Search results for: Metanil Yellow (Aqueous Solution)





Micro-electromembrane extraction using multiple free liquid membranes and acceptor solutions - Towards selective extractions of analytes based on their acid-base strength.
This work investigated selective micro-electromembrane extractions (μ-EMEs) of the colored indicators metanil yellow and congo red (visual proof-of-principle) and the small drug substances nortriptyline, papaverine, mianserin, and citalopram (model analytes) based on their acid-base strength. With two free liquid membranes (FLMs), the target analytes were extracted from aqueous donor solution, across FLM 1 (1-pentanol, 1-ethyl-2-nitrobenzene (ENB) or 4-nitrocumene (4-NC)), into aqueous acceptor solution 1, further across FLM 2 (1-pentanol, ENB or 4-NC), and finally into aqueous acceptor solution 2. All phases had volumes between 1.0 and 1.5 μL and extractions were promoted by 200-300 V d.c. applied across the five-phase μ-EME system formed in a perfluoroalkoxy capillary tubing. The anode was located in acceptor solution 2 and the cathode was located in donor solution for μ-EMEs of acidic analytes, and locations of the electrodes were vice versa for μ-EMEs of basic analytes. After μ-EME, donor solution and acceptor solution 1 and 2 were analyzed by capillary electrophoresis or liquid chromatography-mass spectrometry. The model analytes migrated efficiently in the proposed μ-EME system, their migration behavior was controlled by pH in aqueous solutions and their selective fractionation into acceptor solution 1 and 2 was demonstrated based on their acid-base strength. Under optimal conditions, acceptor solution 2 contained 60% nortriptyline (pK = 10.5) and less than 1% papaverine (pK = 6.0) and acceptor solution 1 contained 17% nortriptyline and 27% papaverine after 15 min of μ-EME. The five-phase μ-EME system was also compatible with human plasma samples. Work is in progress to further increase the fractionation capability, and to implement the concept into microfluidic platforms.
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D Luciferin, free acid *U
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D Luciferin, free acid *U
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Green synthesis of Y2O3:Dy(3+) nanophosphor with enhanced photocatalytic activity.
Facile and green route was employed for the synthesis of Y2O3:Dy(3+) (1-11 mol%) nanostructures (NSs) using Aloe vera gel as fuel. The formation of different morphologies of Y2O3:Dy(3+) NSs were characterized by SEM, TEM and HRTEM. PXRD data and Rietveld analysis evident the formation of single phase Y2O3 with cubic crystal structure. The influence of Dy(3+) ion concentration on the structure morphology, UV absorption, PL emission and photocatalytic activity of NSs were investigated. NSs exhibited an intense warm white emission with CIE chromaticity coordinates (0.32, 0.33) and average CCT value ∼5525 K which corresponds to vertical day light. The control of Dy(3+) ion on Y2O3 matrix influences the photocatalytic decolorization of Metanil Yellow as a model compound was evaluated. The enhanced photocatalytic activities of core shell structured Y2O3:Dy(3+) (1 mol%) was attributed to co-operation effect of dopant concentration, crystallite size, textural properties and capability for reducing electron-hole pair recombination. Further, the recycling catalytic ability of Y2O3:Dy(3+) (1 mol%) nanostructure was also evaluated and found promising photocatalytic performance with negligible decrease in decolorization efficiency even after sixth successive cyclic runs. Considering its green, facile synthesis and recyclable feature from an aqueous solution, the present Y2O3:Dy(3+) (1 mol%) nanophosphor can be considered as one of the ideal photocatalyst for various potential applications.
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Synthesis of magnetic biocomposite for efficient adsorption of azo dye from aqueous solution.
A novel magnetic biocomposite was synthesized using metal chlorides and aquatic macrophytes by co-precipitation method. The resulting product, magnetic biocomposite was characterized by Fourier transform infrared spectra (FTIR), X-ray diffraction (XRD), Energy-dispersive X-ray spectroscopy (EDX) and Scanning electron microscope (SEM). The adsorption performance of the magnetic biocomposite was tested with removal of Metanil Yellow dye from aqueous solution. The effect of influencing parameters such as initial dye concentration, solution pH and agitation were investigated. The equilibrium isotherm was well described by the Langmuir model with the with maximum adsorption capacity of 90.91mg/g. Adsorption kinetics experiments were carried out and the data were well fitted by a pseudo-second-order equation. The results revealed that the magnetic biocomposite could efficiently adsorb the azo dyes from aqueous solution, and the spent adsorbents could be recovered completely by magnetic separation process. Therefore, the prepared magnetic biocomposite could thus be used as promising adsorbent for the removal of azo dyes from polluted water.
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Focused laser lithographic system with sub-wavelength resolution based on vortex laser induced opacity of photochromic material.
A focused laser lithographic system combines with vortex laser induced opacity of photochromic layer to write patterns with linewidth below wavelength. A photochromic layer is formed by coating the mixture of metanil yellow and aqueous PVA solution on the photoresist layer. In our system, the center of a lithographic laser with a 405 nm wavelength coincides with the center of vortex laser with a 532 nm wavelength. When a photochromic layer is illuminated by both lasers simultaneously, the absorbance for the lithographic laser decreases at the hollow region of the vortex laser but increases at its annular region, so that a transparent aperture for the lithographic laser is created and its size could be tuned by changing the power of vortex laser; therefore, the linewidth of written patterns is variable. Experimentally, using a 20× lens (NA = 0.4), this system condenses the linewidth of written patterns from 6614 to 350 nm.
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Degradation of azo dye with dirhodium(II) caprolactamate as heterogeneous catalyst.
The kinetics of the oxidative degradation of an azo dye Metanil Yellow (MY) was investigated in aqueous solution using dirhodium(II) caprolactamate, Rh(2)(cap)(4), as a catalyst in the presence of H(2)O(2) as oxidizing agent. The reaction process was followed by UV/Vis spectrophotometer. The decolorization and degradation kinetics were investigated and both followed a pseudo-first-order kinetic with respect to the [MY]. The effects of various parameters such as H(2)O(2) and dye concentrations, the amount of catalyst and temperature have been studied. The studies show that Rh(2)(cap)(4) is a very effective catalyst for the formation of hydroxyl radicals HO(•) which oxidized and degraded about 92% of MY into CO(2) and H(2)O after 24 h as measured by total carbon analyzer.
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Process development for the batch and bulk removal and recovery of a hazardous, water-soluble azo dye (Metanil Yellow) by adsorption over waste materials (Bottom Ash and De-Oiled Soya).
Bottom Ash and De-Oiled Soya have been used as adsorbents for the removal of a hazardous azo dye-Metanil Yellow from its aqueous solutions. Adsorption of Metanil Yellow on these adsorbents has been studied as function of time, temperature, concentration and pH. Batch adsorption studies, kinetic studies and column operations enabled extraction of lethal dye from wastewaters. Adsorption equilibrium data confirms both Langmuir and Freundlich isotherm models and monolayer coverage of dye over adsorbents. Kinetic data have been employed to calculate specific rate constants, indicating thereby involvement of first order kinetics in the on-going adsorption and activation energy was determined as 0.813 and 1.060 kJ mol(-1) for Bottom Ash and De-Oiled Soya, respectively. For both adsorbents, the adsorption process has been found governing by film diffusion, over the entire concentration range. Column operations have also been performed for the bulk removal of the dye and also to examine the practical utilization of fixed bed adsorption technique in elimination of dangerous effluent. Saturation factors for Bottom Ash and De-Oiled Soya columns have been calculated as 99.15 and 99.38%, respectively. Attempts have also been made to regenerate the dye from the exhausted columns using aqueous sodium hydroxide as eluent.
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Kinetics and thermodynamics of the adsorption of some dyestuffs from aqueous solution by poplar sawdust.
The effect of temperature on the adsorption of metanil yellow (MY) (acidic) and methylene blue (MB) (basic) by poplar sawdust was investigated. In addition, the amounts of NaHCO(3), Na(2)CO(3), NaOH and C(2)H(5)ONa adsorbed by 1g of poplar sawdust to determine its surface acidity were also determined. Kinetical data obtained at different temperatures (293 K, 313 K and 333 K) for the adsorption of each dyestuff by poplar sawdust were applied to the pseudo first-order, the pseudo second-order and the intraparticle diffusion equations, and the rate constants of first-order adsorption (k(1)), the rate constants of second-order adsorption (k(2)) and intraparticle diffusion rate constants (k(p)) at these temperatures were calculated, respectively. In addition, isothermal data obtained at different temperatures (293 K, 313 K and 333 K) for the adsorption of each dyestuff by poplar sawdust were applied to thermodynamical equations, and thermodynamical parameters (DeltaG, DeltaH and DeltaS) were also calculated.
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Competitive adsorption of dye metanil yellow and RB15 in acid solutions on chemically cross-linked chitosan beads.
One kind of adsorbent with a high adsorption capacity for anionic dyes was prepared using ionically and chemically cross-linked chitosan beads. A batch system was applied to study the adsorption behavior of one acid dye (MY, metanil yellow) and one reactive dye (RB15, reactive blue 15) in aqueous solutions by the cross-linked chitosan beads. The adsorption capacities was 3.56 mmol g(-1) (1334 mg g(-1)) for dye MY and 0.56 mmol g(-1) (722 mg g(-1)) for dye RB15 at pH4, 30 degrees C. The Langmuir model agreed very well with the experimental data (R(2)>0.996). The kinetics of adsorption for a single dye and the kinetics of removal of ADMI color value in mixture solutions at different initial dye concentrations were evaluated by the nonlinear first-order and second-order models. The first-order kinetic model fits well with the dynamical adsorption behavior of a single dye for lower initial dye concentrations, while the second-order kinetic model fits well for higher initial dye concentrations. The competitive adsorption favored the dye RB15 in the mixture solution (initial conc. (mM): MY=1.34; RB15=1.36); while it favored the dye MY in the mixture solution (initial conc. (mM): MY=3.00; RB15=1.34) and the adsorption kinetics for dye RB15 has the tendency to shift to a slower first order model.
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Utilization of industrial waste products as adsorbents for the removal of dyes.
A number of low cost adsorbents from steel and fertilizer industries wastes have been prepared and investigated for the removal of anionic dyes such as ethyl orange, metanil yellow and acid blue 113 from aqueous solutions. The results indicate that inorganic wastes, i.e. blast furnace dust, sludge and slag from steel plants are not suitable for the removal of organic materials, whereas a carbonaceous adsorbent prepared from carbon slurry of fertilizer industry was found to adsorb 198, 211 and 219mg/g of ethyl orange, metanil yellow and acid blue 113, respectively. The adsorption of dyes on this adsorbent was studied as a function of contact time, concentration, particle size and temperature by batch method. The adsorption isotherm conformed to Langmuir model and the adsorption was found to be exothermic and physical in nature. Kinetic data conforms to Lagergren's equation with good correlation coefficients varying from 0.9998 to 0.9999 indicating that the adsorption is a first-order process. The adsorption data on carbonaceous adsorbent was compared to a standard activated charcoal sample and it was found that the prepared adsorbent is about 80% as efficient as standard activated charcoal and therefore, can be used as low cost alternative ( approximately 100 US dollars per ton) for colour removal from effluents.
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