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The surface properties of the samples were evaluated using nitrogen sorption, potentiometric titration, thermal analysis, and XPS.
The friction and wear behaviors of the samples were evaluated using a ball-on-disk reciprocating friction and wear tester.
Changes of the chemical composition in the samples were evaluated using UV Vis-NIR and FTIR spectroscopy techniqUV Vis-NIR
The compressive [10] and flexural [11] strengths of the samples were evaluated using a compressive testing machine (Suzpecar, MEM-102/50 t).
Also the quality indexes of the samples were evaluated using the following equation:Qi (quality index)= UTS MPa)+150 log (EL%).
The electrochemical properties of the samples were evaluated using a CHI660D Electrochemical Working Station in a three-electrode system, wherein the samples on NF function as the working electrode (WE), platinum functions as the counter electrode, and saturated calomel electrode (SCE) electrode functions as the reference electrode.
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The intercalation of the samples was evaluated using an X-ray diffraction (Bazgir 2006).
The intercalation of the samples was evaluated using an X-ray Diffraction [3, 7].
The corrosion behavior of the samples was evaluated using immersion test and potentiodynamical polarization test.
The photocatalytic performance of the samples was evaluated using Methylene Blue (MB) as probe pollutant under solar irradiation.
The in vitro antibacterial activity of the samples was evaluated using the Mueller-Hinton Agar disc diffusion method with determination of diameter of inhibition zones in mm.
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