A Micro-Scale Investigation of the Adsorption of Collectors on Bastnaesite
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MME_AFM bastnaesite.pdf
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Final Accepted Manuscript
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Univ Arizona, Dept Min & Geol EngnIssue Date
2019-08-06
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SPRINGER HEIDELBERGCitation
Zhang, J., An, D. & Withers, J. Mining, Metallurgy & Exploration (2019) 36: 957. https://doi.org/10.1007/s42461-019-00118-3Journal
MINING METALLURGY & EXPLORATIONRights
Copyright © Society for Mining, Metallurgy & Exploration Inc. 2019.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
A micro-scale investigation was carried out by applying atomic force microscopy (AFM) to study in situ the adsorption of various collectors, i.e., oleic acid, octanohydroxamic acid (HA), and salicylhydroxamic acid (SHA), on bastnaesite in aqueous solutions. The obtained AFM images show that the surface morphology of bastnaesite changes greatly after it comes into contact with the solutions of the collectors, suggesting that all these collectors can effectively adsorb onto bastnaesite. Increasing temperature can facilitate the adsorption of oleic acid onto bastnaesite. Results from attenuated total reflectance–Fourier transform infrared spectrometry (ATR-FTIR) also show that all of these collectors adsorb strongly onto bastnaesite, with strong absorbance spectra being detected. The ATR-FTIR results confirm those obtained by AFM. In general, hydroxamic acid collectors (HA and SHA) adsorb onto bastnaesite mainly in the form of insoluble metal hydroxamate. This specific adsorption mechanism explains that a high selectivity with a moderate collectivity will be achieved with a hydroxamic acid collector for the flotation of bastnaesite.Note
12 month embargo; published online: 6 August 2019ISSN
2524-3462Version
Final accepted manuscriptSponsors
DoD Office of Navy Research grant [N00014-15-C-0165]; Freeport-McMoRan Copper Gold, Inc.ae974a485f413a2113503eed53cd6c53
10.1007/s42461-019-00118-3
