Amyl Xanthate Adsorption Research Articles

Effects of salinity on xanthate adsorption on sphalerite and bubble–sphalerite interactions

The adsorption of amyl xanthate on sphalerite in NaCl solutions of different concentrations and in saline water (viz. simulated sea water) and the surface properties of treated minerals were investigated. The interactions between xanthate treated sphalerite particles and air bubbles were examined using induction time measurement, which revealed that the salt ions could inhibit the adsorption of xanthate on sphalerite due to the competitive adsorption, but also could compress the electrical double layer at mineral/water interface. The induction time of sphalerite treated in potassium amyl xanthate (PAX) with saline water was shorter than that of sphalerite treated in PAX with NaCl of the same ion concentration, which implies that the water composition (e.g. Ca2+, Mg2+) could play an important role in the bubble–particle interaction. The hydrophobicity, chemical composition, and charge property of PAX treated sphalerite surfaces were characterized using contact angle measurement, Cryo-X-ray photoelectron spectroscopy (Cryo-XPS) and zeta potential determination, respectively, which support the inhibition effect of salt ions on the xanthate adsorption on sphalerite. In the case of saline water, the xanthate decomposition products were confirmed by XPS, which could further lower the hydrophobicity of the treated sphalerite. Our results provide insights into the basic understanding of the salinity effects on the xanthate adsorption on sphalerite and the bubble–mineral interactions in flotation.

Sulfidation of Lead-Loaded Zeolite Microparticles and Flotation by Amylxanthate

The possibility of recovering lead-loaded zeolite Y microparticles (PbY) by flotation after sulfidation was investigated using amyl xanthate (AMX) as the collector. The sulfidation process (by aqueous Na2S) was first studied as a function of the medium composition (Na2S concentration, pH), and the solid phases were characterized by various physicochemical techniques (X-ray photoelectron spectroscopy, high-frequency impedance measurements, and electrochemistry). Progressively increasing the sulfidation level resulted in the concomitant transformation of Pb(II) species ion-exchanged in the zeolite into PbS clusters that were mostly located at the external boundaries of the zeolite particles while remaining attached to the aluminosilicate (PbS-Y). Similar to what occurred for galena particles, the zeolite-supported PbS clusters were likely to adsorb the AMX collector, the remaining (nonsulfided) ion-exchanged Pb(II) species being transformed into a Pb(AMX)2 precipitate when using AMX in large excess. Owing to such AMX adsorption on PbS-Y, the zeolite particles were found to flocculate and to float in the presence of air bubbles. If rather high AMX concentrations (>5 x 10(-3) M) were necessary to ensure the flotation of nonsulfided PbY particles (Walcarius, A.; Lamdaouar, A. M.; El Kacemi, K.; Marouf, B.; Bessiere, J. Langmuir 2001, 17, 2258), significantly lower concentrations (down to 1 x 10(-4) M) gave rise to high flotation yields (ca. 95%) upon PbY sulfidation. It is noteworthy that the sulfidation level should be maintained at a value high enough (>10%) to produce the minimal PbS amount ensuring flotation but not too high (<75%) to avoid conditions that are too reducing and are not compatible with the flotation process. Finally, depression tests seemed to indicate that PbS-Y flotation occurs according to a mechanism similar to that described for the galena mineral.

Adsorption of Amyl Xanthate at Pyrrhotite in the Presence of Nitrogen and Implications in Flotation

AbstractAdsorption of xanthate at pyrrhotite with air and nitrogen, and the effects of cationic species have been investigated. The results have been correlated with flotation of pyrrhotite with air and nitrogen. While the use of nitrogen in place of air causes depression of pyrrhotite the effect is significantly reduced in presence of cationic species. The results are discussed on the basis of a suggested mechanism of the adsorption of xanthate at pyrrhotite.

Adsorption of Amyl Xanthate at Pyrrhotite in the Presence of Nitrogen and Implications in Flotation

Adsorption of Amyl Xanthate at Pyrrhotite in the Presence of Nitrogen and Implications in Flotation