Preparation, Characterization, and Application of Novel Ferric Oxide-Amine Material for Removal of Nitrate and Phosphate in Water

Nguyen, Trung Thanh; Le, Tri Thich; Phan, Phuoc Toan; Nguyen, Nhat Huy

doi:https://doi.org/10.1155/2020/8583543

Journal of Chemistry

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

Research Article | Open Access

Volume 2020 | Article ID 8583543 | https://doi.org/10.1155/2020/8583543

Preparation, Characterization, and Application of Novel Ferric Oxide-Amine Material for Removal of Nitrate and Phosphate in Water

Trung Thanh Nguyen,^1,2Tri Thich Le,^1,2,3Phuoc Toan Phan,^2,3,4and Nhat Huy Nguyen^2,3

Academic Editor: Franck Rabilloud

Received10 Jan 2020

Revised01 Apr 2020

Accepted07 Apr 2020

Published24 Apr 2020

Abstract

Ferric oxide-amine material was synthesized and applied as a novel adsorbent for nitrate and phosphate removal from aqueous solution. The properties of ferric oxide-amine were examined using TGA, FTIR, BET, SEM, EDX, SEM-mapping, and XRD analysis. The results showed that the adsorption using ferric oxide-amine material reached equilibrium after 30 and 60 min for nitrate and phosphate, respectively. The highest nitrate and phosphate adsorption capacities were 131.4 mg nitrate/g at pH 5-6 and 42.1 mg phosphate/g at pH 6. The effects of adsorbent dosage, initial concentrations of nitrate and phosphate, and adsorption temperature were also investigated. Among the three adsorbents of ferric oxide-amine, ferric oxide, and Akualite A420 ion exchange resin, ferric oxide-amine material had the highest adsorption capacity for nitrate and phosphate removal. These results suggest a great potential use of ferric oxide-amine material for water treatment in practical applications.

1. Introduction

Water pollution due to the excessive presence of nitrogen and phosphorus compounds is one of the most frequently faced environmental problems around the world. This is due to the ineffective wastewater treatment and overuse of nitrogen and phosphorus fertilizers in agriculture. High concentrations of nitrate (NO₃⁻) and phosphates (PO₄³⁻) are considered as the main cause of eutrophication [1]. Besides, high level of NO₃⁻ is also one of the risks to human health. It can cause some health problems such as methemoglobinemia, or NO₃⁻ can be converted into nitrosamine (toxic nitrite), which is the reason for increasing the risk of cancer [2].

Many biological, chemical, and physical processes have been applied to remove NO₃⁻ and PO₄³⁻ from water and wastewater [3–6]. In particular, the adsorption process by the ion exchange mechanism is evaluated as an effective, simple, and low-cost method, in which the adsorbent is capable of being recycled many times [7]. Therefore, ion exchange resins have been widely studied in recent years [8–10]. Common materials (e.g., activated carbon, rice husk ash, and bamboo charcoal) and engineered nanomaterials (e.g., iron-carbon oxide nanotube [11] and chitosan/Al₂O₃/Fe₃O₄ [12]) are quite effective for removing NO₃⁻ and PO₄³⁻. However, because of low adsorption capacity, complicated process, and high cost, they have not been employed for practical applications yet. Therefore, a study on the development of a new, inexpensive, and efficient material for simultaneous removal of nitrate and phosphate in water is appreciated.

In this study, ferric oxide was used as a support for synthesis of ferric-amine oxide. The material was then characterized and applied to remove NO₃⁻ and PO₄³⁻ in water. The suitable conditions of NO₃⁻ and PO₄³⁻ adsorption in solution such as pH, contact time, adsorbent dosage, initial concentration, and temperature were determined. Besides, the ability of the material was compared to the original ferric oxide and commercial material available in the market.

2. Materials and Methods

2.1. Chemicals

Lab-grade chemicals such as FeCl₃.6H₂O and urea were from China while H₂SO₄, NaOH, KNO₃, KH₂PO₄, N1-(3-trimethoxysilylpropyl) diethylenetriamine (triamine silane), toluene, and pentane were from Merck. Industrial-grade Akualite A420 resin was from China and DI (deionized) water was from a local water machine in the lab. The nitrate and phosphate aqueous solutions were prepared by dissolving a certain amount of KNO₃ and KH₂PO₄ in DI water.

2.2. Synthesis of Ferric Oxide-Amine

Ferric oxide nanomaterial was prepared by a process adopted from the work of Raul et al. [13, 14]. Typically, 12.5 g (0.1 M) of Fe₂(SO₄)₃·5H₂O was dissolved into 250 mL of double distilled water in a beaker. The beaker was stirred, heated using a magnetic stirrer until the temperature of the solution reached 60°C, and let for 30 min. The solution was then added dropwise to 250 mL of 5.0 M urea solution within 3.5 h under a temperature of 70°C for complete reaction. After that, the temperature was increased to 80°C and maintained until the volume of the solution reduced to half of the initial volume. Subsequently, the brown precipitate formed after cooling the solution to room temperature (25 ± 01°C) was washed repeatedly to remove the excess urea. Finally, the powder form of ferric oxide/hydroxide nanoparticles was obtained after drying the washed precipitate in an oven at 70°C for 4 h.

Ferric oxide-amine was prepared according to a process previously published by Thanh [15]. Ferric oxide was fed into a glass flask containing 150 mL of toluene under stirring for obtaining a homogeneous mixture. Subsequently, 0.3 mL of distilled water per each gram of ferric oxide was added to the flask and mixed for 30 min. The flask was then soaked in a silicone oil bath at 85°C. After that, the mixture was added to triamine silane (3 mL per 1 gram of ferric oxide) for 16 h. After filtering and washing with toluene and pentane, the ferric oxide-amine material was collected and dried at 100°C for 1 h.

2.3. Characterizations

The morphology of ferric oxide-amine was observed by scanning electron microscopy (SEM) while the various elemental compositions of ferric oxide-amine were determined by energy dispersive X-ray analysis (EDX). The surface chemical properties were characterized by Fourier transform infrared spectroscopy (FTIR; Alpha, Bruker). The phase transformation and thermal decomposition of ferric oxide-amine were evaluated by thermogravimetric analysis (TGA, Q500 machine). The specific surface area was determined by the Brunauer-Emmett-Teller method (Porous Materials, BET-202A).

2.4. Batch Adsorption Experiments

The effect of contact time was carried out by adding 30 mg of adsorbent to 50 mL of 50 mg/L nitrate solution or 10 mg/L phosphate solution with adsorption time from 0 to 120 min. The mixture was then filtrated and the water sample was taken for analysis of nitrate and phosphate concentration by UV-visible spectrophotometry. The influencing parameters including contact time, adsorbent dosage, solution pH, initial adsorbate concentration, and temperature were investigated. The adsorption capacity was calculated as follows:where Q_e is the adsorption capacity (mg/g). C_o and C_t are the initial and final concentrations of nitrate or phosphate solution (mg/L), respectively. m is the adsorbent weight (g) and V is the solution volume (L).

3. Results and Discussion

3.1. Characterization of Ferric Oxide-Amine

The surface functional groups of the materials are usually determined by FTIR [16]. In this study, the surface chemical structure of ferric oxide nanomaterials before and after adsorption was determined to clarify the reaction mechanism that occurred on the surface. As showed in Figure 1, all samples had a characteristic peak of Fe-O bond that appeared at a wavenumber of 567 cm⁻¹ [17] while triamine silane peaks were observed at wavenumbers of 1041 and 1122 cm⁻¹ of Si-O in ferric oxide-amine samples [17, 18]. Other peaks in the range of 3384 and 3442 cm⁻¹ were considered as the overlapping of N-H and O-H groups of adsorbed water on the materials [18]. In addition, peaks of -NH₂ appearing at 1626 cm⁻¹ [19] and 1654 cm⁻¹ [18] in ferric oxide-amine samples confirmed the effective grafting of amino groups to ferric oxide nanoparticles. After nitrate and phosphate adsorption, the new peaks appearing at 1384 and 908 cm⁻¹ were considered to be of nitrate [20] and phosphate [21], respectively, proving that the ferric oxide-amine material can adsorb anions such as nitrate and phosphate.

The morphology of ferric oxide-amine and ferric oxide materials was examined by SEM. The flower-shaped structure observed from the attached bunches of ferric oxide in Figure 2(a) became smoother after being grafted by triamine silane (Figure 2(b)), and the particle size of the ferric oxide-amine material became larger than that of the original ferric oxide material. The amine grafting significantly reduces the specific surface area of the material from 145.13 m²/g in ferric oxide to only 14.68 m²/g in ferric oxide material. In addition, this nearly 10-time reduction in the surface area confirmed the effective grafting of a great amine amount on the surface of ferric oxide.

(a)

(b)

The phase transformation and chemical composition of ferric oxide and ferric oxide-amine samples were investigated by thermogravimetric analysis in a wide range of temperatures from 30°C to 900°C. Results in Figure 3 showed that the weight reduction of ferric oxide and ferric oxide-amine was 37% and 56.63%, respectively. There was a light fall in the weight of both materials (4% for ferric oxide and 6% for ferric oxide-amine) at the temperature of 80°C to 150°C, which can be attributed to the release of moisture or dehydration. At 600°C, the weight of ferric oxide changed significantly, possibly because of ferric oxide in the form of γ-hematite (cubic structure) being converted to α-hematite (hexagonal structure) [22, 23]. In addition, the evaporation of water and organic matter in the structure along with the structural change of the ferric oxide occurred at the temperature of 300 and 500°C, which resulted in the decline of ferric oxide-amine weight. The decrease in mass at a temperature of 300 to 350°C is due to the loss of structural water, and at 350 to 500°C due to the restructuring of the oxide and the burning temperature of grafted amine groups on the ferric oxide surface (see Figure 3(b)) [24, 25], proving that ferric oxide-amine material was successfully synthesized.

(a)

(b)

X-ray diffraction spectra of ferric oxide and ferric oxide-amine samples are plotted in Figure 4. The ferric oxide diffraction spectrum had obtuse-angle and low peaks, showing the relatively low crystallinity of the as-synthesized materials without any heat treatment step [13, 26], which was similar for the ferric oxide-amine sample. However, there was a peak with a wide range, and low intensity existed at a low diffraction angle of 20° to 25°, which could be attributed to the presence of a very small amount of silicon oxide in the material [27–29].

EDX and SEM-mapping are two of the most commonly used techniques to evaluate the surface composition and the distribution of elements on the surface of the material. EDX spectrum and elemental mapping of ferric oxide-amine material are exhibited in Figure 5. The sample consists of five elements, which were evenly distributed on the surface of the material. The elemental weight percentage decreased in the order of silicon, carbon, iron, oxygen, and nitrogen, which reflects the amine content of the produced material.

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(b)

3.2. Adsorption of Nitrate and Phosphate onto Ferric Oxide-Amine Material

As presented in Figure 6, the adsorption capacity of ferric oxide-amine increased with the increase of contact time during the test period of 120 min. The adsorption equilibrium of nitrate adsorption was reached after 30 min, which was faster than that of phosphate (60 min). This could be explained by the stronger interaction of the amino-functional groups with nitrate than that with phosphate [18]. The nitrate and phosphate adsorption capacity of ferric oxide-amine were calculated at 100 mgNO₃⁻/g and 40 mgPO₄³⁻/g, respectively. For phosphate removal, the adsorption process has three stages: (i) a rapid increase for the first 30 min by the externally exposed surface of the amine group, (ii) a slow increase for the next 30 min by the internal ferric oxide surface, and (iii) reaching the equilibrium after 60 min when both external and internal surfaces become saturated.

Regarding kinetics study, the nitrate and phosphate adsorption on ferric oxide-amine material was determined by three kinetic models, consisting of pseudo-first-order, pseudo-second-order, and intraparticle diffusion models. The equilibrium adsorption capacity (q_e,exp) of the material was chosen to be 100.51 mgNO₃⁻/g for nitrate and 40.60 mgPO₄³⁻/g for phosphate as taken from the experimental data. Linear equations of kinetic models and correlation coefficients (R²) are shown in Table 1 and Figure 7. On this account, the pseudo-second-order model was considered as the best-fit model to describe the adsorption with the greatest correlation coefficient among the others. Moreover, the calculated adsorption capacity (q_{e, cal}) approximated the experimental adsorption capacity (q_e,exp) and this was correct for both nitrate and phosphate. The adsorption rate constants k were then determined to be 0.00924 (g/mg.min) with nitrate concentration of 50 mg/L and 0.00899 (g/mg.min) with phosphate concentration of 10 mg/L.

It is observed in Figure 8(a) that changes in adsorption capacity of both nitrate and phosphate were followed by changes in solution pH. The nitrate and phosphate adsorption capacity of ferric oxide-amine material reached a peak of over 130 mgNO₃⁻/g and 40 mgPO₄³⁻/g in the pH range of 5-6 and 6, respectively. Regarding nitrate, the increase of H⁺ concentration at pH < 5 impeded the nitrate adsorption, and there is an adsorption competition with SO₄²⁻ anion from H₂SO₄ used to adjust the solution pH [30]. At pH > 6, the nitrate adsorption capacity also decreased on account of an adsorption competition with OH⁻ [31]. In the solution, phosphate anions dissociate into different forms depending on pH. Major forms of phosphate are H₃PO₄, H₂PO₄⁻, HPO₄²⁻, and PO₄³⁻ at pH < 2, 2–7, 7–11, and >11, respectively [30]. In phosphate adsorption at pH < 7, H₂PO₄⁻ was easily bonded to ferric oxide-amine by electrostatic forces (pH < pH_pzc) to increase phosphate adsorption capacity. At high pH, phosphate adsorption capacity decreases due to the adsorption competition with OH⁻. In conclusion, the ferric oxide-amine had the highest adsorption capacity of nitrate and phosphate in the pH range of 5–6 and 6, respectively. The experiment to determine the isoelectric point value of the material in 0.01 N KCl solution is shown in Figure 8(b), where pH_pzc of ferric oxide-amine was determined to be 5.8. At pH < pH_pzc, the adsorbent surface is positively charged, so the adsorption process of nitrate and phosphate anions was based on electrostatic attraction mechanism. However, with the solution pH > pH_pzc, the adsorption capacity decreases because of the negatively charged surface and the competition with OH⁻, which both inhibit the adsorption of anions such as nitrate and phosphate [32].

(a)

(b)

As displayed in Figure 9, the adsorption capacity was greatly influenced by the dosage of ferric oxide-amine. Decreases in adsorption capacity were experienced when the adsorbent dosage increased; however, at the time, the removal efficiency increased and the quality of the output water improved. In terms of nitrate adsorption, an output concentration of 27.10 mgNO₃⁻-N/L was found when 30 mg of absorbent was used, which met the nitrate requirement in column A of QCVN 14:2008/BTNMT. In phosphate adsorption, a good agreement with phosphate concentration in column A (lower than 6 mgPO₄³⁻-P/L) was also witnessed in the output concentration of phosphate. The phosphate adsorption capacity decreased rapidly with the increase of dosage from 5 to 30 mg but then deceased slowly with a further increase of dosage from 30 to 100 mg. Therefore, 30 mg of the material was chosen for subsequent experiments such as the effects of initial adsorbate concentration and solution temperature on adsorption capacity.

The effects of initial nitrate concentration and solution temperature on the adsorption capacity are exhibited in Figure 10(a), showing an increasing trend of adsorption capacity with the increases of initial concentration and temperature. The higher nitrate concentration facilitates the interaction between nitrate ions and adsorption sites of the material. Similarly, the nitrate ions in the solution become more mobile at higher temperatures, increasing the frequency of collisions between the material and the nitrate ions. This can be seen in solutions with a nitrate concentration of 100 mg/L or higher when the solution temperature increased from 20°C to 45°C. In addition, it was seen clearly in Figure 10(b) that similarity to the nitrate adsorption capacity also occurred for phosphate. The phosphate adsorption capacity of the material was directly proportional to the ascending variations in the initial phosphate concentration and solution temperature. Favorable conditions for adsorption such as the increase in the mobility and density of phosphate ions, in short, can promote interaction between them and the material.

(a)

(b)

In this study, the Langmuir and Freundlich isotherm models were used to describe the correlation between nitrate and phosphate on the ferric oxide-amine surface and their equilibrium concentrations in the solution with a constant temperature. The isotherm adsorption parameters of the processes are presented in Table 2. Although both Langmuir and Freundlich models were suitable for describing nitrate adsorption, the Langmuir model was more fit on account of its higher correlation coefficients. Relatively high correlation coefficients of 0.9866 and 0.9982 were found in the Langmuir equation at 30°C for nitrate and phosphate, respectively. These results indicated that the ferric oxide-amine surface had uniformity, and a similar affinity for both nitrate and phosphate ions and the adsorption occurred mainly from the interaction of ions and the functional groups to create monolayer molecules on the ferric oxide-amine surface. The values of n in the Freundlich model indicated the favorable condition for the adsorption process. The maximum adsorption capacities at 30°C were also compared with those reported previously and the results are presented in Table 3. It can be concluded that the maximum adsorption capacity of nitrate onto ferric oxide-amine was the highest among other adsorbents in the literature. However, phosphate adsorption onto this material was lower than that onto MgO-biochar and nano-2D-MgO materials.

As regards adsorption thermodynamics, parameters such as Gibbs free energy (∆G), entropy (∆S), and enthalpy (∆H) obtained using equilibrium constants at different temperatures (i.e., 293, 303, and 318 K) are summarized in Table 4. In general, it is obvious that both nitrate and phosphate adsorption processes had ∆G < 0, proving the self-evolution process under standard conditions. On the other hand, the phosphate adsorption was an exothermic process with ∆H < 0 while the nitrate adsorption was an endothermic process with ∆H > 0 [38]. It is known that, with ∆H <40 kJ/mol, the adsorption process is usually considered as physical adsorption. Besides, the affinity of the adsorbent for nitrate and phosphate is expressed by the value of ∆S [39].

3.3. Competitive Adsorption and Application to Real Wastewater

Some common anions in wastewater such as Cl⁻, SO₄²⁻, and HCO₃⁻ are usually competitors during the adsorption of target nitrate and phosphate. Therefore, to assess the influence level of the competing ions, it is necessary to conduct a test with the solution containing the above anions. The amount of material used was about 30 mg in 50 mL of the solution with nitrate and phosphate concentration of 50 mg/L and 100 mg/L, respectively. As exhibited in Figure 11, the adsorption capacity of ferric oxide-amine was affected at different levels by these anions. Among the anions, sulfate had the greatest influence on phosphate adsorption of the material, making its adsorption capacity reduce by nearly 1/3 from 152.04 mg/g to only 43.74 mg/g. Although chloride has a maximum electronic affinity, sulfate was proven to have a greater competitive effect on phosphate adsorption [40]. Meanwhile, the effect of the other three anions (i.e., chloride, sulfate, and bicarbonate) on the nitrate adsorption capacity of ferric oxide-amine was almost similar. The adsorption capacity, more specifically, decreased by 25% from 135 mg/g to roughly 100 mg/g.

Nitrate and phosphate removal efficiencies from synthetic and real wastewater by ferric oxide-amine material as compared to ferric oxide and anion exchange resin (Akualite A420) are illustrated in Figure 12. The results indicated that all three materials had the ability to simultaneously adsorb nitrate and phosphate anions, especially ferric oxide-amine which had quantitatively superior nitrate adsorption capacity compared to ferric oxide and Akualite A420. In synthetic wastewater (Figure 12(a)), nitrate and phosphate adsorption capacity of the materials can be arranged in descending order as ferric oxide-amine > Akualite A420 > ferric oxide for nitrate and ferric oxide > ferric oxide-amine > Akualite A420 for phosphate. The nitrate adsorption capacity of ferric oxide-amine was 20 times higher than that of ferric oxide and 4 times higher than that of Akualite A420. The phosphate adsorption capacity of ferric oxide-amine (19.43 mg/g) was lower than that of ferric oxide (28.06 mg/g), but it was still 4 times higher than that of Akualite A420. While ferric oxide had the nitrate adsorption capacity much less than the phosphate adsorption capacity, both ferric oxide-amine and Akualite A420 had a nitrate adsorption capacity superior to the phosphate adsorption capacity. In real wastewater (Figure 12(b)), the nitrate adsorption capacity of ferric oxide-amine was still the highest, but it was reduced compared to that of the other materials on this account. There may be some other ions and small amounts of organic matter in the wastewater, which led to adsorption competition as discussed above. The ferric oxide after being grafted with amine-functional groups had much higher adsorption capacity than the original one, but its phosphate adsorption capacity remained the same at 20 mg/g, proving that amine groups mainly interacted with nitrate ions [41] whereas most phosphate ions interacted with ferric oxide [42]. As also depicted in Figure 12(b), it can be said that all ferric oxide, ferric oxide-amine, and Akualite A420 materials can remove the COD content of real wastewater samples. The COD removal efficiency of ferric oxide was the highest one, which was followed by Akualite A420 and then ferric oxide-amine. This also implies that ferric oxide-amine was less affected by organic matter in wastewater than ferric oxide and Akualite A420 under the same conditions.

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(b)

4. Conclusions

Ferric oxide-amine materials were successfully synthesized and characterized by SEM, EDX, FTIR, XRD, TGA, and BET analyses. The equilibrium time for nitrate and phosphate adsorption was 30 min and 60 min, respectively, while the suitable pH was in the range of 5 to 6 for nitrate and pH 6 for phosphate. The adsorption capacity increased with the increase of nitrate and phosphate concentration and temperature but decreased with the increase of adsorbent dosage. When compared with commercial Akualite A420, ferric oxide-amine material showed outstanding nitrate and phosphate adsorption capacity, which can find many applications in water and wastewater treatment.

Data Availability

The experimental data used to support the findings of this study are included in the manuscript. The other data are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Acknowledgments

This research was funded by Vietnam National University Ho Chi Minh City under grant no. A2020-16-01.

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Copyright © 2020 Trung Thanh Nguyen 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.

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