Consider a surface:
Definition:
| q0, q1, ..., qn = Surface area (cm-2) covered by 0, 1, ..., n layers of adsorbed molecules. |
At Equilibrium:
| q0 must remain constant. |
. Rate of Evaporation Rate of Condensation
. . =
from First Layer onto Bare Surface
Similarly, at equilibrium q1 must remain constant.
. Rate of Condensation Rate of Condensation
. . on the Bare Surface on the 1st Layer
+ = +
Rate of Evaporation Rate of Evaporation
from the second layer from the second layer
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. . . | k1Pq0 + k-2q2 = k2Pq1 + k-1q1 |
Substituting into (I) gives
k-2q2 = k2Pq1
Extending this argument to other layers,
Definitions:
Total surface area of the catalyst,
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Total volume of gas adsorbed on surface
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. . . |
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where vm is the volume of gas adsorbed when the entire surface is covered with a complete monolayer.
From (I),
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If we assume that the properties of the 1st, 2nd, ... layers are equivalent, then,
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Similarly,
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| q3 =xq2 =x2q1 |
Generally,
| qi =xqi-1 =xi-1q1 =xi-1yq0 =cxiq0 {c=x/y} |
Substituting into (V),
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Also,
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. . . |
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must be infinite. This means that at P0, x must equal 1.
. . . | g = P0 | (From definition of x) |
. . . | x = P/P0 |
Substituting into VII, we arrive at the recognized form of the BET isotherm,
This can be rearranged to give,