2017
DOI: 10.1016/j.mineng.2017.04.014
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XPS study on the mechanism of starch-hematite surface chemical complexation

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Cited by 149 publications
(37 citation statements)
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“…The Zeta potentials of aegirite and specularite at different pH values were measured, and the result is illustrated in Figure 8. As shown in Figure 8, the Zeta potentials of these two minerals both decreased with the increase of pH value, and the IEP of specularite (2.83) is higher than that of aegirite (2.12), which conforms to the conjecture and previous results [11,40]. As a cationic collector, DDA increases the surface potential when adsorbed on a mineral surface.…”
Section: Surface Charge Of Mineral Surfacesupporting
confidence: 89%
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“…The Zeta potentials of aegirite and specularite at different pH values were measured, and the result is illustrated in Figure 8. As shown in Figure 8, the Zeta potentials of these two minerals both decreased with the increase of pH value, and the IEP of specularite (2.83) is higher than that of aegirite (2.12), which conforms to the conjecture and previous results [11,40]. As a cationic collector, DDA increases the surface potential when adsorbed on a mineral surface.…”
Section: Surface Charge Of Mineral Surfacesupporting
confidence: 89%
“…Based on the type of gangue, iron ore can be classified into three major types: quartz-type, carbonate-type, and silicate-type [3][4][5][6]. The difficulty of quartz-type iron ore separation via flotation is relatively low, and extensive studies have been conducted that mainly focus on the flotation separation of quartz-type oxide iron ore or the novel reagent synthesis and adsorption mechanism [7][8][9][10][11][12]. However, silicate-type iron ore, especially the iron-containing silicate-type iron ores, such as aegirite, chlorite, grunerite, garnet, etc., is difficult to separate due to the similar magnetic and floatability properties between iron-containing silicate and oxidized iron ore [13].…”
Section: Introductionmentioning
confidence: 99%
“…The binding energy of the Ca2p 3/2 peak increases from 348.07 to 348.58 eV, and the binding energy of the Ca2p 1/2 peak also increases from 351.58 to 352.08 eV, showing corresponding chemical shifts of 0.51 and 0.5 eV, relative to the binding energies before PA-Na addition (Figure 11a). When the chemical shift is greater than the experimental error of 0.3 eV, it indicates that a chemical reaction occurs; the greater the chemical shift, the stronger the reaction [38,39]. The increase in the binding energy of the fluorite surface after PA-Na addition implies the existence of a strong force of adsorption on fluorite.…”
Section: Adsorption Energymentioning
confidence: 98%
“…Comparing the fitted C1sX PS spectra of the unmodified ex-pandedH ACS (4a)a nd S350 (4b)s upports to those of Fe-NHC catalysts 1a and 1b ( Figure S10 andS 11), additional carbon peaks at 283.6, 286.1 and 289.2 assigned to CÀC(Ar), C-N and C=Oa re observed. [31] These additional peaks are believed to come from compound (12)a ttached on the expanded HACS.…”
Section: Mçssbauerspectroscopymentioning
confidence: 99%