E ﬀ ects of Ferrous Sulfate Addition on the Selective Flotation of Scheelite over Calcite and Fluorite

: The addition of ferrous sulfate as a depressant for Ca-bearing minerals such as calcite and ﬂuorite during scheelite ﬂotation was investigated to recover scheelite from tungsten mine tailings, using Hallimond-tube ﬂotation tests, zeta-potential measurement and Fourier-transform infrared (FT-IR) analyses. The ﬂotation tests indicate that the selectivity of scheelite recovery was the largest over calcite and ﬂuorite under the following conditions: 0.5 g sample, 50 g / ton AF65, 1 × 10 − 3 M sodium oleate, 1200 g / ton SF2 (sodium silicate and ferrous sulfate) depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL / min air injection rate, 5 min ﬂotation time, and pH 8. The selectivity of scheelite ﬂotation increased when the amount of SF2 depressant addition increased to 1200 g / ton, but it decreased by adding 1400 g / ton SF2, which would result from the precipitation of iron components. In the zeta potential results, the zeta potentials of scheelite with the collector show similar results regardless of the addition of SF2, while the change of zeta potentials of calcite and ﬂuorite by adding NaO collector diminished when SF2 was added. In FT-IR analyses, the spectrum of NaO in scheelite results was observed regardless of the addition of SF2, while the spectra of NaO in calcite and ﬂuorite results disappeared when SF2 was added. These results suggest that the addition of SF2 prevents the adsorption of NaO on the surface of calcite and ﬂuorite. Therefore, the addition of SF2 could enhance the selectivity of scheelite ﬂotation over calcite and ﬂuorite. 10 and 11, respectively, the spectra of calcite and ﬂuorite with the collector (NaO) show the band at 2931.5 and 2910.4 cm − 1 , which are due to the stretching vibration of sodium oleate, indicating good adsorption, but they disappeared in the minerals with the collector after the addition of the depressant (SF2). These results indicate that the addition of SF2 depressant prevents the adsorption of the NaO collector, which shows a good agreement with the experiment results of zeta potential measurement. Therefore, the addition of SF2 depressant could enhance the selectivity of scheelite over Ca-bearing minerals such as calcite and ﬂuorite. on the surface of scheelite was observed regardless of SF2 depressant addition, while the zeta potentials of calcite and ﬂuorite and FT-IR spectra with NaO / SF2 show similar behavior with calcite and ﬂuorite without any ﬂoatation reagents. These results indicate that the addition of SF2 prevents the adsorption of NaO (collector) on the surface of calcite and ﬂuorite, which are regarded as tailing during scheelite ﬂotation, so the selectivity of scheelite ﬂotation could be enhanced by adding the depressant consisting of sodium silicate and ferrous sulfate.


Introduction
The number of abandoned metal mines in South Korea has been found to be 2089, and it was reported that 1268 of the abandoned metal mines have detrimentally affected the environments around the abandoned mines [1]. Sangdong mine is a representative scheelite mine in South Korea, and 12 million tons of tailings was generated during a 40-year operation after it had been abandoned [2,3]. In South Korea, Mine Reclamation Corporation (MIRECO), a state-owned company, has developed technologies to recover valuable materials from tailings [4], which could reduce potential risk of tailings. Although some research was performed to use the tailing of Sandong mine as constructive materials [2], technology for the recovery of valuable materials such as scheelite should be required.
Scheelite has been found to be a representative tungsten ore [5]. Tungsten is being widely used in various industries such as the high-temperature technology, chemical, lighting, X-ray technology, and machine manufacturing industries, owing to its low vapor pressure, high melting point, excellent electricity and thermal conductivity, high density, high abrasion resistance, and excellent X-ray performance [6,7]. Therefore, the recovery of scheelite from tailings is important not only in obtaining tungsten, but also in reducing the volume of tailings. Gravity separation such as jig process has been reported to recover scheelite [8], but, generally, the flotation process has been selected for beneficiation of scheelite [9].
It is known that scheelite can be selectively floated by using fatty acid and a fatty acid derivative as a collector [10,11]. However, since scheelite (CaWO 4 ) contains calcium components, it is closely related to other Ca-bearing minerals such as calcite (CaCO 3 ) and fluorite (CaF 2 ). Scheelite has similar physicochemical properties, such as the existence of the same cations (Ca 2+ ) in the mineral, solubility, hardness, specific gravity, and point of zero charge [12,13], which causes similar chemisorption behavior of the fatty acid and a fatty acid derivative as a collector on the Ca-bearing minerals [9,[14][15][16]. Generally, it has been found that sodium silicate is the most widely used depressant for selective flotation of scheelite [15], and assistant depressant such as ferrous sulfate has been investigated [15,16].
Although the mechanism of the depression of calcite [15] and fluorite [16] during scheelite flotation, using a mixture of sodium silicate and ferrous sulfate as a depressant, was reported by investigating the minerals with X-ray photoelectron spectroscopy (XPS), more experiments will be required to understand the depression mechanism of sodium silicate and ferrous sulfate. Therefore, in the present study, the optimum flotation condition was obtained from Hallimond-tubes flotation tests, and then the effect of ferrous sulfate addition with sodium silicate was investigated with zeta potential measurement and FT-IR analyses using scheelite, calcite and fluorite conditioned at the optimum condition.

Materials
The samples that were used in this study were the concentrates of scheelite (CaWO 4 ), calcite (CaCO 3 ), and fluorite (CaF 2 ), which were obtained from domestic mines such as Sandong mine, Imha mine, and Sinpo mine, respectively. Figure 1 shows the X-ray diffraction (XRD) analysis results for scheelite, calcite, and fluorite. The analysis results show that all the three samples are pure, with almost absolutely no impurities.

Flotation Test Procedures
Flotation tests on singular mineral (scheelite, calcite, and fluorite) were using Hallimond tubes with 300 mL of working volume under the following conditions: 0.5 g mineral sample (75 µm-150 µm), 50 g/ton AF65 as a frother, 1 × 10 −3 M sodium oleate as a collector, 50 mL/min air injection rate, 5-min conditioning for each reagent addition, and 5 min flotation time. The pulp was stirred with a magnetic bar during the conditioning and flotation tests. In a typical run, the pH of 300 mL distilled water with the sample was adjusted at 8 with HCl and NaOH, and then depressant, collector, and frother were added in order. After the flotation tests, the products were collected by filtering with a filter paper and then dried at 105 • C. The floatability (%) was calculated as follows: where M final and M initial indicate mass of final and initial added mineral, respectively.

Zeta Potential and Fourier-Transform Infrared (FTIR) Analyses
The zeta potentials of the mineral particles were measured with Beckman Coulter's Delsa Nano C. The mineral samples were finely ground with an agate mortar, and less than 5 µm particles collected using a filter (pore size: 5 µm) were used. The zeta potential was measured using a 1. NaCl solution as the supporting electrolyte. The pH value was adjusted with HCl and NaOH and was measured after the Zeta potential tests.
The adsorption of the collector and depressants on the surfaces of Ca-bearing minerals was examined using Jasco's FTIR spectrometer. After the 0.5 g mineral sample with less than 200 mesh was added to 300 mL distilled water, the flotation reagents (collector and depressant) were added to the suspension, which was conditioned for 5 min. Then, the solid-liquid separated mineral samples were dried in vacuum before FTIR analyses.

Results and Discussion
Bo et al. reported that sodium silicate forms hydrophilic colloidal silicic acid, which is selectively adsorbed on the surface of calcite and fluorite, and that, in particular, the formation of hydrophilic colloids became smoother in their study when the mixing ratio of sodium silicate and oxalic acid was 3:1 [17]. Based on this finding, the depressant that contains the sodium silicate and oxalic acid in a ratio of 7.5:2.5, 5:5, 2.5:7.5, and 0:10 was used to investigate the effect of the depressants on the floatability of scheelite, calcite and fluorite. Figure 2 shows the floatability of the minerals increased, but the selectivity decreased with decreasing the ratio of sodium silicate.  The difference in floatability was the highest at the 7.5:2.5 sodium silicate-oxalic acid mixing ratio, and the result shows a good agreement with the conventional study [17], where the 3:1 ratio was suggested as an optimum condition. At this ratio of 7.5:2.5, however, the floatabilities of scheelite, calcite and fluorite were 36%, 32% and 29%, respectively. Thus, satisfactory selection efficiency could not be expected when using the depressant of sodium silicate and oxalic acid.
The combination of sodium silicate and ferrous sulfate (SF2) was proposed as a depressant for the selective flotation of scheelite [15,16]. The depressant SF2 was prepared in a ratio of 6:4 to 9:1 of 5% sodium silicate and 1% ferrous sulfate. The flotation tests with SF2 were performed under the following conditions: 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate, 200 g/ton SF2 depressant, 50 mL/min air injection rate, 5 min flotation time, and pH 8, and the results are shown in Figure 3.  The floatability of scheelite decreased but those of calcite and fluorite increased with increasing the ratio of ferrous sulfate. The precipitation was observed in the solution, and the amount of precipitate increased with the ratio of ferrous sulfate. Iron component was detected in the precipitate and iron precipitated due to the oxidation of ferrous to ferric ions by aeration because ferric ion could precipitate over pH 3.5 [18]. At a ratio of 8:2 for sodium silicate and ferrous sulfate, the floatabilities of scheelite, calcite and fluorite were 40.8%, 25.6% and 30.2%, respectively, and the selectivity was the largest at this ratio. The selectivity decreased with increasing the ratio of ferrous sulfate because the effect of ferrous sulfate addition diminished due to the precipitation.
The effects of SF2 depressant dosage on the floatability of scheelite, calcite, and fluorite was investigated under the following conditions: 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate 0-1400 g/ton SF2 depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL/min air The floatability of scheelite decreased but those of calcite and fluorite increased with increasing the ratio of ferrous sulfate. The precipitation was observed in the solution, and the amount of precipitate increased with the ratio of ferrous sulfate. Iron component was detected in the precipitate, and iron precipitated due to the oxidation of ferrous to ferric ions by aeration because ferric ion could precipitate over pH 3.5 [18]. At a ratio of 8:2 for sodium silicate and ferrous sulfate, the floatabilities of scheelite, calcite and fluorite were 40.8%, 25.6% and 30.2%, respectively, and the selectivity was the largest at this ratio. The selectivity decreased with increasing the ratio of ferrous sulfate because the effect of ferrous sulfate addition diminished due to the precipitation.
The effects of SF2 depressant dosage on the floatability of scheelite, calcite, and fluorite was investigated under the following conditions: 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate, 0-1400 g/ton SF2 depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL/min air injection rate, 5 min flotation time, and pH 8, and the results were shown in Figure 4. With increasing SF2 dosage, the floatability of scheelite decreased gradually while those of calcite and fluorite did sharply. That is, when the SF2 dosage increased from 200 to 1200 g/ton, the floatability of scheelite decreased by 7% (from 40.8 to 33.6%) but the floatability of calcite decreased sharply by 21% (from 25.6 to 4.6%) and that of fluorite decreased sharply by approximately 20% (from 30.2 to 10.6%). When the SF2 dosage was 1400 g/ton, the floatability values of calcite and fluorite were around 5%, suggesting an excellent suppressing effect, but that of scheelite was also severely suppressed to around 20%. Since the selectivity is the largest at 1200 g/ton of SF2 dosage, the SF2 dosage was fixed at 1200 g/ton in the following tests. decreased by 7% (from 40.8 to 33.6%) but the floatability of calcite decreased sharply by 21% (from 25.6 to 4.6%) and that of fluorite decreased sharply by approximately 20% (from 30.2 to 10.6%). When the SF2 dosage was 1400 g/ton, the floatability values of calcite and fluorite were around 5%, suggesting an excellent suppressing effect, but that of scheelite was also severely suppressed to around 20%. Since the selectivity is the largest at 1200 g/ton of SF2 dosage, the SF2 dosage was fixed at 1200 g/ton in the following tests. The generally known order of addition of flotation reagents is to add a depressant before a collector. The Ca-bearing minerals were recovered through bulk flotation using the collector sodium oleate, and then selective flotation was performed for scheelite from the bulk flotation product. Therefore, the effect of the order of flotation-reagent addition on the floatability was investigated under the following conditions: 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate, 1200 g/ton SF2 depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL/min air injection rate, 5 min flotation time, and pH 8. The results are shown in Figure 5. The generally known order of addition of flotation reagents is to add a depressant before a collector. The Ca-bearing minerals were recovered through bulk flotation using the collector sodium oleate, and then selective flotation was performed for scheelite from the bulk flotation product. Therefore, the effect of the order of flotation-reagent addition on the floatability was investigated under the following conditions: 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate, 1200 g/ton SF2 depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL/min air injection rate, 5 min flotation time, and pH 8. The results are shown in Figure 5.
decreased by 7% (from 40.8 to 33.6%) but the floatability of calcite decreased sharply by 21% (from 25.6 to 4.6%) and that of fluorite decreased sharply by approximately 20% (from 30.2 to 10.6%). When the SF2 dosage was 1400 g/ton, the floatability values of calcite and fluorite were around 5%, suggesting an excellent suppressing effect, but that of scheelite was also severely suppressed to around 20%. Since the selectivity is the largest at 1200 g/ton of SF2 dosage, the SF2 dosage was fixed at 1200 g/ton in the following tests. The generally known order of addition of flotation reagents is to add a depressant before a collector. The Ca-bearing minerals were recovered through bulk flotation using the collector sodium oleate, and then selective flotation was performed for scheelite from the bulk flotation product. Therefore, the effect of the order of flotation-reagent addition on the floatability was investigated under the following conditions: 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate, 1200 g/ton SF2 depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL/min air injection rate, 5 min flotation time, and pH 8. The results are shown in Figure 5. As shown in Figure 5, the floatability of scheelite was higher than those of calcite and fluorite. The floatability of calcite and fluorite reduced when the depressant was added before the collector, while that of scheelite was enhanced by adding the depressant before the collector, where the selectivity became larger. Therefore, the effect of collector, which was added in the bulk flotation, should be considered to obtain the better selectivity of scheelite. Based on the results, the optimum flotation conditions with high selection efficiency for scheelite are 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate, 1200 g/ton SF2 depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL/min air injection rate, 5 min flotation time, and pH 8, and the addition order of flotation reagents is to add the depressant before the collector. Figures 6-8 show the zeta potential measurement results for scheelite, calcite, and fluorite with or without 1 × 10 −3 M sodium oleate (collector) and 1200 g/ton SF2 (depressant). Each measurement was performed after 5 min conditioning when the collector or the depressant was added, and 1 × 10 −3 M NaCl was added as a supporting solution. In the zeta potentials of scheelite, calcite, and fluorite without the collector and depressant, the measurement results showed that scheelite did not have a point of zero charge (PZC), but that the points of zero charge for calcite and fluorite are 8.6 and 4.7, respectively. Figure 6 indicates the Zeta potential results of scheelite with pH, which shows a good agreement with conventional studies [14,19]. The zeta potentials of scheelite without the collector and depressant are negatively charged over the entire pH range (2)(3)(4)(5)(6)(7)(8)(9)(10)(11), and the zeta potentials are lower negatively when the flotation reagents are added. Since the zeta potentials of scheelite with the collector or with the collector and depressant show similar behaviors over the entire pH range, the addition of depressant does not have a significant effect on the adsorption of the collector on the surface of scheelite.
As shown in Figure 5, the floatability of scheelite was higher than those of calcite and fluorite. The floatability of calcite and fluorite reduced when the depressant was added before the collector, while that of scheelite was enhanced by adding the depressant before the collector, where the selectivity became larger. Therefore, the effect of collector, which was added in the bulk flotation, should be considered to obtain the better selectivity of scheelite. Based on the results, the optimum flotation conditions with high selection efficiency for scheelite are 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate, 1200 g/ton SF2 depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL/min air injection rate, 5 min flotation time, and pH 8, and the addition order of flotation reagents is to add the depressant before the collector. Figures 6-8 show the zeta potential measurement results for scheelite, calcite, and fluorite with or without 1 × 10 −3 M sodium oleate (collector) and 1200 g/ton SF2 (depressant). Each measurement was performed after 5 min conditioning when the collector or the depressant was added, and 1 × 10 −3 M NaCl was added as a supporting solution. In the zeta potentials of scheelite, calcite, and fluorite without the collector and depressant, the measurement results showed that scheelite did not have a point of zero charge (PZC), but that the points of zero charge for calcite and fluorite are 8.6 and 4.7, respectively. Figure 6 indicates the Zeta potential results of scheelite with pH, which shows a good agreement with conventional studies [14,19]. The zeta potentials of scheelite without the collector and depressant are negatively charged over the entire pH range (2)(3)(4)(5)(6)(7)(8)(9)(10)(11), and the zeta potentials are lower negatively when the flotation reagents are added. Since the zeta potentials of scheelite with the collector or with the collector and depressant show similar behaviors over the entire pH range, the addition of depressant does not have a significant effect on the adsorption of the collector on the surface of scheelite.    As shown in Figures 7 and 8, the zeta potentials of the calcite and fluorite only with the collector are the lowest at each pH compared with the zeta potentials of the minerals with or without the collector and depressant. The zeta potentials of calcite and fluorite with or without the collector and depressant show similar behaviors with increasing pH, which indicates that the addition of the SF2 depressant interfered the adsorption of the collector on the surface of minerals. Therefore, the addition of SF2 could enhance the selectivity of scheelite flotation.
FTIR analysis was performed to examine the adsorption of the flotation reagents on the surface of the minerals conditioned at the optimum flotation conditions, and the results were shown in Figures 9-11 for scheelite, calcite, and fluorite, respectively. Figure 9 shows the FTIR analysis results for scheelite, where the spectrum of sodium oleate forms the bands at 1559.1 and 2922.6 cm −1 . The band at 2922.6 cm −1 is known to be formed by the stretching vibrations of CH2 and CH3 [17], and the band at 1559.1 cm −1 is caused by the carbonyl mode (C=O), which mainly indicates a physically adsorbed species [7,20,21]. The spectrum of scheelite without flotation reagents (NaO and SF2) shows the bands in the 650-1000 cm −1 range, and, when the scheelite sample was conditioned in the 1 × 10 −3 M sodium oleate solution, a band was observed at 2871.3 cm −1 , which is similar to the 2922.6 cm −1 of sodium oleate. In the experiment where the SF2 depressant was added before sodium oleate, a band was formed at 2900.7 cm −1 . These results suggest that the chemisorption of sodium oleate on the scheelite is maintained regardless of the addition of SF2. However, in the cases of calcite and fluorite, As shown in Figures 7 and 8, the zeta potentials of the calcite and fluorite only with the collector are the lowest at each pH compared with the zeta potentials of the minerals with or without the collector and depressant. The zeta potentials of calcite and fluorite with or without the collector and depressant show similar behaviors with increasing pH, which indicates that the addition of the SF2 depressant interfered the adsorption of the collector on the surface of minerals. Therefore, the addition of SF2 could enhance the selectivity of scheelite flotation.
FTIR analysis was performed to examine the adsorption of the flotation reagents on the surface of the minerals conditioned at the optimum flotation conditions, and the results were shown in Figures 9-11 for scheelite, calcite, and fluorite, respectively. Figure 9 shows the FTIR analysis results for scheelite, where the spectrum of sodium oleate forms the bands at 1559.1 and 2922.6 cm −1 . The band at 2922.6 cm −1 is known to be formed by the stretching vibrations of CH 2 and CH 3 [17], and the band at 1559.1 cm −1 is caused by the carbonyl mode (C=O), which mainly indicates a physically adsorbed species [7,20,21]. The spectrum of scheelite without flotation reagents (NaO and SF2) shows the bands in the 650-1000 cm −1 range, and, when the scheelite sample was conditioned in the 1 × 10 −3 M sodium oleate solution, a band was observed at 2871.3 cm −1 , which is similar to the 2922.6 cm −1 of sodium oleate. In the experiment where the SF2 depressant was added before sodium oleate, a band was formed at 2900.7 cm −1 . These results suggest that the chemisorption of sodium oleate on the scheelite is maintained regardless of the addition of SF2. However, in the cases of calcite and fluorite, as shown in Figures 10 and 11, respectively, the spectra of calcite and fluorite with the collector (NaO) show the band at 2931.5 and 2910.4 cm −1 , which are due to the stretching vibration of sodium oleate, indicating good adsorption, but they disappeared in the minerals with the collector after the addition of the depressant (SF2). These results indicate that the addition of SF2 depressant prevents the adsorption of the NaO collector, which shows a good agreement with the experiment results of zeta potential measurement. Therefore, the addition of SF2 depressant could enhance the selectivity of scheelite over Ca-bearing minerals such as calcite and fluorite.
indicating good adsorption, but they disappeared in the minerals with the collector after the addition of the depressant (SF2). These results indicate that the addition of SF2 depressant prevents the adsorption of the NaO collector, which shows a good agreement with the experiment results of zeta potential measurement. Therefore, the addition of SF2 depressant could enhance the selectivity of scheelite over Ca-bearing minerals such as calcite and fluorite.   of the depressant (SF2). These results indicate that the addition of SF2 depressant prevents the adsorption of the NaO collector, which shows a good agreement with the experiment results of zeta potential measurement. Therefore, the addition of SF2 depressant could enhance the selectivity of scheelite over Ca-bearing minerals such as calcite and fluorite.

Conclusions
The addition of ferrous sulfate as a depressant for Ca-bearing minerals such as calcite and fluorite during scheelite flotation was investigated using Hallimond-tube flotation tests, zetapotential measurement and FT-IR analyses.
The flotation tests indicate that the selectivity of scheelite recovery was the largest over calcite and fluorite under the following conditions: 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate, 1200 g/ton SF2 (sodium silicate and ferrous sulfate) depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL/min air injection rate, 5 min flotation time, and pH 8. The selectivity of scheelite flotation increased when the amount of SF2 depressant addition increased to 1200 g/ton, but it decreased by adding 1400 g/ton SF2, which would result from the precipitation of iron components.
In the zeta potential and Fourier-transform infrared (FTIR) analyses results of scheelite, calcite, and fluorite conditioned under the optimum conditions, the adsorption of NaO (collector) on the surface of scheelite was observed regardless of SF2 depressant addition, while the zeta potentials of calcite and fluorite and FT-IR spectra with NaO/SF2 show similar behavior with calcite and fluorite without any floatation reagents. These results indicate that the addition of SF2 prevents the adsorption of NaO (collector) on the surface of calcite and fluorite, which are regarded as tailing during scheelite flotation, so the selectivity of scheelite flotation could be enhanced by adding the depressant consisting of sodium silicate and ferrous sulfate.

Conclusions
The addition of ferrous sulfate as a depressant for Ca-bearing minerals such as calcite and fluorite during scheelite flotation was investigated using Hallimond-tube flotation tests, zeta-potential measurement and FT-IR analyses.
The flotation tests indicate that the selectivity of scheelite recovery was the largest over calcite and fluorite under the following conditions: 0.5 g sample, 50 g/ton AF65, 1 × 10 −3 M sodium oleate, 1200 g/ton SF2 (sodium silicate and ferrous sulfate) depressant with the 8:2 ratio of sodium silicate and ferrous sulfate, 50 mL/min air injection rate, 5 min flotation time, and pH 8. The selectivity of scheelite flotation increased when the amount of SF2 depressant addition increased to 1200 g/ton, but it decreased by adding 1400 g/ton SF2, which would result from the precipitation of iron components.
In the zeta potential and Fourier-transform infrared (FTIR) analyses results of scheelite, calcite, and fluorite conditioned under the optimum conditions, the adsorption of NaO (collector) on the surface of scheelite was observed regardless of SF2 depressant addition, while the zeta potentials of calcite and fluorite and FT-IR spectra with NaO/SF2 show similar behavior with calcite and fluorite without any floatation reagents. These results indicate that the addition of SF2 prevents the adsorption of NaO (collector) on the surface of calcite and fluorite, which are regarded as tailing during scheelite flotation, so the selectivity of scheelite flotation could be enhanced by adding the depressant consisting of sodium silicate and ferrous sulfate. Funding: This study was carried out as a research project for the "Establishment of WO 3 flotation concentration conditions in tungsten tailings" of Mineral Reclamation Corporation in 2015. The authors would like to express their sincere gratitude for the support given by such corporation.