Controllable Synthesis of Magnesium Oxysulfate Nanowires with Different Morphologies
© to the authors 2008
Received: 1 September 2008
Accepted: 8 September 2008
Published: 24 September 2008
One-dimensional magnesium oxysulfate 5Mg(OH)2 · MgSO4 · 3H2O (abbreviated as 513MOS) with high aspect ratio has attracted much attention because of its distinctive properties from those of the conventional bulk materials. 513MOS nanowires with different morphologies were formed by varying the mixing ways of MgSO4 · 7H2O and NH4OH solutions at room temperature followed by hydrothermal treatment of the slurries at 150 °C for 12 h with or without EDTA. 513MOS nanowires with a length of 20–60 μm and a diameter of 60–300 nm were prepared in the case of double injection (adding MgSO4 · 7H2O and NH4OH solutions simultaneously into water), compared with the 513MOS with a length of 20–30 μm and a diameter of 0.3–1.7 μm in the case of the single injection (adding MgSO4 · 7H2O solution into NH4OH solution). The presence of minor amount of EDTA in the single injection method led to the formation of 513MOS nanowires with a length of 100–200 μm, a diameter of 80–200 nm, and an aspect ratio of up to 1000. The analysis of the experimental results indicated that the hydrothermal solutions with a lower supersaturation were favorable for the preferential growth of 513MOS nanowires along b axis.
KeywordsMagnesium oxysulfate Nanowires Double injection EDTA Supersaturation
One-dimensional (1D) nanostructured magnesium salts with different morphologies, such as needle , rod , wire , tube , and belt , have attracted much attention because of their unique properties and potential applications in nanotechnical fields. Up to now much work has been focused on the control of the morphologies of 1D 513MOS since it can be used as the reinforcing agent, the flame retardant, or as the precursor for the fabrication of 1D MgO or Mg(OH)2 [6–8].
It was reported that the 513MOS whisker agglomerates with a length of up to 200 μm and a diameter of 0.8–1.2 μm were formed using MgSO4 and Mg(OH)2 or MgO as the reactants [9, 10]. The sector-like 513MOS whiskers with a length of 20–50 μm and a diameter of 0.2–1.0 μm were synthesized using MgSO4 and NaOH as the raw materials [11–13]. Dispersive 1D 513MOS without agglomerates or the sector-like were formed by employing MgSO4 or the mixture of MgSO4 and MgCl2 as the magnesium source and the weak alkali NH4OH as the precipitation agent [14–16]. But little work has been reported on the control of the sizes (length and diameter) of the 1D 513MOS and it is still a challenge to synthesize 1D 513MOS with high aspect ratio and perfect uniformity.
Generally the solution with a lower supersaturation was favorable for the anisotropic or 1D growth of the crystals, which can be achieved by using dilute reactants or chelating agents. For example, it was reported that the presence of EDTA can control the morphologies and sizes of the corresponding particles owing to the chelating effects of EDTA with Ca2+, Zn2+, Ce3+, Fe3+, Co2+, and Bi3+, which can change the forms of the aqueous ions, producing a solution with less free metal ions to control the crystals growth. The growth habits of the crystals can also be altered by the capping effect of EDTA on the surfaces of the crystals.
In the present work the 513 MOS nanowires with high aspect ratio were formed by precipitation of MgSO4and NH4OH solutions at room temperature followed by treatment at hydrothermal conditions. The supersaturations of the solutions were controlled at relatively low levels, which were achieved by controlling the mixing ways of the reactants or addition of EDTA. The preferential orientation of 513MOS nanowires was identified and the related process mechanisms were discussed.
Synthesis of 513MOS Nanowires
Commercial reagents (NH4OH, MgSO4 · 7H2O, and EDTA) with analytical grade provided by Beijing Chemical Regent Factory were used in the experiments.
Three ways were adapted for the formation of the precursor slurries at room temperature: (1) Single injection: 35 mL of 1.0–1.5 mol L−1MgSO4was dropped (3.0 mL min−1) into 20 mL of 5.0–9.0 mol L−1NH4OH; (2) Double injection: 35 mL of 1.0–1.5 mol L−1MgSO4and 20 mL 5.0–9.0 mol L−1NH4OH were dropped (3.0 mL min−1) simultaneously into 5–10 mL water; (3) Single injection in the presence of EDTA: 35 mL of 1.0–1.5 mol L−1MgSO4mixed with varying amount of EDTA was dropped (3.0 mL min−1) into 20 mL of 5–9 mol L−1ammonia.
The slurry formed at room temperature was then transferred to a Teflon-lined stainless steel autoclave with an inner volume of 80 cm3, heated (5 °C min−1) to 150 °C and kept under isothermal condition for 8.0–12.0 h. The autoclave was cooled down to room temperature naturally after hydrothermal treatment and the product was filtrated, washed, and dried at 105 °C for 12.0 h.
The morphology and the microstructure of the samples were examined with the field emission scanning electron microscopy (FESEM, JSM 7401F, JEOL, Japan), the high-resolution transmission electron microscope (HRTEM, JEM-2010, JEOL, Japan) and the selected area electron diffraction (SAED). The crystallization and the composition of the samples were identified by the powder X-ray diffraction (XRD, D/max2500, Rigaku, Japan) using CuKα (λ = 0.154178 nm) radiation. The solution pH was detected by Mettler Toledo Delta 320 pH meter. The concentrations of Mg2+and SO4 2−were analyzed by EDTA titration and barium chromate spectrophotometry (Model 722, Xiaoguang, China), respectively.
Results and Discussion
The presence of EDTA led to the decrease of [Mg2+] (Fig. 5a) and the supersaturation of 513MOS (Fig. 5b), which may be connected with the chelating and/or the capping effects of EDTA. EDTA can form stable chelating complexes with Mg2+. The slow release of Mg2+from the complexes might be favorable for the 1D growth of 513MOS. The varying binding abilities of EDTA on different planes may also inhibit the radial growth and promote the axial growth of the 513MOS nanowires.
The increase of [Mg2+] and the supersaturation of 513MOS within initial 8 h of reaction should be attributed mainly to the dissolution of the Mg(OH)2precursor, and the decrease of [Mg2+] and the supersaturation of 513MOS after 6–10 h of reaction may be connected with the formation of 513MOS. The lower supersaturations of 513MOS achieved in either the double injection route or in the presence of minor amount of EDTA were favorable for the formation of 513MOS nanowires with high aspect ratio.
513MOS nanowires with a length of 20–60 μm and a diameter of 60–300 nm were synthesized via the double injection-hydrothermal reaction and the uniform 513MOS nanowires with a length of 100–200 μm and a diameter of 80–200 nm were formed via single injection EDTA-assisted hydrothermal reaction route. The lower supersaturations of 513MOS achieved in either the double injection route or in the presence of minor amount of EDTA, were favorable for the preferential growth of 513MOS along b axis, leading to the formation of 513MOS nanowires with high aspect ratios.
This work is supported by the National Natural Science Foundation of China (No.50574051).
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