Awaruite, a new large nickel resource: Activation by ammonium sulfate and thiosulfate for flotation

Awaruite is a native nickel-iron alloy with high nickel content and mainly present in serpentinized ultramafic rocks. Recent discoveries have demonstrated the potential for awaruite to contribute to the economics of a nickel deposit. Awaruite selectively floats in weakly acidic conditions with xanth...

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書目詳細資料
發表在:Chemical Engineering Journal Advances
Main Authors: Santiago Seiler, Peter Bradshaw, Bern Klein
格式: Article
語言:英语
出版: Elsevier 2023-03-01
主題:
在線閱讀:http://www.sciencedirect.com/science/article/pii/S2666821122002010
實物特徵
總結:Awaruite is a native nickel-iron alloy with high nickel content and mainly present in serpentinized ultramafic rocks. Recent discoveries have demonstrated the potential for awaruite to contribute to the economics of a nickel deposit. Awaruite selectively floats in weakly acidic conditions with xanthate as collector. However high reagent dosages are required in such conditions since xanthate decomposes and ultramafic rocks are acid consumers. In this work, a novel reagent scheme including ammonium sulfate and sodium thiosulfate is proposed to float awaruite in neutral conditions from ultramafic rocks. Electrochemical studies were carried out on awaruite samples to demonstrate the effect of low concentrations of these reagents on the awaruite surface. The awaruite passivation layer formed in alkaline conditions (natural slurry pH) can, at least, be partially dissolved in the presence of low concentrations of ammonium sulfate and thiosulfate in neutral conditions. After the passivation layer is partially removed, the xanthate collector reacts with the awaruite surface and induces hydrophobicity, thus enabling the awaruite flotation. Microflotation and bench scale flotation tests demonstrate the applicability of the reagent scheme herein proposed. This reagent scheme allows the flotation of awaruite in conditions where xanthate is stable and reduces the acid addition required to adjust the pH.
ISSN:2666-8211