X-Ray Microtomography for 3D Microstructure Characterization of Magnesium Matrix Composite Reinforced with Glassy Carbon Particles

2011 ◽  
Vol 176 ◽  
pp. 119-126 ◽  
Author(s):  
Agnieszka Botor-Probierz ◽  
Anita Olszówka-Myalska ◽  
Sam A. McDonald ◽  
Philip J. Withers
Keyword(s):  
Matrix Composite ◽  
Glassy Carbon ◽  
Volume Fraction ◽  
Sol Gel ◽  
Magnesium Matrix Composite ◽  
Magnesium Matrix ◽  
X Ray ◽  
Carbon Particles ◽  
Az91 Magnesium

The microstructure of novel AZ91 magnesium matrix composite reinforced with glassy carbon particles has been characterized in this study. The composite was produced by hot pressing a mixture of glassy carbon particles and metal powder. Beforehand, the particles were coated with SiO2 by a sol-gel method. Metris X-tek and Xradia MicroXCT laboratory X-ray tomography systems were used to obtain 3D microstructural information (particle-size distribution, volume fraction of particles, phase formation and defects in the form of clusters of particles and pores). These 3D features were validated by 2D scanning electron microscopy (SEM) methods.

Corrosion behavior of in situ (TiC-TiB2)p/AZ91 magnesium matrix composites in Harrison solution

2014 ◽  
Vol 61 (5) ◽  
pp. 319-327 ◽  
Author(s):  
Mohamed Gobara ◽  
Mohamed Shamekh
Keyword(s):  
Mechanical Properties ◽  
Corrosion Behavior ◽  
Matrix Composite ◽  
Electrochemical Impedance ◽  
Magnesium Matrix Composite ◽  
Magnesium Matrix ◽  
Content Type ◽  
X Ray ◽  
Az91 Magnesium

Purpose – This paper aims to study both the mechanical properties and the corrosion behavior of the synthesized in situ (TiC-TiB2) particulates/AZ91 magnesium matrix composite and compare the results with that of the conventional AZ91D alloy. Design/methodology/approach – Scanning electron microscope (SEM) equipped with energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD) were used to study the surface morphology and crystalline structure. Mechanical compression tests were used to investigate the mechanical performance according to ASTM E9-89a. The corrosion behavior of the synthesized magnesium alloy was examined using both electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques in dilute Harrison solutions. Findings – The microstructure of the Mg composite showed a uniform distribution of reinforcing phases. Also, the reinforcing phases were formed without residual intermediate phases. The addition of titanium and boron carbides not only enhanced the mechanical properties of the matrix but also improve its corrosion behavior. Originality/value – This is the first time that magnesium matrix composite has been to synthesized with TiC and TiB2 particulates starting from starting from Ti and B carbides powder without adding aluminium using practical and low-cost technique (in situ reactive infiltration technique). This paper studies the corrosion behavior of synthesized Mg matrix in dilute Harrison solution and compares the results with that of conventional AZ91D.

Sol-gel derived Ba(Mg1/3Ta2/3)O3 thin films: Preparation and structure

1997 ◽  
Vol 12 (3) ◽  
pp. 596-599 ◽  
Author(s):  
Ji Zhou ◽  
Qing-Xin Su ◽  
K. M. Moulding ◽  
D. J. Barber
Keyword(s):  
Thin Films ◽  
Annealing Temperature ◽  
Volume Fraction ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Small Grains

Ba(Mg1/3Ta2/3)O3 thin films were prepared by a sol-gel process involving the reaction of barium isopropoxide, tantalum ethoxide, and magnesium acetate in 2-methoxyethanol and subsequently hydrolysis, spin-coating, and heat treatment. Transmission electron microscopy, x-ray diffraction, and Raman spectroscopy were used for the characterization of the thin films. It was shown that the thin films tend to crystallize with small grains sized below 100 nm. Crystalline phase with cubic (disordered) perovskite structure was formed in the samples annealed at a very low temperature (below 500 °C), and well-crystallized thin films were obtained at 700 °C. Although disordered perovskite is dominant in the thin films annealed below 1000 °C, a low volume fraction of 1 : 2 ordering domains was found in the samples and grows with an increase of annealing temperature.

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