GTBL042-06 GTBL042-Callister-v3 September 28, 2007 21:46
2nd Revise Page
6.5 Factors That Influence Diffusion • 175
0.7 0.8 0.9 1.0 1.1 1.2
Diffusion coefficient (m
2 /s)
10 –12
10 –13
10 –15
10 –14
10 –16
10 –17
Reciprocal temperature (1000/K)
Figure 6.8 Plot of the
logarithm of the diffusion
coefficient versus the
reciprocal of absolute
temperature for the
diffusion of copper in gold.
D= 10 −^14 m^2 /s, the logarithm ofDis –14.0,not 10 −^14. Furthermore, this log-
arithmic scaling affects the readings between decade values; for example, at a
location midway between 10−^14 and 10−^15 , the value is not 5× 10 −^15 but, rather,
10 −^14.^5 =3.2× 10 −^15 .]
Thus, from Figure 6.8, at 1/T 1 =0.8× 10 −^3 (K)−^1 , logD 1 =–12.40, while
for 1/T 2 =1.1× 10 −^3 (K)−^1 , logD 2 =–15.45, and the activation energy, as
determined from the slope of the line segment in Figure 6.8, is
Qd=− 2. 3 R
⎡
⎢
⎢
⎣
logD 1 −logD 2
1
T 1
−
1
T 2
⎤
⎥
⎥
⎦
=− 2 .3(8.31 J/mol-K)
[
− 12. 40 −(− 15 .45)
0. 8 × 10 −^3 (K)−^1 − 1. 1 × 10 −^3 (K)−^1
]
= 194 ,000 J/mol=194 kJ/mol
Now, rather than trying to make a graphical extrapolation to determine
D 0 , a more accurate value is obtained analytically using Equation 6.9b and a
specific value ofD(or logD) and its correspondingT(or 1/T) from Figure 6.8.
Since we know that logD=–15.45 at 1/T=1.1× 10 −^3 (K)−^1 , then
logD 0 =logD+
Qd
2. 3 R
(
1
T
)
=− 15. 45 +
(194,000 J/mol)(1. 1 × 10 −^3 [K]−^1 )
(2.3)(8.31 J/mol-K)
=− 4. 28
Thus,D 0 = 10 −^4.^28 m^2 /s=5.2× 10 −^5 m^2 /s.