Received 18 April 2016; accepted 20 May 2016; published 23 May 2016
The basic concept of native floatability of a mineral is that a naturally hydrophobic surface results when cleavage or fracture occurs between crystal layers which are held together by weak residual bonds―van der Waals forces. It is recognized that the crystalline structure is one of the main factors that determines the wettability of layered silicate minerals such as talc. Talc is a hydrous magnesium silicate, Mg3Si4O10(OH)2 , which is related to the sheet structure of the phyllosilicate (Yehia and Al Wakeel, 2000  ). However, natural floatability of talc is closely related to its three-layer sheet crystal structure (Fuerstenau et al., 2003  and Fuerstenau et al., 2007  ). Positive charge of magnesium layer is compensated from two sides by silicon tetrahedral layers creating the lack of surface polarization responsible for its natural hydrophobicity.
Talc is considered as anisotropic mineral, which when broken, two types of surfaces are formed, one resulting from the easily broken layers and the other resulting from the rupture of ionic bonds within these layers (Ivan et al., 2013  ). The former are termed as “faces”, holding together by weak van der Waals forces, which are hydrophobic and consist of inert −Si−O−Si− groups. The latter are termed as “edges”, which are hydrophilic, consisting of SiOH and MgOH groups, and are held together by ionic bond. However, the edges which are created by rupturing of the covalent bonds are spontaneously reacting with water to form oxidic sites, for example, SiO− that is hydrophilic. On the other hand, the rupture of talc crystals along the faces generates non-polar surfaces, which are characterized by a low energy (El-Midany and Ibrahim, 2010  ; Mierczynska and Beattie, 2013  ). This allows talc to exhibit an inherent hydrophobicity, which is the basis of the separation of talc, by flotation, from other ore constituents in mineral industry. However, the heterogeneous character of talc surface particles has a particular importance in flotation. The face/edge relationship, which depends on the particle size, determines the natural floatability of this mineral (Mierczynska and Beattie, 2013  ). Besides, the solution pH affects the talc floatability. In acidic and alkaline solution, water molecules would hydrate the negatively charged sites (SiO−) on the edges and hence, the talc surface would be more hydrophilic (Yehia and Al Wakeel, 2000  ). At neutral pH, talc surface has a weak affinity for water molecules and air bubbles readily displace any weakly adsorbed water on the uncharged surface.
The size of an individual talc platelet (a few thousand elementary sheets) can vary from approximately 1 micron to over 100 microns depending on the conditions of formation of the deposit. It is this individual platelet size that determines a talc’s lamellarity. A highly lamellar talc will have large individual platelets whereas a microcrystalline talc will have small platelets. The elementary sheets are stacked on top of one another, like flaky pastry, and because the binding forces (Van der Waal’s forces) linking one elementary sheet to its neighbors are very weak, the platelets slide apart at the slightest touch, giving talc its characteristic softness.
Different methods and approaches were investigated by researchers worldwide for the processing of talc- carbonate ores with different proportions of talc, magnesite and dolomite (Houot et al., 1995  ; Marabini et al., 1996  ; Weber, 1998  ; Karlsen et al., 2000  ; Derco and Memeth, 2002  ; Ahmed et al., 2011  ), and CANMET of Canada carried out an intensive R & D work on so many talc and pyrophyllite varieties by applying a wide array of frothers and collectors (Andrews, 1994  ; Wyman, 1973  ).
Talc occurs in the form of veins or lenses in many localities in South and Central Eastern Desert of Egypt (EGSMA, 1991; MQA, 2004). Generally, talc is obtained by either open pit or underground mining. The cost of overburden removal in open pit mining is a major factor in talc mining and waste rock to ore ratios of 40:1 are not uncommon. Processing of low grade varieties is becoming unequivocal and few studies are carried out, on a laboratory scale, to separate both carbonate and iron oxide gangue minerals (Yousef et al., 1995  ; El-Wakeel, 1996  ; Ibrahim, 2003  ; Selim, A.Q., Ibrahim, S.S. and El Manawi, A.W., 2005  ; Hassan et al., 2007  ). This article is a step on the same road for the maximum utilization of the Egyptian talc deposits.
2. Material and Methods
A technological talc sample, about five tonnes, representing Bir Meseh, south of Shalatin locality of the Eastern Desert of Egypt, was kindly supplied by the National Service Sector, Ministry of Defense for investigation. Geologically, the talc deposits of Shalatine locality occur as large fragments of variable sizes enclosed in mafic-ultramafic matrix, or occur as lenses and pockets associating metasediments (Selim et al., 2005). The two associations of talc deposits are restricted to NW-SE shear zones. The rocks within the shear zones are highly brecciated, deformed and extensively altered. The delivered sample represents the previous mentioned genetic types of talc.
Ore characterization was carried out by overall analyses, using XRF model Axios advanced-panalytical and ore microscopy. Attrition scrubbing of the −11 mm crushed ores was carried out in the laboratory using the “Denver D12” flotation cell. In this process, the attritioned product was screened on a 74 μm screen and both oversize and undersize fractions were weighed and analyzed for loss on ignition, L.O.I. This latter size fraction was directed to further fine grinding to improve the degree of liberation of minerals, i.e. until 100% less than 22 μm. Flotation of this superfine feed was conducted in the same conventional subaeration flotation cell. Aerofroth 71 was used as a frother for talc whereas soda ash was tested as selective depressant of carbonate. In the meantime, quaternary amine was employed in the laboratory as a selective collector for talc.
3. Results and Discussion
3.1. Sample Characterization
Complete chemical analysis of the talc sample, supported with the results of the XRD (Figure 1), indicates that it is high in undesirable ingredients, e.g. iron oxides and CaO (Table 1). It is characterized by low MgO content (25.40%), low SiO2 (45.71%), high CaO content (6.32%) and high L.O.I. (11.35%) indicating its low grade (Table 1).
Figure 1. XRD patterns of original Shalatin talc sample.
Table 1. Complete chemical analysis of original Shalatin talc sample.
Mineralogical investigation by XRD, using EVA software, shows that the main sample constitution is talc (48%), dolomite (27%), calcite (6%), chlorite, serpentine, sphene and iron oxides (19%) (Figure 1). Petrography study of the talc sample reveals that the talc sample includes four main lithological groups: steatite group, talc- carbonate group, talc-chlorite group, and ferruginated talc group ( Plate 1 ). This study shows also that the talc sample is characterized by fine-grained talc fragments with apple green color, enclosed in white color harder carbonate matrix.
Plate 1. Petrographic investigation of Shalatin talc sample.
Figure 2. Thermal analysis of original Shalatin talc sample.
On the other hand, Figure 2 illustrates the thermal analysis of the talc sample. Despite the single endothermic peak characteristic of talc at about 950˚C - 1000˚C, the sample demonstrates a sharp endothermic reaction peak at 600˚C associated with an exothermic reaction between 800˚C and 900˚C which is related to dolomite mineral (Figure 2). This corroborates with both the high L.O.I. and CaO contents. Chlorite presence was also confirmed by both XRD and DTA analyses.
High grade steatite, the only mineral shown is talc (Medium grained talc occurs in narrow shear zone parallel to the main foliation planes), B―Photomicrograph of exclusively sheared talc (Notice, the shear foliations and the offset in coarse talc flake “Tc” (Crossed Nicols), C―Coarse flakes of talc “Tc” attacking coarse carbonate crystals “Ca” and corroding it, talc-carbonate rock (Crossed Nicols), D―Photomicrograph shows growth of well developed talc flakes at the expense of mega calcite crystal (Crossed Nicols), E―Microscopic banded structure in the talc-chlorite rock, the upper band rich in opaques and iron staining, the middle band is mainly talc, the lower band consists of talc and chlorite intergrowth (Crossed Nicols), and F-Medium-grained talc contains large amount of opaques (Plane Polarized light).
3.2. Attrition Scrubbing of the Crushed Ores
This technique was suggested as a substitute of the conventional ball or rod milling in talc beneficiation plants by taking advantage of the friable nature of talc, being at the top of Moh’s scale. The objective of this process was to achieve preconcentration of talc by fractional grinding from the harder carbonate impurities. Optimization of the process in the laboratory including verification of the attrition speed, attrition time and pulp density are shown in Figures 3-5.
A. Effect of Changing Motor Speed
Figure 3 illustrates the effect of varying the attritioning motor speed on both the yield and grade of both the under- and oversize products at 50% solid and an optimum attritioning time of 60 min. Evidently, the substantial increase in the process recovery from 69.3% at a motor speed of 1500 rpm to 79.5% at a speed of 2100 rpm was accompanied by an incremental increase in the preconcentrate % L.O.I.
B. Effect of Changing Attritioning Time
At 50% solid, 1500 rpm motor speed and 15 min. attritioning time about 50% by weight of the crushed rock reports to the −200 mesh size with a L.O.I. reaching 8.2% as compared with 14.9% in the oversize product. After 60 min. attritioning time, the weight percent of the talc preconcentrate, −200 mesh, reaches about 69.3% without a pronounced decrease in its grade (Figure 4). This technique, which sounds unconventional in talc processing
Figure 3. Effect of varying impeller speed on attrition scrubbing of talc sample.
Figure 4. Effect of attrition time on talc sample (at 50% solid, 1500 rpm).
Figure 5. Effect of varying solid/liquid ratio on attrition scrubbing of talc sample (at 1500 rpm, 60 min).
technology, looks encouraging in rejecting about 48% of the associating hard carbonaceous impurities (assaying 17.6% L.O.I.) from Shalatin talc sample.
C. Effect of Changing Pulp Density
Figure 5 shows that increasing the% solid in the pulp from 50% to 70% at a motor speed of 1500 rpm and 60 min. attritioning time, the % yield of the talc preconcentrate increases to an optimum of 74.7% at 60% solid with a L.O.I. of 8.5%. But the process becomes, almost, impractical by increasing the% solid in the pulp more than that due to consolidation. Therefore, a talc preconcentrate having about 8.4% L.O.I. was obtained by attrition scrubbing of the −11 mm crushed ore at 60% solid, 1500 rpm motor speed and 60 min. attritioning time, at a yield of about 74.7%.
Carbonate Separation by Flotation
Although the talc surface has a net hydrophobic character, two additional factors must be considered in order to fully appreciate its flotation chemistry. First, there may be a significant number of hydrophilic sites on the talc surface. The second factor is that during size reduction other planes of the crystal may be exposed which do not have a net hydrophobic character. However, due to the anisotropic structure of talc, three types of surfaces will be produced: hydrophobic (faces), partially hydrophobic (faces and edges) and hydrophilic (edges). Accordingly, flotation of talc pre-concentrate for separation of carbonate was studied in the laboratory within three complementary routes as follows:
a―Natural floatability of talc will be achieved for hydrophobic surfaces (faces).
b―Enhanced natural floatability of talc by using a frother for partially hydrophobic surfaces.
c―Conventional talc flotation using a collector (quaternary ammonium salt) for hydrophilic surfaces (edges) in presence of selective carbonate depressant (soda ash).
1. Natural Floatability of Talc
The effect of changing the impeller speed on the natural floatability of talc while changing the pulp pH showed modest recovery of the process and its independence of pH (Table 2). This results in a concentrate assaying about 6% L.O.I. with a recovery of about 32% at an impeller speed of 1200 rpm.
2. Addition of Frother for Partially Hydrophobic Surfaces
Talc mineral, as a predominantly hydrophobic solid, may still possess a number of polar sites. When a meniscus recedes from such a surface it leaves few (if any) isolated water molecules on non-polar sites but clusters of them are around polar sites. This concept explains why talc mineral needs only a fraction of a monolayer of frother to render it floatable. Floatation results as a function of frother concentration at pH 8 (the optimum pH of the natural floatability) are shown in Table 3. By adding Aerofroth 71, the recovery increases significantly with increasing frother concentration but this happens on the prejudice of the grade of the concentrate. By using 300 g/t of the frother a talc concentrate assaying 6.7% L.O.I. was obtained with a yield recovery of 64.71%.
3. Talc Flotation using a Collector for Hydrophilic Surfaces
When using quaternary amine as a selective talc collector, the grade of concentrate is not encouraging (Table 4). Talc concentrate assaying 7.78% L.O.I. was obtained with a yield recovery of 86.88%. But in the presence of soda ash as a selective carbonate depressant, flotation indices relatively improve (Table 5). Cleaner talc concentrate assaying 6.5% L.O.I. but with a lower recovery of 56.35% was obtained using 0.5 kg/t of soda ash and 0.2 kg/t quaternary amine at natural pH.
4. Stepwise Flotation of the −74 μm Size Fraction
According to the above results, stepwise flotation of the −74 μm size fraction was conducted including natural
Table 2. Results of impeller speed of the attrition process on talc sample (−74 um) natural floatability.
Table 3. Effect of Aerofroth 71 addition on talc sample (−74 um) floatability.
Table 4. Flotation using quaternary ammonium salt as a collector.
Table 5. Effect of using soda ash for carbonate depressants in talc flotation using quaternary ammonium salt as a collector.
floatability of talc, addition of frother, collector and depressant. Table 6 shows that three concentrates of talc were produced assaying 5.83%, 6.33% and 7.21% L.O.I. with yield recoveries of 24.22%, 23.17% and 7.32%, respectively.
5. Flotation of the −22 μm Size Fraction
Further grinding of the flotation feed sample was decided to improve these results. Table 7 shows the results of a step flotation of the −22 μm superfine talc pre-concentrate. Using the same conventional type “Denver D 12” flotation cell, this latter superfine feed responded easily to natural floatability without the use of a collector where a first concentrate was obtained assaying 6.6% L.O.I. with a yield recovery of 28.48%. By using soda ash and frother, second concentrate assaying 7.60% L.O.I. was obtained with a yield recovery of 34.43% (Table 7). The needle-like crystals of talc concentrate is shown in Figure 6.
Figure 6. SEM photographs of Shalatine talc concentrate. (a) Needle-like crystals of talc; (b) Talc blades arranged in sheet structure.
Table 6. Step flotation results of the −74 μm scrubbed talc sample.
Table 7. Stepwise flotation results of the −22 μm scrubbed talc sample.
Attrition scrubbing of the −11 mm crushed talc sample was proved to be an unconventional process for separation of the harder carbonate gangue minerals in the +74 μm oversize product and in the production of talc superfine −22 μm as well. Minimization of the carbonate content of talc pre-concentrate by multistage flotation was optimized in the laboratory through natural floatability of the talc and application of a selective carbonate depressant. Fine grinding of the talc to less than 22 μm was imperative to improve the recovery of the process. Flotation of such superfine talc using the conventional “Denver” sub-aeration flotation cell proceeded well with the addition of frother and carbonate depressant without the addition of talc collector. A concentrate assaying 54% SiO2, 33.56% MgO, 1% Fe2O3, 1.44% CaO, and 6.9% L.O.I. with a recovery of 62.91% was obtained. This satisfies the world market requirements for plastics, paints, ceramics and paper also since its brightness is 89.0 and its oil absorption is 20. Evaluation of other flotation products indicates their suitability for both carpets and roofing purposes.
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