As seen in Figure 1 the
relationship between temperature and secondary dendrite space is exhibited
according to the equation above. When the secondary dentrite arm space L
increases from 10?m to 130?m the temperature will increase from 300? to 5,600?
in TiAl. The bigger space expresses that the higher temperature. So the whole
dendtire may be expressed in terms of the whole space changing. Because it is
supposed that Ccom =0.06 and L=20?m the whole space and temperature
will change a certain with the two parameter changing. At the tip of dentrite
the temperature attains high value and then temperature will become low. It
fits to the principle well (Figure 1).

Figure 1: The relationship between
temperature and dentrite second space in TiAl.

(a) v=1860mm/hr;
ls=150mm

(b) v=2860mm/hr;
ls=150mm

(c) v=3860mm/hr;
ls=150mm

(d) v=4860mm/hr;
ls=150mm

(e) v=1860mm/hr;
ls=350mm

(f) v=2860mm/hr;
ls=350mm

(g) v=3860mm/hr;
ls=350mm

(h) v=4860mm/hr;
ls=350mm
Figure 2:
The relationship between cooling rate and dentrite secondary arm space with
various solidified speed v at the two solidified length Ls in TiAl.

Figure 3:
The linear relationship between Gibbs free energy difference and temperature in
TiAl.
As seen in Figure 2(a~h)
when the drawing speed increases from 1860~4860mm/hr with the solidified length
of 150mm and 350 mm the cooling rate will increase from 15K/s, 24K/s, 32K/s
& 40K/s and 7K/s, 10K/s, 13K/s &18K/s at the place of 10?m to 1.5K/s,
2K/s,3K/s &4K/s and 0.5K/s,1K/s, 1.5K/s & 2K/s at the same one of 120?m
in TiAl respectively. At the solidified length to be 350mm it has maximum value
of cooling rate with 40K/s under the condition of 4860mm/hr. Meantime the
minimum cooling rate is 0.5K/s under 1860mm/hr and solidified length of
150mm. It expresses that the cooling
rate decreases with the drawing speed becomes bigger (Figure 2,3).
Gibbs free energy is
defined as below
From Figure 3 DG
decreases with temperature increasing. It decreases with entropy DS maintaining
2.8J/mol/K. This is the result of concentration of liquid and solid in terms of
composition. When DS is 2.8J/ (mol·K) the DG changes from 800J to -2000J with
the temperature increases from 850K to 1900K respectively. G is Gibbs free
energy and DH is enthalpy [3-4]. It is supposed that enthalpy is constant in
this study. It means that when DS becomes big the Gibbs free energy DG will
decrease.
G=
H-T
S (7)
In Ti-Al
H and
S are to be
H=3.3KJ/mol?
S=2.8J/mol/K at 1492?