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Untitled - Aerobib - Universidad Politécnica de Madrid

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46 CHAPTER 2. TRANSPORT PHENOMENA IN GAS MIXTURES<br />

4.0<br />

3.5<br />

3.0<br />

2.5<br />

[D 12<br />

] 1<br />

2.0<br />

1.5<br />

1.0<br />

Rigid spheres<br />

Lennard−Jones potential<br />

0.5<br />

0.0<br />

0 200 400 600 800 1000 1200 1400 1600 1800 2000<br />

T(K)<br />

Figure 2.3: Coefficient [D 12] 1<br />

as a function of temperature in a mixture of N 2 and CO 2, for<br />

rigid spheres and for an interaction potential of Lennard-Jones.<br />

Hence, the influence of mass fractions on the value of D 12 is always small and<br />

can, generally, be neglected by adopting for it the value given by the first approximation.<br />

Frequently, the value given by elementary diffusion theory is approximate<br />

enough. According to it,<br />

D 12 ∼ T 3/2<br />

p . (2.24)<br />

Or else, an empirical formula of the form<br />

D 12 ∼ T n<br />

p , (2.25)<br />

where n is an exponent ranging from 1.5 to 2 whose value is <strong>de</strong>termined empirically.<br />

With respect to thermal diffusion ratio k T , even in the first approximation it is<br />

a complicated function of the molar masses, mass fractions of the species and of the<br />

temperature of the mixture. It is also very much influenced by the laws of molecular<br />

interaction. The expression of the first approximation of k T can be obtained from<br />

Ref. [2], p. 541, where tables for the calculation of their values are also inclu<strong>de</strong>d as<br />

well as a comparison between theoretical and experimental values for many binary<br />

mixtures. It appears that the agreement is not so good for k T as for the other transport<br />

coefficients. When comparing the successive approximations to the value of k T , it is<br />

also verified that in first approximation the error is larger here than for other transport

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