Advances in Materials Science and Engineering

Volume 2014 (2014), Article ID 819745, 9 pages

http://dx.doi.org/10.1155/2014/819745

Research Article

The Synthesis and Physical Properties of Magnesium Borate Mineral of Admontite Synthesized from Sodium Borates

Azmi Seyhun Kipcak,¹ Meral Yildirim,¹ Sureyya Aydin Yuksel,² Emek Moroydor Derun,¹ and Sabriye Piskin¹

¹Department of Chemical Engineering, Faculty of Chemical and Metallurgical Engineering, Yildiz Technical University, Davutpasa Campus, Davutpasa Street No. 127, Esenler, 34210 Istanbul, Turkey

²Department of Physics, Faculty of Arts and Science, Yildiz Technical University, Davutpasa Campus, Davutpasa Street No. 127, Esenler, 34210 Istanbul, Turkey

Received 17 April 2014; Revised 16 July 2014; Accepted 18 July 2014; Published 13 August 2014

Academic Editor: You Song

Copyright © 2014 Azmi Seyhun Kipcak 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.

Abstract.

Magnesium borates are significant compounds due to their advanced mechanical and thermal durability properties. This group of minerals can be used in ceramic industry, in detergent industry, and as neutron shielding material, phosphor of thermoluminescence by dint of their extraordinary specialties. In the present study, the synthesis of magnesium borate via hydrothermal method from sodium borates and physical properties of synthesized magnesium borate minerals were investigated. The characterization of the products was carried out by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) and Raman spectroscopies, and differential thermal analysis and thermal gravimetry (DTA/TG). The surface morphology was examined by scanning electron microscopy (SEM). B₂O₃ content was determined through titration. The electrical resistivity/conductivity properties of products were measured by Picoammeter Voltage Source. UV-vis spectrometer was used to investigate optical absorption characteristics of synthesized minerals in the range 200–1000 nm at room temperature. XRD results identified the synthesized borate minerals as admontite [MgO(B₂O₃)₃·7(H₂O)] with code number “01-076-0540” and mcallisterite [Mg₂(B₆O₇(OH)₆)₂·9(H₂O)] with code number “01-070-1902.” The FT-IR and Raman spectra of the obtained samples were similar with characteristic magnesium borate bands. The investigation of the SEM images remarked that both nano- and microscale minerals were produced. The reaction yields were between 75.1 and 98.7%.

1. Introduction

Magnesium borates are considerable borate minerals by virtue of their high heat resistance, light weight, high elasticity coefficient, birefringent crystal structure, anticorrosion, and antiwear properties [1–4]. Owing to these properties, magnesium borates have extensive usage area and application potentials. Magnesium borates can be used in ceramic industry, in superconducted material production, in detergent composition, in friction reducing additive manufacture, in fluorescent discharge lamps as luminescent material, in ferroelastic material production, in cathode ray tube screens, in X-ray screens, and as thermoluminescent phosphor [5–10]. And also magnesium borates have great potential in areas of electronic ceramics reinforcement, semiconductor material synthesis, and plastics or aluminum/magnesium matrix alloy production [11, 12].

The production methods of magnesium borate minerals can be divided into two by hydrothermal and thermal methods [13]. In previous studies different types of magnesium borate minerals were synthesized. For the syntheses different starting materials were used. MgO and H₃BO₃ were used by Dou et al. [1] to synthesis magnesium borate types of MgO·3B₂O₃·7H₂O and 2MgO·B₂O₃·H₂O. Li et al. [2] prepared Mg₂B₂O₅ by the raw materials of MgBr₂·6H₂O and NaBH₄. Zhu et al. [14] used MgCl₂·6H₂O, H₃BO₃, and NaOH to synthesize MgBO₂(OH). Mg(OH)₂ and H₃BO₃ were used by Elssfah et al. [15] for the purpose of producing Mg₂B₂O₅. MgO, BI₃, and H₃BO₃ were selected as starting materials for synthesis of Mg₂B₂O₅ by Li et al. [16]. Wang et al. [17] used MgNO₃·6H₂O and Na₂B₄O₇·10H₂O for obtaining magnesium borate nanowires. 2MgO·2B₂O₃·MgCl₂·14H₂O and H₃BO₃ were chosen by Zhihong and Mancheng [18] for preparation of 2MgO·B₂O₃·H₂O.

The specific type of magnesium borate mineral, namely, admontite, was synthesized from MgO and H₃BO₃ at 100°C for the reaction times of 120 and 240 minutes by Derun et al. [19]. Also at their other study, Derun and Senberber [20] synthesized pure mcallisterite by using the same raw materials of MgO and H₃BO₃.

The common point to all previous magnesium borate syntheses by hydrothermal method was high reaction temperatures (≥100°C) and extended reaction times, where in literature hydrothermal syntheses are frequently driven in a temperature range of 100–220°C [4]. Furthermore the crystallinities of the obtained minerals were not at the desired levels.

Considering different studies about preparation of magnesium borate in this study, in order to obtain the magnesium borates below 100°C reaction temperature and 120 minutes of reaction time, different combinations and mole ratios of MgCl₂·6H₂O, H₃BO₃, B₂O₃, Na₂B₄O₇·5H₂O, and Na₂B₄O₇·10H₂O were used as raw materials in the hydrothermal synthesis. The mole ratios of raw materials were decided from previous experiments [21]. The main originality of the study is to produce magnesium borate compounds at lower temperatures and shorter reaction times, which leads to less energy consumption and time for a green chemistry approach. Another novelty of this study is the investigation and comparison of the electrical and optical characteristics of bulk and nanowires magnesium borate crystal that were investigated in the literature [16, 22, 23]. The bulk magnesium borate crystal has a wide optical band gap of 5.44 eV according to theoretical calculation [22].

Synthesized magnesium borate minerals were characterized by using X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, Raman spectroscopy, scanning electron microscopy (SEM), and differential thermal analysis and thermal gravimetry (DTA/TG). Electrical and optical properties of the different magnesium borate minerals were investigated with picoammeter voltage source and UV-vis spectrometer techniques, respectively.

2. Materials and Methods

2.1. Preparation and Characterization of the Raw Materials

Magnesium chloride hexahydrate (MgCl₂·6H₂O) was obtained from Merck Chemicals at minimum purity of 98% and particle size below 70 μm. Other reactants were retrieved from Bandırma Boron Works with a particle size below 1 mm. Among these raw materials boric acid (H₃BO₃), tincalconite (Na₂B₄O₇·5H₂O), and borax (Na₂B₄O₇·10H₂O) have a minimum purity of 99.9% and boron oxide (B₂O₃) has a minimum purity of 98%. Since the MgCl₂·6H₂O particle size was fine it was not pretreated, but other raw materials were processed by crushing, grinding through agate mortar (Retsch RM200), and sieving through Fritsch shaker sieve to reduce particle size down to below 70 μm. Then reactants were identified in Philips PANalytical XRD (step: 0.030°, time for step: 0.50 s, scan speed: 0.006°/s, and range: 7–90°) at 45 kV and 40 mA through the X-rays obtained in the Cu-Kα tube.

2.2. Magnesium Borate Synthesis

Some preliminary analyses were carried out using different molar ratios of MgCl₂·6H₂O : Na₂B₄O₇·5H₂O : H₃BO₃ (Mc : T : H) and the use of a molar Mc : T : H ratio of 1 : 1 : 3 throughout the analysis was selected for further experiments [19]. The expected reaction schemes are shown in (1)–(4):

The distilled water used in the experiments was obtained from a “Human Power I+” water treatment system and had a conductivity value of 18.3 mΩ·cm. The reaction temperatures and reaction times were selected between 60–100°C and 30–240 min. The experiments were carried out in a glass reactor and the reaction temperature was set as constant by a temperature control unit.

At the end of the selected reaction times the solution was put in an incubator maintained at 40°C until the excess water evaporated and magnesium borate minerals were crystallized. Then crystallized magnesium borate minerals were washed with pure (96%) ethanol three times to separate unreacted components and byproduct of NaCl. Washed samples were dried in an incubator maintained at 40°C again. The experimental method was shown in Figure 1.

Figure 1: Schematic experimental method.

2.3. Magnesium Borate Characterization Studies

Synthesized magnesium borates were subjected to XRD, FT-IR spectroscopy, and Raman spectroscopy. The parameters used in XRD were the same as those used in Section 2.1; only the range of the patterns was set between 7 and 60°, since the characteristic peaks of magnesium borates are seen in that range.

The characteristic peaks of borate compounds were given in the range of 1500–500 cm⁻¹ [24] so the spectrum ranges in FT-IR and Raman were selected as 1800 cm⁻¹–650 cm⁻¹ and 1800 cm⁻¹–250 cm⁻¹, respectively. Also no peak above 1800 cm⁻¹ was observed in either one of the spectral analyses.

The morphological features of materials, including their structure, morphology, phase, shape, size, and distribution, are affected by their physical and chemical properties [25]. CamScan Apollo 300 Field-Emission SEM was used to observe the surface textures and particle sizes of the synthesized magnesium borate minerals at 20 kV. The detector used was back scattering electron (BEI) and the magnification was set to 10000.

The commercial values of the boron minerals are evaluated from the B₂O₃ content of these minerals. This analysis was carried out using the method reported by Derun et al. [19].

Thermal analysis of a pure admontite selected from the XRD results was studied between the temperature range of 20–720°C with a Perkin Elmer Diamond DTA/TG with a heating rate of 10°C/min in an inert (nitrogen) atmosphere.

In order to investigate and characterize the product obtained after the thermal analysis, admontite mineral was placed in a Protherm MOS 180/4 high temperature furnace with 10°C/min temperature increment to a maximum temperature of 720°C in nitrogen flowing (5 mL/min) atmosphere. After the thermal conversion, the product was analyzed by XRD with the same parameters given in Section 2.3.

Yield analysis was also carried out using the method reported by Derun et al. [19] where MgCl₂·6H₂O was identified as the key component. Experiments were carried out in triplicate in three pure admontite minerals, which have the highest XRD scores in order to calculate the average yields and the standard deviations. The yield calculation of the biphasic samples was carried out based on the phase with the highest molecular weight.

The number of moles of product at the final stage, , was divided by the number of consumed moles of the key reactant to calculate the overall yield, (5). The number of moles of that was consumed was calculated using the initial () and the final () moles of the reactant. The equation then becomes as follows for a batch system [19, 26]:

2.4. Electrical and Optical Properties of Magnesium Borates

The synthesized magnesium borate compounds were pressed under pressure of 30 MPa into pellets with 13 mm diameters and 0.4 mm thickness. Electrical resistivity measurement of synthesized magnesium borate compounds which are coded with “Mc-Bx-B-60-240,” “Mc-T-B-80-60,” and “Mc-Bx-H-100-60” was carried out by standard current voltage measurement at room temperature using Keithley 6487 in dark with thermally evaporated silver contacts on both surfaces of pellets. The optical absorbance spectrum of magnesium borate compounds was taken by Perkin Elmer UV-vis spectrophotometer at room temperature. In this measurement the magnesium borate compounds were dispersed in HCl solution in quartz tube (1 cm × 1 cm).

3. Results

3.1. Results of the Raw Material Characterization

Magnesium source of MgCl₂·6H₂O was determined as “bischofite” (reference code: 01-077-1268). Sodium-boron source of Na₂B₄O₇·5H₂O was determined as “tincalconite” (reference code: 01-079-1529) and another sodium-boron source of Na₂B₄O₇·5H₂O was found as the mixture of both “borax” (reference code: 01-075-1078) and “tincalconite” (reference code: 01-079-1529). Boron sources of H₃BO₃ were determined as “sassolite” (reference code: 01-073-2158) and B₂O₃ was determined as the mixture of two types of “boron oxide” (reference codes: 00-006-0297 and 01-088-2485).

3.2. XRD Results of the Synthesized Magnesium Borates

Synthesized minerals XRD results were given in Table 1. It is seen from the results that the synthesized products were admontite [MgO(B₂O₃)₃·7(H₂O)] and mcallisterite [Mg₂(B₆O₇(OH)₆)₂·9(H₂O)]. The XRD patterns of three pure admontite minerals, which have the highest XRD scores, were represented in Figure 2.

Table 1: XRD scores of the synthesized magnesium borate minerals.

Reaction temperature (°C)
Reaction time (min)
Mc-T-H*
Mc-T-B*
Mc-Bx-H*
Mc-Bx-B*

Admontite
Mcallisterite
Admontite
Mcallisterite
Admontite
Mcallisterite
Admontite
Mcallisterite

60
30
68
64
59
64
67
—
60
—

60
62
68
66
52
68
—
63
—

120
65
35
59
58
64
46
68
—

240
67
55
61
48
63
—
71
—

80
30
61
76
66
40
64
—
65
—

60
65
54
70
—
65
—
64
56

120
56
54
62
56
57
—
60
—

240
49
60
63
45
65
—
65
—

100
30
45
80
47
79
63
—
62
—

60
46
79
49
81
70
—
58
31

120
44
80
39
81
56
44
61
40

240
49
74
48
60
62
—
64
17

*Mc: MgCl₂·6H₂O, T: Na₂B₄O₅(OH)₄·3H₂O, H: H₃BO₃, B: B₂O₃, and Bx: Na₂B₄O₅(OH)₄·8H₂O.

Figure 2: XRD patterns of pure admontite minerals.

As it is seen from Figure 2, the five major characteristic peaks of admontite mineral are seen at all three minerals at around 7°, 17°, 23°, 29°, and 34°. The crystallographic data of synthesized magnesium borates are given in Table 2.

Table 2: Crystallographic data of synthesized magnesium borates.

Mineral name
Admontite
Mcallisterite

Pdf number
01-076-0540
01-070-1902

Chemical formula
MgO(B₂O₃)₃·7(H₂O)
Mg₂(B₆O₇(OH)₆)₂·9(H₂O)

Molecular weight (g/mole)
375.27
768.56

Crystal system
Monoclinic
Rhombohedral

Space group
P21/c (number 14)
Pr3c (number 167)

(Å)
12.6610
11.5490

(Å)
10.0910
11.5490

(Å)
11.3220
35.5670

(°)
90.00
90.00

(°)
109.60
90.00

(°)
90.00
120.00

4.00
6.00

Density (calculated) (g·cm⁻³)
1.83
1.86

The obtained products for Mc-T-H experimental setup were formed in two distinct phases at all reaction temperatures and times. The higher mcallisterite scores were reached at increasing reaction temperatures. For Mc-T-B experimental setup, the obtained products were formed in two distinct phases the same as Mc-T-H set of experiment at all reaction temperatures and times except at 80°C and for the reaction time of 60 minutes. The pure admontite which had the highest crystal score was synthesized at 80°C after 60 minutes. Most of the synthesized minerals were pure admontite for Mc-Bx-H experimental setup apart from synthesis at 60°C and 100°C when the reaction time was 120 minutes. The highest admontite crystal score was achieved at 100°C after 60 minutes. At Mc-Bx-B experimental setup, for all reaction times, the obtained minerals which were produced at 60°C were pure admontite. Also, the highest admontite crystal score for all experimental setups was reached after the reaction of 240 minutes at 60°C.

3.3. FT-IR and Raman Spectral Analysis Results for the Synthesized Products

The FT-IR and Raman spectra of the synthesized magnesium borate minerals were very similar and were also in accordance with Yongzhong et al. [24]. FT-IR and Raman spectra of pure admontite minerals are given in Figures 3 and 4, respectively.

Figure 3: FT-IR spectra of pure admontite minerals.

Figure 4: Raman spectra of pure admontite minerals.

In the FT-IR spectrum, asymmetric stretching of the three-coordinate boron [(B₍₃₎-O)] was observed in the range of 1419 cm⁻¹–1344 cm⁻¹. The peak at between 1229 cm⁻¹ and 1225 cm⁻¹ corresponded to bending of B-O-H [δ(B-O-H)] and the asymmetric stretching of the four-coordinate boron [(B₍₄₎-O)] was observed in the range of 1084 cm⁻¹–999 cm⁻¹. Between the range of 953 cm⁻¹ and 897 cm⁻¹ symmetric stretching of the three-coordinate boron [(B₍₃₎-O)] was observed. The peaks between 856 cm⁻¹ and 805 cm⁻¹ coincided with symmetric stretching of the four-coordinate boron [(B₍₄₎-O)]. Bending of three-coordinate boron [δ(B₍₃₎-O)] was observed at around 671 cm⁻¹.

In the Raman spectrum, the band in the region of 952 cm⁻¹ was asymmetric stretching of the four-coordinate boron [(B₍₄₎-O)]; the bands at around 636 cm⁻¹–635 cm⁻¹ were associated with [B₆O₇(OH)₆]²⁻/[B₃O₃(OH)₄]⁻. The peaks at and below 426 cm⁻¹ belonged to bending of four-coordinate boron [δ(B₍₄₎-O)].

3.4. B₂O₃ Content of the Synthesized Minerals

The B₂O₃ analysis results of the synthesized magnesium borate minerals are given in Table 3. The B₂O₃ content was calculated between 40.00% and 55.39%. In the synthesized pure admontite minerals of coded “Mc-Bx-B-60-240,” “Mc-T-B-80-60,” and “Mc-Bx-H-100-60,” B₂O₃ contents were found as %, %, and %, respectively. Since B₂O₃ content of the admontite mineral is 55.66% [19], the results were close to the literature value.

Table 3: B₂O₃ contents of the synthesized magnesium borate minerals.

Reaction temperature (°C)
Reaction time (min)
B₂O₃ (%)

Mc-T-H
Mc-T-B
Mc-Bx-H
Mc-Bx-B

60
30
51.21 ± 1.87
44.59 ± 1.75
45.73 ± 2.73
43.48 ± 2.28

60
55.39 ± 1.37
53.33 ± 0.79
45.89 ± 2.51
49.92 ± 2.28

120
52.54 ± 0.67
51.65 ± 0.50
45.09 ± 1.82
40.00 ± 1.64

240
53.65 ± 2.16
41.87 ± 1.82
45.48 ± 2.83
52.03 ± 1.59

80
30
54.27 ± 1.59
50.27 ± 2.29
43.48 ± 2.28
46.86 ± 1.14

60
43.48 ± 2.28
54.04 ± 1.37
45.26 ± 1.83
50.89 ± 0.91

120
37.04 ± 2.28
54.42 ± 2.00
48.47 ± 1.14
44.87 ± 1.55

240
43.48 ± 2.28
54.30 ± 0.67
46.83 ± 1.96
45.25 ± 1.59

100
30
53.92 ± 1.79
54.27 ± 2.04
43.48 ± 2.28
43.16 ± 1.37

60
53.18 ± 0.42
54.01 ± 0.25
51.92 ± 2.28
41.97 ± 2.01

120
54.24 ± 1.83
51.89 ± 1.08
50.40 ± 2.05
41.38 ± 1.59

240
53.65 ± 2.16
49.92 ± 2.73
43.48 ± 2.28
40.04 ± 2.28

3.5. Surface Morphology and Particle Size of the Synthesized Admontite

Since the pure admontite minerals XRD scores were very close to each other (Mc-Bx-B-60-240: 71, Mc-T-B-80-60: 70, and Mc-Bx-B-100-60: 70), only “Mc-T-B-80-60” and “Mc-Bx-B-100-60” had been subjected to SEM analyses because of the low reaction times. SEM surface morphology and the particle size of admontite were given in Figure 5.

Figure 5: SEM surface morphology and the particle size of admontite minerals.

Obtained admontite crystals were layered, agglomerated, locally porous, smooth edged in “Mc-T-B-80-60,” and sharp edged in “Mc-Bx-B-100-60.” The size distribution, though varying due to the agglomerated structure, of admontite, of which “Mc-T-B-80-60” and “Mc-Bx-B-100-60” coded minerals particle sizes, was found between 2.04 μm–283.74 nm and 2.38 μm–207.10 nm, respectively.

3.6. Thermal Analysis Results

TG and DTG analyses of a selected (moderate reaction temperature and low reaction time) admontite which has a code of “Mc-T-B-80-60” are shown in Figure 6.

Figure 6: TG and DTG analyses of admontite mineral.

The analysis showed that three endothermic peaks occurred. The first peak that occurred between the temperatures of 40 and 59.47°C was the moisture. So admontite lost its crystal water via a two-step process, where in the first dehydration step the initial, peak, and final temperatures were seen as 59.47°C, 100.10°C, and 129.45°C. In the second step, initial, peak, and final temperatures were found as 129.45°C, 212.06°C, and 710.00°C. Weight decreases were 9.965% and 24.130% for the first and second steps, respectively. Total weight loss was calculated as 34.095%, which is close to theoretical structural water content (33.60%) of admontite mineral. So in the first dehydration step there was small moisture content of 0.495%. According to the found data the dehydration steps of appeared as, which is in a mutual agreement with the study of Derun et al. [19]:

3.7. Thermal Conversion Results of the Synthesized Magnesium Borates

According to thermal conversion results, the calcined magnesium borate lost 33.62% of its weight. This result conformed with the TG analyses and admontite’s theoretical structural water content of 33.60%. XRD results showed that the admontite mineral lost all of its structural water and turned to a dehydrated magnesium borate mineral MgB₄O₇ (pdf 00-031-0787). Before XRD analysis, the calcined admontite was washed with pure ethanol and dried at 40°C to remove B₂O₃ which occurred together with MgB₄O₇ during the calcination. The weight changes before and after leaching showed the equimolar MgB₄O₇ and B₂O₃ conversion.

The crystallographic data obtained from XRD are presented in Table 4 for admontite and MgB₄O₇. The XRD pattern of MgB₄O₇ is given in Figure 7.

Table 4: Crystallographic data of synthesized magnesium borates.

Mineral name
Magnesium borate

Pdf number
00-031-0787

Chemical formula
MgB₄O₇

Molecular weight (g/mole)
179.55

Crystal system
Orthorhombic

Space group
Pbca (number 61)

(Å)
8.5960

(Å)
13.7290

(Å)
7.9560

(°)
90.00

(°)
90.00

(°)
90.00

8.00

Density (calculated) (g·cm⁻³)
2.54

Figure 7: XRD pattern of MgB₄O₇.

At Figure 7 the five major characteristic peaks of MgB₄O₇ are seen at 17°, 20°, 22°, 26°, and 41°.

3.8. Yield Calculation of the Synthesized Magnesium Borates

Reaction yields increased with increasing reaction temperature and time for both sets which is shown in Figure 8. The yields were calculated between 76.2–95.2%, 75.1–92.6%, 82.8–97.2%, and 82.0–98.7% for the sets of “Mc-T-H,” “Mc-T-B,” “Mc-Bx-H,” and “Mc-Bx-B,” respectively.

Figure 8: Reaction yields of synthesized admontite minerals.

The pure admontite minerals yields were found as , , and % for the parameters of “Mc-Bx-B-60-240,” “Mc-T-B-80-60,” and “Mc-Bx-H-100-60,” respectively.

3.9. Results of Electrical and Optical Measurements

The absorption spectra of the magnesium borate mineral of admontite were measured in the wavelength range of 200–1000 nm at room temperature. Figure 9 shows the optical absorption spectra of admontite and calcined admontite. The energy gap of the admontite and calcined admontite was determined from extrapolation of high energy part of absorption spectra as about 4.77 eV and 4.13 eV, respectively.

Figure 9: The optical absorption spectra of admontite and calcined admontite.

Figure 10 shows the current voltage characteristics of the different magnesium borate compounds, which are coded with “Mc-Bx-H-100-60,” “Mc-Bx-B-60-240,” “Mc-T-B-80-60,” and calcined admontite. The resistivity of the compounds is derived to be , , , and  Ω m, respectively, which are obtained from the current voltage curves. The resistivities of the compounds were changed in the range of 10⁷-10⁸ Ω m.

Figure 10: The current voltage characteristics of different magnesium borate compounds.

4. Discussion and Conclusions

In this study for the approach of green chemistry the hydrothermal method at lower reaction temperature and reaction time is conducted in the synthesis of magnesium borates from sodium borates. From the results of this study, contrary to the previous studies, even at 60°C and 30-minute reaction time pure admontite synthesis was accomplished with high crystal scores. Derun et al. [19] reported the highest crystal score as 61 although in this study higher crystal scores were reached even when reducing reaction temperatures and furthermore the yield of obtained synthesized compounds ranged between 75.1 and 98.7%. FT-IR and Raman spectroscopy results showed that the products had characteristic peaks of magnesium borates in both infrared and visible regions. According to SEM results, the particle sizes of synthesized magnesium borate minerals were between 2.38 μm and 207.10 nm.

Also, the electrical conductivity of the magnesium borate compounds was determined in the range of 10⁻⁷-10⁻⁸ (Ω m)⁻¹ with the content of pure admontite minerals yields in the range of 85–94%. Resistivity measurement of bulk magnesium borate has not been studied and conductivity of magnesium borate nanowires is calculated to be about 10⁻⁴ (Ω m)⁻¹ in literature [16]; the wide difference in the conductivity of the magnesium borate obtained by Li et al. and the present study comes from the content of structural water inside the magnesium borates, where in this study MgO(B₂O₃)₃·7(H₂O) type of magnesium borate is synthesized; on the contrary Li et al. synthesized Mg₂B₂O₅ which is a dehydrated type of magnesium borate.

The energy band gaps of admontite and calcined admontite were determined to be about 4.77 eV and 4.13 eV, respectively, where in literature Kumari et al. [3] calculated the energy band gap of magnesium borate to be 4.72 eV, which is in mutual agreement with the obtained energy gap values.

Conflict of Interests

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

Acknowledgment

This research has been supported by Yildiz Technical University Scientific Research Projects Coordination Department with Project number of 2013-07-01-GEP04.

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