Eosin Removal by Cetyl Trimethylammonium-Cloisites: Influence of the Surfactant Solution Type and Regeneration Properties.

The effect of the counteranion of hexadecyltrimethylammonium salts on the physico-chemical properties of organoclays was investigated, using a selected natural clay mineral with a cation exchange capacity of 95 meq/100 g. The uptake amount of C16 cations was dependent on the hexadecyltrimethylammonium (C16) salt solution used, the organoclay prepared from C16Br salt solution exhibited a value of 1. 05 mmole/g higher than those prepared from C16Cl and C16OH salt solutions. The basal spacing of these organoclays was in the range of 1.81 nm to 2.10 nm, indicating a similar orientation of the intercalated surfactants, and could indicated that the excess amount of surfactants, above the cation exchange capacity of 0.95 meq/g could be adsorbed on the external surface of the clay mineral sheets. These organoclays were found to be stable in neutral, acidic, and basic media. The thermal stability of these organoclays was carried out using thermogravimetric analysis and in-situ X-ray diffraction (XRD) techniques. The decomposition of the surfactant occurred at a maximum temperature of 240 °C, accompanied with a decrease of the basal spacing value close to 1.42 nm. The application of these organoclays was investigated to remove an acidic dye, eosin. The removal amount was related to the initial used concentrations, the amount of the surfactants contents, and to the preheated temperatures of the organoclays. The removal was found to be endothermic process with a maximum amount of 55 mg of eosin/g of organoclay. The value decreased to 25 mg/g, when the intercalated surfactants were decomposed. The reuse of these organoclays was limited to four regeneration recycles with a reduction of 20 to 30%. However, noticeable reduction between 35% to 50% of the initial efficiency, was achieved after the fifth cycle, depending of the used organoclays.

A novel green and template free approach for the synthesis of gold nanorice and its utilization as a catalyst for the degradation of hazardous dye.

Herein, we describe a simple, green and template free method for the production of rice shaped gold nanostructures using an aqueous extract of the egg shells of Anas platyrhynchos. The synthesized nanoparticles were characterized by UV-visible, transmission electron microscopy (TEM), selected area electron diffraction pattern (SAED) and FT-IR studies. The UV-visible spectrum of the synthesized gold nanostructures showed a transverse mode surface plasmon resonance peaks (SPR) at around 540nm and a longitudinal mode at 880nm. The TEM and SAED pattern confirmed the morphology, size and crystallographic structure of the synthesized gold nanorice. The synthesized gold nanorice was utilized for the removal of a toxic Eosin Y dye by photodegradation. It was observed that the dye was degraded completely within 1h and the percentage efficiency was found to be 96.1%.

Single stage batch adsorber design for efficient Eosin yellow removal by polyaniline coated ligno-cellulose.

Polyaniline-coated lignin-based adsorbent (PLC) was synthesized and used for uptake of reactive dye eosin yellow (EY) from aqueous solution. The adsorption capability of the adsorbent was found to be more effective than the unmodified adsorbent (LC). In particular, the adsorption capability of the PLC was effective over a wider pH range. This could be owing to its higher point of zero charge, which is more favorable for the uptake of the anionic dye. Adsorption isotherm models suggested a monolayer adsorption was predominant. The mean free energy of adsorption (E(DR)) was found to have values between 8 and 16 kJ mol(-1) which suggests that an electrostatic mechanism of adsorption predominated over other underlying mechanisms. The adsorption process was also found to be spontaneous, with increasing negative free energy values observed at higher temperatures. Chemisorption process was supported by the changes in enthalpy above 40 kJ mol(-1) and by the results of desorption studies. This new adsorbent was also reusable and regenerable over four successive adsorption-desorption cycles. The single stage adsorber design revealed that PLC can be applicable as an effective biosorbent for the treatment of industrial effluents containing EY dye.

Comparison of the efficiency of Cu and silver nanoparticle loaded on supports for the removal of Eosin Y from aqueous solution: Kinetic and isotherm study.

In this study, the efficiency of a novel copper containing ionic liquid based nanoporous organosilica (Cu@IL-ONO) and palladium nanoparticles loaded on activated carbon (Pd-NP-AC) for the removal of Eosin Y from aqueous solution was investigated. The Cu@IL-ONO was prepared by hydrolysis and co-condensation of tetramethoxysilane (TMOS) and 1,3-bis (trimethoxysilylpropyl) imidazolium chloride in the presence of surfactant template following immobilization of copper chloride dihydrate. These materials were characterized by nitrogen adsorption-desorption analysis and scanning electron microscopy (SEM) and subsequently used for the successful removal of Eosin Yellow (EY) from aqueous solution. The effects of pH, contact time, amount of adsorbents, initial dye concentration was optimized and set as following: 0.005g/50mL Cu@IL-ONO and 0.015g/50mL Ag-NP-AC at pH=2 for Cu@IL-ONO and pH=3 for Ag-NP-AC and contact time less than 14min. The experimental removal percentage data at various situations was fitted by conventional isotherm models like Langmuir, Freundlich, Tempkin and Dubinin-Radushkevich (D-R). Judgment based on linear regression coefficient (R(2)) and error analysis show high usability of the Langmuir isotherm for best explanation of experimental data with maximum monolayer adsorption capacities 286 and 250mgg(-1) at room temperatures for Cu@IL-ONO and Ag-NP-AC, respectively. Fitting the corresponding data of removal percentage at various experimental conditions shows the suitability of second order and interparticle diffusion model for interpretation of real data.

Spectral study of fluorone dyes adsorption on chitosan-based polyelectrolyte complexes.

Polyelectrolyte complexes of the chitosan-chondroitin sulfate and chitosan-hyaluronate polycation-polyanion pairs were synthesized and characterized as potential dye adsorbents at different pH levels. Equilibrium isotherm analysis was applied to investigate the efficiency and the mechanism of the adsorption of fluorone dyes (fluorescein, eosin Y, erythrosin B) on the synthesized complexes. The inefficiency of the fluorescein adsorption was proved by two different quantitative spectroscopic methods. The adsorption isotherm for both eosin Y and erythrosin B was adequately described in terms of the Langmuir-Freundlich model. The observed room-temperature phosphorescence of the adsorbed erythrosin B was attributed to the surface inhomogeneity of the synthesized complexes. The revealed variation in the adsorption properties of fluorone dyes was related to the differences in their ionic forms as well as in their polarity and hydrophobicity.

Photocatalytic performance of nitrogen, osmium co-doped TiO2 for removal of eosin yellow in water under simulated solar radiation.

Nitrogen, osmium co-doped TiO2 photocatalysts were prepared by a modified sol-gel method using ammonia as the nitrogen source and osmium tetroxide as the source of osmium. The role of rutile phase OsO2 in enhancing the photocatalytic activity of rutile TiO2 towards the degradation of Eosin Yellow was investigated. The materials were characterised by various techniques that include FTIR, Raman, XRD, SEM, EDS, TEM, TGA and DRUV-Vis. The amorphous, oven dried sample was transformed to the anatase and then the rutile phase with increasing calcination temperature. DRUV-Vis analysis revealed a red shift in absorption with increasing calcination temperature, confirmed by a decrease in the band gap of the material. The photocatalytic activity of N, Os co-doped TiO2 was evaluated using eosin yellow degradation and activity increased with increase in calcination temperature under simulated solar irradiation. The rutile phase of the co-doped TiO2 was found to be more effective in degrading the dye (k(a) = 1.84 x 10(-2) min(-1)) compared to the anatase co-doped phase (k(a) = 9.90 x 10(-3) min(-1)). The enhanced photocatalytic activity was ascribed to the synergistic effects of rutile TiO2 and rutile OsO2 in the N, Os co-doped TiO2.

Biological decolorization of xanthene dyes by anaerobic granular biomass.

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.

Potential biosorbent based on sugarcane bagasse modified with tetraethylenepentamine for removal of eosin Y.

Tetraethylenepentamine (TEPA) modified sugarcane bagasse (SB), a novel biosorbent (TEPA-MSB), was proved to be an effective adsorbent for anionic dyes due to the introduced functional amino groups. FTIR, TG and DSC analysis were employed to characterize the sorbent. The effects of pH, temperature, contact time and initial concentration of dye on the adsorption of eosin Y were investigated. The experimental data fit very well to the Langmuir model, giving a maximum sorption capacity of 399.04 mg/g at 25 °C. And the kinetic data were well described by the pseudo-second-order kinetic model. pH 6 was the optimal pH for eosin Y adsorption, and the maximum adsorption capacity of TEPA-MSB calculated by Langmuir model was 18 times higher than that of SB.

Chemical modification of chitosan by tetraethylenepentamine and adsorption study for anionic dye removal.

To utilize the contribution of introduced amino groups to the adsorption of an anionic dye (eosin Y), a batch adsorption system was applied to study the adsorption of eosin Y from aqueous solution by tetraethylenepentamine (TEPA) modified chitosan (TEPA-CS). Experiments were carried out as a function of particle size, initial pH, agitation rate, adsorbent dosage, agitation period, temperature and initial concentration of eosin Y. The Langmuir and Freundlich models were used to fit the adsorption isotherms. From the values of correlation coefficients (R2), it was observed that the experimental data fit very well to the Langmuir model, giving a maximum sorption capacity of 292.4mg/g at 298K. Kinetic studies showed that the kinetic data were well described by the pseudo-second-order kinetic model. The thermodynamic study revealed negative value of enthalpy change (ΔH°) and free energy change (ΔG°), indicating spontaneous and endothermic nature of the adsorption of eosin Y on to TEPA-CS.

Removal of dye from aqueous solution using a combination of advanced oxidation process and nanofiltration.

In order to have energy and cost effective separation of dyes, a combination of advanced oxidation process (AOP) using Fenton's reagent and nanofiltration (NF) is proposed. Three combinations of AOP and NF are studied using a synthetic solution of eosin dye. Scheme-1 is AOP followed by NF. Scheme-2 is NF followed by AOP. And Scheme-3 is two-step NF. The concentration of eosin dye studied in the first step of each of the schemes is in the range of 70-200mg/l. The operating transmembrane pressures for NF steps are 552, 689 and 828kPa. The crossflow velocities are 0.46, 0.69 and 0.91m/s. The schemes are compared for permeate flux, permeate concentration and duration of operation. In Scheme-1, AOP is conducted for 30min, and then subjected to NF, whereas in Scheme-2, the time needed for AOP is more than 3h to achieve the concentration level of the dye below 1mg/l. Thus, it is found that Scheme-1 is superior to Scheme-2 due to lesser time requirement. However, Scheme-3 involving no AOP, is also suitable for dye separation as the final eosin concentration in the permeate falls below 1mg/l. Scheme-1 is found suitable for dye concentration of 70mg/l and the most appropriate composition of Fenton's reagent is 1665mg/l of H(2)O(2) and 347.5mg/l of FeSO(4)x7H(2)O. Suitable NF operating conditions in step 2 of Scheme-1 is transmembrane pressure of 689kPa and crossflow velocity of 0.91m/s. In Scheme-3, the suitable operating conditions for NF in both the steps are 828kPa transmembrane pressure and 0.91m/s crossflow velocity. Scheme-2 is found to be unsuitable.

Adsorption of eosin dye on activated carbon and its surfactant based desorption.

The performance of activated carbon has been investigated for the adsorption of eosin dye dissolved in water. Eosin is anionic in nature and highly toxic. The effects of initial dye concentration, contact time, pH and temperature on adsorption of eosin by a fixed amount of activated carbon (1.0 g/L) have been studied in batch and column mode. The equilibrium data are successfully fitted to the Freundlich adsorption isotherm. The adsorption rate data are successfully explained by a pseudo second-order kinetic model. Breakthrough curves for column adsorption have also been studied. The regeneration of spent carbon by desorbing the dye has been experimentally investigated applying a surfactant enhanced carbon regeneration (SECR) technique using both cationic and anionic surfactants. An empirical kinetic model for dye desorption from the commercial activated carbon (CAC) using different surfactant and desorption techniques, viz. change in pH, has been proposed. The comparison between the model and the experimental results is found to be satisfactory.

Photocatalytic degradation of two selected textile dye derivatives, eosine yellowish and p-rosaniline, in aqueous suspensions of titanium dioxide.

Thephotocatalytic degradation of two selected textile dye derivatives, eosine yellowish (1) and p-rosaniline (2) has been investigated in aqueous suspensions of titanium dioxide under a variety of conditions. The degradation was studied by monitoring the change in substrate concentration employing UV spectroscopic technique and decrease in Total Organic Carbon (TOC) content as a function of irradiation time under a variety of conditions. The degradation of the dye was studied under different conditions such as pH, catalyst concentration, substrate concentration, different types of TiO2 and in the presence of electron acceptor such as hydrogen peroxide (H2O2), potassium bromate (KBrO3), and ammonium persulphate (NH4)2S2O8) besides molecular oxygen. The degradation rates were found to be strongly influenced by all the above parameters. The photocatalyst Degussa P25 was found to be more efficient as compared with other photocatalyst in the case of p-rosaniline, whereas UV100 was found to be better for the degradation of eosine yellowish. The xanthene dye (1) was found to degrade faster as compared to the triphenylmethane dye (2). The degradation products were analyzed by GC/MS technique and plausible mechanism for the formation of products have been proposed.