Page 138 - Zmist-n4-2015
P. 138

Materials  are  characterized  by a grain size or particulate size of up to about 100 nm.
                  These materials exhibit enhanced mechanical, magnetic, elevated temperature, optical,
                  and excellent catalytic properties [7]. It was reported that the high-energy ball milling
                  has been used to improve particle distribution throughout the matrix [8]. The micro-
                  structure  analysis  of  Al–Al 2O 3  composite  produced  by  mechanical  alloying  method
                  was studied in [9]. In [10] the authors synthesized high volume fraction Al–Al 2O 3 nano
                  composite powders by high-energy milling and studied the characteristics of the milled
                  powders. X-ray diffraction is a convenient method for determining the mean size of
                  crystallites in crystalline bulk materials. The first scientist, Paul Scherrer, published his
                  results in a paper that included what became known as the Scherrer equation in 1981.
                  This can be attributed to the fact that “crystallite size” is not synonymous with “particle
                  size”, while X-Ray diffraction is sensitive to the crystallite size inside the particles.
                      The aim of present work is to prepare aluminium hybrid composite powders that
                  consist of TiO 2 and Gr by using ball milling process. An attempt was made to calculate
                  the grain size, lattice strain, stress, lattice space, lattice constant, dislocation density
                  and unit cell volume of mechanically milled powders. The grain size was calculated by
                  using Williamson-Hall and Scherrer equations. Microstructure analysis was carried out
                  to reveal the presence of reinforcement particles during ball milling.
                      Experimental details. Atomized aluminium (Al) powder size of –325 mesh and
                  purity of 99.7% supplied by Kemphasol, Mumbai, India was used for the matrix mate-
                  rial and rutile phase of titanium-di-oxide (TiO 2) and graphite powders supplied by the
                  Acechemie (India) were used as the reinforcement material. Natural Graphite is a mi-
                  neral  consisting  of  graphitic  carbon.  It  varies  considerably  in  crystallinity.  Natural
                  graphite is an excellent conductor of heat and electricity. It is stable over a wide range
                  of  temperatures.  Graphite  is  a  highly  refractory  material  with  a  high  melting  point
                  (3650°C). The required mass of Al, TiO 2 and Gr were accurately weighed in an electro-
                  nic weighing machine. The powders were milled for 20 h in a ball mill with a speed of
                  100 r/min. The vial of the ball mill is made up of high hardened stainless steel material.
                  Hardened high speed steel balls with a diameter of 10 mm were used and the ball-to-
                  powder  ratio  was  1:1.  X-ray  diffraction  analysis  was  carried  out  using  PANalyti-
                  calX’Pert X-ray diffractometer CuK α target, (λ = 1.5418 Å) to determine the lattice
                  space, lattice constant, grain size, lattice strain, stress, dislocation density and unit cell
                  volume of the milled composite powders by the following equations [11].
                      The grain size was calculated using Williamson-Hall equation:
                                                     kl
                                                          ( 2 sine
                                            b cos q =     +     ) q,                   (1)
                                                     t 
                  where k is the shape factor (0.94); λ is the wavelength of the X-ray used (λ = 1.5406 Å);
                  θ  is  the  Bragg  diffraction  angle  and  β  is  the  FWHM  in  radian;  t  is  the  effective
                  crystallite size; e is the strain value.
                      The Scherrer Equation is given by
                                                      0.94l
                                                  D =       .                            (2)
                                                      b cos q

                      The strain value (e) can be evaluated by using the following relation:
                                                  l       b 
                                             e =              ,                      (3)
                                                         -
                                                  D  sinq   tan q 
                  where D is the grain size.
                      The dislocation density (δ) has been calculated by using the formula:
                                                       15e
                                                   d =    ,                              (4)
                                                       aD
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