in contrast to the higher pH values required to depress pyrite when
using xanthate and other collectors. Essentially this was achieved by
the incorporation in the collector molecule of an O-containing
(ethoxycarbonyl) functional group, thereby augmenting the role of
the S functional group. The introduction of this second functional
group lowers the pKa of the molecule by several orders of magni-
tude compared to that of dialkyl thionocarbamates. This allows the
collector to be effective at lower pH values. (for further discussion,
see Section 5) Further, the second functional group provides for the
formation of more favorable and stronger metal complexes and,
therefore, stronger adsorption. This has been demonstrated by
sequential adsorption studies. For example, AERO 5415 and AERO
5460 promoters have been shown to replace previously adsorbed
dialkyl thionocarbamate from the mineral surface but, on the other
hand, dialkyl thionocarbamate does not replace previously adsorbed
AERO 5415 or AERO 5460 promoters. They are especially effective
for copper-rich minerals such as chalcocite, digenite, covellite and
bornite. They are poor galena collectors, as all thionocarbamates are.
AERO 5415, AERO 5460 promoters
These two collectors are structurally similar, but AERO 5460 promoter
being the higher homologue is the more powerful of the two and,
therefore, especially suitable for the recovery of coarse middlings
particles, whilst being only slightly less selective. Both of these
collectors are now in wide commercial use (both as-is or as compo-
nents of customized formulations) for the flotation of Cu, Cu-Mo
and Cu-Au ores. In most cases, the dosage required of these collectors
is lower than that for the traditional collectors, in addition to pro-
viding considerable savings in lime costs.
Comments
• Being insoluble in water, addition to the grinding circuit or a
conditioning step ahead of flotation may be beneficial. However, in
many cases
AAEERROO 55441155
and
AAEERROO 55446600
promoters are more
readily dispersible than the dialkyl thionocarbamates and allyl
alkyl thionocarbamates (depending upon pH and other condi-
tions). Consequently, in many cases, addition to the head of flota-
tion is possible and indeed may be preferable. The best point of
addition should be determined by laboratory and plant testing.
• Because of their high collecting power in moderately alkaline
circuits, and their high selectivity against iron sulfide minerals,
Flotation of sulfide ores
117