Zeta Potentials Of Cassiterite In Aqueous Solutions

Society for Mining, Metallurgy & Exploration
D. W. McGlashan
Organization:
Society for Mining, Metallurgy & Exploration
Pages:
21
File Size:
666 KB
Publication Date:
Jan 1, 1969

Abstract

Zeta potential changes were determined as a function of pH, metal ion, and surfactant concentrations. Prom the analysis of data, flotation experiments were carried out to correlate float-ability with the differences in zeta potential. Cassiterite in water bears a negative zeta potential, The zeta potential of cassiterite is sensitive to pH changes; the electric double layer arises from the preferential adsorption of H+ and OH- ions and subsequent ionization of the hydroxylated surface. It is suspected that hydronium-ion concentration may cause reversal in the sign of the zeta potential. The ZPC was found to occur at pH 3.4. Metallic ions and the hydrated ions thereof affect the zeta potential of cassiterite in differing degrees of intensity. Without prior activation, sulfonated surfactants do not change the zeta potential of cassiterite. Sodium alkyl aryl sulfonate is especially active on lead-activated cassiterite and ferric-activated cassiteriten Microcalorimetric fiests confimed the activity of ions on cassiterite and showed the hydrated character of cassiterite smfaces. Close correlation between zeta potential and microflotation results was achieved.
Citation

APA: D. W. McGlashan  (1969)  Zeta Potentials Of Cassiterite In Aqueous Solutions

MLA: D. W. McGlashan Zeta Potentials Of Cassiterite In Aqueous Solutions. Society for Mining, Metallurgy & Exploration, 1969.

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