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The specimens were analyzed using micro-CT.
The specimens were analyzed using SEM, EBSD and EDX techniques.
Adhesion failure and strength behavior of the specimens were analyzed using the Response Surface Method.
The specimens were analyzed using Orientation Distribution Function (ODF), optical microscopy and OIM (Orientation Imaging Microscopy).
The specimens were analyzed using X-ray diffraction (XRD), thermogravimetric and differential thermal analyses (TG/DTAs), and nuclear magnetic resonance (NMR).
The specimens were analyzed using methods described previously[ 14].
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Chemical composition of the specimens was analyzed using an EDS as attached on the SEM.
Surface topography of the specimens was analyzed using field emission scanning electron microscope (FE-SEM).
The microstructure of the specimens was analyzed using scanning (SEM) and transmission electron microscopy (TEM) techniques.
The microstructure of the specimens was analyzed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM).
Surface roughness R a of the specimens was analyzed using atomic force microscopy (AFM) with scanning area of 50 μm × 50 μm.
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