Analysis of the Possibility of Using New Types of Protective Coatings and Abrasion-Resistant Linings under the Operating Conditions of the Spiral Classiﬁer at KGHM Polska Mied ´z S.A. Ore Concentration Plant

: A study was carried out to select the appropriate coatings for corrosion protection of the spiral classiﬁer working at KGHM Polska Mied´z S.A. Ore Concentration Plant. The abrasion resistance of selected protective coatings and wear-resistant linings was investigated using a DT-523 rotary abrasion tester with Taber CS-10 rubber abrasive discs. The average weight loss of the coatings after a cycle of 2000 revolutions was determined. Tests of protective coatings using the electrochemical impedance spectroscopy (EIS) technique were carried out to determine the suitability of coatings in the highly saline environment of the aqueous suspension of ground copper ore. During the measurements, changes in resistance, polarising current and capacitance were determined as a function of time for the tested coatings. The linings selected on the basis of laboratory tests were also tested under industrial conditions. Their degrees of wear were characterised. The results obtained indicated the highest abrasion resistance of materials from the polyoleﬁn group (polyethylenes), where the average weight loss did not exceed 5 g/dm 2 . In the case of protective coatings, the highest durability was demonstrated by coatings with additives of ceramic aggregates, phenol-epoxy, and an elastomeric coating based on polyurea, whose average weight loss during the test cycle did not exceed 19 g/dm 2 . EIS measurements showed that the tested coatings were resistant to the aggressive environment of the feedstock. Tests under cathodic polarisation conditions of the samples at a potential below the protection potential showed that they were resistant to a highly saline environment and were also resistant to its alkalinisation resulting from the application of cathodic protection, which will be used to protect the classiﬁer together with protective coatings. Tests carried out under industrial conditions using wear-resistant linings made of plastics have made it possible to analyse the mechanism and degree of wear of the various materials during the operation of the classiﬁer. Measurements of lining wear were made in relation to baseline volumes. Polyurethane, a polymer lining based on MDI and PTMG, and those made of ultra-high-molecular-weight polyethylene with anti-stick additives showed the lowest wear rates.


Introduction
The Ore Concentration Plant (O/ZWR) is an independent unit in the organisational structure of KGHM Polska Miedź S.A., comprising three production regions: Lubin, Polkowice and Rudna. It plays a key role in the copper ore processing sequence. The primary task of O/ZWR is to maximise metal yields and produce concentrates with the quality parameters required by steel plants, at the lowest possible cost [1,2]. of which is enrichment by flotation [4][5][6][7]. As a result of this operation, a concentrate is obtained with a copper content enabling it to be metallurgically processed in the smelting process. Part of the excavated material with a low metal content is flotation waste, which is transported to the tailings pond named Żelazny Most [8]. The technology used in the O/ZWR allows for the effective recovery of copper, silver and other elements from the extracted ore. This is evidenced by high recovery of these metals (up to approximately 90%) and an average copper content in concentrates of 23% with a simultaneous high level of ore processing oscillating around 33 million tonnes of wet weight [9].
The technological operations carried out in O/ZWR require maintaining high availability indicators for machinery and equipment and technical installations. One of the main reasons for their reduced efficiency is the operation under severe corrosion-erosion conditions [10].
Corrosion is the process of destroying materials as a result of electrochemical reactions, while erosion is mechanical destruction. The simultaneous occurrence of corrosion and erosion in an aqueous environment is known as erosion corrosion (EC). The speed of the EC process can be much higher than the sum of the rates of the separate processes. This is called positive synergism-increasing the rate of corrosion by erosion, or enhancing erosion by corrosion [11,12].
An inspection of the classifier systems in O/ZWR showed the need for effective methods of corrosion protection for classifiers [13,14]. For this reason, the development of technology for the anticorrosion protection of classifiers is based on research on the possibility of increasing the effectiveness of anticorrosion protection in grinding-classifier systems by creating conditions for the cooperation of coating protection and wear-resistant linings collaborating additionally with cathodic protection [15,16].
Polymer coatings, whose role is to protect steel structures against corrosion, are most exposed to plastic or elastic stresses arising during operation. Plastic deformation may arise only after exceeding the elastic limit, which, excluding environmental conditions, may be caused by excessive (for a polymer coating) kinetic impact energy. Another possibility is that micro-cutting can occur when the tangential forces to the coating surface are sufficient. An important feature in the course of this process is the hardness of both the factor (dust, stones, sludge, lumps of earth, sand, ice, etc.) and the polymer [17].
Corrosion-erosion phenomena may occur on the working surfaces of the spiral where there is continuous contact (friction) with the ground feed ( Figure 1). The research is therefore focused on protective materials in the form of paint coatings and wear-resistant linings.   The process of segregation of feed grains in terms of their size and weight in the water medium is carried out in spiral classifiers and hydrocyclones [18][19][20][21][22]. There are 29 parallel grinding and classifying systems in O/ZWR, comprising 86 mills and 29 classifiers, each equipped with two spirals, making a total of 58 units. A schematic of the grinding and classifying system is shown in Figure 2 and the basic specifications of the classifier in Table 1. , x FOR PEER REVIEW 3 z 17 The process of segregation of feed grains in terms of their size and weight in the water medium is carried out in spiral classifiers and hydrocyclones [18][19][20][21][22]. There are 29 parallel grinding and classifying systems in O/ZWR, comprising 86 mills and 29 classifiers, each equipped with two spirals, making a total of 58 units. A schematic of the grinding and classifying system is shown in Figure 2 and the basic specifications of the classifier in Table  1.  1500-1650 Overflow Density (g/dm 3 ) 1350-1450 Underflow Density (g/dm 3 ) 2000-2200 The working environment of spiral classifiers is an aqueous suspension of ground copper ore, 95% of whose grain size is less than 1 mm. The excavated material sent to the process consists of three main lithological fractions: shale, dolomite and sandstone, whose average shares in 2020 were 9.83%, 60.70% and 29.47%, respectively. The water used in the technological process comes from the Żelazny Most tailings pond (83%) and water from mine drainage (17%). Data for 2020, coming from the monitoring system for chlorides and sulphates created for KGHM Polska Miedź S.A., show the presence of chloride ions (Cl − ) at the level of 37.6 g/dm 3 , which, together with underground waters, go to the Polkowice area, 1.43 g/dm 3 to the Lubin area and 120.60 g/dm 3 to the Rudna area. In the case of backwaters from the tailings pond Żelazny Most, the chloride (Cl − ) concentration is close to 36.8 g/dm 3 .
Sulphate ions SO4 2− are also another component of water-soluble salts. Their present concentration in mine waters directed to the Polkowice area is 1.67 g/dm 3 , to the Lubin area, 0.96 g/dm 3 and to the Rudna area, 2.43 g/dm 3 , while the backwaters from the tailings pond Żelazny Most contain about 3.4 g/dm 3 of SO4 2-ions. The concentration of sulphate in waters directed to O/ZWR has remained at a similar level for many years and slightly exceeds 3.0 g/dm 3 . The above components cause the process water to be characterised by a very high corrosion aggressiveness [23], and it is necessary to protect the process equipment against corrosion.
The aim of this work was to carry out research to select coatings that could be used in an industrial setting to protect the steel spirals of double-strand classifiers grading copper ore previously subjected to a grinding process. To the authors' knowledge, this type of solution is not used for similar facilities in the ore mining and concentration industry.  The working environment of spiral classifiers is an aqueous suspension of ground copper ore, 95% of whose grain size is less than 1 mm. The excavated material sent to the process consists of three main lithological fractions: shale, dolomite and sandstone, whose average shares in 2020 were 9.83%, 60.70% and 29.47%, respectively. The water used in the technological process comes from theŻelazny Most tailings pond (83%) and water from mine drainage (17%). Data for 2020, coming from the monitoring system for chlorides and sulphates created for KGHM Polska Miedź S.A., show the presence of chloride ions (Cl − ) at the level of 37.6 g/dm 3 , which, together with underground waters, go to the Polkowice area, 1.43 g/dm 3 to the Lubin area and 120.60 g/dm 3 to the Rudna area. In the case of backwaters from the tailings pondŻelazny Most, the chloride (Cl − ) concentration is close to 36.8 g/dm 3 .
Sulphate ions SO 4 2− are also another component of water-soluble salts. Their present concentration in mine waters directed to the Polkowice area is 1.67 g/dm 3 , to the Lubin area, 0.96 g/dm 3 and to the Rudna area, 2.43 g/dm 3 , while the backwaters from the tailings pondŻelazny Most contain about 3.4 g/dm 3 of SO 4 2− ions. The concentration of sulphate in waters directed to O/ZWR has remained at a similar level for many years and slightly exceeds 3.0 g/dm 3 . The above components cause the process water to be characterised by a very high corrosion aggressiveness [23], and it is necessary to protect the process equipment against corrosion.
The aim of this work was to carry out research to select coatings that could be used in an industrial setting to protect the steel spirals of double-strand classifiers grading copper ore previously subjected to a grinding process. To the authors' knowledge, this type of solution is not used for similar facilities in the ore mining and concentration industry. The combined use of coatings and cathodic protection of the classifier is being designed [15], which will be a technological innovation. The research results presented in this paper may be useful for those designing the protection of various industrial facilities that are exposed to the combined erosive and corrosive effects of highly saline environments.

Materials and Methods
Testing of the selected materials was carried out in two groups: plastics and protective coatings. In addition, ordinary uncoated structural steel, which is the backbone-substrate for the installation of the classifier spiral linings, was tested as a comparative benchmark. These material groups included eleven plastic samples, six paint samples and one sample made of ordinary structural steel ( Table 2). For all materials, three samples each were prepared, applied to a substrate of S235 structural steel, measuring 10 × 10 cm and 3 mm thick. The tests were conducted in accordance with EN ISO 7784-2:2016-05 [24]. Taber CS-10 abrasive discs (TABER ® Industries, North Tonawanda, NY, USA) and a load of 10 N per tester arm were used. Prior to testing, central holes were drilled to accommodate the specimens and the size and weight of the specimens were checked to ensure that they met technical requirements, reducing them by machining if necessary. Samples whose size (distance of the edge of the sample from the central hole could not be more than 7.5 cm) or weight (maximum weight of 210 g resulting from the measuring range of the balance used) exceeded the equipment capabilities of the testing apparatus were prepared for the test by mechanical treatment: machining, drilling or grinding.
The masses of samples L, M and N were measured using an analytical balance FA2104 (Yuyao Beyond Dream Commerce Co., Ltd., Zhejiang, China) with an accuracy of 0.1 mg. Samples O, P and R were weighed on a mass comparator with an accuracy of 10 mg due to the significant excess of allowable mass. The coating thickness on metal-backed samples was measured with reference to EN ISO 2808:2020-01 [25]. An ElektroPhysik MiniTest 735 m was used for the measurements. The results of the measurements are shown in Table 3. The thickness of the individual coatings was determined by the manufacturers and adapted to the operating conditions of the spiral classifier. Coat L not be more than 7.5 cm) or weight (maximum weight of 210 g resulting from the measuring range of the balance used) exceeded the equipment capabilities of the testing apparatus were prepared for the test by mechanical treatment: machining, drilling or grinding.

Downloaded from mostwiedzy.pl
The masses of samples L, M and N were measured using an analytical balance FA2104 (Yuyao Beyond Dream Commerce Co., Ltd., Zhejiang, China) with an accuracy of 0.1 mg. Samples O, P and R were weighed on a mass comparator with an accuracy of 10 mg due to the significant excess of allowable mass.

Measuring the Thickness of Tested Coating Samples
The coating thickness on metal-backed samples was measured with reference to EN ISO 2808:2020-01 [25]. An ElektroPhysik MiniTest 735 m was used for the measurements. The results of the measurements are shown in Table 3. The thickness of the individual coatings was determined by the manufacturers and adapted to the operating conditions of the spiral classifier. Samples whose size (distance of the edge of the sample from the central hole could not be more than 7.5 cm) or weight (maximum weight of 210 g resulting from the measuring range of the balance used) exceeded the equipment capabilities of the testing apparatus were prepared for the test by mechanical treatment: machining, drilling or grinding.
The masses of samples L, M and N were measured using an analytical balance FA2104 (Yuyao Beyond Dream Commerce Co., Ltd., Zhejiang, China) with an accuracy of 0.1 mg. Samples O, P and R were weighed on a mass comparator with an accuracy of 10 mg due to the significant excess of allowable mass.

Measuring the Thickness of Tested Coating Samples
The coating thickness on metal-backed samples was measured with reference to EN ISO 2808:2020-01 [25]. An ElektroPhysik MiniTest 735 m was used for the measurements. The results of the measurements are shown in Table 3. The thickness of the individual coatings was determined by the manufacturers and adapted to the operating conditions of the spiral classifier. Coat N not be more than 7.5 cm) or weight (maximum weight of 210 g resulting from the measuring range of the balance used) exceeded the equipment capabilities of the testing apparatus were prepared for the test by mechanical treatment: machining, drilling or grinding. The masses of samples L, M and N were measured using an analytical balance FA2104 (Yuyao Beyond Dream Commerce Co., Ltd., Zhejiang, China) with an accuracy of 0.1 mg. Samples O, P and R were weighed on a mass comparator with an accuracy of 10 mg due to the significant excess of allowable mass.

Measuring the Thickness of Tested Coating Samples
The coating thickness on metal-backed samples was measured with reference to EN ISO 2808:2020-01 [25]. An ElektroPhysik MiniTest 735 m was used for the measurements. The results of the measurements are shown in Table 3. The thickness of the individual coatings was determined by the manufacturers and adapted to the operating conditions of the spiral classifier. Coat O not be more than 7.5 cm) or weight (maximum weight of 210 g resulting from the measuring range of the balance used) exceeded the equipment capabilities of the testing apparatus were prepared for the test by mechanical treatment: machining, drilling or grinding. The masses of samples L, M and N were measured using an analytical balance FA2104 (Yuyao Beyond Dream Commerce Co., Ltd., Zhejiang, China) with an accuracy of 0.1 mg. Samples O, P and R were weighed on a mass comparator with an accuracy of 10 mg due to the significant excess of allowable mass.

Measuring the Thickness of Tested Coating Samples
The coating thickness on metal-backed samples was measured with reference to EN ISO 2808:2020-01 [25]. An ElektroPhysik MiniTest 735 m was used for the measurements. The results of the measurements are shown in Table 3. The thickness of the individual coatings was determined by the manufacturers and adapted to the operating conditions of the spiral classifier. Coat P not be more than 7.5 cm) or weight (maximum weight of 210 g resulting from the measuring range of the balance used) exceeded the equipment capabilities of the testing apparatus were prepared for the test by mechanical treatment: machining, drilling or grinding. The masses of samples L, M and N were measured using an analytical balance FA2104 (Yuyao Beyond Dream Commerce Co., Ltd., Zhejiang, China) with an accuracy of 0.1 mg. Samples O, P and R were weighed on a mass comparator with an accuracy of 10 mg due to the significant excess of allowable mass.

Measuring the Thickness of Tested Coating Samples
The coating thickness on metal-backed samples was measured with reference to EN ISO 2808:2020-01 [25]. An ElektroPhysik MiniTest 735 m was used for the measurements. The results of the measurements are shown in Table 3. The thickness of the individual coatings was determined by the manufacturers and adapted to the operating conditions of the spiral classifier. The test was carried out on a device called a DT-523 rotational abrasion tester (Agencja ANTICORR Gdańsk Sp. z o.o., Gdańsk, Poland) using Taber CS-10-type rubber abrasive discs. For all types of coatings and plastics, 500 preliminary rotations were performed to level the abrasive surface, after which the samples were weighed, taking the indicated weight as the initial weight. This was followed by 2000 rotations each, with samples removed and weighed and abrasive discs cleaned every 500 rotations. The load was 10 N per arm and the number of rotations per minute was 60. Samples numbered O, P and R due to exceeding a mass of 210 g were weighed only in the initial state and after a series of 2000 rotations.

Determination of Resistance of Coatings by Electrochemical Impedance Spectroscopy (EIS)-Laboratory Testing
The resistance of coatings to the environment present in spiral classifiers described in the introduction of this paper was carried out by electrochemical impedance spectroscopy (EIS) for the coating samples designated as L, M, N, O, P and R, which are listed in Table 3. Sycopel's Specstat kit (Sycopel Scientific Ltd, Washington (Tyne and Wear), UK) with a high-impedance ATLAS attachment (Atlas Sollich, Gdańsk, Poland) was used for the tests. The tests were carried out in a two-electrode system, where the working electrode was steel covered with a suitable organic coating and the counter-electrode was a platinum grid. The perturbation signal was a sinusoid with an amplitude of 150 mV. Tests The test was carried out on a device called a DT-523 rotational abrasion tester (Agencja ANTICORR Gdańsk Sp. z o.o., Gdańsk, Poland) using Taber CS-10-type rubber abrasive discs. For all types of coatings and plastics, 500 preliminary rotations were performed to level the abrasive surface, after which the samples were weighed, taking the indicated weight as the initial weight. This was followed by 2000 rotations each, with samples removed and weighed and abrasive discs cleaned every 500 rotations. The load was 10 N per arm and the number of rotations per minute was 60. Samples numbered O, P and R due to exceeding a mass of 210 g were weighed only in the initial state and after a series of 2000 rotations. Downloaded from mostwiedzy.pl

Determination of Resistance of Coatings by Electrochemical Impedance Spectroscopy (EIS)-Laboratory Testing
The resistance of coatings to the environment present in spiral classifiers described in the introduction of this paper was carried out by electrochemical impedance spectroscopy (EIS) for the coating samples designated as L, M, N, O, P and R, which are listed in Table 3. Sycopel's Specstat kit (Sycopel Scientific Ltd, Washington (Tyne and Wear), UK) with a high-impedance ATLAS attachment (Atlas Sollich, Gdańsk, Poland) was used for the tests.
The tests were carried out in a two-electrode system, where the working electrode was steel covered with a suitable organic coating and the counter-electrode was a platinum grid. The perturbation signal was a sinusoid with an amplitude of 150 mV. Tests were carried out in the frequency range from 10 kHz to 1 Hz. A feed taken from a spiral classifier from the Polkowice production area was used as the electrolyte in the study. After analytical testing, the presence of 35.8 g of Cl − /dm 3 was found. The first measurement was taken after 24 h of exposure of the coatings to the aggressive environment. Measurements were repeated every 30 days.
The optimisation program ZSimpWin (V3.10) was used to evaluate the results of the study. As none of the samples tested showed degradation at the level of coating failure and the start of corrosion processes on the steel substrate, the electrical-equivalent circuit [26] shown in Figure 3 was used for the analyses.

Determination of Resistance of Coatings by Electrochemical Impedance Spectroscopy (EIS Laboratory Testing
The resistance of coatings to the environment present in spiral classifiers descri in the introduction of this paper was carried out by electrochemical impedance spect copy (EIS) for the coating samples designated as L, M, N, O, P and R, which are liste Table 3. Sycopel's Specstat kit (Sycopel Scientific Ltd, Washington (Tyne and Wear), U with a high-impedance ATLAS attachment (Atlas Sollich, Gdańsk, Poland) was used the tests. The tests were carried out in a two-electrode system, where the working e trode was steel covered with a suitable organic coating and the counter-electrode w platinum grid. The perturbation signal was a sinusoid with an amplitude of 150 mV. T were carried out in the frequency range from 10 kHz to 1 Hz. A feed taken from a sp classifier from the Polkowice production area was used as the electrolyte in the stu After analytical testing, the presence of 35.8 g of Cl − /dm 3 was found. The first measu ment was taken after 24 h of exposure of the coatings to the aggressive environm Measurements were repeated every 30 days.
The optimisation program ZSimpWin (V3.10) was used to evaluate the results of study. As none of the samples tested showed degradation at the level of coating fail and the start of corrosion processes on the steel substrate, the electrical-equivalent cir [26] shown in Figure 3 was used for the analyses.  The results are presented in the form of the dependence of the changes in resistance and capacitance of coatings during exposure.
In addition to the good resistance to the highly corrosive and erosive environment of the feedstock, the coatings included in the tests are to cooperate with cathodic protection, so tests were also carried out to check whether the phenomena accompanying cathodic protection (alkalisation of the environment in the vicinity of the structure and hydrogen release in the event of possible overprotection near the polarisation anodes-"overprotection") do not adversely affect the condition of the coatings. For this purpose, circular defects were made on the coatings to the steel substrate with a diameter of 1 cm. PVC cups were glued onto the surface of the shells and filled with the feed. A platinised titanium-polarising electrode and an Ag/AgCl reference electrode were also inserted into each dish. After 1 h, the corrosion potentials of the steels were measured and then the test systems were connected to a potentiostat, which maintained the cathodic polarisation of the samples to a potential of −1.1 V vs. Ag/AgCl. During the exposure, changes in the polarising current flowing in the test system were monitored. The prepared samples were left for 30 days and, after this time, the current and the potential of the steel substrate were measured. After a further 30 days, the measurements were repeated and the surfaces of the stripped steel and the immediate surrounding area were analysed to check for any reduction in adhesion of the coating to the substrate.

Determination of Abrasion Resistance of Wear-Resistant Linings-Industrial Tests
Six materials were selected for testing under industrial conditions, including polyurethane, ultra-high-molecular-weight modified polyethylene with anti-adhesion additives, a polymer based on MDI and PTMG, cast polyamide 6, cast polyamide 6 with the addition of molybdenum disulphide, and high-density polyethylene. The criterion for selecting materials for the test was the abrasion resistance test results obtained previously.
The test linings were made in a shape mimicking the outer section of the classifier spiral, allowing the lining to be mounted on the spiral. The tested linings of the shape shown in Figure 4 can be divided into two groups due to their construction. The first had internal cores made of 8 mm-thick structural sheet metal. The purpose of the core fused into the lining was to stiffen it. This group includes polyurethane and polymeric linings based on MDI and PTMG. The second group was coreless linings (Figure 5), whose stiffness did not require additional reinforcements. This group of materials was made by mechanical processing, i.e. milling and drilling.
days and, after this time, the current and the potential of the steel substrate were measured. After a further 30 days, the measurements were repeated and the surfaces of the stripped steel and the immediate surrounding area were analysed to check for any reduction in adhesion of the coating to the substrate.

Determination of Abrasion Resistance of Wear-Resistant Linings-Industrial Tests
Six materials were selected for testing under industrial conditions, including polyurethane, ultra-high-molecular-weight modified polyethylene with anti-adhesion additives, a polymer based on MDI and PTMG, cast polyamide 6, cast polyamide 6 with the addition of molybdenum disulphide, and high-density polyethylene. The criterion for selecting materials for the test was the abrasion resistance test results obtained previously.
The test linings were made in a shape mimicking the outer section of the classifier spiral, allowing the lining to be mounted on the spiral. The tested linings of the shape shown in Figure 4 can be divided into two groups due to their construction. The first had internal cores made of 8 mm-thick structural sheet metal. The purpose of the core fused into the lining was to stiffen it. This group includes polyurethane and polymeric linings based on MDI and PTMG. The second group was coreless linings (Figure 5), whose stiffness did not require additional reinforcements. This group of materials was made by mechanical processing, i.e. milling and drilling.
The base (comparison) lining was the current polyurethane lining. The tested linings were exposed under normal operating conditions of the spiral classifier ( Figure 6).   days and, after this time, the current and the potential of the steel substrate were measured. After a further 30 days, the measurements were repeated and the surfaces of the stripped steel and the immediate surrounding area were analysed to check for any reduction in adhesion of the coating to the substrate.

Determination of Abrasion Resistance of Wear-Resistant Linings-Industrial Tests
Six materials were selected for testing under industrial conditions, including polyurethane, ultra-high-molecular-weight modified polyethylene with anti-adhesion additives, a polymer based on MDI and PTMG, cast polyamide 6, cast polyamide 6 with the addition of molybdenum disulphide, and high-density polyethylene. The criterion for selecting materials for the test was the abrasion resistance test results obtained previously.
The test linings were made in a shape mimicking the outer section of the classifier spiral, allowing the lining to be mounted on the spiral. The tested linings of the shape shown in Figure 4 can be divided into two groups due to their construction. The first had internal cores made of 8 mm-thick structural sheet metal. The purpose of the core fused into the lining was to stiffen it. This group includes polyurethane and polymeric linings based on MDI and PTMG. The second group was coreless linings (Figure 5), whose stiffness did not require additional reinforcements. This group of materials was made by mechanical processing, i.e. milling and drilling.
The base (comparison) lining was the current polyurethane lining. The tested linings were exposed under normal operating conditions of the spiral classifier ( Figure 6).   The base (comparison) lining was the current polyurethane lining. The tested linings were exposed under normal operating conditions of the spiral classifier ( Figure 6). The duration of the test was set at 10 months. During this time, the classifier with technology number K-211 worked 6387 h, while the average working time of one classifier working in the Polkowice area in 2020 was nearly 7500 h. During this period, an estimated 90,5850 Mg of dredged material in the form of an aqueous slurry with a density from 1500 to 1650 g/dm 3 was directed to the classifier, of which approximately 500,000 Mg was transported through the classifier linings, including test linings, towards the spillway.

Determination of Abrasion Resistance of Protective Coatings and Wear Linings-Laboratory Tests
Tests of coatings and linings showed differences in the abrasion resistance of the different materials. The surface view of the tested samples after abrasion testing is shown in Figure 6. View of the installed test linings-before starting the test.
The duration of the test was set at 10 months. During this time, the classifier with technology number K-211 worked 6387 h, while the average working time of one classifier working in the Polkowice area in 2020 was nearly 7500 h. During this period, an estimated 90,5850 Mg of dredged material in the form of an aqueous slurry with a density from 1500 to 1650 g/dm 3 was directed to the classifier, of which approximately 500,000 Mg was The base (comparison) lining was the current polyurethane lining. The tested linings were exposed under normal operating conditions of the spiral classifier ( Figure 6). The duration of the test was set at 10 months. During this time, the classifier with technology number K-211 worked 6387 h, while the average working time of one classifier working in the Polkowice area in 2020 was nearly 7500 h. During this period, an estimated 90,5850 Mg of dredged material in the form of an aqueous slurry with a density from 1500 to 1650 g/dm 3 was directed to the classifier, of which approximately 500,000 Mg was transported through the classifier linings, including test linings, towards the spillway.

Determination of Abrasion Resistance of Protective Coatings and Wear Linings-Laboratory Tests
Tests of coatings and linings showed differences in the abrasion resistance of the different materials. The surface view of the tested samples after abrasion testing is shown in Figure 6. View of the installed test linings-before starting the test. The duration of the test was set at 10 months. During this time, the classifier with technology number K-211 worked 6387 h, while the average working time of one classifier working in the Polkowice area in 2020 was nearly 7500 h. During this period, an estimated 90,5850 Mg of dredged material in the form of an aqueous slurry with a density from 1500 to 1650 g/dm 3 was directed to the classifier, of which approximately 500,000 Mg was transported through the classifier linings, including test linings, towards the spillway.

Determination of Abrasion Resistance of Protective Coatings and Wear Linings-Laboratory Tests
Tests of coatings and linings showed differences in the abrasion resistance of the different materials. The surface view of the tested samples after abrasion testing is shown in

Determination of Abrasion Resistance of Protective Coatings and Wear Linings-Laborato Tests
Tests of coatings and linings showed differences in the abrasion resistance of the d ferent materials. The surface view of the tested samples after abrasion testing is shown          The abrasion resistance results obtained are presented as the weight loss of the s ples after 2000 rotations (before which 500 rotations were carried out to even out the ab sion surface). For samples numbered D1-3 ( Figure 10) and E1-3 (Figure 11), no loss observed, which was most probably caused by the penetration of abrasive particles the structure of the samples.
Tests carried out on the DT-523 rotary abrasion tester showed differences in the a sion resistance of the different materials, as shown in Figures 13 and 14. When consider the samples from the plastics group, two main conclusions can be drawn. The first in cates that the lowest weight losses were achieved by samples C and H. Both samples w ultra-high-molecular-weight polyethylenes.
A further observation indicates that samples D, E and K achieved a weight g which was most likely due to particles from the abrasive disc penetrating the plastic st ture (Figure 13). On the samples, a greenish tarnish could be observed on the abra surface.  The abrasion resistance results obtained are presented as the weight loss of the samples after 2000 rotations (before which 500 rotations were carried out to even out the abrasion surface). For samples numbered D1-3 ( Figure 10) and E1-3 (Figure 11), no loss was observed, which was most probably caused by the penetration of abrasive particles into the structure of the samples.
Tests carried out on the DT-523 rotary abrasion tester showed differences in the abrasion resistance of the different materials, as shown in Figures 13 and 14. When considering the samples from the plastics group, two main conclusions can be drawn. The first indicates that the lowest weight losses were achieved by samples C and H. Both samples were ultra-high-molecular-weight polyethylenes. Downloaded from mostwiedzy.pl cates that the lowest weight losses were achieved by samples C and H. Both samples were ultra-high-molecular-weight polyethylenes.
A further observation indicates that samples D, E and K achieved a weight gain, which was most likely due to particles from the abrasive disc penetrating the plastic structure ( Figure 13). On the samples, a greenish tarnish could be observed on the abraded surface.  Comparing the obtained test results, it should be stated that the highest durability during the conducted tests of abrasion resistance was obtained for samples marked as C and H, i.e. samples from the group of polyolefins (polyethylenes), i.e. materials consisting mainly of carbon and hydrogen. Additives supplementing the material composition of tested samples are trade secrets of the manufacturers. Paint coatings designated as L, M and O also achieved a satisfactory result; however, the losses in their masses were more than four times higher compared to materials made of polyethylene.

Determination of Resistance of Coatings by Electrochemical Impedance Spectroscopy (EIS)-Laboratory Testing
The first measurement, taken two days after the start of exposure, indicates that all tested coatings showed very good barrier properties. During the exposure, none of the tested systems showed a decrease in impedance below the value considered as the limit, i.e., 10 6 Ω. The dynamics of resistance and film capacitance changes were different for the tested coatings. This is due to both the performance properties of the coatings, as well as the varying thicknesses [27,28]. Figure 15 shows example impedance spectra in the form of Nyquist plots obtained for one of the organic coatings tested. Table 4 presents the results of the calculations of the resistance and the capacity of the coating fitted to the equivalent model shown in Figure 3 together with the estimated measurement error. A further observation indicates that samples D, E and K achieved a weight gain, which was most likely due to particles from the abrasive disc penetrating the plastic structure ( Figure 13). On the samples, a greenish tarnish could be observed on the abraded surface.
Among the coatings and structural steel group, three samples with similar weight losses can be observed, i.e., L, M and O, which do not exceed 20 mg after a cycle of 2500 revolutions, as shown in Figure 14. In this group, the most durable coatings were those containing hard additives of ceramic aggregates, phenolic-epoxy and elastomeric coatings based on polyurethane. Other samples tested achieved weight losses of up to nearly 90 mg. It should be noted that ordinary S 235 structural steel lost nearly 25 mg during the entire test cycle.
Comparing the obtained test results, it should be stated that the highest durability during the conducted tests of abrasion resistance was obtained for samples marked as C and H, i.e. samples from the group of polyolefins (polyethylenes), i.e. materials consisting mainly of carbon and hydrogen. Additives supplementing the material composition of tested samples are trade secrets of the manufacturers. Paint coatings designated as L, M and O also achieved a satisfactory result; however, the losses in their masses were more than four times higher compared to materials made of polyethylene.

Determination of Resistance of Coatings by Electrochemical Impedance Spectroscopy (EIS)-Laboratory Testing
The first measurement, taken two days after the start of exposure, indicates that all tested coatings showed very good barrier properties. During the exposure, none of the tested systems showed a decrease in impedance below the value considered as the limit, i.e., 10 6 Ω. The dynamics of resistance and film capacitance changes were different for the tested coatings. This is due to both the performance properties of the coatings, as well as the varying thicknesses [27,28]. Figure 15 shows example impedance spectra in the form of Nyquist plots obtained for one of the organic coatings tested. Table 4 presents the results of the calculations of the resistance and the capacity of the coating fitted to the equivalent model shown in Figure 3 together with the estimated measurement error.

Determination of Resistance of Coatings by Electrochemical Impedance Spectroscopy (EIS)-Laboratory Testing
The first measurement, taken two days after the start of exposure, indicates that all tested coatings showed very good barrier properties. During the exposure, none of the tested systems showed a decrease in impedance below the value considered as the limit, i.e., 10 6 Ω. The dynamics of resistance and film capacitance changes were different for the tested coatings. This is due to both the performance properties of the coatings, as well as the varying thicknesses [27,28]. Figure 15 shows example impedance spectra in the form of Nyquist plots obtained for one of the organic coatings tested. Table 4 presents the results of the calculations of the resistance and the capacity of the coating fitted to the equivalent model shown in Figure 3 together with the estimated measurement error. Figure 15. Example impedance spectra obtained for a selected organic coating (coating "P"). Relative standard error/% 10. 23 5.61 The results for the other tested coatings are presented as the relationship R C = f(t) and C C = f(t) (Figure 16). The typical behaviour of coatings exposed in aggressive environments was evident. There was then an initial drop in the resistance of the coatings, followed by stabilisation at high or very high resistance values, reaching levels ranging from 10,000 Figure 15. Example impedance spectra obtained for a selected organic coating (coating "P"). Relative standard error/% 10. 23 5.61 The results for the other tested coatings are presented as the relationship R C = f(t) and C C = f(t) (Figure 16). The typical behaviour of coatings exposed in aggressive environments was evident. There was then an initial drop in the resistance of the coatings, followed by stabilisation at high or very high resistance values, reaching levels ranging from 10,000 MΩ Downloaded from mostwiedzy.pl for the M coating to around 55,000 MΩ for the O coating. This is related, among other things, to the recommended thickness of the coatings that have been specified to protect the surfaces of spiral classifiers.  The corrosion potential of the steel in the feed ranged from −0.656 to −0.6 Ag/AgCl depending on the sample. Connecting the potentiostat caused the pot the steel substrate to drop very quickly to an assumed level of −1.1 V.
At the end of the exposure, a layer of cathodic deposits was found on the from which the organic coating had been removed, effectively reducing the surf polarised during the tests. The plots of the polarising current versus time (Figure 1 a continuous decrease in the current value. This also demonstrates the lack of n interaction between cathodic and coating protection, as any loss of adhesion of the to the substrate would result in an increase in the current required to polarise the An attempt to mechanically remove the organic coating from the steel surface at ficial failure boundary also failed. The tested coatings were therefore resistant to e mental alkalisation resulting from the application of cathodic protection. The corrosion potential of the steel in the feed ranged from −0.656 to −0.685 V vs. Ag/AgCl depending on the sample. Connecting the potentiostat caused the potential of the steel substrate to drop very quickly to an assumed level of −1.1 V. At the end of the exposure, a layer of cathodic deposits was found on the surface from which the organic coating had been removed, effectively reducing the surface area polarised during the tests. The plots of the polarising current versus time ( Figure 17) show a continuous decrease in the current value. This also demonstrates the lack of negative interaction between cathodic and coating protection, as any loss of adhesion of the coating to the substrate would result in an increase in the current required to polarise the sample. An attempt to mechanically remove the organic coating from the steel surface at the artificial failure boundary also failed. The tested coatings were therefore resistant to environmental alkalisation resulting from the application of cathodic protection.

Determination of Abrasion Resistance of Wear-Resistant Linings-Industrial Tests
Measurements of the degrees of wear of the spiral-mounted linings were taken according to the points indicated in the sketch below ( Figure 18). A view of the linings after exposure is illustrated in Figure 19.
An analysis of the degrees of wear of the tested linings based on the wear measurements shown in Figures 20 and 21 shows that linings made of polyurethane and polymer produced on the basis of MDI and PTMG achieved some of the lowest wear values, which is particularly evident for measurement numbers 4, 5 and 6 ( Figure 21). Downloaded from mostwiedzy.pl

Determination of Abrasion Resistance of Wear-Resistant Linings-Industrial Tests
Measurements of the degrees of wear of the spiral-mounted linings were taken according to the points indicated in the sketch below ( Figure 18). A view of the linings after exposure is illustrated in Figure 19. An analysis of the degrees of wear of the tested linings based on the wear measurements shown in Figures 20 and 21 shows that linings made of polyurethane and polymer produced on the basis of MDI and PTMG achieved some of the lowest wear values, which is particularly evident for measurement numbers 4, 5 and 6 ( Figure 21).

Determination of Abrasion Resistance of Wear-Resistant Linings-Industrial Tests
Measurements of the degrees of wear of the spiral-mounted linings were taken according to the points indicated in the sketch below ( Figure 18). A view of the linings after exposure is illustrated in Figure 19. An analysis of the degrees of wear of the tested linings based on the wear measurements shown in Figures 20 and 21 shows that linings made of polyurethane and polymer produced on the basis of MDI and PTMG achieved some of the lowest wear values, which is particularly evident for measurement numbers 4, 5 and 6 ( Figure 21).  The elastic structure of both materials means that they are able to absorb some of the energy from the pressure force generated by the slurry in the classifier. Additionally noteworthy is the lining made of ultra-high-molecular-weight polyethylene with anti-stick additives, which achieved the lowest wear according to measurement numbers 1 and 2 (Figure 20), which may indicate the low coefficient of friction of this material. The remaining samples achieved a wear (relative to baseline values) above 1 mm for measurements 1, 2 and 3 ( Figure 20       The elastic structure of both materials means that they are able to absorb some of the energy from the pressure force generated by the slurry in the classifier. Additionally noteworthy is the lining made of ultra-high-molecular-weight polyethylene with anti-stick additives, which achieved the lowest wear according to measurement numbers 1 and 2 ( Figure 20), which may indicate the low coefficient of friction of this material. The remaining samples achieved a wear (relative to baseline values) above 1 mm for measurements 1, 2 and 3 ( Figure 20) and above 23 mm for measurements 4, 5 and 6 ( Figure 21).

Conclusions
The results obtained showed that it is possible to use industrially applicable materials that will effectively and permanently protect the classifier spiral from corrosive and erosive environments.
Among the linings tested, ultra-high-molecular-weight polyurethanes and polymeric materials achieved the lowest weight losses. In the case of paint coatings, phenolic-epoxy, polyurea-based elastomeric and those containing hard additions of ceramic aggregates showed the highest durability. All of them showed good barrier properties and resistance to environmental alkalisation resulting from the application of electrochemical protection.
Testing of the linings under industrial conditions confirmed the high erosion resistance of polyurethane and polyethylene-based materials. The optimal solution would be to create a two-material lining consisting of a high-molecular-weight polyethylene with adhesive additives in the front part and a polyurethane or polymeric material in the side part.
During the final selection of paint coatings for the protection of the device, in addition to the abrasion resistance, the possibilities of their cooperation with cathodic protection were taken into account, as well as the weight. As with coatings, the linings used must not exceed the allowable weight, due to the mechanical restrictions mentioned above.