the adsorption of n-octanohydroxamate collector on cu and fe oxide minerals investigated by static secondary ion mass spectrometryn-octanohydroxamate收集器的吸附铜和铁氧化物矿物调查静态二次离子质谱分析.pdfVIP
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the adsorption of n-octanohydroxamate collector on cu and fe oxide minerals investigated by static secondary ion mass spectrometryn-octanohydroxamate收集器的吸附铜和铁氧化物矿物调查静态二次离子质谱分析
Minerals 2012, 2, 493-515; doi:10.3390/min2040493
OPEN ACCESS
minerals
ISSN 2075-163X
/journal/minerals
Article
The Adsorption of n-Octanohydroxamate Collector on Cu and
Fe Oxide Minerals Investigated by Static Secondary Ion Mass
Spectrometry
Alan N. Buckley 1,*, John A. Denman 2 and Gregory A. Hope 3
1 School of Chemistry, University of New South Wales, Sydney, NSW 2052, Australia
2 Ian Wark Research Institute, University of South Australia, Mawson Lakes, SA 5046, Australia;
E-Mail: John.Denman@.au
3 Queensland Micro- and Nanotechnology Centre, School of Biomolecular and Physical Sciences,
Griffith University, Nathan, QLD 4111, Australia; E-Mail: g.hope@.au
* Author to whom correspondence should be addressed; E-Mail: a.buckley@.au;
Tel.: +61-2-9385-4677; Fax: +61-2-9662-1697.
Received: 12 September 2012; in revised form: 26 November 2012 / Accepted: 4 December 2012 /
Published: 10 December 2012
Abstract: The feasibility of investigating the adsorption of n-octanohydroxamate collector
on copper and iron oxide minerals with static secondary ion mass spectrometry has been
assessed. Secondary ion mass spectra were determined for abraded surfaces of air-exposed
copper metal, malachite, pseudomalachite and magnetite that had been conditioned in
aqueous potassium hydrogen n-octanohydroxamate solution, as well as for the corresponding
bulk CuII and FeIII complexes. In each case, the chemical species present at the solid/vacuum
interface of a similarly prepared surface were established by X-ray photoelectron spectroscopy.
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