Surfactant Modified Zeolite from Cyclone Ash as Adsorbent for Removal of Reactive Orange 16 from Aqueous Solution
1Nuclear and Energy Research Institute (IPEN-CNEN/SP), São Paulo, Brazil
Zeolite synthesized from cyclone ash (ZCA) was modified with various loadings of hexadecyltrimethylammonium bromide (HDTMA-Br) and was used as adsorbent to remove Reactive Orange 16 (RO16), an azo reactive dye, from aqueous solution. The RO16 adsorption efficiencies for ZCA and surfactant-modified zeolites from cyclone ash (SMZCAs) were compared. SMZCAs presented higher RO16 adsorption efficiency than ZCA, and SMZCA with higher loading amount of HDTMA-Br exhibited higher RO16 adsorption efficiency. A series of experiments was conducted to examine the effects of contact time, solution pH, and adsorbent dosage on dye removal. The adsorption kinetic of RO16 onto adsorbents was discussed using the pseudo-first order, pseudo-second order and intra-particle diffusion models, and the pseudo-second order model provided the best correlation of the experimental data. The equilibrium adsorption data were well represented by Langmuir isotherm model with maximum adsorption capacity of 0.58 and 12.6 mg g-1 for ZCA and SMZCA, respectively.The toxicity tests of dye solutions before and after the adsorption treatment were evaluated with D. simlis and V.ficheri.
At a glance: Figures
Keywords: reactive azo dye; cyclone ash, zeolite, cationic surfactant
American Journal of Environmental Protection, 2013 1 (1),
Received December 20, 2012; Revised February 19, 2013; Accepted March 02, 2013Copyright © 2013 Science and Education Publishing. All Rights Reserved.
Cite this article:
- Fungaro, Denise A., Sueli I. Borrely, and Terezinha E.M. Carvalho. "Surfactant Modified Zeolite from Cyclone Ash as Adsorbent for Removal of Reactive Orange 16 from Aqueous Solution." American Journal of Environmental Protection 1.1 (2013): 1-9.
- Fungaro, D. A. , Borrely, S. I. , & Carvalho, T. E. (2013). Surfactant Modified Zeolite from Cyclone Ash as Adsorbent for Removal of Reactive Orange 16 from Aqueous Solution. American Journal of Environmental Protection, 1(1), 1-9.
- Fungaro, Denise A., Sueli I. Borrely, and Terezinha E.M. Carvalho. "Surfactant Modified Zeolite from Cyclone Ash as Adsorbent for Removal of Reactive Orange 16 from Aqueous Solution." American Journal of Environmental Protection 1, no. 1 (2013): 1-9.
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In Brazil, the coal used in power plants is pulverized and burned inside a boiler, producing bottom ash (15-20 wt.%) of the bulk solid combustion-by-products produced), which falls inside the boiler, and ﬂy ash (80-85 wt.%) . The fly ash is a fine-grained, powdery particulate material that is carried off in the flue gas and usually collected from the flue gas by means of electrostatic precipitators, baghouses, or mechanical collection devices such as cyclones .
Cyclones are low-cost, low-maintenance centrifugal collectors that are typically used to remove particulates in the size range of 10-100 microns. The cyclone fly ash is the ash fraction that has been carried through the flue gas channels into the cyclone and precipitated there. Technically speaking, cyclone ash is the ash fraction that has been trapped in the cyclone.
During combustion most of the heavy metals in the fuel are retained in the ash. The various ash fractions such as bottom ash, cyclone ash and baghouse filter ash may contain relatively high concentrations of heavy metals . Combustion acts like a thermodynamic separation process for the different inorganic materials in the fuel. Elements with a low volatility will concentrate in the bottom ash, while more volatile elements will concentrate in the fly ash . The consequence of this separation effect in combustion plants is that the different ash fractions have a different chemical composition. Before ash residue can be utilized or disposed of in a landfill, its chemical as well as extraction (leaching) characteristics must be known.
Fly ash from baghouse filter produced in the Brazilian power plant is mostly recycled as cement raw material to be used in civil engineering materials. However, cyclone ash does not ﬁnd at present time a commercial application; rather, it is usually stored in abandoned surface mine or dumped in landﬁlls in the vicinity of the power plant.
The main drawback of coal-fired power plants in Brazil is the high production of ash. The synthesis of zeolites has produced an environmentally friendly and economically viable way of recycling coal fly ash. The initial findings indicate that zeolite synthesized from Brazilian fly ash used as low cost adsorbent has high adsorptive capacity for dyes from water [5, 6, 7].
It is known that although zeolites have little afﬁnity toward organic pollutants, permanent negative charges in their crystal structures enable them to be modiﬁed by cationic surfactants so that they better retain organic pollutants [8, 9, 10].
The most commonly used surfactant for zeolite surface modiﬁcation is hexadecyltrimethylammonium bromide (HDTMA-Br), in which each molecule is composed of a hydrophilic and positively charged head group, and a hydrophobic tail. HDTMA-Br may form monolayers and/or bi-layers on the zeolite surface [11, 12, 13, 14, 15].
It is proposed that cyclone ash be used as raw material for zeolite synthesis. To the best of the authors’ knowledge, the preparation of surfactant-modiﬁed zeolite synthesis from cyclone ash and the removal of dyes by this adsorbent have never been reported. Cyclone ash samples contained larger particles than fabric filter and electrostatic precipitator ash samples and showed lower cytotoxicity, very little mutagenicity and lower concentrations of trace elements [1, 16].
Reactive Orange 16 (RO16) is one of the reactive azo dyes most intensively produced and used globally. High water solubility, excellent coloring properties and covalent bonding with both natural and synthetic textile fibers are the major advantages of this dye class. The reactive dyeing process is accompanied by the loss of 10-50% of the dye due to a hydrolysis reaction involving the vinyl group (dye) under alkaline dyeing conditions, giving rise to a highly colored effluent .
Comparative use of bacterial, algal and protozoan tests to study toxicity of various dyes was evaluated. RO16 was the only dye tested that exhibited mutagenic eﬀects in both the presence and absence of metabolic activation, which indicated that both substitution and frameshift mutations were induced by the compound acting like a direct and indirect mutagen .
In a previous paper  it was proposed, the use of zeolite from fly ash collected in baghouse filter as an adsorbent for the removal of reactive orange 16 from aqueous solution. Continuing the application of this adsorbent, in the present work, we investigated the adsorption capacities of surfactant-modiﬁed zeolite from cyclone fly ash. This study helps to understand the adsorption properties and potential applications of unmodiﬁed and modiﬁed zeolites for dye removal from aqueous environments.
All the reagents used for experimental studies were of analytical grade. The samples of coal fly ash from cyclone filter (CCA) were obtained from a coal-fired power plant located at Figueira County, in Paraná State, Brazil. The quaternary ammonium salt hexadecyltrimethylammonium bromide (HDTMA-Br, Merck), with molar mass mol-1 and minimum 99% active substance, was used. Reactive Orange 16 dye (RO16; C.I. 17757; C20H17N3Na2O11S3; 617.54 g mol-1; λmax = 493 nm) was obtained from Sigma-Aldrich with a dye content of 50% and was used without further puriﬁcation. A stock solution of RO16 was prepared in double distilled water and the solutions for adsorption tests were prepared by diluting it. Concentrations of the aqueous solutions of dye were monitored on UV/Visible spectrophotometer (Varian – model Cary 1E). As shown in Figure 1, RO16 has two sulfonate groups, which have negative charges in aqueous solution.
CCA (30g) was mixed with 240mL of 3.5mol L-1 aqueous NaOH solution in a 300mL Teflon vessel. This mixture was heated to 100°C in oven for 24h. After finishing of the process, the suspension was filtered with 4A quantitative filter paper. The zeolite from cyclone fly ash (ZCA) was repeatedly washed with deionized water until the pH of washing water reach ~ 11 and dried at 50°C for 12h . Twenty-five grams of ZCA were mixed with 0.5L of HDTMA-Br solution at varied concentrations ranged between 0.9mmol L-1 and 20mmol L-1. The mixture of zeolite and HDTMA-Br solution was stirred for 7 h at 120rpm and 25°C. The suspension was filtered and the solid was dried in oven at 50°C for 12h . Zeolites modiﬁed with 0.9, 1.8, 9.0, and 20mmol L-1 of HDTMA-Br solutions were named as SMZCA-0.9, SMZCA-1.8 and SMZCA-20, respectively. SMZCA-20 was selected for characterizations.2.3.Characterization of Materials
Instrumental neutron activation analysis (INAA) was used to determine concentrations of elements of materials. About 100mg of CCA, ZCA, SMZCA-20 and reference material were weighted in polyethylene bags. The accuracy of the results was determined using IAEA standard reference material SOIL-7. For irradiation, the samples, reference material and element standards were simultaneously submitted to a thermal neutron flux in the range of 3.5 to 5.0 x 1012 n cm-2 s-1 for 8 h at the nuclear research reactor IEA-R1 of the Nuclear and Energy Research Institute, (IPEN/CNEN-SP), São Paulo, Brazil. After appropriate decay periods, γ-ray spectra of samples, reference material and element standards were measured using High-purity Ge (HPGe) detector Model POP-TOP (EG&G Ortec, Oak Ridge, TN, USA). This detector was coupled to an EG&G Ortec card and associated electronics. Spectrum analysis was carried out using VISPECT software, in TURBOBASIC language.The particle size of the materials was measured using a laser based particle size analyzer, namely a Malvern MSS Mastersizer 2000 Ver. 188.8.131.52.Adsorption Studies
The adsorption was performed using the batch procedure. Kinetic experiments were carried out by shaking 0.1g of adsorbents ZCA and SMZCA-20 with 10mL of RO16 solutions with an initial concentration of 25mg L-1 at room temperature (25 ± 2°C) in a shaker operated at 120rpm for 1-150min in glass bottles. The samples were withdrawn from the shaker at different time intervals, centrifuged and the concentration in the supernatant solution was determined. For adsorption isotherms, RO16 solutions of different concentrations ranging from 25 to 125mg L-1 for SMZCA-20 and 2.0 to 14.0mg L-1 for ZCA were agitated till the equilibrium was achieved at room temperature (25 ± 2°C). Each experiment was duplicated under identical conditions with maximum deviation was found to be 3%.
The effect of the adsorbent dosage was tested by mixing 0.02-0.2g SMZCA-20 with 10mL of RO16 solution at 50mg L-1 for 60min. The effect of pH on adsorption of dye onto SMZCA-20 was determined over the pH range of 2 to 10.5 at an initial RO16 concentration of 50mg L-1 and the pH was adjusted by adding 0.1 or 0.01mol L-1 of HNO3 or NaOH.
The amount of the dye uptake and percentage of dye removal by the adsorbent were calculated by applying Eqs. (1) and (2), respectively:
where qt is the adsorbed amount of adsorbate per gram of adsorbent at any time t (mg g-1), C0 and Ct the concentrations of the adsorbate in the initial solution and at any time t, respectively (mg L-1); V the volume of the adsorbate solution added (L) and M the amount of the adsorbent used (g).
2.4.1. Kinetic and Equilibrium Models
In order to investigate the mechanism of adsorption, characteristic constants were determined using the linearized form of pseudo-first order (Eq. 3) and pseudo-second order (Eq. 4) kinetic models with equations as follows:
where qeis the amount of dye adsorbed at equilibrium (mg g–1), qt is the amount of dye adsorbed at time t (mg g–1), k1is the rate constant of the pseudo-first-order adsorption (min-1), and k2is the rate constant of the pseudo-second-order kinetics (g mg–1 min–1) [21, 22, 23]. The values of k1andqe were obtained from the slope and intercept respectively of plot of log (qe - qt) versus t for pseudo- first order model. The values of qe and k2 can be determined from the slope and intercept of a plot of t/qt versus t, respectively for pseudo-second-order model.
The initial adsorption rate, h (mg g-1 min-1), as t→0 can be defined as (equation 5):
where k2is the rate constant of the pseudo-second order kinetics (g mg–1 min–1) and qeis the maximum adsorption capacity (mg g-1).
The kinetic results were analyzed by the intraparticle diffusion model to elucidate the diffusion mechanism, which model is expressed as :
where kid is the intraparticle diffusion rate constant (mg g-1 min-0.5). According to Eq. (6), a plot of qt versus t0.5 should be a straight line with a slope kid and intercept C when adsorption mechanism follows the intraparticular diffusion process.
The equilibrium data obtained in the present study were analyzed using the linear forms of the expressions of Langmuir (Eq (7)) and Freundlich (Eq (8)) isotherm models:
where Ce is the equilibrium concentration (mg L-1), qe the amount adsorbed at equilibrium (mg g-1), Q0 is the maximum amount of adsorbate per unit weight of adsorbent to form a complete monolayer on the surface (mg g-1); b is the Langmuir isotherm constant (Lmg-1), related to the affinity of the adsorption sites; KF [(mg g-1) (L mg-1)1/n] and n are the Freundlich constants related to adsorption capacity and adsorption intensity of adsorbents, respectively.
The non-linear regression Chi-square (χ2) test, represented by Eq. (9), was employed as a criterion for the fitting quality due to the inherent bias resulting from linearization of isotherm models .
where qe exp is the equilibrium capacity of the adsorbent obtained from experiment (mg g−1), and qe calc is the equilibrium capacity obtained by calculating from the model (mg g−1). A low value of χ2 indicates that experimental data fit better to the value from the model.2.5. Toxicity Assessments
Young individuals of Daphnia similis were exposed to different concentration of dye (from 6.25mg L-1 to 100.0mg L-1), during 48h. The concentrations that could lead to the immobilization of 50% of the organisms (EC50) were calculated from the number of immobile organisms per sample concentration and by applying statistical tests with the program Trimmed Spearman Karber . The experiment with the bioluminescent bacteria Vibrio fischeri was performed with the Microtox System, model M-500 from Microbics, exposing the samples to concentrations between 10.23mg L-1 and 81.90mg L-1 during 15min. The statistical analysis was carried out with proper statistics program by Microbics (version 7.82), that calculates the values of EC50 based on the reduction of the 50% of light emitted by the microorganism after exposure .
3. Results and Discussion3.1. Effect of Initial Surfactant on Dye Adsorption
In order to investigate the effect of HDTMA concentration on removal of RO16 HDTMA concentration was used as 0.9, 1.8, 9.0 and 20mmol L-1 while initial RO16 concentration was 10 mg L-1. As it can be seen from Table 1 and Figure 2, with augmentation of HDTMA, removal efficiency of RO16 enhanced and maximum dye removal was observed at 20mmol L-1 surfactant concentration.
Thus treatment of zeolite with initial concentration of 20mmol L-1 of surfactant appears to be the optimal loading for RO16 removal and was selected to be used in remaining experiments. The theoretical critical micelle concentration (CMC) of HDTMA-Br is about 0.9mmol L-1  and this initial concentration exceeds the critical micelle concentration of the surfactant. It is therefore envisaged that these micelles attach as such to the external surface and then rearrange to form a patchy mono-layer and/or bi-layers that tends to impart anionic exchange and hydrophobic characteristics to the adsorbent .3.2. Characterization of the Materials
The characterizations of ZCA and SMZCA-20 have been described in detail in previous paper . Some important physicochemical characteristics of ZCA and SMZCA-20 materials with respect to this study are shown in Table 2.
The XRD analyses of two zeolitic materials showed that hydroxysodalite (ICDD 00-011-0401) was the major zeolitic phase with peaks of quartz (ICDD001-0649) and mullite (ICDD002-0430) of fly ash that remained after the alkaline hydrothermal treatment. The structural parameters of SMZCA-20 are very close to that of corresponding parent zeolite which indicate that the crystalline nature of the zeolite material remained intact after required chemical treatment with HDTMA molecules and heating treatment for drying .
Laser granulometric analysis results for CCA, ZCA and SMZCA-20 samples are reported both as absolute and cumulative volumetric distributions (Figure 3). The particle size distributions of materials are given in Table 3. These distributions specify that the majority of particles (90%) lie below 174.8, 291.8 and 230.0µm in case of CCA, ZCA and SMZCA-20, respectively. The Sauter mean diameter (D[3, 2]) was 24.3 µm for CCA, 23.9 µm for ZCA and 20.7µm for SMZCA-20. The D[3, 2] values are indicative of the active surface area of the materials, therefore based on these results it would seem appropriate to consider SMZCA-20 as having better adsorption potential than others materials. The particle size of the modified zeolite is as a function of the amount and the molecular size of surfactant added.
Fly ash has a broad size distribution with diameters spanning more than three orders of magnitude. The median diameters of ashsamples from six representative coals collected in cyclones and baghouses of american coal fired power plants were between 1.2-3.4µm and 0.4-1.2µm, respectively .
The grain size distribution of fly ash sample from a Brazilian power plant (Presidente Medici Power Plant or UTPM-446 MW) collected from electrostatic precipitator was determined. The continuous interval of particle sizes was between 0.5 and 600µm, and the average diameter was 49.30µm. Ninety percent of the particles have diameters smaller than 232µm, while the finest particles (< 5 µm) correspond to ~ 1% of the total mass of the sample .
Table 4 presents the trace elemental concentration in CCA, ZCA and SMZCA-20 samples obtained by instrumental neutron activation analyses. A considerable reduction in the elements contents was attained in the fly ash zeolitization for arsenic and zinc that decreased between 86-90% and 16-25%, respectively. A significant amount of Na element is incorporated in the zeolitic products after hydrothermal treatment with NaOH solution due to entrapment of sodium ions to neutralize the negative charge on aluminosilicate gel . The presence of bromide in the modified zeolitic material was detected. The positive charge of cation HDTMA adsorbed on the surface of the zeolite is counterbalanced by anions bromide. The other elements are present in approximately the same amount in the three samples.
The high concentrations of As, Fe and Zn are due to the high content of pyrite of the feed coal. Concentrations of U are relatively high because the area near Figueira coal-ﬁred power plant is rich in uranium, with an average of 0.148% U3O8 in calcitic sandstone above the coal seam [1, 31].3.3. dsorption Knetics
To determine the equilibration concentration and time, the adsorption of the RO16 onto zeolites was studied as a function of contact time. These experiments were performed against time (range 10-80min for ZCA and 1-60min for SMZCA-20) and the effect of equilibrium time on the adsorption of RO16 onto the unmodiﬁed and modiﬁed zeolites is presented in Figure
It should be pointed out that apparent equilibrium was reached after 120min for ZCA. The adsorption of RO16 onto modiﬁed zeolite was almost instantaneous and an apparent equilibrium was reached within the ﬁrst 5min. The adsorption capacities of unmodiﬁed zeolite are low and when zeolite was modiﬁed with HDTMA-Br, the adsorption capacities were increased remarkably. The degree of removal of RO16 was 100% for concentrations < 25.0mg L-1 using SMZCA-20.
It is important to be able to predict the rate at which contamination is removed from aqueous solutions in order to design an adsorption treatment plant. Aiming at evaluating the adsorption kinetics of RO16 onto zeolites, the pseudo-ﬁrst order, pseudo-second order and intraparticle diffusion kinetic models were used to ﬁt the experimental data, according to the kinetic model equations (3) to (6). The values of kinetic constants for RO16 adsorption onto unmodiﬁed zeolite and surfactant-modiﬁed zeolite are presented in Table 5.
Table 5. Kinetic parameters for the removal of RO16 by zeolite from cyclone ash and surfactant-modiﬁed zeolite
It is obvious from Table 5 that the correlation coefﬁcients R2 for the linear plots of the pseudo-second order model is 0.999 which is higher than the correlation coefﬁcients R1 for the pseudo-ﬁrst order and the calculated qe values are in agreement with experimental qe values. This indicates that the adsorption kinetic is better represented by the pseudo-second order model.
The intraparticle rate constants were obtained from the plot of q versus t0.5 and the results are given in Table 5. The C values indicate that the line did not pass through the origin. It has been reported by various researchers that when the plots do not pass through the origin, this is indicative of some degree of boundary layer control and further shows that the intraparticle diffusion is not only the rate controlling step, but some other processes may also control the rate of adsorption.3.4. Adsorption Isotherm
Langmuir and Freundlich models were applied to describe equilibrium adsorption isotherms for RO16 onto the ZCA and SMZCA-20 samples at 25°C, and the ﬁts of the theoretical models to the experimental values are shown in Figure. 5. The isotherm constants, their correlation coefﬁcients and value of Chi-square test calculated from Eq. (7)-(9) are given in Table 6. For analysis of data using linear regression, the fitness of the model is often evaluated based on the value of the correlation coefficients (R2). Both Langmuir and Freundlich isotherms give similar R2 values for ZCA and SMZCA-20. Despite this, the χ2 values for Freundlich were very large, mainly for ZCA, suggesting that the isotherm constants of Freundlich obtained from the linear regression do not describe well the equilibrium data.
The RO16 maximun adsorption capacity (Q0) of the ZCA sample is 0.580mg g-1. After surface modiﬁcation with HDTMA, dye ion removal is greatly enhanced to 12.6mg g-1. Adsorption by zeolite is negligible presumably because of the strong dipole interaction between zeolite and water, which excludes organic solutes from this portion of the zeolite.
The measurements of pHPZC revealed that surfactant-modified zeolite sample surface acquires a negative charge in water at natural pH (Table 2). The negative charge of SMZCA-20 is probably due to the formation of a patchy bilayer on the number of exchangeable active sites on the external zeolite surface .
The adsorption of RO16 onto SMZCA-20 with patchy bilayer coverage is attributed to multiple mechanisms, such as, electrostatic interaction, hydrogen bonding, hydrophobic interaction and ion exchange. Hydrophobic interaction and hydrogen bonding are suggested to be the predominant mechanisms. Hydrophobic interaction involves the hydrophobic tails of HDTMA and the hydrophobic functional groups of RO16 molecules, and this mechanism is of London-Van der Waals type .
A large number of hydrogen bonds between C or N of HDTMA and alkyl, aromatic and sulphonic groups of RO16 also is responsible for the effective adsorption. The aromatic and sulfonate groups of organic compounds and their planar shape and delocalized -bonds interact strongly with ammonium centers of HDTMA [33, 34, 35].
A comparison of the adsorption maxima of RO16 on zeolite from cyclone fly ash (ZCA) and surfactant modified zeolite from cyclone ash (SMZCA-20) with those of some low cost adsorbents reported in the literature is given in Table 7. As seen in Table 7, the SMZCA-20 had comparable adsorption performances with chitosan cross-linked beads.Although activated carbon from waste materials [36, 37, 38] and various types of sludge  presents high efﬁciency in the removal of RO16, the obtaining of these adsorbents requires optimization of the preparation process involving several steps anduse of relatively expensive chemical reagents .
Adsorption capacity for unmodified zeolites increased with decreasing adsorbent particle size. Zeolites from baghouse ash have smaller particle size than zeolitesfrom cyclone ash. The increase in adsorption capacity with decreasing adsorbent particle size is attributable to molecules adsorbing principally in the exterior region close to the external particle surface . The speciﬁc external surface area (surface area per unit mass) available for adsorption would be greater for smaller adsorbent particles. The values of BET surface area were 69.3 and 39.0m2 g-1 for zeolite from baghouse fly ash and zeolite from cyclone ash, respectively.
The inﬂuence of SMZCA-20 dosage on RO16 removal was studied and the results are presented in Figure. 6. As the adsorbent dosage increased, a greater surface area and a greater number of binding sites should be available for the constant amount of RO16, which results in the percentage removal of RO16 increasing with increasing SMZCA-20 dose. The highest amount of dye removal was attained for adsorbent dose of 10g L-1. For adsorbent dosages higher than this value, the percentage of the dye removal and the amount of dye uptake per gram of adsorbent (qe) remained almost constant.
The effect of pH on the RO16 anions uptake by SMZCA-20 is shown in Figure 7. The amount adsorbed remained constant in the pH interval between 2 to 9 and increased with the medium pH 10. The hydrophobic interactions between RO16 and HDTMA chains appears to be the most important mechanism involved in anionic dye adsorption in the case where the pH does not play any role on adsorption process. The increase in RO16 removal in pH 10 may be due to strong basic nature of the loaded HDTMA on ZCA.3.7. Acute Toxicity Test
The dye toxicity was evaluated for dye solutions before and after the adsorption processes with D. simlis and V. ficheri.In the present study, toxicity was evaluated at RO16 concentrations of 6.25-100mg L-1 and 10.23-81.90mg L-1 for to determine EC50 ranges forD. simlis and V. ficheri, respectively.
The results indicate that the EC50 of RO16 were 16.72 and 92.10mg L-1 for V. ficheri and D. simlis, respectively.This means that the concentration values of the dye used are considered toxic to the aquatic environment and that color removal is required. After treatment of RO16 by SMZCA-20, EC50 value was 0.32mg L-1 for D. simlis and 1.32 for mg L-1 V. ficheri. One possible reason for this increase in toxicity after treatment could be due to the presence of residual surfactant in the effluent. This hypothesis was confirmed by toxicity tests carried out with dyes solutions after adsorption process using unmodified zeolite from fly ash. It was observed that acute effects were substantially reduced or was eliminated after the adsorption treatment [6, 46, 47].
This study investigated the equilibrium and the dynamics the adsorption of an anionic dye, which is namely Reactive Orange 16 dye, RO16, onto unmodified zeolite (ZCA) and surfactant-modiﬁed zeolite (SMZCA) that were synthesized from cyclone ash. The best conditions were established with respect to contact time, adsorbent dose and pH to saturate the available sites located on the SMZCA surface. The pseudo-second order kinetic model agrees very well with the dynamic behavior for the adsorption of RO16 onto adsorbents. The experimental data ﬁtted well to the Langmuir adsorption isotherm.The ecotoxicity studies showed the wastewater contaminated with dyes after treatment with modified-surfactant zeolite should not be discarded directly into water bodies, but can be used as non-potable water reuse. Although zeolite synthesized from cyclone ash showed little adsorption for RO16, surface modiﬁed zeolite material proved to be an effective adsorbent for the adsorption of anionic azodye compound from wastewater.
The authors are grateful to Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for financial support and to Carbonífera do Cambuí (Figueira Power Plant) for providing cyclone fly ash samples for this study.
|||Depoi, F.S., Pozebon, D. and Kalkreuth, W.D. “Chemical characterization of feed coals and combustion-by-products from Brazilian power plants,” International Journal of Coal Geology, 76, 227-236, 2008.|
|||Shanthakumar, S., Singh, D.N. and Phadke, R.C. “Flue gas conditioning for reducing suspended particulate matter from thermal power stations,” Progress in Energy and Combustion Science, 34, 685-695, 2008.|
|||Silva, L.F.O. and da Boit, K.M. “Nanominerals and nanoparticles in feed coal and bottom ash: implications for human health effects,” Environmental Monitoring and Assessment, 174, 187-197, 2011.|
|In article||CrossRef PubMed|
|||Font, O., Córdoba, P., Leiva, C., Romeo, L.M., Bolea, I., Guedea, I., Moreno, N., Querol, X., Fernandez, C. and Díez, L.I., “Fate and abatement of mercury and other trace elements in a coal fluidised bed oxy combustion pilot plant,” Fuel, 95, 272-281, 2012.|
|||Fungaro, D.A., Bruno, M. and Grosche, L.C. “Adsorption and kinetic studiesof methylene blue on zeolite synthesized from fly ash,” Desalination and Water Treatmen, 2, 231-239, 2009.|
|||Fungaro, D.A., Grosche, L.C., Pinheiro, A.S., Izidoro, J.C. and Borrely, S.I. “Adsorption of methylene blue from aqueous solution on zeolitic material and the improvement as toxicity removal to living organisms,” Orbital, 2, 235-247, 2010.|
|||Fungaro, D.A., Yamaura, M. and Carvalho, T.E.M. “Adsorption of anionic dyes from aqueous solution on zeolite from fly ash-iron oxide magnetic nanocomposite,” Journal of Atomic and Molecular Sciences, 2, 305-316, 2011.|
|||Bowman, B.S. “Applications of surfactant-modiﬁed zeolites to environmental remediation.Review,” Microporous Mesoporous Materials, 6, 43-56, 2003.|
|||Haggerty, G.M. and Bowman, R.S. “Sorption of chromate and other inorganic anions by organo-zeolite,” Environmental Science & Technology, 28, 452-458, 1994.|
|In article||CrossRef PubMed|
|||Li, Z. and Bowman, R.S. “Counterion effects on the sorption of cationic surfactant and chromate on natural clinoptilolite,” Environmental Science & Technology, 31, 2407-2412, 1997.|
|||Fungaro, D.A. and Borrely, S.I. “Synthesis and characterization of zeolite from coal ashes modified by cationic surfactant,” Cerâmica, 58, 77-83, 2012. (in Portuguese with English abstract)|
|||Guan, H., Bestland, E., Zhu, C., Zhu, H., Albertsdottir, D., Hutson, J., Simmons, C.T., Ginic-Markovic, M., Tao, X. and Ellis, A.V. “Variation in performance of surfactant loading and resulting nitrate removal among four selected natural zeolites,” Journal of Hazardous Materials, 183, 616-621, 2010.|
|In article||CrossRef PubMed|
|||Li, Z.H. “Sorption kinetics of hexadecyltrimethylammonium on natural clinoptilolite,” Langmuir, 15, 6438-6445, 1999.|
|||Li, Z.H. and Bowman, R.S. “Sorption of perchloroethylene by surfactant-modiﬁed zeolite as controlled by surfactant loading,” Environmental Science & Technology, 32, 2278-2282, 1998.|
|||Rozic, M., Sipusic, D.I., Sekovanic, L., Miljanic, S., Curkovic, L. and Hrenovic, J. “Sorption phenomena of modiﬁcation of clinoptilolite tuffs by surfactant cations,” Journal of Colloid and Interface Science, 331, 295-301, 2009.|
|In article||CrossRef PubMed|
|||Mumford, J.L. and Lewtas, J. “Evaluation of ﬂy ash collection methods for short-term bioassay studies of ﬂuidized-bed coal combustion,” Environmental Science & Technology, 18, 765-768, 1984.|
|||Easton, JR. The dye maker’s view. Society of Dyers and Colourists; The Alden Press, Oxford, 9-21, 1995.|
|||Novotny, C., Dias, N., Kapanen, A., Malachova, K., Vandrovcova, M., Itavaara, M. and Lima, N.” Comparative use of bacterial, algal and protozoan tests to study toxicity of azo- and anthraquinone dyes,” Chemosphere, 63, 1436-1442, 2006.|
|In article||CrossRef PubMed|
|||Carvalho, T.E.M., Fungaro, D.A., Magdalena, C.P. and Cunico. P. “Adsorption of indigo carmine from aqueous solution using coal fly ash and zeolite from fly ash,” Journal of Radioanalytical and Nuclear Chemistry,289, 617-626, 2011.|
|||Henmi, T., “Increase in cation exchange capacity of coal fly ash by alkali treatment,” Clay Science, 6, 277-282, 1987.|
|||Blanchard, G., Maunaye, M.and Martim, G. “Removal of heavy metals from waters by means of natural zeolites,” Water Research 18, 1501-1507,1984.|
|||Ho, Y.S. and McKay, G. “Sorption of dye from aqueous solution by peat,” Chemical Engineering Journal, 70, 115-12, 1998.|
|||Ho, Y.S. and McKay, G. “Pseudo-second order model for sorption processes,” Process Biochemistry, 34, 451-465, 1999.|
|||Weber, W.J. and Morris, J.C. “Kinetics of adsorption carbon from solutions,” Journal Sanitary Engeering Division Proceedings.American Society of Civil Engineers, 89, 31-60, 1963.|
|||Ho, Y.S. “Selection of optimum sorption isotherm,” Carbon, 42, 2115-2116, 2004.|
|||CETESB - Companhia Ambiental do Estado de São Paulo. “Água: Testes de toxicidade aguda com Daphnia similis” Claus, 1976(Cladocera, Crustácea). L5.019-1, São Paulo, 28 pp, 1986.|
|||CETESB - Companhia Ambiental do Estado de São Paulo. “Bioensaio de toxicidade aguda com Photobacterium phosphoreum. Sistema Microtox” São Paulo, 1987.|
|||Ghosal, S., Ebert, J.L. and Self.S.A. “Chemical composition, size distributions for fly ashes”,Fuel Processing Technology, 44, 81-94, 1995.|
|||Pires, M. and Querol, X. “Characterization of Candiota (South Brazil) coal and combustion by-product,” International Journal of Coal Geology, 60, 57-72, 2004.|
|||Murayama, N., Yamamoto, H., and Shibata, J. “Mechanism of zeolite synthesis from fly ash by alkali hydrothermal reaction,” International Journal of Mineral Processing, 64, 1-17, 2002.|
|||Flues, M., Camargo, I.M.C., Figueiredo Filho, P.M., Silva, P.S.C. and Mazzilli, B.P. “Evaluation of radionucletides concentration in Brazilian Coals” Fuel, 86, 807–812, 2007.|
|||Dong, Y, Wu, D.Y., Chen, XC and Lin, Y. “Adsorption of bisphenol A from water by surfactant-modiﬁed zeolite,” Journal of Colloid and Interface Science, 348, 585- 59, 2010.|
|In article||CrossRef PubMed|
|||Sheng, G., Xu, S., Boyd, S.A. “Mechanism(s) controlling sorption of neutral organic contaminants by surfactant-derived and natural organic matter,” Environmental Science & Technology, 30:1553-1557, 1996.|
|||Custelcean, R. and Jackson, J.E. “Dihydrogen bonding: structures, energetics, and dynamics,” Chemical Reviews, 101, 1963-1980, 2001.|
|In article||CrossRef PubMed|
|||Stefov, V., Pejov, L. and Soptrajanov, B. “Experimental and quantum chemical study of pyrrole self-association through N–H… [π] hydrogen bonding.” Journal of MolecularStructure, 649, 231-243, 2003.|
|||Lee, J.W., Choi, S.P., Thiruvenkatachari, R., Shim, W.G. and Moon, H. “Submerged microﬁltration membrane coupled with alum coagulation/powdered activated carbon adsorption for complete decolorization of reactive dyes,” Water Reseaerch, 40, 435-444, 2006.|
|In article||CrossRef PubMed|
|||Calvete, T., Lima, E.C., Cardoso, N.F., Vaghetti, J.C., Dias S.L., and Pavan, F.A. “Application of carbon adsorbents prepared from Brazilian-pine fruit shell for the removal of reactive orange 16 from aqueous solution: Kinetic, equilibrium, and thermodynamic studies,” Journal of Environmental Management, 91, 1695-706, 2010.|
|In article||CrossRef PubMed|
|||Ramachandran, P., Vairamuthu, R., Ponnusamy, S. “Adsorption isotherms, kinetics, thermodynamics and desorption studies of reactive orange16 on activated carbon derived from Ananas comosus (L.) Carbon,” Journal of Engineering & Applied Sciences; 6, 15-26, 2011.|
|||Won, S.W., Choi, S.B. and Yun, Y.S. “Performance and mechanism in binding of Reactive Orange 16 to various types of sludge,” Biochemical Engineering Journal, 28, 208-214, 2006.|
|||Dias, J.M., Alvim-Ferraz, M.C.M., Almeida, M.F., Rivera-Utrilla, J. and Sanchez-Polo, M. “Waste materials for activated carbon preparation and its use in aqueous-phase treatment: a review,” Journal of Environmental Management, 85, 833-846, 2007.|
|In article||CrossRef PubMed|
|||Suteu, D., Malutan, T. and Bilba, D. “Agricultural waste corn cob as a sorbent for removing reactive dye orange 16: equilibrium and kinetic study,” Cellulose Chemistry and Technology, 45,413-420, 2011.|
|||Kimura, I.Y., Laranjeira, M.C.M., Fávere, V.T. and Furlan, L. “The interaction between reactive dye containing vinylsulfone group and chitosan microspheres,” International Journal of Polymeric Materials, 51, 759-768, 2002.|
|||Wong, S.Y., Tan, Y.P., Abdullah A.H. and Ong, S.T. “The Removal of Basic and Reactive Dyes using Quartenized Sugar Cane Bagasse,” Journal of Physical Science 20, 59-74, 2009.|
|||Fungaro, D. A.; Yamaura, M.; Carvalho, T. E. M.; “Adsorption of anionic dyes from aqueous solution on zeolite from fly ash-iron oxide magnetic nanocomposite,” Journal of Atomic and Molecular Sciences, 2, 305-316.2011.|
|||Ando, N., Matsui, Y., Kurotobi, Y., Nakano, Y., Matsushita, T. and Ohno, K. “Comparison of natural organic matter adsorption capacities of super-powdered activated carbon and powdered activated carbon,” Water Research, 44, 4127-4136, 2010.|
|In article||CrossRef PubMed|
|||Magdalena, C.P. “Adsorption of reactive remazol red RB dye of aqueous solution using zeolite of the coal ash and evaluation of acute toxicity with Daphnia similis,”|
|||http://pelicano.ipen.br/PosG30/TextoCompleto/Carina%20Pitwak%20Magdalena_M.pdf, 2010 (in Portuguese with English abstract).|
|||Ferreira,C.P. “Studies on the adsorption of reactive black 5 dye of aqueous solution using zeolite of the coal ashes,”|
|||http://pelicano.ipen.br/PosG30/TextoCompleto/Patricia%20Cunico%20Ferreira_M.pdf, 2011 (in Portuguese with English abstract).|