scholarly journals Nondestructive Methodology for Identification of Local Discontinuities in Aluminide Layer-Coated Mar 247 during Its Fatigue Performance

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3824
Author(s):  
Dominik Kukla ◽  
Mateusz Kopec ◽  
Kehuan Wang ◽  
Cezary Senderowski ◽  
Zbigniew L. Kowalewski
Keyword(s):  
Eddy Current ◽  
Chemical Vapor ◽  
Nickel Superalloy ◽  
Fatigue Performance ◽  
Protective Atmosphere ◽  
Coarse Grain ◽  
X Ray ◽  
Fine Grain ◽  
Aluminide Layer

In this paper, the fatigue performance of the aluminide layer-coated and as-received MAR 247 nickel superalloy with three different initial microstructures (fine grain, coarse grain and column-structured grain) was monitored using nondestructive, eddy current methods. The aluminide layers of 20 and 40 µm were obtained through the chemical vapor deposition (CVD) process in the hydrogen protective atmosphere for 8 and 12 h at the temperature of 1040 °C and internal pressure of 150 mbar. A microstructure of MAR 247 nickel superalloy and the coating were characterized using light optical microscopy (LOM), scanning electron microscopy (SEM) and X-ray energy dispersive spectroscopy (EDS). It was found that fatigue performance was mainly driven by the initial microstructure of MAR 247 nickel superalloy and the thickness of the aluminide layer. Furthermore, the elaborated methodology allowed in situ eddy current measurements that enabled us to localize the area with potential crack initiation and its propagation during 60,000 loading cycles.

scholarly journals Aluminide Thermal Barrier Coating for High Temperature Performance of MAR 247 Nickel Based Superalloy

Coatings ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 48
Author(s):  
Mateusz Kopec ◽  
Dominik Kukla ◽  
Xin Yuan ◽  
Wojciech Rejmer ◽  
Zbigniew L. Kowalewski ◽  
...  
Keyword(s):  
High Temperature ◽  
Stress Amplitude ◽  
Aluminide Coating ◽  
Chemical Vapor ◽  
Fatigue Tests ◽  
Protective Atmosphere ◽  
X Ray ◽  
Nickel Based Superalloy ◽  
Barrier Coating ◽  
Aluminide Layer

In this paper, mechanical properties of the as-received and aluminide layer coated MAR 247 nickel based superalloy were examined through creep and fatigue tests. The aluminide layer of 20 µm was obtained through the chemical vapor deposition (CVD) process in the hydrogen protective atmosphere for 8 h at the temperature of 1040 °C and internal pressure of 150 mbar. A microstructure of the layer was characterized using the scanning electron microscopy (SEM) and X-ray Energy Dispersive Spectroscopy (EDS). It was found that aluminide coating improve the high temperature fatigue performance of MAR247 nickel based superalloy at 900 °C significantly. The coated MAR 247 nickel based superalloy was characterized by the stress amplitude response ranging from 350 MPa to 520 MPa, which is twice as large as that for the uncoated alloy.

Analysis of Cracking Process in Conditions of High-Temperature Creep of Castings Form the Modified Superalloy IN-713C

2013 ◽  
Vol 212 ◽  
pp. 247-254
Author(s):  
Marek Cieśla ◽  
Franciszek Binczyk ◽  
Marcin Mańka
Keyword(s):  
High Temperature ◽  
Creep Resistance ◽  
Nickel Superalloy ◽  
Morphological Properties ◽  
Coarse Grain ◽  
High Temperature Creep ◽  
Temperature Creep ◽  
Fine Grain ◽  
Initiation And Propagation ◽  
Cracking Process

mpact of complex modification and filtration during pouring into moulds on durability has been evaluated in this study in conditions of high-temperature creep of castings made from nickel superalloy IN-713C post production rejects. The conditions of initiation and propagation of cracks in the specimens were analysed with consideration of morphological properties of material macro-, micro-and substructure. It has been demonstrated that in conditions of high-temperature creep at temperature 980°C with stress σ =150 MPa creep resistance of the IN-713C superalloy increases significantly with the increase of macrograin size. Creep resistance of specimens made of coarse grain material was significantly higher than the resistance of fine grain material.

In situ x-ray scattering study of PbTiO3 chemical-vapor deposition

2002 ◽  
Vol 80 (10) ◽  
pp. 1809-1811 ◽  
Author(s):  
M. V. Ramana Murty ◽  
S. K. Streiffer ◽  
G. B. Stephenson ◽  
J. A. Eastman ◽  
G.-R. Bai ◽  
...  
Keyword(s):  
Chemical Vapor Deposition ◽  
Vapor Deposition ◽  
Chemical Vapor ◽  
X Ray ◽  
X Ray Scattering ◽  
Scattering Study ◽  
Ray Scattering

Synthesis of YBa2Cu3O7−δ with clean grain boundaries by a modified aerosol decomposition process

1992 ◽  
Vol 7 (12) ◽  
pp. 3175-3184 ◽  
Author(s):  
Yuan-Liang Wang ◽  
Z.Q. Tan ◽  
Yimei Zhu ◽  
A.R. Moodenbaugh ◽  
M. Suenaga
Keyword(s):  
Grain Boundaries ◽  
Decomposition Method ◽  
Flow Reactor ◽  
Superconducting Transition ◽  
X Ray ◽  
Grain Sizes ◽  
Fine Grain ◽  
Precursor Powders ◽  
X Ray Absorption

A modified aerosol decomposition method was developed for producing sintered YBa2Cu3O7−δ (1-2-3) pellets having sharp superconducting transition Tc's at ∼90 K, fine grain sizes, and clean grain boundaries. This method used “precursor” powders, which were produced with an aerosol flow reactor at 550 °C, instead of in situ produced 1-2-3 powders commonly processed at 880–1000 °C. As determined by x-ray absorption and powder diffraction studies, the 1-2-3 powders produced by the modified route contain less cation disorders than the in situ produced powders. The disorder is speculated to be the cause of Tc-suppression and broadening. It cannot be removed unless high sintering temperatures were used (>950 °C), which resulted in large grains and impurities and cracks at grain boundaries.

Improved Structural Quality and Carrier Decay Times in GaN Epitaxy on SiN and TiN Porous Network Templates

2006 ◽  
Vol 527-529 ◽  
pp. 1505-1508
Author(s):  
Ümit Özgür ◽  
Y. Fu ◽  
Cole W. Litton ◽  
Y.T. Moon ◽  
F. Yun ◽  
...  
Keyword(s):  
Chemical Vapor ◽  
Structural Quality ◽  
Threading Dislocation ◽  
X Ray Diffraction ◽  
Porous Network ◽  
X Ray ◽  
Radiative Efficiency ◽  
Decay Times ◽  
Threading Dislocation Density

Improved structural quality and radiative efficiency were observed in GaN thin films grown by metalorganic chemical vapor deposition on in situ-formed SiN and TiN porous network templates. The room temperature carrier decay time of 1.86 ns measured for a TiN network sample is slightly longer than that for a 200 μm-thick high quality freestanding GaN (1.73 ns). The linewidth of the asymmetric X-Ray diffraction (XRD) (1012) peak decreases considerably with the use of SiN and TiN layers, indicating the reduction in threading dislocation density. However, no direct correlation is yet found between the decay times and the XRD linewidths, suggesting that point defect and impurity related nonradiative centers are the main parameters affecting the lifetime.

Real-Time X-Ray Scattering Studies of Surface Structure During Metalorganic Chemical Vapor Deposition of GaN

MRS Bulletin ◽  
1999 ◽  
Vol 24 (1) ◽  
pp. 21-25 ◽  
Author(s):  
G. Brian Stephenson ◽  
Jeffrey A. Eastman ◽  
Orlando Auciello ◽  
Anneli Munkholm ◽  
Carol Thompson ◽  
...  
Keyword(s):  
Chemical Vapor Deposition ◽  
Surface Structure ◽  
Real Time ◽  
Vapor Phase ◽  
Vapor Deposition ◽  
Chemical Vapor ◽  
X Rays ◽  
Production Scale ◽  
X Ray

Vapor-phase processes such as chemical vapor deposition (CVD) and reactive ion etching are the primary methods for the production-scale synthesis and processing of many high-quality thin-film materials. For example, these processes are widely used in the microelectronics industry for synthesis and lithography of the various semiconducting, insulating, and conducting layers in devices. Understanding the means of controlling the microstructure and composition of these materials is of great technological interest. However a difficulty often encountered in developing vapor-phase processes is an undesirable dependence on trial-and-error methods for optimizing the many process parameters. These parameters include gas composition, flow rate, pressure, and substrate temperature, all of which are typically changing with time. This reliance on empirical methods can be attributed to the tremendous chemical and physical complexity of vapor-phase processes and the lack of appropriate in situ measurement techniques for the vapor-phase environment.We have initiated a program to apply synchrotron x-ray analysis techniques as real-time probes of film and surface structure during vapor-phase processing. X-rays have a combination of properties which makes them particularly well-suited for these studies. Unlike electrons, x-rays have a sufficiently low absorption to penetrate vapor-phase processing environments and chamber walls. Unlike visible light, x-rays have wavelengths and energies suitable for study of atomic-scale structure and chemistry. A growing number of in situ synchrotron x-ray investigations of film growth and processing demonstrate the power of these techniques.

IN SITU X-RAY SCATTERING STUDIES OF CHEMICAL VAPOR DEPOSITION

1989 ◽  
Vol 50 (C7) ◽  
pp. C7-159-C7-168
Author(s):  
P. H. FUOSS ◽  
D. W. KISKER ◽  
S. BRENNAN ◽  
J. L. KAHN ◽  
G. RENAUD ◽  
...  
Keyword(s):  
Chemical Vapor Deposition ◽  
Vapor Deposition ◽  
Chemical Vapor ◽  
X Ray ◽  
X Ray Scattering ◽  
Ray Scattering

scholarly journals Changing Contents of Carbon Hybridizations in Amorphous Hydrogenated Carbon Layers (a-C:H) on Sustainable Polyhydroxybutyrate (PHB) Exhibit a Significant Deterioration in Stability, Depending on Thickness

2019 ◽  
Vol 5 (3) ◽  
pp. 52 ◽  
Author(s):  
Torben Schlebrowski ◽  
Lucas Beucher ◽  
Hadi Bazzi ◽  
Barbara Hahn ◽  
Stefan Wehner ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Chemical Vapor ◽  
Drift Spectroscopy ◽  
Significant Deterioration ◽  
X Ray ◽  
Diffuse Reflectance Infrared ◽  
X Ray Absorption ◽  
Amorphous Hydrogenated Carbon

PHB is a biodegradable polymer based on renewable raw materials that could replace synthetic polymers in many applications. A big advantage is the resulting reduction of the waste problem, as well as the conservation of fossil resources. To arrange it for various applications, the surface is arranged by plasma-enhanced chemical vapor deposition (PECVD) with amorphous hydrogenated carbon layers (a-C:H). Here, on a 50 µm thick PHB-foil, a-C:H layers of different thicknesses (0–500 nm) were deposited in 50 nm steps. Surface topography was investigated by scanning electron microscopy (SEM), chemical composition by diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy and wettability checked by contact angle. In addition, layers were examined by synchrotron supported X-ray photoelectron spectroscopy (XPS) and near edge X-ray absorption fine structure (NEXAFS), which revealed thickness dependent changes of the sp2/sp3 ratio. With increasing thickness, even the topography changes show internal, stress-induced phenomena. The results obtained provide a more detailed understanding of the predominantly inorganic a-C:H coatings on (bio)polymers via in situ growth.

Chemical Vapor Functionalization of ZnO Nanocrystals

2010 ◽  
Vol 1260 ◽  
Author(s):  
Moazzam Ali ◽  
Marty D. Donakowski ◽  
Markus Winterer
Keyword(s):  
Gas Phase ◽  
Diffuse Reflectance ◽  
Chemical Vapor ◽  
X Ray Diffraction ◽  
X Ray ◽  
Zno Nanocrystals ◽  
In Series ◽  
Lower Temperature ◽  
Diffuse Reflectance Infrared

AbstractChemical Vapor Functionalization (CVF) is a method in which nanocrystals undergo in situ functionalization in the gas phase. In CVF, two reactors are used in series. The first reactor consists of a hot quartz tube (1073 K) where ZnO nanocrystals are synthesized in the gas phase from diethylzinc and oxygen. The second reactor, connected at the exit of the first one and kept at lower temperature (673 K), is used as functionalization chamber. At the connecting point of the two reactors, vapors of organic functionalizing agents are injected which react with the surface of ZnO nanocrystals. ZnO nanocrystals have been functionalized by 1-hexanol, n-hexanoic acid, n-hexanal and 1-hexylamine. Functionalized ZnO nanocrystals have been characterized by Dynamic Light Scattering, X-ray Diffraction and Diffuse Reflectance Infrared Fourier Transform Spectroscopy.

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