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Article

Effect of the Mineralogical Composition of Sandstones on the Wear of Mining Machinery Components

1
Faculty of Mining, Safety Engineering and Industrial Automation, Silesian University of Technology, Akademicka 2 Street, 44-100 Gliwice, Poland
2
Faculty of Mechanical Engineering and Robotics, AGH University of Cracow, 30-059 Cracow, Poland
3
Łukasiewicz Research Network—Institute of Ceramics and Building, Refractory Materials Division in Gliwic, Materials, Toszecka 99 Street, 44-100 Gliwice, Poland
*
Author to whom correspondence should be addressed.
Coatings 2024, 14(7), 859; https://doi.org/10.3390/coatings14070859
Submission received: 25 May 2024 / Revised: 3 July 2024 / Accepted: 5 July 2024 / Published: 9 July 2024
(This article belongs to the Collection Feature Paper Collection in Corrosion, Wear and Erosion)

Abstract

:
The paper provides and comments on the results of studies of the effect of sandstone-based abrasives and quartz sand alone on the wear of martensitic surfaces of wear-resistant steels. The wear process was examined on a ring-on-ring test rig seeking to determine the mass decrement parameter which characterised wear. In addition, SEM microscopy, optical profilometry and XRF analysis were used to analyse the abrasives used and damaged surfaces. The tests were conducted for three sandstone varieties, Carboniferous, Permian, and Cretaceous, and they made it possible to determine that the most intense process of deterioration of wear-resistant steels took place in the presence of quartz sand grain, while less intense wear was observed in the case of sandstone-based abrasives. The mass decrement values established in the presence of the sandstones in question did not differ significantly between individual sandstone varieties. Based on a surface damage analysis, the basic damage mechanism was found to be micro-scratching; however, with regard to the sandstones examined, it was also determined that individual grains could be pressed into surface irregularities and that films of soft hematite cement developed in the Permian sandstone and that inclusions of carbonaceous matter were formed in the Carboniferous sandstone. With reference to the wear process observations, a wear model was described for the surface of the steels examined in the presence of sandstone-based abrasives. This model presents the possibility of capturing wear products by unstable binder layers and changing the form of wear from three-body to two-body.

1. Introduction

Considerable tribological wear is observed in mining machinery components working under harsh environmental conditions, which can be attributed to diverse causes, including the effect of aggressive abrasive materials. One of the main expectations held by companies that operate mining machines is the capacity to ensure their adequate availability. Excessive wear of machinery and equipment components is an issue typical of both underground and open-cast mining. Consequently, the elements most prone to damage include, for example, the liners of bins or buckets in excavators, power train caterpillars, or drive chains and drums of mining conveyors. The factors that link the aforementioned components are the presence of grain of different sandstone sorts in the zone where these elements work together and the widespread use of wear-resistant steel grades in their production.
This paper focuses on the overall body of problems pertaining to the operation of mining material handling machines used while dog headings are being driven [1,2], which represents a very complex range of subjects on account of the variety of issues and limitations experienced in the process, these being of geological and mining as well as technical nature. The work conducted in these headings is among the most labour- and time-intensive kinds. Dog headings, and the opening-out ones in particular, are currently driven in rocks characterised by very unfavourable parameters. What appears to be a relevant factor to this process is the type of rock-building minerals, since their hardness affects the rate of abrasion and wear of cutting tools. Additionally, the presence of specific concretions, such as those of spherosiderite, in rock banks causes intense sparking while mining operations are being performed, which poses a very serious threat in underground mines.
The equipment used for rock loosening and output haulage while driving tunnels or headings can be considerably diversified. It may comprise various types of conveyors, including scraper and belt conveyors, self-propelled machines moving on tyred wheels, excavators, roadheaders, loaders, or haulage cars [3]. In operation, individual components of these machines are exposed to factors that reinforce their surface damage [4,5]. Friction is one of the main causes of degradation of transport machinery components [6], yet an equally important degradation factor is the effect of abrasive material, the presence of which can significantly intensify the processes of deterioration of the surfaces comprising a given tribological system (Figure 1). When combined, both these factors can induce an abrasive wear process. Abrasive wear can be defined as a process of deterioration and removal of material from the surface of a solid body, accompanied by a change in volume and the associated mass decrement [7,8,9]. An extreme case of abrasive wear can be a change in the structure and mechanical properties of elements engaged in friction or even their physical degradation (Figure 2A).
However, what proves to be more frequent is the effect of either dry (Figure 2B) or wet abrasive material (Figure 2C,D), which can cause significant material decrement precisely at the point of impact of this degradation factor. Material decrement in the surface layer can be due to such processes as micro-ridging, micro-scratching, micro-fatigue, and micro-cracking [10]. In the case of abrasives composed of minerals characterised by considerable hardness, damage is typically attributable to micro-scratching or micro-ridging.
The adverse effect of hard mineral abrasives on the surface of machine components has been extensively explored and discussed in the literature on the subject [10,11,12,13,14,15]. However, clastic materials are often non-homogeneous and may contain materials of inherently diversified wear (abrasion) properties [16,17,18]. Lawrowski [19] claims that the abrasive wear mechanism depends on the proportion between the hardness of the metal wearing away (HM) and the hardness of the abrasive (HA). Where HM/HA > 0.6, a less aggressive chemical-mechanical form of abrasion occurs, but where HM/HA < 0.6, edges of the abrasive grains cause surface micro-abrasion.
As aforementioned, the mineral composition of the rock mass in which dog headings are driven can be diversified and variable along the entire driving section. This is precisely the situation presented and discussed by Mucha [20] using an example of driving through a mass of rock and coal in order to develop an inclined ventilation drift in one of the Polish coal mines. The geological cross-sections provided in Figure 3 formed layers of coal and sandstone (left-hand figure) and sandstone alone (right-hand figure).
It is common that underground headings are driven in sandstone-containing rock formations [3]. Sandstones [21,22,23,24] represent a group of clastic rocks which—on account of the grain size of the clastic material—are classified as psammitic. There are generally two groups of components found in the structure of sandstones: allogenic minerals, forming what is referred to as the grain skeleton, and authigenic minerals, contained in the binding matter commonly known as cement. There is also a separate group known as the matrix, comprising allogenic grains of a size below the lower limit of the fraction which represents the grain skeleton. The allogenic grains include weathering-resistant minerals derived from the comminution of older rocks, and these are primarily quartz, feldspar (most commonly represented by orthoclase, albite, and oligoclase), mica (mainly muscovite, less commonly biotite), and heavy minerals such as zircon and garnets. The authigenic minerals, on the other hand, are formed where sediment develops, during either sedimentation or diagenesis. These include opal, chalcedony, carbonates, clayey minerals, iron oxides, and hydroxides.
Sandstones can be classified according to diverse criteria [25]. Considering the grain size diversity of the grain skeleton, sandstones can be broken down into coarse-grained (1–2 mm), medium-grained (0.5–1 mm), fine-grained (0.25–0.5 mm), and very fine-grained (0.10–0.25 mm) sandstones. The sandstone varieties depending on the mineralogical composition are either monomineral, quartz being their main component, or polymineral. As per Folk’s [26] classification, polymineral sandstones include arkose (containing numerous feldspar grains besides quartz) and greywacke sandstones rich in rock clast and clayey minerals. According to Petitjohn [27], on the other hand, the breakdown of sandstones should also be based on the fraction of the matrix, besides the mineralogical composition. Such an assumption leads to the division into arenytes (containing up to 15% of matrix by vol.) and wackes (containing 15–75% of matrix by vol.).
Sandstones can also be subdivided on account of the mineralogical composition of cement, which essentially affects their physical and mechanical properties, and so there can be siliceous, calcareous, clayey, ferruginous, and other sandstones. The mineralogical composition of cement determines the sandstone colour, which also plays an important role, especially in construction stone production. Therefore, for instance, one can distinguish between white (Cretaceous), red (Permian), pink (Triassic), and green (Cretaceous) sandstones.
There is a relatively plentiful body of research on the mechanical properties of sandstones. These characteristics, including fatigue strength, susceptibility to cracking, and axial load behaviour, as well as the failure mechanisms of sandstones, have been studied by numerous authors, some of whom are Z. Song et al. [28], Bagde and Petroš [29,30,31], Song, H et al. [32], Cai et al. [33], Y. Zhao et al. [34], Vaneghi et al. [35], Yang et al. [36,37,38], G. Zhao et al. [39], Liu et al. [40], Ray et al. [41], Feng et al. [42], Figarska-Warchoł et al. [43], and Li et al. [44]. The abrasiveness of sandstones, on the other hand, has been addressed in papers [45,46,47,48,49,50,51,52,53,54,55].
In order to counteract the excessive abrasive wear of working surfaces in the machinery and equipment operated while driving dog headings and tunnels, typically caused by the effect of rocks, including sandstones, wear-resistant steels are used in production. These steel grades are classified as martensitic, weldable, resistant to abrasive wear, and characterised by very high strength parameters [56,57,58]. Their anti-wear properties have been examined relatively extensively in terms of the potential impact of quartz grains or rock mixtures forming different variations of mineral aggregates [15,16,17,57,58,59,60,61,62,63,64].
In their studies released to date, the authors have analysed the effects of quartz sand [65], coal [66], and siltstones [67], as well as their mixtures with quartz sand [68], on the wear of wear-resistant steels. This body of research has allowed them to conclude that the content of low-hardness minerals in the rock material can exert a fundamental impact on the underlying damage mechanism of the steel grades in question, thereby determining the intensity of their wear. The role of rocks such as siltstone or coal may consist in changing the three-body form of abrasive wear to the less intense two-body form of wear of the grains embedded in the material wearing away. Furthermore, clayey minerals and coal show a tendency to be pressed into surface irregularities and can immobilise steel wear products. Consequently, in the processes of abrasive wear of martensitic steels in the presence of sandstones composed, as aforementioned, primarily of quartz and cement, the damage mechanism at play may not necessarily be solely the one typical of hard grain, such as quartz. Based on that observation, Wieczorek et al. [69] proposed a wear model for mixtures of hard grains and soft phases, dedicated to elements of tunneling machinery. In the case of sandstones, specific wear mechanisms, as well as the interactions between wear processes, can be complex [70] and conditioned by the components comprising a given tribological system [71,72,73,74].
The primary objectives of the research addressed in this paper were as follows:
  • To identify the mechanisms of surface damage of wear-resistant steels in the presence of sandstones featuring different kinds of mineral cement;
  • To determine the effect of the fraction of quartz in the sandstones examined on the wear of wear-resistant steels;
  • To define the interaction between the damage mechanism and the sandstone cement type.
In pursuit of the main research objectives, the following studies were conducted:
  • Mineralogical and chemical identification of the analysed abrasive material based on microscopic observations of thin plates using a scanning electron microscope, as well as analysis of chemical composition by X-ray fluorescence (XRF);
  • Wear testing of wear-resistant steels in the presence of comminuted sandstone grains and quartz sand;
  • Identification of the surface damage mechanisms observed in the samples based on scanning microscopy observations and EDS analysis.
Besides quartz sand, three sandstone types were used in the studies:
  • Carboniferous sandstone obtained from the Piast-Ziemowit hard coal mine in Bieruń;
  • Permian ferruginous sandstone from the Lower Silesian deposits found in the district of Kłodzko;
  • Sandstone from the bottom Godulian strata extracted in the town of Wisła, dating back to the Upper Cretaceous.
In order to achieve the objectives of their research, the authors focused on identifying the mineralogical composition of the sandstones under consideration. Additionally, they compared the results obtained in the studies they had conducted with the results pertaining to the effect of quartz sand grains. With reference to the preliminary research, it should also be concluded that the literature on the subject lacks analyses of the impact of the mineralogical composition of sandstones on the damage mechanisms of wear-resistant steels, which makes the research addressed in this paper and its results novel, given the current state of knowledge in the field of wear processes.

2. Experimental Details

The research was divided into three phases: identification of the materials and abrasives used, basic wear tests, and analysis of surface damage (the research scheme is presented in Figure 4).
In addition to quartz sand, three types of sandstone were used for the research:
  • Carboniferous sandstone from the mine workings of KWK Piast-Ziemowit in Bieruń;
  • Ferruginous sandstone dating from the Permian originating from Lower Silesian deposits in the Kłodzko district;
  • Sandstone from the lower Godula beds in Vistula, dating to the Upper Cretaceous.
Thin plates of material were used to perform transmitted light microscopy observations by means of the OPTA-TECH LAB-40 HAL polarised light diagnostic microscope featuring an image analyser.
In order to determine the chemical composition of the sandstones by X-ray fluorescence (XRF) in line with the EN ISO 12677: 2011 standard, the samples were ground to a grain size of less than 63 μm using a tungsten carbide-lined mill. The samples were dried, and then the relevant loss on ignition was determined at the temperature of 1025 °C. Roasted to a constant mass, the samples were melted using an off-the-shelf mixture of lithium tetraborate, lithium metaborate, and lithium bromide (66.67%, 32.83%, and 0.5%) of a flux purity suitable for XRF (from Spex, Metuchen, NJ, USA). The sample-to-flux weight ratio was 1:9. Thus prepared, the samples were measured using the PANalytical MagiX PW2424 spectrometer calibrated with a series of certified reference materials, i.e., JRRM 121-135, JRRM 201-210, and JRRM 301-310 (Technical Association of Refractories, Tokyo, Japan).
The surface of the steel and sandstone samples was subject to observations at the fracture, conducted using the SEM AXIA ChemiSEM scanning electron microscope from ThermoFisher Scientific with a fully integrated EDS spectrometer using secondary electron (SE) detection at an accelerating voltage of 15 kV and magnification ranging from ×50 to ×2000. The chemical composition in micro-areas was subject to a qualitative analysis by energy-dispersive X-ray spectroscopy (EDS) at an accelerating voltage of 15 kV. For testing purposes, the sandstone samples were sputtered with gold using the SPT-20 COXEM sputter coater, while surface texture examinations were performed using the Profilm3D optical profilometer from Filmetrics Inc. (San Diego, CA, USA).
The tribological test samples were made from a wear-resistant steel with the trade name of RAEX400. The main material data of the steel subject to the tests are provided in Table 1, while its chemical composition is provided in Table 2. Detailed information on the steel used in the studies can be found in papers [68,69]. The surface profilogram of the RAEX400 steel is shown in Figure 5.
The abrasive wear tests were conducted at a ring-on-ring type test rig (Figure 6A,B). One of the characteristics of the test [68,69] was the constant presence of comminuted grains of sand or the sandstones analysed. Two ring-shaped samples of the RAEX400 steel (Figure 6C) were fixed in the upper and lower holders of the test rig so as to arrange them parallel to each other and to prevent them from moving in the holders.
Prior to the testing, the abrasive material subject to the tests was ground to a grain size of less than 100 μm and placed in an amount corresponding to 1 cm3 between the faces of the samples. While exerting its impact on the steel surfaces, the abrasive continued to grind out. The samples were cleaned and weighed before and after a 10 min wear cycle to determine their mass decrement, while fresh abrasive was added between the test samples before the start of each cycle. For each abrasive variant and each load value, three test series were performed, each consisting of eight wear cycles. The parameters characterising the wear tests are provided in Table 3.
Based on the mass measurements conducted after the 10 min wear cycle, the mass decrement of sample WM was determined according to Formula (1):
W M = M B S _ E n d M B S _ S t a r t + M U S _ E n d M U S _ S t a r t
where MBS_Start—mass of the bottom sample before the test in g, MBS_End—end mass of the bottom sample in g, MUS_Start—mass of the upper sample before the test in g, and MUS_End—end mass of the upper sample in g.
Measurement uncertainty was determined using Student’s T method for confidence level equal to 0.95 and number of tests n = 3. The relative measurement uncertainty was less than 3% for all the cases considered.

3. Results

3.1. Identification Tests

Carboniferous sandstone (Figure 7A) is characterised by its grey colour, medium-grained texture, and low degree of sorting. The sandstone texture is compact, typically chaotic, only locally with directional texture marked by the presence of fine-grained parallel layers of carbonaceous matter. In a sample comprising chunks of material, sandstone reacts with HCl when exposed to cold, which implies that there is calcite (CaCO3) in the mineralogical composition of the cement, and moreover, a distinct odour of mortar is released when the rock comes into contact with water, which, in turn, indicates the presence of clayey minerals.
Permian sandstone (Figure 7B) is red in colour, which indicates the presence of iron oxides, mainly hematite (Fe2O3), in the mineralogical composition of the cement. The structure of this sandstone is medium-grained with a low degree of sorting. Its texture is chaotic and typically compact, yet fine pores can be observed locally on the rock surface. This sandstone is also brittle.
Cretaceous sandstone (Figure 7C) displays a light grey colour and a fine-grained texture with a high degree of sorting of the clastic material. The texture of the sandstone is compact and chaotic. Macroscopic examinations reveal that, besides quartz, there are lamellae of muscovite with a characteristic pearly lustre in the mineralogical composition of the sandstone clast.
In order to identify the structure and mineralogical composition of the sandstones under consideration, transmitted light microscopic observations were conducted using a scanning electron microscope. Figure 8 and Figure 9 are microphotographs of the grain surface and microstructure of the Carboniferous sandstone, Figure 10 and Figure 11 show the Permian sandstone, while Figure 12 and Figure 13 show the Cretaceous sandstone.
Having performed the microscopic observations and spot EDS measurements, the authors also established the surface distribution of elements. A sample distribution obtained for the Permian sandstone is shown in Figure 14, and the elements were mapped for the sandstones studied (Figure 15). Figure 16 shows the surface of the quartz sand used in the studies. Additionally, the sandstones subject to testing were also analysed for chemical composition (Table 4).
The microscopic observations showed that the composition of the clastic material of the studied sandstones is similar. The dominant mineral is quartz, as also plagioclase, muscovite, and biotite were distinguished. However, differences are observed in the quantitative ratio of aggregate material to the binder and in the mineral composition of the binder.
The binder of the Carboniferous and Cretaceous sandstones represents a porous type, while in the Permian sandstone, basal binder was observed. In all sandstones, binder creates a mixed cement type; no matrix type was found. In the Cretaceous sandstone, similarly to the Carboniferous sandstone, the cement is of the mixed clay–carbonate–silica type, but the participation of a mineral belonging to the clay mineral group—glauconite—is worth noting. The most characteristic feature of glauconite in the microareas is its green colour under parallel polarizers (Figure 13).
In the Carboniferous sandstone, chalcedony, clay minerals, and carbonate minerals were distinguished among the cement components. Chalcedony forms microcrystalline aggregates, and the individual grains show optical properties similar to quartz; they are colourless, with zero or weakly positive relief, and do not present cleavage. Clay minerals form microcrystalline aggregates with dark grey interference colours. Carbonates are colourless with variable relief; during crossed polarizers, they have interference colours of the fourth order (Figure 9). In the Permian sandstone, the main components of the cement are oxidised iron compounds, represented primarily by hematite with a characteristic red colour (Figure 11).

3.2. Wear Tests

Figure 16 illustrates the behaviour of mass decrement as a function of testing time for the sandstone varieties and quartz sand examined, while Figure 17 provides a comparison of wear curves for the sandstone varieties in question.
The wear test results obtained imply the following findings:
  • The greatest wear was observed for homogeneous hard mineral abrasives (quartz sand);
  • All the wear values obtained for the wear-resistant steel in the presence of quartz sand and for all load values are very similar;
  • The differences in the mass decrement caused by the presence of Permian, Carboniferous, and Cretaceous sandstone are inconsiderable and cannot be graded in terms of the intensity of their effect on the wear-resistant steel.

3.3. Surface Analysis after Wear Tests

Once the wear tests had been completed, the next stage in the research consisted of assessing the effects of the abrasive materials on the surface of the steel samples tested. For this purpose, microscopic observations of the steel surfaces were performed by optical profilometry and scanning electron microscopy. What could be found on the surface of all the steel samples tested in the presence of three types of sandstone and quartz sand was the wear forms typical of hard abrasives, forming scratches whose presence was caused by the impact of quartz grains. This can be clearly seen in the profilograms provided in Figure 18.
What these profilograms also demonstrate for all the three sandstone varieties studied is surface zones characterised by plastic minerals, forming the sandstone cement, having been partially pressed into scratches that developed earlier. However, the images of the surface of the wear-resistant steel wearing away in the presence of sandstone grains (Figure 19, Figure 20 and Figure 21) reveal far more forms of damage.
In numerous cases of the steel tested in the presence of the Carboniferous sandstone-based abrasive, it was observed that, due to the wear caused by the presence of grains between mating surfaces, the carbonaceous substance had been pressed into the scratches formed on the surface, but finer crumbs thereof were also found to have mixed with some harder components of the abrasive material showing on the steel surface (Figure 19). Visible in this figure are also quartz grains embedded in the surface either directly or via a layer of coal previously pressed in.
The microphotographs of the steel samples exposed to the impact of the Permian sandstone-based abrasive clearly show that scratches were filled by hematite (Fe2O3), which is the main component of the sandstone cement (Figure 20). The remaining, nonpressed part of the haematite-rich cement was subjected to the effect of friction. Affected by load and relative surface motion, the abrasive material displayed a tendency to aggregate into larger lumps, mostly typically found in surface chipping areas.
The surface of the steel samples exposed to the effect of the Cretaceous sandstone abrasive showed relatively the greatest signs of wear. Clearly visible are the scratches created by the abrasive action of quartz (Figure 21) as well as the crushed quartz grains embedded in the steel surface, surrounded by clusters of mineral cement.
Figure 22 shows examples of the damage that the wear-resistant steel surface sustained following the wear tests in the presence of quartz sand. The effect of the grain, as observed on the surface of the test samples, was damage in the form of numerous extensive scratches. Between these scratches, patches of smoothed surface or small pinpoint cavities can be seen. No embedded quartz sand grains or any films of pressed-in mineral grain were found on the surface of the test samples.

4. Discussion

Quartz is the primary mineral forming the grain skeleton of all the sandstone varieties examined. Quartz grains are characterised by diversified sizes ranging between 0.1 mm and 1 mm as well as varying degrees of roundness. Alongside rounded-edge samples, sharp-edged grains could also be discerned, especially in the Cretaceous sandstone. With the polarisers arranged in parallel, the quartz grains appear colourless with weakly positive relief; their surface is predominantly scratched and covered with a lattice of irregular cracks. With the crossed polarisers in use, first-order grey interference colours characteristic of quartz are visible, but one can also observe some optical anomalies caused by the dynamic deformations to the quartz lattice. The foregoing causes wavy light extinction, which means that the surface of individual grains is not extinguished uniformly but rather in a fragmented fashion instead, which manifests itself as locally extinct patches within the grain.
Mica can be found primarily in the Cretaceous sandstone, with incidental occurrences in the Carboniferous and Permian sandstone. This group is represented by well-preserved grains of muscovite, forming elongated idiomorphic shapes, often twisted upon contact with other minerals. With the parallel polarisers in use, muscovite is colourless and non-pleochroic, showing distinctive unidirectional cleavage. With the crossed polarisers, second- and even third-order interference colours are marked, characteristic of muscovite. In addition to muscovite, biotite is found in the Cretaceous sandstone. Biotite grains are highly weathered, typically with jagged edges, while well-preserved idiomorphic crystals can rarely be observed. With the polarisers arranged in parallel, biotite appears to be characterised by a brown colour and pronounced pleochroism, with unidirectional cleavage visible on the grain surface. With the crossed polarisers in use, biotite shows simple light dimming and second-order interference colours.
The feldspar group is represented mainly by plagioclases, identified in all the sandstones studied. They form fine grains showing grey interference colours and characteristic polysynthetic twinning. Heavy minerals were mainly observed in the Carboniferous sandstone, and these included zircon, found to have formed well-rounded colourless grains with characteristic black pleochroic rims. With the polarisers crossed, zircon shows fourth-order interference colours.
The binding matter in the Carboniferous and Cretaceous sandstone represents the porous type, while it is primary in nature in the Permian sandstone. It is a mixed cement type, and no matrix-type cement was observed. In the Carboniferous sandstone, chalcedony, clayey minerals, and carbonate-based minerals were found among the cement components. Chalcedony forms microcrystalline aggregates whose individual grains show optical characteristics similar to those of quartz: they are colourless and non-pleochroic, with zero or weakly positive relief, showing no cleavage. With the crossed polarisers in use, they are characterised by grey interference colours of the first order. Clayey minerals form microcrystalline aggregates with dark grey interference colours. Carbonates are colourless with variable relief, and with the crossed polarisers in use, they show fourth-order interference colours.
The main component of the Permian sandstone’s cement is oxidised iron compounds, represented primarily by hematite with a characteristic red colour. In the Cretaceous sandstone, as in the Carboniferous one, the cement is of mixed clay–carbonate–silica type, but what is particularly noteworthy about it is the fraction of glauconite, belonging to the group of clayey minerals. The most characteristic feature of glauconite is its green colour observed in the microscopic image with the polarisers in the parallel arrangement.
In the Carboniferous sandstone, the texture was confirmed to be compact (Figure 7A), and furthermore, clasts of carbonaceous matter were found among the sandstone’s structural components (Figure 8). The microphotographs of the Permian sandstone clearly show the presence of ferruginous cement which, on account of the clast-to-cement ratio, is primary in nature (Figure 10). On the other hand, among the components of the clastic material, well-preserved irregular quartz grains could be observed (Figure 11). The microscopic analysis of the surface of the Cretaceous sandstone revealed micropores that were not discernible in the macroscopic observations (Figure 12). The quartz grains were also found to be characterised by a much smaller size compared to the quartz forming the Carboniferous and Permian sandstone, which had already been established during the macroscopic observations, implying that the structure of the Cretaceous sandstone should be categorised as fine-grained (Figure 13).
The analysis of the chemical composition of the sandstones examined showed that their dominant component is silica (SiO2), whose content in the Carboniferous and Cretaceous sandstone is 88.53% and 83.14%, respectively, while the smallest content of this component was identified in the Permian sandstone—80.27%. Silica occurs alongside the oxides of aluminium (Carboniferous sandstone—3.83%, Permian sandstone—5.09%, Cretaceous sandstone—8.06%), iron (most found in the Permian sandstone (11.81%) and least (0.35%) in the Carboniferous sandstone), and potassium (Carboniferous sandstone—0.67%, Permian sandstone—0.43%, Cretaceous sandstone—1.41%). The other oxides are present in smaller amounts, their content not exceeding 1%. The loss on ignition implies that admixtures of organic matter are present in the sandstone composition, found in the largest content in the Carboniferous sandstone (4.73%).
In their previous papers [4,64,65,66,67,68], the authors demonstrated that the fraction of quartz, or possibly also of the SiO2 + Al2O3 complex, in abrasive mixtures has a decisive impact on the rate of wear of wear-resistant steels. The study addressed in this paper also served to establish a relation between the wear rate and the fraction of quartz (SiO2) expressed in per cent (Figure 23).
Figure 23 shows that, within the range of 80–88% of the SiO2 content, the increase in mass decrement is relatively small, and not until the quartz content nears 100% does the abrasive material cause significantly greater wear. One should seek the rationale behind the above observation in the potential interactions between the hard particles of the abrasive material (crushed quartz grains) and the relatively soft cement or carbonaceous inclusions.
As implied by the figures showing the steel surface affected by sand grains, processes of intense abrasion caused by hard mineral grains take place while the material is wearing away (Figure 22). Meanwhile, these grains are subject to comminution, and yet such particles of reduced size continue to abrade the steel surface and generate wear products, i.e., loosened fragments of steel. The surface deterioration processes observed in all the sandstones containing hematite-based cement or carbon inclusions besides quartz grains proceed differently compared to the cases where quartz sand alone is present.
First and foremost, the grains of the minerals that make up sandstone become comminuted and subsequently mixed. At the same time, two different processes take place. On the one hand, during the relative motion of the surface of the samples, the steel surface is being abraded by sandstone grain fragments, forming metallic wear products (process accompanied by continuous grain comminution), and on the other hand, the aforementioned motion of the surface of the samples causes the soft components (e.g., hematite cement or carbonaceous inclusions) to separate, which leads to the formation of discontinuous layers on the steel surface. As a consequence of the effect of quartz grains, they are driven into the surface either directly or through the cement layer previously formed or through inclusions. The embedment of grains in the surface is facilitated by the formation of cement-filled cavities into which the former are pressed under the pressure of the upper sample, the outcome of which is a partial change in the form of abrasive wear from the three-body to the two-body type. The latter form is characterised by a lower intensity of wear compared to the former [9,11].
The loosened wear products along with non-embedded grain fragments may be subject to further comminution, or they can continue to cut the mating surfaces as well as break into the dynamically developing discontinuous layer of cement and inclusions, thus becoming inactive.
Based on the studies conducted by the authors, a model of wear of wear-resistant steel in the presence of sandstone grains was proposed (Figure 24).
The wear model envisages a four-stage steel surface deterioration process:
Stage I: Initial condition—non-comminuted quartz grains placed in the test head.
Stage II: Initial cutting of the steel surface by comminuted and non-comminuted mineral grain and initial compaction of the cement and inclusions under the effect of load and relative motion of the samples.
Stage III: Further cutting by grains and simultaneous formation of layers of soft sandstone components, facilitated by the temperature increase on the surface of the samples.
Stage IV: Further filling of cavities by cement films, formation of pockets capturing larger quartz grains, and inactivation of small grain fragments and wear products by cement films. In the wear model presented above, the hard sandstone fractions are the wear-intensifying factors, and their effects are as follows:
  • Surface abrasion by hard mineral grains and wear products;
  • Capacity for the formation of extensive surface cracks between abrasion areas as a consequence of aggregate accumulation in surface cracking areas.
On the other hand, the material-forming fractions can mitigate the wear process to some extent by the following:
  • Facilitating the settling of mineral abrasive grains in surface damage areas and partially converting the three-body form of abrasive wear into two-body abrasive wear;
  • Enabling limited capture of hard abrasive particles by discontinuous cement films;
  • Limiting oxygen access to the loosened steel surface fragments via consolidated cement fractions.

5. Conclusions

Based on the studies conducted by the authors, the following findings were obtained:
(1)
The form of damage to mating surfaces depends on the type of abrasive material introduced between them:
  • For abrasive material based on quartz sand, micro-scratching was found to be the primary steel damage mechanism, the secondary one being the smoothing effect of highly comminuted wear products.
  • For the sandstone-based abrasive, signs of abrasion of the steel surface by grain fragments, as well as formation of films comprising minerals forming the sandstone cement (clayey minerals, hematite) and carbonaceous substance, were observed.
(2)
What could also be noticed in the sandstones was the deposition of hard grains, mainly of quartz, in the damaged surface areas, which was facilitated by the presence of soft cement-building minerals (clayey minerals, hematite) and, in the case of Carboniferous sandstone, the presence of carbonaceous matter inclusions.
(3)
On the surfaces worn in the presence of sandstones, discontinuous and irregular films of cement and carbonaceous inclusions were formed under load.
(4)
The following conclusions were drawn with reference to the volumetric wear values measured:
  • The most extensive wear was observed in the presence of hard mineral abrasives (quartz sand);
  • The wear values obtained for wear-resistant steels in the presence of all three sandstone varieties studies were very similar to one another. Moreover, the average consumption determined for the tested sandstones was 72% lower compared to the consumption observed for quartz sand.
(5)
Additionally, models of wear in the presence of sandstone-based abrasive material were provided in the paper.
In conveyors intended for use in mining workings, wear-resistant steels are supplied according to the specifications of the users of these machines. As a rule, they require a steel surface hardness of not less than 400 HB. Based on the presented results, it is recommended to increase the surface hardness to the range of 475–505 HB while maintaining the weldability of the sheets used. The increased cost of purchasing sheets of increased hardness should be returned in the form of an increase in the failure-free operation time of wear-resistant steels.

Author Contributions

Conceptualization, A.N.W. and I.J.; methodology, A.N.W.; investigation, A.N.W., A.G., M.K., and A.P.; formal analysis, I.J., A.G., and M.K.; resources, K.M., K.F., M.K., and A.P.; writing—original draft preparation, A.N.W. and I.J.; writing—review and editing, K.F.; funding acquisition, A.N.W. and K.F. All authors have read and agreed to the published version of the manuscript.

Funding

The article was written as part of the research work of the Department of Mining Mechanization and Robotization of the Silesian University of Technology No. 06/020/BK_21/0052 under the title “Identification of the mechanisms of the impact of abrasive on the basis of sedimentary rocks accompanying coal seams on the surface of friction nodes”.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding authors.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Tribological system [5]; designations: 1—relative motion inducing element, 2—element subject to kinematic forcing, 3—intermediate layer, 4—further surrounding, D—disturbances, Fn—load, I—preset input values (X), O—effective output values (Y), RP—residual processes, T—friction forces, v1 and v2—surface velocities of elements 1 and 2.
Figure 1. Tribological system [5]; designations: 1—relative motion inducing element, 2—element subject to kinematic forcing, 3—intermediate layer, 4—further surrounding, D—disturbances, Fn—load, I—preset input values (X), O—effective output values (Y), RP—residual processes, T—friction forces, v1 and v2—surface velocities of elements 1 and 2.
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Figure 2. Examples of the effect of environmental conditions observed while driving underground dog headings on elements of haulage machinery: (A) example of critical damage to a conveyor track, (B) conveyor track covered with dry rocky abrasive material, (C) conveyor deck plate with visible scratches, (D) chain links covered with a sticky mixture of rock and water; designations: 1—deck plate abrasion.
Figure 2. Examples of the effect of environmental conditions observed while driving underground dog headings on elements of haulage machinery: (A) example of critical damage to a conveyor track, (B) conveyor track covered with dry rocky abrasive material, (C) conveyor deck plate with visible scratches, (D) chain links covered with a sticky mixture of rock and water; designations: 1—deck plate abrasion.
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Figure 3. Examples of geological cross-sections of an underground dog heading; designations: yellow—sandstone, black—coal (based on [20]).
Figure 3. Examples of geological cross-sections of an underground dog heading; designations: yellow—sandstone, black—coal (based on [20]).
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Figure 4. Diagram of the experiment setup.
Figure 4. Diagram of the experiment setup.
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Figure 5. Surface profilogram of the RAEX400 steel sample prior to wear testing.
Figure 5. Surface profilogram of the RAEX400 steel sample prior to wear testing.
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Figure 6. Tribotester; (A) test rig, (B) testing head, (C) sample, (D) bottom holder with abrasive material.
Figure 6. Tribotester; (A) test rig, (B) testing head, (C) sample, (D) bottom holder with abrasive material.
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Figure 7. Samples of the sandstones subject to the tests.
Figure 7. Samples of the sandstones subject to the tests.
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Figure 8. Carboniferous sandstone surface: (A) microscopic view (×30, SEM); (B) microscopic view (×1000, SEM); (C) EDS analysis results for item 1 with chemical analysis.
Figure 8. Carboniferous sandstone surface: (A) microscopic view (×30, SEM); (B) microscopic view (×1000, SEM); (C) EDS analysis results for item 1 with chemical analysis.
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Figure 9. Microphotograph of Carboniferous sandstone (in transmitted light, crossed polarisers, ×100); designations: q—quartz, cl—clayey minerals; c—carbonates, ch—chalcedony, zr—zirconium.
Figure 9. Microphotograph of Carboniferous sandstone (in transmitted light, crossed polarisers, ×100); designations: q—quartz, cl—clayey minerals; c—carbonates, ch—chalcedony, zr—zirconium.
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Figure 10. Permian sandstone surface: (A) microscopic view (×44, SEM); (B) microscopic view (×1000, SEM); (C) EDS analysis results for item 1 with chemical analysis.
Figure 10. Permian sandstone surface: (A) microscopic view (×44, SEM); (B) microscopic view (×1000, SEM); (C) EDS analysis results for item 1 with chemical analysis.
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Figure 11. Microphotograph of Permian sandstone (in transmitted light, crossed polarisers, ×100); designations: q—quartz, h—hematite.
Figure 11. Microphotograph of Permian sandstone (in transmitted light, crossed polarisers, ×100); designations: q—quartz, h—hematite.
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Figure 12. Cretaceous sandstone surface: (A) microscopic view (×44, SEM); (B) microscopic view (×1000, SEM); (C) EDS analysis results for item 1 with chemical analysis.
Figure 12. Cretaceous sandstone surface: (A) microscopic view (×44, SEM); (B) microscopic view (×1000, SEM); (C) EDS analysis results for item 1 with chemical analysis.
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Figure 13. Microphotograph of Cretaceous sandstone (in transmitted light; (left) parallel polarisers, (right) crossed polarisers, ×100); designations: q—quartz, cl—clayey minerals, c—carbonates, f—feldspars, ch—chalcedony, m—muscovite, bt—biotite, g—glaukonite.
Figure 13. Microphotograph of Cretaceous sandstone (in transmitted light; (left) parallel polarisers, (right) crossed polarisers, ×100); designations: q—quartz, cl—clayey minerals, c—carbonates, f—feldspars, ch—chalcedony, m—muscovite, bt—biotite, g—glaukonite.
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Figure 14. Element distribution on the Permian sandstone surface (elements designated in figures).
Figure 14. Element distribution on the Permian sandstone surface (elements designated in figures).
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Figure 15. Element maps identified for the sandstones studied.
Figure 15. Element maps identified for the sandstones studied.
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Figure 16. Behaviour of mass decrement (WM) of wear-resistant steel as a function of testing time established for the sandstone varieties and quartz sand examined.
Figure 16. Behaviour of mass decrement (WM) of wear-resistant steel as a function of testing time established for the sandstone varieties and quartz sand examined.
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Figure 17. Comparison of curves of mass decrement (WM) of wear-resistant steel for the sandstone varieties examined: (A) for 0.094 MPa of load, (B) for 0.125 MPa of load.
Figure 17. Comparison of curves of mass decrement (WM) of wear-resistant steel for the sandstone varieties examined: (A) for 0.094 MPa of load, (B) for 0.125 MPa of load.
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Figure 18. Profilograms of the surface of wear-resistant steel wearing away in the presence of sandstone clast, as determined for a load of 0.125 MPa.
Figure 18. Profilograms of the surface of wear-resistant steel wearing away in the presence of sandstone clast, as determined for a load of 0.125 MPa.
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Figure 19. Surfaces of wear-resistant steel (A,B) wearing away under a load of 0.125 MPa in the presence of Carboniferous sandstone clast: a—scratches, b—clasts of carbonaceous matter, c—coal-filled surface cracks, d—carbonaceous films, e—quartz grain embedded in carbonaceous film, f—quartz grain embedded in surface, g—groove.
Figure 19. Surfaces of wear-resistant steel (A,B) wearing away under a load of 0.125 MPa in the presence of Carboniferous sandstone clast: a—scratches, b—clasts of carbonaceous matter, c—coal-filled surface cracks, d—carbonaceous films, e—quartz grain embedded in carbonaceous film, f—quartz grain embedded in surface, g—groove.
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Figure 20. Surface of wear-resistant steel wearing away under a load of 0.125 MPa in the presence of Permian sandstone clast: a—scratches, d—hematite films, e—quartz grain embedded in hematite film.
Figure 20. Surface of wear-resistant steel wearing away under a load of 0.125 MPa in the presence of Permian sandstone clast: a—scratches, d—hematite films, e—quartz grain embedded in hematite film.
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Figure 21. Surface of wear-resistant steel wearing away under a load of 0.125 MPa in the presence of Cretaceous sandstone clast: a—scratches, d—carbonaceous films, e—quartz grain embedded in carbonaceous film.
Figure 21. Surface of wear-resistant steel wearing away under a load of 0.125 MPa in the presence of Cretaceous sandstone clast: a—scratches, d—carbonaceous films, e—quartz grain embedded in carbonaceous film.
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Figure 22. Surface of wear-resistant steel wearing away under a load of 0.125 MPa in the presence of quartz sand grain: a—scratches.
Figure 22. Surface of wear-resistant steel wearing away under a load of 0.125 MPa in the presence of quartz sand grain: a—scratches.
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Figure 23. Curves of final mass decrement (WM) of wear-resistant steel in a function of content of quartz in the sandstone varieties examined and of quartz sand (behaviour established for the loads of 0.094 MPa and 0.125 MPa).
Figure 23. Curves of final mass decrement (WM) of wear-resistant steel in a function of content of quartz in the sandstone varieties examined and of quartz sand (behaviour established for the loads of 0.094 MPa and 0.125 MPa).
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Figure 24. Model of wear in the presence of sandstone, developed for the sample/counter-sample system studied: (A) Stage I, (B) Stage II, (C) Stage III, (D) Stage IV; designations: 1—bottom sample, 2—top sample, 3—lateral test head surface, 4—hard fractions in sandstone (quartz), 5—cement and inclusions in sandstone, 6—fragments of grain and wear products, 7—discontinuous layer of cement and inclusions, 8—grain fragment driven directly into the surface, 9—scratch on the sample surface, 10—scratch filled with cement film, 11—grain fragment driven into the surface and embedded in a pocket.
Figure 24. Model of wear in the presence of sandstone, developed for the sample/counter-sample system studied: (A) Stage I, (B) Stage II, (C) Stage III, (D) Stage IV; designations: 1—bottom sample, 2—top sample, 3—lateral test head surface, 4—hard fractions in sandstone (quartz), 5—cement and inclusions in sandstone, 6—fragments of grain and wear products, 7—discontinuous layer of cement and inclusions, 8—grain fragment driven directly into the surface, 9—scratch on the sample surface, 10—scratch filled with cement film, 11—grain fragment driven into the surface and embedded in a pocket.
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Table 1. Mechanical properties of the steel tested.
Table 1. Mechanical properties of the steel tested.
Mechanical PropertiesTensile Strength TS, MPaElongation A, %Minimum Temperature for Which the Steel Impact Strength V is 30 J, °CHardness, HB
RAEX400125010−40383–403
Table 2. Chemical composition of the tested steel [mass%].
Table 2. Chemical composition of the tested steel [mass%].
CMnSiSPNiCrMoBNb
0.2881.140.4360.01240.00420.07820.4570.1220.0063<0.004
Table 3. Main parameters of the wear tests.
Table 3. Main parameters of the wear tests.
ParameterValue
Contact surface area S, mm2785.3
Compressing stress σ, MPa for
Quartz sand0.0310.0620.0940.125
Carboniferous sandstone 0.0940.125
Permian sandstone0.0310.0620.0940.125
Cretaceous sandstone 0.0940.125
Tests duration, min8 × 10
Sliding distance, m1390
Rotational speed of the moving sample, RPM149.1
Average linear speed of the moving sample, m/s0.29
Number of test repetitions for each variant3
Outside diameter of the sampleØ (54,954–55,000) mm
Inside diameter of the sampleØ (45,000–45,025) mm
Sample width (B)for upper lid B = 10 mm,
for lower lid B = 6 mm
Table 4. Results of analysis of chemical composition of studied sandstones.
Table 4. Results of analysis of chemical composition of studied sandstones.
Component, %Carboniferous SandstonePermian SandstoneCretaceous Sandstone
SiO288.53 ± 2.2180.27 ± 2.0183.14 ± 2.08
Al2O33.83 ± 0.195.09 ± 0.258.06 ± 0.40
Fe2O30.35 ± 0.1711.81 ± 0.592.88 ± 0.14
TiO20.17 ± 0.090.23 ± 0.120.37 ± 0.19
MnO 0.02 ± 0.010.01 ± 0.010.04 ± 0.02
CaO0.62 ± 0.310.03 ± 0.020.25 ± 0.12
MgO0.49 ± 0.250.09 ± 0.050.66 ± 0.33
Na2O0.53 ± 0.260.01 ± 0.011.63 ± 0.16
K2O0.67 ± 0.330.43 ± 0.221.41 ± 0.14
P2O50.01 ± 0.010.09 ± 0.040.07 ± 0.03
loss on ignition *4.73 ± 0.472.42 ± 0.241.86 ± 0.19
* loss on ignition determined at 1025 °C.
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Wieczorek, A.N.; Jonczy, I.; Filipowicz, K.; Kuczaj, M.; Pawlikowski, A.; Mucha, K.; Gerle, A. Effect of the Mineralogical Composition of Sandstones on the Wear of Mining Machinery Components. Coatings 2024, 14, 859. https://doi.org/10.3390/coatings14070859

AMA Style

Wieczorek AN, Jonczy I, Filipowicz K, Kuczaj M, Pawlikowski A, Mucha K, Gerle A. Effect of the Mineralogical Composition of Sandstones on the Wear of Mining Machinery Components. Coatings. 2024; 14(7):859. https://doi.org/10.3390/coatings14070859

Chicago/Turabian Style

Wieczorek, Andrzej N., Iwona Jonczy, Krzysztof Filipowicz, Mariusz Kuczaj, Arkadiusz Pawlikowski, Kamil Mucha, and Anna Gerle. 2024. "Effect of the Mineralogical Composition of Sandstones on the Wear of Mining Machinery Components" Coatings 14, no. 7: 859. https://doi.org/10.3390/coatings14070859

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