Abstract

Tellurium (Te), a critical element for photovoltaic technologies, commonly occurs as a trace constituent in pyrite, which is typically depressed during copper porphyry flotation process and discarded to tailings. Selective flotation of pyrite offers a promising route to enhance Te production within the copper supply chain, although its recovery is often limited by surface oxidation and hydrophilic passivation. This study establishes a mechanistic framework to improve flotation of Te-bearing pyrite from copper sulfide tailings. Micro flotation tests designed using Box–Behnken response surface methodology revealed significant nonlinear and synergistic effects of pH, potassium amyl xanthate (PAX), methyl isobutyl carbinol (MIBC), and activators (NaHS, Na2S, CuSO4). Dual sulfidization with NaHS–Na2S at pH 9.0 yielded optimal performance, with a cubic regression model (R2 = 0.91) accurately capturing reagent interactions. Surface analysis using zeta potential, contact angle, total organic carbon adsorption, and X-ray photoelectron spectroscopy demonstrated that sulfidization suppressed oxidized species and enriched reduced sulfur surface states (S2−/S0), thereby enhancing xanthate chemisorption. Bench-scale flotation with controlled potential activation validated these findings, achieving ∼90% pyrite recovery and ∼82% Te recovery. Overall, this work elucidates the surface-chemical mechanisms controlling Te-bearing pyrite flotation and demonstrates a viable pathway for Te recovery from sulfide tailings.

Department(s)

Mining Engineering

Publication Status

Full Text Access

Comments

U.S. Department of Energy, Grant 37989

Keywords and Phrases

Box–Behnken response surface methodology; Contact angle measurement; Critical minerals; Froth flotation; Pyrite; Tailings; Tellurium; X-ray photoelectron spectroscopy; Zeta potential

International Standard Serial Number (ISSN)

1873-3794; 1383-5866

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 2026 Elsevier, All rights reserved.

Publication Date

19 Jul 2026

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