Sulphur-induced collectorless flotation

It has been reported that although pyrite is only slightly floatable in self-induced flotation, the floatability is pronounced if sodium sulphur is added, which is called sulphur-induced collectorless flotation. As can be seen from... 

Figure 3.4 Sulphur-induced collectorless flotation recovery of marmatite as a fimction of Na2S concentration...

Figure 3.5 Sulphur-induced collectorless flotation recovery of pynhotites, jamesonite and marmatite as a function of NaaS concentration at pH = 8.8...

The h-pH diagrams of surface oxidation of arsenopyrite and pyrite are shown in Fig. 2.16 and Fig. 2.17, respectively. Figure 2.16 shows that jBh-pH area of self-induced collectorless flotation of arsenopyrite is close to the area forming sulphur. The reactions producing elemental sulphur determine the lower limit potential of flotation. The reactions producing thiosulphate and other hydrophilic species define the upper limit of potential. In acid solutions arsenopyrite demonstrates wider potential region for collectorless flotation, but almost non-floatable in alkaline environment. It suggests that the hydrophobic entity is metastable elemental sulphur. However, in alkaline solutions, the presence of... 

Pyrite and arsenopyrite have similar oxidation and self-induced collectorless flotation behavior. It is generally suggested that anodic oxidation of pyrite occurs according to reactions (2-24) in acidic solutions (Lowson, 1982 Heyes and Trahar, 1984 Trahar, 1984 Stm et al., 1991 Chander et al., 1993). The oxidation of pyrite in basic solutions takes place according to reactions (2-25). Since pyrite is flotable only in strong acidic solutions, it seems reasonable to assume that reaction (2-24) is the dominant oxidation at acidic solutions. Whereas pyrite oxidizes to oxy-sulfur species with minor sulphur in basic solutions. 

Abstract The sodium sulphide-induced collectorless flotation of several minerals are first introduced in this chapter. The results obtained are that sodium sulphide-induced collectorless flotation of sulphide minerals is strong for pyrite while galena, jamesonite and chalcopyrite have no sodium sulphide-induced collectorless flotability. And the nature of hydrophobic entity is then determined through J h-pH diagram and cyclic voltammogram, which is element sulphur. It is further proved widi the results of surface analysis and sulphur-extract. In the end, the self-induced and sodium sulphide-induced collectorless flotations are compared. And it is found that the order is just reverse in sodium sulphide-induced flotation to the one in self-induced collectorless flotation. 

From the Eqs. (3-1) to (3-13), the h-pH diagram of sodium sulphide solution is constructed with element sulphxir as metastable phase considering the presence of barrier (about 300kJ/mol) or overpotential (about 3.114 mV) of sulphide oxidation to sulphate and shown in Fig. 3.7. It is obvious that the lower limit of potential of sodium sulphide-induced collectorless flotation of pyrite, pyrrhotite and arsenopyrite at various pH agree well with the potential defined respectively by reactions of Eq. (3-9) producing elemental sulphur. The initial potential... 

Sun et al. (1993a) reported the effects HS ion concentration on the adsorption of HS , the amount of extracted sulphur and sulphur-induced flotation of pyrite as shown in Fig. 3.11. The results show that dining sodium sulphide-induced collectorless flotation, it involves the adsorption of HS ion on the mineral and the HS" adsorbed can be oxidized into sulphur to render pyrite and arsenopyrite surface hydrophobic due to the fact that the adsorption density of HS" ion increases with the HS" ion concentration and the amount of extracted sulphur and hence the flotation rate increases with the increase of adsorption density. It suggests that the mechanism of sodium sulphide-induced collectorless flotation of pyrite takes place hy reactions ... 

Fuerstenau (1980) found that sulphide minerals are naturally floatable in the absence of oxygen. Yoon (1981) ever attributed the natural floatability of some sulphide minerals to their very low solubility. Finkelstein et al. (1975) considered that the natural floatability of sulphide minerals are due to the formation of elemental sulphur and related to the thickness of formation of elemental sulphur at the surface. Some authors reported that the hydrophobic entity in collectorless flotation of sulphide minerals were the metal-deficient poly sulphide (Buckley et al., 1985). No matter whichever mechanism, investigators increasingly concluded that most sulphide minerals are not naturally floatable and floated only under some suitable redox environment. Some authors considered that the natural floatability of sulphide minerals was restricted to some special sulphide minerals such as molybdenite, stibnite, orpiment etc. owing to the effects of crystal structure and the collectorless floatability of most sulphide minerals could be classified into self-induced and sulphur-induced floatability (Trahar, 1984 Heyes and Trahar, 1984 Hayes et al., 1987 Wang et al., 1991b, c Hu et al, 2000). 

Heyes and Trahar (1984) leached pyrite with cyclohexane and compared the extract with a sulphur-containing solution of cyclohexane in a UV spectra photometer as shown in Fig. 1.4, indicating that sulphur was present at the mineral surface. Therefore, the inherent hydrophobicity and natural floatability once thought to be typical of sulphides is now thought to be restricted to sulphides such as molybdenite and other minerals or compound with special structural features. The collectorless floatability that most sulphide minerals showed came from the self-induced or sulphur-induced flotation at certain pulp potential range and certain conditions. 

Figure 10.11 presents the sehematic flowsheets of potential controlled flotation separation to recover chalcopyrite and pyrite from a copper-sulphur ore. Flowsheet I is collectorless flotation of chalcopyrite and then collector floatation of pyrite. Flowsheet II is collectorless flotation of chalcopyrite and then sodium sulphide-induced flotation of pyrite. Batch flotation results are illustrated in Table 10.5. It is evident that both flowsheets are suitable for flotation separation of copper-sulphur ore. The feed ore assayed 0.38% Cu and about 6% S, the copper concentrate obtained assayed 18%- 19% Cu with a recovery of 89%. For sulphur concentrate, the grade is 37%-43% S with a recovery of 82% - 85%. Interestingly, flie grade of sulphur concentrate is higher using sodium sulphide induced flotation than collector flotation. 

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