Removal of reactive black 5 dye from aqueous solutions by Fe3O4@SiO2-APTES nanoparticles

Document Type : Research Paper

Authors

1 Department of Environmental Sciences and Engineering, Faculty of Natural Resources, University of Guilan, Sowmeh Sara, Guilan, Iran and Dept. of Water Eng. and Environment, University of Guilan. Rasht, Iran

2 Department of Chemistry, Faculty of Science, University of Guilan, Rasht, Iran

3 Department of Environmental Health Engineering, School of Health, Guilan University of Medical Sciences, Rasht, Iran and Research Center of Health and Environment, Guilan Unversity of Medical Sciences, Rasht, Iran

Abstract

In this study, Fe3O4@SiO2-APTES nanoparticles were successfully synthesized via a one-pot route in order to remove reactive black 5 dye from aqueous solutions. To obtain optimal conditions on the dye removal efficiency, the effects of various parameters were investigated including solution pH, initial dye concentration, and absorbent dosage. According to the experimental results, the removal efficiency of the dye decreased with increasing in pH and initial dye concentration, as well as with decreased adsorbent dosage. In fact, about 100.00 % of reactive black 5 was removed from aqueous solution using Fe3O4@SiO2-APTES NPs at the adsorbent amount of 0.4 g L-1 and  pH = 3 in 90 min. The kinetics were found well match with pseudo-second-order equation. The isotherm analysis indicated that the equilibrium data were well fitted to the Langmuir isotherm model, showing a monolayer adsorption manner of the dyes on homogeneous surface of nanoparticles. Also, the results of absorbent recycling showed that this nanoparticle could be reused up to 6 times with high efficiency.

Keywords


[Research]

 

Removal of reactive black 5 dye from aqueous solutions by Fe3O4@SiO2-APTES nanoparticles

 

Bozorgpanah Kharat Z.1, Mohammadi Galangash M.1*, Ghavidast A.­­ 2, Shirzad-Siboni M.3

 

1. Department of Environmental Sciences and Engineering, Faculty of Natural Resources, University of Guilan, Sowmeh Sara, Guilan, Iran and Dept. of Water Eng. and Environment, University of Guilan. Rasht, Iran

2. Department of Chemistry, Faculty of Science, University of Guilan, Rasht, Iran

3. Department of Environmental Health Engineering, School of Health, Guilan University of Medical Sciences, Rasht, Iran and Research Center of Health and Environment, Guilan Unversity of Medical Sciences, Rasht, Iran

 

* Corresponding author’s E-mail: m_mohammadi@guilan.ac.ir             (Received: Feb. 06. 2018 Accepted: May 31. 2018)

ABSTRACT

In this study, Fe3O4@SiO2-APTES nanoparticles were successfully synthesized via a one-pot route in order to remove reactive black 5 dye from aqueous solutions. To obtain optimal conditions on the dye removal efficiency, the effects of various parameters were investigated including solution pH, initial dye concentration, and absorbent dosage. According to the experimental results, the removal efficiency of the dye decreased with increasing in pH and initial dye concentration, as well as with decreased adsorbent dosage. In fact, about 100.00 % of reactive black 5 was removed from aqueous solution using Fe3O4@SiO2-APTES NPs at the adsorbent amount of 0.4 g L-1 and  pH = 3 in 90 min. The kinetics were found well match with pseudo-second-order equation. The isotherm analysis indicated that the equilibrium data were well fitted to the Langmuir isotherm model, showing a monolayer adsorption manner of the dyes on homogeneous surface of nanoparticles. Also, the results of absorbent recycling showed that this nanoparticle could be reused up to 6 times with high efficiency.

 

Key words: Fe3O4@SiO2-APTES nanoparticles, Reactive Black 5, Kinetic, Isotherm.


INTRODUCTION

Due to limited availability of fresh water resources and growth of industrial development, large quantities of effluents are generated and wastewater treatment became as one of the main priorities for preservation of the aquatic ecosystems (Agarwal et al. 2016). Among the various industries, paper, food, pharmaceutical, leather and especially the textile industries, are producing high volume of colored wastewater and have to be specific treated before released into the environment (Madrakian et al. 2013). The most of the dyes which are used in the industries are of organic origin and can cause allergy, skin irritation and genetic mutations for humans and animals (Gholivand et al. 2015). By the growing production of these dyes, the

 

discharge of dye effluents at high concentration and strong color has caused serious environmental pollution, because many of these dyes are toxic and unruly to biodegradation. Due to the chemically and light stable characteristics of dye wastes, a wide range of techniques have been developed for management of related issues. So far, various physical, chemical and biological methods have been investigated for the treatment of colored wastewater, such as coagulation and flocculation, chemical oxidation, membrane filtration, electrochemical purification, advanced oxidation, enzymatic decomposition, ultrasonic waves and electrochemical degradation (Karadag et al. 2007; Zhang &Kong2011). Beside the several methods of purification, absorption technology is one of the most effective methods for removing dye from textile sewage due to its simplicity, high efficiency, flexibility, low cost, insensibility to toxic compounds and the availability of a wide range of adsorbents (Robinson et al. 2011). The results of studies on neutral red (Qu et al. 2008; Iram et al. 2010), methylene blue (Yang et al. 2008 ; Zhang  & Kong 2011), methyl orange (Zhu et al. 2010), reactive blue 19 and reactive red 198 (Moussavi &  Mahmoudi  2009), reactive orange 16 (Ramachandran et al. 2011), acid orange 7 (Sheshmani et al. 2014)  and acid red 18 (Zhang et al. 2014) have illustrated that adsorption methods especially by nanomaterial are increasing  for the efficiency purification systems. Among different nanostructure materials, magnetic nanoparticles (NPs), as compared with other materials, have a widespread use in removing dye from industrial wastewater. Magnetic NPs have high thermal, mechanical stability, easy separation of NPs from the dye and the reusability of these NPs are another advantage of their use in absorbing industrial dyes (Mohagheghian et al. 2015). Iron oxide NPs are eco-friendly materials that have been investigated in recent years as effective adsorbents in adsorption of dye pollutants from wastewater (Zhang & Kong 2011). Ease to use, affordable, rapid absorption response, the high surface-to-volume ratio of magnetic NPs and their adequate level to trap components of dye contaminants have led to a wide application of these materials (Ghoreishian et al. 2014).

The reactive black 5 (RB-5) as an azo-reactive dyes is the most varied of water-soluble artificial dyes and because of easy to use and low energy consumption is used extensively in the textile industries (Demirbas &Nas2009). High resistance to aerobic decomposition and water solubility of RB-5 has made it difficult to treat by conventional biological treatment processes (Vijayaraghavan & yan 2008; Shirzad-Siboni et al. 2014). In recent years, various adsorbents such as activated carbon (Choi et al. 2008), chitosan (Chen & Huang 2010), fly ash (Eren & Acar 2007), modified zeolite (Karadag et al. 2007) and graphite oxide (Travlou et al. 2013) have been used to remove  RB-5 dye. Regarding the high volume of dye sewage production in Iran and its harmful effects, this study was conducted to synthesis magnetic amino-coated silica iron oxide NPs of Fe3O4@SiO2-APTES NPs to remove RB-5 dye from water. In order to achieve the highest absorption efficiency, the effects of some parameters were studied such as, pH, RB-5 concentration and absorbent dosage. In addition, the adsorption isotherm, kinetics, thermodynamics feature and the reusability of the adsorbents are also analyzed to evaluate the economic values.

 

MATERIALS AND METHODS

The following reagents were purchased (Merck, Germany) and used without further modification: ferric chloride hexahydrate (FeCl3.6H2O), ferrous chloride tetrahydrate (FeCl2.4H2O), ammonia (NH3, 25 wt %), tetraethyl orthosilicate (TEOS) and 3-Aminopropyl triethoxysilane (APTES). The RB-5 dye was supplied from Alvan Sabet Co., Iran. The properties of RB-5 dyes are shown in Table 1. In the experiment, deionized water was used for all sample preparation process. The initial pH of solution was adjusted by the addition of 0.1 M NaOH or HCl and also using a pH meter device (WTW, Germany). The external magnet was used to remove NPs from the aqueous solution. The X-ray diffraction (XRD) patterns were recorded in air at ambient temperature by Phillips (pw-1840) X-ray diffractometer with Cu-Kα radiation source (λ = 1.54056 Å) at 40 KV voltage and 25 mA current in a wide angle range (2θ = 20-70).

 

The synthesis of Fe3O4@SiO2-APTES NPs

Firsty, the synthesis of iron oxide NPs (Fe3O4 NPs) was carried out using co-precipitation method in alkaline conditions .So that, 1.08 g FeCl3.6H2O and 0.39 g FeCl3.6H2O were dissolved with deionized water in three necked bottom flask and stirred heavily under argon gas at 80 °C. Then, the ammonia was added dropwise via a dropping funnel under mechanical stirring. The reaction was refluxed at 80 °C for 5 h at argon atmosphere. Then, black precipitate Fe3O4 was formed and separated from the reaction medium using an external magnet of 1.4 T (Mohagheghian et al. 2015) and washed with deionized water. Then, 1 g of synthesized Fe3O4 NPs was dispersed with 50 mL of deionized water under argon atmosphere for 10 min. After reaching the temperature to 80 °C, 1 mL of TEOS was added in 20 mL of EtOH, and the reaction was continued for 24 h in inert conditions. Thereafter, the black powder Fe3O4@SiO2 NPs formed and separated from the reaction medium using the external magnet, then was washed with H2O and EtOH three times. Subsequently, this achieved NPs suspended in 10 mL of EtOH and stirred heavily for 15 min under N2 gas. Then, 0.37 mL APTES in 25 mL EtOH was added drop-wise to resulting mixture under mechanical stirring. The reaction was refluxed at 80 °C for 8 h at argon atmosphere. The resulted mixture was cooled and the solid was separated magnetically and then washed with EtOH and H2O several times (3 × 50 mL). The precipitate was then dried in oven at 50 °C for 8 h and the black nanopowder Fe3O4@SiO2-APTES NPs was obtained.

 

 

Table 1. The properties of RB-5 dye.

Chemical structure

Molar mass

Color index number

lmax

 

991.82 g mol-1

20.505

597

 

 

Removal efficiency

The effect of parameter changes such as pH, absorbent dose and dye concentration was investigated on absorption efficiency. To evaluate the effect of pH on the dye removal efficiency of RB-5, we examined different values, ranging 3-9 with RB-5 concentration 20 mg L-1 and adsorbent dosage 0.3 g L-1. After reaching pH 3 as optimum pH, the adsorption of dye on Fe3O4@SiO2-APTES NPs was examined by changing the quantity of adsorbent range from 0.1 through 0.4 g L-1, with the dye concentration of 20 mg L-1, room temperature (25 ± 1 °C) and pH = 3, hence, 0.4 g L-1 was obtained as an optimum dose of absorbent. Finally, the effects of initial dye concentrations on the rate of adsorption by Fe3O4@SiO2-APTES NPs were studied in different initial RB-5 concentrations of 20-80 mg L-1 under the 0.4 g L-1 absorbent and pH = 3 at different times (Ballav et al. 2015). The removed amount of dye by Fe3O4@SiO2-

 

APTES NPs and removal efficiency were calculated by Eqs. 1 and 2, respectively (Eren & Acar 2007), where q is the adsorption capacity (mg g-1), Ci, C0 and Ce are the initial, outlet, and equilibrium concentrations of dye (mg L-1), V (L) is the volume of dye solution and M (g) is the total amount of Fe3O4@SiO2-APTES NPs.

                                              (1)                                                                                                     

Removal efficiency (%) =            (2)

The efficiency of recycled Fe3O4@SiO2 APTES NPs

After performing the parameters optimization tests, all the used adsorbent to dye removal experiments were collected and regenerated with 0.1 M sodium hydroxide solution (NaOH). The adsorption-desorption experiments were carried out under optimal conditions (pH = 3, initial RB-5 concentration = 20 mg L-1, adsorbent dose = 0.4 g L-1). The result showed the recovered adsorbent reused for at least six successive removal processes with removal efficiency higher than 80%, displaying the stability of adsorbent (Mohagheghian et al. 2015).

 

Kinetic studies

The kinetic experiments of the adsorption process were carried out at different concentrations of RB5 (20-80 mg L-1), 0.4 g L-1 NPs, pH = 3 and at different contact times. The pseudo-first order and pseudo-second-order kinetic models were applied in order to find an efficient model for the description of adsorption mechanism (Liu & Liu 2008). In absorption kinetics equations, qe is the absorption capacity at equilibrium (mg g-1), qt is the absorption capacity at different time (mg g-1), K1 is equal to the speed coefficient (min-1) and K2 is the velocity coefficient (g mg -1min-1) (Samarghandi et al. 2011). Kinetic equations are presented in Table 2.

 

Equilibrium studies

To evaluation of adsorption isotherms, the adsorption experiments of RB-5 on the Fe3O4@SiO2-APTES NPs with 20 mg L -1 RB-5 as an initial concentration using various adsorbent dosages (0.005 - 1 g L-1) at pH = 3 for 24 h and also at 20, 30 and 45 °C are given in Fig. 6. The equilibrium adsorption data were evaluated according to the renowned models Langmuir and Freundlich isotherms (Sadaf & Bhatti 2014).

Isothermic equations are presented in Table 2. In isotherm models, Ce is equal to the equilibrium concentration (mg L-1), qe is the equivalence of absorption capacity at equilibrium time (mg g-1), K is the equation of equation (L mg-1) and qm is the equal to the maximum absorption capacity (mg g-1) (Geetha et al. 2014). The adsorption isotherm process favorability was also evaluated using the dimensionless separation factor ( ) that were calculated using the following equation [67]:

 

 

                                                     (3)                                                                                                                  

 

The adsorption process can be defined as favorable (0 <  < 1), unfavorable (1 < ), linear (  = 1) and irreversible in nature (  = 0) (Ballav et al. 2015).

 

 

Table 2. The equations of isotherm and kinetic used in this study.

Isotherm equations

Kinetic models

Freundlich isotherm

 

Pseudo-first order

 

Langmuir isotherm

 

 

Pseudo-second order

 

 

 


RESULTS

Adsorbent characterization

The FT-IR spectrum of prepared Fe3O4@SiO2-APTES (red line) compared with Fe3O4 NPs (black line) and Fe3O4@SiO2 NPs (violet line) is shown in Fig. 1. The typical absorption peaks at 567 is related to thestretching vibration of

 

Fe-O bond and also overlap with stretching bonds of Si-O-Fe. The characteristic absorption bands at 1000, 3417 and 2869-2906 cm-1 are corresponded to C-N, N-H and C-H stretching modes of the alkyl chain, respectively and the N‐H bending mode appeared at 1627 cm-1 thatconfirm the successful coating of APTES on Fe3O4@SiO2 surfaces. Fig. 2, shows the X-ray diffraction (XRD) patterns of Fe3O4@SiO2-APTES. The sharp diffraction peaks with 2θ at 30.3° (220), 35.6° (311), 43.3° (400), 53.9o (422), 57.2° (511) and 62.5° (440) are observed, indicating that the Fe3O4@SiO2-APTES NPs have highly crystalline cubic spinel structure of the magnetite.

The average crystallite size D was determined by the Scherrer formula, D = /(βcosθ), where λ = 1.54 ˚A is the wavelength of Cu-Kα radiation used, β is the full width at half-maximum (FWHM) intensity of the diffraction line, θ is the Bragg angle for the measured hkl peak and K is a constant equal to 0.94. The particle sizes of the magnetite calculated using the Scherrer equation was 15.7 nm.

 

 

 

Fig. 1. The FT-IR spectra of Fe3O4@SiO2-APTES (red line), Fe3O4@SiO2 NPs (violet line) and Fe3O4 NPs (black line).

 

Fig. 2. TheXRD image of Fe3O4@SiO2-APTES NPs.

 

Fig. 3 shows the transmission electron microscopy (TEM) images of the Fe3O4@SiO2-APTES microspheres. The TEM images obviously show that the functional group (with light color) is immobilized on the surface of Fe3O4@SiO2 NPs (with dark color). The synthesized Fe3O4@SiO2-APTES NPs showed a spherical shape with an average diameter of about < 20 nm, however, the NPs tended to aggregate to large particle. This value is in good agreement with that obtained from XRD patterns (Scherrer equation = 15.7 nm).

 

 

 

Fig. 3. The TEM micrographs of synthesized Fe3O4@SiO2-APTES NPs.

 

 

The effect of solution pH

The effect of pH on the RB-5 (20 mg L-1) adsorption onto Fe3O4@SiO2-APTES NPs (0.3 g L-1) was investigated between pH 3 to 9, and the results are depicted in Fig. 4.

The removal efficiency decreased from 96.45 to 29.14% by increasing the solution pH from 3 to 9. The interactions between Fe3O4@SiO2-APTES NPs and RB-5 dye are shown in Fig. 4b.

 

 

The effect of adsorbent dosage

The influence of adsorbent dosage on the removal efficiency for RB-5 was investigated at various amounts of Fe3O4@SiO2-APTES NPs in the range of 0.1-0.4 g L-1 at pH 3 (Fig. 5). Indeed, the removal efficiency increased from 43.9 to 100% by increasing the adsorbent dosage from 0.1 to 0.4 g L-1 over the entire reaction time (1-120 min).

 

The effect of initial RB-5 concentration

The effect of initial RB-5 concentration on the removal efficiency was studied by varying the initial RB-5 concentration (20, 40, 60, 80 mg L-1)

 

 

 

at constant adsorbent dosage (0. 4 g L-1) and at pH 3 (Fig. 6). By increasing initial RB-5 concentration from 20 to 80 mg L-1, the RB-5 removal efficiency decreased from 100 to 54.7%.

 

The recovery of Fe3O4@SiO2-APTES NPs

While RB-5 dye adsorption on the Fe3O4@SiO2-APTES is a reversible process, it is possible for regeneration or activation of adsorbent to reuse (Fig. 7).

The desorption ability of NaOH 0.1 M was found higher than the other solvents.

The results showed that desorption efficiency higher than 80% after six cycles can be attained in a short time of 1 min and in a one-step elution using 3 mL of NaOH 0.1 M, as shown in Fig. 7. Furthermore, after seven cycles of the desorption-adsorption process, the high magnetic sensitivity of Fe3O4@SiO2-APTES still retained and was collected from the solution using a magnet of 1.4 T. Therefore, the Fe3O4@SiO2-APTES can be potentially used as a magnetic adsorbent for further dye adsorption from water.

 

 

 

Fig. 4. (a) The effect of pH on the removal of RB-5 dye and (b) main interactions between Fe3O4@SiO2-APTES NPs and RB-5 dye.

 

 

Fig. 5. The effect of adsorbent dosage on the removal of RB-5 dye.

 

 

 

 

Fig. 6. The effect of initial RB-5 concentration.

 

Fig. 7. The results of reusability test for the removal of RB-5 dye by Fe3O4@SiO2-APTES NPs (pH = 3, initial dye concentration = 20 mg L-1, adsorbent dose = 0.4 g L-1).

 

 

 

 

Kinetic and equilibrium studies

Adsorption kinetic experiments were performed at different RB-5 concentration 20, 40, 60 and 80 mg L-1, at constant adsorbent dosage 0.4 g L-1 and at pH = 3.

The kinetics and isotherms parameters are shown in Tables 3 and 4. The kinetic data for RB-5 adsorption showed the best fitting (R2 = 0.997) with the pseudo-second order model. The values of correlation coefficient R2 = 0.995, R2 = 0.987 and R2 = 0.973 at 20, 35 and 45 oC indicate that sorption of the RB-5 by

 

 

 

Fe3O4@SiO2-APTES NPs follows the Langmuir isotherm. In these temperatures, interaction between the RB-5 and Fe3O4@SiO2-APTES NPs is probably larger due to the presence of a higher number of potential adsorption sites. However, at high temperatures, the interaction between RB-5 and Fe3O4@SiO2-APTES NPs is weakened due to decrease in electrostatic and van der Waal interactions (Mohammadi Galangash et al. 2016).The Langmuir and Freundlich isotherm charts are displayed at 20 °C in Figs. 8 and 9.

 

Table 3. The kinetic parameters for removal of RB-5 dye by Fe3O4@SiO2-APTES NPs.

Concentration  mg L-1

Pseudo-first order

Pseudo-second-order

 

qe(exp)

k1

qe(cal)

R2

k2

qe(cal)

R2

20

50

0.0215

51

0.0063

0.004007

52.63158

0.9947

40

85.101

0.0216

86.1

0.4818

0.001511

87.719

0.9855

60

106.32

0.0244

107.3

0.48

0.001336

109.89

0.979

80

109.4366

0.0032

108.8

0.4838

0.001047

114.9425

0.9748

 

Table 4. The isotherm parameters for the adsorption of RB-5 dye by Fe3O4@SiO2-APTES NPs.

Temperature

Freundich isotherm

Langmuir isotherm

oC

KF

N

R2

qm

KL

R2

RL

20

35.07519

5.327651

0.8734

56.49718

1.041176

0.9957

0.045822

35

46.78429

2.85144

0.8848

116.2791

8.77551

0.9875

0.005665

45

43.05266

2.650411

0.9732

119.0476

6.774194

0.9734

0.007327

 

 

 

Fig. 8. Langmuir isotherm chart at 20 °C (pH = 3 and initial dye concentration = 20 mg L-1).

 

 

Fig. 9. Freundich isotherm chart at 20 ° C (pH = 3 and initial dye concentration = 20 mg L-1).

 

 

DISCUSSION

In absorption studies, after synthesis and characterization of adsorbent, some parameters and models are evaluated to achieve the kind of adsorption process in the environment and the economic value of the prepared adsorbent. Kinetic evaluation is necessary to determine the rate and degree of dye removal efficiency (Soltani & Entezari 2013) and kinetic models are used to determine the absorption and penetration mechanisms (Salmani et al. 2011). As shown in Table 4, by increasing the initial concentration of RB-5 from 20 to 80 mg L-1, the K2 and R2 ratios in the pseudo-second order kinetics were decreased from 0.004 to 0.001 g mg-1 min-1 and from 0.9947 to 0.9748, respectively. Also, qe (mg g-1) increased from 52.63 to 114.94 mg g-1. These results show that the absorption process of RB-5 using Fe3O4@SiO2-APTES NPs is more consistent with the Pseudo-second order model (R2 = 0.9999). This model shows a chemical absorption (Wang et al. 2004).

The findings of Azizian (2004) and Xu et al. (2016) are consistent with the results of the present study.

The isothermal studies are carried out to explain the reaction between adsorbent and pollutant as well as the removal capacity (Alizadeh et al. 2012).

The Table 5 can be explained such that RB-5 absorption process is more compatible with Langmuir model (R2 = 0.9957). The maximum

 

 

 

absorption capacity at 20 °C was  56.497 mg g-1. Also, at this temperature, the amount of RL factor was found 0.045 which is between 0 and 1 and this indicates the desirability of the absorption process (Farrokhi et al. 2014). The obtained results were consistent with those of Mohagheghian et al. (2015) and Mohammadi Galangash et al. (2016) on the removal of Azo dye by modified magnetic NPs.

The results also point out that the NPs have a homogeneous surface, and all of the absorbing sites are similar in surface and also the RB-5 absorption mechanism on Fe3O4@SiO2-APTES NPs is monolayer and the adsorption sites in NPs surface have the same energy (Poursaberi & Hassanisadi 2013). The pH of the aqueous solution is an important effect on the surface charge of the adsorbents, the degree of ionization and speciation of the adsorbents. Therefore, in most water and wastewater treatment studies, this factor is always carefully considered. The results of this study, as shown in Fig. 4, illustrate that by increasing the pH, the absorption rate efficiency by the NPs has a decreasing trend, and these results are very consistent with those of Xu et al. (2016), Ballav et al. (2015) and Ballav et al. (2015).

The increased efficiency of the removal of RB-5 dye by Fe3O4@SiO2-APTES NPs at acidic pH can be associated with an increase in positive H+ ion in the environment versus the reduction of negative OH- ions. Because RB-5 is an anionic dye, at low pH, and the adsorbent surface with positive charge, so a strong electrostatic interaction occurs between amine in the positively-charged groups on the adsorbent surface and negative RB-5 molecules. In other words, by decreasing the pH, the number of sites with positive charge on NPs increases, so these places tend to absorb dye due to electrostatic gravity (Geetha et al. 2014). Therefore, by increasing in pH, the removal efficiency of the RB-5 decreases, as shown schematically in Fig. 4b (Manimekalai et al. 2015). Subsequently, the adsorption of dye on Fe3O4@SiO2-APTES NPs was investigated by changing the quantity of adsorbent on dye removal. The results of removal process showed that, by increasing the amount of adsorbent dosage from 0.1 to 0.4 g L-1, the removal of dye performance had an aggregate trend. Apparently, by increasing the amount of active sites, the absorption process will be increased. But how long will this process last? Its response is shown in Fig. 5 that the removal rate of RB-5 at all doses was rapid in the first stages of contact time and then it was slowed down step by step. This kind of absorption process is consistent with results of Mohammadi Galangash et al. (2016). The rapid adsorption at the initial reaction time may be attributed to the easy availability of active sites for RB-5 molecules. As the active sites are occupied by RB-5, adsorption rates will be reduced due to less availability of active locates on the adsorbent surfaces (Xue et al. 2009). The concentration of the pollutant also plays an important role in the absorption process. By increasing the initial RB-5 concentration from 20 to 80 mg L-1, the RB-5 removal efficiency was decreased. Similar observations were also reported for the removal of other dyes (Xue et al. 2009; Vimonses et al. 2009). These results can be explained with the fact that the adsorbent has a limited number of active sites, which would become saturated above a certain pollutant concentration (Zhu et al. 2010). Therefore, we can determine, based on the optimum absorbent dose rate, the maximum removable concentration of pollutant with proper efficiency for our operational planning (Fig. 6). As the amount of consumed NPs is considered in their economic assessment, the recycling potential and frequency of NPs recovery are other important factors that are very important for the economic justification of produced NPs (Mohammadi Galangash et al. 2016). According to Fig. 7, the reusability of adsorbent was examined and adsorption capacity of RB-5 by regenerated of Fe3O4@SiO2-APTES NPs was maintained with proper efficiency up to six consecutive runs. Therefore, it can be recommended as a plausible adsorbent for treatment of the organic dyes. Regeneration of Fe3O4@SiO2-APTES NPs by NaOH can be due to the weak electrostatic bond between the adsorbent and RB-5 dye in alkaline medium. As a result, the exchange of hydroxide ions and negative charge dye molecules will be occurred (Agarwal et al. 2016).

In fact, the RB-5 molecules on the surface of Fe3O4@SiO2-APTES could be replaced with hydroxyl of the basic solution in adsorbent washing step. Under higher removal cycles, removal efficiency decrease may be due to oxidation, losing or dissolving some a mounts of the adsorbent through the following steps.

The adsorption capacity of Fe3O4@SiO2-APTES for the removal of RB-5 has been compared with other adsorbents reported in literature and the values of qmax have been listed in Table 5 (Kalkan et al. 2014; Mook et al. 2015; Samadi et al. 2015; Amin et al. 2015; Munagapati et al. 2018).

Therefore, noteworthy, the Fe3O4@SiO2-APTES has important potential to remove RB-5 from aqueous solution.

Furthermore, the magnetic properties of Fe3O4@SiO2-APTES make it as a more efficient adsorbent for the removal of contaminant from aqueous solution.

 

 

 

 

Table 5. Comparison of various adsorbents for RB-5 removal.

Adsorbents

qm

(mg g-1)

Adsorbent dosage

(g L-1)

Concentration (mg L-1)

Best fit isotherm

Ref.

BPPa

49.2

0.60

300

Langmuir

Munagapati et al. 2018

Palm Shellb

25.1

3.0

40

Langmuir

Mook et al. 2015

LMSFc

322.58

1.0

5

Langmuir

Kalkan et al. 2014

MWCNd

36.2

0.50

50

Freundlich

Samadi et al. 2015

BCe

34.01

0.50

170

Freundlich

Amin et al. 2015

Fe3O4@SiO2-APTES

56.497

0.40

20

Langmuir

This work

a Banana Peel Powder

b Activated Carbon Derived from Biomass Waste

c Laccase-Modified Silica Fume

d Multi-Walled Carbon Nanotubes

e Bentonite Clay

 

 

Agarwal, S , Tyagi, I , Gupta, VK , Mashhadi, S  & Ghasemi, M  2016, Kinetics and thermodynamics of     Malachite Green dye removal from aqueous phase using iron nanoparticles loaded on ash. Journal of Molecular Liquids, 223: 1340-1347.
Alizadeh, A, Khodaei, M, Beygzadeh, Kordestani, D & Feyzi, M 2012, Biguanide-functionalized Fe3 O4/SiO2 magnetic nanoparticles: an efficient heterogeneous organosuperbase catalyst for various organic transformations in aqueous media. Bulletin of the Korean Chemical Society, 33: 2546-2552.
Amin, MT, Alazba, AA & Shafiq, M  2015, Adsorptive removal of reactive black 5 from wastewater using bentonite clay: isotherms, kinetics and thermodynamics, Sustainability, 7: 15302-15318.
Azizian, S 2004, Kinetic models of sorption: a theoretical analysis. Journal of Colloid and Interface Science, 276: 47-52.
Ballav, N, Debnath, S, Pillay, K & Maity, A 2015, Efficient removal of Reactive Black from aqueous solution using polyaniline coated ligno-cellulose composite as a potential adsorbent. Journal of Molecular Liquids, 209: 387-396.
Chen, AH & Huang, YY 2010, Adsorption of Remazol Black 5 from aqueous solution by
 
 
 
       the templated crosslinked-chitosans. Journal of Hazardous Materials, 177: 668-675.
Choi, HD, Shin, MC, Kim, DH, Jeon, CS & Baek, K 2008, Removal characteristics of Reactive Black 5 using surfactant-modified activated carbon. Desalination, 22: 290-298.
Demirbas, E & Nas, MZ 2009, Batch kinetic and equilibrium studies of adsorption of Reactive Blue 21 by fly ash and sepiolite. Desalination, 243: 8-21.
Eren, Z & Acar, FN 2007, Equilibrium and kinetic mechanism for Reactive Black 5 sorption onto high lime Soma fly ash. Journal of Hazardous Materials, 143: 226-232.
Farrokhi, M, Hosseini, SC, Yang, J & Shirzad-Siboni, M 2014, Application of ZnO-Fe3O4 nanocomposite on the removal of azo dye from aqueous solutions: kinetics and equilibrium studies. Water, Air, and Soil Pollution Journal, 225: 1-12.
Galangash, MM, Kolkasaraei, ZN, Ghavidast, A & Shirzad-Siboni, M 2016, Facile synthesis of methyl propylaminopro- panoate functionalized magnetic nanoparticles for removal of acid red 114 from aqueous solution. RSC Advances, 6: 113492-113502.
Geetha, K, Velmani, N & Syed Shabudeen, PS  2014, Estimation of Acid Red 114 adsorption using Ceiba Pentradenta wood bark based activated carbon modified using phosphoric acid. Journal of Chemical and Pharmaceutical Research, 6:26-39.
Gholivand, MB, Yamini, Y, Dayeni, M, Seidi, S & Tahmasebi, E 2015, Adsorptive removal of alizarin red-S and alizarin yellow GG from aqueous solutions using polypyrrole-coated magnetic nanoparticles. Journal of Environmental Chemical Engineering, 3: 529-540.
Ghoreishian, SM, Badii, K, Norouzi, M, Rashidi, A, Montazer, M, Sadeghi, M & Vafaee, M  2014, Decolorization and mineralization of an azo reactive dye using loaded nanophotocatalysts on spacer fabric: kinetic study and operational factors. Journal of the Taiwan Institute of Chemical Engineers, 45: 2436–2446.
Iram, M, Guo, C, Guan, Y, Ishfaq, A & Liu, H 2010, Adsorption and magnetic removal of neutral red dye from aqueous solution using Fe3O4 hollow nanospheres. Journal of Hazardous Materials, 181: 1039-1050.
Kalkan, E, Nadaroğlu, H, Celebi, N & Tozsin, G 2014, Removal of textile dye Reactive Black 5 from aqueous solution by adsorption on laccase-modified silica fume, Desalination and Water Treatment, 52: 6122-6134.
Karadag, D, Turan, M, Akgul, E, Tok, S & Faki, A 2007, Adsorption equilibrium and kinetics of Reactive Black 5 and reactive red 239 in aqueous solution onto surfactant-modified zeolite. Journal of Chemical and Engineering Data, 52: 1615-1620.
Liu, Y, & Liu, Y J 2008, Biosorption isotherms, kinetics and thermodynamics. Separation and Purification Technology, 61: 229-242.
Madrakian, T, Afkhami, A, Mahmood-Kashani, H & Ahmadi M 2013, Adsorption of some cationic and anionic dyes on magnetite nanoparticles-modified activated carbon from aqueous solutions: equilibrium and kinetics study. Journal of Iranian Chemical Society, 10: 481-9.
Manimekalai, T, Sivakumar, N & Periyasamy, S  2015, Catalytic Pyrolysis of Plastic Waste into Activated Carbon and its Adsorption Studies on Acid Red 114 as Model Organic Pollutant. International Journal of Chemical Technology Research, 8: 333-348.
Mohagheghian, A, Vahidi-Kolur, R, Pourmohseni, M, Yang, JK & Shirzad-Siboni, M  2015, Application of scallop SHELL-Fe3O4 nano-composite for the removal azo dye from aqueous solutions. Water, Air, and Soil Pollution, 226: 1-16.
Mook, WT, Aroua, MK & Szlachta, M 2015, Palm shell-based activated carbon for removing reactive black 5 dye: equilibrium and kinetics studies, Bioresources, 11: 1432-1447.
Moussavi, G, Mahmoudi, M 2009, Removal of azo and anthraquinone reactive dyes from industrial wastewaters using MgO nanoparticles. Journal of Hazardous Materials, 168: 806-812.
Munagapati, VS, Yarramuthi, V, Kim, Y, Lee, KM & Kim, DS  2018, Removal of anionic dyes (Reactive Black 5 and Congo Red) from aqueous solutions using Banana Peel Powder as an adsorbent, Ecotoxicology and Environmental Safety, 148: 601-607.
Poursaberi, T & Hassanisadi, M  2013 Magnetic removal of Reactive Black 5 from wastewater using ionic liquid grafted magnetic nanoparticles. Clean Soil. Air, Water Journal, 41: 1208-1215.
Qu, S, Huang, F, Yu, S, Chen, G & Kong, J 2008, Magnetic removal of dyes from aqueous solution using multi-walled carbon nanotubes filled with Fe2O3 particles. Journal of Hazardous Materials, 160: 643-647.
Ramachandran, P, Vairamuthu, R &  Ponnusamy, S  2011, Adsorption isotherms, kinetics, thermodynamics and desorption studies of reactive orange16 on activated carbon derived from ananascomosus (L) carbon. ARPN Journal of Engineering and Applied Sciences, 6: 100-110.
Robinson, T, McMullan, G, Marchant, R & Nigam, P 2011, Remediation of dyes in textile effluent: a critical review on current treatment technologies with a proposed alternative. Bioresource Technology, 77: 247-255.
Samadi, MT, Zolghadrnasab, H, Godini, K, Poormohammadi, A, Ahmadian, M & Shanesaz, S  2015, Kinetic and adsorption studies of reactive black 5 removal using multi-walled carbon nanotubes from aqueous solution, Der Pharma Chemica, 7: 267-274.
Samarghandi, M, Azizian, S, Siboni, MS, Jafari, S & Rahimi, S 2011, Removal of divalent nickel from aqueous solutions by adsorption onto modified holly sawdust: equilibrium and kinetics. Iranian Journal of Environmental Health Science and Engineering, 8: 167–174. 
Sheshmani, S, Ashori, A &  Hasanzadeh, S 2014, Removal of Acid Orange 7 from aqueous solution using magnetic graphene/ chitosan: A promising nano-adsorbent. International Journal of Biological Macromolecules, 68: 218-224.
Sadaf, S & Bhatti, HN 2014, Batch and fixed bed column studies for the removal of Indosol Yellow BG dye by peanut husk. Journal of the Taiwan Institute of Chemical Engineers, 45: 541–553.
Salmani, MH, Aboueyan, M, Ehrampoush, M H, Zare, HR & Sazvari, M  2011, Ability of iron oxide nanoparticles in ion silver removal from synthetic wastewater, TOLOO-E-BEHDASHT, 10: 62-69.
Soltani, T & Entezari, M 2013, Solar photocatalytic degradation of RB5 by ferrite bismuth nanoparticles synthesized via ultrasound. Ultrasonics Sonochemistry, 20: 1245-1253.
Travlou, NA, Kyzas, GZ, Lazaridis, NK & Deliyanni, EA  2013, Graphite oxide/chitosan composite for reactive dye removal. Chemical Engineering Journal, 217: 256-265.
Vijayaraghavan, K & Yun, YS 2008, Biosorption of CI Reactive Black 5 from aqueous solution using acid-treated biomass of brown seaweed Laminaria sp. Dyes and Pigments, 76: 726–732.
Vimonses, V, Lei, S, Jin, B, Chow, CW  & Saint, C  2009, Adsorption of congo red by three Australian kaolins. Applied Clay Science, 43: 465-472.
Wang, LK, Hung, YT, Lo, HH &  Yapijakis, C 2004, Handbook of industrial and hazardous wastes treatment. CRC Press.
Xu, ZLiW, Xiong, Z, Fang, JLiY, Wang, Q &  Zeng, Q 2016, Removal of anionic dyes from aqueous solution by adsorption onto amino functionalized magnetic nanoads- orbent. Desalination and Water Treatment, 57: 7054-7065.
Xue, Y, Hou, H & Zhu, S 2009, Adsorption removal of reactive dyes from aqueous solution by modified basic oxygen furnace slag: isotherm and kinetic study. Chemical Engineering Journal, 147: 272–279.
Yang, N, Zhu, S, Zhang, D & XuS 2008, Synthesis and properties of magnetic Fe3O4-activated carbon nanocomposite particles for dye removal. Materials Letters, 62: 645-647.
Zhang, Z & Kong, J 2011, Novel magnetic Fe3O4@C nanoparticles as adsorbents for removal of organic dyes from aqueous solution. Journal of Hazardous Materials, 193: 325-329.
Zhang, YR, Shen, SL, Wang, SQ , Huang, J , Su, P , Wang, QR , Zhao, BX  2014, A dual function magnetic nanomaterial modified with lysine for removal of organic dyes from water solution. Chemical Engineering Journal, 239: 250-256.
Zhu, HY, Jiang, R & Xiao, L 2010, Adsorption of an anionic azo dye by chitosan/kaolin/γ-Fe2O3 composites. App- lied Clay Science, 48: 522-526.