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International Journal of Photoenergy
Volume 2012 (2012), Article ID 608298, 5 pages
Synthesis and Characterization of Iron Oxide Nanoparticles and Applications in the Removal of Heavy Metals from Industrial Wastewater
1School of Chemical & Life Sciences, Singapore Polytechnic, 500 Dover Road, Singapore 139651
2Advanced Material Technology Centre, Singapore Polytechnic, 500 Dover Road, Singapore 139651
Received 16 January 2012; Accepted 17 February 2012
Academic Editor: Stéphane Jobic
Copyright © 2012 Zuolian Cheng et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
This study investigated the applicability of maghemite (γ-Fe2O3) nanoparticles for the selective removal of toxic heavy metals from electroplating wastewater. The maghemite nanoparticles of 60 nm were synthesized using a coprecipitation method and characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectroscopy (EDX). Batch experiments were carried out for the removal of Pb2+ ions from aqueous solutions by maghemite nanoparticles. The effects of contact time, initial concentration of Pb2+ ions, solution pH, and salinity on the amount of Pb2+ removed were investigated. The adsorption process was found to be highly pH dependent, which made the nanoparticles selectively adsorb this metal from wastewater. The adsorption of Pb2+ reached equilibrium rapidly within 15 min and the adsorption data were well fitted with the Langmuir isotherm.
With heavy metal pollution becoming one of the most serious environmental problems, various methods for heavy metal removal from wastewater have been extensively studied during the past decades, such as chemical precipitation, electrochemical techniques, membrane filtration, ion exchange, and adsorption . To date, considerable research attention has been paid to the removal of heavy metals from contaminated water via adsorption process. In theory, the adsorption process can offer flexibility in design and operation and in many cases will produce high-quality treated effluent. In addition, as the adsorption is sometimes reversible and adsorbent can be regenerated by suitable desorption process, various types of adsorbents have found application in the removal of heavy metals, including activated carbon [2, 3], carbon nanotubes [4–6], polymeric adsorbents , metal oxides , and bioadsorbents [9–12]. Among these adsorbents, iron-based magnetic nanomaterials have distinguished themselves by their unique properties, such as larger surface area-volume ratio, diminished consumption of chemicals, and no secondary pollutant. However, with another special property of this kind magnetic materials are realized and utilized in the context of environmental remediation. More and more magnetic separation has been combined with adsorption for the removal of heavy metals from contaminated water at laboratory scales [13–15]. Especially in industries, magnetic separation is desirable because it can overcome many drawbacks occurring in the membrane filtration, centrifugation, or gravitational separation and is easy to achieve a given level of separation just via external magnetic field.
Iron oxides exit in many forms in nature, with magnetite (Fe3O4), hematite (α-Fe2O3) and maghemite (γ-Fe2O3), being most probably common and important technologically . It has been reported that surface effects have a strong influence on the magnetic properties of iron oxide nanoparticles . As the surface area of iron-oxide-based magnetic materials decreased, their responses to external magnetic field decreased, making it difficult to recover the adsorbents after treatment has been completed . On the other hand, it has also been noted that the adsorption capacities of adsorbents rely largely on the available surface areas, and the increase of the surface area is normally obtained by the decrease of the particle size of adsorbents. As a result, there is a need to synthesize such absorbents with proper particles sizes for the removal of heavy metals from industrial wastewater.
Up to now, there are several methods that can be used to synthesize iron-oxide-based nanomaterials. These methods include hydrothermal synthesis [18, 19], thermal decomposition [20, 21], co-precipitation [22, 23], sol-gel method , and colloidal chemistry method . Among these synthesis methods, coprecipitation has proven to be the most promising method for the production of nanomaterials as the procedure is relatively simple and the particles can be obtained with controlled particle size.
The specific objective of the present study was (1) to synthesize γ-Fe2O3 nanoparticles using a modified method, which involved urea as a uniformity precipitation reagent, (2) to characterize γ-Fe2O3 nanoparticles synthesized using different kinds of analytical instruments, and (3) to evaluate synthesized γ-Fe2O3 nanoparticles as adsorbents to remove heavy metals such as Pb2+ from industrial wastewater.
2.1. Preparation and Characterization of γ-Fe2O3 Nanoparticles
The synthesis of γ-Fe2O3 nanoparticles involves the following steps: (1) a designated molar ratio of iron chloride and urea was dissolved in deionized water; (2) the mixture was continuously stirred for 45 min at 90°C in a water bath before it was cooled to room temperature; (3) the produced precipitation was centrifuged and washed by deionized water and followed by ethanol; (4) after being dried at 75°C for 4 hours, the collected powder was slowly calcined to 650°C in air and dwelt for 2 hours. The resultant product of γ-Fe2O3 nanoparticles was obtained for subsequent characterization.
A scanning electron microscope (SEM, JEOL JEM2010, Japan) was used to characterize the structure properties of the synthesized materials. The element composition of the synthesized materials was identified by an energy dispersive X-ray spectroscopy system (EDX) coupled to the SEM. The crystallization phase analysis was executed by a powder X-ray diffraction (XRD) (Philips PW-1830, Netherlands). Magnetization measurement was carried out with a vibration sample magnetometer (VSM) at room temperature.
2.2. Removal of Heavy Metals from Wastewater
A stock solution containing Pb2+ was prepared by dissolving a known quantity of lead nitrate (Pb(NO3)2) in deionized water. Batch adsorption studies were performed by mixing 0.5 g of γ-Fe2O3 with 50 mL of solutions of varying Pb2+ concentrations (50, 100, and 150 mg/L) in 100 mL glass vials. The adsorption on γ-Fe2O3 was first studied at pH values of 2.5 to 6.5 to investigate the effects of pH values on the Pb2+ adsorption. 0.1 M HCl and 0.1 M NaOH solutions were used to adjust the pH values of water samples. The pH values of water samples were stable over the the experiment period. All the adsorption experiments were carried out at a room temperature of and were performed in triplicate. The total aqueous concentrations of Pb2+ were measured using an inductively coupled plasma-optical emission spectrometer (ICP-OES, Thermo, icap 6000). Sample dilution was conducted before the ICP-OES measurement, where necessary.
3. Results and Discussion
3.1. Synthesis and Characterization of γ-Fe2O3
The crystalline grain size is mainly determined by both the formation energy of growth unit and the lattice energy, besides different synthesis conditions. In the present study, Fe2O3 nanoparticles were synthesized by varying pH values, ageing time, the mass ratio of FeCl3 and urea, and so forth. Figure 1(a) shows an SEM image of the synthesized γ-Fe2O3, confirming that the particles obtained were indeed in the nanometer range. Upon ageing for different durations, it was observed that the grain size increased with increasing ageing time. The smallest grain size ( nm) was obtained after ageing for 45 minutes. In addition, strong peaks for Fe and O can be observed in the spectrum illustrated in Figure 1(b) for particles after ageing time of 45 min. The insert of Figure 1(b) reveals that the O/Fe atomic ratio of the γ-Fe2O3 analyzed was 1.56, which was relatively consistent with the theoretical O/Fe atomic ratio of 1.50.
The magnetization with respect to applied field was recorded at room temperature. The hysteresis loop, shown in Figure 2, suggested a weak magnetic nature of the samples with little hysteresis. The weak magnetism might be caused by the presence of α-Fe2O3 as detected by XRD. From Figure 2, the MS was calculated to be 0.025 emu/g and the HC to be 1250 Oe.
Figure 3 shows the results of XRD analysis for the synthesized nanoparticles that were obtained with different initial concentrations of FeCl3. It indicates that the particles consist of γ-Fe2O3 (peaks denoted by *) and α-Fe2O3 (peaks denoted by #). It also indicates that a concentration of 0.02 M of FeCl3 resulted in the particles with the smallest Z-average diameter. Therefore, 0.02 M was the optimized concentration for FeCl3.
3.2. Effect of Adsorption Time and Initial Concentration
The adsorption of Pb2+ onto γ-Fe2O3 nanoparticles was monitored for 120 min. The initial Pb2+ concentrations were 50, 100, and 150 mg/L, respectively. The initial pH value of water samples was 5.5, and the solution temperature was . As seen in Figure 4, Pb2+ ions were adsorbed onto γ-Fe2O3 nanoparticles rapidly, and equilibrium was established within 30 minutes. This could be due to the small size of γ-Fe2O3 nanoparticles, which was favorable for the diffusion of Pb2+ ions from bulk solution onto the active sites of the solid surface. External adsorption dominated and no pore diffusion was observed to slow down the adsorption rate. Despite the short equilibrium time, a 24-h contact time was adopted for the subsequent experiment to ensure that adsorption equilibrium was achieved. The short equilibrium time was in agreement with that reported by other researchers for the adsorption of other metal ions onto iron oxide nanoparticles [25–27]. This is in contrast to other conventional porous adsorbents in which adsorption occurs through pore diffusion steps, which in turn slow down the adsorption rate. The γ-Fe2O3 nanoparticles are nonporous adsorbents, as confirmed by the surface area and porosity measurements, where only external adsorption occurred. This type of adsorption mass transfer requires less time to reach the equilibrium . This result is promising as equilibrium time plays a major role in economic viability for wastewater treatment plant. Furthermore, as shown in Figure 4, the amount adsorbed of Pb2+ increased with the increase in the initial concentration of Pb2+ in water samples. This can be attributed to the increase in the ion occupancy number, which favors the adsorption process.
3.3. Effect of pH
It is well known that pH is one of the most important factors that affect the adsorption process of heavy metals in water samples. The experiments were carried out to find the optimum pH on the adsorption of Pb2+ ions onto γ-Fe2O3 nanoparticles using different initial pH values of 2.5 to 6.5. The experimental pH values of up to 6.5 were chosen as precipitation of lead hydroxide would occur at pH values equal to or higher than 7.0, even though other variables such as the amount of nanoparticles were fixed . Therefore, it was not feasible to carry out the adsorption experiments for Pb2+ at pH > 6.5 without introducing some uncertainties to the results. Figure 5 shows the effects of pH on the adsorption of Pb2+. As observed in the graph, the removal efficiency of Pb2+ ions from watersamples by the γ-Fe2O3 nanoparticles was clearly pH dependent and the highest adsorption efficiency was obtained at pH ≥5.5. Lee et al. also observed a similar pH effect for the adsorption of Pb2+ onto bulk iron oxides in water samples . It indicated that a water sample with a higher pH value was favorable for the deprotonation of sorbent surface [31, 32]. Increased deprotonation could result in the increase of negatively charged sites, which enhanced the attractive forces between the sorbent surface and the Pb2+ ions. Therefore, it will result in the increase in the adsorption capacity. On the other hand, in a water sample with lower pH, the positively charged sites dominate and this could enhance the repulsion forces existing between the sorbent surface and the Pb2+ ions and therefore decrease the adsorption of Pb2+ ions.
3.4. Effects of Salinity
Increasing NaCl salinity from 0% to 3.5% (the salinity of seawater) had no effects on the removal of Pb2+ by γ-Fe2O3 nanoadsorbents. This suggested that no interaction occurred among NaCl, Pb2+ and γ-Fe2O3 nanoadsorbents, and the complexation of Pb2+, and Cl− was much weaker than the coordination between Pb2+ and the adsorptive sites on the surfaces of γ-Fe2O3 nanoadsorbents.
This study showed that the prepared γ-Fe2O3 nanoparticles could be used as an alternate to the conventional adsorbents for the removal of metal ions from wastewater with high removal efficiency within a very short time. The removal of Pb2+, as a typical metal ion commonly present in wastewater, by adsorption onto γ-Fe2O3 nanoparticles was successfully accomplished. Adsorption was very rapid and equilibrium was achieved within 15 min. It also showed that adsorption was highly dependent on the initial concentration of Pb2+ and initial pH value. Maximum removal efficiency was achieved at pH 5.5 at room temperature. Increasing NaCl from 0% to 3.5% (the salinity of seawater) had no effects on the adsorption of Pb2+ on γ-Fe2O3 nanoparticles. The adsorption isotherms were also determined and were appropriately described by both Langmuir and Freundlich models, with a better fitting to the Langmuir model than the Freundlich model. Therefore, γ-Fe2O3 nanoparticles were recommended as fast, effective, and inexpensive nanoadsorbents for rapid removal and recovery of metal ions from industrial wastewater.
This work was supported by the Ministry of Education Innovation Fund of Singapore (MOE2008-IF-1-010).
- F. Fu and Q. Wang, “Removal of heavy metal ions from wastewaters: a review,” Journal of Environmental Management, vol. 92, no. 3, pp. 407–418, 2011.
- K. C. Kang, S. S. Kim, J. W. Choi, and S. H. Kwon, “Sorption of Cu2+ and Cd2+ onto acid- and base-pretreated granular activated carbon and activated carbon fiber samples,” Journal of Industrial and Engineering Chemistry, vol. 14, no. 1, pp. 131–135, 2008.
- A. Jusoh, L. Su Shiung, N. Ali, and M. J. M. M. Noor, “A simulation study of the removal efficiency of granular activated carbon on cadmium and lead,” Desalination, vol. 206, no. 1–3, pp. 9–16, 2007.
- Y. Li, F. Liu, B. Xia et al., “Removal of copper from aqueous solution by carbon nanotube/calcium alginate composites,” Journal of Hazardous Materials, vol. 177, no. 1–3, pp. 876–880, 2010.
- M. I. Kandah and J. L. Meunier, “Removal of nickel ions from water by multi-walled carbon nanotubes,” Journal of Hazardous Materials, vol. 146, no. 1-2, pp. 283–288, 2007.
- Y. H. Li, Z. Di, J. Ding, D. Wu, Z. Luan, and Y. Zhu, “Adsorption thermodynamic, kinetic and desorption studies of Pb2+ on carbon nanotubes,” Water Research, vol. 39, no. 4, pp. 605–609, 2005.
- A. Dabrowski, Z. Hubicki, P. Podkocielny, and E. Robens, “Selective removal of the heavy metal ions from waters and industrial wastewaters by ion-exchange method,” Chemosphere, vol. 56, no. 2, pp. 91–106, 2004.
- Z. Ai, Y. Cheng, L. Zhang, and J. Qiu, “Efficient removal of Cr(VI) from aqueous solution with Fe@Fe2O3 core-shell nanowires,” Environmental Science and Technology, vol. 42, no. 18, pp. 6955–6960, 2008.
- T. Aman, A. A. Kazi, M. U. Sabri, and Q. Bano, “Potato peels as solid waste for the removal of heavy metal copper(II) from waste water/industrial effluent,” Colloids and Surfaces B, vol. 63, no. 1, pp. 116–121, 2008.
- S. J. Köhler, P. Cubillas, J. D. Rodríguez-Blanco, C. Bauer, and M. Prieto, “Removal of cadmium from wastewaters by aragonite shells and the influence of other divalent cations,” Environmental Science and Technology, vol. 41, no. 1, pp. 112–118, 2007.
- P. Pavasant, R. Apiratikul, V. Sungkhum, P. Suthiparinyanont, S. Wattanachira, and T. F. Marhaba, “Biosorption of Cu2+, Cd2+, Pb2+, and Zn2+ using dried marine green macroalga Caulerpa lentillifera,” Bioresource Technology, vol. 97, no. 18, pp. 2321–2329, 2006.
- M. Souiri, I. Gammoudi, H. B. Ouada et al., “Escherichia coli-functionalized magnetic nanobeads as an ultrasensitive biosensor for heavy metals,” Procedia Chemistry, vol. 1, no. 1, pp. 1027–1030, 2009.
- J. T. Mayo, C. Yavuz, S. Yean et al., “The effect of nanocrystalline magnetite size on arsenic removal,” Science and Technology of Advanced Materials, vol. 8, no. 1-2, pp. 71–75, 2007.
- C. T. Yavuz, J. T. Mayo, W. W. Yu et al., “Low-field magnetic separation of monodisperse Fe3O4 nanocrystals,” Science, vol. 314, no. 5801, pp. 964–967, 2006.
- J. Hu, G. Chen, and I. M. C. Lo, “Removal and recovery of Cr(VI) from wastewater by maghemite nanoparticles,” Water Research, vol. 39, no. 18, pp. 4528–4536, 2005.
- A. S. Teja and P. Y. Koh, “Synthesis, properties, and applications of magnetic iron oxide nanoparticles,” Progress in Crystal Growth and Characterization of Materials, vol. 55, no. 1-2, pp. 22–45, 2009.
- T. Neuberger, B. Schöpf, H. Hofmann, M. Hofmann, and B. Von Rechenberg, “Superparamagnetic nanoparticles for biomedical applications: possibilities and limitations of a new drug delivery system,” Journal of Magnetism and Magnetic Materials, vol. 293, no. 1, pp. 483–496, 2005.
- V. Sreeja and P. A. Joy, “Microwave-hydrothermal synthesis of γ-Fe2O3 nanoparticles and their magnetic properties,” Materials Research Bulletin, vol. 42, no. 8, pp. 1570–1576, 2007.
- T. J. Daou, G. Pourroy, S. Bégin-Colin et al., “Hydrothermal synthesis of monodisperse magnetite nanoparticles,” Chemistry of Materials, vol. 18, no. 18, pp. 4399–4404, 2006.
- K. Simeonidis, S. Mourdikoudis, M. Moulla et al., “Controlled synthesis and phase characterization of Fe-based nanoparticles obtained by thermal decomposition,” Journal of Magnetism and Magnetic Materials, vol. 316, no. 2, pp. e1–e4, 2007.
- W. Zhou, K. Tang, S. Zeng, and Y. Qi, “Room temperature synthesis of rod-like FeC2O4·2H2O and its transition to maghemite, magnetite and hematite nanorods through controlled thermal decomposition,” Nanotechnology, vol. 19, no. 6, Article ID 065602, 2008.
- W. Yu, T. Zhang, J. Zhang, X. Qiao, L. Yang, and Y. Liu, “The synthesis of octahedral nanoparticles of magnetite,” Materials Letters, vol. 60, no. 24, pp. 2998–3001, 2006.
- I. Nedkov, T. Merodiiska, L. Slavov, R. E. Vandenberghe, Y. Kusano, and J. Takada, “Surface oxidation, size and shape of nano-sized magnetite obtained by co-precipitation,” Journal of Magnetism and Magnetic Materials, vol. 300, no. 2, pp. 358–367, 2006.
- P. D. Cozzoli, E. Snoeck, M. A. Garcia et al., “Colloidal synthesis and characterization of tetrapod-shaped magnetic nanocrystals,” Nano Letters, vol. 6, no. 9, pp. 1966–1972, 2006.
- A. Uheida, M. Iglesias, C. Fontàs et al., “Sorption of palladium(II), rhodium(III), and platinum(IV) on Fe3O4 nanoparticles,” Journal of Colloid and Interface Science, vol. 301, no. 2, pp. 402–408, 2006.
- A. Uheida, G. Salazar-Alvarez, E. Björkman, Z. Yu, and M. Muhammed, “Fe3O4 and γ-Fe2O3 nanoparticles for the adsorption of Co2+ from aqueous solution,” Journal of Colloid and Interface Science, vol. 298, no. 2, pp. 501–507, 2006.
- H. Sun, X. Zhang, Q. Niu, Y. Chen, and J. C. Crittenden, “Enhanced accumulation of arsenate in carp in the presence of titanium dioxide nanoparticles,” Water, Air, and Soil Pollution, vol. 178, no. 1–4, pp. 245–254, 2007.
- P. K. Dutta, A. K. Ray, V. K. Sharma, and F. J. Millero, “Adsorption of arsenate and arsenite on titanium dioxide suspensions,” Journal of Colloid and Interface Science, vol. 278, no. 2, pp. 270–275, 2004.
- T. K. Naiya, A. K. Bhattacharya, and S. K. Das, “Adsorption of Pb(II) by sawdust and neem bark from aqueous solutions,” Environmental Progress, vol. 27, no. 3, pp. 313–328, 2008.
- S. Z. Lee, L. Chang, H. H. Yang, C. M. Chen, and M. C. Liu, “Adsorption characteristics of lead onto soils,” Journal of Hazardous Materials, vol. 63, no. 1, pp. 37–49, 1998.
- P. Roonasi and A. Holmgren, “An ATR-FTIR study of sulphate sorption on magnetite; rate of adsorption, surface speciation, and effect of calcium ions,” Journal of Colloid and Interface Science, vol. 333, no. 1, pp. 27–32, 2009.
- S. B. Johnson, G. V. Franks, P. J. Scales, D. V. Boger, and T. W. Healy, “Surface chemistry-rheology relationships in concentrated mineral suspensions,” International Journal of Mineral Processing, vol. 58, no. 1–4, pp. 267–304, 2000.