Page 42 - Read Online
P. 42

Park et al. J Mater Inf 2023;3:5  https://dx.doi.org/10.20517/jmi.2022.37        Page 5 of 25

               Table 2. Compositions used in the present experimental investigation
                                                              Experimental technique
                Sample  Composition   Differential scanning   Contact angle     Electromagnetic levitation
                      (X )
                        Sn
                                   calorimetry             measurement          technique
                I     0.365        Yes                     Yes                  Yes
                II    0.414        Yes                     Yes                  No
                III   0.523        Yes                     Yes                  No
                IV    0.653        Yes                     Yes                  No
                V     0.727        Yes                     Yes                  No

































                                     Figure 2. Experimental apparatus for the electromagnetic levitation test.


               temperature was held at 1,600 °C for 2 min for mixing Fe and Sn. After a predetermined time passed, the RF
               generator was turned off and the droplet was cooled down to room temperature in the furnace to prevent
               oxidation.


               Differential scanning calorimetry
               All differential scanning calorimetry (DSC) measurements in the present study were carried out in a
               NETZSCH DSC 404F1 Pegasus with an Rh furnace (T  = 1,650 °C) and a Pt sensor with thermocouples of
                                                             max
               type S. Alumina crucibles with lids (85 µl) were used for all experiments. The protective tube of the Rh
               furnace was purged permanently with Ar 5.0 (purity 99.999%). To minimize oxygen levels at high
               temperatures, a Zr getter was placed directly below the DSC sensor. By this, oxygen is absorbed by the getter
               material at temperatures above 350 °C. The experimental setup was calibrated by measuring the melting
               points of NETZCH’s standards of pure metals In, Bi, Al, Ag, Au, Ni, and Co. More detailed information on
               the used equipment can be found in the references [48,49] .

               The DSC signal strongly depends on the (i) sample mass, (ii) the applied heating rate (HR) and (iii) the heat
               consumption/release (∆H) during the phase transformation . It was expected from thermodynamic
                                                                     [48]
               calculations  that by crossing the liquidus phase boundary (Liquid  + Liquid  ↔ Liquid) during scanning,
                         [19]
                                                                                 2
                                                                         1
   37   38   39   40   41   42   43   44   45   46   47