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Synthesis of nanocrystalline MgO particles by combustion followed by annealing method using hexamine as a fuel.

1. Introduction

Magnesium Oxide (designated as MgO) is a semiconductor/insulator which crystallizes in rock salt/sodium chloride (NaCl) type cubic structure [1]. Like MgO, many binary oxides, for instance, CaO, SrO, BaO, NiO, and CoO, also crystallize in rock salt structure [1]. MgO is an attractive material which has many potential applications [2-15], such as water purification, optoelectronics, microelectronics, and additive in heavy fuel oil, paint, gas separation, bactericides, and insulator in industrial cables, crucibles, and refractory materials. Further, it has been used as an oxide barrier in spin tunneling devices as well as substrate in super conducting and ferroelectric film. The MgO nanoparticles have high catalytic activity. Due to high specific surface area of nano-MgO materials, they are found to catalyze efficiently in variety of organic reactions [16-18].

Several preparation routes [2-6, 9,19-31], namely, combustion, microwave assisted synthesis, spinning disk reactor, wet chemical method, nonaqueous sol-gel method, chemical synthesis, microwave assisted sol-gel synthesis, surfactant assisted precipitation method, electrospinning technique, colloidal synthesis, rf impulse discharge plasma, hard templating pathway, sol-gel method, and microwave hydrothermal process, have been reported for the preparation of nano-MgO materials. For these synthesis methods, in literature, there are a variety of precursors, namely, magnesium nitrate, glycine, Mg[(CHCOO).sub.2] and ethylene glycol, Mg[Cl.sub.2] and NaOH, magnesium foil, toluene and Mg[Cl.sub.2] x 6[H.sub.2]O, ammonia, polyvinyl alcohol, polyvinyl pyrrolidone, magnesium acetate tetrahydrate, Mg particle, tungsten wire, trioctylphosphine oxide (TOPO) and bis(cyclopentadienyl)magnesium (Cp2Mg), Mg rod electrode, and magnesium acetate, which have been reported for the preparation of MgO nanoparticles. Further, to prepare MgO nanomaterials, various fuels [2-15], namely, glycine, urea, combination of urea, glycine, and cellulose, propane, and 1,3 propane diol, have been used. Among these different fuels, urea [4, 8, 10-12, 14, 15] is the most commonly used fuel in the preparation of nano-MgO particles. In literature, for the synthesis of nano-MgO materials, magnesium nitrate and urea with the molar ratio 1: 1.67 have been used as the oxidizer and fuel, respectively [4, 8, 10-12, 14, 15]. The (average) crystalline sizes of 1560 nm [7], 16-19 nm [11], and 38 nm [14] have been reported for the MgO particles by different research group. The particle size obtained from microimages (SEM/TEM) has showed 300-350 nm (SEM) [7] and 20-25 (TEM) [4]. The combination of urea, glycine, and cellulose with the molar ratios 1 : 1.67 : 1.11 : 0.42 has showed the lowest particle size of 6.9 nm (XRD) and 5nm (TEM) [6]. In addition to the reported various fuels [2-15], there are several efficient fuels which are available to perform the combustion synthesis. Hexamine is one of the efficient fuels to synthesize the nanoscale materials. To the best of our knowledge, there is no report available in literature on the synthesis of nano-MgO materials by hexamine as the fuel by combustion method. In this paper, we report the synthesis and characterization of nanocrystalline MgO particles by combustion method using hexamine as a fuel and magnesium nitrate as the precursor.

2. Experimental Procedure

The nanocrystalline MgO particles were prepared by combustion method using magnesium nitrate and hexamine (see the flow chart in Figure 1). The commercially available Mg[(N[O.sub.3]).sub.2] x 6[H.sub.2]O was first dissolved in minimum quantity of deionised water. Then this solution was stirred at 300 rpm for few minutes. After that, the fuel, hexamine ([C.sub.6][H.sub.12][N.sub.4]), dissolved in minimum quantity of deionised water was mixed to the magnesium nitrate solution and stirred well. Then, the solution combustion mixture was heated slowly in heating mantle until it gets ignited. When the temperature reached about 190[degrees]C, combustion flame appeared. Figure 2 shows the observation of flame during the combustion of nitrate and fuel. After completion of combustion, the crude brown color powder was obtained. The obtained combustion product was annealed at 800[degrees]C for 3 hrs in a groove rolled muffle furnace. After completion of annealing, the furnace was cooled to room temperature by switching off the power. The annealed product was white in color and taken for characterizations. The phase identification and purity of the annealed materials were tested by powder XRD and FT-IR spectroscopy. The photoluminescence (PL) property of the MgO powder sample was performed in a spectrofluorometer (ELICO SL 174) using 150 Watt Xenon Arc lamp as the excitation light source. The NIR spectrum of MgO powder was performed in a NIR Spectrophotometer (ELICO SL 153) using Quartz halogen lamp as the light source. The microstructural images and the elements present in the combustion-annealed MgO materials were performed in the scanning electron microscope, SEM (Jeol model; JSM-6390LV), attached with Energy Dispersive X-ray Analyzer (JED-2300).

3. Results and Discussion

3.1. XRD Pattern of Nano-MgO Powder. In the present work, Mg[(N[O.sub.3]).sub.2] x 6[H.sub.2]O is used as oxidizer and [C.sub.6][H.sub.12][N.sub.4] is used as reducing agent. Similar to the oxidation number concept, the valency of the oxidizing elements is considered as negative and the reducing elements as positive in solution combustion calculations [32]. Accordingly, the elemental valency of C, H, and Mg is +4, +1, and +2, respectively, and the oxidizing valency of oxygen is taken as -2. The valency of nitrogen is assumed to be zero. Based on this concept, the oxidizing valency of magnesium nitrate and the reducing valency of hexamine can be calculated as Mg[(N[O.sub.3]).sub.2] x 6[H.sub.2]O = [+2 - 12 + 0] = -10 and [C.sub.6][H.sub.12][N.sub.4] = + 24 + 12 + 0 = 36. According to the equivalence ratio theory, for the combustion of magnesium nitrate and hexamine mixture, the molar ratio becomes 10/36 = 0.28.

That is, [[PHI].sub.e] = [summation](Coefficient of oxidizing elements in specific formula * valency)/(-1)(Coefficient of reducing elements in specific formula * valency) = 10/36 = 0.28. The 1: 0.28 molar ratio of nitrate and hexamine is taken for the formation of MgO in the present combustion reaction. In order to see the variation in fuel concentration on the phase purity and particle size of MgO nanomaterial under different molar ratios, for example, 1 : 0.1, 1 : 0.2, 1 : 0.28, 1 : 0.4, 1 : 0.5, 1: 0.75, and 1: 1 conditions, the combustion syntheses were carried out. However, no significant effects are seen on their physical properties.

The powder XRD analyses were performed in the 2[theta] range between 20 and 80[degrees] using Cu [K.sub.[alpha]] radiation. In Figure 3, the powder XRD patterns of both as-prepared and annealed MgO nanopowder are presented. From these XRD patterns, we observe that the annealed material is crystallized in single phase with cubic symmetry. The Bragg reflections are indexed on the basis of space group, Fm-3m (225), Z = 4 with cubic lattice parameter, and a ~ 0.4210(4) nm for the annealed sample. This present value is in good accordance with the literature reports. The Bragg reflections such as (111), (002), (202), (113), and (222) are seen in the 2[theta] range between 20 and 80[degrees]. All reflections are sharp with slight broadening. These reflect the crystalline nature of MgO nanopowder. The average crystalline size of 22 nm is obtained for the annealed nanocrystalline MgO powder from the Debye Scherrerformula using the XRD powder data [33].

3.2. FT-IR Spectrum of Nano-MgO Powder. The typical FTIR spectrum for the annealed MgO powder is depicted in Figure 4. From FT-IR analysis, the stretching vibration mode for the Mg-O-Mg compound is seen in the range of 487-677 [cm.sup.-1] as a broad band. Two distinct bands are seen at the wave number ranges of 1014-1073 [cm.sup.-1] and 1567-1641 [cm.sup.-1] and are attributed to the bending vibration of absorbed water molecule and surface hydroxyl group (-OH), respectively. A broad vibration band is seen in the wavenumber range 3325-3650 [cm.sup.-1] due to O-H stretching vibration of absorbed water molecule and surface hydroxyl group [11]. This is due to the aerial adsorptions of water molecule onto the MgO surface when it is exposed to atmosphere. The FT-IR absorption peak seen at the wavenumber 1420 [cm.sup.-1] is assigned to the asymmetric stretching of the carbonate ion, C[O.sub.3.sup.2-] species [11].

3.3. Optical Properties of Nano-MgO Powder. The PL emission spectrum of annealed nanocrystalline MgO powder is shown in Figure 5. The PL emission spectrum was recorded at 385 nm as an excitation wavelength with bandwidth equal to 5nm and scanning rate equal to 200nm/sec. The PL emission spectrum reveals three emission peaks at 432, 465, and 495 nm in 400-500 nm emission band range, in which the 432 nm emission arises from the defect band transition and [sup.3][B.sub.1u] [right arrow] [sup.1][A.sub.g] from [F.sub.2.sup.2+] defect centre occupied in [D.sub.2h] symmetry [11, 34]. The 465 and 495nm blue emissions are owing to the recombination of electrons with oxygen vacancies (i.e., F centre). These vacancies are possibly generated by various factors, namely, unbalanced oxygenation during self-ignition, subsequential crystallization process, and Mg vacancies and interstitials [11, 35]. Figure 6 depicts the NIR spectrum of annealed nano-MgO powder as a function of wavelength. Quite similar to the report of Jeevanandam et al. [36], our NIR spectrum of nano-MgO powder shows higher reflectance value in the region 800-1300 nm. This is due to the smaller crystalline size of combustion-annealed nano-MgO powder. Owing to the higher reflectance of nano-MgO, it can be used as NIR reflective pigments [36].

3.4. Microstructure Analysis of MgO by SEM. In order to see the morphology and the particle size of the annealed MgO, the SEM images were taken in the scanning electron microscope (SEM; Jeol model JSM-6390LV instrument) (see Figures 7(a)-7(d)). The SEM images are shown in different magnifications. The SEM results reveal that the annealed MgO nanomaterials are seemingly porous and highly agglomerated with the nanoentities. Thus the particle size of MgO could not be seen accurately from the present SEM results (Figure 8). Due to the porous nature of MgO, the combustion-annealed MgO nanomaterials may play a major role in gas sensing application.

4. Conclusion

From our present work, it is concluded that it is easy to prepare MgO nanoparticles by combustion method using magnesium nitrate as oxidizer and hexamine as a fuel. The obtained white color MgO materials were analyzed using various characterization techniques. The XRD pattern confirmed the crystallinity and phase purity of the annealed nano-MgO powder. The average particle size calculated from the diffraction peaks was found to be 22 nm. The SEM result revealed that the powder is porous and agglomerated with polycrystallite nanoparticles. The MgO materials obtained by combustion-annealing method using hexamine may prove potential applications in pigments, catalyst, water purification, optoelectronics, bactericides, substrate, insulator, crucibles, and refractory materials.

http://dx.doi.org/10.1155/2014/841803

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The author S. Balamurugan is thankful to DST-SERB, Government of India, for the research Grant (Sanction no. CS-108/2011) under the Fast Track-Young Scientist award scheme. Further, the authors are thankful to Noorul Islam Centre for Higher Education for the encouragement.

Received 28 January 2014; Accepted 18 May 2014; Published 3 June 2014

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S. Balamurugan, (1) L. Ashna, (2) and P. Parthiban (1)

(1) Advanced Nanomaterials Research Laboratory, Department of Nanotechnology, Noorul Islam Centre for Higher Education, Kumaracoil, Thuckalay, Tamil Nadu 629180, India

(2) Department of Biotechnology, Udaya School of Engineering, UdayaNagar, Vellamodi, Ammandivilai, Tamil Nadu 629 204, India

Correspondence should be addressed to S. Balamurugan; scandium.chemistry@gmail.com

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Title Annotation:Research Article
Author:Balamurugan, S.; Ashna, L.; Parthiban, P.
Publication:Journal of Nanotechnology
Article Type:Report
Date:Jan 1, 2014
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