1992
DOI: 10.1016/0169-4332(92)90173-u
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XPS studies of xanthate adsorption on pyrite

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Cited by 55 publications
(26 citation statements)
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“…The C 1s peak II can also be attributed to CAO in adsorbed xanthate (Deng et al, 2013;Ikumapayi et al, 2012). The C 1s III is reported to be attributed to C@O (Hu et al, 2012) or hydrocarbon species on oxidized (insulating) mineral surfaces (Khmeleva et al, 2005), which is also close to the binding energy of solid CS 2 (Ranta et al, 1981) and dixanthogen (Szargan et al, 1992). Compared with the C 1s spectra of sphalerite treated in PAX with Milli-Q water and NaCl (Fig.…”
Section: Cryo-xps Analysismentioning
confidence: 84%
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“…The C 1s peak II can also be attributed to CAO in adsorbed xanthate (Deng et al, 2013;Ikumapayi et al, 2012). The C 1s III is reported to be attributed to C@O (Hu et al, 2012) or hydrocarbon species on oxidized (insulating) mineral surfaces (Khmeleva et al, 2005), which is also close to the binding energy of solid CS 2 (Ranta et al, 1981) and dixanthogen (Szargan et al, 1992). Compared with the C 1s spectra of sphalerite treated in PAX with Milli-Q water and NaCl (Fig.…”
Section: Cryo-xps Analysismentioning
confidence: 84%
“…5b) also indicates that the binding energy of metal-deficient species is lower than that of the sulfur in xanthate, which suggests dixanthogen is involved in the adsorbed xanthate species, since the reported binding energy of dixanthogen (162.7-164.5 eV (Buckley et al, 2003;Ranta et al, 1981;Szargan et al, 1992)) is higher than that of chemisorbed xanthate and metal-xanthate, e.g. 162.6 eV for lead-xanthate (Buckley and Woods, 1990), 162.4-162.5 eV for copper-xanthate (Buckley et al, 2003;Mielczarski et al, 1996) and 162-162.3 eV for silver-xanthate (Buckley and Woods, 1995).…”
Section: àmentioning
confidence: 88%
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“…Au, Cr, Mo, Pd, Zn) [17][18][19][20][21] and radionuclides (Am) [22]. Researchers have conducted experiments on the adsorption of glucose for bacterial adhesion in bioleaching process [23], xanthate for froth floatation to separate minerals from coal and mine tailing piles [24], phospholipids for the inhibition of surface oxidation [25], and surfactants for chlorobenzene removal [26] to verify diverse reaction mechanisms of the chemical compounds on pyrite surfaces. Surface charge of an interface between adsorbent and adsorbate can be developed by release and uptake of the interfacial ions (H + , OH 2+ , O 2À and OH À ).…”
Section: Introductionmentioning
confidence: 99%