Solution combustion synthesis of high surface area Li2TiO3 nanostructure particles: Effect of nitric acid and NaCl addition

Author(s):  
Hoora Kaspoor ◽  
Ahmad Reza Abbasian ◽  
Mahdi Shafiee Afarani
2013 ◽  
Vol 757 ◽  
pp. 85-98 ◽  
Author(s):  
L.D. Jadhav ◽  
S.P. Patil ◽  
A.P. Jamale ◽  
A.U. Chavan

Solution combustion synthesis technique is one of the novel techniques used to prepare nanoparticles, multi-component ceramic oxides and nanocomposites with properties better than conventionally prepared one and these materials have been used for various applications such as sensors, catalysts, and materials for solid oxide fuel cell (SOFCs). In the present work, the method has been used to prepare nanoparticles of 10 mol% Gd doped ceria (GDC) and Cu and its oxides. The oxidant to fuel (O/F) ratio is found to affect the powder properties and even compositional homogeneity. In glycine-nitrate combustion synthesis of GDC, as revealed by XRD studies, phase pure nanoparticles with crystallite size in the range 9-12nm were obtained for all the O/F ratios. TEM measurements of calcined powder showed hexagonal shaped particles of roughly 20nm size. The exothermicity was increased with the oxidant to fuel ratio resulting in high surface area and soft agglomerates. A slightly lean O/F ratio gives surface area of 73 m2/g and soft agglomerates (D50= 5.34 mm), which eventually results into high sintering density at low temperature. Raman Spectra of GDC showed a sharp and intense peak at 467 cm−1which corresponds to CeO2due to F2gsymmetry of the cubic phase. In combustion synthesis of copper nitrate and citirc acid, the compositional homogenity and phase purity was affected by the oxidant to fuel ratio. The combustion at stoichiometric O/F ratio gives Cu nano particles, lean O/F ratio gives nanoparticles of Cu, CuO and Cu2O and rich ratio gives pure CuO nanoparticles. These nanoparticles have been studied with different characterization techniques like XRD, TG-DTA, SEM, TEM, FT-IR and Raman.


2011 ◽  
Vol 80-81 ◽  
pp. 332-336 ◽  
Author(s):  
Yan Xia ◽  
Mei Huang ◽  
Jun Ming Guo ◽  
Ying Jie Zhang

Effect of nitric acid and the burning time on the liquid combustion synthesis of spinel LiMn2O4 has been studied, using lithium nitrite and Manganese acetate as raw a material. The results show that the main phases are all LiMn2O4, which can be obtained at 400-600 oC. Before modified, the impurity is Mn3O4 or Mn2O3. After modified, the impurity is only Mn3O4. The aggregation obviously reduced after adding nitric acid, it is indicated that the crystalline increased. With the increasing temperatures, the modified particle size was increased and the aggregation reduced. The initial discharge capacity and cycle stability improved at some extent too. Its first discharge capacity was 104.6, 112.8 and 117.7mAh/g synthesized at 400, 500, 600 oC, respectively, and the 30th capacity retention rate were 84.89%, 80.67% and 73.24%.


2014 ◽  
Vol 617 ◽  
pp. 187-190 ◽  
Author(s):  
Te Wei Chiu ◽  
Yi Wei Feng

In this study, the effects of glycine-nitrate ratios and postcombustion chemical treatment on the phase evolution and surface area of CuCrO2powders were investigated. The pure phase of CuCrO2powders was obtained at a glycine-nitrate ratio of 1.2–1.4. When the glycine-nitrate ratio was higher than 1.9, the Cu ions were reduced to Cu(0) and the phase of Cu metal and Cr2O3were observed. However, when the glycine-nitrate ratio was lower than 1.1, the Cu ions were partially maintained as Cu(2+), and a bluish residue was observed. As-combusted CuCrO2powder with a high surface area (50 m2/g) was obtained at a glycine-nitrate ratio of 1.2. Furthermore, a high surface area (> 60 m2/g) was obtained by leaching as-combusted CuCrO2powder with diluted nitric acid.


2020 ◽  
Vol 221 ◽  
pp. 462-475
Author(s):  
V. Danghyan ◽  
T. Orlova ◽  
S. Roslyakov ◽  
E.E. Wolf ◽  
A.S. Mukasyan

2018 ◽  
Vol 2018 ◽  
pp. 1-8 ◽  
Author(s):  
Imarally V. de S. R. Nascimento ◽  
Willams T. Barbosa ◽  
Raúl G. Carrodeguas ◽  
Marcus V. L. Fook ◽  
Miguel A. Rodríguez

The objective of this work has been the synthesis of wollastonite by solution combustion method. The novelty of this work has been obtaining the crystalline phase without the need of thermal treatments after the synthesis. For this purpose, urea was used as fuel. Calcium nitrate was selected as a source of calcium and colloidal silica served as a source of silicon. The effect of the amount of fuel on the combustion process was investigated. Temperature of the combustion reaction was followed by digital pyrometry. The obtained products were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and specific surface area. The results showed that the combustion synthesis provides nanostructured powders characterized by a high surface area. When excess of urea was used, wollastonite-2M was obtained with a submicronic structure.


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