1. Introduction
Since China is one of the countries with a large number of mineral resources, it is vital to ensure the normal production and continuous running of minerals. As a highly hazardous material, spontaneous combustion of sulfide ore is one of the most serious forms of disasters faced by the metal mining process, which, in addition to causing the loss of mineral resources, leads to serious damage to the environment [
1,
2,
3,
4]. With the increasing depth of minerals mining, in particular, the problem of rising ground temperature is significant, which will lead to a high possibility of spontaneous combustion and fire accidents [
5]. According to statistics, approximately 5–10% of nonferrous metal or polymetallic sulfide ore, and 20–30% of pyrite in China have spontaneous combustion and fire hazards [
6]. The composition of sulfide ores is relatively complex, but the main components that can contribute to spontaneous combustion are pyrite, colloidal pyrite, chalcopyrite, etc. [
7,
8]. Sulfur in these sulfide minerals is the decisive factor for spontaneous combustion in accordance with the mechanism of oxidation and spontaneous combustion [
9,
10]. Therefore, there is a growing focus on research into desulfurization to curb spontaneous combustion.
It has been proven that microbial desulfurization could be applied to sulfur-ore fire fighting, with the advantages of simple operation, cheap raw materials, mild reaction conditions, and less environmental pollution, compared with other technologies. Hence, many scholars have shifted their attention to microbial desulfurization technology [
11].
This technology is currently used in three main fields: petroleum desulfurization, wastewater desulfurization, and coal desulfurization [
12,
13,
14,
15,
16,
17]. Owing to their success, in the field of metal sulfide ores, microbial desulfurization dates back to 1947, when Colmer et al. [
18] found that
Thiobacillus ferrooxidans could accelerate the oxidation of pyrite in coal. Then, Silverman and Stevens began to utilize
Thiobacillus ferrooxidans to remove pyrite from coal [
19,
20]. Recently, some researchers conducted experiments to find a negative correlation between the particle size of sulfide ore and desulfurization [
21]. Additionally, studies have reported on the utilization of surfactants to strengthen the microbial desulfurization effect [
22]. Although various aspects of microbial desulfurization were studied, its efficiency and rate remain low due to the interaction between microorganisms and a relatively complex process on the ore surface, and there is a certain obstruction when the bacterial solution is in contact with the ore [
23].
In recent years, ultrasound has become increasingly popular and widely used as a novel technical tool in mining-related experiments [
24,
25,
26,
27,
28]. Some studies have found that ultrasound could change the potential of the ore and have a crushing effect on selected ore particles, as well as change the pH and temperature of the pulp. Furthermore, it was found that not only the sulfur and iron elements on the surface of the ore were chemically displaced, but the relative density of anions and cations on the surface also changed to some extent by using an ultrasonic treatment on pyrite. Hence, the study showed that ultrasonic treatment could change the hydrophobicity and hydrophilicity of metal sulfides, in addition to significantly improving floatability [
29,
30,
31]. In addition, ultrasonic treatment could greatly improve the interface area for the reaction, increase the effective local concentration of the reactive species, and enhance the mass transfer in the interface area. Therefore, it led to a significant increase in solubility [
32,
33]. Regrettably, there is still a gap in research related to the combination of ultrasound and microorganisms to remove sulfur from sulfide ores.
Therefore, using ultrasonic treatment to enhance the techniques for microbial desulfurization is an important research direction. Based on the above considerations, an experimental scheme was designed with ore samples collected from a pyrite mine in China as the experimental materials. Firstly, a steepest-climb experiment was conducted to quickly reach the response surface center to ensure that the subsequent response surface fitting equation was accurate and valid. Then, a Box–Behnken experiment was performed with a response surface center to find the best factor level combination for the following experiments. Finally, microbial desulfurization experiments of sulfide ores were carried out by ultrasonic treatment, focusing on the effect of particle size, ultrasonic treatment time, and ultrasonic power on desulfurization rate. In summary, this study has important theoretical and practical significance for the sustainability of the minerals.
2. Materials and Methods
2.1. Sources of Ore Samples
Compared with other types of ores, elemental sulfur in sulfide ores is an important internal factor in the occurrence of spontaneous combustion of the ore, and its content will cause sulfide ores to have a faster oxidation rate. Therefore, to prevent spontaneous combustion fire accidents at the root, we need to focus on the high sulfur content of the ore itself.
The presence of elemental sulfur in sulfide ores is in the form of organic and inorganic sulfur, with inorganic sulfur consisting mainly of sulfides (FeS, FeS2) and sulfates (CaSO4, BsSO4, FeSO4). Reducing the occurrence of spontaneous combustion accidents in sulfide ores from the endogenous point of view mainly requires reducing the content of inorganic sulfur (FeS, FeS2) in the ore.
From the microbiological point of view, for inorganic sulfur desulfurization mechanism can be roughly divided into the direct action of bacteria, indirect action of bacteria, and compound action of bacteria. By cultivating bacteria with elemental sulfur as the main nutrient and through a series of reactions, the sulfur content of sulfide ore can be fundamentally reduced.
Therefore, in this paper, we selected sulfide ore as the subject. The sulfide ore samples (mainly containing pyrite) were collected from Tongshan, Anhui Province, China. Many cases of accidents due to spontaneous combustion of sulfide ore have been reported in Tongshan, which brought large economic losses and casualties, so the selection of ore samples from this site is beneficial to provide a basis for production practice. Mineral composition analysis shows that the main elements of the sulfur ore samples were sulfur, iron, oxygen, and silicon, with small amounts of calcium, barium, magnesium, and other elements. The main compositions of the sulfide ore samples are listed in
Table 1.
2.2. Strain and Medium
In the previous experimental studies, the desulfurization rate of
Acidithiobacillus caldus (
A.c.) was higher than all other bacteria, so
A.c. was selected as the primary strain for the experiment. The medium used for
A.c. was 9K medium. The specific composition of this medium is shown in
Figure 1. Briefly, 5 g of sulfide mineral powder was added to the medium and incubated at 43 °C for 5 days (the rotating speed of a constant temperature shaker was set at 170 r/min) until the bacteria count reached a certain number. All chemicals were of analytical grade.
2.3. Optimization of Experimental Conditions
2.3.1. Design of the Steepest Climb Experiment
Aiming to determine the response surface center, the steepest-climb experiment was designed. All three factors have a positive climbing direction, so their levels should be gradually increased in the experiment. According to the effect value analysis, the following incremental steps were set: (A) particle size of ore sample as 20, (B) the speed of the shaker as 10, and (C) the dosage of bacterial solution as 10. Specifically, as the level value gradually increased by one unit, each of the three factors should increase by the increment indicated in their corresponding steps. The experimental level design of the steepest-climb experiment is shown in
Table 2.
Five groups of experimental samples were set up, with two samples in each group. The specific process of the experiment was as follows:
- (1)
A sufficient quantity of ore samples of sizes 60–80 mesh, 80–100 mesh, 100–120 mesh, 120–140 mesh, and 140–160 mesh were taken for the experiment; then, 20 g of ore samples were taken from each bottle according to size and numbered and acidified with pH = 1 sulfuric acid; each size of ore samples was then dipped in sulfuric acid for 1–2 days to bring their surface pH down to 2.5.
- (2)
A quantitative amount of bacterial solution and leaching aid was added to the experimental ore samples, and the leaching aid was diluted to a concentration of 0.01% using the culture medium, with the bacterial solution: leaching aid = 5:1. The initial sulfur concentration test samples were extracted.
- (3)
The mixed ore samples and desulfurization solution were sealed and put into a shaker, with the temperature set at 35 °C. The sulfur concentration test samples were extracted for 5 days.
2.3.2. Design of the Box–Behnken Experiment
Aiming to find the best factor level combination, a Box–Behnken experiment was designed with three factors and three levels. The upper, lower, and zero levels were set for three factors, where the zero level was set based on the response surface center, +1 means upper level, and −1 means lower level. The experimental level design of the Box–Behnken experiment is shown in
Table 3.
In total, 15 groups of experimental samples were set up, and the specific procedure was as follows:
- (1)
A sufficient quantity of ore samples of 100–120 mesh, 120–140 mesh, and 140–160 mesh were taken for the experiment; then, 20 g of each sample was taken from each bottle of the three numbered sizes and acidified with pH = 1 sulfuric acid. Each particle size of the samples was then dipped in sulfuric acid for 1–2 days to bring the samples’ surface pH down to 2.5.
- (2)
A quantitative amount of bacterial solution and leaching aid was added to the experimental ore samples, and the leaching aid was diluted to a concentration of 0.01% using the culture medium, with the bacterial solution: leaching aid = 5:1. The initial sulfur concentration test samples were extracted.
- (3)
The mixed ore samples and desulfurization solution were sealed and put into a shaker, with the temperature set at 35 °C. The sulfur concentration test samples were extracted for 5 days. All 15 sets of experimental samples are shown in
Figure 2.
2.4. Microbial Desulfurization Experiments of Sulfide Ores Using Ultrasonic Treatment
In this experiment, we explored the influence of ultrasonic treatment on the effect of microbial desulfurization. The ultrasonic device is shown in
Figure 3. Meanwhile, the control variable method was adopted to study the main factors affecting microbial desulfurization by ultrasonic treatment, which include the particle size of ore samples, the ultrasonic action time, and the ultrasonic power. The sulfur content in sulfide ore and the desulfurization rate of microorganisms were analyzed under different parameter conditions so that we could find the optimal parameter conditions.
The experimental flow and setups of microbial desulfurization experiments of sulfide ores using ultrasonic treatment are shown in
Figure 3.
Firstly, the ore sample was mixed with distilled water proportionally to make the ore sample treated more fully. Then, the ore sample reacted under ultrasonic conditions. As the pH in the ore slurry was not suitable for the survival of bacteria, it needed to be acidified before adding bacteria. After acidification, bacterial solution and leach were added proportionally, and it was incubated in a constant temperature shaker for 5 days. Additionally, the supernatant was taken daily to calculate the sulfur content of the solution and desulfurization rate.
2.4.1. Experiment of the Effect of the Particle Size of Ore Sample on Desulfurization Rate
The particle size of the ore sample affected the reaction between the sulfur of the ore and the microorganism. Thus, the specific process of the experiment was as follows:
- (1)
Four different particle sizes of 60–80 mesh, 80–100 mesh, 100–120 mesh, and 120–140 mesh were selected. Then, 20 g of each of the ore samples was added to distilled water to form a slurry for ultrasonic treatment and then filtered dry and acidified to make the pH of the ore samples 2.0.
- (2)
The incubated bacterial solution was mixed with the same amount of 9K medium (diluted at a ratio of 1:10). Combined with the previous research results, leach (diluted to 0.005%) was added to the bacterial solution.
- (3)
After pretreatment with ultrasonic power of 200 W and an action time of 30 min, 111 mL of A.c. was added and incubated in a constant temperature shaker at 35 °C and 175 r/min for 5 days (111 mL of A.c. and 175 r/min for shaker were determined by the Box–Behnken experiment).
The design of the experiment on the effect of the particle size of ore sample on desulfurization rate is shown in
Table 4.
2.4.2. Experiment of the Effect of the Ultrasonic Action Time on Desulfurization Rate
In this experiment, the best desulfurization effect of particle size 120–140 mesh was selected (according to the results of the experiment on the effect of the particle size of ore sample on desulfurization rate); other conditions remained unchanged, and ultrasonic action time was used as a variable to study the effect of the ultrasonic action time on desulfurization rate. According to the results of the previous pre-experiments, there was an obvious difference in the desulfurization effect when choosing 1 min, 2 min, and 3 min. Hence, the minimum ultrasonic action time was set to 30 min, and the incremental step was 10 min.
The design of the experiment on the effect of the ultrasonic action time on the desulfurization rate is shown in
Table 5.
2.4.3. Experiment of the Effect of the Ultrasonic Power on Desulfurization Rate
In this experiment, ultrasonic power was used as a variable to study the effect of ultrasonic power on the desulfurization rate. Ultrasonic power was set to 100 W, 200 W, 300 W, and 400 W. Ultrasonic action time was set to 50 min, but other conditions remained unchanged.
The design of the experiment on the effect of the ultrasonic power on the desulfurization rate is shown in
Table 6.