1. Introduction
Serious environmental risk are associated with mining wastes in a form of liquid and solid waste, which contain potentially toxic elements such as cadmium (Cd), copper (Cu), zinc (Zn), lead (Pb), chromium (Cr), arsenic (As), and vanadium (V) [
1,
2,
3]. Among these environmental concerns are the solubilization of sulphides from pyritic mine tailings, which often results in acid mine drainages [
4,
5].
The Gauteng province of South Africa is characterized by numerous mine tailing dumps which are a result of previously active mining activities. Several decades of mining activities in the Gauteng Province of South Africa has had and continues to have a negative impact on ecosystems through the pollution of soils and water with high levels of potentially toxic metals such as As, Pb, and Al, as is the case with the old gold mine tailings in Blesbokspruit, Ekurhuleni South Africa [
6,
7,
8,
9]. Previous studies have reported cases of health-related complications among dwellers who reside nearer to these mine tailing sites as a result of the contamination of agricultural soils, water sources, and atmospheric air by these mine tailings and effluents [
10,
11,
12,
13,
14,
15,
16].
Most gold mine tailings are composed mainly of industrial sand (i.e., silica) and silica sand is best described as a granular material that is composed of majorly quartz and trace amounts of coal, clay and other minerals [
17]. In some instances, it is referred to as either quartz or industrial sand and is widely applied in many engineering applications. When silica sand is present in metallic materials, it could serve as a source of crevice corrosion on such metals. Silica sand is mechanically and chemically purified quartz sand, from which various products are made using processes such as hydro classification and thermal treatments [
17]. The industrial application of silica sand is largely dependent on parameters such as the grain size, refractories, texture, and shape of the sample to be used [
18]. Over the years, silica sand has remained a vital component in various engineering projects and applications including building product and abrasive, glass making and hydraulic fracturing of oil wells [
17,
18]. The essential Silicon Dioxide (SiO
2) required for glass formulation is provided by silica sand, which makes silica the basic component in all forms of glass. Although the production of glass requires a variety of different materials, silica represents over 75% of the final product [
19]. Silica is hard, chemically inert and has a high melting point, which could be linked to the strength of the bonds between the atoms. These are prized qualities in applications like foundries and filtration systems. Quartz is the most common silica crystal; it may be transparent to translucent and has a vitreous luster, hence it is used in glassmaking and ceramics.
In 2003, South Africa based on silica as a mineral was reported to have 20 producers, 3 dormant mines, 2 decommissioned mines and 5 fume silica producers with most of the mining operations being in an opencast form [
20]. The extracted silica sands are mostly from pegmatites, quartz massifs, veins or quartzites which are in the Western Cape, Mpumalanga and Gauteng regions [
21]. The United States of America recorded an increase in silica sand production between 1996 and 1997 from 2.5 to 28.5 metric tons of which 37% was used in the manufacture of glass, 23% as foundry sand, 6% for hydraulic fracturing, and 5% as abrasives [
22]. Continued usage of different forms of glass by individuals and organizations has necessitated an increasing global demand for the number of glass plants and industries [
23,
24,
25,
26].
As a waste disposal mechanism, the process of vitrification which involves the immobilization and encapsulation of radioactive and other types of hazardous materials at high temperatures (between 1100–1600 °C) result in such materials melting into a liquid which, on cooling, transforms to an amorphous, glass-like solid [
27]. This process could be employed if the obtained glass is recycled in high-value applications [
28]. A herald of materials such as industrial wastes [
29], fly ashes [
30], sewage sludge [
31] and pyrolized shales [
32] are involved in some of these applications. The usage of the aforementioned materials is advantageous in that they have undergone diverse industrial processes that leave them with good homogeneity and finer particle size.
The production of glass using gold mine tailings as a major raw material could help decrease the volume of waste exposed to atmospheric processes thus averting ecological pollution while at the same time, contributing to economic earnings. Reports from previous studies on the physicochemical composition of mine tailings generated during the extraction of gold show close features with those frequently used raw materials in glassmaking processes [
33,
34]. The various environmental issues resulting from gold mine tailings had called for several scientific investigations to resolve the environmental burden that emanates from mine tailings. Some tailings dams have been partially or completely reclaimed leaving contaminated footprints. Some studies evaluated the potential to reuse mine tailings to produce bricks or ceramics [
35,
36]. In a recent study on gold tailings dam, it was found that the topsoil was highly acidified and only a minor portion of contaminants was bioavailable with the potential harm of phytotoxic contaminants such as Co, Ni, and Zn complicating rehabilitation measures as they limit the soil function [
37]. In addition, soil samples from this study area in a recent investigation revealed trace element concentrations, which often exceeded background concentrations in soils [
38]. Therefore, in a bid to extract value from gold mine tailings, this study was aimed at the quantification and qualification of gold mine tailings as a potential cheap silica source for the manufacture of glass.
2. Materials and Methods
2.1. Site Description and Sample Collection
The study area (
Figure 1) was situated in the eastern region of the East Rand Basin within the Blesbokspruit catchment (26°10′12″S, 28°27′52″E) in the Gauteng province of South Africa.
The materials used in this study included gold mine tailings (MT) that were logically collected from four different spots at an interval of 100 m for a fair representation of the area. Each sample was separately and carefully collected using a disinfected auger to drill vertically downwards to a depth of 20 cm. This process was repeated at the different spots before transferring approximately 10 kg of each tailings material in labelled polyethylene bags designated MT1–MT4 for the purposes of identification. The tagged tailings samples were transported to the laboratory for preparation and further analysis.
2.2. Sieve Analysis (Granulometric Distribution)
Analysis of the grain-size of the silica sand from MT samples was determined using an electric sieving machine model (Filtra Vibracion SL–FTL 0200) operated under conditions of 230 V (50/60 Hz) 2 A–400 W with a standard set of sieves. This was done to provide information on the percentage ideal fraction of the sample. 250 g of MT were weighed from each sample bag and thoroughly mixed in a pan for homogeneity to make a combined weight of 1000 g. The set of sieves utilised was in the range of (10–150 Mesh), which is equivalent to 2000–105 microns. 1000 g of as received gold tailings material was properly dried in an oven at 100 °C for 30 min to ensure easy separation. Arrangement of the set of sieves was in ascending order of Mesh number with the pan at the bottom for the collection of the finest particles. The dried sample was poured onto the sieve at the top (10 Mesh), covered with a lid, and carefully fixed onto the electric sieve shaker, and subsequently agitated for 15 min. Each sieve beginning from the top was removed and the retained grain size was poured on a clean white paper. A brush was used to ensure all sand particles retained in each sieve were removed onto the paper. The weight of each collected grain size was determined using a Top pan balance model (Sartorius). The percentage retention of grain size was subsequently calculated [
39,
40].
2.3. Determination of Moisture Content and pH
Using a clean crucible, 24.95 g of a composite MT was poured and weighed (W
1) using an analytical balance. With the aid of an oven operated at 105 °C, the crucible containing the sample was heated for 1 h after which the new weight (W
2) was checked. The difference between both weights was determined and expressed as a percentage.
The aim of measuring and controlling the moisture content of the samples is to ensure minimal casting defects that are associated with too much or too little organic materials within silica materials.
The pH of the samples was electronically determined using a Crison multimeter (model MM 41) of ± 0.1 percent sensitivity that was calibrated using a buffer solution [
41]. A representative sample of the tailings sediments was air-dried at room temperature for 6 h. Afterward, using a chemical balance, 25 g of the dried sediments were weighed and poured into a clean beaker. This was done in triplicate. Subsequently, 40 mL of distilled water was added to each beaker using a volumetric cylinder. The solution was stirred with a glass rod and allowed to sit for 30 min. While waiting, the pH meter was calibrated according to the manufacturer’s instructions using two buffer solutions (pH 4.0 and pH 7.0). Before taking the pH readings of the sample, the mixtures were stirred again immediately. Precaution was taken not to place the electrode(s) directly in the sediment layer at the bottom of the beaker. Hence, the electrode(s) were positioned in the solution just above the sediment layer. After the initial reading (use), the electrode(s) were properly triple rinsed with distilled water before testing mixtures in beakers 2 and 3, respectively. The pH readings for the three mixtures were recorded to the nearest 0.1 pH unit and the average reported.
2.4. Determination of Clay Content
2.465 kg of composite MT were introduced into a clean head pan containing water and the mixture thoroughly rubbed using bear hands. Decantation of the brown water from the mixture was done and repeated several times until a clear water colouration was observed in the mixture. The water was then decanted leaving behind wet sand, which was air blown in a pressurized vacuum. The cake-like structure obtained was oven-dried at a temperature of 100 °C for 3 h [
22]. The dried sample was reweighed and expressed as a percentage.
2.5. Grain Morphology Test
The shape of silica sand is an important factor in the manufacture of glass products. Using an electronic microscope model (Olympus BX41), the shape of a composite MT was revealed to ascertain their suitability for glass production.
2.6. Specific Gravity Test
With the aid of a specific gravity tester (model DH-300L), the specific gravity of a composite MT was directly obtained by introducing a very small sample into the equipment, which automatically conducted the test and displayed the values digitally on a visual display unit.
2.7. Determination of Metal Oxides Concentration
X-ray fluorescence (XRF) using a Sequential X-ray Spectrophotometer (XRF; Rigaku ZSX PrismusII) was used to determine the chemical compositions of each MT. The spectrometer was calibrated by a set of more than 60 international standards. 10 g of each of the four collected pulverised MT samples was mixed with a selected binder (PVC dissolved in toluene) before being pelletized using a mould at very high pressure. The pellets were oven-dried at 50 °C for 1 h and subsequently placed in the sample compartment (Analyzer) of the spectrophotometer equipped with an end window 4 KW Rh-anode X-ray tube-powered at a voltage and current of 40 KV and 60 mA for heavy elements while the light elements were at 30 KV and 100 mA, respectively.
2.8. Determination of Mineralogy
Using approximately 5 g of the oven-dried pulverized combination of the four collected representative MT samples, the XRD patterns were determined using a powder X-ray Diffractometer Model Rigaku Ultima IV with CuKα radiation (40 kV and 40 mA) having a scanning range of 4–100° with a 0.017° 2Ɵ step scan and a 50 s measuring time. The XRD aided the determination of the mineralogical composition of the material components and qualitative and quantitative phase analysis of multiphase mixtures. Individual reflection, as displayed by the X-ray diffraction, corresponded to a mineral. With peaks distinctly separated from each other, their heights were used to determine the orientation of identified minerals in the mixture. Mineral analysis of the gold tailings samples by X-ray diffraction was based on the identification of various peaks and by comparison of their relative heights. Respective phase levels were identified as semi-quantitative estimates based on their relative peak heights using a PAN analytical X’Pert High Score software. A wavelength of 1.5406 was employed in the calculation of the diffraction angles.
2.9. Removal of Metals through Leaching
For the best outcomes, two acids were utilised, nitric (HNO
3) and sulphuric (H
2SO
4) [
42,
43]. In the first instance, 40 g of composite MT was weighed and poured into a 250 mL flask which was followed by the introduction of 100 mL of 1M nitric acid. The mixture was agitated at 850 rpm using a magnetic stirrer on a hot plate at a temperature of 80 °C for 60 min. Evaporation was prevented during the process by placing a watch glass over the flask. The samples were filtered using a Whatman filter paper and the residue thoroughly washed using a solution of 10% (2.5M) Sodium hydroxide (NaOH). The leaching process described above was done in duplicate. This was to further remove potential residual impurities from the silica sand surface. A subsequent filtration of the mixture was done followed by drying of the residue in an oven for 3 h [
44,
45]. A similar process was repeated using 100 mL of 1M sulphuric acid and the percentage concentrations of metal oxides in each sample were evaluated using the procedure described in
Section 2.7.
2.10. Qualification Analysis as Glass Sand
The qualification of extracted silica sand as potential glass sand was examined by the making of actual glass using silica from composite MT. Glass products were made from extracted silica sand from composite raw MT, water treated MT obtained from
Section 2.4, and aid-treated samples from
Section 2.9 using CaCO
3 and Na
2CO
3 as fluxing agents. The mixtures were then heated in a muffle furnace at a temperature range of 1500–1600 °C for 2 h. Four batches utilising each category of silica sand with a total mixture of 50 g in the ratio of 3:2:1 for silica, calcium carbonate, and sodium carbonate were used for the glass production. The mixtures were poured in four crucibles and carefully placed in the muffle furnace [
46]. The role of the soda is to reduce the melting point of the silica sand, which in the long run will minimize energy consumption during manufacture. Unfortunately, industrial practices have discovered a drawback to the use of soda as it produces a kind of glass that would dissolve in water. However, the addition of limestone will mitigate the negative effect of soda [
47].
Table 1 describes the batch compositions for glass production.