Synthesis of magnesium aluminate spinel nano-powders by co-precipitation method

2015 ◽  
Vol 19 (sup9) ◽  
pp. S9-20-S9-23
Author(s):  
H. Li ◽  
Y. Q. Liu ◽  
H. Liu ◽  
Z. J. Yang
Processes ◽  
2019 ◽  
Vol 7 (10) ◽  
pp. 741 ◽  
Author(s):  
Nguyen ◽  
Lee

Synthesis of magnesium aluminate spinel (MgAl2O4) was investigated by employing ball milling and co-precipitation methods. The starting materials (aluminum hydroxides) were obtained from the purified sodium hydroxide leaching solution of black dross. The characteristics of the synthesized spinel was analyzed through X-ray diffraction (XRD), scanning electron microscopy (SEM) images. In this work, the effect of calcination temperature and time on the formation of spinel by the two methods was compared. Calcination temperature showed a great effect on the formation of spinel in both methods. The results showed that the co-precipitation method has many advantages over the ball milling method. In ball milling method, complete conversion of the starting materials to spinel was impossible even at 1500 °C, while complete conversion to spinel was accomplished at 1000 °C for 5 h by the co-precipitation method. The average size of the spinel synthesized at these optimum conditions of the co-precipitation method was about 17 nm. A process can be developed to synthesize spinel from the black dross which is regarded as hazardous materials.


2015 ◽  
Vol 659 ◽  
pp. 159-163
Author(s):  
Sarut Teerasoradech ◽  
Karn Serivalsatit

Magnesium aluminate spinel (MgAl2O4) or spinel ceramics have been widely used in engineering fields due to its attractive properties, such as high mechanical strength, good optical properties, and high refractoriness. Precipitation is one of the most common techniques for preparing spinel nanopowders because it offers many advantages including low cost, simple method, and ease of mass production. However, severe agglomeration usually takes place during water removal process, i.e. washing and drying. These hard agglomerates deteriorate sinterability of nanopowders. In this study, spinel nanopowders were prepared by co-precipitation method. The remaining water in the precipitated precursor was removed by washing the precipitated precursor with organic solvents, i.e. ethanol and acetone-toluene-acetone. Conventional drying process was also performed for comparison. The characteristics of the obtained spinel nanopowders were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and dynamic light scattering (DLS) method. The results showed that the water removal process did not have any significant effects on phases of the dried precursors and the calcined powders. However, washing the precipitate precursor with organic solvent is the most effective process to prepare spinel nanopowders with low degree of agglomeration. Whereas, removing water by conventional drying process led to the formation of hard agglomerates. Furthermore, the effects of water removal process on sinterability of the spinel nanopowders were also reported.


2015 ◽  
Vol 659 ◽  
pp. 310-314
Author(s):  
Karn Serivalsatit ◽  
Thanataon Pornpatdetaudom ◽  
Adison Saelee ◽  
Sarut Teerasoradech

A wide application of magnesium aluminate spinel powder has attracted a number of studies concerning the preparation of magnesium aluminate spinel powder. In this study, a precursor for magnesium aluminate spinel was synthesized by a homogeneous precipitation method using urea as a precipitant. The precursor and the calcined powders were characterized by X-ray diffractometry, Fourier transform infrared spectroscopy, scanning electron microscopy, and transmission electron microscopy. After precipitation, the precursor was magnesium aluminium hydrate carbonate compound. By calcining, the precursor decomposed to MgO and an amorphous phase after calcining at 600°C. The formation of magnesium aluminate spinel via a reaction between MgO and the amorphous phase was observed after calcining over 800°C. The equiaxed magnesium aluminate spinel nanoparticles with particle size of 20-40 nm were obtained after calcining at 1100°C for 2 hours. Sinterability of the obtained magnesium aluminate spinel nanoparticles was also investigated by sintering compacts of magnesium aluminate spinel nanoparticles in the temperature interval of 1300-1650°C. Sintering temperature of 1600°C allowed the fabrication of dense magnesium aluminate spinel ceramics with relative density >95%.


2016 ◽  
Vol 690 ◽  
pp. 224-229 ◽  
Author(s):  
Adison Saelee ◽  
Sirithan Jiemsirilers ◽  
Supatra Jinawath ◽  
Karn Serivalsatit

Magnesium aluminate spinel (MgAl2O4) is widely used in many engineering applications due to its high melting point (2135°C), high mechanical strength, chemical inertness, and good optical properties. Precipitation method is recognized as a convenient and cost-effective method for the synthesis of nanopowders. In this present work, MgAl2O4 nanopowders were prepared by precipitation method using ammonium hydrogen carbonate as a precipitant. The precipitated precursors were a mixture of ammonium dawsonite (NH4Al (OH)2CO3·H2O) and hydrotalcite (Mg6Al2(CO3)(OH)16·4H2O). After calcining at 1100°C for 2 hours, The MgAl2O4 nanopowders with particle size of 20-170 nm were obtained. The sinterability of the MgAl2O4 nanopowders was evaluated by sintering compacts of the MgAl2O4 nanopowders at temperature of 1300-1650°C for 2 hours. The relative density of the sintered MgAl2O4 ceramics reached about >97% of theoretical density after sintering at 1500°C for 2 hours. The Vicker’s hardness of the sintered ceramics reached a value of 1414 HV (13.9 GPa) after sintering at 1650°C for 2 hours.


2015 ◽  
Vol 7 (2) ◽  
pp. 1393-1403
Author(s):  
Dr R.P VIJAYALAKSHMI ◽  
N. Manjula ◽  
S. Ramu ◽  
Amaranatha Reddy

Single crystalline nano-sized multiferroic BiFeO3 (BFO) powders were synthesized through simple chemical co-precipitation method using polyethylene glycol (PEG) as capping agent. We obtained pure phase BiFeO3 powder by controlling pHand calcination temperature. From X-ray diffraction studies the nanoparticles were unambiguously identified to have a rhombohedrally distorted perovskite structure belonging to the space group of R3c. No secondary phases were detected. It indicates single phase structure. EDX spectra indicated the appearance of three elements Bi, Fe, O in 1:1:3. From the UV-Vis diffuse reflectance spectrum, the absorption cut-off wavelength of the BFO sample is around 558nm corresponding to the energy band gap of 2.2 eV. The size (60-70 nm) and morphology of the nanoparticles have been analyzed using transmission electron microscopy (TEM).   Linear M−H behaviour and slight hysteresis at lower magnetic field is observed for BiFeO3 nanoparticles from Vibrating sample magnetometer studies. It indicates weak ferromagnetic behaviour at room temperature. From dielectric studies, the conductivity value is calculated from the relation s = L/RbA Sm-1 and it is around 7.2 x 10-9 S/m.


2020 ◽  
Vol 3 (1) ◽  
pp. 30-33
Author(s):  
Muthulakshmi M ◽  
Madhumitha G

Nanotechnology is a field of applied science focused on design, synthesis and characterization of nanomaterials. The nickel and magnesium have improved their applications in transparent electrodes and nano electronics. In addition, magnesium oxide has moisture resistance and high melting point properties. In the present work has been carried out in the development of green crystalline powder of nickel doped magnesium oxide nanoparticles by Co-precipitation method, from the mixture of nickel chloride and magnesium chloride with KOH as solvent. From the XRD results, crystalline size of the particle can be observed. Spherical structure of Ni doped MgO nanoparticles were indicated by SEM results and powdered composition of samples were obtained from FTIR. EDAX represents the peak composition of the nanoparticle. The above analytical techniques have confirmed that the Ni doped MgO nanoparticles obtained from the mixture of NiCl2 and MgCl2.


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