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W. Richard Bowen and Nidal Hilal 4

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94 3. QUANTIFICATION OF PARTICLE–BUBBLE INTERACTIONs<br />

3.5.2 Effect of Surfactant on Particle–Bubble Interactions<br />

During the froth flotation process, surfactant compounds are commonly<br />

added to the flotation chamber to modify bubble–particle<br />

attachment <strong>and</strong> increase mineral recovery. A number of AFM-based<br />

measurements have been carried out to assess the effect of surfactants in<br />

solution on particle–bubble interactions <strong>and</strong> hence, presumably, on flotation<br />

efficiency.<br />

Preuss <strong>and</strong> Butt [36, 48] studied the effects of adding two surfactants,<br />

sodium dodecyl sulphate (SDS) <strong>and</strong> dodecyltrimethylammonium bromide<br />

(DTAB), to solution when carrying out measurements between<br />

both hydrophobic <strong>and</strong> hydrophilic particles with air bubbles. When<br />

hydrophilic silica particles were allowed to approach the bubble in aqueous<br />

solution without surfactant present, repulsive forces were measured<br />

prior to contact, as reported previously for hydrophilic silica particles [37,<br />

39]. As the concentration of SDS in solution was increased, this repulsive<br />

force also increased <strong>and</strong> the decay length became decreased. As SDS has<br />

a negative charge in solution, as do the silica–water <strong>and</strong> air–water interfaces,<br />

the most likely explanation was that the repulsion was electrostatic<br />

in origin <strong>and</strong> increased with increasing quantities of SDS at the interfaces.<br />

When the effects of DTAB were investigated long-range forces between<br />

the particles <strong>and</strong> the bubbles occurred, <strong>and</strong> adhesion was observed when<br />

retracting the particle, most probably due to DTAB coating the silica surface<br />

<strong>and</strong> increasing its hydrophobicity.<br />

When silanized hydrophobic silica particles were used, capillary forces<br />

were dominant, with large adhesions on the order of 70 mN m �1 detected<br />

upon particle retraction [36, 48]. In the absence of SDS, small repulsive<br />

forces were measured on approach, probably due to electrostatic repulsion.<br />

When SDS was introduced, adhesion appeared to be dependent<br />

upon the maximum force used to press the particle into the bubble, reaching<br />

a threshold value of approximately 6 mN m �1 for an SDS concentration<br />

of 5.6 mM. Below this threshold value no adhesion was seen, with no<br />

hysteresis between the approach <strong>and</strong> the retract parts of the force curves,<br />

suggesting that the SDS was reducing the interaction between the particle<br />

<strong>and</strong> the bubble. As the loading force increased above the threshold, a<br />

jump-in event occurred <strong>and</strong> high adhesion was observed. This threshold<br />

force was increased, as the SDS concentration was increased as illustrated<br />

in Figure 3.5. When the effects of DTAB were investigated, they were<br />

found to follow a similar trend to that seen with SDS. At concentrations<br />

�6 or 12 mM, for SDS or DTAB, respectively, formation of the TPC was no<br />

longer observed for the load forces that were reached [36, 48]. The most<br />

likely explanation for this behaviour is that a surfactant film was built up<br />

between particle <strong>and</strong> bubble, preventing TPC formation. As the surfactant<br />

concentration was increased, this film would most likely be thicker <strong>and</strong>

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