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W. Richard Bowen and Nidal Hilal 4

W. Richard Bowen and Nidal Hilal 4

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Bubble<br />

3.2 PARTICLE–BUBBLE INTERACTIONs 83<br />

Hydration<br />

layers<br />

between the particle <strong>and</strong> the bubble will add a hydrodynamic component<br />

to the attachment kinetics. In flotation, if the time required for this film to<br />

rupture (the induction time) is less than the actual contact time, then the<br />

particle will be unable to attach to the bubble [4]. Further approach will<br />

cause the hydration layers to become thinner <strong>and</strong> less stable. As this layer<br />

becomes destabilised, the particle <strong>and</strong> bubble will be allowed to attach<br />

directly, leading to the formation of a three phase contact (TPC) line. The<br />

more hydrophobic the particle surface, the thinner <strong>and</strong> less stable any<br />

hydration layer will be. Consequently, the more hydrophobic in character<br />

a particle is, the more readily it will attach to air bubbles in solution. This<br />

is the mechanism by which the flotation of fine particles is achieved [1, 2].<br />

Derjaguin <strong>and</strong> Dukhin [5] explain that the main thermodynamic parameter<br />

involved in the particle–bubble interaction is the disjoining pressure,<br />

which is defined by them as the derivative of the free energy with respect<br />

to the thickness h of this wetting layer per unit area. This disjoining pressure<br />

is formed by a combination of pressures:<br />

P � N � A � S<br />

( h) ( h) ( h) ( h)<br />

Particle<br />

Bulk fluid<br />

layer<br />

FIGurE 3.1 Simple illustration of a basic particle–bubble interaction. On approach<br />

there are three fluid layers present between the particle <strong>and</strong> the bubble. These are hydration<br />

layers on both the particle <strong>and</strong> the bubble (represented by the dashed line) <strong>and</strong> a layer<br />

of bulk fluid in the middle. The confinement <strong>and</strong> drainage of this bulk fluid layer leads to a<br />

hydrodynamic component to the interactions.<br />

(3.1)<br />

where P is the disjoining pressure, N the ionic double layer repulsion<br />

per unit area, A the contribution due to van der Waals interactions per<br />

unit area <strong>and</strong> S (h) the contribution of particle surface hydrophobicity to<br />

the disjoining pressure. S (h) will tend towards zero for very hydrophobic<br />

surfaces.<br />

As described by Sutherl<strong>and</strong> [6, 7], the probability of a particle being<br />

collected during flotation (P) is a composite of the probability of particle–<br />

bubble collision (P c), the probability of such a collision leading to adhesion

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