Removal of Congo Red dye from its aqueous solution using natural coagulants

The textile dyeing industry consumes large quantities of water and produces large volumes of wastewater from different processes in dyeing and finishing processes. The low-cost, easily available naturally prepared coagulants like Surjana seed powder (SSP), Maize seed powder (MSP) and Chitosan as an ideal alternative to recent expensive coagulant methods for Congo Red (CR) dye removal has been investigated in this study. Various process parameters like pH, coagulant dose, flocculation time and temperature and also its optimization were exploited. The maximum percentage CR removal was found to be 98.0, 94.5 and 89.4 for SSP, Chitosan and MSP, respectively, at pH 4.0, coagulant dose of 25 mg/l, flocculation time 60 min and temperature of 340 K. The Sludge Volume Index (SVI) and turbidity were calculated for these parameters including process optimization. SSP found more preferable for CR removal and Chitosan was a better coagulant, which corresponds to SVI than the other coagulants investigated.     

The effect of gamma radiation on biodegradability of morpholine in aqueous solution

The effect of -radiation on the aqueous solution of morpholine was studied on the basis of UV spectrum measurement, COD /chemical oxygen demand/, TOC /total organic carbon/ and STOD /short-term oxygen demand/ determination and Pitter's kinetic test of biodegradation. The biodegradability of the model solution after irradiation became substantially worse.     

Role of reactive intermediates in the radiolytic degradation of Acid Red 1 in aqueous solution

The role of reactive intermediates of water radiolysis (e_aq⁻, H, HO, O₂⁻/HO₂) in decoloration and mineralization of aqueous solutions of Acid Red 1 dye was investigated. The decoloration is highly effective in the reactions of e_aq⁻ and H, and less effective in HO reactions. The O₂⁻/HO₂ pair does not take part in decoloration. For mineralization, which is an oxidative degradation, HO radicals are needed: the efficiency increases with the dissolved oxygen concentration. The reactions of the O₂⁻/HO₂ radical pair slightly increase the rate of mineralization. Iron and copper ions (possible constituents of waste waters) in low concentration do not influence the reactions.     

Gamma radiolysis of anthraquinone dye aqueous solution

The decoloration of Acid Blue 62 in aqueous solution was mainly attributed to the attack of the e _aq ^– and OH radicals on the dye molecule. The mechanisms of these reactions were investigated in detail including the influence of pH, dose rate and oxygen.     

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

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 °C), dosimetric response was found to be stable up to 22 days while at higher temperature (ca. 30 °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 °C) in dark.     

The radiation-induced degradation of a diazo dye in aqueous solution,II

The effect of -radiation on the color intensity of aerated, deaerated and oxygenated aqueous solutions of a diazo dye (Helion Red 8B) has been investigated. The decoloration yields of Helion Red 8B neutral aqueous solution, G(-Dye), for the nitrogen-, oxygen- and aerated-saturated solutions were found to be 0.77, 0.46 and 0.36 in the respective early stage. The rate constant for the reaction of the OH radical with the HR8B dye, obtained from competition kinetics using ethanol, was found to be 1.3·10¹⁰ M^–1·s^–1. In aerated solutions (pH 3), the G(-Dye) decreased markedly upon the addition of a very small amount of ethanol. Suggestions are made for possible use of the dye as a radiation dosimeter in the dose range of 0.1 to 2 kGy.     

The effect of cation size on ion pairing of methyl orange dye with tetraalkylammonium and benzyltrialkylammonium ions in aqueous solution

Formation constants have been measured by a solvent distribution method for the ion pairing of an arene sulfonate, methyl orange dye, with two series of quaternary ammonium ions: R₄N⁺(R=Et,n-Pr,n-Bu, andn-Pent) and C₆H₅CH₂R₃N⁺ (R=Me, Et,n-Pr,n-Bu,n-Pent, andn-Hex). Ion pairing increases dramatically as the length of the R group increases beyond butyl. Using a hard-sphere model for contact ion pairs, it is estimated that coulombic attraction contributes about –kT to the binding free energy and decreases slightly with increasing size of R₄N⁺. Other factors related to solvation effects, of which cosphere overlap predominates, contribute from –2kT to –7kT of binding energy. Plots of logK for association as a function of cation size show an inflection with decreasing slope between R=propyl and R=butyl. Possible causes for the inflection are considered.     

Enhanced visible-light-driven photodegradation of Acid Orange 7 azo dye in aqueous solution using Fe-N co-doped TiO2

FeN -co-doped TiO₂ photocatalysts are prepared by sol–gel method using titanium tetraisopropoxide, urea and iron(II) acetylacetonate as precursors of titania, nitrogen and iron, respectively. The prepared samples are analysed from chemical-physical point of view by X-ray diffraction (XRD), Raman spectroscopy, UV–Vis diffuse reflectance spectroscopy (UV–Vis DRS), specific surface area measurements and scanning electron microscopy (FESEM). UV–Vis DRS spectra evidence that the co-doping of TiO₂ with N and Fe leads to the narrowing of the band gap value (2.7 eV) with respect to Fe-doped TiO₂ (2.8 eV) and N-doped TiO₂ (2.9–3 eV). XRD patterns show that photocatalysts are mainly in anatase phase and Fe and N ions are successfully incorporated into the TiO₂ lattice. The average crystallite size of Fe-N co-doped TiO₂ is slightly lower than the other samples and equal to about 7 nm and the specific surface area of the co-doped sample results to be 117 m² g⁻¹. Photocatalytic performances of all prepared samples are evaluated by analysing the degradation of Acid Orange 7 azo dye under visible light irradiation. Photocatalytic efficiency obtained using FeN co-doped TiO₂ strongly increases compared to undoped TiO₂, N-doped TiO₂ and Fe-doped TiO₂ photocatalysts. In detail, using the co-doped photocatalyst, dye discoloration and mineralization result equal to about 90 and 83% after 60 min of LEDs visible light irradiation, underlining the best performances of the FeN co-doped TiO₂ photocatalyst both in terms of treatment time and electric energy consumption.     

Removal of an azo-metal complex textile dye from colored aqueous solutions using an agro-residue

The pine leaves which are an agricultural residue were used in its natural form as biosorbent for the removal of Acid Yellow 220 (AY 220) dye from aqueous solutions. The sorption experiments were carried out as a function of solution pH, biosorbent dosage, biosorbent size, dye concentration, temperature, contact time and ionic strength. The sorption isotherms closely followed the Langmuir model. The monolayer sorption capacity of the pine leaves for AY 220 was found as 40.00 mg g^{− 1}. It was shown that pseudo-second order equation could best describe the sorption kinetics. The thermodynamic data indicated that the sorption system was spontaneous, endothermic and physical process. Based on the results of present investigation, the pine leaves could be used as a suitable alternative biosorbent for the elimination of AY 220 from aqueous solutions.     

The rheology of lignosulfonate-stabilized dispersions of a textile dye

Rheological measurements of typical industrial, aqueous dispersion of a mono-azo dye stabilized with lignosulfonates were interpreted by means of the Ree-Eyring model to evaluate the degree of flocculation, the degree of agglomeration, and the particle—particle interaction energy between agglomerates. The effects of pH, ionic strength, temperature, and sample age on these parameters were measured. Mechanism underlying these effect were deduced from the above results when combined with electrophoretic mobilities of the dispersed phase and the properties of lignosulfonate solutions. In additions, the ξ potentials and Debye lengths demonstrated that the controlled flocculation in concentrated dispersion is predominantly due to steric stabilization, whereas deflocculation and stabilization of the dispersion after dilution with water is due to electrostatic repulsion.     

Geopolymeric adsorbents from fly ash for dye removal from aqueous solution

Adsorbents from coal fly ash treated by a solid-state fusion method using NaOH were prepared. It was found that amorphous aluminosilicate geopolymers would be formed. These fly ash-derived inorganic polymers were assessed as potential adsorbents for removal of some basic dyes, methylene blue and crystal violet, from aqueous solution. It was found that the adsorption capacity of the synthesised adsorbents depends on the preparation conditions such as NaOH:fly-ash ratio and fusion temperature with the optimal conditions being at 1.2:1 weight ratio of Na:fly-ash at 250-350 degrees C. The synthesised materials exhibit much higher adsorption capacity than fly ash itself and natural zeolite. The adsorption isotherm can be fitted by Langmuir and Freundlich models while the two-site Langmuir model producing the best results. It was also found that the fly ash derived geopolymeric adsorbents show higher adsorption capacity for crystal violet than methylene blue and the adsorption temperature influences the adsorption capacity. Kinetic studies show that the adsorption process follows the pseudo second-order kinetics.     

The influence of radio-frequency radiation on thermal stability of bovine serum albumin in aqueous solution

Protein unfolding events were studied by differential scanning calorimetry (DSC) for bovine serum albumin (BSA) aqueous solutions exposed to radio-frequency radiation. No immediate effect of this radiation on thermal unfolding of BSA was observed. The differences between irradiated and control samples have appeared during the storage of BSA solution. The irradiated samples changed faster than non-irradiated. Our results indicated that the age-related changes were stronger for 3.5 and 5 MHz than for 247 MHz frequency and dependent on energy power of radiation. Deconvolution of DSC traces allowed to study the effect of radio-frequency radiation on each component transition. This revised version was published online in July 2006 with corrections to the Cover Date.     

UV radiation effects on flavocytochrome b2 in dilute aqueous solution

A dilute aqueous solution of flavocytochrome b2 when exposed to inactivating doses of UV radiation at 280 nm underwent reversible loss in activity both under aerated and deaerated conditions. The active site as well as the substrate binding sites were found to be modified in the irradiated enzyme. Irradiation of the enzyme in the UV-C range resulted in partial unfolding of the polypeptide framework. Destruction and/or modification of both tryptophan and tyrosine residues as well as heme moieties took place. Preliminary laser flash photolysis studies suggest that the initial photo-ionization takes place with tryptophan and tyrosine residues with the formation of excited states and radicals, and then rapid transfer of electrons takes place to histidyl and cystinyl sites which might have eventually been altered in the process.     

High energy induced decoloration and mineralization of Reactive Red 120 dye in aqueous solution: A steady state and pulse radiolysis study

Gamma radiation induced decoloration and degradation of aqueous solution of Reactive Red 120 dye (RR-120) have been investigated under different experimental conditions. Rate constants for the reaction of hydrated electron and hydroxyl radical with RR-120 were determined to be 1.2×10¹⁰ and 7.9×10⁹ mol^?1 dm³ s^?1, respectively, by pulse radiolysis technique. The decoloration and degradation efficiency were measured in terms of % decoloration and % TOC, respectively. Decoloration was observed to be most efficient under reducing condition, where the radiolytic yield for the decoloration of dye was determined to be 0.14 μmol/J. The extent of decoloration for both aerated and oxygen saturated solution was almost identical, whereas it decreased in N₂O saturated solution as well as N₂ saturated solution. For a solution having 10.56 μg/ml total organic carbon (TOC) at a dose of 3 kGy, 48% mineralization takes place in oxygen saturated solution whereas under aerated condition same was observed to be lowered to 38%.     

Photocatalytic degradation of carcinogenic Congo red dye in aqueous solution,antioxidant activity and bactericidal effect of NiO nanoparticles

Journal of the Iranian Chemical Society - Face-centered cubic structure of nickel oxide (NiO) nanoparticles with 30&nbsp;nm average size was synthesized by co-precipitation method with some...     

Gamma radiolysis of an aqueous anthraquinone dye solution in the presence of oxygen

Experiments with Acid Blue 62 as a model compound for dyes were performed under steady-state conditions, using deoxygenated solutions as well as those saturated with N₂O, oxygen or oxygen mixed with N₂O. The yield of decoloration served as an indicator for the degradation process. Oxygen seems to inhibit radiation-induced decomposition of the dye in aqueous solution.     

Spectrophotometric investigation of the hetero-association of caffeine and thiazine dye in aqueous solution

The self-association of thiazine dye, Methylene Blue (MB), and its hetero-association with Caffeine (CAF), were studied in aqueous solution by means of spectrophotometry in the visible range of spectrum. Concentration and temperature dependences of molar absorption of the interacting molecules were used to analyse dynamic equilibrium in solution in terms of two-component model of molecular hetero-association. The magnitudes of equilibrium dimerization and hetero-association constants as well as thermodynamic parameters, enthalpy and entropy, were determined. The calculation of the fraction of different types of associates in the mixed solution, containing Methylene Blue and Caffeine, was done. It was concluded that the hetero-association of Methylene Blue and Caffeine molecules results in lower effective concentration of the dye in solution, which may account for the alteration of its biological activity.     

Adsorption of strontium from aqueous solution using activated carbon produced from textile sewage sludges

Different types of activated carbons were prepared by changing the activation temperatures (400–700 °C) and impregnation ratio (sewage sludge: KOH; 1:1, 1:2) and the removal of Sr⁺² from aqueous solution was determined. The maximum adsorption yield (12.11 mg/g) was obtained at 500 °C for 1 h carbonization conditions with impregnation ratio of 1:1. The affecting parameters were analyzed by using central composite design method. The selected parameters were initial pH, temperature, initial strontium concentration and carbon dosage. The analysis of variance was performed in 95% confidence level and checked to fitting of experimental value and predicted value. The significant F was P < 0.05 with a model F value of 19.94 which revealed that this regression is statistically significant. The results of regression analysis indicated that pH and temperature parameters were not individually statistically significant for Sr⁺²sorption. However, the efficiency of strontium sorption increases with the increase in carbon dosage and decreases with the Sr⁺² concentration. Influences of initial pH and temperature, pH and Sr⁺² concentration, temperature and carbon dosage and Sr⁺² concentration and carbon dosage on the adsorption process were considered statistically significant. Adsorption of strontium was described by Freundlich isotherm as a physical adsorption (E = 7.2 kJ/mol). The adsorption reactions were calculated as endothermic, spontaneous and favorable reactions.