Solution Combustion Synthesis: Role of Oxidant to Fuel Ratio on Powder Properties

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.

2007 ◽  
Vol 1056 ◽  
Author(s):  
Luiz G. Jacobsohn ◽  
Bryan L. Bennett ◽  
Stephanie C. Sitarz ◽  
Ozan Ugurlu ◽  
Ana L. Lima Sharma ◽  
...  

ABSTRACTIn this work we explore the uniqueness of solution combustion synthesis (SCS) technique to produce luminescent nanostructured materials with metastable phases. We synthesized Gd2O3:Eu with the high-temperature phase and induced phase transformation toward the room temperature phase to investigate the effects of structural transformation on the luminescent properties. SCS is based on exothermic redox reactions that undergo self-sustaining combustion, yielding powders composed of agglomerates of nanocrystals with typical dimensions of tens of nanometers. Synthesis of materials through SCS occurs in conditions far from thermodynamic equilibrium and, due to the high temperatures achieved during combustion, metastable crystallographic phases can be formed. Eu-doped Gd2O3 was obtained with base-centered monoclinic structure and average nanocrystal size of 35 nm as determined by Debye-Scherre analysis. Phase transformation to the cubic structure was induced by isothermal annealing at 1000 oC for up to 152 hrs and followed by x-ray diffraction (XRD). Luminescence excitation and emission spectra were obtained as a function of annealing time. The transformation from monoclinic to cubic structure was followed by the behavior of the (111) monoclinic/(222) cubic intensity ratio. The ratio value for the as-prepared material is 6, decreasing fast to 3 after 5 hrs. annealing, and reaching a value of 0.1 after 152 hrs. Concomitant to the structural transformation, nanocrystal size was followed for both crystalline phases. The average nanocrystal size for the cubic phase increases from 27 to 47 nm from 1 to 152 hrs., respectively. On the other hand, nanocrystals with the monoclinic phase remained with a constant size around 38 nm. Overall, variation in size is small due to the low connectivity among nanocrystals resulting from the low isostatic pressure employed to prepare the pellets, together with the non-uniform shape of the agglomerates. Photoluminescence excitation spectra are dominated by a broad centered near 278 nm and assigned to the O2-Eu3+ charge transfer band. Photoluminescence emission results present the 5D0-7FJ (with J = 0-4) transitions of Eu3+ ions. The behavior of these bands was investigated as a function of annealing time and subsequently related to the structural changes.


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

QJM ◽  
2020 ◽  
Vol 113 (Supplement_1) ◽  
Author(s):  
H Ibrahim

Abstract Nowadays there are more interesting with nanotechnology and its applications in several sectors specially in medicine for diagnoses, therapeutic and research biomedical tools. It can be defined as any process or technique used to produce material in nano-scale structure with particle size ranged from 1-100 nm. The utilization of nanotechnology in human health benefits known as nano medicine. So that nanotechnology has firmly entered the drug delivery realm to maximize drug therapeutic activity and minimize its undesirable side effects. Herein we deal with both nanoparticles and nano-fibers and their applications in medical field. Nano-particles have unique properties from its small size with high surface area therefore it provides larger than particle numbers from that prepared with convention methods. In addition, nanoparticles can be used to improve various drug bio-availability from its biodegradability and bio-compatibility. Nano-fibers have huge surface area to volume ratio which increase its performance in several applications. Nano-fiber produced via electrospinning process (simple and have high production rate). It can be used in many applications such as water filtration, tissue engineering scaffold, wounds, fiber composites, drug release and protective clothes.


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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