Oxidation Behavior of NiAl Produced by Gel Combustion Synthesis

2016 ◽  
Vol 701 ◽  
pp. 122-126
Author(s):  
Tammy Anne Gonsalvez ◽  
Abreeza Manap ◽  
Nurfanizan Afandi ◽  
Halina Misran
Keyword(s):  
Combustion Synthesis ◽  
Oxidation Behavior ◽  
Mixed Oxides ◽  
Synthesis Method ◽  
Mass Gain ◽  
Isothermal Oxidation ◽  
X Ray Diffraction ◽  
Gel Combustion ◽  
Before And After ◽  
Different Temperatures

This paper presents the results of a study of the oxidation behavior of NiAl produced by gel combustion synthesis calcined at two different temperatures. The objective is to compare the oxide growth rates, oxide scale composition, morphology and elemental composition of the sample powder subjected to isothermal oxidation and calcined at 1050 °C and 1300 °C for 1, 2, 4 and 10 hours by means of mass gain measurements, X-ray diffraction (XRD), field emission scanning electron microsocopy (FESEM) and energy-dispersive spectrometry (EDX) in order to investigate the reliability of the gel combustion synthesis method and evaluate the effect of calcination temperature on the oxidation behaviour of the powder. It was found that for the sample calcined at 1300°C the sample was made up mainly of metastable and stable alumina before oxidation and stable alpha alumina after oxidation whereas for the powder calcined at 1050°C the sample was mainly composed of detrimental mixed oxides before and after oxidation. Overall findings indicate that the oxidation behavior of the powder calcined at 1300°C is more protective compared to the powder calcined at 1050°C.

Investigating the High Temperature Oxidation Behavior of TiAl-Based Alloys with Nickel and Ruthenium Additions

2014 ◽  
Vol 1019 ◽  
pp. 294-301
Author(s):  
H.C. Mantyi ◽  
L.A. Cornish ◽  
Lesley H. Chown ◽  
I. Alain Mwamba
Keyword(s):  
Room Temperature ◽  
Oxidation Behavior ◽  
Mass Gain ◽  
Isothermal Oxidation ◽  
X Ray Diffraction ◽  
Mechanically Alloyed ◽  
Temperature Oxidation ◽  
X Ray ◽  
High Temperature Oxidation Behavior ◽  
Titanium Aluminium

Pure powders of titanium, aluminium, nickel and ruthenium were mechanically alloyed and melted in a button arc furnace under an argon atmosphere to produce two alloys of composition Ti-52.5Al-10.0Ni (at.%) and Ti-52.5Al-10.0Ni-0.2Ru (at.%). The alloys were then cut and metallographically prepared. Scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD) were used to characterize the samples. Thermogravimetric analysis (TGA) was used to analyze the oxidation behavior from room temperature up to 1050°C. The alloys were also oxidized in air at 1050°C for 120 hours. The Ti-52.5Al-10.0Ni (at.%) alloy formed dendrites of γ-TiAl (55.6 at.% Al) surrounded by a eutectic of γ-TiAl + Al3NiTi2 (τ3) phases. The Ti-52.5Al-10.0Ni-0.2Ru (at.%) alloy formed dendrites of γ-TiAl (53.6 at.% Al) surrounded by a eutectic of γ-TiAl + Al3NiTi2 (τ3). The ruthenium was mostly in solid solution (0.3 at.%) in the Al3NiTi2 (τ3) phase, although traces of it were present in the dendrites (0.1 at.% Ru). When oxidized in air from room temperature to 1050°C, the as-cast Ti-52.5Al-10.0Ni-0.2Ru (at.%) had a mass gain of 0.60% and the as-cast Ti-52.5Al-10.0Ni (at.%) had a mass gain of 0.97%. Isothermal oxidation of both alloys at 1050°C for 120 hours formed mixed metal oxides of TiO2+Al2O3 on the surface.

scholarly journals Isothermal Oxidation Behavior of Novel Al2O3 / NiCrAlY / Ti3Al System at 850�C

2020 ◽  
Vol 71 (5) ◽  
pp. 106-116
Author(s):  
Alexandra Banu ◽  
Alexandru Paraschiv ◽  
Simona Petrescu ◽  
Irina Atkinson ◽  
Elena Maria Anghel ◽  
...  
Keyword(s):  
Oxidation Resistance ◽  
Oxidation Behavior ◽  
Mass Gain ◽  
Isothermal Oxidation ◽  
Thermal Barrier ◽  
The Novel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Aerospace Applications

The novel Al2O3 / NiCrAlY /alfa2-Ti3Al system obtained by APS technique was tested against long (500h) isothermal oxidation at 850�C in air for prospective use in aerospace applications. EDX-SEM, X-ray diffraction (XRD) and Raman investigations were conducted to substantiate structural, textural and mass gain modifications underwent by the Al2O3 / NiCrAlY /alfa2-Ti3Al system in comparison with bare alfa2-Ti3Al and NiCrAlY /alfa2-Ti3Al system. Improved oxidation resistance of the double-coated system is based on moderate oxygen and thermal barrier role played by the mixture of delta - and alfa-Al2O3 present in the top ceramic coat.

Flameless Solution Combustion Synthesis of Al3+ Doped LiMn2O4

2011 ◽  
Vol 186 ◽  
pp. 7-10 ◽  
Author(s):  
Gui Yang Liu ◽  
Jun Ming Guo ◽  
Bao Sen Wang ◽  
Ying He
Keyword(s):  
Combustion Synthesis ◽  
Synthesis Method ◽  
Solution Combustion Synthesis ◽  
Xrd Analysis ◽  
Cycling Performance ◽  
X Ray Diffraction ◽  
Solution Combustion ◽  
Electrochemical Test ◽  
Micro Morphology ◽  
Better Than

Single phase Al3+ doped LiMn2O4 has been prepared by flameless solution combustion synthesis method at 600oC for 1h. X-ray diffraction (XRD) and scanning electric microscope (SEM) were used to determine the phase composition and micro morphology of the products. XRD analysis indicates that the purities increase and the lattice parameters of the products decrease with increasing Al3+ content. Electrochemical test indicates that the cycling performance of the products with Al3+ doping are better than that of the product without Al3+ doping. The product LiAl0.10Mn1.90O4 gets the best electrochemical performance. At the current density of 30mA/g, the initial discharge capacity of LiAl0.10Mn1.90O4 is 124.8mAh/g, and after 20 cycles, the capacity retention is more than 89%. SEM investigation indicates that the particles of LiAl0.10Mn1.90O4 are sub-micron in size and well dispersed.

Optimized Preparation of Fe2O3/Al2O3 Composite with Sol-Gel Combustion Synthesis Method Based on Orthogonal Experimental Design

2011 ◽  
Vol 341-342 ◽  
pp. 215-220
Author(s):  
Bao Wen Wang ◽  
Chuan Chang Gao ◽  
Hai Bo Zhao ◽  
Chu Guang Zheng
Keyword(s):  
Experimental Design ◽  
Combustion Synthesis ◽  
Ignition Temperature ◽  
Sintering Temperature ◽  
Sol Gel ◽  
Synthesis Method ◽  
Influential Factor ◽  
Molar Ratio ◽  
Orthogonal Experimental Design ◽  
Gel Combustion

Fe2O3/Al2O3 composite at the mass ratio of 3:2 was prepared by sol-gel combustion synthesis using urea as fuel. The optimized preparation parameters were determined by the robust orthogonal experimental design (OED) method. Standard L9(34) orthogonal array was adopted, and the four factors were determined as the molar ratio of oxidizer nitrates to fuel urea Ф, relative amount of the deionized water added Rw, ignition temperature and sintering temperature. Range analysis of the relative importance of those four factors on the mean weight loss rate for the reduction of synthesized Fe2O3/Al2O3 with 50 vol% H2 indicated that the most influential factor was Ф, sintering temperature, Rw and ignition temperature in the descending order. And the optimized preparation parameters for Fe2O3/Al2O3 composite were Ф=1, Rw=7.5, ignition and sintering temperatures stabilized as 600°C and 950°C,respectively. Finally, the reaction characteristics of Fe2O3/Al2O3 prepared by SGCS and the other two reference methods (including sol-gel method and mechanical mixing method) were compared and the results verified that the optimized SGCS was the best option to synthesize Fe2O3/Al2O3 composite with good reaction performance.

Temperature Dependence of LiMn2O4 Prepared by a Solution Combustion Synthesis in the System of Acetate Salts and Acetic Acid

2012 ◽  
Vol 485 ◽  
pp. 465-468
Author(s):  
Li Li Zhang ◽  
Gui Yang Liu ◽  
Jun Ming Guo ◽  
Bao Sen Wang ◽  
Ying He
Keyword(s):  
Acetic Acid ◽  
Combustion Synthesis ◽  
Raw Materials ◽  
Synthesis Method ◽  
Solution Combustion Synthesis ◽  
Electrochemical Performances ◽  
Metal Foil ◽  
X Ray Diffraction ◽  
Solution Combustion ◽  
Acid Ratio

Spinel LiMn2O4 have been prepared by the solution combustion synthesis method using acetate salts as raw materials and acetic acid as fuel. The phase compositions of the as-prepared products were determined by X-ray diffraction (XRD). The electrochemical performance of the products was tested by using a coin-type half battery versus lithium metal foil as anode material. XRD results suggested that the purities of the products prepared at 500oC are higher than these of the products prepared at 600oC. For the products prepared at 500oC, the purities of the products increase with increasing acetic acid ratios. But for the products prepared at 600oC, the purities of the products decrease with increasing acetic acid ratios. The performance tests indicated that the electrochemical performances of the products prepared at 500oC are better than these of the products prepared at 600oC. The product prepared at 500oC with the acetic acid ratio of 1.0 gets the best performance. The initial capacity of it reaches to 124.8mAh/g at the current density of 75mA/g, and after 50 cycles, the capacity retention is 93.7%.

Synthesis and Characterization of Porous Mo-W Oxide Nanostructures

2008 ◽  
Vol 8 (12) ◽  
pp. 6445-6450
Author(s):  
F. Paraguay-Delgado ◽  
Y. Verde ◽  
E. Cizniega ◽  
J. A. Lumbreras ◽  
G. Alonso-Nuñez
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Synthesis Method ◽  
Atomic Ratio ◽  
High Specific Surface Area ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Before And After

The present study reports the synthesis method, microstructure characterization, and thermal stability of nanostructured porous mixed oxide (MoO3-WO3) at 550 and 900 °C of annealing. The material was synthesized using a hydrothermal method. The precursor was prepared by aqueous solution using ammonium heptamolibdate and ammonium metatungstate, with an atomic ratio of Mo/W = 1. The pH was adjusted to 5, and then the solution was transferred to a teflon-lined stainless steel autoclave and heated at 200 °C for 48 h. The resultant material was washed using deionized water. The specific surface area, morphology, composition, and microstructure before and after annealing were studied by N2 physisorption, scanning electron microscopy (SEM), analytical transmission electron microscopy (TEM), and X-Ray diffraction (XRD). The initial synthesized materials showed low crystallinity and high specific surface area around (141 m2/g). After thermal annealing the material showed higher crystallinity and diminished its specific surface area drastically.

LiAl0.1Mn1.9O4 Prepared by a Solution Combustion Synthesis Using Acetate as Raw Materials and Acetic Acid as Fuel: Effect of Further Calcination Time

2012 ◽  
Vol 485 ◽  
pp. 473-477
Author(s):  
Gui Yang Liu ◽  
Jun Ming Guo ◽  
Li Li Zhang ◽  
Jing Wang ◽  
Bao Sen Wang ◽  
...  
Keyword(s):  
Combustion Synthesis ◽  
Raw Materials ◽  
Synthesis Method ◽  
Solution Combustion Synthesis ◽  
Metal Foil ◽  
X Ray Diffraction ◽  
Calcination Time ◽  
Solution Combustion ◽  
X Ray ◽  
Discharge Capacities

LiAl0.1Mn1.9O4 materials were prepared by a solution combustion synthesis method. In order to improve the purity of the products, the effect of further calcination time was investigated. The phase compositions of the as-prepared products were determined by X-ray diffraction (XRD). The electrochemical performance of the products was tested by using a coin-type half battery versus lithium metal foil as anode material. XRD results suggested that the main phase of the products was LiAl0.1Mn1.9O4, and there was a trace amount Mn2O3 impurity in some of the products. The purity, crystallinity and grain size of the LiAl0.1Mn1.9O4 were increased with increasing further calcination time. Electrochemical experiments demonstrate that the initial discharge capacities of the products with further calcination time of 0, 6, 12 and 24h were 93.7, 105.7, 114.0 and 120.6mAh/g, and about 89.8, 89.5, 89.2 and 88.3% of the initial capacities were retained after 25 cycles, respectively. Further calcination time can enhance the initial capacity, but is not favorable for the cycle ability of the products.

Effect of Post-Deposition Annealing on some Optical Properties of Thermally-Evaporated V2O5 Thin Film

2012 ◽  
Vol 329 ◽  
pp. 139-145
Author(s):  
S.A. Aly
Keyword(s):  
Optical Properties ◽  
Amorphous State ◽  
X Ray Diffraction ◽  
Post Deposition Annealing ◽  
X Ray ◽  
Spectral Behaviour ◽  
Before And After ◽  
Different Temperatures ◽  
Reflectance Measurements ◽  
Post Deposition

A Vanadium Pentoxide Sample with a Film Thickness of 75 Nm Has Been Thermally Evaporated on Unheated Glass Substrate Using V2O5High Purity Powder. the Sample Was Subjected to a Subsequent Post-Deposition Annealing in Air at Different Temperatures for a Period of One Hour. the Optical Properties Were Studied by Transmittance and Reflectance Measurements. the Integrated Visible ,TVis, and Solar, TSol, Transmittance Were Calculated. the Spectral Behaviour of the Refractive Index as Well as the Absorption Coefficient before and after Post-Deposition Heat-Treatment Was Also Reported. X-Ray Diffraction Confirmed that the Film in the as-Deposited as Well as after Annealing up to 400 °C Is in the Amorphous State.

Ni Doped LiMn2O4 Prepared by a Flameless Combustion Synthesis

2012 ◽  
Vol 625 ◽  
pp. 251-254 ◽  
Author(s):  
Gui Yang Liu ◽  
Bao Sen Wang ◽  
Ying He ◽  
Jun Ming Guo
Keyword(s):  
Combustion Synthesis ◽  
Raw Materials ◽  
Synthesis Method ◽  
Solution Combustion Synthesis ◽  
Electrochemical Performances ◽  
X Ray Diffraction ◽  
Galvanostatic Charge ◽  
Solution Combustion ◽  
Limn2o4 Spinel ◽  
X Ray

In this paper, LiNixMn2−xO4 materials were prepared by solution combustion synthesis method using acetic salts as raw materials and acetic acid as fuel. The phase structures are characterized by X-ray diffraction (XRD). Electrochemical performances of the materials are investigated by galvanostatic charge/discharge methods. XRD results revealed that the main phase of the products with increasing Ni3+ content is LiMn2O4, and there is a trace amount of Mn3O4 found in the product with Ni3+ content of 0.05. Electrochemical experiments showed that the capacity and the cyclability of the LiNixMn2−xO4 materials decrease with increasing Ni3+ content. Ni3+ doping has no significantly improvement for the capacity and the cyclability of the LiMn2O4 spinel.

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