2005
DOI: 10.1016/j.minpro.2005.06.006
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On the cathodic reaction coupled with the oxidation of xanthates at the pyrite/aqueous solution interface

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Cited by 66 publications
(49 citation statements)
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“…Pyrite surface is readily oxidized and is considered to be of heterogeneous nature after oxidation, and is composed of mosaics of both hydroxide and bare pyrite as shown in Fig. 8(a) [8]. Immersion of pyrite in acid solutions leads to the dissolution of Fe 2+ in the solution or near the surface, leaving behind a hydrophobic iron-deficient sulfur-rich layer.…”
Section: Discussionmentioning
confidence: 99%
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“…Pyrite surface is readily oxidized and is considered to be of heterogeneous nature after oxidation, and is composed of mosaics of both hydroxide and bare pyrite as shown in Fig. 8(a) [8]. Immersion of pyrite in acid solutions leads to the dissolution of Fe 2+ in the solution or near the surface, leaving behind a hydrophobic iron-deficient sulfur-rich layer.…”
Section: Discussionmentioning
confidence: 99%
“…Alkyl xanthates, known to selectively interact with sulfides and render their surfaces hydrophobic, are the most extensively used collectors in the flotation of base metal sulfide minerals [3,4]. Pyrite responds strongly with xanthates (X À ) in acidic to neutral pH conditions and it is generally acknowledged that dixanthogen (X 2 , oxidation product of xanthate ions) is the main product responsible for pyrite flotation [3,8]. The formation of dixanthogen is an electrochemical process involving charge transfer between pyrite and xanthate accompanied by the reduction of ferric hydroxides species on pyrite surface formed by surface oxidation [8][9][10].…”
Section: Introductionmentioning
confidence: 99%
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“…It reverses the positive surface charge of pyrite in acid pH pulps, and gets it more negative at neutral and alkaline pHs with increasing the xanthate concentration [4,[8][9][10]. There DA VID PUBLISHING D is a general consensus that xanthate makes pyrite hydrophobic adsorbing as dixanthogen and, meanwhile, the loss of positive charge associated with surface ferric hydroxide on the surface resulting in the negative increase in the zeta potential of pyrite.…”
Section: Introductionmentioning
confidence: 99%
“…Laajalehto et al (1999) demonstrated that the new phase on the copper activated pyrite was probably a chalcopyrite type (CuFeS2), and the reduction of Cu 2+ was compensated by the oxidation of iron when chalcopyrite was formed. proposed (Leppinen 1990, Buckley 1994, Valdivieso et al 2005. However, the adsorption of collector on un-activated pyrite surface is minimal at alkaline conditions.…”
Section: Pyrite Activation Mechanism By Copper Ionsmentioning
confidence: 99%