low radiation doses and changes linearly for high radiation doses. Also the K* value (the efficiency coefficient of dye radiolysis) was calculated and compared for the different dye compounds e.g. for FO, FY and FV dyes, the K* values were found to range from 5.5x10 9 to 1.92x10 -7 mol·L -1 '·cm -1 . In addition to the study of a single dye compound in solution, mixtures of different dyes (3 dyes) were also subjected to g-ray irradiation simulating more closely actual waste effluents. Also the effect of some

Biodegradation of Methylene Blue Dye by Sequential Treatment Using Anaerobic Hybrid Reactor and Submerged Aerobic Fixed Film Bioreactor

Science.gov (United States)

Farooqi, Izharul H.; Basheer, Farrukh; Tiwari, Pradeepika

2017-12-01

Laboratory scale experiments were carried out to access the feasibility of sequential anaerobic/aerobic biological treatment for the biodegradation of Methylene Blue (MB) dye. Anaerobic studies were performed using anaerobic hybrid reactor (consisting of UASB and Anaerobic filter) whereas submerged aerobic fixed film reactor was used as aerobic reactor. Degradation of MB dye was attempted using neutralized acetic acid (1000 mg/L) as co-substrate. MB dye concentration was stepwise increased from 10 to 70 mg/L after reaching steady state in each dye concentration. Such a gradual increase in the dye concentration helps in the proper acclimatization of the sludge to dyes thereby avoiding the possible inhibitory effects to biological activities at high dye concentrations. The overall treatment efficiency of MB through sequential anaerobic-aerobic reactor operation was 90% at maximum attempted dye concentration of 70 mg/L. The effluent from anaerobic reactor was analysed for intermediate biodegradation products through HPLC. It was observed that catechol, quinone, amino pyrine, 1,4 diamino benzene were present. However they were absent in final effluent.

Uniform silica nanoparticles encapsulating two-photon absorbing fluorescent dye

International Nuclear Information System (INIS)

Wu Weibing; Liu Chang; Wang Mingliang; Huang Wei; Zhou Shengrui; Jiang Wei; Sun Yueming; Cui Yiping; Xu Chunxinag

2009-01-01

We have prepared uniform silica nanoparticles (NPs) doped with a two-photon absorbing zwitterionic hemicyanine dye by reverse microemulsion method. Obvious solvatochromism on the absorption spectra of dye-doped NPs indicates that solvents can partly penetrate into the silica matrix and then affect the ground and excited state of dye molecules. For dye-doped NP suspensions, both one-photon and two-photon excited fluorescence are much stronger and recorded at shorter wavelength compared to those of free dye solutions with comparative overall dye concentration. This behavior is possibly attributed to the restricted twisted intramolecular charge transfer (TICT), which reduces fluorescence quenching when dye molecules are trapped in the silica matrix. Images from two-photon laser scanning fluorescence microscopy demonstrate that the dye-doped silica NPs can be actively uptaken by Hela cells with low cytotoxicity. - Graphical abstract: Water-soluble silica NPs doped with a two-photon absorbing zwitterionic hemicyanine dye were prepared. They were found of enhanced one-photon and two-photon excited fluorescence compared to free dye solutions. Images from two-photon laser scanning fluorescence microscopy demonstrate that the dye-doped silica NPs can be actively uptaken by Hela cells.

Measuring the Photocatalytic Breakdown of Crystal Violet Dye using a Light Emitting Diode Approach

Science.gov (United States)

Ryan, Robert E.; Underwood, Lauren W.; O'Neal, Duane; Pagnutti, Mary; Davis, Bruce A.

2009-01-01

A simple method to estimate the photocatalytic reactivity performance of spray-on titanium dioxide coatings for transmissive glass surfaces was developed. This novel technique provides a standardized method to evaluate the efficiency of photocatalytic material systems over a variety of illumination levels. To date, photocatalysis assessments have generally been conducted using mercury black light lamps. Illumination levels for these types of lamps are difficult to vary, consequently limiting their use for assessing material performance under a diverse range of simulated environmental conditions. This new technique uses an ultraviolet (UV) gallium nitride (GaN) light emitting diode (LED) array instead of a traditional black light to initiate and sustain photocatalytic breakdown. This method was tested with a UV-resistant dye (crystal violet) applied to a titanium dioxide coated glass slide. Experimental control is accomplished by applying crystal violet to both titanium dioxide coated slides and uncoated control slides. A slide is illuminated by the UV LED array, at various light levels representative of outdoor and indoor conditions, from the dye side of the slide. To monitor degradation of the dye over time, a temperature-stabilized white light LED, whose emission spectrum overlaps with the dye absorption spectrum, is used to illuminate the opposite side of the slide. Using a spectrometer, the amount of light from the white light LED transmitted through the slide as the dye degrades is monitored as a function of wavelength and time and is subsequently analyzed. In this way, the rate of degradation for photocatalytically coated versus uncoated slide surfaces can be compared. Results demonstrate that the dye absorption decreased much more rapidly on the photocatalytically coated slides than on the control uncoated slides, and that dye degradation is dependent on illumination level. For photocatalytic activity assessment purposes, this experimental configuration and

Evaluation of concordance between labelling and content of 52 hair dye products: overview of the market of oxidative hair dye.

Science.gov (United States)

Antelmi, Annarita; Bruze, Magnus; Zimerson, Erik; Engfeldt, Malin; Young, Ewa; Persson, Lena; Foti, Caterina; Sörensen, Östen; Svedman, Cecilia

2017-04-01

Hair dyes contain strong allergens and are widely available. Correct labelling is a necessity in order to provide information about the contents. To compare the labelling and content of hair dyes. In total, 52 hair dyes, from 11 different countries, were bought over the counter. High-pressure liquid chromatography was used for the analysis of p-phenylenediamine (PPD), toluene-2,5-diamine (2,5-TDA), and three oxidation products of PPD. There was good agreement between labelling and content, although seven of the 52 products (13.5%) studied were incorrectly labelled. There were differences in the geographical use of PPD and 2,5-TDA; 2,5-TDA was more common in European products, while PPD was more common in products purchased outside Europe and was present in higher concentrations. All dyes purchased in Europe contained PPD and 2,5-TDA at levels within the limits defined by European legislation, however, levels were higher in some products purchased outside Europe. Only a small group of hair dyes sold in Europe were mislabelled. Further improvement in labelling, by providing the concentration of chemicals, may facilitate products to be purchased both locally and within the global market, when travelling or on the internet.

Removal of Azo Dye from Synthetic Wastewater Using Immobilized Nano-Diatomite Within Calcium Alginate

Directory of Open Access Journals (Sweden)

AA Khodabandelou

2016-03-01

Full Text Available Introduction: The presence of organic dyes, discharged by textile industries, in aqueous environments can cause detrimental effects on aquatic life and subsequently human health. Therefore, the decolorization of aquatic environments is mandatory to protect the environment. For this reason, in the present study, nano-sized diatomite was immobilized within calcium alginate as a nanocomposite adsorbent for removing organic azo dye (Direct blue 15 from aqueous solutions.  Methods: First of all, Iranian diatomite was grinded in a planetary ball mill equipped with tungsten carbide cup for 20 h to achieve nanoparticles of the diatomite. For the immobilization of nanostructured diatomite, a 2% sodium alginate solution was used. Scanning electron microscopy (SEM, X-ray diffraction (XRD and Fourier transform infra-red (FT-IR spectroscopy were used to characterize immobilized nano-diatomite. Fifty milliliter Erlenmeyer flasks were used as batch flow mode experimental reactors. Working solutions were prepared by the dilution of stock solution (1 g/L to desired concentrations. The effect of different operational parameters including contact time, initial pH, adsorbent dosage and initial dye concentration along with kinetic and isotherm of the adsorption were evaluated. After each experiment, the residual concentration of the dyes was measured spectrophotometrically. Results: As results, the adsorption of organic dye increased with increasing contact time and adsorbent dosage, while increasing initial dye concentrations resulted in decreasing the adsorption. The adsorption of DB-15 was favored at basic PH. The immobilization of diatomite led to enhancing the adsorption of  DB-15 compared to diatomite alone. According to the obtained correlation coefficient, the adsorption of DB-15 obeyed pseudo-second order kinetic model and Langmuir isotherm model. The maximum adsorption capacity of diatomite/alginate nanocomposite for the adsorption of DB-15 were found

Low cost removal of reactive dyes using wheat bran

International Nuclear Information System (INIS)

Cicek, Fatma; Ozer, Dursun; Ozer, Ahmet; Ozer, Ayla

2007-01-01

In this study, the adsorption of Reactive Blue 19 (RB 19), Reactive Red 195 (RR 195) and Reactive Yellow 145 (RY 145) onto wheat bran, generated as a by-product material from flour factory, was studied with respect to initial pH, temperature, initial dye concentration, adsorbent concentration and adsorbent size. The adsorption of RB 19, RR 195 and RY 145 onto wheat bran increased with increasing temperature and initial dye concentration while the adsorbed RB 19, RR 195 and RY 145 amounts decreased with increasing initial pH and adsorbent concentration. The Langmuir and Freundlich isotherm models were applied to the experimental equilibrium data depending on temperature and the isotherm constants were determined by using linear regression analysis. The monolayer covarage capacities of wheat bran for RB 19, RR 195 and RY 145 dyes were obtained as 117.6, 119.1 and 196.1 mg/g at 60 deg. C, respectively. It was observed that the reactive dye adsorption capacity of wheat bran decreased in the order of RY 145 > RB 19 > RR 195. The pseudo-second order kinetic and Weber-Morris models were applied to the experimental data and it was found that both the surface adsorption as well as intraparticle diffusion contributed to the actual adsorption processes of RB 19, RR 195 and RY 145. Regression coefficients (R 2 ) for the pseudo-second order kinetic model were higher than 0.99. Thermodynamic studies showed that the adsorption of RB 19, RR 195 and RY 145 dyes onto wheat bran was endothermic in nature

Color-sensitive photoconductivity of nanostructured ZnO/dye hybrid films prepared by one-step electrodeposition

International Nuclear Information System (INIS)

Oekermann, T.; Yoshida, T.; Tada, H.; Minoura, H.

2006-01-01

Nanostructured ZnO/dye hybrid films prepared by one-step electrodeposition have been investigated in conductivity and photoconductivity measurements in view of applications in dye-sensitized solar cells (DSSC) and in optoelectronics. Highly porous ZnO/eosin Y films, which were obtained at potentials < - 0.9 V vs. SCE, were found to have a very high conductivity already in the dark, probably because of a higher n-doping, which is due to a higher concentration of Zn atoms in the film. On the other hand, less porous or non-porous films, which were obtained at more positive potentials and in which the dye molecules are located within the ZnO crystals, were found to show a much higher sensitivity to illumination with visible light in photoconductivity measurements due to a higher absolute photoconductivity and a lower conductivity in the dark

Color-sensitive photoconductivity of nanostructured ZnO/dye hybrid films prepared by one-step electrodeposition

Energy Technology Data Exchange (ETDEWEB)

Oekermann, T. [Gifu University, Graduate School of Engineering, Yanagido 1-1, Gifu 501-1193 (Japan) and University of Hannover, Institute of Physical Chemistry and Electrochemistry, Callinstrasse 3-3A, 30167 Hannover (Germany)]. E-mail: torsten.oekermann@pci.uni-hannover.de; Yoshida, T. [Gifu University, Graduate School of Engineering, Yanagido 1-1, Gifu 501-1193 (Japan)]. E-mail: yoshida@apchem.gifu-u.ac.jp; Tada, H. [Institute for Molecular Science, Okazaki National Research Institutes, Myodaiji, Okazaki 444-8585 (Japan); Minoura, H. [Gifu University, Graduate School of Engineering, Yanagido 1-1, Gifu 501-1193 (Japan)

2006-07-26

Nanostructured ZnO/dye hybrid films prepared by one-step electrodeposition have been investigated in conductivity and photoconductivity measurements in view of applications in dye-sensitized solar cells (DSSC) and in optoelectronics. Highly porous ZnO/eosin Y films, which were obtained at potentials < - 0.9 V vs. SCE, were found to have a very high conductivity already in the dark, probably because of a higher n-doping, which is due to a higher concentration of Zn atoms in the film. On the other hand, less porous or non-porous films, which were obtained at more positive potentials and in which the dye molecules are located within the ZnO crystals, were found to show a much higher sensitivity to illumination with visible light in photoconductivity measurements due to a higher absolute photoconductivity and a lower conductivity in the dark.

DYEING OF WOOL YARNS WITH LAURUS NOBILIS L. BERRIES

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ERKAN Gökhan

2016-05-01

Full Text Available Nowadays natural dyes have been attracted by many researchers and firms due to demands on sustainable and nontoxic products. In this study the mature berries of bay laurel (Laurus nobilis L. were collected from trees located Kuşadası Turkey. The berries dried at 25oC and % 20-25 relative humidity. Dried berries milled and extracted with ethanol. Extracted dye was used. Three mordanting procedure (pre, meta and post mordanting and two concentrations were applied to wool yarns. Cupric sulfate, ferric sulfate, potassium dichromate and alum was used as mordant Color strength and colorimetric values were measured by Konica-Minolta 3600D spectrophotometer. Fastness to washing, perspiration and light were applied according to ISO 105C06 (A1S, ISO 105E04 and ISO 105B02 (method 2 respectively. The highest color strength (K/S value was 16.6405 and was obtained in the case of premordanting with cupric sulfate at 2 gr/L concentration. If the a* and b* values were examined, the conditions at highest color strength, the yarns had yellow color with a reddish hue. Generally, the fastness properties were moderate and good results were obtained in the case of premordanting procedure. The results show us ethanol extract of bay laurel berries can be used for dyeing of woolen products.

Efficient dye-sensitized solar cells from mesoporous zinc oxide nanostructures sensitized by N719 dye

Science.gov (United States)

Kumara, G. R. A.; Deshapriya, U.; Ranasinghe, C. S. K.; Jayaweera, E. N.; Rajapakse, R. M. G.

2018-03-01

Dye-sensitized solar cells (DSCs) have attracted a great deal of attention due to their low-cost and high power conversion efficiencies. They usually utilize an interconnected nanoparticle layer of TiO2 as the electron transport medium. From the fundamental point of view, faster mobility of electrons in ZnO is expected to contribute to better performance in DSCs than TiO2, though the actual practical situation is quite the opposite. In this research, we addressed this problem by first applying a dense layer of ZnO on FTO followed by a mesoporous layer of interconnected ZnO nanoparticle layer, both were prepared by spray pyrolysis technique. The best cell shows a power conversion efficiency of 5.2% when the mesoporous layer thickness is 14 μm and the concentration of the N719 dye in dye coating solution is 0.3 mM, while a cell without a dense layer shows 4.2% under identical conditions. The surface concentration of dye adsorbed in the cell with a dense layer and that without a dense layer are 5.00 × 10‑7 and 3.34 × 10‑7 mol/cm2, respectively. The cell with the dense layer has an electron lifetime of 54.81 ms whereas that without the dense layer is 11.08 ms. As such, the presence of the dense layer improves DSC characteristics of ZnO-based DSCs.

Utilization of a new optical sensor unit to monitor the electrochemical elimination of selected dyes in water

Science.gov (United States)

Valica, M.; Černá, T.; Hostin, S.

2017-10-01

This paper presents results obtained by developed optical sensor, which consist from multi-wavelength LED light source and two photodetectors capable of measuring the change in optical signal along two different optical paths (absorbance and reflectance measurements). Arduino microcomputer was used for light source management and optical signal data measuring and recording. Analytical validation of developed optical sensor is presented in this paper. The performance of the system has been tested with varying water solution of dyes (malachite green, methyl orange, trypan red). These results show strong correlations between the optical signal response and colour change from the dyes. Sensor was used for continual in-situ monitoring of electrochemical elimination of selected dyes (current density 15.7 mA cm-2, electrolyte volume 4 L and NaCl concentration 2 g L-1). Maximum decolorization level varies with each dye. For malachite green was obtain 92,7 % decolorization (25 min); methyl orange 90,8% (8,5 min) and trypan red 84,7% decolorization after 33 min of electrochemical treatment.

Decolorization of different textile dyes by Penicillium simplicissimum and toxicity evaluation after fungal treatment

Directory of Open Access Journals (Sweden)

L.R. Bergsten-Torralba

2009-12-01

Full Text Available The objective of this study was to investigate the capacity of decolorization and detoxification of the textile dyes Reactive Red 198 (RR198, Reactive Blue 214 (RB214, Reactive Blue 21 (RB21 and the mixture of the three dyes (MXD by Penicillium simplicissimum INCQS 40211. The dye RB21, a phthalocyanine, was totally decolorized in 2 days, and the others, the monoazo RR198, the diazo RB214 and MXD were decolorized after 7 days by P. simplicissimum. Initially the dye decolorization involved dye adsorption by the biomass followed by degradation. The acute toxicity after fungal treatment was monitored with the microcrustacean Daphnia pulex and measured through Effective Concentration 50% (EC50. P. simplicissimum reduced efficiently the toxicity of RB21 from moderately acutely toxic to minor acutely toxic and it also reduced the toxicity of RB214 and MXD, which remained minor acutely toxic. Nevertheless, the fungus increased the toxicity of RR198 despite of the reduction of MXD toxicity, which included this dye. Thus, P. simplicissimum INCQS 40211 was efficient to decolorize different textile dyes and the mixture of them with a significant reduction of their toxicity. In addition this investigation also demonstrated the need of toxicological assays associated to decolorization experiments.

Performance variation from triphenylamine- to carbazole-triphenylamine-rhodaniline-3-acetic acid dyes in dye-sensitized solar cells

Energy Technology Data Exchange (ETDEWEB)

Yang, Chien-Hsin, E-mail: yangch@nuk.edu.tw [Department of Chemical and Materials Engineering, National University of Kaohsiung, Kaohsiung 811, Taiwan (China); Lin, Wen-Churng [Department of Environmental Engineering, Kun Shan University, Tainan 710, Taiwan (China); Wang, Tzong-Liu; Shieh, Yeong-Tarng; Chen, Wen-Janq; Liao, Shao-Hong; Sun, Yu-Kuang [Department of Chemical and Materials Engineering, National University of Kaohsiung, Kaohsiung 811, Taiwan (China)

2011-10-17

Highlights: {yields} We synthesized an organic dye of carbazole-rhodaniline-3-acetic acid-triphenylamine. {yields} A dye-sensitized solar cell is fabricated using this dye with efficiency of 4.64%. {yields} Carbazole donor in the dye molecule provides electron in increasing efficiency. {yields} Two rhodaniline-3-acetic acids play a key role in increasing efficiency. {yields} AC impedance proves this dye's effect on enhancing charge transfer in TiO{sub 2}. - Abstract: Organic dyes have been synthesized which contain an extra-electron donor (carbazole) and electron acceptors (rhodaniline-3-acetic acid) on triphenylamines (TPA). Photophysical, electrochemical, and theoretical computational methods have categorized these compounds. Nanocrystalline TiO{sub 2}-based dye-sensitized solar cells (DSSCs) are fabricated using these dye molecules as light-harvesting sensitizers. The overall efficiency of sensitized cells has 4.64% relative to a cis-di(thiocyanato)-bis(2,2'-bipyridyl)-4,4'-dicarboxylate ruthenium (II) (N3 dye)-sensitized device (7.83%) fabricated and measured under the same conditions. Carbazole-electron donation in the dye molecules plays a key role in the increased efficiency. Two rhodaniline-3-acetic acid groups appear to help convey the charge transfer from the excited dye molecules to the conduction band of TiO{sub 2}, leading to a higher efficiency of devices using such a dye. Electrochemical impedance supports this dye's effect on enhancing charge transfer in TiO{sub 2} (e{sup -}). Computations on this dye compound also indicate the larger charge transfer efficiency in the electronically excited state.

DYE-SENSITIZED PHOTOPOLYMERIZATION OF METHYL METHACRYLATE INITIATED BY COUMARIN DYE/IODONIUM SALT SYSTEM

Institute of Scientific and Technical Information of China (English)

Fang Gao; Yong-yuan Yang

1999-01-01

The photosensitive initiating system composed of 7-diethylamino-3-(2'-benzimidazolyl)coumarin dye (DEDC) and diphenyliodonium hexafluorophosphate (DIHP) which act as the sensitizer and the initiator respectively, can be used to initiate the polymerization of methyl methacrylate (MMA). The results showed that when exposed to visible light, coumarin dye/iodonium salt undergoes quick electron transfer from DEDC to DIHP and free radicals are produced. The visible light photoinduced reaction between DEDC and DIHP is mainly through the excited singlet state of DEDC and thus it is a little sensitive to O2. The influence of concentration of DEDC, DIHP and MMA on the rate of photopolymerization of MMA was also investigated.

Synthesis, dyeing performance on polyester fiber and antimicrobial studies of some novel pyrazolotriazine and pyrazolyl pyrazolone azo dyes

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Hala F. Rizk

2017-05-01

Full Text Available 5-Amino-4-heterylazo-3-phenyl-1H-pyrazoles (2a–d were diazotized and coupled with malononitrile to give pyrazoloazo malononitrile which by heating in glacial acetic acid gave novel pyrazolo[5,1-c][1,2,4]triazine dyes (3a–d. Also, some diazopyrazolyl pyrazolone dyes (4a–h were synthesized by diazotization of 2a–d and coupled with some pyrazolone derivatives. The structure of the synthesized dyes was determined by elemental analysis and spectral data. All the synthesized compounds were applied as disperse dyes and their dyeing performance on polyester fabric was studied. The fastness and colorimetric properties were measured. The results revealed that the monoazo dyes have good fastness and good to moderate affinity to polyester fabric than diazo dyes. In addition, the synthesized dyes were screened for their antimicrobial activities against Staphylococcus aureus, Pseudomonas aeruginosa (Gram positive, Bacillus subtitles, Escherichia coli (Gram negative and Candida albicans, Aspergillus niger (Fungi. The results revealed that most of the prepared dyes have high antibacterial activity.

Modified coal fly ash as low cost adsorbent for removal reactive dyes from batik industry

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Taufiq Agus

2018-01-01

Full Text Available The removal of reactive dyes on modified coal fly ash has been investigated during a series of batch adsorption experiments. Physical characteristics of modified coal fly ash was characterized by Brunauer Emmett Teller (BET surface area analysis, X-ray powder diffraction (XRD, Fourier transform infrared spectrophotometer (FT-IR, and scanning electron microscope (SEM. The effects of operational parameters such as initial dye concentration (50–200 mg/L, solution pH (4–10 and adsorbent dosage (50–200 mg/L were studied. The adsorption experiments indicated that modified coal fly ash was effective in removing of Remazol Blue. The percentage removal of dyes increased while the modified fly ash dosage increased. The percentage removal of dyes increased with decreased initial concentration of the dye and also increased with amount of adsorbent used. The optimum of removal of dyes was found to be 94% at initial dye concentration 50 g/mL, modified fly ash dosage 250 g/mL, and pH of 2.0.

Biostimulative effects of Nd:YAG Q-switch dye on normal human fibroblast cultures: study of a new chemosensitizing agent for the Nd:YAG laser

International Nuclear Information System (INIS)

Castro, D.J.; Saxton, R.E.; Fetterman, H.R.; Castro, D.J.; Ward, P.H.

1987-01-01

Kodak Q-switch II is a new chemical with an absorption maxima at 1051 nm, designed to be used as an Nd:YAG dye laser. The potential for this dye as a new chemosensitizing agent in the treatment of connective tissue diseases and wound healing with low energy Nd:YAG laser was examined. Two normal fibroblast cell lines were tested for sensitivity to various levels of this dye in vitro. These cells were exposed to Q-switch II dye at concentrations of 0.01, 0.1, 1, 10, 50, and 100 micrograms/ml for 1 and 24 hours. Cell viability was assessed by the trypan blue exclusion test. Cell duplication and DNA synthesis were measured by the incorporation of [ 3 H]-thymidine at 6 and 24 hours postexposure to Q-switch II dye. At concentrations up to 10 micrograms/ml, both cell lines tested showed no changes in cell viability. However, at concentrations equal or higher than 50 micrograms/ml, more than 40% of the fibroblasts incorporated trypan blue after 24 hours of exposure to this dye, indicating significant cell destruction. The results indicate that Q-switch II dye is nontoxic to normal human fibroblast cultures and showed significant biostimulative effects on cell duplication at concentrations equal to or lower than 10 micrograms/ml. Further studies will be required to determine the usefulness of Q-switch II dye as a new photochemosensitizing agent for potential biostimulation of wound healing and/or treatment of connective tissue diseases with the Nd:YAG laser (near infrared, 1060 nm) at nonthermal levels of energies

Graft polymerization using radiation-induced peroxides and application to textile dyeing

Energy Technology Data Exchange (ETDEWEB)

Enomoto, Ichiro, E-mail: enomoto.ichiro@iri-tokyo.j [Tokyo Metropolitan Industrial Technology Research Institute, KFC Bldg., 12F, 1-6-1, Yokoami, Sumida-ku, Tokyo 130-0015 (Japan); School of Engineering, University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan); Katsumura, Yosuke [School of Engineering, University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan); Advanced Science Research Center, Japan Atomic Energy Agency, 2-4 Shirakata Shirane, Tokai-mura, Ibaraki 319-1195 (Japan); Kudo, Hisaaki [School of Engineering, University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan); Soeda, Shin [Tokyo Metropolitan Industrial Technology Research Institute, KFC Bldg., 12F, 1-6-1, Yokoami, Sumida-ku, Tokyo 130-0015 (Japan)

2011-02-15

To improve the dyeing affinity of ultra high molecular weight polyethylene (UHMWPE) fiber, surface treatment by radiation-induced graft polymerization was performed. Methyl methacrylate (MMA), acrylic acid (AA) and styrene (St) were used as the monomers. The grafting yields as a function of storage time after irradiation were examined. Although the grafting yield of St after the sulfonation processing was quite low compared with those of MMA and AA, it was successfully dyed to a dark color with a cationic dye. Some acid dyes can dye the grafted fiber with AA. The acid dye is distributed to the amorphous domains of the AA grafted fiber. The dyeing concentration depended on the grafting yield, and the higher the grafting yield the darker the dye color.

Graft polymerization using radiation-induced peroxides and application to textile dyeing

International Nuclear Information System (INIS)

Enomoto, Ichiro; Katsumura, Yosuke; Kudo, Hisaaki; Soeda, Shin

2011-01-01

To improve the dyeing affinity of ultra high molecular weight polyethylene (UHMWPE) fiber, surface treatment by radiation-induced graft polymerization was performed. Methyl methacrylate (MMA), acrylic acid (AA) and styrene (St) were used as the monomers. The grafting yields as a function of storage time after irradiation were examined. Although the grafting yield of St after the sulfonation processing was quite low compared with those of MMA and AA, it was successfully dyed to a dark color with a cationic dye. Some acid dyes can dye the grafted fiber with AA. The acid dye is distributed to the amorphous domains of the AA grafted fiber. The dyeing concentration depended on the grafting yield, and the higher the grafting yield the darker the dye color.

Solid waste from leather industry as adsorbent of organic dyes in aqueous-medium

International Nuclear Information System (INIS)

Oliveira, Luiz C.A.; Goncalves, Maraisa; Oliveira, Diana Q.L.; Guerreiro, Mario C.; Guilherme, Luiz R.G.; Dallago, Rogerio M.

2007-01-01

The industrial tanning of leather usually produces considerable amounts of chromium-containing solid waste and liquid effluents and raises many concerns on its environmental effect as well as on escalating landfill costs. Actually, these shortcomings are becoming increasingly a limiting factor to this industrial activity that claims for alternative methods of residue disposals. In this work, it is proposed a novel alternative destination of the solid waste, based on the removal of organic contaminants from the out coming aqueous-residue. The adsorption isotherm pattern for the wet blue leather from the Aurea tanning industry in Erechim-RS (Brazil) showed that these materials present high activity on adsorbing the reactive red textile dye as well as other compounds. The adsorbent materials were characterized by IR spectroscopy and SEM and tested for the dye adsorption (reactive textile and methylene blue dyes). The concentrations of dyes were measured by UV-vis spectrophotometry and the chromium extraction from leather waste was realized by basic hydrolysis and determined by atomic absorption. As a low cost abundant adsorbent material with high adsorption ability on removing dye methylene blue (80 mg g -1 ) and textile dye reactive red (163 mg g -1 ), the leather waste is revealed to be a interesting alternative relatively to more costly adsorbent materials

Solid waste from leather industry as adsorbent of organic dyes in aqueous-medium

Energy Technology Data Exchange (ETDEWEB)

Oliveira, Luiz C.A. [Universidade Federal de Lavras, Depto. de Quimica, Caixa Postal 37, CEP 37200.000, Lavras-MG (Brazil)]. E-mail: luizoliveira@ufla.br; Goncalves, Maraisa [Universidade Federal de Lavras, Depto. de Quimica, Caixa Postal 37, CEP 37200.000, Lavras-MG (Brazil); Oliveira, Diana Q.L. [Universidade Federal de Lavras, Depto. de Quimica, Caixa Postal 37, CEP 37200.000, Lavras-MG (Brazil); Guerreiro, Mario C. [Universidade Federal de Lavras, Depto. de Quimica, Caixa Postal 37, CEP 37200.000, Lavras-MG (Brazil); Guilherme, Luiz R.G. [Universidade Federal de Lavras, Depto. de Ciencia do solo, CEP 37200.000, Lavras-MG (Brazil); Dallago, Rogerio M. [URI-Campus Erechim, Av. 7 Setembro 1621, Centro, CEP 99700-000, Depto de Quimica, Erechim-RS (Brazil)

2007-03-06

The industrial tanning of leather usually produces considerable amounts of chromium-containing solid waste and liquid effluents and raises many concerns on its environmental effect as well as on escalating landfill costs. Actually, these shortcomings are becoming increasingly a limiting factor to this industrial activity that claims for alternative methods of residue disposals. In this work, it is proposed a novel alternative destination of the solid waste, based on the removal of organic contaminants from the out coming aqueous-residue. The adsorption isotherm pattern for the wet blue leather from the Aurea tanning industry in Erechim-RS (Brazil) showed that these materials present high activity on adsorbing the reactive red textile dye as well as other compounds. The adsorbent materials were characterized by IR spectroscopy and SEM and tested for the dye adsorption (reactive textile and methylene blue dyes). The concentrations of dyes were measured by UV-vis spectrophotometry and the chromium extraction from leather waste was realized by basic hydrolysis and determined by atomic absorption. As a low cost abundant adsorbent material with high adsorption ability on removing dye methylene blue (80 mg g{sup -1}) and textile dye reactive red (163 mg g{sup -1}), the leather waste is revealed to be a interesting alternative relatively to more costly adsorbent materials.

Effects of operational parameters on the removal of brilliant green dye from aqueous solutions by electrocoagulation

Directory of Open Access Journals (Sweden)

Barun Kumar Nandi

2017-05-01

Full Text Available This paper presents an experimental study on the removal of brilliant green dye from aqueous solutions in a batch stirred electrocoagulation (EC reactor using iron electrodes. The main objectives of the experiments were to investigate the effects of the various operating parameters, such as current density, inter electrode distance, initial dye concentration, pH of the solution, EC duration and salt (NaCl concentrations on the brilliant green dye removal efficiency from synthetic wastewater containing in batch EC process. The experimental results showed that 99.59% dye removal was observed for initial dye concentration of 100 mg/L with current density of 41.7 A/m2, initial pH of 4.0 at the end of 30 min of operation. It was observed that, an increase in current density, time of operation and decrease in inter electrode distance improved the dye removal efficiency. Optimum pH for highest dye removal was 4.0–10.0. It was also observed that increase in salt (NaCl concentration in the solution reduces the specific electrical energy consumption (SEEC.

Color removal from acid and reactive dye solutions by electrocoagulation and electrocoagulation/adsorption processes.

Science.gov (United States)

Bellebia, S; Kacha, S; Bouberka, Z; Bouyakoub, A Z; Derriche, Z

2009-04-01

In this study, electrocoagulation of Marine Blue Erionyl MR (acid dye) and electrocoagulation followed by adsorption of Brilliant Blue Levafix E-BRA (reactive dye) from aqueous solutions were investigated, using aluminum electrodes and granular activated carbon (GAC). In the electrocoagulation and adsorption of dyestuff solutions, the effects of current density, loading charge, pH, conductivity, stirring velocity, contact time, and GAC concentration were examined. The optimum conditions for the electrocoagulation process were identified as loading charges 7.46 and 1.49 F/m3, for a maximum abatement of 200 mg/L reactive and acid dye, respectively. The residual reactive dye concentration was completely removed with 700 mg/L GAC. The results of this investigation provide important data for the development of a combined process to remove significant concentrations of recalcitrant dyes from water, using moderate activated carbon energy and aluminum consumption, and thereby lowering the cost of treatment.

Optimal decolorization and kinetic modeling of synthetic dyes by Pseudomonas strains.

Science.gov (United States)

Yu, J; Wang, X; Yue, P L

2001-10-01

Pseudomonas spp were isolated from an anaerobic-aerobic dyeing house wastewater treatment facility as the most active azo-dye degraders. Decolorization of azo dyes and non-azo dyes including anthraquinone, metal complex and indigo was compared with individual strains and a bacterial consortium consisting of the individual strain and municipal sludge (50 50wt). The consortium showed a significant improvement on decolorization of two recalcitrant non-azo dyes, but little effect on the dyes that the individual strains could degrade to a great or moderate extent. Decolorization of Acid violet 7 (monoazo) by a Pseudomonas strain GM3 was studied in detail under various conditions. The optimum decolorization activity was observed in a narrow pH range (7-8), a narrow temperature range (35-40 degrees C), and at the presence of organic and ammonium nitrogen. Nitrate had a severe inhibitory effect on azo dye decolorization: 10 mg/L led to 50% drop in decolorization activity and 1000 mg/L to complete activity depression. A kinetic model is established giving the dependence of decolorization rate on cell mass concentration (first-order) and dye concentration (half order). The rate increased with temperature from 10 to 35 C, which can be predicted by Arrhenius equation with the activation energy of 16.87 kcal/mol and the frequency factor of 1.49 x 10(11) (mg L)1/2/g DCM min.

Dyeing of Polyester with Disperse Dyes: Part 2. Synthesis and Dyeing Characteristics of Some Azo Disperse Dyes for Polyester Fabrics

Directory of Open Access Journals (Sweden)

Alya M. Al-Etaibi

2016-06-01

Full Text Available The goal of this study was to utilize carrier for accelerating the rate of dyeing not only to enhance dyeing of polyester fabrics dyed with disperse dyes 3a,b, but also to save energy. Both the color strength expressed as dye uptake and the fastness properties of the dyed fabrics were evaluated.

Adsorption of methylene blue dye from aqueous solution by sugar extracted spent rice biomass.

Science.gov (United States)

Ur Rehman, Muhammad Saif; Kim, Ilgook; Han, Jong-In

2012-10-15

This study was aimed at using sugar extracted spent rice biomass (SRB) as a potential adsorbent to remove methylene blue (MB) dye from aqueous solution. The SRB was used without any modification. A three factor full factorial experimental design (2(3)) was employed to investigate the effect of factors (adsorbent dose, dye concentration, temperature) and their interaction on the adsorption capacity and color removal. Two levels for each factor were used; adsorbent dose (0.25-0.5g/100mL), dye concentration (25-50mg/L), and temperature (25-45°C). Initial dye concentration and adsorbent dosage were found as significant factors for the adsorption of MB dye. Langmuir isotherm (R(2)>0.998) best explained the equilibrium of MB adsorption on SRB with monolayer adsorption capacity of 8.13mg/g. The pseudo-second order model (R(2)>0.999) was best fitted to explain the adsorption kinetics. Thermodynamic investigation revealed that the adsorption process was spontaneous, endothermic, and was feasible to treat dyeing wastewater. Copyright © 2012 Elsevier Ltd. All rights reserved.

Nano-dyeing

Directory of Open Access Journals (Sweden)

Ning Cui-Juan

2016-01-01

Full Text Available Dyeing nanofibers is a frontier of both modern textile engineering and nanotechnology. This paper suggest a feasible method for dyeing nanofibers with a natural red (Roselle Calyx by bubble electrospinning. Reactive dye (Red S3B and acid dye (Red 2B were also used in the experiment for comparison. The dyeing process was finished during the spinning process.

A study of charge transfer kinetics in dye-sensitized surface conductivity solar cells

Energy Technology Data Exchange (ETDEWEB)

Friedrich, Dennis

2011-05-15

The efficiency of the quasi-solid-state dye-sensitized solar cell developed by Junghaenel and Tributsch, the so-called Nano Surface Conductivity Solar Cell (NSCSC), was improved from 2% to 3.5% introducing a compact TiO{sub 2} underlayer, modifying the surface of the mesoporous TiO{sub 2} electrode, optimizing the deposition process of the electrolyte film, and replacing the platinum counter electrode by a carbon layer. Space-resolved photocurrent images revealed the importance of a homogeneous distribution of the electrolyte film. An uneven dispersion led to localized areas of high and low photocurrents, whereas the latter were attributed to an insufficient concentration of the redox couple. Impedance spectroscopy was performed on cells containing different concentrations of the redox couple. By modeling the spectra using an equivalent circuit with a transmission line of resistive and capacitive elements, the characteristic parameters of electron transport in the TiO{sub 2}, such as diffusion length and electron lifetime were obtained. The measurements indicated that the transport of the positive charge to the counter electrode is the main process limiting the efficiency of the cells. Excess charge carrier decay in functioning devices was analyzed by contactless transient photoconductance measurements in the microwave frequency range (TRMC). The lifetime of the photogenerated charge carriers was observed to decrease with increasing applied potential, reaching its maximum close to the opencircuit potential of the cell, where the photocurrent density was minimal, i.e. the potential dependent decay observed was limited by the injection of electrons into the front contact. The functioning of this NSCSC indicated that the transport of the positive charge occurs by solid-state diffusion at the surface of the TiO{sub 2} particles. TRMC measurements on subset devices in the form of sensitized TiO{sub 2} layers revealed charge carrier kinetics strongly dependent on the

Micro-Fluidic Dye Ring Laser - Experimental Tuning of the Wavelength and Numerical Simulation of the Cavity Modes

DEFF Research Database (Denmark)

Gersborg-Hansen, Morten; Balslev, Søren; Mortensen, Niels Asger

2006-01-01

We demonstrate wavelength tuning of a micro-fluidic dye ring laser. Wavelength tunability is obtained by controlling the liquid dye concentration. The device performance is modelled by FEM simulations supporting a ray-tracing view.......We demonstrate wavelength tuning of a micro-fluidic dye ring laser. Wavelength tunability is obtained by controlling the liquid dye concentration. The device performance is modelled by FEM simulations supporting a ray-tracing view....

Random laser emission at dual wavelengths in a donor-acceptor dye mixture solution

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Sunita Kedia

Full Text Available The work was aimed to generate random laser emissions simultaneously at two wavelengths in a weakly scattering system containing mixture of binary dyes, rhodamine-B (Rh-B and oxazine-170 (O-170 dispersed with ZnO nano-particles serving as scattering centres. Random lasing performances for individual Rh-B dye were extensively studied for varying small signal gain/scatterer density and we found lasing threshold to significantly depend upon number density of dispersed nano-particles. In spite of inefficient pumping, we demonstrated possibility of random lasing in O-170 dye solution on account of resonance energy transfer from Rh-B dye which served as donor. At optimum concentrations of fluorophores and scatterer in dye mixture solution, incoherent random lasing was effectively attained simultaneously at two wavelengths centered 90 nm apart. Dual-emission intensities, lasing thresholds and rate of amplifications could be controlled and made equivalent for both donor and acceptor in dye mixture solution by appropriate choice of concentrations of dyes and scatterers. Keywords: Random lasing, Energy transfer, Rhodamine-B, Oxazine-170, Zinc oxide

Removal of methylene blue dye from wastewater by using supported liquid memberane technology

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Ashraf Muhammad Waqar

2016-06-01

Full Text Available The present work describes the application of Supported Liquid Membrane (SLM technology towards the removal and recovery of a cationic dye (Methylene Blue from aqueous solutions. Natural and non-toxic vegetable oils have been impregnated on microporous polymeric films of polyvinylidene fluoride (PVDF to constitute a liquid membrane. Different parameters affecting the transport, like pH of feed solution, acid concentration in the strip solution, initial dye concentration, oil types and stirring speeds have been investigated. Highest value of flux (1.7 × 10−5 mg/cm2/sec1 for methylene blue dye was achieved with sunflower oil impregnated on the PVDF support, with pH maintained at 12 in the feed solution and 0.3 M hydrochloric acid concentration in the strip solution. It took 6 hours to transport maximum amount of dye under optimum conditions.

Extraction and Characterization of Natural Dye from Green Walnut Shells and Its Use in Dyeing Polyamide: Focus on Antibacterial Properties

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Mohammad Mirjalili

2013-01-01

Full Text Available Extraction of dyes from walnut using Soxhlet apparatus has been studied. The color components extracted and isolated from walnut shells were characterized by column chromatography, thin layer chromatography (TLC, nuclear magnetic resonance (NMR, mass spectroscopy (MS, and infrared (IR techniques. Natural dye extract obtained from the walnut was used in dyeing polyamide fabrics with different mordants. The dyed fabrics were evaluated for antibacterial activity against pathogenic strains of Gram-positive (Staphylococcus aureus and Gram-negative (Escherichia coli bacteria. As such, the relationship between antibacterial activity and dye concentration is investigated. Durability of antibacterial activity to laundering is also discussed. Results indicate that the polyamide dyed with walnut displayed excellent antibacterial activity in the presence of ferric sulfate, cupric sulfate, and potassium aluminum sulfate and exhibited good and durable fastness properties.

Pengaruh konsentrasi pigmen indigo pada pewarnaan (dyeing dan pengulangan warna (topping pada kulit bludru

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Emiliana Kasmudjiastuti

2007-06-01

Full Text Available Paste indigo pigment having blue colour was produced from fermentation of indigofera tinctoria leaves and twigs. Having was very popular dye and was used especially in textile industries and leather industries of fur. The aim of the study was to the optimum concentration of indigo pigmen on dyeing of suede leather. The materials used in study were crust suede leather, indigo pigmen, wetting agent, soda ash, ammonia, formic acid sulfonated oil, and redactors such as palm sugar. The dying of leather using indigo pigmen was principally similar with common dyeing and pH of indigo is 11.5, however pH on several steps must adjusted. Variation of the concentration of in dyeing was 0.5, 1, and 1.5% respectively. Performance test were of conducted for dye penetration, colour rub fastness (dry, wet, sweat resistant, and sun light resistant for 6, 13, and 20 hours respectively. The results showed that the optimum concentration of pigmen indigo was 9% dyeing and 1 % for topping with level dye, indicated appropriate penetration dye into the cross-section leather, no fading was performed by dry colour fastness test (score 4/5 and wet colour fastness test (score 4, good sweat resistant (score 5, no colour fading on the exposure to sun light for 20 hours (score 4.

Photoelectrochemical studies of dye-sensitized solar cells using organic dyes

Energy Technology Data Exchange (ETDEWEB)

Marinado, Tannia

2009-10-15

The dye-sensitized solar cell (DSC) is a promising efficient low-cost molecular photovoltaic device. One of the key components in DSCs is the dye, as it is responsible for the capture of sunlight. State-of-the-art DSC devices, based on ruthenium dyes, show record efficiencies of 10-12 %. During the last decade, metal-free organic dyes have been extensively explored as sensitizers for DSC application. The use of organic dyes is particularly attractive as it enables easy structural modifications, due to fairly short synthetic routes and reduced material cost. Novel dye should in addition to the light-harvesting properties also be compatible with the DSC components. In this thesis, a series of new organic dyes are investigated, both when integrated in the DSC device and as individual components. The evaluation methods consisted of different electrochemical and photoelectrochemical techniques. Whereas the light-harvesting properties of the dyes were fairly easily improved, the behavior of the dye integrated in the DSC showed less predictable photovoltaic results. The dye series studied in Papers II and IV revealed that their dye energetics limited vital electron-transfer processes, the dye regeneration (Paper II) and injection quantum yield (Paper IV). Further, in Papers III-VI, it was observed that different dye structures seemed to alter the interfacial electron recombination with the electrolyte. In addition to the dye structure sterics, some organic dyes appear to enhance the interfacial recombination, possibly due to specific dye-redox acceptor interaction (Paper V). The impact of dye sterical modifications versus the use of coadsorbent was explored in Paper VI. The dye layer properties in the presence and absence of various coadsorbents were further investigated in Paper VII. The core of this thesis is the identification of the processes and properties limiting the performance of the DSC device, aiming at an overall understanding of the compatibility between the

Two-phase flow measurements using a photochromic dye activation technique

International Nuclear Information System (INIS)

Kawaji, M.

1998-01-01

A novel flow visualization method called photochromic dye activation (PDA) technique has been used to investigate flow structures and mechanisms in various two-phase flow regimes. This non-intrusive flow visualization technique utilizes light activation of a photochromic dye material dissolved in a clear liquid and is a molecular tagging technique, requiring no seed particles. It has been used to yield both quantitative and qualitative flow data in the liquid phase in annular flow, slug flow and stratified-wavy flows. (author)

Estimation of presynaptic calcium currents and endogenous calcium buffers at the frog neuromuscular junction with two different calcium fluorescent dyes.

Science.gov (United States)

Samigullin, Dmitry; Fatikhov, Nijaz; Khaziev, Eduard; Skorinkin, Andrey; Nikolsky, Eugeny; Bukharaeva, Ellya

2014-01-01

At the frog neuromuscular junction, under physiological conditions, the direct measurement of calcium currents and of the concentration of intracellular calcium buffers-which determine the kinetics of calcium concentration and neurotransmitter release from the nerve terminal-has hitherto been technically impossible. With the aim of quantifying both Ca(2+) currents and the intracellular calcium buffers, we measured fluorescence signals from nerve terminals loaded with the low-affinity calcium dye Magnesium Green or the high-affinity dye Oregon Green BAPTA-1, simultaneously with microelectrode recordings of nerve-action potentials and end-plate currents. The action-potential-induced fluorescence signals in the nerve terminals developed much more slowly than the postsynaptic response. To clarify the reasons for this observation and to define a spatiotemporal profile of intracellular calcium and of the concentration of mobile and fixed calcium buffers, mathematical modeling was employed. The best approximations of the experimental calcium transients for both calcium dyes were obtained when the calcium current had an amplitude of 1.6 ± 0.08 pA and a half-decay time of 1.2 ± 0.06 ms, and when the concentrations of mobile and fixed calcium buffers were 250 ± 13 μM and 8 ± 0.4 mM, respectively. High concentrations of endogenous buffers define the time course of calcium transients after an action potential in the axoplasm, and may modify synaptic plasticity.

Kinetics of leather dyeing pretreated with enzymes: role of acid protease.

Science.gov (United States)

Kanth, Swarna Vinodh; Venba, Rajangam; Jayakumar, Gladstone Christopher; Chandrababu, Narasimhan Kannan

2009-04-01

In the present investigation, kinetics of dyeing involving pretreatment with acid protease has been presented. Application of acid protease in dyeing process resulted in increased absorption and diffusion of dye into the leather matrix. Enzyme treatment at 1% concentration, 60 min duration and 50 degrees C resulted in maximum of 98% dye exhaustion and increased absorption rate constants. The final exhaustion (C(infinity)) for the best fit of CI Acid Black 194 dye has been 98.5% with K and r2 values from the modified Cegarra-Puente isotherm as 0.1033 and 0.0631. CI Acid Black 194 being a 2:1 metal complex acid dye exhibited higher absorption rate than the acid dye CI Acid Black 210. A reduction in 50% activation energy calculated from Arrhenius equation has been observed in enzyme assisted dyeing process of both the dyes that substantiates enhanced dye absorption. The absorption rate constant calculated with modified Cegarra-Puente equation confirm higher rate constants and faster kinetics for enzyme assisted dyeing process. Enzyme treated leather exhibited richness of color and shade when compared with control. The present study substantiates the essential role of enzyme pretreatment as an eco-friendly leather dyeing process.

Dye sensitization of antimony-doped CdS photoelectrochemical solar cell

Energy Technology Data Exchange (ETDEWEB)

El Zayat, M.Y.; Saed, A.O.; El-Dessouki, M.S. [Department of Physics, Faculty of Science, Cairo University, Giza (Egypt)

2002-01-31

Sb-doped CdS single crystal was used as a photoanode to fabricate a photoelectrochemical solar (PECS) cell. The three organic dyes; eosin, thymol blue and rhodamin 6G were used as sensitizers in (PECS) cell. In the absence of the dye, the results showed that with Sb-doped CdS single crystal electrode, a higher power conversion efficiency 9.27% has been achieved compared to 5.7-7.4% for pure crystal. Application of the dye in PECS cell increases the efficiency to about 13%. The efficiency reaches its maximum value when the dye concentration is (2.5x10{sup -5})M, sufficient to cover the surface of the semiconductor electrode with a continuous monolayer of the dye. Exceeding this value resulted in a gradual decrease of the efficiency from its maximum value. Mott-Schottky plots gave a doping density of 3.14x10{sup 17}cm{sup -3} and a space charge width of 4.95x10{sup -6}cm for the sample used. A flat-band potential equal to -0.84V, independent of both frequency and pH, was also predicted. Cyclic voltammetry (c.v.) measurements showed an anodic current peak at 0.4V vs. SCE. The disappearance of this peak after excess addition of the reducing agent Na{sub 2}S, indicates that this peak is due to the PEC corrosion of the semiconductor electrode.

Removal of reactive dyes from wastewater by shale

Directory of Open Access Journals (Sweden)

Jareeya Yimrattanabovorn

2012-02-01

Full Text Available Colored textile effluents represent severe environmental problems as they contain mixture of chemicals, auxiliariesand dyestuffs of different classes and chemical constitutions. Elimination of dyes in the textile wastewater by conventionalwastewater treatment methods is very difficult. At present, there is a growing interest in using inexpensive and potentialmaterials for the adsorption of reactive dyes. Shale has been reported to be a potential media to remove color from wastewaterbecause of its chemical characteristics. In this study, shale was used as an adsorbent. The chosen shale had particlesizes of : A (1.00 < A < 2.00 mm, B (0.50 < B < 1.00 mm, C (0.25 < C < 0.50 mm, D (0.18 < D < 0.25 mm and E (0.15 < E < 0.18mm. Remazol Deep Red RGB (Red, Remazol Brilliant Blue RN gran (Blue and Remazol Yellow 3RS 133% gran (Yellow wereused as adsorbates. Batch adsorption experiments were performed to investigate the effect of contact time, pH, temperatureand initial dye concentration. It was found that the equilibrium data were best described by the Langmuir isotherm model,with the maximum monolayer adsorption capacities of 0.0110-0.0322 mg/g for Red, 0.4479-1.1409 mg/g for Blue and 0.0133-0.0255 mg/g for Yellow, respectively. The maximum adsorption capacity of reactive dye by shale occurred at an initial pH of 2,initial concentration of 700 Pt-Co and temperature 45°C. Reactive dye adsorption capacities increased with an increase of theinitial dye concentration and temperature whereas with a decrease of pH. The fixed bed column experiments were appliedwith actual textile wastewater for estimation of life span. The results showed that COD and color removal efficiencies of shalefix bed column were 97% and 90%, respectively. Also the shale fixed bed columns were suitable for using with textile effluentfrom activated sludge system because of their COD and color removal efficiencies and life expectancy comparison using withdyebath wastewater and raw

Use of the ultrasonic cavitation in wool dyeing process: Effect of the dye-bath temperature.

Science.gov (United States)

Actis Grande, G; Giansetti, M; Pezzin, A; Rovero, G; Sicardi, S

2017-03-01

The present work aims to study the effect of the liquid temperature on the performance of ultrasounds (US) in a dyeing process. The approach was both theoretical and experimental. In the theoretical part the simplified model of a single bubble implosion is used to demonstrate that the "maximum implosion pressure" calculated with the well known Rayleigh-Plesset equation for a single bubble can be correlated with the cavitation intensity experimentally measured with an Ultrasonic Energy Meter (by PPB Megasonics). In particular the model was used to study the influence of the fluid temperature on the cavitation intensity. The "relative" theoretical data calculated from the implosion pressure were satisfactorily correlated with the experimental ones and evidence a zone, between 50 and 60°C, were the cavitation intensity is almost constant and still sufficiently high. Hence an experimental part of wool dyeing was carried out both to validate the previous results and to verify the dyeing quality at low temperatures (40-70°C) in presence of US. A prototype dyeing equipment able to treat textile samples with US system of 600W power, was used. The dyeing performances in the presence and absence of US were verified by measuring ΔE (colour variation), R e,% (reflectance percentage), K/S (colour strength) and colour fastness. The US tests performed in the temperature range of 40-70°C were compared with the conventional wool dyeing at 98°C. The obtained results show that a temperature close to 60°C should be chosen as the recommended US dyeing condition, being a compromise between the cavitation intensity and the kinetics which rules the dyestuff diffusion within the fibres. Copyright © 2016 Elsevier B.V. All rights reserved.

(MTT) dye reduction assay.

African Journals Online (AJOL)

to inhibit proliferation of HeLa cells was determined using the 3443- dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) dye reduction assay. Extracts from roots of Agathisanthemum bojeri, Synaptolepis kirkii and Zanha africana and the leaf extract of Physalis peruviana at a concentration of 10 pg/ml inhibited cell ...

Biological decolorization of xanthene dyes by anaerobic granular biomass.

Science.gov (United States)

Apostol, Laura Carmen; Pereira, Luciana; Pereira, Raquel; Gavrilescu, Maria; Alves, Maria Madalena

2012-09-01

Biodegradation of a xanthene dyes was investigated for the first time using anaerobic granular sludge. On a first screening, biomass was able to decolorize, at different extents, six azo dye solutions: acid orange 7, direct black 19, direct blue 71, mordant yellow 10, reactive red 2 and reactive red 120 and two xanthene dyes--Erythrosine B and Eosin Y. Biomass concentration, type of electron donor, induction of biomass with dye and mediation with activated carbon (AC) were variables studied for Erythrosine B (Ery) as model dye. Maximum color removal efficiency was achieved with 4.71 g VSS L⁻¹, while the process rates were independent of the biomass concentration above 1.89 g VSS L⁻¹. No considerable effects were observed when different substrates were used as electron donors (VFA, glucose or lactose). Addition of Ery in the incubation period of biomass led to a fivefold increase of the decolorization rate. The rate of Ery decolorization almost duplicated in the presence of commercial AC (0.1 g L⁻¹ AC₀). Using different modified AC samples (from the treatment of AC₀), a threefold higher rate was obtained with the most basic one, AC(H₂), as compared with non-mediated reaction. Higher rates were obtained at pH 6.0. Chemical reduction using Na₂S confirmed the recalcitrant nature of this dye. The results attest that decolorization of Ery is essentially due to enzymatic and adsorption phenomena.

Characteristics of dye-sensitized solar cells using natural dye

Energy Technology Data Exchange (ETDEWEB)

Furukawa, Shoji, E-mail: furukawa@cse.kyutech.ac.j [Graduate School of Computer Science and Systems Engineering, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka-shi, Fukuoka-ken 820-8502 (Japan); Iino, Hiroshi; Iwamoto, Tomohisa; Kukita, Koudai; Yamauchi, Shoji [Graduate School of Computer Science and Systems Engineering, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka-shi, Fukuoka-ken 820-8502 (Japan)

2009-11-30

Dye-sensitized solar cells are expected to be used for future clean energy. Recently, most of the researchers in this field use Ruthenium complex as dye in the dye-sensitized solar cells. However, Ruthenium is a rare metal, so the cost of the Ruthenium complex is very high. In this paper, various dye-sensitized solar cells have been fabricated using natural dye, such as the dye of red-cabbage, curcumin, and red-perilla. As a result, it was found that the conversion efficiency of the solar cell fabricated using the mixture of red-cabbage and curcumin was about 0.6% (light source: halogen lamp), which was larger than that of the solar cells using one kind of dye. It was also found that the conversion efficiency was about 1.0% for the solar cell with the oxide semiconductor film fabricated using polyethylene glycol (PEG) whose molecular weight was 2,000,000 and red-cabbage dye. This indicates that the cost performance (defined by [conversion efficiency]/[cost of dye]) of the latter solar cell (dye: red-cabbage) is larger by more than 50 times than that of the solar cell using Ruthenium complex, even if the effect of the difference between the halogen lamp and the standard light source is taken into account.

Application of thin film cellulose composite membrane for dye wastewater reuse

KAUST Repository

Puspasari, Tiara; Peinemann, Klaus-Viktor

2016-01-01

artificial dye effluents. In the experiments using a feed containing Congo Red and high NaCl concentration, the membrane featured impressive dye removal with zero salt rejection combined with high flux. More interestingly, the membrane reached as much as 600

Decolourisation of chemically different dyes by enzymes from spent ...

African Journals Online (AJOL)

The optimum veratryl alcohol concentration for RBBR was 4 mM. Based on the effect of hydrogen peroxide on the rate of decolourisation of each dye, the dyes could be divided into two groups. From the results of the present study, it could be concluded that the enzymes extracted from the spent compost of P. sajor-caju ...

Adsorption Of Blue-Dye On Activated Carbons Produced From Rice ...

African Journals Online (AJOL)

The activated carbons prepared were used for the adsorption of blue-dye of concentration ranging from 100 to 2000 mg/l from aqueous solution. The results obtained indicated that ferric chloride-activated carbons produced from coconut coirpith are better adsorbents for blue-dye than those prepared from rice husk.

Color pollution control in textile dyeing industry effluents using tannery sludge

Directory of Open Access Journals (Sweden)

Sajjala Sreedhar Reddy

2008-12-01

Full Text Available Effective treatment of dyestuff containing textile dyeing industry effluents require advanced treatment technologies such as adsorption for the removal of dyestuffs. Powdered commercial coal based activated carbon has been the most widely used adsorbent for the removal of dyestuffs from dyeing industry effluents. As an alternative to commercial coal based activated carbon, activated carbon prepared from dried tannery sludge was used as an adsorbent for dyestuff removal from simulated textile dying industry effluent in this study. The color removal performance of tannery sludge derived activated carbon and commercial coal based activated carbon has been investigated using parameters such as adsorbent dosage, initial dye concentration, pH and temperature. It was found that tannery sludge derived activated carbon exhibits dye removal efficiency that is about 80–90 % of that observed with commercial coal based activated carbon. The amount of dye adsorbed on to tannery sludge derived activated carbon is lower compared with commercial activated carbon at equilibrium and dye adsorption capacity increased with increase of initial dye concentration and temperature, and deceasing pH. It was found that the Langmuir isotherm appears to fit the isotherm data better than the Freundlich isotherm. The leachate of heavy metals from tannery sludge derived activated carbon to the environment is very low, which are within the standard limit of industrial effluent and leachable substances.

Removal of Acid Red 18 dye from Aqueous Solutions Using Nanoscale Zero-Valent Iron

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Ahmad Reza Yari

2015-08-01

Full Text Available Background and Purpose:Organic dyes with a complex structure are often toxic, carcinogenic, mutagenic, non-biodegradation and stable in the environment and if released to the environment without treatment can endanger the environment and human health. The aim was to evaluate the performance nanoscalezero-valent iron (NZVI in the removal of dye acid red 18 (AR18 from aqueous solutions. Materials and Methods:This study was conducted at the laboratory scale. In this study, the removal efficiency of AR18 from a synthetic solution by NZVI was investigated. As well as the effect of solution pH, dye concentration, the concentration of NZVI and contact time in decolorization efficiency was investigated. Results:The results show that in pH = 3, contact time of 80 minutes, dye concentration of 25 mg/l and concentration of NZVI of 2 g/l, the removal efficiency was about 94%. Conclusion:According to the results of experiments, NZVI has high efficiency in removal of AR18 from aqueous solution.

Co-encapsulation of enzyme and sensitive dye as a tool for fabrication of microcapsule based sensor for urea measuring.

Science.gov (United States)

Kazakova, Lyubov I; Shabarchina, Lyudmila I; Sukhorukov, Gleb B

2011-06-21

Enzyme based micron sized sensing system with optical readout was fabricated by co-encapsulation of urease and dextran couple with pH sensitive dye SNARF-1 into polyelectrolyte multilayer capsules. Co-precipitation of calcium carbonate, urease and dextran followed up by multilayer film coating and Ca-extracting by EDTA resulted in the formation of 3.5-4 micron capsules, what enable the calibrated fluorescence response to urea in concentration range from 10(-6) to 10(-1) M. The presence of urea can be monitored on a single capsule level as illustrated by confocal fluorescent microscopy. Variations in urease:dye ratio in capsules, applicability and limits of use of that type multi-component microencapsulated sensors are discussed.

Conduction and TSC properties of LB films adsorbing cyanine dyes; Cyanine shikiso kyuchaku LB maku ni okeru denki dendo oyobi netsushigeki denryu tokusei

Energy Technology Data Exchange (ETDEWEB)

Shinbo, K.; Kato, K.; Kaneko, F.; Kobayashi, S. [Niigata University, Niigata (Japan)

1995-05-20

The electric properties were investigated for phosphatidic acid (PA) LB films adsorbing cyanide dyes (NK-3) with sandwich electrodes. PA LB adsorbing the dyes and the monolayers of Cd salt without the dyes are deposited using subphases, containing various concentrations of the dyes and containing CdCl2 instead of the dyes, respectively. Conduction currents are measured at room temperature for the PA LB film devices. Increases in the conduction currents are observed in the LB films containing the dyes. Furthermore, the conduction currents remarkably increase using the Au upper electrode. The current(I) vs. voltage (V) properties nearly follow the Poole conduction, log(I)-V. Therefore, the conduction currents are very complicated and are thought to be due to composite mechanisms in the film and at the interface. TSC measurements are used to examine the dipolar polarizations in the PA LB films, in the temperature region between 150 K and 300 K. Remarkable increase of TSCs are observed above 260 K for the devices containing the dyes. The TSCs are caused by the dipolar polarizations, and increase with the quantity of the dyes contained in the LB devices and/or aggregations of the dyes. The results are useful for applications of ultrathin film devices in the future. 16 refs., 11 figs., 3 tabs.

Tests of rhodamine WT dye for toxicity to oysters and fish

Science.gov (United States)

Parker, Garald G.

1973-01-01

Because of the toxicity to oyster larvae and eggs of rhodamine B dye in concentrations greater than 1 mg/l in earlier tests, there was a concern that rhodamine WT, a similar tracer dye, would have a detrimental effect on marine life being developed under the aquaculture program of the Lummi Indian Tribe near Bellingham, Wash. Tests showed that 48-hour exposures at 24° C of 11,000 oyster eggs per liter and 6,000 12-day-old larvae per liter, in sea water with concentrations of rhodamine WT ranging from 1 μg/l to 10 mg/l, resulted in development of the eggs to normal straight-hinge larvae and no abnormalities in the larvae development. Tests made on the smolt of both silver salmon and Donaldson trout, with the fish held for 17.5 hours in a tankfull of sea water with a dye concentration of 10 mg/l at 22°C showed no mortalities or respiratory problems. With the concentration increased to 375 mg/l, and the time extended an additional 3.2 hours, still no mortalities or abnormalities were noted. The fish remained healthy in dye-free water when last checked a month after the test.

Levitated droplet dye laser

DEFF Research Database (Denmark)

Azzouz, H.; Alkafadiji, L.; Balslev, Søren

2006-01-01

a high quality optical resonator. Our 750 nL lasing droplets consist of Rhodamine 6G dissolved in ethylene glycol, at a concentration of 0.02 M. The droplets are optically pumped at 532 nm light from a pulsed, frequency doubled Nd:YAG laser, and the dye laser emission is analyzed by a fixed grating...

Characteristics of a Broadband Dye Laser Using Pyrromethene and Rhodamine Dyes

Science.gov (United States)

Tedder, Sarah A.; Danehy, Paul M.; Wheeler, Jeffrey L.

2011-01-01

A broadband dye laser pumped by a frequency-doubled Nd:YAG laser with a full-width half-maximum (FWHM) from 592 to 610 nm was created for the use in a dual-pump broadband CARS system called WIDECARS. The desired broadband dye laser was generated with a mixture of Pyrromethene dyes as an oscillator gain medium and a spectral selective optic in the oscillator cavity. A mixture of Rhodamine dyes were used in the amplifier dye cell. To create this laser a study was performed to characterize the spectral behavior of broadband dye lasers created with Rhodamine dyes 590, 610, and 640, Pyrromethene dyes 597 and 650 as well as mixture of these dyes.

Removal of Basic Red 46 dye from aqueous solution by adsorption onto Moroccan clay

International Nuclear Information System (INIS)

Karim, A. Bennani; Mounir, B.; Hachkar, M.; Bakasse, M.; Yaacoubi, A.

2009-01-01

In this study, Moroccan crude clay of Safi, which was characterized by X-ray diffraction, is used as adsorbent for the investigation of the adsorption kinetics, isotherms and thermodynamic parameters of the Basic Red 46 (BR46) in aqueous solutions at various dye concentrations, adsorbent masses and pH values. The results showed that the adsorption capacity of the dye increased by initial dye concentration and pH values. Two kinetic models (the pseudo-first-order and the pseudo-second-order) were used to calculate the adsorption rate constants. The adsorption kinetics of the basic dye followed pseudo-second-order model. The experimental data isotherms were analyzed using the Langmuir, Freundlich and Dubinin-Radushkevish equations. The monolayer adsorption capacity for BR46 dye is 54 mg/g of crude clay. Nearly 20 min of contact time was found to be sufficient for the dye adsorption to reach equilibrium. Thermodynamical parameters were also evaluated for the dye-adsorbent system and revealed that the adsorption process is exothermic in nature.

OPTIMIZATION OF DYEING PARAMETERS TO DYE COTTON WITH CARROT EXTRACTION

Directory of Open Access Journals (Sweden)

MIRALLES Verónica

2017-05-01

Full Text Available Natural dyes derived from flora and fauna are believed to be safe because of non-toxic, non-carcinogenic and biodegradable nature. Furthermore, natural dyes do not cause pollution and waste water problems. Natural dyes as well as synthetic dyes need the optimum parameters to get a good dyeing. On some occasions, It is necessary the use of mordants to increase the affinity between cellulose fiber and natural dye, but there are other conditions to optimize in the dyeing process, like time, temperature, auxiliary porducts, etc. In addition, the optimum conditions are different depends on the type of dye and the fiber nature. The aim of this work is the use of carrot extract to dye cotton fabric by exhaustion at diverse dyeing conditions. Diffferent dyeing processes were carried out to study the effect of pH condition and the temperature, using 7, 6 and 4 pH values and 95 ºC and 130ºC for an hour. As a result some images of dyed samples are shown. Moreover, to evaluate the colour of each sample CIELAB parameters are analysed obtained by reflexion spectrophotometre. The results showed that the temperature used has an important influence on the colour of the dyed sample.

Construction of an integrated enzyme system consisting azoreductase and glucose 1-dehydrogenase for dye removal.

Science.gov (United States)

Yang, Yuyi; Wei, Buqing; Zhao, Yuhua; Wang, Jun

2013-02-01

Azo dyes are toxic and carcinogenic and are often present in industrial effluents. In this research, azoreductase and glucose 1-dehydrogenase were coupled for both continuous generation of the cofactor NADH and azo dye removal. The results show that 85% maximum relative activity of azoreductase in an integrated enzyme system was obtained at the conditions: 1U azoreductase:10U glucose 1-dehydrogenase, 250mM glucose, 1.0mM NAD(+) and 150μM methyl red. Sensitivity analysis of the factors in the enzyme system affecting dye removal examined by an artificial neural network model shows that the relative importance of enzyme ratio between azoreductase and glucose 1-dehydrogenase was 22%, followed by dye concentration (27%), NAD(+) concentration (23%) and glucose concentration (22%), indicating none of the variables could be ignored in the enzyme system. Batch results show that the enzyme system has application potential for dye removal. Copyright © 2012 Elsevier Ltd. All rights reserved.

Study of the Direct Red 81 Dye/Copper(II-Phenanthroline System

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Elsa Walger

2018-01-01

Full Text Available Recovered papers contain several chromophores, such as wood lignin and dyes. These have to be eliminated during paper recycling in order to produce white paper. Hydrogen peroxide under alkaline conditions is generally used to decolorize lignin, but its effect on dyes is limited. Copper(II-phenanthroline (Cu-Phen complexes can activate the oxidation of lignin by hydrogen peroxide. Hydrogen peroxide may also be activated during recycled fiber bleaching, thus enhancing its color-stripping efficiency towards unoxidizable azo dyes. The purpose of this paper was to determine the effect of Cu-Phen complexes on a model azo dye, Direct Red 81 (DR81, in aqueous solution. Different Cu-Phen solutions (with different initial Cu:Phen molar ratios were prepared and mixed with the dye at different pHs. The geochemical computer program PHREEQC allowed precise calculation of the theoretical distribution between different possible coordinates (CuPhenOH+, Cu(Phen22+, CuPhen(OH2, Cu(Phen32+, etc. depending on pH and initial concentrations. UV-vis spectroscopic measurements were correlated with the major species theoretically present in each condition. The UV absorbance of the system was mainly attributed to the Cu-Phen complex and the visible absorbance was only due to the dye. Cu-Phen appeared to reduce the color intensity of the DR81 dye aqueous solution under specific conditions (more effective at pH 10.7 with Cu:Phen = 1:1, probably owing to the occurrence of a coordination phenomenon between DR81 and Cu-Phen. Hence, the ligand competition between phenanthroline and hydroxide ions would be disturbed by a third competitor, which is the dye molecule. Further investigation proved that the DR81 dye is able to form a complex with copper-phenanthroline, leading to partial color-stripping. This new “color-stripping effect” may be a new opportunity in paper and textile industries for wastewater treatment.

FACTORS AFFECTING THE REMOVAL OF A BASIC AND AN AZO DYE FROM ARTIFICIAL SOLUTIONS BY ADSORPTION USING ACTIVATED CARBON

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H Albroomi

2014-10-01

Full Text Available Decolourisation of wastewater, particularly from textile industries, is one of the major environmental concerns these days. Current methods for removing dyes from wastewater are costly and cannot effectively be used to treat wide range of such wastewater. This work describes the use of commercial available granular activated carbon (GAC as an efficient adsorbent material for dyes removal. Aqueous solutions of various basic dye Methylene Blue (MB and azo-dye Tartrazine with concentrations 5-20 mg l–1 and 10-100 mg l–1, respectively, were shaken with certain amount of GAC to determine the adsorption capacity and removal efficiencies. The effects of adsorbent dose, initial pH, initial dye concentration, agitation speed and contact time on dyes removal efficiencies have been studied. Maximum dye concentration was removed from the solution within 60-90 min after the beginning of every experiment. Adsorption parameters were found to fit well into Langmuir and Freundlich adsorption isotherms models with correlation coefficient (R2 > 0.99 in the concentration range of MB and TZ studied.

Removal of reactive dyes from aqueous solutions by a non-conventional and low cost agricultural waste: adsorption on ash of Aloe Vera plant

Directory of Open Access Journals (Sweden)

Mohammad Malakootian

2014-08-01

Full Text Available Dyes are an important class of pollutants and disposal of them in precious water resources must be avoided. Among various methods adsorption occupies a prominent place in dye removal. The aim of this study is to evaluate adsorption of dye Reactive Red 198 and Blue 19 (RR-198 & RB-19 (on to Aloe Vera plant ash from aqueous solutions. In this research Aloe Vera ash was prepared at laboratory conditions and then after shredding, screened by ASTM standard sieve with 60 -200 mesh sizes and the effects of pH (3-12, adsorbent dose (0.1-1 g/L, contact time (10-60 min, initial dye concentration (10-160 mg/L and temperature were investigated in the experiment. In different samples Dye concentration was measured by spectrophotometer at 592 nm and 520 nm wavelength for RR198 and RB19 respectively. Also the Langmuir and Freundlich adsorption isotherms were determined in order to describe the relations between the colored solutions and the adsorbent. The results of this study showed that acidic conditions were more conducive to enhance the hydrolysis rate than basic ones as the decomposition was optimum at pH 3. The adsorption rate of RR-198 and RB-19 dyes was increased by increasing of initial dye concentration, increasing of adsorbent dose in 0.1 to 0.4 mg/L. Dye solution was decolorized in a relatively short time (20 min. The efficiencies for RR-198 and RB- 19 reactive dyes were 82.68% and 90.42% respectively. The maximum adsorption capacity (qmax has been found to be 80.152 mg/g for RR-198 reactive dye and 88.452 mg/g for Blue 19 reactive dye. Adsorption isotherms were examined by Freundlich and Langmuir isotherm that finally showed the Freundlich multilayer isotherm has better accordance with dates. The results indicate that Aloe Vera ash plant as a natural and inexpensive adsorbent is a suitable adsorbent for the adsorption of textile dyes.

Decolorization of direct poly azo dye with nanophotocatalytic UV/NiO process

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Ali Assadi

2012-01-01

Full Text Available Aims: The aim of the present study is to investigate the efficiency of ultraviolet/ nickel oxide (UV/NiO system as one form of advanced oxidation processes (AOP for decolorization of red poly azo. Materials and Methods: This study was conducted as a laboratory scale in a batch mode. Ultraviolet radiation was provided by a low pressure (11 W UV lamp. Effects of various factors including pH, different irradiation durations, different concentration of nickel oxide, and initial dye concentration were evaluated. Results: The results of the UV/NiO system′s assessment showed that UV light alone cannot remove DR 80 dye. Nickel oxide is an effective catalyst in the decolorization of dye with the nanophotocatalytic process. The decolorization efficiency increases with decreasing pH value and the optimum pH value is 4. Fainally, the highest removal efficiency achieved by UV/NiO process for DR 80 dye with concentrations of 25 mg/l and 50 mg/l was 94.3% and 82.2%, respectively. UV/NiO-based decolorization process follows pseudo-second-order reaction kinetics. Conclusions: From the findings of the present study, it can be concluded that UV/NiO process is an effective technique for decolorization of poly azo dye, DR 80, in aqueous solutions.

Kinetics of γ-rays induced decoloration of textile dye aqueous solutions

International Nuclear Information System (INIS)

Perkowski, J.; Ledakowicz, S.; Nowicki, L.

1987-01-01

The γ-rays induced decoloration of aqueous solutions of commercial dyes has been studied. Four chemical classes of dyes were applied. The initial dye concentration and the irradiation dose rate ranged from 0.025 to 0.250 g/dm 3 and 0.014 to 2.0 Gy/s respectively. On the base of obtained experimental data the kinetic paramaters in the proposed rate equation were calculated. 8 refs., 8 figs., 2 tabs. (author)

Adsorption of reactive dyes from aqueous solutions by fly ash: Kinetic and equilibrium studies

International Nuclear Information System (INIS)

Dizge, N.; Aydiner, C.; Demirbas, E.; Kobya, M.; Kara, S.

2008-01-01

Adsorption kinetic and equilibrium studies of three reactive dyes namely, Remazol Brillant Blue (RB), Remazol Red 133 (RR) and Rifacion Yellow HED (RY) from aqueous solutions at various initial dye concentration (100-500 mg/l), pH (2-8), particle size (45-112.5 μm) and temperature (293-323 K) on fly ash (FA) were studied in a batch mode operation. The adsorbent was characterized with using several methods such as SEM, XRD and FTIR. Adsorption of RB reactive dye was found to be pH dependent but both RR and RY reactive dyes were not. The result showed that the amount adsorbed of the reactive dyes increased with increasing initial dye concentration and contact time. Batch kinetic data from experimental investigations on the removal of reactive dyes from aqueous solutions using FA have been well described by external mass transfer and intraparticle diffusion models. It was found that external mass transfer and intraparticle diffusion had rate limiting affects on the removal process. This was attributed to the relatively simple macropore structure of FA particles. The adsorption data fitted well with Langmuir and Freundlich isotherm models. The optimum conditions for removal of the reactive dyes were 100 mg/l initial dye concentration, 0.6 g/100 ml adsorbent dose, temperature of 293 K, 45 μm particle size, pH 6 and agitation speed of 250 rpm, respectively. The values of Langmuir and Freundlich constants were found to increase with increasing temperature in the range 135-180 and 15-34 mg/g for RB, 47-86 and 1.9-3.7 mg/g for RR and 37-61 and 3.0-3.6 mg/g for RY reactive dyes, respectively. Different thermodynamic parameters viz., changes in standard free energy, enthalpy and entropy were evaluated and it was found that the reaction was spontaneous and endothermic in nature

Novel organic dyes based on phenyl-substituted benzimidazole for dye sensitized solar cells

Energy Technology Data Exchange (ETDEWEB)

Saltan, Gözde Murat [Department of Chemistry, Faculty of Arts and Science, Celal Bayar University, Yunus Emre, 45140 Manisa (Turkey); Dinçalp, Haluk, E-mail: haluk.dincalp@cbu.edu.tr [Department of Chemistry, Faculty of Arts and Science, Celal Bayar University, Yunus Emre, 45140 Manisa (Turkey); Kıran, Merve; Zafer, Ceylan [Solar Energy Institute, Ege University, Bornova, 35100 Izmir (Turkey); Erbaş, Seçil Çelik [Celal Bayar University, Materials Engineering Department, Faculty of Engineering, Yunus Emre, 45140 Manisa (Turkey)

2015-08-01

Two new sensitizers derived from benzimidazole core for dye-sensitized solar cell (DSSC) applications were designed and synthesized as D–π–A structures, in which two phenyl-substituted benzimidazole group, a phenyl ring and a cyanoacrylic acid were used as the electron donor, π-conjugated linkage and the electron acceptor, respectively. Effect of methoxy- and N,N-dimetylamino- moieties attached to the phenyl groups of benzimidazole were investigated by means of optical and photovoltaic measurements. The compounds exhibit broad absorption maximum at 387 nm with the tail extending up to 500 nm on TiO{sub 2}-coated thin film. The longer wavelength absorption band around 360 nm and the much longer decay components could be attributed to the existence of charge transfer state of the dyes in solutions. DSSC device fabricated by using methoxy substituted dye (BI5a) as a sensitizer shows much better incident photon-to-current conversion efficiency (IPCE) of 64% giving cell efficiency of 2.68%. - Graphical abstract: Display Omitted - Highlights: • Long decay times suggest the delayed fluorescence caused by the existence of ICT. • The best solar energy conversion efficiency was obtained for BI5a dye (2.68%). • More fluorescent BI5a dye gives higher photocurrent generation.

Novel organic dyes based on phenyl-substituted benzimidazole for dye sensitized solar cells

International Nuclear Information System (INIS)

Saltan, Gözde Murat; Dinçalp, Haluk; Kıran, Merve; Zafer, Ceylan; Erbaş, Seçil Çelik

2015-01-01

Two new sensitizers derived from benzimidazole core for dye-sensitized solar cell (DSSC) applications were designed and synthesized as D–π–A structures, in which two phenyl-substituted benzimidazole group, a phenyl ring and a cyanoacrylic acid were used as the electron donor, π-conjugated linkage and the electron acceptor, respectively. Effect of methoxy- and N,N-dimetylamino- moieties attached to the phenyl groups of benzimidazole were investigated by means of optical and photovoltaic measurements. The compounds exhibit broad absorption maximum at 387 nm with the tail extending up to 500 nm on TiO 2 -coated thin film. The longer wavelength absorption band around 360 nm and the much longer decay components could be attributed to the existence of charge transfer state of the dyes in solutions. DSSC device fabricated by using methoxy substituted dye (BI5a) as a sensitizer shows much better incident photon-to-current conversion efficiency (IPCE) of 64% giving cell efficiency of 2.68%. - Graphical abstract: Display Omitted - Highlights: • Long decay times suggest the delayed fluorescence caused by the existence of ICT. • The best solar energy conversion efficiency was obtained for BI5a dye (2.68%). • More fluorescent BI5a dye gives higher photocurrent generation

Efficiency-limiting processes in cyclopentadithiophene-bridged donor-acceptor-type dyes for solid-state dye-sensitized solar cells

KAUST Repository

Hinkel, Felix

2018-01-26

The charge generation and recombination processes in three novel push-pull photosensitizers for dye-sensitized solar cells (DSSCs) are studied by ps–μs transient absorption (TA) and quasi-steady-state photoinduced absorption (PIA) spectroscopy. The three cyclopentadithiophene-based photosensitizer dye molecules exhibit comparably low power conversion efficiencies ranging from 0.8% to 1.7% in solid-state DSSCs. We find that the photocurrents increase in the presence of Li-salt additives. Both TA and PIA measurements observe long-lived dye cations created by electron injection from the dyes’ excited state for two dyes from the series. However, the third dye shows significantly lower performance as a consequence of the less efficient electron injection even after the addition of Li-salts and faster electron-hole recombination on the ns-μs time scale. In essence, the prerequisites for this class of donor-π bridge-acceptor photosensitizers to reach higher charge generation efficiencies are a combination of strong dipole moments and fine tuning of the electronic landscape at the titania-dye interface by Li-salt addition.

Efficiency-limiting processes in cyclopentadithiophene-bridged donor-acceptor-type dyes for solid-state dye-sensitized solar cells

KAUST Repository

Hinkel, Felix; Kim, Yoojin M.; Zagraniarsky, Yulian; Schlü tter, Florian; Andrienko, Denis; Mü llen, Klaus; Laquai, Fré dé ric

2018-01-01

The charge generation and recombination processes in three novel push-pull photosensitizers for dye-sensitized solar cells (DSSCs) are studied by ps–μs transient absorption (TA) and quasi-steady-state photoinduced absorption (PIA) spectroscopy. The three cyclopentadithiophene-based photosensitizer dye molecules exhibit comparably low power conversion efficiencies ranging from 0.8% to 1.7% in solid-state DSSCs. We find that the photocurrents increase in the presence of Li-salt additives. Both TA and PIA measurements observe long-lived dye cations created by electron injection from the dyes’ excited state for two dyes from the series. However, the third dye shows significantly lower performance as a consequence of the less efficient electron injection even after the addition of Li-salts and faster electron-hole recombination on the ns-μs time scale. In essence, the prerequisites for this class of donor-π bridge-acceptor photosensitizers to reach higher charge generation efficiencies are a combination of strong dipole moments and fine tuning of the electronic landscape at the titania-dye interface by Li-salt addition.

Z-scan and optical limiting properties of Hibiscus Sabdariffa dye

Science.gov (United States)

Diallo, A.; Zongo, S.; Mthunzi, P.; Rehman, S.; Alqaradawi, S. Y.; Soboyejo, W.; Maaza, M.

2014-12-01

The intensity-dependent refractive index n 2 and the nonlinear susceptibility χ (3) of Hibiscus Sabdariffa dye solutions in the nanosecond regime at 532 nm are reported. More presicely, the variation of n 2, β, and real and imaginary parts of χ (3) versus the natural dye extract concentration has been carried out by z-scan and optical limiting techniques. The third-order nonlinearity of the Hibiscus Sabdariffa dye solutions was found to be dominated by nonlinear refraction, which leads to strong optical limiting of laser.

Response surface methodological approach for the decolorization of simulated dye effluent using Aspergillus fumigatus fresenius.

Science.gov (United States)

Sharma, Praveen; Singh, Lakhvinder; Dilbaghi, Neeraj

2009-01-30

The aim of our research was to study, effect of temperature, pH and initial dye concentration on decolorization of diazo dye Acid Red 151 (AR 151) from simulated dye solution using a fungal isolate Aspergillus fumigatus fresenius have been investigated. The central composite design matrix and response surface methodology (RSM) have been applied to design the experiments to evaluate the interactive effects of three most important operating variables: temperature (25-35 degrees C), pH (4.0-7.0), and initial dye concentration (100-200 mg/L) on the biodegradation of AR 151. The total 20 experiments were conducted in the present study towards the construction of a quadratic model. Very high regression coefficient between the variables and the response (R(2)=0.9934) indicated excellent evaluation of experimental data by second-order polynomial regression model. The RSM indicated that initial dye concentration of 150 mg/L, pH 5.5 and a temperature of 30 degrees C were optimal for maximum % decolorization of AR 151 in simulated dye solution, and 84.8% decolorization of AR 151 was observed at optimum growth conditions.

Removal of rhodamine B (a basic dye) and thoron (an acidic dye) from dilute aqueous solutions and wastewater simulants by ion flotation.

Science.gov (United States)

Shakir, Kamal; Elkafrawy, Ahmed Faouzy; Ghoneimy, Hussein Fouad; Elrab Beheir, Shokry Gad; Refaat, Mamdoh

2010-03-01

The present work deals with removal, by ion flotation, of two dyes: a basic dye (rhodamine B (RB)) and an acidic one (thoron (TH)) from dilute aqueous solutions and simulated wastewaters. These dyes are widely used for analytical and biological staining purposes. Besides, RB is commonly used in dyeing of various industrial products. Therefore, wastewaters emanating from chemical and radiochemical laboratories, and biomedical and biological research laboratories may be contaminated with RB and TH. Ion flotation of these dyes has been investigated over a wide range of pH using the anionic surfactant, sodium lauryl sulfate (NaLS) and the cationic surfactant, cetyltrimethylammonium bromide (CTAB) as collectors. Successful removals could be achieved for RB and TH with the anionic collector, NaLS, and the cationic collector, CTAB, respectively. In addition to the effects of pH and type of collector on the efficiency of removal of each dye, the effects of collector and dye concentrations, frother dosage, ionic strength, bubbling time period and presence of foreign salts were investigated and the optimal removal conditions have been established. Removals exceeding 99.5 % and 99.9% could be achieved for RB and TH, respectively. The results obtained are discussed with respect to dissociation of dye, type of collector, ionic strength and sign and magnitude of charge of added foreign ions. Kinetics of flotation were also studied. Further studies demonstrate that under optimum conditions the developed flotation processes can be applied for the treatment of dye-contaminated wastewaters simulated to those generated at dyeing industries and radiochemical laboratories. Copyright 2009 Elsevier Ltd. All rights reserved.

Parameters affecting the photocatalytic degradation of dyes using TiO2: a review

Science.gov (United States)

Reza, Khan Mamun; Kurny, ASW; Gulshan, Fahmida

2017-07-01

Traditional chemical, physical and biological processes for treating wastewater containing textile dye have such disadvantages as high cost, high energy requirement and generation of secondary pollution during treatment process. The advanced oxidation processes technology has been attracting growing attention for the decomposition of organic dyes. Such processes are based on the light-enhanced generation of highly reactive hydroxyl radicals, which oxidize the organic matter in solution and convert it completely into water, CO2 and inorganic compounds. In this presentation, the photocatalytic degradation of dyes in aqueous solution using TiO2 as photocatalyst under solar and UV irradiation has been reviewed. It is observed that the degradation of dyes depends on several parameters such as pH, catalyst concentration, substrate concentration and the presence of oxidants. Reaction temperature and the intensity of light also affect the degradation of dyes. Particle size, BET-surface area and different mineral forms of TiO2 also have influence on the degradation rate.

Estimation of presynaptic calcium currents and endogenous calcium buffers at the frog neuromuscular junction with two different calcium fluorescent dyes

Directory of Open Access Journals (Sweden)

Dmitry eSamigullin

2015-01-01

Full Text Available At the frog neuromuscular junction, under physiological conditions, the direct measurement of calcium currents and of the concentration of intracellular calcium buffers—which determine the kinetics of calcium concentration and neurotransmitter release from the nerve terminal—has hitherto been technically impossible. With the aim of quantifying both Ca2+ currents and the intracellular calcium buffers, we measured fluorescence signals from nerve terminals loaded with the low-affinity calcium dye Magnesium Green or the high-affinity dye Oregon Green BAPTA-1, simultaneously with microelectrode recordings of nerve-action potentials and end-plate currents. The action-potential-induced fluorescence signals in the nerve terminals developed much more slowly than the postsynaptic response. To clarify the reasons for this observation and to define a spatiotemporal profile of intracellular calcium and of the concentration of mobile and fixed calcium buffers, mathematical modeling was employed. The best approximations of the experimental calcium transients for both calcium dyes were obtained when the calcium current had an amplitude of 1.6 ± 0.08 рА and a half-decay time of 1.2 ± 0.06 ms, and when the concentrations of mobile and fixed calcium buffers were 250 ± 13 µM and 8 ± 0.4 mM, respectively. High concentrations of endogenous buffers define the time course of calcium transients after an action potential in the axoplasm, and may modify synaptic plasticity.

[Decolorization of the azo dye reactive red X-3B by an Al-Cu bimetallic system].

Science.gov (United States)

Fan, Jin-hong; Ma, Lu-ming; Wang, Hong-wu; Wu, De-li

2008-06-01

The decoloration mechanism and kinetics of the azo dye reactive red X-3B by an Al-Cu bimetallic system were investigated by measuring the dye removal, the TOC removal and the aniline concentration, and by adding EDTA as control experiments. The results showed the colority removal rate of X-3B reached 83% in the near neutral pH medium for 30 min and 96.4% for 120 min, in which, about 34% was due to the X-3B reduced to aniline, and about 20% and 30% was due to the flocculating of aluminum ions and surface adsorption of aluminum-fillings respectively. The decolorization of dyeing wastewater is a gradual reaction process, which first adsorbs a large number of dyeing ingredients and then carries out inner electrolysis reduction, improved effectively by the flocculating action of aluminum ions. The decolorization reaction appears to be a pseudo first-order reaction and increases with rising temperature.

Application of thin film cellulose composite membrane for dye wastewater reuse

KAUST Repository

Puspasari, Tiara

2016-09-22

The use of low cost membranes with high salt/dye selectivity and high flux is ideal for an economic and eco-friendly treatment of dye wastewater. Here, regenerated cellulose membranes prepared from trimethylsilyl cellulose are studied for treating artificial dye effluents. In the experiments using a feed containing Congo Red and high NaCl concentration, the membrane featured impressive dye removal with zero salt rejection combined with high flux. More interestingly, the membrane reached as much as 600 LMH flux at 80 °C and 4 bar while maintaining high dye rejection close to 98%. In prolonged experiments up to 75 h the membrane exhibited good antifouling behavior with nearly 100% flux recovery. This study may provide a promising alternative of dye effluent treatment where high amounts of monovalent salts are present. © 2016

Removal of Malachite Green Dye by Mangifera indica Seed Kernel Powder

Science.gov (United States)

Singh, Dilbagh; Sowmya, V.; Abinandan, S.; Shanthakumar, S.

2017-11-01

In this study, batch experiments were carried out to study the adsorption of Malachite green dye from aqueous solution by Mangifera indica (mango) seed kernel powder. The mango seed kernel powder was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. Effect of various parameters including pH, contact time, adsorbent dosage, initial dye concentration and temperature on adsorption capacity of the adsorbent was observed and the optimized condition for maximum dye removal was identified. Maximum percentage removal of 96% was achieved with an adsorption capacity of 22.8 mg/g at pH 6 with an initial concentration of 100 mg/l. The equilibrium data were examined to fit the Langmuir and Freundlich isotherm models. Thermodynamic parameters for the adsorption process were also calculated.

Dye mixtures for ultrafast wavelength shifters

Energy Technology Data Exchange (ETDEWEB)

Gangopadhyay, S.; Liu, L.; Palsule, C.; Borst, W.; Wigmans, R. [Texas Tech Univ., Lubbock, TX (United States). Dept. of Physics; Barashkov, N. [Karpov Inst. of Physical Chemistry, Moscow (Russian Federation)

1994-12-31

Particle detectors based on scintillation processes have been used since the discovery of radium about 100 years ago. The fast signals that can be obtained with these detectors, although often considered a nice asset, were rarely essential for the success of experiments. However, the new generation of high energy particle accelerators require particle detectors with fast response time. The authors have produced fast wavelength shifters using mixtures of various Coumarin dyes with DCM in epoxy-polymers (DGEBA+HHPA) and measured the properties of these wavelength shifters. The particular mixtures were chosen because there is a substantial overlap between the emission spectrum of Coumarin and the absorption spectrum of DCM. The continuous wave and time-resolved fluorescence spectra have been studied as a function of component concentration to optimize the decay times, emission peaks and quantum yields. The mean decay times of these mixtures are in the range of 2.5--4.5 ns. The mean decay time increases with an increase in Coumarin concentration at a fixed DCM concentration or with a decrease in DCM concentration at a fixed Coumarin concentration. This indicates that the energy transfer is radiative at lower relative DCM concentrations and becomes non-radiative at higher DCM concentrations.

Dye mixtures for ultrafast wavelength shifters

International Nuclear Information System (INIS)

Gangopadhyay, S.; Liu, L.; Palsule, C.; Borst, W.; Wigmans, R.

1994-01-01

Particle detectors based on scintillation processes have been used since the discovery of radium about 100 years ago. The fast signals that can be obtained with these detectors, although often considered a nice asset, were rarely essential for the success of experiments. However, the new generation of high energy particle accelerators require particle detectors with fast response time. The authors have produced fast wavelength shifters using mixtures of various Coumarin dyes with DCM in epoxy-polymers (DGEBA+HHPA) and measured the properties of these wavelength shifters. The particular mixtures were chosen because there is a substantial overlap between the emission spectrum of Coumarin and the absorption spectrum of DCM. The continuous wave and time-resolved fluorescence spectra have been studied as a function of component concentration to optimize the decay times, emission peaks and quantum yields. The mean decay times of these mixtures are in the range of 2.5--4.5 ns. The mean decay time increases with an increase in Coumarin concentration at a fixed DCM concentration or with a decrease in DCM concentration at a fixed Coumarin concentration. This indicates that the energy transfer is radiative at lower relative DCM concentrations and becomes non-radiative at higher DCM concentrations

Laser Dyes

Indian Academy of Sciences (India)

amplification or generation of coherent light waves in the UV,. VIS, and near IR region. .... ciency in most flashlamp pumped dye lasers. It is used as reference dye .... have led to superior laser dyes with increased photostabilities. For instance ...

Fabrication and characterization of mixed dye: Natural and synthetic organic dye

Science.gov (United States)

Richhariya, Geetam; Kumar, Anil

2018-05-01

Mixed dye from hibiscus sabdariffa and eosin Y was employed in the fabrication of dye sensitized solar cell (DSSC). Nanostructured mesoporous film was prepared from the titanium dioxide (TiO2). The energy conversion efficiency of hibiscus, eosin Y and mixed dye was obtained as 0.41%, 1.53% and 2.02% respectively. Mixed DSSC has shown improvement in the performance of the cell as compared to hibiscus and eosin Y dye due to addition of synthetic organic dye. This illustrates the effect of synthetic organic dyes in performance enhancement of natural dyes. It has been credited to the improved absorption of light mainly in higher energy state (λ = 440-560 nm) when two dyes were employed simultaneously as was obvious from the absorption spectra of dyes adsorbed onto TiO2 electrode. The cell with TiO2 electrode sensitized by mixed dye gives short circuit current density (Jsc) = 4.01 mA/cm2, open circuit voltage (Voc) = 0.67 V, fill factor (FF) = 0.60 and energy conversion efficiency (η) of 2.02%.

Binding affinities of cationic dyes in the presence of activated charcoal and anionic surfactant in the premicellar region

Science.gov (United States)

Ali, Farman; Ibrahim, Muhammad; Khan, Fawad; Bibi, Iram; Shah, Syed W. H.

2018-03-01

Binding preferences of cationic dyes malachite green and methylene blue in a mixed charcoal-sodium dodecyl sulfate system have been investigated using UV-visible absorption spectroscopy. The dye adsorption shows surfactant-dependent patterns, indicating diverse modes of interactions. At low surfactant concentration, a direct binding to charcoal is preferred. Comparatively greater quantities of surfactant lead to attachment of dye-surfactant complex to charcoal through hydrophobic interactions. A simple model was employed for determination of equilibrium constant K eq and concentration of dye-surfactant ion pair N DS for both dyes. The values of binding parameters revealed that malachite green was directly adsorbed onto charcoal, whereas methylene blue was bound through surfactant monomers. The model is valid for low surfactant concentrations in the premicellar region. These findings have significance for material and environmental sciences.

Removal of azo and anthraquinone reactive dyes from industrial wastewaters using MgO nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Moussavi, Gholamreza, E-mail: Moussavi@modares.ac.ir [Department of Environmental Health, School of Medical Sciences, Tarbiat Modares University, Tehran (Iran, Islamic Republic of); Mahmoudi, Maryam [Department of Environmental Health, School of Medical Sciences, Tarbiat Modares University, Tehran (Iran, Islamic Republic of)

2009-09-15

In the present investigation, a porous MgO powder was synthesized and tested for the removal of dyes from aqueous solution. The size of the MgO particles was in the range of 38-44 nm, with an average specific surface area of 153.7 m{sup 2}/g. Adsorption of reactive blue 19 and reactive red 198 was conducted to model azo and anthraquinone dyes at various MgO dosages, dye concentrations, solution pHs and contact times in a batch reactor. Experimental results indicate that the prepared MgO powder can remove more than 98% of both dyes under optimum operational conditions of a dosage of 0.2 g, pH 8 and a contact time of 5 min for initial dye concentrations of 50-300 mg/L. The isotherm evaluations revealed that the Langmuir model attained better fits to the experimental equilibrium data than the Freundlich model. The maximum predicted adsorption capacities were 166.7 and 123.5 mg of dye per gram of adsorbent for RB 19 and RR 198, respectively. In addition, adsorption kinetic data followed a pseudo-second-order rate for both tested dyes.

Binding of phenazinium dye safranin T to polyriboadenylic acid: spectroscopic and thermodynamic study.

Directory of Open Access Journals (Sweden)

Ankur Bikash Pradhan

Full Text Available Here, we report results from experiments designed to explore the association of the phenazinium dye safranin T (ST, 3,7-diamino-2,8-dimethyl-5-phenylphenazinium chloride with single and double stranded form of polyriboadenylic acid (hereafter poly-A using several spectroscopic techniques. We demonstrate that the dye binds to single stranded polyriboadenylic acid (hereafter ss poly-A with high affinity while it does not interact at all with the double stranded (ds form of the polynucleotide. Fluorescence and absorption spectral studies reveal the molecular aspects of binding of ST to single stranded form of the polynucleotide. This observation is also supported by the circular dichroism study. Thermodynamic data obtained from temperature dependence of binding constant reveals that association is driven by negative enthalpy change and opposed by negative entropy change. Ferrocyanide quenching studies have shown intercalative binding of ST to ss poly-A. Experiments on viscosity measurements confirm the binding mode of the dye to be intercalative. The effect of [Na⁺] ion concentration on the binding process suggests the role of electrostatic forces in the complexation. Present studies reveal the utility of the dye in probing nucleic acid structure.

55 cases of allergic reactions to hair dye: a descriptive, consumer complaint-based study

DEFF Research Database (Denmark)

Søsted, H; Agner, T; Andersen, Klaus Ejner

2002-01-01

themselves, and adverse reactions to hair dye may not necessarily be recorded by the health care system, unless the reactions are especially severe. Based on this assumption, we suspected that hair dye dermatitis was occurring more frequently than reported in the literature. Consumer complaint-based data......Severe facial and scalp dermatitis following the use of permanent hair dyes has been reported in several cases. Para-phenylenediamine (PPD) is known as a potent contact allergen, and PPD is allowed in hair dye at a concentration of 6%. Hair dye reactions are usually diagnosed by the patients...

The role of FRET in solar concentrator efficiency and color tunability

Energy Technology Data Exchange (ETDEWEB)

Balaban, Benjamin, E-mail: bbalaban@ucsc.edu; Doshay, Sage; Osborn, Melissa; Rodriguez, Yvonne; Carter, Sue A., E-mail: sacarter@ucsc.edu

2014-02-15

We demonstrate concentration-dependent Förster-type energy transfer in a luminescent solar concentrator (LSC) material containing two high quantum yield laser dyes in a PMMA matrix. FRET heterotransfer is shown to be approximately 50% efficient in the regime of 2×10{sup −3}molal acceptor dye by weight in the host polymer. The two dyes used have been well studied for solar concentrator applications: BASF's Lumogen Red 305, and Exciton Chemical Company's DCM both demonstrate desirable stability, quantum yield, and complementary absorption spectra. We demonstrate how multiple-dye LSC devices employing FRET increase the absorption of air mass 1.5 solar irradiance without affecting the self-absorption properties of the film. Color tunability may be achieved through the addition of additional absorbers while minimizing the impact on waveguide efficiency. -- Highlights: • Förster Resonance Energy Transfer is demonstrated in a two-dye luminescent solar concentrator. • Donor-acceptor pair distance is related to the dye concentration in PMMA. • FRET's benefit to waveguide transport losses and color tunability is discussed.

Treatment of dyeing wastewater including reactive dyes (Reactive ...

African Journals Online (AJOL)

Fungal growth was not observed at pH 2. Maximum fungal decolourisation ocurred at pH 3 for anionic reactive dyes (RR, RBB, RB) and pH 6 for cationic MB dye. The fungal dye bioremoval was associated with the surface charge of the fungus due to electrostatic interactions. Growing R. arrhizus strain decolourised 100% of ...

Point and planar LIF for velocity-concentration correlations in a jet in cross flow

DEFF Research Database (Denmark)

Meyer, Knud Erik; Özcan, Oktay; Larsen, Poul Scheel

2002-01-01

Simultaneous measurements of velocities and concentration with Planar Laser Induced Fluorescense (PLIF) combined with Particle Image Velocimetry (PIV) are compared to similar measurements with pointwise Laser Induced Fluorescense (LIF) made with a slightly modified standard Laser Doppler Anemometer......, since these involve areas with high velocity- and concentration gradients, which in turn amplifies the effect of a finite measurement volume in the two measurement systems. In addition, the concentration measurement was realized by injecting clean water into the dye seeded main flow. This "inverse...

Mixed ZnO-TiO2 Suspended Solution as an Efficient Photocatalyst for Decolonization of a Textile Dye from Waste Water

Directory of Open Access Journals (Sweden)

Mohammad Ali Mooji

2015-03-01

Full Text Available Introduction: Textile industries produce large volume of colored dye effluents which are toxic and removal of dyes from wastewater is a significant environmental issue. Advanced oxidation process (AOPs is alternative method for the complete degradation many organic pollutants. ZnO and TiO2 are important photocatalysts with high catalytic activity that have attracted much research attention. Material and Methods: Mixed ZnO/TiO2 was prepared with mixing of ZnO and TiO2 (20, 40, 60, 80 % (w/w. 20 mL of dye solution (80 mgL-1 for DB71 containing the appropriate quantity of photocatalyst was magnetically stirred under UV irradiation. Photocatalytic study was carried out to evaluate the effect of UV (400 W, ZnO/TiO2 weight percent (20, 40, 60, 80 % (w/w, pH (2.3 – 9.2, irradiation time of (10 – 70 min, initial dye concentration of (10, 40, 80 mg/L and ZnO/TiO2 dosage of (0.2 – 1.6 g/L on removal of dye. Dye concentration was monitored spectrophotometrically by measuring the dye absorbance at 285 nm. Results: In comparison with TiO2 or ZnO as photocatalyst, mixed photocatalyst (ZnO/TiO2 is more efficient catalyst for degradation of dye under UV irradiation Results show that approximately 90 % of Direct Blue 71 has been eliminated after 70 minutes and optimized condition ((pH = 6.4, ZnO/TiO2 (50% w/w, 1.25 g/L. Experiments showed, the noticeable decolorization of dye solution can be done without any oxidation agent with mixed ZnO/TiO2 photocatalyst.

Extraction of antioxidant pigments from dye sorghum leaf sheaths

NARCIS (Netherlands)

Kayode, A.P.P.; Bara, C.A.; Dalode-Vieira, G.; Linnemann, A.R.; Nout, M.J.R.

2012-01-01

Extraction of antioxidant biocolorant pigments from leaf sheaths of dye sorghum was optimized. Effects of temperature and ethanol concentration of the extraction solvent on the concentrations of the 3-deoxyanthocyanidins, total phenolics and total anthocyanins, and the colour parameters of the

Homogeneous plate based antibody internalization assay using pH sensor fluorescent dye.

Science.gov (United States)

Nath, Nidhi; Godat, Becky; Zimprich, Chad; Dwight, Stephen J; Corona, Cesear; McDougall, Mark; Urh, Marjeta

2016-04-01

Receptor-mediated antibody internalization is a key mechanism underlying several anti-cancer antibody therapeutics. Delivering highly toxic drugs to cancer cells, as in the case of antibody drug conjugates (ADCs), efficient removal of surface receptors from cancer cells and changing the pharmacokinetics profile of the antibody drugs are some of key ways that internalization impacts the therapeutic efficacy of the antibodies. Over the years, several techniques have been used to study antibody internalization including radiolabels, fluorescent microscopy, flow cytometry and cellular toxicity assays. While these methods allow analysis of internalization, they have limitations including a multistep process and limited throughput and are generally endpoint assays. Here, we present a new homogeneous method that enables time and concentration dependent measurements of antibody internalization. The method uses a new hydrophilic and bright pH sensor dye (pHAb dye), which is not fluorescent at neutral pH but becomes highly fluorescent at acidic pH. For receptor mediated antibody internalization studies, antibodies against receptors are conjugated with the pHAb dye and incubated with the cells expressing the receptors. Upon binding to the receptor, the dyes conjugated to the antibody are not fluorescent because of the neutral pH of the media, but upon internalization and trafficking into endosomal and lysosomal vesicles the pH drops and dyes become fluorescent. The enabling attributes of the pHAb dyes are the hydrophilic nature to minimize antibody aggregation and bright fluorescence at acidic pH which allows development of simple plate based assays using a fluorescent reader. Using two different therapeutic antibodies--Trastuzumab (anti-HER2) and Cetuximab (anti-EGFR)--we show labeling with pHAb dye using amine and thiol chemistries and impact of chemistry and dye to antibody ration on internalization. We finally present two new approaches using the pHAb dye, which will be

Bio-degradation of synthetic textile dyes by thermophilic lignolytic fungal isolates

Directory of Open Access Journals (Sweden)

Nidhi Sahni

2014-10-01

Full Text Available Synthetic dyes are extensively used in different industries like textile dyeing, paper, printing, color, photography, pharmaceutics and cosmetics. These are generally toxic and carcinogenic in nature. If not treated, they will remain in nature for a long period of time as they are recalcitrant. Among these, azo dyes represent the largest and most versatile class of synthetic dyes. Approximately 10-15% of the dyes are released into the environment during manufacture and usage. Various methods are used for dye removal viz. physical, chemical, electrochemical and biological. Advantage of chemical, electrochemical and biological methods over physical involves the complete destruction of the dye, but chemical and electrochemical methods are found to be expensive and have operational problems. So the biological method is preferred over other methods for degradation/decolorization of dyes. In the present study, thermophilic lignolytic fungal culture was isolated from compost/soil/digested slurry/plant debris, were subjected for acclimatization to Remazol Brilliant Blue (RBB at 0.05% concentration, in the malt extract broth (MEB. The most promising fungal isolates were used for further dye degradation studies. The results suggest that the isolates T10, T14 and T17 as a useful tool for degradation of reactive dyes.

Rationalization of dye uptake on titania slides for dye-sensitized solar cells by a combined chemometric and structural approach.

Science.gov (United States)

Gianotti, Valentina; Favaro, Giada; Bonandini, Luca; Palin, Luca; Croce, Gianluca; Boccaleri, Enrico; Artuso, Emma; van Beek, Wouter; Barolo, Claudia; Milanesio, Marco

2014-11-01

A model photosensitizer (D5) for application in dye-sensitized solar cells has been studied by a combination of XRD, theoretical calculations, and spectroscopic/chemometric methods. The conformational stability and flexibility of D5 and molecular interactions between adjacent molecules were characterized to obtain the driving forces that govern D5 uptake and grafting and to infer the most likely arrangement of the molecules on the surface of TiO2. A spectroscopic/chemometric approach was then used to yield information about the correlations between three variables that govern the uptake itself: D5 concentration, dispersant (chenodeoxycholic acid; CDCA) concentration, and contact time. The obtained regression model shows that large uptakes can be obtained at high D5 concentrations in the presence of CDCA with a long contact time, or in absence of CDCA if the contact time is short, which suggests how dye uptake and photovoltaic device preparation can be optimized. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Toxicity Reduction of Reactive Red Dye-238 Using Advanced Oxidation Process by Solar Energy

Directory of Open Access Journals (Sweden)

Riyad Al-Anbari

2017-09-01

Full Text Available Decolorization of red azo dye (Cibacron Red FN-R from synthetic wastewater has been investigated as a function of solar advanced oxidation process. The photocatalytic activity using ZnO as a photocatalysis has been estimated. Different parameters affected the removal efficiency, including pH of the solution, initial dye concentration and H2O2 concentration were evaluated to find out the optimum value of these parameters. The results proved that the optimal pH value was 8 and the most efficient H2O2 concentration was 100mg/L. Toxicity reduction percent for effluent solution was also monitored to assess the degradation process. This treatment method was able to strongly reduce the color and toxicity of reactive red dye-238 to about (99 and 80 % respectively. It can be concluded, from these experiments, that the using of ZnO as a photocatalysis was exhibited as economical and efficient treatment method to remove reactive red dye-238 from aqueous solution.

The Application of Low-Cost Adsorbent for Reactive Blue 19 Dye Removal from Aqueous Solution: Lemna Minor

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Davoud Balarak

2015-10-01

Full Text Available Background & Aims of the Study: Due to widespread use and adverse effect of dyes, the removal of dyes from effluents is necessary. This study was aimed to remove the reactive blue 19 dye removal from aqueous solution by dried Lemna minor. Materials and Methods:  The effect of various parameters including contact time, solution pH, adsorbent dosage and dye concentration was investigated in this experimental-lab study, Also, the isotherm and kinetic studies was performed for RB19 dye adsorption process. Results: The results indicated that RB19 dye removal efficiency increases by increasing of contact time and adsorbent dosage. The equilibrium time was 75 min ad the maximum dye removal efficiency was obtained in pH=3. Also, the dye removal efficiency decreases by increasing of pH and initial concentration. It was found that the equilibrium data was best follow by Langmuier isotherm. Also, the pseudo-second-kinetic model was best applicable for RB 19 dye adsorption. Conclusion: It can be concluded that the dried Lemna minor can be considered as an effective adsorbent to remove the RB19 dye.

Sonochemical degradation of Basic Blue 41 dye assisted by nanoTiO2 and H2O2

International Nuclear Information System (INIS)

Abbasi, Mahmood; Asl, Nima Razzaghi

2008-01-01

The sonolysis of Basic Blue 41 dye in aqueous solution was performed at 35 kHz using ultrasonic power of 160 W and aqueous temperature of 25 + 1 o C within 180 min. The TiO 2 nanoparticles were used as a catalyst to assist the sonication process. The effect of experimental parameters such as pH, H 2 O 2 concentration and initial dye concentration on the reaction were investigated. It was recognized that in lower pH values the dye removal rate decreased. However, dye removal increased via increase in H 2 O 2 concentration and lowering the initial dye concentration. All intermediate compounds were detected by integrated gas chromatography-mass spectrometry (GC/MS) and also ion chromatograph (IC). During the decolorization, all nitrogen atoms and aromatic groups of Basic Blue 41 were converted to urea, nitrate, formic acid, acetic acid and oxalic acid, etc. Kinetic studies revealed that the degradation process followed pseudo-first order mechanism with the correlation coefficient (R 2 ) of 0.9918 under experimental conditions. The results showed that power ultrasound can be regarded as an appropriate tool for degradation of azo dyes to non-toxic end products

Kinetics and mechanism of azo dye destruction in advanced oxidation processes

International Nuclear Information System (INIS)

Wojnarovits, L.; Palfi, T.; Takacs, E.

2007-01-01

The kinetics and mechanism of dye destruction in advanced oxidation processes is discussed on the example of Apollofix Red (Ar-28) radiolysis in aqueous solution. When the reactive intermediate reacts with the color bearing part of the molecule causing with nearly 100% efficiency destruction of the conjugation, the dose dependence, or time dependence of color disappearance is linear. In this case, spectrophotometry can be used to follow-up dye decomposition. Linear dependence was observed when hydrated electrons or hydrogen atoms reacted with the dye. In hydroxyl radical reactions some colored products form with spectra similar to those of the starting dye molecules. For that reason, spectrophotometry gives false result about the intact dye molecule concentration. Analysis by the HPLC reveals logarithmic time dependence in agreement with a theoretical model developed

Removal of Dye in Wastewater by Adsorption-Coagulation Combined System with Hibiscus sabdariffa as the Coagulant

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Hoong Ho Nicholas Jian

2018-01-01

Full Text Available The conventional process to treat dye wastewater is the physicochemical treatment such as coagulation, flocculation and adsorption process. A new approach has been demonstrated to treat Congo red dye wastewater, which is the adsorption-coagulation hybrid process. Natural coagulant extracted from Hibiscus sabdariffa seeds is used as the coagulant while activated carbon is used as the adsorbent in this case study. The objective of this experiment is to study the significant factors that will affect the efficiency of dye removal. Then, the optimum conditions for the hybrid process is determined using Respond Surface Methodology (RSM. The variables are pH, initial dye concentration, coagulant dosage and adsorbent dosage while the response of experiment is the dye removal percentage. A three-level and four-variable Box-Behnken design (BBD is used for the RSM. A total of 27 sets of experimental results is required to determine the optimum conditions. Jar test is used to conduct the experiment with the addition of coagulant and adsorbent simultaneously. Based on the regression model analysis and ANOVA, the highly significant factors that contribute to the dye removal efficiency through adsorption-coagulation hybrid process are pH of solution and initial dye concentration. The RSM results shows that the optimised process parameters for adsorption-coagulation hybrid process with Hibiscus sabdariffa seeds as the coagulant and activated carbon as the adsorbent are pH 2, initial dye concentration of 385 ppm, coagulant dosage of 209 mg/L and adsorbent dosage of 150 mg/L. The dye removal reaches up to 96.67% under optimum parameters.

Plant waste materials from restaurants as the adsorbents for dyes

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Pavlović Marija D.

2015-01-01

Full Text Available This paper has demonstrated the valorization of inexpensive and readily available restaurant waste containing most consumed food and beverage residues as adsorbents for methylene blue dye. Coffee, tea, lettuce and citrus waste have been utilized without any pre-treatment, thus the adsorption capacities and dye removal efficiency were determined. Coffee waste showed highest adsorbent capacity, followed by tea, lettuce and citrus waste. The dye removal was more effective as dye concentration increases from 5 up to 60 mg/L. The favorable results obtained for lettuce waste have been especially encouraged, as this material has not been commonly employed for sorption purposes. Equilibrium data fitted very well in a Freundlich isotherm model, whereas pseudo-second-order kinetic model describes the process behavior. Restaurant waste performed rapid dye removal at no cost, so it can be adopted and widely used in industries for contaminated water treatment.

Dye adsorption mechanisms in TiO2 films, and their effects on the photodynamic and photovoltaic properties in dye-sensitized solar cells.

Science.gov (United States)

Hwang, Kyung-Jun; Shim, Wang-Geun; Kim, Youngjin; Kim, Gunwoo; Choi, Chulmin; Kang, Sang Ook; Cho, Dae Won

2015-09-14

The adsorption mechanism for the N719 dye on a TiO2 electrode was examined by the kinetic and diffusion models (pseudo-first order, pseudo-second order, and intra-particle diffusion models). Among these methods, the observed adsorption kinetics are well-described using the pseudo-second order model. Moreover, the film diffusion process was the main controlling step of adsorption, which was analysed using a diffusion-based model. The photodynamic properties in dye-sensitized solar cells (DSSCs) were investigated using time-resolved transient absorption techniques. The photodynamics of the oxidized N719 species were shown to be dependent on the adsorption time, and also the adsorbed concentration of N719. The photovoltaic parameters (Jsc, Voc, FF and η) of this DSSC were determined in terms of the dye adsorption amounts. The solar cell performance correlates significantly with charge recombination and dye regeneration dynamics, which are also affected by the dye adsorption amounts. Therefore, the photovoltaic performance of this DSSC can be interpreted in terms of the adsorption kinetics and the photodynamics of oxidized N719.

Design and Application of Electrochemical Processes for Decolorization Treatment of Nylanthrene Red dye Bearing Wastewaters

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D. Marmanis

2016-04-01

Full Text Available The purpose of this paper is the investigation of the capability of electrochemical methods, such as electrocoagulation, electrooxidation and electro-Fenton for decolorization and degradation of synthetic aqueous solutions and actual dye house effluents containing nylanthrene red reactive dye. All electrochemical experiments with the synthetic dye solutions were conducted in electrochemical cell of volume 500 ml containing 200 mL of dye solution at concentration 50 mg/L and interelectrode distance of 1 cm. The three different electrochemical processes were analyzed, and their removal efficiencies were measured and evaluated. In addition, a flow diagram is designed for a continuously operated electrochemical process for remediation of synthetic and actual dye house effluents laden with nylanthrene dye. In the electrocoagulation process with aluminum electrodes, the colored aqueous dye solution was treated at the applied current densities of 5, 10 and 15 mA/cm2 and was quantitatively decolorized in 11, 9 and less than 6 minutes of electroprocessing time respectively. The electrooxidation process conducted with Ti/Pt and boron doped diamond (BDD electrodes, at the applied current density of 10 mA/cm2 led to the quantitative decolorization and destruction of the dye in 25 and 15 min respectively. In the electro-Fenton process with iron electrodes, supply of added hydrogen peroxide and applied current density of 10 mA/cm2, complete decolorization and degradation of the nylanthrene red dye occurred in 6 min. The actual polyamide textile dyeing effluent of same volume 200 mL with initial turbidity of 114 NTU and COD of 1755 mg/L was treated by electrocoagulation at the same applied current density of 10 mA/cm2. The turbidity was quantitatively eliminated in only 10 min, while COD was reduced by 74.5 % in 40 minutes of electrolysis time.

Theoretical study of indoline dyes for dye-sensitized solar cells

International Nuclear Information System (INIS)

Ham, Ho Wan; Kim, Young Sik

2010-01-01

Indoline dye sensitizers were designed and studied theoretically to increase molar extinction coefficients in the visible to near infrared region for solar-cell devices. To gain insight into dye sensitizers' structural, electronic, and optical properties, DFT/TDDFT calculations were performed on a series of dye sensitizers derived from the D149. The good agreement between the experimental and TDDFT calculated absorption spectra of the D149 sensitizer allowed us to provide a detailed assessment of the main spectral features of a series of dye sensitizers. Increase in the conjugation length resulted in a more red-shifted spectral response and less positive oxidation potential than that of the D149. The dye with the dimethylfluorene group showed stronger absorption bands due to a large dipole moment. The calculated dipoles for the dye series correlate well with the observed strong absorption bands of the electronic spectra. These results provided useful clues for the molecular engineering of efficient organic dye sensitizers.

Dose determination with nitro blue tetrazolium containing radiochromic dye films by measuring absorbed and reflected light

DEFF Research Database (Denmark)

Kovács, A.; Baranyai, M.; Wojnárovits, L.

2000-01-01

determination in a wide dose range both by absorbance and reflectance measurements. The concept of measuring reflected light from dose labels has been discussed earlier and emerged recently due to the requirement of introducing semiquantitative label dose indicators for quarantine control. The usefulness...... of the method was studied using the newly developed radiochromic dye films as well as already existing ones. (C) 2000 Elsevier Science Ltd. All rights reserved....

Advanced treatments for the removal of a textile dye

International Nuclear Information System (INIS)

Almazan S, P. T.

2016-01-01

In this work, the remove a dye from aqueous solution and the treatment of textile wastewater using natural and iron and copper modified materials and advanced oxidation by Fenton and photo-Fenton heterogeneous processes are presented. Clay and activated carbon were modified using Fe and Cu electrodes at ph values of 7 and 2 respectively. The materials were characterized by scanning electronic microscopy (Sem), electron X-ray dispersive spectroscopy (EDS), X-ray diffraction and specific area (Bet), the optimum ph for clay modifications with Fe and Cu was 7, whereas for copper modified activated carbon was 2, because de elemental analysis indicated that under the above conditions the content of evaluated metals is highest. The specific area for natural and iron and copper modified clay samples was 5.97, 131.30 and 78.44 m"2/g, whereas for natural and copper modified activated carbon at ph 2 was 654.85 and 647.61 m"2/g. Dye and wastewater used in this study were obtained from a laundry where jeans are manufactured in Almoloya del Rio in Mexico State. Dye was characterized by infrared spectrophotometry and UV-Vis and it was compared with a standard of potassium indigo trisulfonate and it was observed that both spectra were identical, whereby the dye used in this study is an indigo dye with a maximum absorption band at 591 nm. The characterization of wastewater shows a low biodegradability index (0.25) indicating the presence of non-biodegradability organic matter, and a high concentration of phosphorous was found (93.7 mg/L). A compound parabolic concentrator (CPC-2D) was built to concentrate UV radiation from sunlight and applied in photo-Fenton heterogeneous process obtaining concentrated UV-A and UV-B radiation of 54.29±0.71 and 1.65±0.37 W/m"2 respectively. Iron modified clay (Mt-Fe-7) and copper modified activated carbon (Ac-Cu-2) was used as catalyst in the photo-Fenton process with hydrogen peroxide. The results show that using 1.5 g of catalyst, a

Synthesis and characterization of organic dyes with various electron-accepting substituents for p-type dye-sensitized solar cells.

Science.gov (United States)

Weidelener, Martin; Powar, Satvasheel; Kast, Hannelore; Yu, Ze; Boix, Pablo P; Li, Chen; Müllen, Klaus; Geiger, Thomas; Kuster, Simon; Nüesch, Frank; Bach, Udo; Mishra, Amaresh; Bäuerle, Peter

2014-11-01

Four new donor-π-acceptor dyes differing in their acceptor group have been synthesized and employed as model systems to study the influence of the acceptor groups on the photophysical properties and in NiO-based p-type dye-sensitized solar cells. UV/Vis absorption spectra showed a broad range of absorption coverage with maxima between 331 and 653 nm. Redox potentials as well as HOMO and LUMO energies of the dyes were determined from cyclic voltammetry measurements and evaluated concerning their potential use as sensitizers in p-type dye-sensitized solar cells (p-DSCs). Quantum-chemical density functional theory calculations gave further insight into the frontier orbital distributions, which are relevant for the electronic processes in p-DSCs. In p-DSCs using an iodide/triiodide-based electrolyte, the polycyclic 9,10-dicyano-acenaphtho[1,2-b]quinoxaline (DCANQ) acceptor-containing dye gave the highest power conversion efficiency of 0.08%, which is comparable to that obtained with the perylenemonoimide (PMI)-containing dye. Interestingly, devices containing the DCANQ-based dye achieve a higher V(OC) of 163 mV compared to 158 mV for the PMI-containing dye. The result was further confirmed by impedance spectroscopic analysis showing higher recombination resistance and thus a lower recombination rate for devices containing the DCANQ dye than for PMI dye-based devices. However, the use of the strong electron-accepting tricyanofurane (TCF) group played a negative role in the device performance, yielding an efficiency of only 0.01% due to a low-lying LUMO energy level, thus resulting in an insufficient driving force for efficient dye regeneration. The results demonstrate that a careful molecular design with a proper choice of the acceptor unit is essential for development of sensitizers for p-DSCs. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Rhodamine-WT dye losses in a mountain stream environment

Science.gov (United States)

Bencala, Kenneth E.; Rathburn, Ronald E.; Jackman, Alan P.; Kennedy, Vance C.; Zellweger, Gary W.; Avanzino, Ronald J.

1983-01-01

A significant fraction of rhodamine WT dye was lost during a short term multitracer injection experiment in a mountain stream environment. The conservative anion chloride and the sorbing cation lithium were concurrently injected. In-stream rhodamine WT concentrations were as low as 45 percent of that expected, based on chloride data. Concentration data were available from shallow‘wells’dug near the stream course and from a seep of suspected return flow. Both rhodamine WT dye and lithium were nonconservative with respect to the conservative chloride, with rhodamine WT dye closely following the behavior of the sorbing lithium.Nonsorption and sorption mechanisms for rhodamine WT loss in a mountain stream were evaluated in laboratory experiments. Experiments evaluating nonsorption losses indicated minimal losses by such mechanisms. Laboratory experiments using sand and gravel size streambed sediments show an appreciable capacity for rhodamine WT sorption.The detection of tracers in the shallow wells and seep indicates interaction between the stream and the flow in the surrounding subsurface, intergravel water, system. The injected tracers had ample opportunity for intimate contact with materials shown in the laboratory experiments to be potentially sorptive. It is suggested that in the study stream system, interaction with streambed gravel was a significant mechanism for the attenuation of rhodamine WT dye (relative to chloride).

Biochemical study of some environmental pollutants dyes Part II: disperse dyes

International Nuclear Information System (INIS)

Shakra, S.; Ahmed, F.A.; Fetyan, N.A.

2005-01-01

This work was aimed to develop a method for removal of the dyes color from the textile wastewater that is well be much less costly than the other chemical or physical methods used. It therefore included: 1. Preparation of three disperses dyes. 2. Isolation of dyes degradable microorganisms from wastewater effluents and soil after adding 200 ppm of each dye individually. 3. Decolorisation and biodegradation of the dyes in liquid culture of the isolated bacteria (Bacillus thuringiensis). 4. Identification of the probable byproducts by different instruments. 5. Toxicity assessment of the dyes and their biodegraded products

Development of the plastic solid-dye cell for tunable solid-state dye lasers and study on its optical properties

Energy Technology Data Exchange (ETDEWEB)

Ko, Do Kyeong; Lee, Jong Min; Cha, Byung Heon; Yi, Jong Hoon; Lee, Kang Soo; Kim, Sung Ho; Lim, Gwon

2000-01-01

We have fabricated solid-state dyes with Copolex NK-55, which is the base element of plastic lens, and PMMA. We have measured the longevity of solid-state dyes doped in both polymers and found that PMMA has better properties than Coploex NK-55. We have realized the tuning range of 560-620 nm by doping rhodamine 6Gand rhodamin B in the manufactured solid-state dye laser oscillators. In the standing-wave cavity we achieved the slop efficiency of 10.8 percent and in the grazing incidence cavity, 1.2 percent. We have constructed a very compact grazing- incidence cavity which is only 6 cm long and the linewidth of the laser was less than 1.5 GHz with 3-ns pulse duration. And we have fabricated disk-type solid-state dye cell and installed it in the cavity in which the dye cell can be translated and rotated with the help of the two steeping motors. By this we could constantly changed the illuminated area of the dye cell and , therefore, were able to achieve long time operation and to use almost the entire region of the solid-state dye cell. (author)

Development of the plastic solid-dye cell for tunable solid-state dye lasers and study on its optical properties

International Nuclear Information System (INIS)

Ko, Do Kyeong; Lee, Jong Min; Cha, Byung Heon; Yi, Jong Hoon; Lee, Kang Soo; Kim, Sung Ho; Lim, Gwon

2000-01-01

We have fabricated solid-state dyes with Copolex NK-55, which is the base element of plastic lens, and PMMA. We have measured the longevity of solid-state dyes doped in both polymers and found that PMMA has better properties than Coploex NK-55. We have realized the tuning range of 560-620 nm by doping rhodamine 6G and rhodamin B in the manufactured solid-state dye laser oscillators. In the standing-wave cavity we achieved the slop efficiency of 10.8 percent and in the grazing incidence cavity, 1.2 percent. We have constructed a very compact grazing- incidence cavity which is only 6 cm long and the linewidth of the laser was less than 1.5 GHz with 3-ns pulse duration. And we have fabricated disk-type solid-state dye cell and installed it in the cavity in which the dye cell can be translated and rotated with the help of the two steeping motors. By this we could constantly changed the illuminated area of the dye cell and , therefore, were able to achieve long time operation and to use almost the entire region of the solid-state dye cell. (author)

Effect of indigo dye effluent on the growth, biomass production and phenotypic plasticity of Scenedesmus quadricauda (Chlorococcales).

Science.gov (United States)

Chia, Mathias A; Musa, Rilwan I

2014-03-01

The effect of indigo dye effluent on the freshwater microalga Scenedesmus quadricauda ABU12 was investigated under controlled laboratory conditions. The microalga was exposed to different concentrations of the effluent obtained by diluting the dye effluent from 100 to 175 times in bold basal medium (BBM). The growth rate of the microalga decreased as indigo dye effluent concentration increased (p Scenedesmus, which means it can be considered an important biomarker for toxicity testing.

Configuration of organic dye excimers in nanoporous SiO2 matrices

International Nuclear Information System (INIS)

Sorokin, A.V.; Gnap, B.A.; Bespalova, I.I.; Yefimova, S.L.; Malyukin, Yu.V.

2016-01-01

The effect of cyanine dye 3,3′-dioctadecyloxacarbocyanine perchlorate (DiO) and benzimidazole dye 4-dimethylamino-1,8-naphthoylene-1′,2′-benzimidazole (DNBI) accumulation in nanoporous silica matrices on the dyes luminescence properties has been studied. For both dyes, ground state dimer formation with perpendicular transition dipoles at high dye concentrations has been considered as a result of restricted geometry of the nanoscale pores. The dimer excitation leads to excimer formation revealing by appearance of new long-wavelength luminescence band and shortening the dye luminescence lifetime. In the excimer luminescence excitation spectra two additional bands have been observed, one of which is bathochromically shifted relatively to the absorption band and another one is hypsocromically shifted. Using the Kasha exciton model it was shown that the excimers possess oblique transition dipoles configuration. - Highlights: • Organic dye molecules are efficiently accumulated in nanoporous silica matrices. • Restricted geometry of SiO 2 nanopores provokes excimerization of both cyanine and benzimidazole dyes. • The excimers reveal configuration of oblique dimers. • The excimers are originated from ground state dimers with a perpendicular arrangement of transition dipoles.

STATISTICAL INVESTIGATION OF ADSORPTION OF TWO REACTIVE TEXTILE DYES BY VARIOUS ADSORBENTS

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Ümmühan DANIŞ

2002-03-01

Full Text Available Textile industry, in which uses the dyestuffs containing coloured and complex chemical compounds, is both water consumer and water pollutant. The removal of these compounds from the wastewaters is one of the most important problems in the textile industry. In this study, the adsorption of two reactive dyes (Red Px and Yellow P onto Aşkale and Balkaya lignites, Bensan clay and powdered active carbon (PAC from aqueous solution was statistically investigated. The adsorption time, dye concentration, solid/liquid ratio and mixing rate were chosen as parameters. The effects of these parameters on the amount of dye adsorbed by the adsorbents were determined. The results obtained have been statistically evaluated by using the stepwise method and SPSS Sortware version (9.1. The experimental observations and statistical evaluations shown that the effective parameters on the adsorption are equilibrium dye concentration and solid/liquid ratio. It was found that the adsorptive behaviours of both lignites and clay are similar to each other, but powdered active carbon displays different adsorptive behaviour. Finally, the empirical equations showing the relation between amount of dye adsorbed and the effective parameters were developed.

Investigation of adsorption and inhibitive effect of acid red GRE (183 dye on the corrosion of carbon steel in hydrochloric acid media

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M. Abd El-raouf

2015-09-01

Full Text Available The adsorption and corrosion inhibitive effect of acid red GRE (183 dye on carbon steel alloy in 1 M HCl solutions was studied using various techniques. Results of weight loss, Tafel polarization measurements and electrochemical impedance spectroscopy (EIS techniques show that this compound has fairly good inhibiting properties for steel corrosion in acidic bath; with efficiency around 96% at a concentration of 50 ppm. The inhibition is of a mixed anodic–cathodic nature. Factors affecting the corrosion process have been calculated and discussed. Acid red GRE (183 dye was shown to be an inhibitor in the acidic corrosion. Inhibition efficiency increased with acid red GRE (183 dye concentration but decreased with rise in temperature, corrosion inhibition is attributed to the adsorption of acid red GRE (183 dye on the carbon steel surface via a physical adsorption mechanism. Langmuir isotherm is found to provide an accurate description of the adsorption behavior of the investigated azo compound. The nature of the protective film was investigated using SEM and EDX techniques.

Assessment of the Dyeing Properties of the Pigments Produced by Talaromyces spp.

Science.gov (United States)

Morales-Oyervides, Lourdes; Oliveira, Jorge; Sousa-Gallagher, Maria; Méndez-Zavala, Alejandro; Montañez, Julio Cesar

2017-07-05

The high production yields of pigments by Talaromyces spp. and their high thermal stability have implied that industrial application interests may emerge in the food and textile industries, as they both involve subjecting the colourants to high temperatures. The present study aimed to assess the potential application of the pigments produced by Talaromyces spp. in the textile area by studying their dyeing properties. Dyeing studies were performed on wool. The dyeing process consisted of three stages: scouring, mordanting, and dyeing. Two different mordants (alum, A; ferric chloride, F) were tested at different concentrations on fabric weight (A: 5, 10, 15%; F: 10, 20, 30%). The mordanting process had a significant effect on the final colour of the dyed fabrics obtained. The values of dyeing rate constant ( k ), half-time of dyeing ( t 1/2 ), and sorption kinetics behaviour were evaluated and discussed. The obtained results showed that pigments produced by Talaromyces spp. could serve as a source for the natural dyeing of wool textiles.

Assessment of the Dyeing Properties of the Pigments Produced by Talaromyces spp.

Science.gov (United States)

Oliveira, Jorge; Sousa-Gallagher, Maria; Montañez, Julio Cesar

2017-01-01

The high production yields of pigments by Talaromyces spp. and their high thermal stability have implied that industrial application interests may emerge in the food and textile industries, as they both involve subjecting the colourants to high temperatures. The present study aimed to assess the potential application of the pigments produced by Talaromyces spp. in the textile area by studying their dyeing properties. Dyeing studies were performed on wool. The dyeing process consisted of three stages: scouring, mordanting, and dyeing. Two different mordants (alum, A; ferric chloride, F) were tested at different concentrations on fabric weight (A: 5, 10, 15%; F: 10, 20, 30%). The mordanting process had a significant effect on the final colour of the dyed fabrics obtained. The values of dyeing rate constant (k), half-time of dyeing (t1/2), and sorption kinetics behaviour were evaluated and discussed. The obtained results showed that pigments produced by Talaromyces spp. could serve as a source for the natural dyeing of wool textiles. PMID:29371555

Interactions of Fluorescein Dye with Spherical and Star Shaped Gold Nanoparticles.

Science.gov (United States)

Pal, Gopa Dutta; Paul, Somnath; Bardhan, Munmun; Ganguly, Tapan

2018-04-01

UV-vis absorption, FT-IR, steady state fluorescence and fluorescence lifetime measurements were made on Fluorescein dye (Fl dye) molecules in presence of gold nanoparticles of different morphologies: spherical gold nanoparticles (GNP) and star shaped gold nanoparticles (GNS). The experimental observations demonstrate that Fl dye molecules form dimers when adsorbed on nanosurface of spherical gold particles. On the other hand possibly due to lack of adsorption on the surface of GNS the dye molecules were unable to form dimers. The projected tips on the surface of GNS may possibly hinder the dyes to adsorb on the surface of this nanoparticle. From the spectral analysis and measurements of thermodynamic parameters it is inferred that two different types of ground state interactions occur between Fl-dye-GNP and Fl dye-GNS systems. Both the observed negative values of the thermodynamic parameters ΔH and ΔS in the case of the former system predict the possibility of occurrences of hydrogen bonding interactions between two neighboring Fl dye molecules when adsorbed on the nanosurface of GNP. On the other hand in Fl dye-GNS system electrostatic interactions appear to occur, as evidenced from negative ΔH and positive value of ΔS, between the positive charges residing on the tips of the nanoparticles and anionic form of Fl dye. It has been concluded that as the adsorption of organic dyes on solid surfaces is prerequisite for the degradation of dye pollutants, the present experimental observations demonstrate that GNP could be used as a better candidate than GNS in degradation mechanism of the xanthenes dyes.

Experimental Study of Dye Removal from Industrial Wastewater by Membrane Technologies of Reverse Osmosis and Nanofiltration

Directory of Open Access Journals (Sweden)

Mohammad Fadhil Abid

2012-12-01

Full Text Available Currently, biological method has been utilized in the treatment of wastewater -containing synthetic dyes used by textile industries in Iraq. The present work was devoted to study the operating feasibility using reverse osmosis (RO and nanofiltration (NF membrane systems as an alternative treatment method of wastewater discharged from Iraqi textile mills. Acid red, reactive black and reactive blue dyes were selected, based on the usage rate in Iraq. Effects of dye concentration, pH of solution, feed temperature, dissolved salts and operating pressure on permeate flux and dye rejection were studied. Results at operating conditions of dye concentration?=?65 mg/L, feed temperature?=?39?C and pressure?=?8 bar showed the final dye removal with RO membrane as 97.2%, 99.58% and 99.9% for acid red, reactive black and reactive blue dyes, respectively. With NF membrane, the final dye removal were as 93.77%, 95.67%, and 97% for red, black and blue dyes, respectively. The presence of salt (particularly NaCl in the dye solution resulted in a higher color removal with a permeate flux decline. It was confirmed that pH of solution had a positive impact on dye removal while feed temperature showed a different image. A comparison was made between the results of dye removal in biological and membrane methods. The results showed that membrane method had higher removal potential with lower effective cost. The present study indicates that the use of NF membrane in dye removal from the effluent of Iraqi textile mills is promising.

Recording membrane potential changes through photoacoustic voltage sensitive dye

Science.gov (United States)

Zhang, Haichong K.; Kang, Jeeun; Yan, Ping; Abou, Diane S.; Le, Hanh N. D.; Thorek, Daniel L. J.; Kang, Jin U.; Gjedde, Albert; Rahmim, Arman; Wong, Dean F.; Loew, Leslie M.; Boctor, Emad M.

2017-03-01

Monitoring of the membrane potential is possible using voltage sensitive dyes (VSD), where fluorescence intensity changes in response to neuronal electrical activity. However, fluorescence imaging is limited by depth of penetration and high scattering losses, which leads to low sensitivity in vivo systems for external detection. In contrast, photoacoustic (PA) imaging, an emerging modality, is capable of deep tissue, noninvasive imaging by combining near infrared light excitation and ultrasound detection. In this work, we develop the theoretical concept whereby the voltage-dependent quenching of dye fluorescence leads to a reciprocal enhancement of PA intensity. Based on this concept, we synthesized a novel near infrared photoacoustic VSD (PA-VSD) whose PA intensity change is sensitive to membrane potential. In the polarized state, this cyanine-based probe enhances PA intensity while decreasing fluorescence output in a lipid vesicle membrane model. With a 3-9 μM VSD concentration, we measured a PA signal increase in the range of 5.3 % to 18.1 %, and observed a corresponding signal reduction in fluorescence emission of 30.0 % to 48.7 %. A theoretical model successfully accounts for how the experimental PA intensity change depends on fluorescence and absorbance properties of the dye. These results not only demonstrate the voltage sensing capability of the dye, but also indicate the necessity of considering both fluorescence and absorbance spectral sensitivities in order to optimize the characteristics of improved photoacoustic probes. Together, our results demonstrate photoacoustic sensing as a potential new modality for sub-second recording and external imaging of electrophysiological and neurochemical events in the brain.

Formic acid enhanced effective degradation of methyl orange dye in aqueous solutions under UV-Vis irradiation.

Science.gov (United States)

Wang, Jingjing; Bai, Renbi

2016-09-15

Developing efficient technologies to treat recalcitrant organic dye wastewater has long been of great research and practical interest. In this study, a small molecule, formic acid (FA), was applied as a process enhancer for the degradation of methyl orange (MO) dye as a model recalcitrant organic pollutant in aqueous solutions under the condition of UV-Vis light irradiation and air aeration at the ambient temperature of 25 °C. It was found that the decolouration of the dye solutions can be rapidly achieved, reducing the time, for example, from around 17.6 h without FA to mostly about less than 2 h with the presence of FA. The mineralization rate of MO dye reached as high as 81.8% in 1.5 h in the case of initial MO dye concentration at 25 mg L(-1), which is in contrast to nearly no mineralization of the MO dye for a similar system without the FA added. The study revealed that the generation of the H2O2 species in the system was enhanced and the produced OH radicals effectively contributed to the degradation of the MO dye. Process parameters such as the initial concentration of MO dye, FA dosage and solution pH were all found to have some effect on the degradation efficiency under the same condition of UV-Vis light irradiation and air aeration. The MO dye degradation performance was found to follow a first-order reaction rate to the MO dye concentration in most cases and there existed a positive correlation between the reaction rate constant and the initial FA concentration. Compared to the traditional H2O2/UV-Vis oxidation system, the use of FA as a process-enhancing agent can have the advantages of low cost, easy availability, and safe to use. The study hence demonstrates a promising approach to use a readily available small molecule of FA to enhance the degradation of recalcitrant organic pollutants, such as MO dye, especially for their pre-treatment. Copyright © 2016 Elsevier Ltd. All rights reserved.

Synthesis, characterization and dyeing behavior of heterocyclic acid dyes and mordent acid dyes on wool and silk fabrics

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Patel Hitendra M.

2012-01-01

Full Text Available Novel heterocyclic acid and mordent acid dyes were synthesized by the coupling of diazonium salt solution of different aromatic amines with 2- butyl-3-(4-hydroxybenzoylbenzofuran. The resulting heterocyclic acid dyes were characterized by spectral techniques, i.e., elemental analysis, IR, 1HNMR, 13C-NMR spectral studies and UV- visible spectroscopy. The dyeing performance of all the heterocyclic acid dyes was evaluated on wool and silk fabrics. The dyeing of chrome pre treated wool and silk fabrics showed better hues on mordented fabrics. Dyeing of wool and silk fabrics resulted in pinkish blue to red shades with very good depth and levelness. The dyed fabrics showed excellent to very good light, washing, perspiration, sublimation and rubbing fastness.

Insights into the Mechanism of a Covalently Linked Organic Dye-Cobaloxime Catalyst System for Dye-Sensitized Solar Fuel Devices.

Science.gov (United States)

Pati, Palas Baran; Zhang, Lei; Philippe, Bertrand; Fernández-Terán, Ricardo; Ahmadi, Sareh; Tian, Lei; Rensmo, Håkan; Hammarström, Leif; Tian, Haining

2017-06-09

A covalently linked organic dye-cobaloxime catalyst system based on mesoporous NiO is synthesized by a facile click reaction for mechanistic studies and application in a dye-sensitized solar fuel device. The system is systematically investigated by photoelectrochemical measurements, density functional theory, time-resolved fluorescence, transient absorption spectroscopy, and photoelectron spectroscopy. The results show that irradiation of the dye-catalyst on NiO leads to ultrafast hole injection into NiO from the excited dye, followed by a fast electron transfer process to reduce the catalyst. Moreover, the dye adopts different structures with different excited state energies, and excitation energy transfer occurs between neighboring molecules on the semiconductor surface. The photoelectrochemical experiments also show hydrogen production by this system. The axial chloride ligands of the catalyst are released during photocatalysis to create the active sites for proton reduction. A working mechanism of the dye-catalyst system on the photocathode is proposed on the basis of this study. © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

Waste sizing solution as co-substrate for anaerobic decolourisation of textile dyeing wastewaters

NARCIS (Netherlands)

Bisschops, I.; Santos, dos A.B.; Spanjers, H.

2005-01-01

Dyeing wastewaters and residual size are textile factory waste streams that can be treated anaerobically. For successful anaerobic treatment of dyeing effluents, a co-substrate has to be added because of their low concentration of easily biodegradable compounds. Starch-based size contains easily

Modified magnetite nanoparticles with cetyltrimethylammonium bromide as superior adsorbent for rapid removal of the disperse dyes from wastewater of textile companies

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Ali Asghar Rajabi

2016-01-01

Full Text Available This paper reports application of cetyltrimethylammonium bromide (CTAB coated magnetite nanoparticles (Fe3O4 NPs as a novel adsorbent for removal of two types of disperse dyes, including disperse red 167, and disperse blue 183, from wastewater of textile companies. The effect of parameters including type of surfactant, pH of solution, surfactant concentration, and amount of salt, was investigated and optimized. The obtained results showed that the ratio of initial dye concentration to CTAB amounts has critical effect on removal processes so that removal efficiencies higher than 95% can be achieved even at high concentration of dyes as high as 500 mg l-1 when the ratio is optimum. Removal of dyes is very fast, and equilibrium is reached at times less than 10 min even for high concentration of the dyes. Very high adsorbent capacity (as high as 2000 mg g-1 was yielded for maximum tested concentration of the dyes (500 mg g-1. The obtained result was confirmed by thermogravimetric analysis data. This study showed that CTAB coated Fe3O4 NPs is a very efficient adsorbent for removal of dyes from wastewater of textile companies and has high capacity under optimum conditions.

Ozonation of azo dyes (Orange II and Acid Red 27) in saline media

International Nuclear Information System (INIS)

Silva, Alessandra C.; Pic, Jean Stephane; Sant'Anna, Geraldo L.; Dezotti, Marcia

2009-01-01

Ozonation of two azo dyes was investigated in a monitored bench scale bubble column reactor (8.5-L), varying liquid media salt content (0, 1, 40 and 100 g L -1 , NaCl). In experiments with Orange II pH was varied (5, 7.5 and 9) but ozonation of Acid Red 27 was performed at pH 7.5. Ozone self-decomposition rate-constant increased with salt concentration. Color removal was very effective and fast achieved under all experimental conditions. For the two azo dyes tested, more than 98% of color intensity was removed in 30-min ozonation assays. However, only partial mineralization of azo dyes (45%-Orange II; 20%-Acid Red 27) was attained in such experiments. The degree of mineralization (TOC removal) was negatively affected by salt concentration. Biodegradation assays conducted by respirometry revealed the inhibitory effect of dye degradation products formed during ozonation.

Fabrication of Electrospun Polyamide-6/Chitosan Nanofibrous Membrane toward Anionic Dyes Removal

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Mozhdeh Ghani

2014-01-01

Full Text Available Nanofibrous filter media of polyamide-6/chitosan were fabricated by electrospinning onto a satin fabric substrate and characterized by scanning electron microscopy (SEM, Fourier transform infrared spectroscopy (FTIR, and water contact angle (WCA. Anionic dye removal capability of the filter was investigated for Solophenyl Red 3BL and Polar Yellow GN, respectively, as acidic and direct dyes were investigated with respect to solution parameters (pH and initial dye concentration and membrane parameters (electrospinning time and chitosan ratio through filtration system. Experiments were designed using response surface methodology (RSM based on five-level central composite design (CCD with four parameters to maximize removal efficiency of the filter media. Moreover, the effect of parameters and their likely interactions on dye removal were investigated by mathematically developed models. The optimum values for solution pH, initial dye concentration, electrospinning time, and chitosan ratio were predicted to be 5, 50 mg/L, 4 hr, 30% and 5, 100 mg/L, 4 hr, 10%, respectively, for achieving 96% and 95% removal of Solophenyl Red 3BL and Polar Yellow GN. Evaluation of the estimation capability of applied models revealed that the models have a good agreement with experimental values. This study demonstrated that polyamide-6/chitosan nanofibrous membrane has an enormous applicable potential in dye removal from aqueous solutions.

Adsorption and desorption of cationic malachite green dye on cellulose nanofibril aerogels.

Science.gov (United States)

Jiang, Feng; Dinh, Darren M; Hsieh, You-Lo

2017-10-01

Ultra-light aerogels have been assembled from cellulose nanofibrils into hierarchically macroporous (several hundred μm) honeycomb cellular structure surrounded with mesoporous (8-60nm) thin walls. The high specific surface (193m 2 /g) and surface carboxyl content (1.29mmol/g) of these aerogels were demonstrated to be highly capable of removing cationic malachite green (MG) dye from aqueous media. The rapid MG adsorption was driven by electrostatic interactions and followed a pseudo-second-order adsorption kinetic and monolayer Langmuir adsorption isotherm. At a low 1:5mg/mL aerogel/MG ratio, both initial MG adsorption rate (2.3-59.8mgg -1 min -1 ) and equilibrium adsorption capacity (53.0-203.7mgg -1 ) increased with increasing initial MG concentrations from 10 to 200mg/L, reaching a maximum adsorption of 212.7mgg -1 . The excellent dye removal efficiency was demonstrated by complete MG removal through four repetitive adsorptions at a low 1:5mg/mL aerogel/MG ratio and 10mg/L dye concentration as well as 92% MG adsorption in a single batch at one order of magnitude higher10:5mg/mL aerogel/MG ratio and 100mg/L dye concentration. The adsorbed MG in aerogels could be desorbed in aqueous media by increasing ionic strength, demonstrating facile recovery of both dye and aerogel as well as the robust capability of this aerogel for repetitive applications. Copyright © 2017 Elsevier Ltd. All rights reserved.

Factor Affecting Textile Dye Removal Using Adsorbent From Activated Carbon: A Review

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Mohammad Razi Mohd Adib

2017-01-01

Full Text Available Industrial company such as textile, leather, cosmetics, paper and plastic generated wastewater containing large amount of dye colour. The removal of dye materials are importance as the presence of this kind of pollutant influence the quality of water and makes it aesthetically unpleasant. As their chemical structures are complicated, it is difficult to treat dyes with municipal waste treatment operations. Even a small quantity of dye does cause high visibility and undesirability. There have been various treatment technique reviewed for the removal of dye in wastewater. However, these treatment process has made it to another expensive treatment method. This review focus on the application of adsorbent in dye removal from textile wastewater as the most economical and effective method, adsorption has become the most preferred method to remove dye. The review provides literature information about different basis materials used to produce activated carbon like agricultural waste and industrial waste as well as the operational parameters factors in term of contact time, adsorbent dosage, pH solution and initial dye concentration that will affect the process in removing textile dye. This review approach the low cost and environmental friendly adsorbent for replacing conventional activated carbon.

Electrochemical treatment of Orange II dye solution-Use of aluminum sacrificial electrodes and floc characterization

International Nuclear Information System (INIS)

Mollah, M. Yousuf A.; Gomes, Jewel A.G.; Das, Kamol K.; Cocke, David L.

2010-01-01

Electrocoagulation (EC) of Orange II dye in a flow through cell with aluminum as sacrificial electrodes was carried out under varying conditions of dye concentration, current density, flow rate, conductivity, and the initial pH of the solution in order to optimize the operating parameters for maximum benefits. Maximum removal efficiency of 94.5% was obtained at the following conditions: dye concentration = 10 ppm, current density = 160 A/m 2 , initial pH 6.5, conductance = 7.1 mS/cm, flow rate = 350 mL/min, and concentration of added NaCl = 4.0 g/L of dye solution. The EC-floc was characterized using Fourier transform infrared spectroscopy, scanning electron microscopy/energy dispersive X-ray spectroscopy, and powder X-ray diffraction techniques. The removal mechanism has been proposed that is in compliance with the Pourbaix diagram, solubility curve of aluminum oxides/hydroxides, and physico-chemical properties of the EC-floc.

Electrochemical treatment of Orange II dye solution-Use of aluminum sacrificial electrodes and floc characterization

Energy Technology Data Exchange (ETDEWEB)

Mollah, M. Yousuf A. [Department of Chemistry, University of Dhaka, Dhaka-1000 (Bangladesh); Gomes, Jewel A.G., E-mail: jewel.gomes@lamar.edu [Dan F. Smith Department of Chemical Engineering, Lamar University, P.O. Box 10053, Beaumont, TX 77710 (United States); Das, Kamol K.; Cocke, David L. [Gill Chair of Chemical Engineering, Lamar University, P.O. Box 10053, Beaumont, TX 77710 (United States)

2010-02-15

Electrocoagulation (EC) of Orange II dye in a flow through cell with aluminum as sacrificial electrodes was carried out under varying conditions of dye concentration, current density, flow rate, conductivity, and the initial pH of the solution in order to optimize the operating parameters for maximum benefits. Maximum removal efficiency of 94.5% was obtained at the following conditions: dye concentration = 10 ppm, current density = 160 A/m{sup 2}, initial pH 6.5, conductance = 7.1 mS/cm, flow rate = 350 mL/min, and concentration of added NaCl = 4.0 g/L of dye solution. The EC-floc was characterized using Fourier transform infrared spectroscopy, scanning electron microscopy/energy dispersive X-ray spectroscopy, and powder X-ray diffraction techniques. The removal mechanism has been proposed that is in compliance with the Pourbaix diagram, solubility curve of aluminum oxides/hydroxides, and physico-chemical properties of the EC-floc.

Ultrasound-assisted dyeing of cellulose acetate.

Science.gov (United States)

Udrescu, C; Ferrero, F; Periolatto, M

2014-07-01

The possibility of reducing the use of auxiliaries in conventional cellulose acetate dyeing with Disperse Red 50 using ultrasound technique was studied as an alternative to the standard procedure. Dyeing of cellulose acetate yarn was carried out by using either mechanical agitation alone, with and without auxiliaries, or coupling mechanical and ultrasound agitation in the bath where the temperature range was maintained between 60 and 80 °C. The best results of dyeing kinetics were obtained with ultrasound coupled with mechanical agitation without auxiliaries (90% of bath exhaustion value at 80 °C). Hence the corresponding half dyeing times, absorption rate constants according to Cegarra-Puente modified equation and ultrasound efficiency were calculated confirming the synergic effect of sonication on the dyeing kinetics. Moreover the apparent activation energies were also evaluated and the positive effect of ultrasound added to mechanical agitation was evidenced by the lower value (48 kJ/mol) in comparison with 112 and 169 kJ/mol for mechanical stirring alone with auxiliaries and without, respectively. Finally, the fastness tests gave good values for samples dyed with ultrasound technique even without auxiliaries. Moreover color measurements on dyed yarns showed that the color yield obtained by ultrasound-assisted dyeing at 80 °C of cellulose acetate without using additional chemicals into the dye bath reached the same value yielded by mechanical agitation, but with remarkably shorter time. Copyright © 2014 Elsevier B.V. All rights reserved.

Graphene oxide based CdSe photocatalysts: Synthesis, characterization and comparative photocatalytic efficiency of rhodamine B and industrial dye

International Nuclear Information System (INIS)

Ghosh, Trisha; Lee, Jeong-Ho; Meng, Ze-Da; Ullah, Kefayat; Park, Chong-Yeon; Nikam, Vikram; Oh, Won-Chun

2013-01-01

Highlights: ► CdSe–graphene is synthesized by hydrothermal method. ► Three molar solutions of CdSe were used making three different composites. ► RhB and Texbrite MST-L were used as sample dye solutions. ► Texbrite MST-L is photo degraded in visible light. ► UV-spectroscopic analysis was done to measure degradation. - Abstract: CdSe–graphene composites were prepared using simple “hydrothermal method” where the graphene surface was modified using different molar solutions of cadmium selenide (CdSe) in aqueous media. The characterization of CdSe–graphene composites were studied by X-ray diffraction (XRD), energy dispersive X-ray (EDX), scanning electron microscope (SEM), and with transmission electron microscope (TEM). The catalytic activities of CdSe-composites were evaluated by degradation of rhodamine B (RhB) and commercial industrial dye “Texbrite MST-L (TXT-MST)” with fixed concentration. The degradation was observed by the decrease in the absorbance peak studied by UV spectrophotometer. The decrease in the dye concentration indicated catalytic degradation effect by CdSe–graphene composites

Decolorization of Reactive Blue 19 Dye from Textile Wastewater by the UV/H2O2 Process

Science.gov (United States)

Rezaee, Abbas; Taghi Ghaneian, Mohammad; Jamalodin Hashemian, Sayed; Moussavi, Gholamreza; Khavanin, Ali; Ghanizadeh, Ghader

Photo-oxidation of dyes is a new concern among researchers since it offers an attractive method for decoloration of dyes and breaks them into simple mineral forms. An advanced oxidation process, UV/H2O2, was investigated in a laboratory scale photoreactor for decolorization of the Reactive blue 19 (RB19) dye from synthetic textile wastewater. The effects of operating parameters such as hydrogen peroxide dosage, pH, initial dye concentration and UV dosage, on decolorization have been evaluated. The RB19 solution was completely decolorized under optimal hydrogen peroxide dosage of 2.5 mmol L-1 and low-pressure mercury UV-C lamps (55 w) in less than 30 min. The decolorization rate followed pseudo-first order kinetics with respect to the dye concentration. The rate increased linearly with volumetric UV dosage and nonlinearly with increasing initial hydrogen peroxide concentration. It has been found that the degradation rate increased until an optimum of hydrogen peroxide dosage, beyond which the reagent exerted an inhibitory effect. From the experimental results, the UV/H2O2 process was an effective technology for RB19 dye treatment in wastewater.

Thermodynamic Study of the Ion-Pair Complexation Equilibria of Dye and Surfactant by Spectral Titration and Chemometric Analysis

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Hakimeh Abbasi Awal

2017-12-01

Full Text Available Surfactant-dye interactions are very important in chemical and dyeing processes. The dyes interact strongly with surfactant and show new spectrophotometric properties, so the UV-vis absorption spectrophotometric method has been used to study this process and extract some thermodynamic parameters. In this work, the association equilibrium between ionic dyes and ionic surfactant were studied by analyzing spectrophotometric data using chemometric methods. Methyl orange and crystal violet were selected as a model of cationic and anionic dyes respectively. Also sodium dodecyl sulphate and cetyltrimethylammonium bromide were selected as anionic and cationic surfactant, respectively. Hard model methods such as target transform fitting (TTF classical multi-wavelength fitting and soft model method such as multivariate curve resolution (MCR were used to analyze data that were recorded as a function of surfactant concentration in premicellar and postmicellar regions. Hard model methods were used to resolve data using ion-pair model in premicellar region in order to extract the concentration and spectral profiles of individual components and also related thermodynamic parameters. The equilibrium constants and other thermodynamic parameters of interaction of dyes with surfactants were determined by studying the dependence of their absorption spectra on the temperature in the range 293–308 K at concentrations of 5 × 10−6 M and 8 × 10−6 M for dye crystal violet and methyl orange, respectively. In postmicellar region, the MCR-ALS method was applied for resolving data and getting the spectra and concentration profiles in complex mixtures of dyes and surfactants.

Analysis of solvent dyes in refined petroleum products by electrospray ionization mass spectrometry

Science.gov (United States)

Rostad, C.E.

2010-01-01

Solvent dyes are used to color refined petroleum products to enable differentiation between gasoline, diesel, and jet fuels. Analysis for these dyes in the hydrocarbon product is difficult due to their very low concentrations in such a complex matrix. Flow injection analysis/electrospray ionization/mass spectrometry in both negative and positive mode was used to optimize ionization of ten typical solvent dyes. Samples of hydrocarbon product were analyzed under similar conditions. Positive electrospray ionization produced very complex spectra, which were not suitably specific for targeting only the dyes. Negative electrospray ionization produced simple spectra because aliphatic and aromatic moieties were not ionized. This enabled screening for a target dye in samples of hydrocarbon product from a spill.

Decolorization of basic dye solutions by electrocoagulation: an investigation of the effect of operational parameters.

Science.gov (United States)

Daneshvar, N; Oladegaragoze, A; Djafarzadeh, N

2006-02-28

Electrocoagulation (EC) is one of the most effective techniques to remove color and organic pollutants from wastewater, which reduces the sludge generation. In this paper, electrocoagulation has been used for the removal of color from solutions containing C. I. Basic Red 46 (BR46) and C. I. Basic Blue 3 (BB3). These dyes are used in the wool and blanket factories for fiber dyeing. The effect of operational parameters such as current density, initial pH of the solution, time of electrolysis, initial dye concentration and solution conductivity were studied in an attempt to reach higher removal efficiency. The findings in this study shows that an increase in the current density up to 60-80 A m(-2) enhanced the color removal efficiency, the electrolysis time was 5 min and the range of pH was determined between 5.5 and 8.5 for two mentioned dye solutions. It was found that for, the initial concentration of dye in solutions should not be higher than 80 mg l(-1) in order to achieve a high color removal percentage. The optimum conductivity was found to be 8 mS cm(-1), which was adjusted using proper amount of NaCl with the dye concentration of 50 mg l(-1). Electrical energy consumption in the above conditions for the decolorization of the dye solutions containing BR46 and BB3 were 4.70 kWh(kgdye removed)(-1) and 7.57 kWh(kgdye removed)(-1), respectively. Also, during the EC process under the optimized conditions, the COD decreased by more than 75% and 99% in dye solutions containing BB3 and BR46, respectively.

Characterization of aqueous rose bengal dye solution for the measurement of low doses of gamma radiation

International Nuclear Information System (INIS)

Hasan Mahmood Khan; Khan, A.A.

2010-01-01

Aqueous solution of rose bengal dye has been studied spectrophotometrically as a gamma-ray dosimeter for the measurement of low doses of radiation. The useful dose range was found to be from 50 to 1000 Gy when the measurements were made at 549 nm. The effects of temperature and light conditions on the stability of response during post-irradiation storage were also investigated. When stored in dark at room temperature, the dosimetric solutions showed a stable response up to 22 days. The storage of irradiated solutions in diffused sunlight showed a stable response only up to 6 days. When exposed to direct sunlight, very prominent and fast bleaching of dye solution occurred. At low storage temperature (ca. 11 deg C), dosimetric response was found to be stable up to 22 days while at higher temperature (ca. 30 deg C), the response of dosimetric solution was stable only up to 6 days. The rose bengal aqueous solution showed promising characteristics as a low dose radiation dosimeter when stored at lower temperatures (<25 deg C) in dark. (author)

Studies on Dyeing Performance of Novel Acid Azo Dyes and Mordent Acid Azo Dyes Based on 2,4-Dihydroxybenzophenone

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Bharat C. Dixit

2009-01-01

Full Text Available Novel acid azo and mordent acid azo dyes have been prepared by the coupling of diazo solution of different aminonaphthol sulphonic acids and aromatic amino acids with 2,4-dihydroxybenzophenone. The resultant dyes were characterized by elemental analysis as well as IR and 1H NMR spectral studies. The UV-visible spectral data have also been discussed in terms of structure property relationship. The dyeing assessments of all the dyes were evaluated on wool and silk textile fibers. The dyeing of chrome pretreated wool and silk have also been monitored. The result shows that better hue was obtained on mordented fiber. Results of bactericidal studies of chrome pretreated fibers revealed that the toxicity of mordented dyes against bacteria is fairly good. Dyeing on wool and silk fibers resulted in yellowish pink to reddish brown colourations having excellent light fastness and washing fastness.

WATERLESS DYEING [REVIEW

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DEVRENT Nalan

2015-05-01

Full Text Available The textile industry is believed to be one of the biggest consumers of water. Water consumption and exhaustion in dyeing textile materials in conventional methods is an important environmental problem. The cost of waste water treatment will cause a prominent problem in the future as it does today. Increasing consideration of ecologic consequences of industrial processes as well as legislation enforcing the avoidance of environmental problems have caused a reorientation of thinking and promoted projects for replacement of conventional technologies. One of these new technologies is dyeing in supercritical fluids. Dyeing with supercritical carbon dioxide is a favourable concept considering the value of water as a natural resource and the cost of waste water treatment. This dyeing method offers many advantages over conventional aqueous dyeing: During this dyeing process no water is used, therefore there is no waste water problem, no other chemicals are required; the carbon dioxide can be recycled; the dystuff which is not adsorbed on the substrate can be collected and reused; The necessary energy consumption in this process is relatively lower than is needed to heat water in conventional methods of dyeing. Due to unnecessary of drying process, it helps to save both energy and time; and dyeing cycle is shorter compared with traditional methods. In addition carbon dioxide is non-toxic and non-flammable. Supercritical fluid, supercritical dyeing, disperse dyestuffs, solid-fluid equilibrium

Modulating fluorescence quantum yield of highly concentrated fluorescein using differently shaped green synthesized gold nanoparticles

International Nuclear Information System (INIS)

John, Jisha; Thomas, Lincy; Kurian, Achamma; George, Sajan D.

2016-01-01

The interaction of dye molecules with differently shaped nanoparticles is of great interest owing to the potential applications in areas of bioimaging, sensing and photodynamic therapy (biology) as well as solar cells (photonics) applications. For such applications, noble metallic nanoparticles are commonly employed to either enhance or quench the luminescence of a nearby fluorophore. However, in most of the studies, the dye concentration is limited to avoid self-quenching. This paper reports the influence of differently shaped gold nanoparticles (spherical, bean and star), prepared via green synthesis, on the emission behavior as well as on the fluorescence quantum yield of fluorescein dye at concentrations for which self-quenching occurs. The emission behavior is probed via laser based steady state fluorescence whereas quantum yield is measured using a dual beam laser based thermal lens technique. The experimentally observed fluorescence quenching with a concomitant increase in thermal lens signal in the vicinity of nanoparticles are explained in terms of nonradiative energy transfer between the donor and the acceptor. Further, the influence of pH of the prepared gold nanofluid on the absorption, emission as well as quantum yield are also accounted. These studies elucidate that even at high concentrations of dye, the gold nanoparticle and its shape clearly influences the optical properties of nearby dye molecules and thus can be exploited for future applications. - Highlights: • Green synthesis of differently shaped gold nanoparticles. • Tailoring emission properties of fluorescein with respect to nanoparticle concentration and shape. • Tailoring the quantum yield of highly concentrated fluorescein with nanoparticles.

Adsorption of the reactive azo dyes onto NH4Cl-induced activated carbon

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Sakine Shekoohiyan

2016-03-01

Full Text Available Background: The efficacy of NH4Cl-induced activated carbon (NAC was examined in order to adsorb RR198, an azo reactive model dye, from an aqueous solution. Methods: The effects of pH (3 to 10, adsorbent dose (0.1 to 1.2 g/L, dye concentration and contact time on the adsorption efficiency were investigated. Results: The results showed that the removal of dye was highest at a solution pH of 7 and a powder dose of 1.1 g/L. The 85.9%, 72.6% and 65.4% removal of RR198 was obtained for a concentration of 25, 50 and 100 mg/L, respectively, at a relatively short contact time of 30 minutes, and at optimum pH and NAC concentrations of 1 g/L. The experimental data for kinetic analysis illustrated a best fit to the pseudo-second-order model. The study data on equilibrium were modeled using Langmuir, Freundlich and Dubinin–Radushkevich models; the Langmuir equation provided the best fit for the data. Conclusion: Therefore, the NAC appears to be an efficient and appropriate adsorbent for the removal of reactive azo dyes from waste streams.

Significance of hair-dye base-induced sensory irritation.

Science.gov (United States)

Fujita, F; Azuma, T; Tajiri, M; Okamoto, H; Sano, M; Tominaga, M

2010-06-01

Oxidation hair-dyes, which are the principal hair-dyes, sometimes induce painful sensory irritation of the scalp caused by the combination of highly reactive substances, such as hydrogen peroxide and alkali agents. Although many cases of severe facial and scalp dermatitis have been reported following the use of hair-dyes, sensory irritation caused by contact of the hair-dye with the skin has not been reported clearly. In this study, we used a self-assessment questionnaire to measure the sensory irritation in various regions of the body caused by two model hair-dye bases that contained different amounts of alkali agents without dyes. Moreover, the occipital region was found as an alternative region of the scalp to test for sensory irritation of the hair-dye bases. We used this region to evaluate the relationship of sensitivity with skin properties, such as trans-epidermal water loss (TEWL), stratum corneum water content, sebum amount, surface temperature, current perception threshold (CPT), catalase activities in tape-stripped skin and sensory irritation score with the model hair-dye bases. The hair-dye sensitive group showed higher TEWL, a lower sebum amount, a lower surface temperature and higher catalase activity than the insensitive group, and was similar to that of damaged skin. These results suggest that sensory irritation caused by hair-dye could occur easily on the damaged dry scalp, as that caused by skin cosmetics reported previously.

Homogenous and heterogenous advanced oxidation of two commercial reactive dyes.

Science.gov (United States)

Balcioglu, I A; Arslan, I; Sacan, M T

2001-07-01

Two commercial reactive dyes, the azo dye Reactive Black 5 and the copper phythalocyanine dye Reactive Blue 21, have been treated at a concentration of 75 mg l(-1) by titanium dioxide mediated photocatalytic (TiO2/UV), dark and UV-light assisted Fenton (Fe2+/H2O2) and Fenton-like (Fe3+/H2O2) processes in acidic medium. For the treatment of Reactive Black 5, all investigated advanced oxidation processes were quite effective in terms of colour, COD as well as TOC removal. Moreover, the relative growth inhibition of the azo dye towards the marine algae Dunaliella tertiolecta that was initially 70%, did not exhibit an increase during the studied advanced oxidation reactions and complete detoxification at the end of the treatment period could be achieved for all investigated treatment processes. However, for Reactive Blue 21, abatement in COD and UV-VIS absorbance values was mainly due to the adsorption of the dye on the photocatalyst surface and/or the coagulative effect of Fe3+/Fe2+ ions. Although only a limited fraction of the copper phythalocyanine dye underwent oxidative degradation, 47% of the total copper in the dye was already released after 1 h photocatalytic treatment.

Comparison of activated carbon and bottom ash removal of reactive dye from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Dincer, A.R.; Gunes, Y.; Karakaya, N.; Gunes, E. [Trakya University, Tekirdag (Turkey). Dept. of Environmental Engineering

2007-03-15

The adsorption of reactive dye from synthetic aqueous solution onto granular activated carbon (GAC) and coal-based bottom ash (CBBA) were studied under the same experimental conditions. As an alternative to GAC CBBA was used as adsorbent for dye removal from aqueous solution. The amount of Vertigo Navy Marine (VNM) adsorbed onto CBBA was lower compared with GAC at equilibrium and dye adsorption capacity increased from 0.71 to 3.82 mg g{sup -1}, and 0.73 to 6.35 mg g{sup -1} with the initial concentration of dye from 25 to 300 mg l{sup -1} respectively. The initial dye uptake of CBBA was not so rapid as in the case of GAC and the dye uptake was slow and gradually attained equilibrium.

Concentration Dependence of Gold Nanoparticles for Fluorescence Enhancement

Science.gov (United States)

Solomon, Joel; Wittmershaus, Bruce

Noble metal nanoparticles possess a unique property known as surface plasmon resonance in which the conduction electrons oscillate due to incoming light, dramatically increasing their absorption and scattering of light. The oscillating electrons create a varying electric field that can affect nearby molecules. The fluorescence and photostability of fluorophores can be enhanced significantly when they are near plasmonic nanoparticles. This effect is called metal enhanced fluorescence (MEF). MEF from two fluorescence organic dyes, Lucifer Yellow CH and Riboflavin, was measured with different concentrations of 50-nm colloidal gold nanoparticles (Au-NP). The concentration range of Au-NP was varied from 2.5 to 250 pM. To maximize the interaction, the dyes were chosen so their emission spectra had considerable overlap with the absorption spectra of the Au-NP, which is common in MEF studies. If the dye molecules are too close to the surface of Au-NP, fluorescence quenching can occur instead of MEF. To try to observe this difference, silica-coated Au-NP were compared to citrate-based Au-NP; however, fluorescence quenching was observed with both Au-NP. This material is based upon work supported by the National Science Foundation under Grant Number NSF-ECCS-1306157.

Effective biotransformation and detoxification of anthraquinone dye reactive blue 4 by using aerobic bacterial granules.

Science.gov (United States)

Chaudhari, Ashvini U; Paul, Dhiraj; Dhotre, Dhiraj; Kodam, Kisan M

2017-10-01

Treatment of textile wastewater containing anthraquinone dye is quite a huge challenge due to its complex aromatic structure and toxicity. Present study deals with the degradation and detoxification of anthraquinone dye reactive blue 4 using aerobic bacterial granules. Bacterial granules effectively decolorized reactive blue 4 at wide range of pH (4.0-11.0) and temperature (20-55 °C) as well as decolorized and tolerated high concentration of reactive blue 4 dye upto 1000 mg l -1 with V max 6.16 ± 0.82 mg l -1 h -1 and K m 227 ± 41 mg l -1 . Metagenomics study evaluates important role of Clostridia, Actinobacteria, and Proteobacterial members in biotransformation and tolerance of high concentrations of reactive blue 4 dye. Up-regulation of xenobiotic degradation and environmental information processing pathways during dye exposure signifies their noteworthy role in dye degradation. Biotransformation of dye was confirmed by significant decrease in the values of total suspended solids, biological and chemical oxygen demand. The metabolites formed after biotransformation was characterized by FT-IR and GC-MS analysis. The reactive blue 4 dye was found to be phytotoxic, cytotoxic and genotoxic whereas its biotransformed product were non-toxic. This study comprehensively illustrates that, bacterial aerobic granules can be used for eco-friendly remediation and detoxification of wastewater containing high organic load of anthraquinone dye. Copyright © 2017 Elsevier Ltd. All rights reserved.

A novel biosorbent for dye removal: Extracellular polymeric substance (EPS) of Proteus mirabilis TJ-1

Energy Technology Data Exchange (ETDEWEB)

Zhang Zhiqiang [State Key Laboratory of Pollution Control and Resource Reuse, Key Laboratory of Yangtze River Water Environment of Ministry of Education, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China); Laboratoire de Sciences Analytiques (UMR CNRS 5180), Universite Claude Bernard Lyon 1, Universite de Lyon, 69622 Villeurbanne Cedex (France); Xia Siqing [State Key Laboratory of Pollution Control and Resource Reuse, Key Laboratory of Yangtze River Water Environment of Ministry of Education, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China)], E-mail: siqingxia@mail.tongji.edu.cn; Wang Xuejiang; Yang Aming; Xu Bin; Chen Ling; Zhu Zhiliang; Zhao Jianfu [State Key Laboratory of Pollution Control and Resource Reuse, Key Laboratory of Yangtze River Water Environment of Ministry of Education, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China); Jaffrezic-Renault, Nicole; Leonard, Didier [Laboratoire de Sciences Analytiques (UMR CNRS 5180), Universite Claude Bernard Lyon 1, Universite de Lyon, 69622 Villeurbanne Cedex (France)

2009-04-15

This paper deals with the extracellular polymeric substance (EPS) of Proteus mirabilis TJ-1 used as a novel biosorbent to remove dye from aqueous solution in batch systems. As a widely used and hazardous dye, basic blue 54 (BB54) was chosen as the model dye to examine the adsorption performance of the EPS. The effects of pH, initial dye concentration, contact time and temperature on the sorption of BB54 to the EPS were examined. At various initial dye concentrations (50-400 mg/L), the batch sorption equilibrium can be obtained in only 5 min. Kinetic studies suggested that the sorption followed the internal transport mechanism. According to the Langmuir model, the maximum BB54 uptake of 2.005 g/g was obtained. Chemical analysis of the EPS indicated the presence of protein (30.9%, w/w) and acid polysaccharide (63.1%, w/w). Scanning electron microscopy (SEM) images showed that the EPS with a crystal-linear structure was whole enwrapped by adsorbed dye molecules. FTIR spectrum result revealed the presence of adsorbing groups such as carboxyl, hydroxyl and amino groups in the EPS. High-molecular weight of the EPS with more binding-sites and stronger van der Waals forces together with its specific construct leads to the excellent performance of dye adsorption. The EPS shows potential board application as a biosorbent for both environmental protection and dye recovery.

A novel biosorbent for dye removal: Extracellular polymeric substance (EPS) of Proteus mirabilis TJ-1

International Nuclear Information System (INIS)

Zhang Zhiqiang; Xia Siqing; Wang Xuejiang; Yang Aming; Xu Bin; Chen Ling; Zhu Zhiliang; Zhao Jianfu; Jaffrezic-Renault, Nicole; Leonard, Didier

2009-01-01

This paper deals with the extracellular polymeric substance (EPS) of Proteus mirabilis TJ-1 used as a novel biosorbent to remove dye from aqueous solution in batch systems. As a widely used and hazardous dye, basic blue 54 (BB54) was chosen as the model dye to examine the adsorption performance of the EPS. The effects of pH, initial dye concentration, contact time and temperature on the sorption of BB54 to the EPS were examined. At various initial dye concentrations (50-400 mg/L), the batch sorption equilibrium can be obtained in only 5 min. Kinetic studies suggested that the sorption followed the internal transport mechanism. According to the Langmuir model, the maximum BB54 uptake of 2.005 g/g was obtained. Chemical analysis of the EPS indicated the presence of protein (30.9%, w/w) and acid polysaccharide (63.1%, w/w). Scanning electron microscopy (SEM) images showed that the EPS with a crystal-linear structure was whole enwrapped by adsorbed dye molecules. FTIR spectrum result revealed the presence of adsorbing groups such as carboxyl, hydroxyl and amino groups in the EPS. High-molecular weight of the EPS with more binding-sites and stronger van der Waals forces together with its specific construct leads to the excellent performance of dye adsorption. The EPS shows potential board application as a biosorbent for both environmental protection and dye recovery

REMOVAL OF REMAZOL ROSSO RB DYE FROM AQUEOUS EFFLUENTS BY HOMOGENOUS FENTON OXIDATION PROCESSES

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Carmen Zaharia

2014-06-01

Full Text Available The paper presents some data from our laboratory-setup experiments of homogenous oxidative processes with hydrogen peroxide (i.e. advanced Fenton oxidation processes applied for Remazol Rosso RB dye-containing aqueous systems, especially textile effluents. Therefore, some different operating parameters (including pH, concentration of dye, H2O2 and ferrous ions, oxidation time, temperature, stirring regime, among its were tested for determination of the best performance in effluent decoloration and dye removal, meaning the optimal values of each studied parameters for highest decoloration or dye removal.

Increased light harvesting in dye-sensitized solar cells with energy relay dyes

KAUST Repository

Hardin, Brian E.

2009-06-21

Conventional dye-sensitized solar cells have excellent charge collection efficiencies, high open-circuit voltages and good fill factors. However, dye-sensitized solar cells do not completely absorb all of the photons from the visible and near-infrared domain and consequently have lower short-circuit photocurrent densities than inorganic photovoltaic devices. Here, we present a new design where high-energy photons are absorbed by highly photoluminescent chromophores unattached to the titania and undergo Förster resonant energy transfer to the sensitizing dye. This novel architecture allows for broader spectral absorption, an increase in dye loading, and relaxes the design requirements for the sensitizing dye. We demonstrate a 26% increase in power conversion efficiency when using an energy relay dye (PTCDI) with an organic sensitizing dye (TT1). We estimate the average excitation transfer efficiency in this system to be at least 47%. This system offers a viable pathway to develop more efficient dye-sensitized solar cells.

Radiation degradation adsorption treatment of some toxic dyes present in wastewater

International Nuclear Information System (INIS)

Dessouki, A.M.; Hegazy, E.A.; El-Kelesh, N.A.

2000-01-01

The degradation kinetics due to gamma irradiation of aqueous solutions of some organic pollutants (reactive yellow dye, acidic yellow Dye and fast yellow Dye) were investigated. A combined treatment of gamma irradiation and conventional methods was applied and is much more effective than either alone. Factors affecting the radiolysis of the pollutants such as concentration, irradiation dose, dose rate and ph of the solutions was studied. Radiochemical degradation yields were calculated to elucidate the mechanism of the degradation process. Also, the feasibility of using granular activated carbon (GAC), ion exchange resins (Merck I, III, Iv) for the removal of these pollutants from aqueous solution were studied. Synergistic treatment of the dye solutions by irradiation methods showed that the saturation of the dye solutions with nitrogen did not enhance the radiation degradation of the dyes, while addition of O 2 , H 2 O 2 or Na Ocl resulted in remarkable enhancement. Adsorption of the dyes into GAC and some ion-exchangers, showed that GAC has the highest adsorption capacity compared with ion-exchangers. Irradiation followed by adsorption resulted in the removal of these toxic pollutants from wastewater

Radiation degradation adsorption treatment of some toxic dyes present in wastewater

International Nuclear Information System (INIS)

Al-Dousougi, A. M.; Hijarzi, A. A.; Al-Qalash, N. A. A.

2002-01-01

The degradation kinetics due to gamma irradiation of aqueous solutions of some organic pollutants (Reactive Yellow Dye, acidic yellow dye and fast yellow dye) were investigated. A combined treatment of gamma irradiation and conventional methods was applied and is much more effective than either alone. Factors affecting the radiolysis of the pollutants such as concentration, irradiation dose, dose rate, and pH of the solutions was studied. Radiochemical degradation yields were calculated to elucidate the mechanism of the degradation process. Also, the feasibility of using granular Activated carbon (GAC), ion exchange resins (Metck I, II, III, IV) for the removal of these pollutants from aqueous solutions were studied. Synergistic treatment of the dye solutions by irradiation methods showed that the saturation of the dye solutions with nitrogen did not enhance the radiation degradation of the dyes, while addition of O 2 , H 2 O 2 or NaOCI resulted in remarkable enhancement. Adsorption of the dyes onto GAC and some ion-exchangers, showed that GAC has the highest adsorption capacity compared with ion-exchangers. Irradiation followed by adsorption resulted in the removal of these toxic pollutants from wastewater. (author)

Radiation degradation-adsorption treatment of some toxic dyes present in wastewater

International Nuclear Information System (INIS)

El-Kelesh, N.A.; Dessouki, A.M.; Amer, S.I.

2002-01-01

The radiolysis or three toxic dyes, viz. Reactive Yellow 3, Reactive Black 39, and Basic Blue 26, was investigated as a function of the dye concentration, pH, irradiation dose and dose rate. The radiolytic degradation was more pronounced with Reactive yellow 3 and Reactive Black 39 than with Basic Blue 26. The degree of degradation could be increased by combining the irradiation procedure with the conventional treatment, such as addition of oxygen or hydrogen peroxide; addition of nitrogen, on the other hand, resulted in no change. A pH drop was observed and tentatively attributed to the degradation of the dye molecules to lower molecular weight compounds such as organic acids. The primary radiolysis products as well as the secondary products are responsible for the degradation of the dye chromophore. Experiments with the adsorption or exchange of the dyes on GAC, some ion exchange resins and polymeric membranes were carried out to find that the polymeric membranes have the highest adsorption capacity for the pollutants except the basic dye. The combined treatment by irradiation and adsorption resulted in a complete removal of the toxic dyes in question

Ultrafast photodynamics of the indoline dye D149 adsorbed to porous ZnO in dye-sensitized solar cells.

Science.gov (United States)

Rohwer, Egmont; Richter, Christoph; Heming, Nadine; Strauch, Kerstin; Litwinski, Christian; Nyokong, Tebello; Schlettwein, Derck; Schwoerer, Heinrich

2013-01-14

We investigate the ultrafast dynamics of the photoinduced electron transfer between surface-adsorbed indoline D149 dye and porous ZnO as used in the working electrodes of dye-sensitized solar cells. Transient absorption spectroscopy was conducted on the dye in solution, on solid state samples and for the latter in contact to a I(-)/I(3)(-) redox electrolyte typical for dye-sensitized solar cells to elucidate the effect of each component in the observed dynamics. D149 in a solution of 1:1 acetonitrile and tert-butyl alcohol shows excited-state lifetimes of 300±50 ps. This signature is severely quenched when D149 is adsorbed to ZnO, with the fastest component of the decay trace measured at 150±20 fs due to the charge-transfer mechanism. Absorption bands of the oxidized dye molecule were investigated to determine regeneration times which are in excess of 1 ns. The addition of the redox electrolyte to the system results in faster regeneration times, of the order of 1 ns. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Waste metal hydroxide sludge as adsorbent for a reactive dye.

Science.gov (United States)

Santos, Sílvia C R; Vílar, Vítor J P; Boaventura, Rui A R

2008-05-30

An industrial waste sludge mainly composed by metal hydroxides was used as a low-cost adsorbent for removing a reactive textile dye (Remazol Brilliant Blue) in solution. Characterization of this waste material included chemical composition, pH(ZPC) determination, particle size distribution, physical textural properties and metals mobility under different pH conditions. Dye adsorption equilibrium isotherms were determined at 25 and 35 degrees C and pH of 4, 7 and 10 revealing reasonably fits to Langmuir and Freundlich models. At 25 degrees C and pH 7, Langmuir fit indicates a maximum adsorption capacity of 91.0mg/g. An adsorptive ion-exchange mechanism was identified from desorption studies. Batch kinetic experiments were also conducted at different initial dye concentration, temperature, adsorbent dosage and pH. A pseudo-second-order model showed good agreement with experimental data. LDF approximation model was used to estimate homogeneous solid diffusion coefficients and the effective pore diffusivities. Additionally, a simulated real effluent containing the selected dye, salts and dyeing auxiliary chemicals, was also used in equilibrium and kinetic experiments and the adsorption performance was compared with aqueous dye solutions.

Application of edible paraffin oil for cationic dye removal from water using emulsion liquid membrane.

Science.gov (United States)

Zereshki, Sina; Daraei, Parisa; Shokri, Amin

2018-05-18

Using an emulsion liquid membrane based on edible oils is investigated for removing cationic dyes from aqueous solutions. There is a great potential for using edible oils in food industry extraction processes. The parameters affecting the stability of the emulsion and the extraction rate were studied. These parameters were the emulsification time, the stirring speed, the surfactant concentration, the internal phase concentration, the feed phase concentration, the volume ratio of internal phase to organic phase and the treat ratio. In order to stabilize the emulsion without using a carrier, edible paraffin oil and heptane are used at an 80:20 ratio. The optimum conditions for the extraction of methylene blue (MB), crystal violet and methyl violet (CV and MV) cationic dyes using edible paraffin oil as an environment friendly solvent are represented. A removal percentage of 95% was achieved for a mixture of dyes. The optimum concentration of sodium hydroxide in the internal phase, which results a stabile emulsion with a high stripping efficiency of 96%, was 0.04 M. An excellent membrane recovery was observed and the extraction of dyes did not decrease up to seven run cycles. Copyright © 2018 Elsevier B.V. All rights reserved.

Incorporating Multiple Energy Relay Dyes in Liquid Dye-Sensitized Solar Cells

KAUST Repository

Yum, Jun-Ho

2011-01-05

Panchromatic response is essential to increase the light-harvesting efficiency in solar conversion systems. Herein we show increased light harvesting from using multiple energy relay dyes inside dye-sensitized solar cells. Additional photoresponse from 400-590 nm matching the optical window of the zinc phthalocyanine sensitizer was observed due to Förster resonance energy transfer (FRET) from the two energy relay dyes to the sensitizing dye. The complementary absorption spectra of the energy relay dyes and high excitation transfer efficiencies result in a 35% increase in photovoltaic performance. © 2011 Wiley-VCH Verlag GmbH& Co. KGaA.

Dyes for displays

Science.gov (United States)

Claussen, U.

1984-01-01

The improvement of contrast and visibility of LCD by two different means was undertaken. The two methods are: (1) development of fluorescent dyes to increase the visibility of fluorescent activated displays (FLAD); and (2) development of dichroic dyes to increase the contrast of displays. This work was done in close cooperation with the electronic industry, where the newly synthesized dyes were tested. The targets for the chemical synthesis were selected with the help of computer model calculations. A marketable range of dyes was developed. Since the interest of the electronic industries concerning FLAD was low, the investigations were stopped. Dichroic dyes, especially black mixtures with good light fastness, order parameter, and solubility in nematic phases were developed. The application of these dyes is restricted to indoor use because of an increase of viscosity below -10 C. Applications on a technical scale, e.g., for the automotive industry, will be possible if the displays work at temperatures down to -40 C. This problem requires a complex optimization of the dye/nematic phase system.

Dye stability and performances of dye-sensitized solar cells with different nitrogen additives at elevated temperatures - Can sterically hindered pyridines prevent dye degradation?

Energy Technology Data Exchange (ETDEWEB)

Tuyet Nguyen, Phuong; Lund, Torben [Department of Science, Systems and Models, Roskilde University, 4000 Roskilde (Denmark); Rand Andersen, Anders [University of Southern Denmark, Institute of Sensors, Signals and Electrotechnics (SENSE), Niels Bohrs Alle 1, 5230 Odense M (Denmark); Danish Technological Institute, Plastics Technology, Gregersensvej 2630 Taastrup (Denmark); Morten Skou, Eivind [University of Southern Denmark, Department of Chemical Engineering, Biotechnology and Enviromental Technology, Niels Bohrs Alle 1, 5230 Odense M (Denmark)

2010-10-15

The homogeneous kinetics of the nucleophilic substitution reactions between the ruthenium dye N719 and eight pyridines and 1-methylbenzimidazole have been investigated in 3-methoxypropionitrile at 100 C. The half lives of N719 with the additives 4-tert-butylpyridine (0.5 M) and 1-methylbenzimidazole (0.5 M) were 57 and 160 h, respectively. Sterically hindered pyridines like 2,6-lutidine did not react with N719. The efficiencies of dye-sensitized solar cells (DSC, area=8.0 cm{sup 2}) prepared with 1-methylbenzimidazole (MBI), 4-tert-butylpyridine (4-TBP), 2,6-lutidine and without any additive were 7.1%, 6.2%, 6.0% and 4.8%, respectively. The cells were stored in dark at 85 C and their I-V curves and impedance spectra were measured at regular time intervals. The N719 dye degradation in the cells were monitored by a new dye extraction protocol combined with analysis of the dye extract by HPLC coupled to mass spectrometry. After 300 h storage in dark at 85 C 40% of the initial amount of N719 dye was degraded in DSC cells prepared with MBI and the efficiency was decreased to 40% of its initial value. DSC cells prepared with 2,6-lutidine or no additives showed smaller thermal dye and efficiency stability at elevated temperatures than DSC cells prepared with the none sterically hindered additives MBI and 4-TBP. In the cells prepared with 2,6-lutidine or no additive higher contents of the iodo products [RuL{sub 2}(NCS)(iodide)]{sup +} and [RuL{sub 2}(3-MPN)(iodide)]{sup +} were found than in cells prepared with 4-TBP and MBI. It is suggested that sterically hindered pyridines have smaller complexation constants with I{sub 3}{sup -} than unsterically hindered additives. This may explain the observed faster nucleophilic substitution rates of uncomplexed I{sub 3}{sup -} with N719 in DSC cells prepared with sterically hindered pyridines. The EIS analysis showed that the lifetime of the injected electrons in the TiO{sub 2}{tau}{sub eff} is reduced by a thermally induced change

Production of Superoxide in Bacteria Is Stress- and Cell State-Dependent: A Gating-Optimized Flow Cytometry Method that Minimizes ROS Measurement Artifacts with Fluorescent Dyes.

Science.gov (United States)

McBee, Megan E; Chionh, Yok H; Sharaf, Mariam L; Ho, Peiying; Cai, Maggie W L; Dedon, Peter C

2017-01-01

The role of reactive oxygen species (ROS) in microbial metabolism and stress response has emerged as a major theme in microbiology and infectious disease. Reactive fluorescent dyes have the potential to advance the study of ROS in the complex intracellular environment, especially for high-content and high-throughput analyses. However, current dye-based approaches to measuring intracellular ROS have the potential for significant artifacts. Here, we describe a robust platform for flow cytometric quantification of ROS in bacteria using fluorescent dyes, with ROS measurements in 10s-of-1000s of individual cells under a variety of conditions. False positives and variability among sample types (e.g., bacterial species, stress conditions) are reduced with a flexible four-step gating scheme that accounts for side- and forward-scattered light (morphological changes), background fluorescence, DNA content, and dye uptake to identify cells producing ROS. Using CellROX Green dye with Escherichia coli, Mycobacterium smegmatis , and Mycobacterium bovis BCG as diverse model bacteria, we show that (1) the generation of a quantifiable CellROX Green signal for superoxide, but not hydrogen peroxide-induced hydroxyl radicals, validates this dye as a superoxide detector; (2) the level of dye-detectable superoxide does not correlate with cytotoxicity or antibiotic sensitivity; (3) the non-replicating, antibiotic tolerant state of nutrient-deprived mycobacteria is associated with high levels of superoxide; and (4) antibiotic-induced production of superoxide is idiosyncratic with regard to both the species and the physiological state of the bacteria. We also show that the gating method is applicable to other fluorescent indicator dyes, such as the 5-carboxyfluorescein diacetate acetoxymethyl ester and 5-cyano-2,3-ditolyl tetrazolium chloride for cellular esterase and reductive respiratory activities, respectively. These results demonstrate that properly controlled flow cytometry coupled

The removal of reactive dyes using high-ash char

Directory of Open Access Journals (Sweden)

Moreira R.F.P.M.

2001-01-01

Full Text Available The thermodynamics and kinetics of adsorption of reactive dyes on high-ash char was studied. Equilibrium data were obtained using the static method with controlled agitation at temperatures in the range of 30 to 60ºC. The Langmuir isotherm model was used to describe the equilibrium of adsorption, and the equilibrium parameters, R L, in the range of 0 to 1 indicate favorable adsorption. The amount of dye adsorbed increased as temperature increased from 30 to 40ºC, but above 40ºC the increase in temperature resulted in a decrease in the amount of dye adsorbed. The kinetic data presented are for controlled agitation at 50 rpm and constant temperature with dye concentrations in the range of 10 ppm to50 ppm. The film mass transfer coefficient, Kf, and the effective diffusivity inside the particle, De, were fitted to the experimental data. The results indicate that internal diffusion governs the adsorption rate.

[Adsorption of a dye by sludges and the roles of extracellular polymeric substances].

Science.gov (United States)

Kong, Wang-sheng; Liu, Yan

2007-12-01

This paper investigated the adsorption of a dye, acid turquoise blue A, by four kinds of sludges including activated sludge, anaerobic sludge, dried activated sludge, and dried anaerobic sludge, respectively. The roles of extracellular polymeric substances (EPS) including the soluble EPS (SEPS) and bound EPS (BEPS) for the biosorption of activated sludge and anaerobic sludge were further studied. Results show that the relation between four kinds of sludge adsorption amount and remained concentration of the dye fitted well both Freundlich model (R2: 0.921-0.995) and Langmuir model (R2: 0.958-0.993), but not quite fitted BET model (R2: 0.07-0.863). The adsorption capability of dried anaerobic sludge ranked the highest, and dried activated sludge was the lowest. According to Langmuir isotherm, the maximum adsorption amount of dried anaerobic, anaerobic, activated, and dried activated sludge was 104 mg/g, 86 mg/g, 65 mg/g, 20 mg/g, respectively. The amount of the dye found in EPS for both activated sludge and anaerobic sludge were over 50%, illustrating that EPS adsorption was predominant in adsorption of the dye by sludge. The amount of adsorbed dye by BEPS was greater than that by SEPS for anaerobic sludge, but for activated sludge the result was quite opposite. The amount of adsorbed dye by unit mass SEPS was much higher than the corresponding values of BEPS for both sludges. The average amount of adsorbed dye by unit mass SEPS was 52 times of the corresponding value of BEPS for activated sludge, and 10 times for anaerobic sludge. The relation between adsorption amount of dye by BEPS from anaerobic sludge and remained concentration of the dye in mixed liquor was best fitted to Langmuir model (R2: 0.9986).

Electrochemical degradation of reactive dyes at different DSA compositions

Energy Technology Data Exchange (ETDEWEB)

Silva, Rodrigo G. da; Aquino Neto, Sydney; Andrade, Adalgisa R. de, E-mail: ardandra@ffclrp.usp.b [Universidade de Sao Paulo (FFCLRP/USP), Ribeirao Preto, SP (Brazil). Fac. de Filosofia Ciencias e Letras. Dept. de Quimica

2011-07-01

This paper investigates the electrochemical oxidation of the reactive dyes reactive blue 4 (RB-4) and reactive orange 16 (RO-16) on RuO{sub 2} dimensionally stable anode (DSA) electrodes. Electrolysis was achieved under galvanostatic control as a function of supporting electrolyte and electrode composition. The electrolyses, performed in either the presence or absence of NaCl, were able to promote efficient color removal; moreover, at low chloride concentration (0.01 mol L{sup -1}), total color removal was obtained after just 10 min of electrolysis, and a significant increase in total dye combustion was achieved for all the studied anodes in chloride medium (reaching ca. 80% - chemical oxygen demand - COD removal). No significant enhancement in dye color removal or mineralization was observed upon increasing chloride concentration. The influence of oxide composition on dye elimination seems to be significant in both media (with or without chloride), being Ti/Ru{sub 0.30}Ti{sub 0.70}O{sub 2}, the most active material for organic compound oxidation. The oxygen evolution reaction was shown to be a limiting reaction in both supporting electrolytes; i.e., NaCl and Na{sub 2}SO{sub 4}, and its competition with organic compound oxidation remained an obstacle. The adsorbable organo halogens formation study revealed that there is slight consumption of the undesirable species formed within the first minutes of the electrolysis, being Ti/(RuO{sub 2}){sub 0.70}(Ta{sub 2}O{sub 5}){sub 0.30} the most environmentally friendly composition. Both anode composition and chloride concentration affect the formation of these undesirable compounds. (author)

Selective Adsorption and Separation of Organic Dyes with Spherical Polyelectrolyte Brushes and Compressed Carbon Dioxide.

Science.gov (United States)

Zhang, Rui; Yu, Zhenchuan; Wang, Lei; Shen, Qizhe; Hou, Xiaoyan; Guo, Xuhong; Wang, Junwei; Zhu, Xuedong; Yao, Yuan

2017-10-04

Dye-containing wastewater has caused serious environmental pollution. Herein, rationally designed spherical polyelectrolyte brushes (SPBs) with cationic charges, polystyrene-poly(2-aminoethylmethacrylate hydrochloride) (PS-PAEMH) as the absorbent, and compressed carbon dioxide as the antisolvent are proposed for the separation of the anionic dye eosin Y (EY) from a solution of mixed dyes. The adsorption behavior of EY onto PS-PAEMH was highly dependent on CO 2 pressure, contact time, and initial concentration. The maximum adsorption capacity of PS-PAEMH was 335.20 mg g -1 . FTIR and UV/Vis measurements proved that the electrostatic interactions between EY and PS-PAEMH played an important role in the absorbance process. The adsorption process fitted the pseudo-second-order kinetic model and Freundlich isotherm model very well. The combined dye and polymer brush could be easily separated through ion exchange by adding an aqueous solution of NaCl. Recovered PS-PAEMH retained a high adsorption capacity even after ten cycles of regeneration. This method provides a simple and effective way to separate ionic materials for environmental engineering. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Batch Removal of Acid Blue 292dye by Biosorption onto Lemna minor: Equilibrium and Kinetic Studies

Directory of Open Access Journals (Sweden)

Ali Joghataei

2016-12-01

Full Text Available Background: Recently, there has been a great concern about the consumption of dyes because of their toxicity, mutagenicity, carcinogenicity, and persistence in the aquatic environment. Therefore, the aim of this study was to determine the feasibility of using Lemna minor for Acid Blue 292 (AB292 dye removal from aqueous solution and to determine the optimal conditions. Methods: This experimental study was conducted in the batch systems to investigate the effects of parameters such as contact time, initial concentration of dye, pH and Lemna minor biomass dose. Isotherms and kinetic studies of dye adsorption were performed using equilibrium data. Results: According to the results, a maximum removal efficiency of 98.5% was obtained at pH of 3 and the contact time of 90 min; initial dye concentration 10 mg/L and adsorbent dose 3g/L. The adsorption data was best fitted to the Langmuir isotherm and pseudo-second order kinetic model. Conclusion: The results showed that Lemna minor could be used as a cost-effective adsorbent for removing AB292 dye from textile wastewater efficiently.

Ultrasound for low temperature dyeing of wool with acid dye.

Science.gov (United States)

Ferrero, F; Periolatto, M

2012-05-01

The possibility of reducing the temperature of conventional wool dyeing with an acid levelling dye using ultrasound was studied in order to reach exhaustion values comparable to those obtained with the standard procedure at 98 °C, obtaining dyed samples of good quality. The aim was to develop a laboratory method that could be transferred at industrial level, reducing both the energy consumption and fiber damage caused by the prolonged exposure to high temperature without the use of polluting auxiliary agents. Dyeings of wool fabrics were carried out in the temperature range between 60 °C and 80 °C using either mechanical or ultrasound agitation of the bath and coupling the two methods to compare the results. For each dyeing, the exhaustion curves of the dye bath were determined and the better results of dyeing kinetics were obtained with ultrasound coupled with mechanical stirring. Hence the corresponding half dyeing times, absorption rate constants according to Cegarra-Puente modified equation and ultrasonic efficiency were calculated in comparison with mechanical stirring alone. In the presence of ultrasound the absorption rate constants increased by at least 50%, at each temperature, confirming the synergic effect of sonication on the dyeing kinetics. Moreover the apparent activation energies were also evaluated and the positive effect of ultrasound was ascribed to the pre-exponential factor of the Arrhenius equation. It was also shown that the effect of ultrasound at 60 °C was just on the dye bath, practically unaffecting the wool fiber surface, as confirmed by the results of SEM analysis. Finally, fastness tests to rubbing and domestic laundering yielded good values for samples dyed in ultrasound assisted process even at the lower temperature. These results suggest the possibility, thanks to the use of ultrasound, to obtain a well equalized dyeing on wool working yet at 60°C, a temperature process strongly lower than 98°C, currently used in industry

DYEING COTTON WITH EISENIA BICYCLIS AS NATURAL DYE USING DIFFERENT BIOMORDANTS

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BONET Mª Ángeles

2015-05-01

Full Text Available Natural dyes are known for their use in coloring of food substrate, leather as well as natural protein fibers like wool, silk and cotton as major areas of application since pre-historic times. Nowadays, there has been revival of the growing interest on the application of natural dyes on natural fibers due to worldwide environmental consciousness. Some researchers focus their studies on the improvement of these dyes using mordants. Most works use metallic mordants like aluminum or iron are used, but some of them are hazardous. In this work we used a biomordant to solve environmental problems caused by metallic mordants. The effects of chitosan weight molecular in mordanting on the dyeing characteristics and the UV protection property were examined in this study. Chitosan mordanted Eisenia Bicyclis dyed cotton showed better dyeing characteristic and higher UV protection property compared with undyed cotton fabric. To analyze the differences of the dyeing, reflection spectrophotometer was used, evaluating the results of CIELAB color difference values and the strength color (in terms of K/S value. We conclude that the type of chitosan used affect the dyeing efficiency and the UV protection, showing different behavior between dye sample using chitosan with low or medium molecular weight.

Photostability of low cost dye-sensitized solar cells based on natural and synthetic dyes

Science.gov (United States)

Abdou, E. M.; Hafez, H. S.; Bakir, E.; Abdel-Mottaleb, M. S. A.

2013-11-01

This paper deals with the use of some natural pigments as well as synthetic dyes to act as sensitizers in dye-sensitized solar cells (DSSCs). Anthocyanin dye extracted from rosella (Hibiscus sabdariffa L.) flowers, the commercially available textile dye Remazole Red RB-133 (RR) and merocyanin-like dye based on 7-methyl coumarin are tested. The photostability of the three dyes is investigated under UV-Vis light exposure. The results show a relatively high stability of the three dyes. Moreover, the photostability of the solid dyes is studied over the TiO2 film electrodes. A very low decolorization rates are recorded as; rate constants k = 1.6, 2.1 and 1.9 × 10-3 min-1 for anthocyanin, RR and coumarin dyes, respectively. The stability results favor selecting anthocyanin as a promising sensitizer candidate in DSSCs based on natural products. Dyes-sensitized solar cells are fabricated and their conversion efficiency (η) is 0.27%, 0.14% and 0.001% for the anthocyanin, RR and coumarin dyes, respectively. Moreover, stability tests of the sealed cells based on anthocyanin and RR dyes are done under continuous light exposure of 100 mW cm-2, reveals highly stable DSSCs.

Use of Titanium Dioxide Photocatalysis on the Remediation of Model Textile Wastewaters Containing Azo Dyes

Directory of Open Access Journals (Sweden)

Josino Costa Moreira

2011-12-01

Full Text Available The photocatalytic degradation of two commercial textile azo dyes, namely C.I Reactive Black 5 and C.I Reactive Red 239, has been studied. TiO2 P25 Degussa was used as catalyst and photodegradation was carried out in aqueous solution under artificial irradiation with a 125 W mercury vapor lamp. The effects of the amount of TiO2 used, UV-light irradiation time, pH of the solution under treatment, initial concentration of the azo dye and addition of different concentrations of hydrogen peroxide were investigated. The effect of the simultaneous photodegradation of the two azo dyes was also investigated and we observed that the degradation rates achieved in mono and bi-component systems were identical. The repeatability of photocatalytic activity of the photocatalyst was also tested. After five cycles of TiO2 reuse the rate of colour lost was still 77% of the initial rate. The degradation was followed monitoring the change of azo dye concentration by UV-Vis spectroscopy. Results show that the use of an efficient photocatalyst and the adequate selection of optimal operational parameters may easily lead to a complete decolorization of the aqueous solutions of both azo dyes.

Identification of changes in the inorganic matrix of dye sensitized solar cells during preparation

Energy Technology Data Exchange (ETDEWEB)

Graaf, Harald; Maedler, Carsten; Kehr, Mirko; Baumgaertel, Thomas [Institute of Physics, Chemnitz University of Technology, Reichenhainer Str. 70, 09126 Chemnitz (Germany); Oekermann, Torsten [Institute of Physical Chemistry and Electrochemistry, Leibniz University Hannover, 30167 Hannover (Germany)

2009-12-15

Nanoporous zinc oxide films can be prepared by electrochemical co-deposition with the dye eosin Y (EY) as template. A subsequent desorption of the dye with aqueous KOH is a key step for the increased efficiency of such dye sensitized solar cells (DSSC). In this contribution, the partial dissolving and reorganization of the zinc oxide film during the desorption step has been studied in detail by X-ray diffraction, Kelvin probe force microscopy, and atomic force microscopy (AFM) as well as scanning electron microscopy. It is found that the reorganization leads to an enhancement of crystal orientation and a reduction of the defect concentration at the surface of zinc oxide, being a possible reason for suppressed recombination of electrons in these films. Also, an increased defect concentration in ZnO was found when co-deposited with EY. For these co-deposited films, AFM investigations showed a coverage of the surface with dye aggregates. High resolution AFM investigations revealed the nanocrystalline and highly porous structure of the inorganic matrix after desorption of the dye. Photographs of the organic/inorganic hybrid thin film material were investigated in this study. Left side: film directly after deposition, right side: after desorption of the organic dye. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

Electroadsorption of acilan blau dye from textile effluents by using activated carbon-perlite mixtures.

Science.gov (United States)

Koparal, A S; Yavuz, Y; Bakir Ogütveren, U

2002-01-01

The feasibility of the removal of dye stuffs from textile effluents by electroadsorption has been investigated. An activated carbon-perlite mixture with a ratio of 8:1 for bipolarity has been used as the adsorbent. Conventional adsorption experiments have also been conducted for comparison. A bipolar trickle reactor has been used in the electroadsorption experiments. The model wastewater has been prepared by using acilan blau dye. Initial dye concentration, bed height between the electrodes, applied potential, flowrate, and the supporting electrolyte concentration have been examined as the parameters affecting the removal efficiency. A local textile plant effluent has been treated in the optimum values of these parameters obtained from the experimental studies. Adsorption kinetics and the amount of adsorbent required to reach the maximum removal efficiency have also been investigated and mass-transfer coefficients have been calculated for adsorption and electroadsorption. The results showed that a removal efficiency of up to 100% can be achieved with energy consumption values of 1.58 kWh/m3 of wastewater treated. However, energy consumption decreases to 0.09 kWh/m3 if an exit dye concentration of 4.65 mg/L is accepted. It can be concluded from this work that this method combines all of the advantages of the activated-carbon adsorption and electrolytic methods for the removal of dyes from wastewater.

Thermomechanical and Photophysical Properties of Crystal-Violet-Dye/H2O Based Dissolutions via the Pulsed Laser Photoacoustic Technique

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Vicente Torres-Zúñiga

2014-01-01

Full Text Available Different thermoelastic parameters, for example, the acoustic attenuation and the speed of sound, are fundamental for instrumental calibration and quantitative characterization of organic-based dissolutions. In this work, these parameters as functions of the concentration of an organic dye (crystal-violet: CV in distillated water (H2O based dissolutions are investigated. The speed of sound was measured by the pulsed-laser photoacoustic technique (PLPA, which consists in the generation of acoustic-waves by the optical absorption of pulsed light in a given material (in this case a liquid sample. The thermally generated sound-waves traveling through a fluid are detected with two piezoelectric sensors separated by a known distance. An appropriate processing of the photoacoustic signals allows an adequate data analysis of the generated waves within the system, providing an accurate determination of the speed of sound as function of the dye-concentration. The acoustic attenuation was calculated based on the distance of the two PZT-microphones to an acoustic-source point and performing linear-fitting of the experimental data (RMS-amplitudes as function of the dye-concentration. An important advantage of the PLPA-method is that it can be implemented with poor or null optical transmitting materials permitting the characterization of the mechanical and concentration/aggregate properties of dissolved organic compounds.

MODELING OF TUBULAR ELECTROCHEMICAL REACTOR FOR DYE REMOVAL

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V. VIJAYAKUMAR

2017-06-01

Full Text Available The aim of the present investigation is to model a tubular electrochemical reactor for the treatment of synthetic dye wastewater. The tubular reactor was modeled and solved by finite difference method. For the model solution, the column was divided into 11 nodes in the axial direction and the variation in the radial direction has been neglected. An initial dye concentration of 200 mg L-1was taken in the reservoir. The reactor was operated in a batch with recirculation operation. Based on preliminary experiments all parameters have been optimized. The model simulation is compared with the experimental value and it is observed that the model fairly matches well with the experiment. The modeling of tubular electrochemical reactors for dye waste water treatment could be useful in the design and scale up of electrochemical process.

Quantum dot-dye hybrid systems for energy transfer applications

International Nuclear Information System (INIS)

Ren, Ting

2010-01-01

In this thesis, we focus on the preparation of energy transfer-based quantum dot (QD)-dye hybrid systems. Two kinds of QD-dye hybrid systems have been successfully synthesized: QD-silica-dye and QD-dye hybrid systems. In the QD-silica-dye hybrid system, multishell CdSe/CdS/ZnS QDs were adsorbed onto monodisperse Stoeber silica particles with an outer silica shell of thickness 2-24 nm containing organic dye molecules (Texas Red). The thickness of this dye layer has a strong effect on the total sensitized acceptor emission, which is explained by the increase in the number of dye molecules homogeneously distributed within the silica shell, in combination with an enhanced surface adsorption of QDs with increasing dye amount. Our conclusions were underlined by comparison of the experimental results with Monte-Carlo simulations, and by control experiments confirming attractive interactions between QDs and Texas Red freely dissolved in solution. New QD-dye hybrid system consisting of multishell QDs and organic perylene dyes have been synthesized. We developed a versatile approach to assemble extraordinarily stable QD-dye hybrids, which uses dicarboxylate anchors to bind rylene dyes to QD. This system yields a good basis to study the energy transfer between QD and dye because of its simple and compact design: there is no third kind of molecule linking QD and dye; no spacer; and the affinity of the functional group to the QD surface is strong. The FRET signal was measured for these complexes as a function of both dye to QD ratio and center-to-center distance between QD and dye by controlling number of covered ZnS layers. Data showed that fluorescence resonance energy transfer (FRET) was the dominant mechanism of the energy transfer in our QD-dye hybrid system. FRET efficiency can be controlled by not only adjusting the number of dyes on the QD surface or the QD to dye distance, but also properly choosing different dye and QD components. Due to the strong stability, our QD-dye

Quantum dot-dye hybrid systems for energy transfer applications

Energy Technology Data Exchange (ETDEWEB)

Ren, Ting

2010-07-01

In this thesis, we focus on the preparation of energy transfer-based quantum dot (QD)-dye hybrid systems. Two kinds of QD-dye hybrid systems have been successfully synthesized: QD-silica-dye and QD-dye hybrid systems. In the QD-silica-dye hybrid system, multishell CdSe/CdS/ZnS QDs were adsorbed onto monodisperse Stoeber silica particles with an outer silica shell of thickness 2-24 nm containing organic dye molecules (Texas Red). The thickness of this dye layer has a strong effect on the total sensitized acceptor emission, which is explained by the increase in the number of dye molecules homogeneously distributed within the silica shell, in combination with an enhanced surface adsorption of QDs with increasing dye amount. Our conclusions were underlined by comparison of the experimental results with Monte-Carlo simulations, and by control experiments confirming attractive interactions between QDs and Texas Red freely dissolved in solution. New QD-dye hybrid system consisting of multishell QDs and organic perylene dyes have been synthesized. We developed a versatile approach to assemble extraordinarily stable QD-dye hybrids, which uses dicarboxylate anchors to bind rylene dyes to QD. This system yields a good basis to study the energy transfer between QD and dye because of its simple and compact design: there is no third kind of molecule linking QD and dye; no spacer; and the affinity of the functional group to the QD surface is strong. The FRET signal was measured for these complexes as a function of both dye to QD ratio and center-to-center distance between QD and dye by controlling number of covered ZnS layers. Data showed that fluorescence resonance energy transfer (FRET) was the dominant mechanism of the energy transfer in our QD-dye hybrid system. FRET efficiency can be controlled by not only adjusting the number of dyes on the QD surface or the QD to dye distance, but also properly choosing different dye and QD components. Due to the strong stability, our QD-dye

Kinetics of photocurrent generation and an efficient charge separation of a dye-sensitized n-Cu2O/p-CuSCN junction photoelectrode in a solid-state photovoltaic cell

International Nuclear Information System (INIS)

Fernando, C A N; Kumara, N T R N; Gamage, T N

2010-01-01

A Cu/n-Cu 2 O/dye/p-CuSCN junction photoelectrode is fabricated to produce a solid-state dye-sensitized photovoltaic cell. Samples are characterized by XRD, SEM and surface resistivity measurements. Photocurrent generation is found due to light absorption of n-Cu 2 O thin film and dye sensitization between p-CuSCN and the dye. Kinetics of the photocurrent generation of the dye sensitization is studied solving the rate equations by the iteration method obtaining a relationship for the photocurrent quantum efficiency (Φ) depending on the surface concentration (D o ) of the dye and the rate constants of the reactions with connection to the dye sensitization process. The solution obtained in the steady state by iteration is found to be of the form Φ = AD o −BD o 2 (A and B are constants related to the reaction rates of the photocurrent generation process and the concentration of the n-Cu 2 O film). The variation of the n-Cu 2 O concentration with photocurrent is presented. A photocurrent enhancement is observed for the Cu/n-Cu 2 O/dye/p-CuSCN photovoltaic cell compared to that of Cu/n-Cu 2 O, Cu/p-CuSCN/dye and Cu/n-Cu 2 O/p-CuSCN photovoltaic cells. Good rectification characteristics are observed for the Cu/n-Cu 2 O/p-CuSCN photoelectrode compared to that of Cu/n-Cu 2 O and Cu/p-CuSCN photoelectrodes. Photocurrent enhancement is found due to the efficient charge separation process at the n–p junction. Energy band structures of the n–p junction are proposed according to the onset potentials which are used to discuss the mechanism of the efficient charge separation suppressing the recombination process

Uptake of Cationic Dyes from Aqueous Solution by Biosorption Using Granulized Annona squmosa Seed

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T. Santhi

2009-01-01

Full Text Available A new, low cost, locally available biomaterial was tested for its ability to remove cationic dyes from aqueous solution. A sample of granulized Annona squmosa seeds had been utilized as a sorbent for uptake of three cationic dyes, methylene blue (MB, methylene red (MR and malachite green (MG. The effects of various experimental parameters (e.g., contact time, dye concentration, adsorbent dose and pH were investigated and optimal experimental conditions were ascertained. Above the value of initial pH 5, three dyes studied could be removed effectively. The isothermal data fitted the Langmuir model in the case of MB sorption and the Freundlich model for all three dyes sorption. The biosorption processes followed the pseudo first order rate kinetics. The results in this study indicated that granulized Annona squmosa seed was an attractive candidate for removing cationic dyes from the dye wastewater.

LASERS, ACTIVE MEDIA: The aqueous-polyelectrolyte dye solution as an active laser medium

Science.gov (United States)

Akimov, A. I.; Saletskii, A. M.

2000-11-01

The spectral, luminescent, and lasing properties of aqueous solutions of a cationic dye rhodamine 6G with additions of anion polyelectrolytes — polyacrylic and polymethacrylic acids — are studied. It is found that the energy and spectral properties of lasing of these solutions depend on the ratio of concentrations of polyelectrolyte and molecules. It is also found that the lasing parameters of aqueous-polyelectrolyte dye solutions can be controlled by changing the structure of the molecular system. The variation in the structure of aqueous-polyelectrolyte dye solutions of rhodamine 6G resulted in an almost five-fold increase in the lasing efficiency compared to that in aqueous dye solutions.

Interaction of anthraquinone dyes with lysozyme: Evidences from spectroscopic and docking studies

International Nuclear Information System (INIS)

Paramaguru, G.; Kathiravan, A.; Selvaraj, S.; Venuvanalingam, P.; Renganathan, R.

2010-01-01

The interaction between lysozyme and anthraquinone dyes such as Alizarin Red S, Acid blue 129 and Uniblue was studied using steady state, time resolved fluorescence measurements and docking studies. Addition of anthraquinone dyes effectively quenched the intrinsic fluorescence of lysozyme. Fluorescence quenching of lysozyme by dyes has revealed the formation of complex. The number of binding sites (n) and binding constant (K) for all the three dyes was calculated by relevant fluorescence quenching data. Based on Foerster's non-radiative energy transfer theory, distance (r 0 ) between the donor (lysozyme) and acceptor (dyes) as well as the critical energy transfer distance (R 0 ) has also been calculated. The interaction between dyes and lysozyme occurs through static quenching mechanism as confirmed by time resolved spectroscopy. The conformational change of lysozyme has been analyzed using synchronous fluorescence measurement. Finally, docking studies revealed that specific interactions were observed with the residue of Trp 62.

Dye-enhanced laser welding for skin closure.

Science.gov (United States)

DeCoste, S D; Farinelli, W; Flotte, T; Anderson, R R

1992-01-01

The use of a laser to weld tissue in combination with a topical photosensitizing dye permits selective delivery of energy to the target tissue. A combination of indocyanine green (IG), absorption peak 780 nm, and the near-infrared (IR) alexandrite laser was studied with albino guinea pig skin. IG was shown to bind to the outer 25 microns of guinea pig dermis and appeared to be bound to collagen. The optical transmittance of full-thickness guinea pig skin in the near IR was 40% indicating that the alexandrite laser should provide adequate tissue penetration. Laser "welding" of skin in vivo was achieved at various concentrations of IG from 0.03 to 3 mg/cc using the alexandrite at 780 nm, 250-microseconds pulse duration, 8 Hz, and a 4-mm spot size. A spectrum of welds was obtained from 1- to 20-W/cm2 average irradiance. Weak welds occurred with no thermal damage obtained at lower irradiances: stronger welds with thermal damage confined to the weld site occurred at higher irradiances. At still higher irradiances, local vaporization occurred with failure to "weld." Thus, there was an optimal range of irradiances for "welding," which varied inversely with dye concentration. Histology confirmed the thermal damage results that were evident clinically. IG dye-enhanced laser welding is possible in skin and with further optimization may have practical application.

Phosphorescence and delayed fluorescence properties of fluorone dyes in bio-related films

International Nuclear Information System (INIS)

Penzkofer, A.; Tyagi, A.; Slyusareva, E.; Sizykh, A.

2010-01-01

Graphical abstract: The spectral and temporal phosphorescence and delayed fluorescence behaviour of five fluorescein dyes in gelatine, starch, and chitosan is studied and basic parameters are determined. Research highlights: → Phosphorescence quantum yields of fluorone dyes in bio-related films are measured at room temperature. → Delayed fluorescence quantum yields of fluorone dyes in bio-related films are measured at room temperature. → Phosphorescence lifetimes of fluorone dyes in bio-related films are measured at room temperature. → Delayed fluorescence lifetimes of fluorone dyes in bio-related films are measured at room temperature. → General theory of short-pulse excited phosphorescence and delayed fluorescence is presented and relevant parameters are extracted. - Abstract: The phosphorescence and delayed fluorescence behaviour of the fluorone dyes disodium fluorescein (FL, uranine), 4,5-dibromofluorescein (DBF), eosin Y (EO), erythrosine B (ER), and rose bengal (RB) in bio-films of gelatine, starch, and chitosan at room temperature is studied. Phosphorescence and delayed fluorescence quantum yields and lifetimes were measured. The singlet-triplet dynamics is described and applied to the fluorone dyes for parameter extraction. For uranine films at room temperature no phosphorescence could be resolved. The efficiency of singlet-triplet intersystem crossing increased in the order φ ISC (DBF) ISC (EO) ISC (ER) ISC (RB) due to the heavy atom effect on spin-orbit coupling. The phosphorescence quantum yields increased in the order φ P (DBF) P (EO) P (RB) P (ER). The phosphorescence lifetimes followed the order τ P (DBF) > τ P (EO) > τ P (ER) > τ P (RB).

CW-laser induced microchannels in dye-polymethacrylic acid films

OpenAIRE

M.A. Camacho-López

2007-01-01

In this work we report on the formation of microchannels on dye-polymethacrylic acid films using a cw-laser. A focalized beam of a He-Ne laser (632.8 nm emission line) was used to form microchannels on the films. It was found that there exists a laser power density threshold for a pit formation that depends on the dye concentration. The dimensions of the laser-induced channels are dependent on the laser power density. Microchannel formation in the transparent polymethacrylic acid films was no...

Skin sensitization quantitative risk assessment for occupational exposure of hairdressers to hair dye ingredients.

Science.gov (United States)

Goebel, Carsten; Diepgen, Thomas L; Blömeke, Brunhilde; Gaspari, Anthony A; Schnuch, Axel; Fuchs, Anne; Schlotmann, Kordula; Krasteva, Maya; Kimber, Ian

2018-06-01

Occupational exposure of hairdressers to hair dyes has been associated with the development of allergic contact dermatitis (ACD) involving the hands. p-Phenylenediamine (PPD) and toluene-2,5-diamine (PTD) have been implicated as important occupational contact allergens. To conduct a quantitative risk assessment for the induction of contact sensitization to hair dyes in hairdressers, available data from hand rinsing studies following typical occupational exposure conditions to PPD, PTD and resorcinol were assessed. By accounting for wet work, uneven exposure and inter-individual variability for professionals, daily hand exposure concentrations were derived. Secondly, daily hand exposure was compared with the sensitization induction potency of the individual hair dye defined as the No Expected Sensitization Induction Levels (NESIL). For PPD and PTD hairdresser hand exposure levels were 2.7 and 5.9 fold below the individual NESIL. In contrast, hand exposure to resorcinol was 50 fold below the NESIL. Correspondingly, the risk assessment for PPD and PTD indicates that contact sensitization may occur, when skin protection and skin care are not rigorously applied. We conclude that awareness of health risks associated with occupational exposure to hair dyes, and of the importance of adequate protective measures, should be emphasized more fully during hairdresser education and training. Copyright © 2018 Elsevier Inc. All rights reserved.

High Excitation Transfer Efficiency from Energy Relay Dyes in Dye-Sensitized Solar Cells

KAUST Repository

Hardin, Brian E.

2010-08-11

The energy relay dye, 4-(Dicyanomethylene)-2-methyl-6-(4- dimethylaminostyryl)-4H-pyran (DCM), was used with a near-infrared sensitizing dye, TT1, to increase the overall power conversion efficiency of a dye-sensitized solar cell (DSC) from 3.5% to 4.5%. The unattached DCM dyes exhibit an average excitation transfer efficiency (EÌ?TE) of 96% inside TT1-covered, mesostructured TiO2 films. Further performance increases were limited by the solubility of DCM in an acetonitrile based electrolyte. This demonstration shows that energy relay dyes can be efficiently implemented in optimized dye-sensitized solar cells, but also highlights the need to design highly soluble energy relay dyes with high molar extinction coefficients. © 2010 American Chemical Society.

Removal of Reactive-dyes from Textile Plant Effluents Using Polyvinyl Alcohol-coated Active Carbon obtained from Sesame Seeds

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Sheida Moradi- Nasab

2016-09-01

Full Text Available In this study, the adsorption of active carbon derived from waste sesame seeds coated with polyvinyl alcohol (AC/PVA was investigated for removing red 198 and blue 19 reactive dyes from textile effluents. The batch process was carried out to identify such parameters as pH, adsorbent dose, contact time, and initial dye concentration involved in the dye removal adsorption capacity of AC/PVA. Also, batch kinetic and isotherm experiments were conducted. Results indicated that the maximum dye removal was obtained in an acidic pH over 90 min of contact time and that adsorption rates followed the pseudo-second-order kinetics. Blue and red dye concentrations were determined using the spectrophotometric method at 590 and 517 nm, respectively. It may be concluded that AC/PVA is capable of removing blue and red reactive dyes and can be used as an efficient, cheap, and accessible adsorbent for treating textile effluents.

Removal of Reactive Red 141 Dye from Synthetic Wastewater by Electrocoagulation Process: Investigation of Operational Parameters

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Elham Rahmanpour Salmani

2016-01-01

Full Text Available Release of textile industries waste especially their dying effluent impose a serious pollution on the environment. Reactive dyes are one of the most used dyes which are recalcitrant to conventional treatment processes. In the performed project, the effectiveness of electrocoagulation process was studied on decolorization. RR141 was selected as model dye and treatment process was performed in a simple batch of electrocoagulation (EC cell using iron electrodes. Central Composite Design (CCD was used to plan study runs. Experiments were done under 5 levels of various operational parameters at bench scale. Initial concentration of dye was varied among 50 and 500ppm, pH ranging from 4-12; retention time was ranged between 3-30 minutes, 1-3cm was selected as the distance between electrodes, and current intensity studied under the range of 5-30 mA/cm2. EC treatment process of dyestuff wastewater was satisfactory at high levels of current density, pH, and retention time. While increasing the initial dye concentration and electrodes gap had a negative effect on decolorization performance. Determined optimal conditions to treat 200ml of sample were including pH: 9.68, electrode gap: 1.58cm, dye concentration: 180ppm, retention time: 10.82 minutes, and current intensity: 22.76mA/cm2. Successful removal of the model dye about 99.88% was recorded in the mentioned values of variables. Simple design and operation of the experiments can be an interesting option for implementation and applying of inexpensive electrocoagulation treatment process which was successful to reach nearly a complete decolorization.

Henna (Lawsonia inermis L.) Dye-Sensitized Nanocrystalline Titania Solar Cell

International Nuclear Information System (INIS)

Jasim, Kh.E.; Al-Dallal, Sh.; Hassan, A.M.

2012-01-01

Low-cost solar cells have been the subject of intensive research activities for over half century ago. More recently, dye-sensitized solar cells (DSSCs) emerged as a new class of low-cost solar cells that can be easily prepared. Natural-dye-sensitized solar cells (NDSSCs) are shown to be excellent examples of mimicking photosynthesis. The NDSSC acts as a green energy generator in which dyes molecules adsorbed to nanocrystalline layer of wide bandgap semiconductor material harvest photons. In this paper we investigate the structural, optical, electrical, and photovoltaic characterization of two types of natural dyes, namely, the Bahraini Henna and the Yemeni Henna, extracted using the Soxhlet extractor. Solar cells from both materials were prepared and characterized. It was found that the levels of open-circuit voltage and short-circuit current are concentration dependent. Further suggestions to improve the efficiency of NDSSC are discussed

Henna (Lawsonia inermis L. Dye-Sensitized Nanocrystalline Titania Solar Cell

Directory of Open Access Journals (Sweden)

Khalil Ebrahim Jasim

2012-01-01

Full Text Available Low-cost solar cells have been the subject of intensive research activities for over half century ago. More recently, dye-sensitized solar cells (DSSCs emerged as a new class of low-cost solar cells that can be easily prepared. Natural-dye-sensitized solar cells (NDSSCs are shown to be excellent examples of mimicking photosynthesis. The NDSSC acts as a green energy generator in which dyes molecules adsorbed to nanocrystalline layer of wide bandgap semiconductor material harvest photons. In this paper we investigate the structural, optical, electrical, and photovoltaic characterization of two types of natural dyes, namely, the Bahraini Henna and the Yemeni Henna, extracted using the Soxhlet extractor. Solar cells from both materials were prepared and characterized. It was found that the levels of open-circuit voltage and short-circuit current are concentration dependent. Further suggestions to improve the efficiency of NDSSC are discussed.

Degradation of direct azo dye by Cucurbita pepo free and immobilized peroxidase.

Science.gov (United States)

Boucherit, Nabila; Abouseoud, Mahmoud; Adour, Lydia

2013-06-01

Enzymatic decolourization of the azo dye, Direct Yellow (DY106) by Cucurbita pepo (courgette) peroxidase (CP) is a complex process, which is greatly affected by pH, temperature, enzyme activity and the concentrations of H2O2 and dye. Courgette peroxidase was extracted and its performance was evaluated by using the free-CP (FCP) and immobilized-CP (ICP) forms in the decolourization of DY106. Immobilization of peroxidase in calcium alginate beads was performed according to a strategy aiming to minimize enzyme leakage and keep its activity at a maximum value by optimizing sodium alginate content, enzyme loading and calcium chloride concentration. The initial conditions at which the highest DY106 decolourization yield was obtained were found at pH 2, temperature 20 degrees C, H2O2 dose 1 mmol/L (FCP) and 100 mmol/L (ICP). The highest decolourization rates were obtained for dye concentrations 50 mg/L (FCP) and 80 mg/L (ICP). Under optimal conditions, the FCP was able to decolorize more than 87% of the dye within 2 min. While with ICP, the decolourization yield was 75% within 15 min. The decolourization and removal of DY106 was proved by UV-Vis analysis. Fourier transform infrared (FT-IR) spectroscopy analysis was also performed on DY106 and enzymatic treatment precipitated byproduct.

Degradation of textile dyes by cyanobacteria.

Science.gov (United States)

Dellamatrice, Priscila Maria; Silva-Stenico, Maria Estela; Moraes, Luiz Alberto Beraldo de; Fiore, Marli Fátima; Monteiro, Regina Teresa Rosim

Dyes are recalcitrant compounds that resist conventional biological treatments. The degradation of three textile dyes (Indigo, RBBR and Sulphur Black), and the dye-containing liquid effluent and solid waste from the Municipal Treatment Station, Americana, São Paulo, Brazil, by the cyanobacteria Anabaena flos-aquae UTCC64, Phormidium autumnale UTEX1580 and Synechococcus sp. PCC7942 was evaluated. The dye degradation efficiency of the cyanobacteria was compared with anaerobic and anaerobic-aerobic systems in terms of discolouration and toxicity evaluations. The discoloration was evaluated by absorption spectroscopy. Toxicity was measured using the organisms Hydra attenuata, the alga Selenastrum capricornutum and lettuce seeds. The three cyanobacteria showed the potential to remediate textile effluent by removing the colour and reducing the toxicity. However, the growth of cyanobacteria on sludge was slow and discoloration was not efficient. The cyanobacteria P. autumnale UTEX1580 was the only strain that completely degraded the indigo dye. An evaluation of the mutagenicity potential was performed by use of the micronucleus assay using Allium sp. No mutagenicity was observed after the treatment. Two metabolites were produced during the degradation, anthranilic acid and isatin, but toxicity did not increase after the treatment. The cyanobacteria showed the ability to degrade the dyes present in a textile effluent; therefore, they can be used in a tertiary treatment of effluents with recalcitrant compounds. Copyright © 2016 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. All rights reserved.

Anaerobic azo dye reduction

OpenAIRE

Zee, van der, F.P.

2002-01-01

Azo dyes, aromatic moieties linked together by azo (-N=N-) chromophores, represent the largest class of dyes used in textile-processing and other industries. The release of these compounds into the environment is undesirable, not only because of their colour, but also because many azo dyes and their breakdown products are toxic and/or mutagenic to life. To remove azo dyes from wastewater, a biological treatment strategy based on anaerobic reduction of the azo dye...