W. Richard Bowen and Nidal Hilal 4
W. Richard Bowen and Nidal Hilal 4
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>