Oxidation Behaviour of Intermetallic Compounds Based on Ti-Al System

1994 ◽  
Vol 364 ◽  
Author(s):  
A. Tomasi ◽  
S. Gialanella ◽  
P. G. Orsini ◽  
M. Nazmy
Keyword(s):  
Oxidation Kinetics ◽  
Fixed Time ◽  
Isothermal Oxidation ◽  
Operating Conditions ◽  
Weight Changes ◽  
X Ray Diffraction ◽  
Time Intervals ◽  
Surface Stability ◽  
X Ray ◽  
The Stability

AbstractIn this study we present some results regarding phase and surface stability, with particular reference to the oxidation, of Ti alloys based on the γ-TiAl phase.We investigated the stability of the metallic phases with TG and DSC methods, according to the temperature range over which the relevant transformations do occur. These tests were particularly useful to select times and temperatures for precipitation hardening treatments and also to evaluate the oxidation resistance.The isothermal oxidation kinetics were followed with a thermobalance (TG) for time up to 25 hours and, for longer treatments, we put the samples in a furnace and measured their weight changes at fixed time intervals. The microstructure of the oxide scale was investigated with scanning electron microscopy and energy dispersion X-ray analysis and mapping. The identification of the crystalline phases was carried out with X-ray diffraction analysis.The obtained results afford clear information on the predominant phenomena assisting the observed oxidation kinetics and give indications on the operating conditions suitable for these materials.

Isothermal oxidation of bulk Zr2Al3C4 at 500 to 1000 °C in air

2008 ◽  
Vol 23 (2) ◽  
pp. 359-366 ◽  
Author(s):  
L.F. He ◽  
Z.J. Lin ◽  
Y.W. Bao ◽  
M.S. Li ◽  
J.Y. Wang ◽  
...  
Keyword(s):  
Activation Energy ◽  
Raman Spectra ◽  
Oxidation Kinetics ◽  
Oxidation Behavior ◽  
Oxygen Affinity ◽  
Isothermal Oxidation ◽  
Oxide Scales ◽  
X Ray Diffraction ◽  
X Ray ◽  
Parabolic Law

The isothermal oxidation behavior of Zr2Al3C4 in the temperature range of 500 to 1000 °C for 20 h in air has been investigated. The oxidation kinetics follow a parabolic law at 600 to 800 °C and a linear law at higher temperatures. The activation energy is determined to be 167.4 and 201.2 kJ/mol at parabolic and linear stages, respectively. The oxide scales have a monolayer structure, which is a mixture of ZrO2 and Al2O3. As indicated by x-ray diffraction and Raman spectra, the scales formed at 500 to 700 °C are amorphous, and at higher temperatures are α-Al2O3 and t-ZrO2 nanocrystallites. The nonselective oxidation of Zr2Al3C4 can be attributed to the strong coupling between Al3C2 units and ZrC blocks in its structure, and the close oxygen affinity of Zr and Al.

Degradation of glass polymers due to successive exposure to acid rain and UV radiation

2015 ◽  
Vol 11 (2) ◽  
pp. 2979-2989
Author(s):  
Abbas H ◽  
M. M. El-Tonsy ◽  
Aqeel. Abdul jalil. Ali. Shumis
Keyword(s):  
Uv Radiation ◽  
Chain Scission ◽  
Glassy Polymers ◽  
Optical Parameters ◽  
X Ray Diffraction ◽  
Time Intervals ◽  
X Ray ◽  
Before And After ◽  
The Stability ◽  
Environmental Element

Utilization of polymer products for outdoor applications is continuously increasing. So the stability of polymers against environmental degradation became top of interests for many researchers. The effect of environmental elements on the polymers stability has been studied, but individually. A solution against an environmental element may conflict with a solution against other element. Therefore current study aimed to clarify a sort of these conflicts. Polymethylmethacrylate (PMMA) films as example of glassy polymers are exposed to acid rains and Ultraviolet (UV) radiation in sequenced method for different time intervals. The effects on both structural and optical parameters are deduced from the measurements of Infrared spectra, X-ray diffraction charts, refractive indices and optical dispersion of samples before and after treatments. Chain scission is found to reduce the transparency of the samples. Acid rains are found to enhance the transparency of PMMA films by disordering chain fragments that are released by chain scission. Lot of experimental data are given in many coloured graphs.

Isothermal Oxidation Behavior of FGH720Li Superalloy at Service Temperatures

2021 ◽  
Vol 1035 ◽  
pp. 96-101
Author(s):  
Yue Tang ◽  
Zi Chao Peng ◽  
Xu Qing Wang ◽  
Guo Jun Ma ◽  
Dan Wu
Keyword(s):  
Oxidation Kinetics ◽  
Oxidation Behavior ◽  
Isothermal Oxidation ◽  
Elemental Distribution ◽  
X Ray Diffraction ◽  
Cross Sectional ◽  
X Ray ◽  
Parabolic Law ◽  
Medium Layer ◽  
Oxidation Layers

The oxidation behavior of FGH720Li(P/M Udimet720Li) superalloy was investigated under static atmosphere in temperature ranging from 600°C to 730°C. The oxidation kinetics, composition and morphology of the oxidation layers were characterized by means of isothermal oxidation tests, X-ray diffraction(XRD), scanning electron microscopy（SEM）and energy dispersive X-ray spectroscopy(EDS). The results showed that the oxidation kinetics curves of FGH720Li superalloy followed the parabolic law. The results of cross-sectional morphology and elemental distribution indicated that the oxidation layer could be divided into three parts：porous Cr2O3 outer layer, dense Cr2O3 medium layer and oxidation affected zone with nail-like Al2O3 inner layer. The oxidation process was primarily controlled by the diffusion of chromium and oxygen through the oxide scale.

Fractionation of polymethylene chains: An electron crystallographic investigation

1986 ◽  
Vol 44 ◽  
pp. 794-795
Author(s):  
Douglas L. Dorset
Keyword(s):  
Cross Section ◽  
Binary Systems ◽  
Linear Chain ◽  
Pure Component ◽  
Organic Substrates ◽  
Crystallographic Investigation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molecular Sizes ◽  
The Stability

A variety of linear chain materials exist as polydisperse systems which are difficultly purified. The stability of continuous binary solid solutions assume that the Gibbs free energy of the solution is lower than that of either crystal component, a condition which includes such factors as relative molecular sizes and shapes and perhaps the symmetry of the pure component crystal structures.Although extensive studies of n-alkane miscibility have been carried out via powder X-ray diffraction of bulk samples we have begun to examine binary systems as single crystals, taking advantage of the well-known enhanced scattering cross section of matter for electrons and also the favorable projection of a paraffin crystal structure posited by epitaxial crystallization of such samples on organic substrates such as benzoic acid.

scholarly journals A Superhydrophobic, Antibacterial, and Durable Surface of Poplar Wood

Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1885
Author(s):  
Xinyu Wu ◽  
Feng Yang ◽  
Jian Gan ◽  
Zhangqian Kong ◽  
Yan Wu
Keyword(s):  
Stearic Acid ◽  
Antibacterial Properties ◽  
Alkali Resistance ◽  
Poplar Wood ◽  
X Ray Diffraction ◽  
X Ray ◽  
Different Temperatures ◽  
Acid And Alkali Resistance ◽  
The Stability

The silver particles were grown in situ on the surface of wood by the silver mirror method and modified with stearic acid to acquire a surface with superhydrophobic and antibacterial properties. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and X-ray energy spectroscopy (XPS) were used to analyze the reaction mechanism of the modification process. Scanning electron microscopy (SEM) and contact angle tests were used to characterize the wettability and surface morphology. A coating with a micro rough structure was successfully constructed by the modification of stearic acid, which imparted superhydrophobicity and antibacterial activity to poplar wood. The stability tests were performed to discuss the stability of its hydrophobic performance. The results showed that it has good mechanical properties, acid and alkali resistance, and UV stability. The durability tests demonstrated that the coating has the function of water resistance and fouling resistance and can maintain the stability of its hydrophobic properties under different temperatures of heat treatment.

scholarly journals Synthesis of Bis(Carboranyl)amides 1,1′-μ-(CH2NH(O)C(CH2)n-1,2-C2B10H11)2 (n = 0, 1) and Attempt of Synthesis of Gadolinium Bis(Dicarbollide)

Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1321
Author(s):  
Yasunobu Asawa ◽  
Aleksandra V. Arsent’eva ◽  
Sergey A. Anufriev ◽  
Alexei A. Anisimov ◽  
Kyrill Yu. Suponitsky ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Single Crystal ◽  
Quantum Chemical Calculations ◽  
Quantum Chemical ◽  
X Ray Diffraction ◽  
Stable Conformation ◽  
Acyl Chlorides ◽  
X Ray ◽  
Cesium Fluoride ◽  
The Stability

Bis(carboranyl)amides 1,1′-μ-(CH2NH(O)C(CH2)n-1,2-C2B10H11)2 (n = 0, 1) were prepared by the reactions of the corresponding carboranyl acyl chlorides with ethylenediamine. Crystal molecular structure of 1,1′-μ-(CH2NH(O)C-1,2-C2B10H11)2 was determined by single crystal X-ray diffraction. Treatment of bis(carboranyl)amides 1,1′-μ-(CH2NH(O)C(CH2)n-1,2-C2B10H11)2 with ammonium or cesium fluoride results in partial deboronation of the ortho-carborane cages to the nido-carborane ones with formation of [7,7′(8′)-μ-(CH2NH(O)C(CH2)n-7,8-C2B9H11)2]2−. The attempted reaction of [7,7′(8′)-μ-(CH2NH(O)CCH2-7,8-C2B9H11)2]2− with GdCl3 in 1,2-dimethoxy- ethane did not give the expected metallacarborane. The stability of different conformations of Gd-containing metallacarboranes has been estimated by quantum-chemical calculations using [3,3-μ-DME-3,3′-Gd(1,2-C2B9H11)2]− as a model. It was found that in the most stable conformation the CH groups of the dicarbollide ligands are in anti,anti-orientation with respect to the DME ligand, while any rotation of the dicarbollide ligand reduces the stability of the system. This makes it possible to rationalize the design of carborane ligands for the synthesis of gadolinium metallacarboranes on their base.

scholarly journals Multi-Scale Studies of 3D Printed Mn–Na–W/SiO2 Catalyst for Oxidative Coupling of Methane

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 290
Author(s):  
Tim Karsten ◽  
Vesna Middelkoop ◽  
Dorota Matras ◽  
Antonis Vamvakeros ◽  
Stephen Poulston ◽  
...  
Keyword(s):  
Oxidative Coupling ◽  
Oxidative Coupling Of Methane ◽  
Operating Conditions ◽  
Homogeneous Distribution ◽  
Silica Support ◽  
X Ray Diffraction ◽  
Cross Sectional ◽  
X Ray ◽  
Multi Scale ◽  
3D Printed

This work presents multi-scale approaches to investigate 3D printed structured Mn–Na–W/SiO2 catalysts used for the oxidative coupling of methane (OCM) reaction. The performance of the 3D printed catalysts has been compared to their conventional analogues, packed beds of pellets and powder. The physicochemical properties of the 3D printed catalysts were investigated using scanning electron microscopy, nitrogen adsorption and X-ray diffraction (XRD). Performance and durability tests of the 3D printed catalysts were conducted in the laboratory and in a miniplant under real reaction conditions. In addition, synchrotron-based X-ray diffraction computed tomography technique (XRD-CT) was employed to obtain cross sectional maps at three different positions selected within the 3D printed catalyst body during the OCM reaction. The maps revealed the evolution of catalyst active phases and silica support on spatial and temporal scales within the interiors of the 3D printed catalyst under operating conditions. These results were accompanied with SEM-EDS analysis that indicated a homogeneous distribution of the active catalyst particles across the silica support.

scholarly journals Facile Organometallic Synthesis of Fe-Based Nanomaterials by Hot Injection Reaction

Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1141
Author(s):  
Georgia Basina ◽  
Hafsa Khurshid ◽  
Nikolaos Tzitzios ◽  
George Hadjipanayis ◽  
Vasileios Tzitzios
Keyword(s):  
Room Temperature ◽  
Colloidal Particles ◽  
Iron Pentacarbonyl ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
Organometallic Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Hot Injection ◽  
The Stability

Fe-based colloids with a core/shell structure consisting of metallic iron and iron oxide were synthesized by a facile hot injection reaction of iron pentacarbonyl in a multi-surfactant mixture. The size of the colloidal particles was affected by the reaction temperature and the results demonstrated that their stability against complete oxidation related to their size. The crystal structure and the morphology were identified by powder X-ray diffraction and transmission electron microscopy, while the magnetic properties were studied at room temperature with a vibrating sample magnetometer. The injection temperature plays a very crucial role and higher temperatures enhance the stability and the resistance against oxidation. For the case of injection at 315 °C, the nanoparticles had around a 10 nm mean diameter and revealed 132 emu/g. Remarkably, a stable dispersion was created due to the colloids’ surface functionalization in a nonpolar solvent.

scholarly journals Study of Corrosion Resistance and Degradation Mechanisms in LiTiO2-Li2TiO3 Ceramic

Crystals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 753
Author(s):  
Dmitriy Shlimas ◽  
Artem L. Kozlovskiy ◽  
Maxim Zdorovets
Keyword(s):  
Degradation Mechanism ◽  
Diffraction Method ◽  
Large Mass ◽  
Time Frame ◽  
X Ray Diffraction ◽  
Acidic Media ◽  
X Ray ◽  
Mass Losses ◽  
The Stability ◽  
Thermal Sintering

The interest in lithium-containing ceramics is due to their huge potential as blanket materials for thermonuclear reactors for the accumulation of tritium. However, an important factor in their use is the preservation of the stability of their strength and structural properties when under the influence of external factors that determine the time frame of their operation. This paper presents the results of a study that investigated the influence of the LiTiO2 phase on the increasing resistance to degradation and corrosion of Li2TiO3 ceramic when exposed to aggressive acidic media. Using the X-ray diffraction method, it was found that an increase in the concentration of LiClO4·3H2O during synthesis leads to the formation of a cubic LiTiO2 phase in the structure as a result of thermal sintering of the samples. During corrosion tests, it was found that the presence of the LiTiO2 phase leads to a decrease in the degradation rate in acidic media by 20–70%, depending on the concentration of the phase. At the same time, and in contrast to the samples of Li2TiO3 ceramics, for which the mechanisms of degradation during a long stay in aggressive media are accompanied by large mass losses, for the samples containing the LiTiO2 phase, the main degradation mechanism is pitting corrosion with the formation of pitting inclusions.

Polydomain Structure of Epitaxial PbTiO3 films on MgO

1997 ◽  
Vol 493 ◽  
Author(s):  
S. P. Alpay ◽  
A. S. Prakash ◽  
S. Aggarwal ◽  
R. Ramesh ◽  
A. L. Roytburd ◽  
...  
Keyword(s):  
Domain Structure ◽  
Pulsed Laser ◽  
Laser Deposition ◽  
X Ray Diffraction ◽  
X Ray ◽  
Theoretical Predictions ◽  
The Stability ◽  
Increasing Temperature ◽  
Stable Domains ◽  
Domain Stability

ABSTRACTA PbTiO3(001) film grown on MgO(001) by pulsed laser deposition is examined as an example to demonstrate the applications of the domain stability map for epitaxial perovskite films which shows regions of stable domains and fractions of domains in a polydomain structure. X-ray diffraction studies indicate that the film has a …c/a/c/a… domain structure in a temperature range of °C to 400°C with the fraction of c-domains decreasing with increasing temperature. These experimental results are in excellent agreement with theoretical predictions based on the stability map.

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