“…At different stages of milling (5,10,15,20,40, 60, 80 and 100 h), small batch of the milled powder was taken out of the vessel for testing. The characteristics of the powders were exam- ined by different methods including: particle morphology by scanning electron microscopy (Philips XL30 SEM and TSCAN VEGA II XMU, Czech Republic); particle size distribution by laser particle size analyzer (Mastersizer 2000, Malvern Instruments); powder density by standard Hall method (ASTM Standard B 417 and MPIF 28); microstructure by optical and electron microscopy (SEM and field-emission TEM, Philips CM200-FEG); chemical analysis by inductive coupled plasma spectroscopy (ICP, Jobin Yvon Emission, JY 138, Edison, New Jersey, USA), atomic absorption spectroscopy (AAS, Varian Techtron AA6, Mulgrave, Victoria, Australia) and energy dispersive X-ray (EDX); crystallite size and lattice strain by X-ray diffraction according to Williamson-Hall method [22][23]; phase transformation by differential thermal analysis (DTA Netzsch STA 409PC/PG, Burlington, MA, USA).…”