Received date: June 28, 2017; Accepted date: July 06, 2017; Published date: July 16, 2017
Citation: Moustafa IMI, Abdelhamid MR (2017) Synthesis of MgO Nanoparticles from Different Organic Precursors; Catalytic Decontamination of Organic Pollutants and Antitumor Activity. J Material Sci Eng 6: 359. doi: 10.4172/2169-0022.1000359
Copyright: © 2017 Moustafa IMI, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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The present work deals with the synthesis of nanostructured MgO from different organic precursors, by a facile precipitation method as catalysts for the decontamination of Malathion (stimulant of chemical warfare agents) (VX) and orange G as organic pollutants. The as-prepared nanoparticles were obtained by thermal decomposition of the oxalate, tartarate, citrate, succinate, malate, malonate and glycinate precursors at ≈650°C and were characterized by thermal analysis, FTIR, X-ray diffraction, high resolution transmission electron microscope (HRTEM) and absorption spectra. The morphology and crystal sizes were found to be highly affected by the starting organic precursors. The results revealed that the prepared inexpensive magnesium oxides have high potential as catalysts for photo degradation of both Malathion and orange G from water samples. Inhibitory activity against Breast Carcinoma MCF-7 cell line was detected using some selected nanosized MgO and compared to that of Vinblastine as a standard drug.
Nano sized MgO; Catalytic photo degradation; VX stimulant (Malathion); Orange G; Antitumor activity
Researches on the synthesis and application of nanomaterials had experienced tremendous growth in recent years, owing to their unique properties making them suitable for applications in almost every field of science [1-11]. Photocatalytic degradation of dyes and toxic organic materials from aqueous solution is considered one of the most effective methods for water treatment especially using nanosized metal oxides as catalysts [12-18]. Nanocrystalline MgO is an interesting functional material due to its low heat capacity, chemical inertness, optical transparency and high thermal stability. Due to its high surface area, it is used as an efficient adsorbent for numerous toxic chemicals and acid gases. Recently, MgO nanoparticles have shown promise for application in tumor treatment and also have considerable potential as an antibacterial agent [19-24]. In the present work and in continuity to our previous work , we study the effect of starting organic precursors on the crystal size and morphology of nanosized MgO. The prepared nanooxides were tested successfully as adsorbents for the decontamination of Malathion as stimulant of chemical warfare agents (CWA) (VX) and orange G as organic pollutant. Inhibitory activity against Breast Carcinoma MCF-7 cell line was also tested using some selected nanosized MgO.
Synthesis of magnesium oxide nanoparticles
AR grade chemicals obtained from Merck and Aldrich were used for the preparation of the nano particles of magnesium oxide (M1-M7). The individual oxides were prepared via the precipitation method by titration of 50 ml of 0.1 M magnesium acetate drop by drop to 50 ml of 0.2 M of different organic acids viz. oxalic acid (M1), tartaric acid (M2), citric acid (M3), succinic acid (M4), malic acid (M5), malonic acid (M6) and glycine (M7), respectively. The mixtures were stirred for 1 hr. and the precipitates formed were filtered, washed thoroughly using bidistilled water, air dried, thoroughly grounded in agate mortar and finally dried at 120°C for two hours in the form of fine powder. The powder so obtained was annealed at 650°C for six hours in muffle furnace to obtain the corresponding nanosized magnesium oxides.
FT-IR spectra of both of the precipitated and ignited samples were recorded on a Nicolet iSio FT-IR spectrophotometer in the 4000-400 cm−1 region using KBr disk technique (Chemistry department, Faculty of science, Benha University, Egypt). Electronic absorption spectra of the prepared nanooxides were recorded on a Jasco (V-530) UV-Vis spectrophotometer (Chemistry department, Faculty of Science, Benha University, Egypt). Thermogravimetric analysis (TG-DT) for the organic precursors was recorded on Shimadzu TA-60 WS thermal analysis (Micro analytical unit, Menofia University, Shebin El-Kom, Egypt). Elemental analysis for C and H of the nanooxides were carried out using Elementer Vario EL III Carlo Erba 1108 instrument (The Regional Center for Mycology and Biotechnology, Al-Azhar University, Cairo, Egypt). X-ray powder diffraction (XRD) was recorded on a 18 kW diffractometer (Bruker; model D8 Advance) with monochromated Cu Kα radiation (λ) 1.54178 Å (Central metallurgical research institute, Helwan, Egypt). The HR-TEM images of some selected nanooxides were taken on a transmission electron microscope (JEOL; model 1200 EX) at an accelerator voltage of 220 kV (Egyptian Petroleum Research Institute, Cairo, Egypt).
Photocatalytic degradation of Orange G dye
For a typical photocatalytic experiment, 100 mg of the nanosized photocatalyst was added to 25 ml of 20 ppm aqueous dye solution which was kept in dark for 6 hrs to allow the system to reach an adsorption desorption equilibrium then 2 ml of 0.5 M hydrogen peroxide solution was added. The degradation process was investigated in a Pyrex beaker under the UV illumination using a 250 W xenon arc lamp (Thoshiba, SHLS-002) (λ=365 nm). After recovering the catalyst by centrifugation, the absorption spectra of the clear solution was measured at 485 nm (λmax for Orange G dye) at different time intervals using a UV-Vis spectrophotometer.
Photocatalytic degradation of Malathion
The photocatalytic degradation of 0.06 ml/l of Malathion solution was performed using the smallest crystal sized magnesium oxide (M7) sample (prepared from glycine). For a typical experiment, 100 mg of the nanooxide sample was added to 25 ml of 0.06 ml/l Malathion solution which was kept in dark for 6 hrs. The degradation process was investigated as previously mentioned for Orange G dye and the concentration of the remaining pollutant was followed up by measuring absorption spectra at 238, 265 nm (λmax for Malathion) at different time intervals.
Antitumor activity against Breast Carcinoma MCF-7 cell line was measured for some selected samples at The Regional Center for Mycology and Biotechnology, Al-Azhar University, Cairo, Egypt and compared to that of Vinblastine as a standard drug. The number of viable cells and the percentage of viability were calculated as where ODt is the mean optical density of the wells treated with the tested samples and ODc is the mean optical density of the untreated cells. The relation between surviving cells and drug concentration is plotted to get the survival curve of each tumor cell line after treatment with the nanooxides. The 50% inhibitory concentration (IC50), the concentration required to cause toxic effect in 50% of intact cells, was estimated from graphic plots of the dose response curve for each concentration.
Thermogravimetric analysis: The thermogravimetric-differential thermal analysis was performed on the organic precursors to follow their thermal decomposition to the final oxide forms. Inspection of the thermograms (Figure 1) showed that the organic precursors were thermally degraded through three main steps. The first within the temperature range 66.75-184.78°C due to the dehydration of humidity and crystallinity water (this step is sometimes a composite of two steps). The beginning of the thermal degradation of the unhydrous compounds took place within the second step within the temperature range 114.72-344.33°C by the evolution of gases such as N2 and CO2. Complete decomposition of the organic precursors occurred in the third step within the range 232.99-565.99°C which led to the formation of the nanosized MgO as final product. Example of thermal decomposition process of tartaric acid precursor is represented as:
Fourier transforms infrared spectra (FTIR): The FTIR spectra of the magnesium-organic precursors were studied and compared to those of the corresponding nanooxides. The most important band frequencies (cm-1) are listed in Table 1. The spectra of the organic precursors show weak absorption bands within the wavenumber ranges 3373-3430 cm-1 and 1033-1171 cm-1 due to the stretching and bending vibrations of the trace water molecule, respectively. These two bands appeared within the ranges 2955-3430 cm-1 and 1032-1176 cm-1 as very weak bands in the spectra of the ignited samples. The strong bands within the range 1570-1677cm-1are due to the stretching vibration of C=O group (VC=O). These bands, more or less, disappeared in case of calcinated samples. It is worthy to mention that there is a shift in the IR active mode, which is due to nano size grain. For a nano size grain, the atomic arrangement on the boundaries differ greatly from that of the bulk crystals, both in coordination number and bond lengths, showing some extent of disorder . Crystal symmetry is thus, degraded in nano size grains. The degradation in crystal symmetry results in the shifting of the IR active mode .
|Compound||IR frequency (cm-1)|
Table 1: IR frequencies (cm-1) of some important groups in the organic precursors and the corresponding nanooxides.
X-ray diffraction analysis (XRD): The X-ray diffraction patterns of the nano sized magnesium oxides are shown in Figure 2. The XRD sharp lines reveal that the oxide nanoparticles are crystalline. The relative crystalline sizes are determined from the XRD lines broadening using the Scherrer equation . From calculation, the average crystalline size was found to be 44.8, 33.94, 44.60, 46.32, 47.16, 60.80 and 53.64 nm for magnesium oxides (M1-M7), respectively (Table 2). The phase purity of all the samples was established by comparison of the X-ray diffraction patterns with JCPDS international data value.
|Sample||Precursor||crystal size (nm)||Phase produced by XRD||Card No.||Crystal system|
Table 2: Effect of organic acids and glycine precursors on the crystal size and morphology of the prepared nanooxides.
High resolution transmission electron microscopy (HRTEM): The micro structural analysis of the synthesized samples calcined at 650°C for 6 hours was investigated using HRTEM. The HRTEM images of some selected samples are shown in Figure 3. It can be seen from the graphs that magnesium nanoparticles have narrow size distribution and are rectangular rode shapes with weak agglomeration. The average particle sizes ranged from 33.93-60.80 nm.
Optical analysis: A fundamental property of nanosized metal oxides is the band gap energy. The band gap energy is the energy separation between the filled valence band and the empty conduction band. Optical excitation of electrons across the band gap is strongly allowed, producing an abrupt increase in the absorption at the wavelength corresponding to the band gap energy. The UV-Visible spectra allow direct determination of band gap using the relation between the absorption coefficient (α) and the incident photon energy (hv) represented by Tauc equation :
Where, A is a constant, Eg is the band gap of the material and exponent n depends on the type of transition, n is either 2 for an indirect transition or ½ for a direct transition. Here the transition is direct so, n is taken to be ½. The value of optical band gap is calculated by plotting the relation between (αhv) 2 vs. hv and extrapolating the straight line portion to the hv axis. The extrapolation of linear portion to the hv axis gives values of energy gap for magnesium oxide nano particles. The obtained Eg values (within the range 2.91-3.12 eV) show the semiconductor nature of the samples and are in an excellent agreement with the reported data .
Photocatalytic degradation of organic G dye: The photodegradation efficiency of selected zirconium oxide nanoparticle (sample M3; prepared from citric acid as organic precursor) was tested using Orange G (OG) as model. The experiments were done at different conditions, namely; (UV+H2O2+M3), (UV+H2O2), (UV only), (UV+M3) where best results were obtained in the case of (UV+H2O2+M3). At periodic intervals of time, aliquots of the sample were withdrawn and the absorption spectra were recorded. Clearly, the absorbance decreases and the photodegradation efficiency increases (reaching a plateau) as a function of time (Figure 4). The results showed that the maximum percent of degradation of OG dye was 93% after 210 min indicating the very high efficiency of the nanoparticle used.
Decomposition of chemical warfare agents on metal oxides: Metal oxides demonstrate superior ability to adsorb and decompose CWA compared to pure metal surfaces. This is often attributed to reactive sites on the metal oxide surface through which organophosphonate species (nerve agents) can adsorb and subsequently undergo a hydrolysis reaction. The use of MgO nanoparticle, M7, (prepared from glycine as precursor) as catalyst for the decontamination of VX stimulant Malathion was carefully investigated. The effect of different factors affecting the removal efficiency, such as: time, pH, temperature and initial dose of Malathion was studied. The results obtained (Figures 5 and 6) showed that such nanooxides have high ability for the removal of this pollutant from water samples.
Inhibitory activity against Breast Carcinoma MCF-7 cell line was detected using some selected nanosized metal oxides viz; M2 and M3 and M7 and compared to that of Vinblastine as a standard drug. The relation between surviving cells and drug concentration is plotted to get the survival curve of each tumor cell line after treatment with the nanooxides. The 50% inhibitory concentration (IC50), the concentration required to cause toxic effect in 50% of intact cells, was estimated from graphic plots of the dose response curve for each concentration. The results are represented graphically in Figure 7 and the lethal concentrations (IC50) values are listed in Table 3.
Table 3: Lethal concentration (IC50) of the nanosized oxides M2, Z3 and MZ7.
Inspection of the cytotoxic data, it is found that magnesium oxide M2 (prepared from tartaric acid) is, in general, more effective than those of M3 (prepared from citric acid) and M7 (prepared from glycine). Shier  suggested that compounds having IC50 values 10- 25 μg/ml are considered to have weak cytotoxic activities, while those having intermediate values (ranging from 5-10 μg/ml) are classified as moderately active. On the other hand, compounds with IC50 values less than 5 μg/ml are considered to be very active. Consequently, the nanosized metal oxides under study are considered to have weak activity with IC50 values higher than 213 μg/ml.
MgO nanoparticles (M1-M7) were prepared by precipitation of Mg as oxalate, tartarate, citrate, succinate, malate, malonate and glycinate then ignition at 650oC. The magnesium-organic precursors and the corresponding nanooxides were characterized by thermal analysis and different spectroscopic techniques. The morphology and crystal sizes were found to be highly affected by the starting organic precursors. The optical energy gaps (Eg) calculated from electronic absorption spectra ranged from 2.91 to 3.12 eV suggesting the semiconductor nature of the nanooxides. The results revealed that the prepared inexpensive magnesium oxides have high potential as catalysts for photo degradation of both Malathion and orange G from water samples. Inhibitory activity against Breast Carcinoma MCF-7 cell line was detected using some selected nanosized MgO and compared to that of Vinblastine as a standard drug.
We would like to acknowledge the financial support from the MSP (Management of Scientific Projects), Benha University, Benha, Egypt (project presented by I. M. Ibrahim).
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