Adsorptive Removal of Iron Using SiO<sub>2</sub> Nanoparticles Extracted from Rice Husk Ash

Nguyen, Tan Tai; Ma, Hoa Thai; Avti, Pramod; Bashir, Mohammed J. K.; Ng, Choon Aun; Wong, Ling Yong; Jun, Hieng Kiat; Ngo, Quang Minh; Tran, Ngoc Quyen

doi:https://doi.org/10.1155/2019/6210240

Journal of Analytical Methods in Chemistry

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Abstract Introduction Materials and Methods Results and Discussion Conclusion Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2019 | Article ID 6210240 | https://doi.org/10.1155/2019/6210240

Adsorptive Removal of Iron Using SiO₂ Nanoparticles Extracted from Rice Husk Ash

Tan Tai Nguyen,¹Hoa Thai Ma,²Pramod Avti,³Mohammed J. K. Bashir,⁴Choon Aun Ng,⁴Ling Yong Wong,⁴Hieng Kiat Jun,⁵Quang Minh Ngo,^6,7,8and Ngoc Quyen Tran^10,9

Academic Editor: Jaroon Jakmunee

Received13 Dec 2018

Revised18 Mar 2019

Accepted15 Apr 2019

Published02 Jun 2019

Abstract

In this work, SiO₂ nanoparticles were prepared by the sol-gel method after sodium silicate was extracted from rice husk ash (RHA) under various experimental conditions such as types of acids, NaOH concentration, dissolved time, and temperature and used for removal of Fe²⁺ ions from aqueous solutions. The extracted SiO₂ was morphologically and chemically characterized and showed a surface area of 78 m²/g and uniform pores of 2.71 nm, offering high adsorption capacity for Fe²⁺ ions. The influence of pH, contact time, and amount of adsorbent was studied in order to establish the best conditions for the Fe²⁺ adsorption and removal. Furthermore, the adsorption data were fitted with an exponential shape curve for all the three variable parameters that affect the adsorption process. The best results were obtained for pH 5, 20 min contact time, and 0.5 g adsorbent dose. The loading adsorption capacity was 9 mg of Fe²⁺ ions/g SiO₂ in the concentration range 0.1–1.0 mgL⁻¹. In addition, the synthesized SiO₂ with the size of around 50 nm can be used for specific heavy metal removal and drug delivery, after modification of the SiO₂ surface with various functional groups.

1. Introduction

In the past few decades, absorptive materials have been developed for removal of heavy metal ions including Hg²⁺, Cu²⁺, Pb²⁺, Zn²⁺, Cd²⁺, and Fe²⁺ from the environmental and biological system due to their toxicity [1–5]. Among all of the heavy metals mentioned, Fe²⁺ ions widely existed in underground water and they are commonly used for household activity in the South of Viet Nam. Long-term drinking water containing high level of Fe²⁺ ions may cause kidney disease, cancer, and anemia along with metabolism disorders [6–12]. Until now, a great deal of effort has been developed for Fe²⁺ ion collection using various techniques, for instance, membrane technology, chemical precipitation coagulation, ion exchange, and electrolytic reduction [13–21]. However, it was known that these methods have several drawbacks such as long time for operation, low capacity for removal, and low thermal and mechanical stability [17, 19, 21]. Among these methods, the adsorption-based technique is a promising technique for removal of Fe²⁺ ions due to its high efficiency, easy operation, cost-effectiveness, and environmental-friendly method. Therefore, several adsorptive materials for removal of Fe²⁺ ions have been widely investigated such as rice husk, activated carbon, fly ash, zeolites, and agricultural by-products [22–27]. It is worth to mention that silica dioxide (SiO₂) is a promising adsorptive material due to peculiar properties such as porous structure and large surface area. In addition, there are several methods to prepare silica nanoparticles (SNPs) from different agents such as synthesis of nanosilica via the precipitation method with the SNP size of around 50 nm [28, 29] and synthesis of SNPs based on the sol-gel method using rice husk with SNP size of 15 to 90 nm [30–33]. In Viet Nam, the average rice husk produced was around 42 billion tons per year. After burning at high temperature, it became rice husk ash (RHA), which contained a very high amount of silica (approximately 90%). Note that the presence of silica in rice husk had been known since 1938 [34].

In this work, we presented the SNPs efficiency in Fe²⁺ ion adsorption, with SNPs extracted from RHA in brick-kiln industry. We used the sol-gel method for extraction of SNPs under certain controlled conditions such as acid, base, pH, and stirring speed. The physicochemical properties of SNPs were studied for applications of removal of Fe²⁺ ions. The SNPs synthesized could find potential applications including environment for removal of heavy metals and biomedicine for drug delivery.

2. Materials and Methods

2.1. Agents

Rice husk ash (RHA) was taken from brick-kiln industry. Hydrochloric acid (HCl), nitric acid (HNO₃), sulfuric acid (H₂SO₄), sodium hydroxide (NaOH), iron(II) sulfate, heptahydrate (FeSO₄·7H₂O), hydroxylamide (H₂NO), and 1,10 phenanthroline (C₁₂H₈N₂) were purchased from Sigma-Aldrich. All agents were diluted in distilled water (DI water).

2.2. Methods

2.2.1. Extraction of SiO₂ Nanoparticles

SNPs were extracted from RHA based on the sol-gel method. Figure 1 illustrates the procedure for extraction of SiO₂ nanoparticles. The extraction process could be briefly described: Firstly, RHA of 2 g was collected from brick-kiln industry and then washed with DI water for removal of dirt. Secondly, RHA was soaked in the sodium hydroxide solvent under stirring at the speed of 400 rpm to generate sodium silicate. The RHA-induced sodium silicate was filtered to remove the nonreactive impurities. Finally, the sodium silicate solution obtained was cooled at room temperature and added to acid under vigorous stirring in order to initiate the hydrolysis-condensation reaction at pH∼7. The gel obtained was then dispersed in ethanol, washed with DI water (three times), and dried at 110°C for 2 h to remove remaining surfactants. The SNPs synthesized were stored in a desiccator for further characterizations. In this work, the effect of acids, NaOH concentration, dissolved time, and temperature was studied.

(a)

(b)

(c)

(d)

2.2.2. Fe²⁺ Ion Adsorption Study

The adsorption of Fe²⁺ metal ions from aqueous solution was studied at room temperature. The influence of pH, adsorption time, and mass of adsorbed material was investigated. Consequently, the pH was changed from 3 to 7; adsorption time was set up from 5 to 25 min with increment of 5 min; and mass of SiO₂ varied between 0.1, 0.5, 1.0, 1.5, and 2.0 g.

For Fe²⁺ ion adsorption measurement, a standard curve was plotted using the concentrations of Fe²⁺ solution in the range of 0.2, 0.4, 0.6, 0.8, and 1.0 ppm. The standard Fe²⁺ solution was generated by mixing FeSO₄·7H₂O with 1 ml hydroxylamine hydrochloride, 5 ml phenanthroline, and acetate buffer solution (pH = 3.5). The standard solution generated was kept for 15 min and measured by using a UV-Vis spectrum analyzer. The adsorption capacity () and the adsorption efficiency () were estimated using the following equation, respectively:where are the initial concentration and concentration of equilibrium of Fe²⁺ ions in solution, respectively, is the mass of the adsorbent used, and is the volume of solution.

2.2.3. Physicochemical and Morphological Characterization

Five analytical techniques were used for physicochemical characterization of SiO₂ extracted and adsorption of Fe²⁺ ions: energy dispersive X-ray spectroscopy (EDS) for the elemental composition of SiO₂ extracted, transmission electron microscopy (TEM) for ultrastructural analysis; Fourier transform infrared spectroscopy (FT-IR) for characterization of functional groups in the range 4000–500 cm⁻¹, ultraviolet-visible spectroscopy (UV-Vis) for determination concentration of solution, surface area measurement by the BET method, and pore size distribution by BJH (Micrometrics ASAP 2010).

3. Results and Discussion

In this work, we used 2 g of RHA for synthesis of nanosilica particles. To optimize the conditions for nanosilica synthesis, the effect of dissolved temperature, concentration of sodium hydroxide, concentration of acids, and dissolved time was investigated. The stirring speed of 400 rpm was kept during all the process. Note that each square point in Figures 2 and 3 represents the average value of the three repeated experimental results.

(a)

(b)

(c)

(d)

(a)

(b)

(c)

(d)

3.1. Effect of Acids

The efficiency of SiO₂ extracted using different acids for neutralization is presented in Figure 2(a). We used three different acids including sulfuric acid, nitric acid, and hydrochloric acid with the same concentration of 3 M for precipitation. The results obtained showed that the extracted efficiency was 58%, 75%, and 76%, respectively. It should be noted that no significant difference was observed using HCl and HNO₃ for precipitation. The results were better than those of H₂SO₄, caused by slow gelation process of silica when sodium silicate reacted with H₂SO₄. Thus, HCl was chosen for further study. Herein, concentration of NaOH, temperature, stirring speed, and dissolved time was 3.5 M, 70°C, 400 rpm, and 120 min, respectively. Then, the effect of concentration of HCl was studied in the range from 1 to 5 M. The results showed the highest efficiency of 82%, due to increase in concentration of acids. In addition, the efficiency also depended on the amount of silicate in RHA. So, the optimizing concentration of HCl used was 4 M.

3.2. Effect of NaOH

In order to optimize the condition for nanosilica synthesis, an effect of NaOH concentration was investigated. The experiments were performed with NaOH concentration series of 2.0, 2.5, 3.0, 3.5, and 4 M; the dissolved time, concentration of HCl, temperature, and stirring speed were fixed at 120 min, 4 M, 70°C, and 400 rpm, respectively. The results showed that the concentration of NaOH was directly proportional to the efficiency. And, the efficiency of silica synthesized was obtained around 81% at NaOH concentration of 3.5 M as seen in Figure 2(b). This led us believe that the efficiency can be enhanced by controlling the other factors.

3.3. Effect of Dissolved Time

Based on the above results, the concentration of NaOH chosen was 3.5 M for further investigating dissolved time. Dissolved time of RHA in NaOH solution was set as a series of 60, 90, 120, 150, and 180 min. Figure 2(c) shows that the amount of SiO₂ extracted was gradually increased. Efficiency increased from 70, 82, and 83% for the first, second, and third hours, respectively. The results showed that the amount of SiO₂ extracted was saturated at 120 min. This was because of the restricted amount of silicate on RHA under burning conditions in brick-kiln industry.

3.4. Effect of Temperature

The influence of temperature on the extraction of SiO₂ from RHA was illustrated in Figure 2(d). This study had been performed using the temperature range from 60°C to 100°C with an interval increment of 10°C. The amount of SiO₂ extracted had increased with temperature and presented a maximum around 90°C and remained until 100°C. The maximum of extraction mass of SiO₂ was 1.66 g SiO₂ in this experiment, corresponding to 83% of efficiency. The efficiency was not higher than that of the other work, due to impurity of RHA in brick-kiln industry under variant conditions in comparison with RHA produced at laboratory with standard conditions [35].

The FT-IR spectrum showed strong adsorption bands at 1069 and 794 cm⁻¹ that corresponded to the symmetric and asymmetric Si-O-Si vibration as seen in Figure 4(a), respectively. After extraction of SiO₂, it was clear that the spectrum differs from the RHA, showing a deeper signal between 1069 and 794 cm⁻¹ due to increase in amount of SiO₂ extracted. In addition, an adsorption peak at 3450 cm⁻¹ was associated with the O-H bonds of the silanol groups. Moreover, the main elements consisted of Si, O, and Na with weight concentrations of 23, 75, and 2%, respectively. The small remaining Na was due to unperfect washing. The surface analysis of TEM showed that SiO₂ had a spherical shape with the diameter of around 50 nm. In addition, BET and BJH analyses of SiO₂ showed the specific surface area of 78 m²/g with a pore size of 2.7 nm. This led us to believe that the extracted SiO₂ could be used for removal of heavy metal applications.

(a)

(b)

(c)

(d)

The adsorption of Fe²⁺ ions by the synthesized SiO₂ was analyzed. Figure 3(b) shows the relation of the loading capacity (mg·g⁻¹) and adsorption efficiency as a function of pH. At pH < 4, Figure 3(b) presents a low adsorption capacity due to competition between H⁺ ions and Fe²⁺ ions. For pH > 4, concentration of H⁺ decreased, offering the adsorption of Fe²⁺ ions. The adsorption phenomena could be explained by the charge of SiO₂ dependent on the pH of the surrounding medium. When the pH of the surrounding medium increased, negative charges on the surface of SiO₂ increased, leading to enhanced electrostatic interaction capacity between SiO₂ and Fe²⁺ ions as follows:

The adsorption of Fe²⁺ ions on SiO₂ was found between pH 4 and 5. At pH > 5, the small change in adsorption of Fe²⁺ ions resulted from the precipitation of Fe²⁺ and small volume of the pore on SiO₂ surface. Furthermore, the removal of Fe²⁺ ions was also associated with contact time as seen in Figure 3(c). Results showed that the maximum adsorption efficiency occurred within 20 min with 0.5 g loading mass of SiO₂ and the maximum adsorption capacity was around 9 mg/g (efficiency of 99%). This result was better than other works using other adsorbents as depicted in Table 1 [36–38]. Note that the higher adsorption capacity would be caused by an increase in the number of active -OH sites on the SNPs surface as presented in Figure 4(a) as well as the surface area and the pore volume of the synthesized SiO₂.

We fitted the exponential shape curves of the form of to the measurement data in Figures 3(b)–3(d) to confirm the characteristic exponential shape of adsorption capacity with variable parameters including pH, time, and mass during adsorption process. Unlike the Langmuir and Freundlich isothermal model, this fitting equation could be used to estimate minimum possible adsorption capacity () of the adsorbent. As shown in Table 2, the minimum possible adsorption capacity was 7.7, 7.8, and 0.5 mg/g for the case of time change (Figure 3(c)), mass change (Figure 3(c)), and pH change (Figure 3(b)), respectively. We saw that there was large difference in minimum possible adsorption capacity between pH with the other ones. This was due to the fact that there was competitive adsorption occurring between Fe²⁺ ions and H⁺ ions into SNPs at low pH as we already discussed based on equation (2). Moreover, the correlation coefficients (R²) were both higher than 0.95 indicating that the exponential adsorption data fit well into the model.

The use of the synthesized silica nanoparticles may offer several benefits for drug delivery and adsorption of heavy metals in environment, as mentioned below. Firstly, silica nanoparticles can eliminate the toxicity in comparison with the other particles linked with magnetic nanoparticles or silver nanoparticles when they are introduced into human body for treatment. Secondly, the synthesis process of silica nanoparticles can also be applied for generation of an insulating layer to control electron tunneling between particles, which may be important in charge transfer or magneto-optics. Thirdly, surface modification via functional group immobilization is being pursued with great interest since it can provide unique opportunities to engineer the interfacial of solid substrates while retaining particles’ basic geometry. Moreover, the extracted SiO₂ can be conjugated with various functional groups for specific target detection such as heavy metal ions (Pb²⁺, Cu²⁺, and Cr⁶⁺) for environmental applications. Finally, the surface area of synthesized SiO₂ can be increased by using cetyltrimethyl ammonium bromide (CTAB) to enhance capability for drug delivery and heavy metal adsorption.

4. Conclusion

We presented the extraction process of SNPs from RHA under different conditions like types of acids, NaOH concentration, dissolved time, and temperature. The results showed that the extraction efficiency was around 83% with purity of 98% and surface area of 78 m²/g. Moreover, the Fe²⁺ ion adsorption capacity of the SiO₂ extracted from RHA was studied under different conditions including pH, contact time, and adsorbent mass. We obtained a maximum loading adsorption capacity of 9 mg Fe²⁺/g SiO₂ at pH 5 with 20 min of contact time. The adsorption efficiency can be enhanced by modification of SiO₂ with functional groups. In addition, the synthesized SiO₂ with the size of around 50 nm can be used for biomedical applications such as drug delivery.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Acknowledgments

This research was supported by Tra Vinh University under Basic Science Research Fund No. 181/HĐ.HĐCN-ĐHTV.

References

D. L. Gutnick and H. Bach, “Engineering bacterial biopolymers for the biosorption of heavy metals; new products and novel formulations,” Applied Microbiology and Biotechnology, vol. 54, no. 4, pp. 451–460, 2000.
View at: Publisher Site | Google Scholar
G. Renard, M. Mureseanu, A. Galarneau, D. A. Lerner, and D. Brunel, “Immobilisation of a biological chelate in porous mesostructured silica for selective metal removal from wastewater and its recovery,” New Journal of Chemistry, vol. 29, no. 7, pp. 912–918, 2005.
View at: Publisher Site | Google Scholar
M. Mureseanu, N. Cioatera, I. Trandafir, I. Georgescu, F. Fajula, and A. Galarneau, “Selective Cu²⁺ adsorption and recovery from contaminated water using mesoporous hybrid silica bio-adsorbents,” Microporous and Mesoporous Materials, vol. 146, no. 1–3, pp. 141–150, 2011.
View at: Publisher Site | Google Scholar
F. Ge, M.-M. Li, H. Ye, and B.-X. Zhao, “Effective removal of heavy metal ions Cd²⁺, Zn²⁺, Pb²⁺, Cu²⁺ from aqueous solution by polymer-modified magnetic nanoparticles,” Journal of Hazardous Materials, vol. 211-212, pp. 366–372, 2012.
View at: Publisher Site | Google Scholar
F. Ke, L.-G. Qiu, Y.-P. Yuan et al., “Thiol-functionalization of metal-organic framework by a facile coordination-based postsynthetic strategy and enhanced removal of Hg²⁺ from water,” Journal of Hazardous Materials, vol. 196, pp. 36–43, 2011.
View at: Publisher Site | Google Scholar
B. Halliwel, “Antioxidants in human health and disease,” Annual Review of Nutrition, vol. 16, no. 1, pp. 33–50, 1996.
View at: Publisher Site | Google Scholar
B. Halliwell and J. M. C. Gutteridge, “Oxygen toxicity, oxygen radicals, transition metals and disease,” Biochemical Journal, vol. 219, no. 1, pp. 1–14, 1984.
View at: Publisher Site | Google Scholar
B. Halliwell, “Reactive oxygen species in living systems: source, biochemistry, and role in human disease,” The American Journal of Medicine, vol. 91, no. 3, pp. S14–S22, 1991.
View at: Publisher Site | Google Scholar
B. Halliwell, “Free radicals and antioxidants: a personal view,” Nutrition Reviews, vol. 52, no. 8, pp. 253–265, 1994.
View at: Publisher Site | Google Scholar
S. L. Simpson and G. E. Batley, “Disturbances to metal partitioning during toxicity testing of iron(II)-rich estuarine pore waters and whole sediments,” Environmental Toxicology and Chemistry, vol. 22, no. 2, pp. 424–432, 2003.
View at: Publisher Site | Google Scholar
I. I. Somers and J. W. Shive, “The iron-manganese relation in plant metabolism,” Plant Physiology, vol. 17, no. 4, pp. 582–602, 1942.
View at: Publisher Site | Google Scholar
L. H. A. Rahman, R. M. E. Khatib, L. A. E. Nasr, and A. M. Abu-Dief, “Synthesis, physicochemical studies, embryos toxicity and DNA interaction of some new Iron (II) Schiff base acid complexes,” Journal of Molecular Structure, vol. 1040, pp. 9–18, 2013.
View at: Publisher Site | Google Scholar
V. A. Elrod, K. S. Johnson, and K. H. Coale, “Determination of subnanomolar levels of iron(II) and total dissolved iron in seawater by flow injection and analysis with chemiluminescence detection,” Analytical Chemistry, vol. 63, no. 9, pp. 893–898, 1991.
View at: Publisher Site | Google Scholar
F. Jaouen, S. Marcotte, J. P. Dodelet, and G. Lindbergh, “Oxygen reduction catalysts for polymer electrolyte fuel cells from the pyrolysis of iron acetate adsorbed on various carbon supports,” Journal of Physical Chemistry B, vol. 107, no. 6, pp. 1376–1386, 2003.
View at: Publisher Site | Google Scholar
S. O. Pehkonen, Y. Erel, and M. R. Hoffmann, “Simultaneous spectrophotometric measurement of iron(II) and iron(III) in atmospheric water,” Environmental Science & Technology, vol. 26, no. 9, pp. 1731–1736, 1992.
View at: Publisher Site | Google Scholar
S. Kagaya, Y. Araki, N. Hirai, and K. Hasegawa, “Coprecipitation with yttrium phosphate as a separation technique for iron(III), lead, and bismuth from cobalt, nickel, and copper matrices,” Talanta, vol. 67, no. 1, pp. 90–97, 2005.
View at: Publisher Site | Google Scholar
L. C. Roberts, S. J. Hug, T. Ruettimann, M. M. BIllah, A. W. Khan, and M. T. Rahman, “Arsenic removal with iron(II) and iron(III) in waters with high silicate and phosphate concentrations,” Environmental Science & Technology, vol. 38, no. 1, pp. 307–315, 2004.
View at: Publisher Site | Google Scholar
S. P. Burke and S. A. Banwart, “A geochemical model for removal of iron(II)(aq) from mine water discharges,” Applied Geochemistry, vol. 17, no. 4, pp. 431–443, 2002.
View at: Publisher Site | Google Scholar
G. Muñiz, V. Fierro, A. Celzard, G. Furdin, G. Gonzalez-Sánchez, and M. L. Ballinas, “Synthesis, characterization and performance in arsenic removal of iron-doped activated carbons prepared by impregnation with Fe(III) and Fe(II),” Journal of Hazardous Materials, vol. 165, no. 1–3, pp. 893–902, 2009.
View at: Publisher Site | Google Scholar
W. Chen, R. Parette, J. Zou, F. S. Cannon, and B. A. Dempsey, “Arsenic removal by iron-modified activated carbon,” Water Research, vol. 41, no. 9, pp. 1851–1858, 2007.
View at: Publisher Site | Google Scholar
T. L. Theis and P. C. Singer, “Complexation of iron(II) by organic matter and its effect on iron(II) oxygenation,” Environmental Science & Technology, vol. 8, no. 6, pp. 569–573, 1974.
View at: Publisher Site | Google Scholar
S. Cetin and E. Pehlivan, “The use of fly ash as a low cost, environmentally friendly alternative to activated carbon for the removal of heavy metals from aqueous solutions,” Colloids and Surfaces A: Physicochemical and Engineering Aspects, vol. 298, no. 1-2, pp. 83–87, 2007.
View at: Publisher Site | Google Scholar
C. Quintelas, Z. Rocha, B. Silva, B. Fonseca, H. Figueiredo, and T. Tavares, “Biosorptive performance of an Escherichia coli biofilm supported on zeolite NaY for the removal of Cr(VI), Cd(II), Fe(III) and Ni(II),” Chemical Engineering Journal, vol. 152, no. 1, pp. 110–115, 2009.
View at: Publisher Site | Google Scholar
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.
View at: Publisher Site | Google Scholar
M. Hua, S. Zhang, B. Pan, W. Zhang, L. Lv, and Q. Zhang, “Heavy metal removal from water/wastewater by nanosized metal oxides: a review,” Journal of Hazardous Materials, vol. 211-212, pp. 317–331, 2012.
View at: Publisher Site | Google Scholar
T. G. Chuah, A. Jumasiah, I. Azni, S. Katayon, and S. Y. Thomas Choong, “Rice husk as a potentially low-cost biosorbent for heavy metal and dye removal: an overview,” Desalination, vol. 175, no. 3, pp. 305–316, 2005.
View at: Publisher Site | Google Scholar
A. B. Jusoh, W. H. Cheng, W. M. Low, A. Nora’aini, and M. J. M. M. Noor, “Study on the removal of iron and manganese in groundwater by granular activated carbon,” Desalination, vol. 182, no. 1–3, pp. 347–353, 2005.
View at: Publisher Site | Google Scholar
N. Thuadaij and A. Nuntiya, “Synthesis and characterization of nanosilica from rice husk ash prepared by precipitation method,” Nanotechnology, vol. 7, no. 1, 2008.
View at: Google Scholar
U. Kalapathy, A. Proctor, and J. Shultz, “An improved method for production of silica from rice hull ash,” Bioresource Technology, vol. 85, no. 3, pp. 285–289, 2002.
View at: Publisher Site | Google Scholar
Y. Qu, Y. Tian, B. Zou et al., “A novel mesoporous lignin/silica hybrid from rice husk produced by a sol-gel method,” Bioresource Technology, vol. 101, no. 21, pp. 8402–8405, 2010.
View at: Publisher Site | Google Scholar
U. Kalapathy, A. Proctor, and J. Shultz, “A simple method for production of pure silica from rice hull ash,” Bioresource Technology, vol. 73, no. 3, pp. 257–262, 2000.
View at: Publisher Site | Google Scholar
J. P. Nayak, S. Kumar, and J. Bera, “Sol-gel synthesis of bioglass-ceramics using rice husk ash as a source for silica and its characterization,” Journal of Non-Crystalline Solids, vol. 356, no. 28–30, pp. 1447–1451, 2010.
View at: Publisher Site | Google Scholar
T. Witoon, M. Chareonpanich, and J. Limtrakul, “Synthesis of bimodal porous silica from rice husk ash via sol-gel process using chitosan as template,” Materials Letters, vol. 62, no. 10-11, pp. 1476–1479, 2008.
View at: Publisher Site | Google Scholar
J. I. Martin, “The desilification of rice hull and a study of the products obtained,” Lousiana State University, Baton Rouge, LA, USA, 1938, M.S. thesis.
View at: Google Scholar
D. Z. Zhao, S. B. Jing, J. N. Xu et al., “Recycle adsorption of Cu²⁺ on amine-functionalized mesoporous silica monolithic,” Chemical Research in Chinese Universities, vol. 29, no. 4, pp. 793–797, 2013.
View at: Publisher Site | Google Scholar
S. R. Shukla, R. S. Pai, and A. D. Shendarkar, “Adsorption of Ni(II), Zn(II) and Fe(II) on modified coir fibres,” Separation and Purification Technology, vol. 47, no. 3, pp. 141–147, 2006.
View at: Publisher Site | Google Scholar
B. Acemioglu, “Removal of Fe(II) ions from aqueous solution by Calabrian pine bark wastes,” Bioresource Technology, vol. 93, no. 1, pp. 99–102, 2004.
View at: Publisher Site | Google Scholar
W. S. W. Ngah, S. Ab Ghani, and A. Kamari, “Adsorption behaviour of Fe(II) and Fe(III) ions in aqueous solution on chitosan and cross-linked chitosan beads,” Bioresource Technology, vol. 96, no. 4, pp. 443–450, 2005.
View at: Publisher Site | Google Scholar

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Journal of Analytical Methods in Chemistry

Adsorptive Removal of Iron Using SiO2 Nanoparticles Extracted from Rice Husk Ash

Abstract

1. Introduction

2. Materials and Methods

2.1. Agents

2.2. Methods

2.2.1. Extraction of SiO2 Nanoparticles

2.2.2. Fe2+ Ion Adsorption Study

2.2.3. Physicochemical and Morphological Characterization

3. Results and Discussion

3.1. Effect of Acids

3.2. Effect of NaOH

3.3. Effect of Dissolved Time

3.4. Effect of Temperature

4. Conclusion

Data Availability

Conflicts of Interest

Acknowledgments

References

Copyright

Adsorptive Removal of Iron Using SiO₂ Nanoparticles Extracted from Rice Husk Ash

2.2.1. Extraction of SiO₂ Nanoparticles

2.2.2. Fe²⁺ Ion Adsorption Study