Chemistry > Surface Chemistry > 4.0 Adsorption Isotherms

  Surface Chemistry
    1.0 Introduction
    2.0 Adsorption
    3.0 Factors affecting adsorption of gases by solids
    4.0 Adsorption Isotherms
    5.0 Applications of Adsorption
    6.0 Types of Solutions
    7.0 Colloidal System
    8.0 Coagulation of colloidal solutions
    9.0 Emulsions
    10.0 Catalysis
    11.0 Zeolites as shape-selective catalysts
    12.0 Enzyme as catalysts

4.1 Freundlich adsorption isotherm
Freundlich gave an empirical relationship between the quantity of gas adsorbed by a given amount of solid adsorbent surface and pressure of the gas at a particular temperature. It states that $$\frac{x}{m} = k{p^{1/n}}$$
where $x$ is the weight of the gas adsorbed by $m$ gm of the adsorbent at a pressure $p$;
thus $x/m$ represents the amount of gas adsorbed per gm (unit mass) of the adsorbent,
$k$ and $n$ are constants at a particular temperature and for a particular adsorbent and adsorbate (gas) :
$n$ is always greater than one, indicating that the amount of the gas adsorbed does not increase as rapidly as the pressure.

When $n = 1$, $$\frac{x}{m} = kp$$ $$\frac{x}{m} \propto p$$
This is observed in lower pressure range. When $n$ is large, $\frac{x}{m} = k$ (independent of pressure). This is observed at high pressure when saturation point is reached as shown in figure $2$.

Taking logarithm of the equation $$\frac{x}{m} = k{p^{1/n}}$$
$$\log \frac{x}{m} = \log k + \frac{1}{n}\log p$$
Graph between $\left( {\log \frac{x}{m}} \right)$ and $\log p$ is a straight line with $slope\frac{1}{n}$ and intercept $\log k$ as shown in figure $3$.
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