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Article

Influence of Chromium Concentration on the Abrasive Wear of Ni-Cr-B-Si Coatings Applied by Supersonic Flame Jet (HVOF)

1
Tribology Center, Faculty of Industrial Engineering, Technical University–Sofia, 8 Kl. Ohridski Blvd, 1757 Sofia, Bulgaria
2
South Ural State University, 76 Prospekt Lenina, 454080 Chelyabinsk, Russia
3
SciBuCom 2 Ltd., P.O. Box 249, 1113 Sofia, Bulgaria
*
Author to whom correspondence should be addressed.
Metals 2021, 11(6), 915; https://doi.org/10.3390/met11060915
Submission received: 20 April 2021 / Revised: 18 May 2021 / Accepted: 25 May 2021 / Published: 4 June 2021
(This article belongs to the Special Issue Amorphous and High-Entropy Alloy Coatings)

Abstract

:
This research work studies the characteristics of wear and wear resistance of composite powder coatings, deposited by supersonic flame jet (HVOF), which contain composite mixtures Ni-Cr-B-Si having different chromium concentrations—9.9%, 13.2%, 14%, 16%, and 20%, at one and the same size of the particles and the same content of the remaining elements. The coating of 20% Cr does not contain B and Si. Out of each powder composite, coatings have been prepared without any preliminary thermal treatment of the substrate and with preliminary thermal treatment of the substrate up to 650 °C. The coatings have been tested under identical conditions of dry friction over a surface of solid, firmly-attached, abrasive particles using tribological testing device “Pin-on-disk”. Results have been obtained and the dependences of the hardness, mass wear, intensity of the wearing process, and absolute and relative wear resistance on the Cr concentration under identical conditions of friction. It has been found out that for all the coatings the preliminary thermal treatment of the substrate leads to a decrease in the wear intensity. Upon increasing Cr concentration the wear intensity diminishes and it reaches minimal values at 16% Cr. In the case of coatings having 20% Cr concentration, the wear intensity is increased, which is due to the absence of the components B and Si in the composite mixture, whereupon no inter-metallic structures are formed having high hardness and wear resistance. The obtained results have no analogues in the current literature and they have not been published by the authors.

1. Introduction

The basic priorities of contemporary engineering science and practice refer to enhancement of energy effectiveness and functionality of the industrial systems in harmonic coexistence with clean environment, preservation of natural resources, and improving of the quality of life. These priorities are connected with the genesis of tribology as contemporary science and technology for contact processes of friction, wear, and greasing in the technical systems [1,2,3]. The lowering of the wear intensity in the machines appears to be the central task of tribology tribological technologies. It is the reason for more than 85% of the machine failures, huge expenses of materials, and human resources for spare parts, consumables, and expenses for maintenance in the process of operation. The decrease in the wear intensity results not only in lower financial expenses, but also decrease in extraction of raw materials from the natural environment, which is directly connected with the equilibrium in eco-systems [4,5,6,7,8,9,10].
The abrasive and erosive wear are the most dangerous types of wear in the machines for ore mining, road construction, agricultural technique, energy production, transportation, aircraft building, and space technology. They are the reason for more than 50% of all the technical failures due to wear of machine components and the expenses due to it in the world reach 1–4% of the gross domestic product GDP of the developed industrial countries in the world. The problem of abrasive and erosive wear resistance of tribological materials is of exceptional importance and actuality, which is evidenced by the fact that there exist 17 active standards ASTM, concerning the abrasive wear and at least 4 standards connected with the erosion wear.
It is of special importance for the high wear resistance of tribology materials to combine high hardness and plasticity, which are mutually self-excluding aspects and they cannot be achieved by most of the conventional tribology technologies [11,12,13,14,15,16,17,18,19,20,21,22,23,24].
The composite powder coatings, deposited by means of supersonic flame jet-HVOF (High Velocity Oxy-Fuel) are a new generation of tribo-materials, allowing to achieve a wide range of combining mechanical and tribological characteristics—high adhesion strength, density, hardness, wear resistance, and corrosion stability. The powder particles obtain high kinetic and thermal energy in the flame jet, passing over into semi-plastic and/or plastic state in the form of droplets or particles, and they interact with the substrate being deformed, whereupon they form thin lamellas. Upon their collision with roughness of the substrate the particles’ droplets are being cooled down, forming adhesion bonds with the surface, and cohesion bonds between each other leading to generation of the laminar structure of the composite coating. Due to the high velocity and low contact time of the particles with oxygen under definite conditions they do not form oxides, which, in fact, is a prerequisite for good tribological properties of the coatings [25,26]. HVOF-coatings are the object of intensive investigations and they are continuously being improved [27,28,29,30,31,32,33,34,35,36,37,38,39,40,41]. The results of studies of the authors and those of other researchers show that the mechanical and tribological characteristics of the HVOF-coatings, depend not only on the parameters of the technological regime of deposition, but also to a great extent they depend on the chemical composition and on the concentrations of the chemical elements in the powder composite material, the size of the particles, and on the temperature of the substrate. The results also depend on the type and the dimensions of the contact (point type, linear type, planar type) [29,31,35]. The papers [35,36] present interesting results concerning the ceramic coatings with aluminum oxide matrix (Al2O3) with matrix of 3% titanium oxide (TiO2) and zirconium oxide (ZrO2) matrix with 30% calcium oxide (CaO) on the basis of non-alloy structural steel of the S235JR class. The buffer layer is obtained on the basis of Ni-Al-Mo powder. The complex investigations including metallographic tests, phase composition, microhardness, adhesion of coating to the base, resistance to abrasion, and heat shock show that these coatings have high abrasive and erosion wear resistance and resistance towards thermal impact load. In the paper [37] the results of the investigation of the mechanical properties of aluminum coatings are presented by the same Authors. The coatings are strengthened with carbon materials with nano-dimensions: carbon nanotubes Nanocyl NC 7000 (0.5 w.% and 1 w.%) and (carburate 0.5 w.%). It has been proved that the applied coatings with nano-carbon particles, will be an effective alternative of coatings applied with laser technology and might be additionally improved and successfully applied in the automotive, aviation, and space technology.
According to the specialized literature the most widely used in the practice high quality powder metal composites, known as “super alloys”, can be divided into two large groups: powder composites based on nickel (nickel-chromium-boron-silicon (Ni-Cr-B-Si)) and powder composites based on cobalt (tungsten-cobalt-chromium alloys). The chromium at high temperatures is involved into contact interactions with the carbon, silicon, and boron, whereupon it forms new inter-metallic structures. It forms with the carbon solid high-melting structure (Cr3C2) having a green color, which is not dissolved in acids and which attributes to the coating high corrosion stability. Chromium forms with the oxygen some oxides (CrO3, Cr2O3), which are characterized by high level of hardness and fragility [33,34].
In the paper [40], the influence of the dimensions of the abrasive particles has been presented on the abrasive stability on the coatings of 40WC/Co, applied by three technological regimes: high velocity oxygen fuel (HVOF), high energy plasma spray (HEPS), and high velocity plasma spray (HVPS) with the use of nanostructured experimental powders. The most important results are: first—the coatings applied by HVOF have the best wear resistance, while the HVPS coatings have the worst wear resistance; and second—the greater the size of the abrasive particles, the lower the abrasion resistance of the coatings.
Thermospray coatings based on tungsten, nickel, and their compounds are widely used in extreme operating conditions due to their high resistance to wear and oxidation at high temperatures [39,40,41]. Work [39] is an in-depth study of the influence of process primers on friction, abrasion resistance, and corrosion of U.Co coatings deposited on aluminum alloy AA 7050 by HVOF process.
The present publication represents the results from an investigation about the influence of chromium concentration on the abrasion wear of Ni-Cr-B-Si coatings, deposited by means of supersonic flame jet on a substrate with and without thermal treatment of the substrate.

2. Materials and Technology

The investigated coatings are obtained in the following consecutive steps: preparation of the powder compositions, preparation of the substrate, application of the coatings with HVOF technology, measurement of the thickness and the hardness of the obtained coatings, preparation of the samples for testing of the abrasive wear, and calculation of the characteristic of the wear (Figure 1).
Ten types of coatings were prepared on the basis of five composite powder mixtures with nickel matrix, united in five series A, B, C, D, E (Table 1). The serial composition A, B, C, D containing different concentration of Chromium—9.9%, 13.2%, 14%, 16%, and approximately the same composition of the other chemical elements—Si, B, Fe, Cu, Mo, etc. The composite mixture of series E (sample No 9 and No 10) contain 20% Cr and 80% Ni, i.e., in it are not included other elements, present in the compositions A, B, C, D, respectively.
From each of the series, we applied two types of coatings; without preliminary thermic processing of the substrate (cold HVOF process); and with preliminary heating of the substrate in thermic chamber at a temperature of 650 °C for 60 min. The coatings with thermic processing of the substrate are denoted with PHS.
All the coatings have been deposited on a substrate of one and the same material-steel of chemical composition: C—0.15%; S—0.025%; Mn—0.8%; P—0.011%; Si—0.21%; Cr—0.3%; Ni—0.3% and hardness 193.6–219.5 HV.
The particles in all the powder composites have one and the same size—45 ± 2.5 µm. Before placing of the powder composite inside the system for thermal spraying, it is heated for 30 min at temperature 150 °C in thermal chamber for removing the moisture and the other adsorbed organic molecules.
In order to increase the adhesion strength of the coatings, the substrate is heated preliminarily in three stages: cleaning, erosion with abrasive particles (blasting), and mechanical treatment. The cleaning is aimed at the removal of mechanical contaminants, adsorbed organic molecules, moisture, and other components, and it is carried out using a solvent. The extraction of the adsorbed gas molecules and elements in the depth of the surface layer is achieved by burning of the surface of the substrate with a flame to reach 100 °C at a distance of the nozzle 40 mm and at an angle of 45° or with vapor spraying device. After this operation, again the surface is cleaned with a solvent.
Upon erosion of the surface of the substrate (blasting) one can achieve a definite level of roughness of the substrate, which is of essential importance for the level of the adhesion strength of the coating. We used abrasive material “Grit”, in accordance with the requirements of the standard ISO 11126, having granular composition of the abrasive material in the following percentage ratio: 3.15 ÷ 1.4 mm—9.32%; 1.63 ÷ 0.5 mm—16.4%; 1.4 ÷ 1.0 mm—15.8%; 1.0 ÷ 0.63 mm—39.6%; 0.5 ÷ 0.315 mm—9.32%; 0.315 ÷ 0.16 mm—9.32%; particles having sizes below 0.15 mm of the various fractions—up to 100% of the following chemical compounds: SiO2—41%, combined in the form of silicates; AlO—8.3%, MgO—6.6%, CaO—5.5%, and MnO—0.4%.
The system for blasting has the following technical parameters: input pressure 8 atm; operating pressure in the nozzle—4 atm; diameter of the nozzle 7 mm; distance between the nozzle and the surface—30 mm; angle of interaction of the jet with the surface—90°.
The coatings have been deposited using the device MICROJET + Hybrid, which makes use of fuel mixture of acetylene and oxygen. The parameters of the technological regime of deposition of the coatings are listed in Table 2.
In case of deposition of coatings without thermal treatment (cold HVOF process), the surface of the substrate is heated using flame having temperature up to 200 °C, which is measured by Laser infrared thermometer INFRARED with an error of 0.5 °C.
The coating is deposited in several layers. In the case of the first layer the nozzle is situated at an angle of 45° and at a distance from the substrate 10 mm, while in the consecutive layers—at a distance of 25 mm. Coatings have been prepared having thickness within the range from 393 µm up to 415 µm. The thickness of the coatings is measured by a portable device Pocket Leptoskop 2021 Fe in 10 points on the surface and the mean arithmetic value is taken (Table 1). The accuracy of the apparatus is 1 µm.
After polishing all surfaces, the coatings have the same roughness Ra = 0.450–0.455 µm, which is measured by recording the profile diagram using profile metering device “TESA Rugosurf 10-10G” with an error of 0.005 µm.
The hardness of the coatings is measured by hardness-metering device “Bambino” based on the scale of Rockwell (HRC) taking the mean arithmetic value out of three measurements for each sample in order to eliminate some possible effects of segregation.

3. Experimental Procedures

The abrasive wear of the coatings is studied under conditions of dry friction during sliding along the surface with firmly attached abrasive particles.
The methodology consists in measurement of the mass wear of the coatings after a definite pathway of friction (number of cycles) under set permanent conditions-loading, sliding velocity, kinds of the abrasive, temperature of the environment. The mass of the samples before and after a definite pathway of friction is measured by electric balance WPS 180/C/2 with an accuracy of 0.1 mg. In each experiment, with each sample, the abrasive surface is replaced and prior to each measurement the sample is cleaned, removing mechanical and organic particles, thereafter it is dried up using ethyl alcohol in order to prevent the electrostatic effect.
After measuring of the mass wear the wear process characteristics are calculated-reduced intensity of the wear process, the absolute or the relative wear resistance.
The mass wear in mg is obtained as the difference between the initial mass of the sample m o and its mass m i   after a definite number of cycles of friction:
m = m o m i
The wear rate of the wear process i r represents the mass wear m of the coating per unit of loading P and per unit of path length L of friction. It is measured in mg/Nm and it is estimated by the formula:
i r = m P L
The absolute abrasive wear resistance   I r is represented as the reciprocal value of the reduced wear rate and it has dimension Nm/mg, i.e.,
I r = 1 i r = P L m
The relative wear resistance R i j is dimensionless quantity and it represents the ratio between the wear resistance of the tested sample I r i and the wear resistance of a sample, taken as a standard I r j , determined during identical regimes of friction, i.e.,
R i j = I r i I r j
The abrasive wear is studied using tribological tester “Pin-on-disc” in case of plane-like contact using the functional scheme, shown in Figure 2. The studied sample with coating 1 (pin) is firmly attached in the holder 2 of the loading head 8, in such a way that the frontal surface of the sample is in contact with the abrasive surface 3, fixed to a horizontal disc 4. The disc 4 is driven by the electric motor 6 and it is rotating around its central vertical axis at constant angle velocity. The normal loading pressure P is adjusted by means of the lever system in the center of the contact plate between the sample and the abrasive surface. The pathway length of friction as a number of cycles (N) is selected and then measured by the turnover number metering device 7. The abrasive surface 3 is modeled by impregnated corundum P 320 of hardness 9.0 on the scale of Moos, whereupon the requirement of the standard for minimum 60% higher hardness of the abrasive is observed with respect to that of the surface layer of the tested materials.
The investigation of all the coatings has been carried out using a set of the following parameters of the regime of friction: loading 4.5 N, nominal contact surface area 2.25 × 10−6 m2; nominal contact pressure 2.0 N/cm2, sliding velocity of 0.155 m/s; type of the abrasive surface Corundum P 320, temperature of the environment 21 °C.

4. Experimental Results and Discussion

Applying the above-described methodology and the device experimental results have been obtained for the mass wear process, the wear rate, and the absolute and the relative wear resistance for all the studied coatings, listed in Table 1.
In Table 3, we give the results of the mass wear rate at a friction path 20, 40, 60 and 80 m.
In accordance with the data in Table 3 the kinetic curves have been plotted in regard to the mass wear for all coatings with and without thermal treatment of the substrate, represented in the Figure 3, Figure 4, Figure 5, Figure 6 and Figure 7. Each plotted graph represents regression equations of the wearing process as a function of the length of the friction pathway m = m ( L ) and the value of the wear rate i r at friction pathway length L = 80 m. It is seen, that in the case of dry abrasive friction, the dependence of the mass wear as a function of the sliding pathway has linear character for coatings with and without thermal treatment of the substrate.
The second observation in the analysis of these curves refers to the fact that the wear of all coatings having thermal treatment of the substrate is less than the wear of the coatings without any thermal treatment of the substrate.
Figure 8 represents graphically the dependence of the wear rate on the concentration of chromium for coatings without thermal treatment of the substrate and for coatings with thermal treatment of the substrate for one and the same friction pathway length L = 80 m.
The curves have non-linear character with a clearly expressed minimum of the wear rate at 16% concentration of Cr for coatings with and without thermal treatment. In the first section, in which the chromium concentration is changing within the range from 9.9% to 16% upon increasing of the chromium concentration, the wear rate decreases down to reaching a minimal value at chromium concentration 16%, respectively, for coatings without thermal treatment of the substrate i r = 0.91 × 10−2 mg/Nm and for coatings with thermal treatment of the substrate i r = 0.49 × 10−2 mg/Nm. In the second section, at higher chromium concentration (20%) (coatings Ni80-20Cr and Ni80-20Cr:PHS), the wear rate is increasing sharply. In spite of the higher chromium concentration the increase in the wear is due to the absence of the elements B, Si, Cu, and the others, which are contained in the other coatings. These elements in the process of contact interaction of the flame jet with the substrate at the high temperature are forming inter-metallic compounds with the chromium, which lead to decrease in the wear rate.
The curve of the dependence of the wear resistance on the concentration of chromium in coatings without thermal treatment and with thermal treatment of the substrate is reciprocal to the curve of wear intensity (Figure 9).
Figure 10 shows the diagram of the wear resistance of all the tested coatings, which gives clear evidence, that the lowest wear resistance is displayed by coatings having the lowest concentration of chromium without thermal treatment of the substrate i r = 0.24 × 102 Nm/mg, while the greatest wear resistance is manifested by the coatings having 16% content of chromium with thermal treatment of the substrate I r = 2.04 × 102 Nm/mg.
Table 4 represents results on the relative wear resistance, calculated by the Formula (4). The last two columns reflect the results respectively for the influence of the thermal treatment of the substrate and the effect of chromium concentration in the powder composites. These results are represented in the form of diagrams in Figure 11 and Figure 12.
The strongest influence on the wear resistance is observed for the thermal treatment of the substrate in the case of the coating NiBSi-16Cr:PHS, having concentration of chromium at 16%, for which the wear resistance is 1.84 times higher than that of the same coating without thermal treatment of the support. Next to it, follows the coating NiBSi-14Cr:PHS with concentration of chromium at 14%. For the remaining coatings the influence of the thermal treatment is almost one and the same ranging from 1.14 to 1.21.
The influence of the concentration of chromium upon the abrasive wear resistance of the coatings is the greatest in the cases of the coatings NiBSi-16Cr:PHS and NiBSi-16Cr (16% Cr). For coating with thermal treatment (the coating NiBSi-16Cr:PHS) the wear resistance is increased 7.29 times, while for the same coating without thermal treatment (the coating NiBSi-16Cr) it is increased 4.58 times, which is an extraordinary result. Another good result is the increase in the wear resistance of the coatings NiBSi-16Cr:PHS and Ni80-20Cr:PHS, which becomes higher almost to the same degree, respectively 1.68 and 1.67 times. The results on the wear resistance correlate with the hardness of the coatings having different concentrations of Cr (Figure 13).
Figure 14 illustrates the diagram of the interconnection between the abrasive wear resistance and the hardness of the tested coatings.

5. Regression Models

The experimental curve of the dependence of the wear intensity i r on the chromium concentration in the range 9.9 % w 16 % is considered (Figure 14).
The section of the curve where w > 16 % is not considered because it includes coatings No 9 and No 10 (Ni80-20Cr and Ni80-20Cr:PHS) with different chemical composition from the other coatings. These coatings contain only nickel (80%) and chromium (20%), which does not give us reason to analyze them in parallel with the other coatings.
Experimental results for the wear intensity at more points on the curve in Figure 8 are presented in Table 5. Graphically, the dependence of the wear intensity on the percentage of chromium is shown in Figure 15.
Based on the regression analysis, analytical dependences of the wear rate on the chromium concentration were obtained, presented as second- and third-degree polynomials.
For coatings without heat treatment of the substrate the dependence has the following form
i r ( w ) = a 3 w 3 + a 2 w 2
The results are presented on the next Figure 16.
The Adjusted R Square is 0.745894827 and shows that 74.58% of the variance of the intensity of wear is predictable from chosen factors (w3, w2) which are adequately included in the model. The value of the significance F with significance level 0.05 is 0.00012 < 0.05 (0.012% < 5%), i.e., the results are reliable (statistically significant) and the model is adequate. p-values of the coefficients of the regression equations with level of significance 0.05 are smaller than 0.000032, i.e., they are smaller than 0.05, which means that the coefficients are statistically significant, and the adequacy of the model is confirmed.
For coatings without heat treatment of the substrate the dependence has the following form:
i r ( w ) = b 3 w 3 + b 2 w 2
The results are presented on the Figure 17.
The Adjusted R Square is 0.74616892 and shows that 74.62% of the variance of the intensity of wear is predictable from chosen factors (w3, w2), i.e., they are adequately included in the model. The value of the significance F with significance level 0.05 is 0.00011 < 0.05 (0.011% < 5%), i.e., the results are reliable (statistically significant) and the model is adequate. P-values of the coefficients of the regression equations with level of significance 0.05 are smaller than 0.000019, i.e., they are smaller than 0.05, which means that the coefficients are statistically significant, and the adequacy of the model is confirmed.

6. Conclusions

The present research work represents comparison of results for the characteristics of the wear process and the wear resistance of composite powder coatings, deposited by means of supersonic flame jet (HVOF), which contain composite mixtures Ni-Cr-B-Si having different concentrations of chromium—9.9%, 13.2%, 14%, 16%, and 20%—at one and the same size of the particles (45 µm) and equal content of the other elements, boron and silicon. The coating, prepared to have 20% Cr, does not contain the elements B and Si. Each powder composition was applied to obtain coating without preliminary thermal treatment of the substrate and with preliminary thermal treatment of the substrate up to 650 °C. The coatings have been tested under identical regimes of dry friction along the surface with firmly attached abrasive particles using a tribo-tester “Pin-disc”.
Results have been obtained on the dependence of the mass wear as a function of the length of the pathway of friction, the variation of the wear rate depending on the concentration of chromium for coatings without thermal treatment of the substrate and with thermal treatment of the substrate.
It has been ascertained that for all coatings the preliminary thermal treatment of the substrate leads to a decrease in the wear rate.
It has been shown that upon increasing the concentration of chromium the wear rate is decreasing non-linearly, whereupon it reaches minimal values at 16% Cr. In the case of coatings having 20% concentration of Cr the wear rate is higher, which is due to the absence of the components B and Si in the composite mixture. In this case no new inter-metallic structures are formed, having high hardness and high wear resistance. A diagram of the interconnection between the hardness of the coatings and their abrasive wear resistance is represented.
The destruction of the surface of the coating due to abrasive wear is mechanical in nature. The main mechanisms of abrasive wear are two-plastic deformation and micro-cutting. At a low concentration of chromium in the coating, its hardness is lower, the abrasive particles penetrate into the coating, and initially, part of the material is pushed out, forming scratches and grooves on the surface of the coating. Due to the repeated cyclic interaction, the material separates from the surface and the intensity of wear increases as a result of the formation of submicro- and micro-cracks from fatigue. With a higher chromium content in the coating, the hardness of the coating is higher than the presence of chromium intermetalloid compounds. In this case, the abrasive wear takes place by the mechanism of micro-cutting of the surface layer of the coating, in which very thin and shallow scratches are observed and the wear rate is significantly lower.
Based on the regression analysis, analytical dependences of the wear rate on the chromium concentration were obtained for coatings without heat treatment and coatings with heat treatment of the substrate, presented as polynomials of second and third degree.

Author Contributions

Conceptualization, Z.K. and M.K.; methodology, M.K.; software, Y.S.; validation, Z.K., M.K. and Y.S.; formal analysis, Z.K.; investigation, M.K.; resources, Z.K.; data curation, Y.S.; writing—original draft preparation, M.K.; writing—review and editing, Z.K.; visualization, M.K.; supervision, M.K.; project administration, M.K.; funding acquisition, Z.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Scheme of preparation and research of HVOF-coatings.
Figure 1. Scheme of preparation and research of HVOF-coatings.
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Figure 2. Schematic diagram of abrasive wear testing on pin-disc tribometer.
Figure 2. Schematic diagram of abrasive wear testing on pin-disc tribometer.
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Figure 3. Mass wear vs. sliding distance for NiBSi-9.9Cr and NiBSi-9.9Cr: PHS coatings.
Figure 3. Mass wear vs. sliding distance for NiBSi-9.9Cr and NiBSi-9.9Cr: PHS coatings.
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Figure 4. Mass wear vs. sliding distance for NiBSi-13.2Cr and NiBSi-13.2Cr: PHS coatings.
Figure 4. Mass wear vs. sliding distance for NiBSi-13.2Cr and NiBSi-13.2Cr: PHS coatings.
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Figure 5. Mass wear vs. sliding distance for NiBSi-14Cr and NiBSi-14Cr: PHS coatings.
Figure 5. Mass wear vs. sliding distance for NiBSi-14Cr and NiBSi-14Cr: PHS coatings.
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Figure 6. Mass wear vs. sliding distance for NiBSi-16Cr and NiBSi-16Cr: PHS coatings.
Figure 6. Mass wear vs. sliding distance for NiBSi-16Cr and NiBSi-16Cr: PHS coatings.
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Figure 7. Mass wear vs. sliding distance for Ni80-20Cr and Ni80-20Cr: PHS coatings.
Figure 7. Mass wear vs. sliding distance for Ni80-20Cr and Ni80-20Cr: PHS coatings.
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Figure 8. Dependence of wear rate on the concentration of chromium in the tested HVOF-coatings.
Figure 8. Dependence of wear rate on the concentration of chromium in the tested HVOF-coatings.
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Figure 9. Dependence of wear resistance on the concentration of chromium in the tested HVOF coatings.
Figure 9. Dependence of wear resistance on the concentration of chromium in the tested HVOF coatings.
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Figure 10. Diagram of the abrasive wear resistance of the tested coatings.
Figure 10. Diagram of the abrasive wear resistance of the tested coatings.
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Figure 11. Diagram of the influence of the heat treatment of the substrate on the wear resistance of the tested coatings.
Figure 11. Diagram of the influence of the heat treatment of the substrate on the wear resistance of the tested coatings.
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Figure 12. Diagram of the influence of Cr concentration on the wear resistance of the tested coatings.
Figure 12. Diagram of the influence of Cr concentration on the wear resistance of the tested coatings.
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Figure 13. Diagram of the influence of Cr concentration on the hardness of the tested coatings.
Figure 13. Diagram of the influence of Cr concentration on the hardness of the tested coatings.
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Figure 14. Diagram of abrasive wear resistance and hardness of the tested coatings.
Figure 14. Diagram of abrasive wear resistance and hardness of the tested coatings.
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Figure 15. Dependence of wear rate on chromium concentration range from 9.9% to 16%.
Figure 15. Dependence of wear rate on chromium concentration range from 9.9% to 16%.
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Figure 16. Analytical dependences of the wear rate on the chromium concentration for coatings without heat treatment, i r ( w ) = 0.00599819 w 3 + 0.099501902 w 2 .
Figure 16. Analytical dependences of the wear rate on the chromium concentration for coatings without heat treatment, i r ( w ) = 0.00599819 w 3 + 0.099501902 w 2 .
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Figure 17. Analytical dependences of the wear rate on the chromium concentration for coatings with heat treatment, i r ( w ) = 0.005371987 w 3 + 0.087400503 w 2 .
Figure 17. Analytical dependences of the wear rate on the chromium concentration for coatings with heat treatment, i r ( w ) = 0.005371987 w 3 + 0.087400503 w 2 .
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Table 1. Description, chemical composition, hardness, and thickness of the tested coatings.
Table 1. Description, chemical composition, hardness, and thickness of the tested coatings.
SeriesSampleCoating
Designation
DescriptionChemical Composition, wt. %Hardness
HRC
Thickness
µm
A1NiBSi-9.9CrCoatings without heat treatment of the substrateCr: 9.9; Si:3.1; B:1.7; Fe:3.2; C: 0.35; Mo: 3; Cu:3;
Ni Balance
55–56410–415
2NiBSi-9.9Cr:PHSCoatings with heat treatment of the substrate58–59400–412
B3NiBSi-13.2CrCoatings without heat treatment of the substrateCr: 13.2; Si: 3.98; B: 2.79; Fe: 4.6; Co: 0.03; C: 0.63;
Ni: Balance
56–57395–400
4NiBSi-13.2Cr:PHSCoatings with heat treatment of the substrate59–60408–414
C5NiBSi-14CrCoatings without heat treatment of the substrateCr: 14; Si:4.2; B:2,9; Fe:4,6; C:0.6; Mo:2,5; Cu:2,4;
Ni: Balance
57–58395–406
6NiBSi-14Cr:PHSCoatings with heat treatment of the substrate59–60400–405
D7NiBSi-16CrCoatings without heat treatment of the substrateCr:16; Si:4; B:3.4; Fe:2.7; C:0.6; Mo:3; Cu:3;
Ni: Balance
58–59394–405
8NiBSi-16Cr:PHSCoatings with heat treatment of the substrate61–62404–410
E9Ni80-20CrCoatings without heat treatment of the substrateCr: 20; Ni: 8054–55400–408
10Ni80-20Cr:PHSCoatings with heat treatment of the substrate57–60393–403
Table 2. Technological regime parameters for HVOF coating deposition.
Table 2. Technological regime parameters for HVOF coating deposition.
ParameterTechnological Regime
Propylene/oxygen ratio55/100%
Particle velocity1000 m/s
Spraying distance100 mm
Impact angle90°
Air pressure from compressor5 bar
N2 pressure in the proportioning device4 bar
Powder feed rate22 g/min
Table 3. Abrasive wear and wear rate of tested coatings.
Table 3. Abrasive wear and wear rate of tested coatings.
SampleCoating
Designation
Number of Cycles
100200300400
Sliding Distance, m
20406080
Mass Wear, [mg]//Wear Rate, [mg/Nm]
1NiBSi-9.9Cr4.7
5.22 × 10−2
8.5
4.71 × 10−2
12.7
4.71 × 10−2
15.3
4.24 × 10−2
2NiBSi-9.9Cr:PHS3.2
3.56 × 10−2
5.8
3.22 × 10−2
11.2
4.15 × 10−2
12.6
3.51 × 10−2
3NiBSi-13.2Cr4.4
4.89 × 10−2
7.9
4.4 × 10−2
10.6
3.93 × 10−2
12.3
3.42 × 10−2
4NiBSi-13.2Cr:PHS3.5
3.89 × 10−2
7.1
3.96 × 10−2
9.8
3.62 × 10−2
10.4
2.89 × 10−2
5NiBSi-14Cr4.0
4.44 × 10−2
6.0
3.33 × 10−2
7.6
2.82 × 10−2
10.5
2.91 × 10−2
6NiBSi-14Cr:PHS3.1
3.44 × 10−2
4.2
2.33 × 10−2
5.8
2.16 × 10−2
7.6
2.11 × 10−2
7NiBSi-16Cr1.5
1.67 × 10−2
2.2
1.22 × 10−2
2.8
1.04 × 10−2
3.3
0.91 × 10−2
8NiBSi-16Cr:PHS0.9
1.0 × 10−2
1.2
0.67 × 10−2
1.6
0.58 × 10−2
1.8
0.49 × 10−2
9Ni80-20Cr2.9
3.22 × 10−2
5.6
3.11 × 10−2
7.6
2.82 × 10−2
10.4
2.89 × 10−2
10Ni80-20Cr:PHS1.8
2.0 × 10−2
4.1
2.22 × 10−2
6.3
2.33 × 10−2
9.1
2.51 × 10−2
Table 4. Relative abrasive wear resistance of the tested coatings.
Table 4. Relative abrasive wear resistance of the tested coatings.
SeriesSampleCoating
Designation
Wear Resistance, mN/mg
in the Sliding Distance 80 m
Relative Abrasive Wear Resistance
Influence of Heat Treatment of the SubstrateInfluence of the Concentration of Cr, %
A1NiBSi-9.9Cr0.24 × 102R1,1 = 1R1,1 = 1
2NiBSi-9.9Cr:PHS0.28 × 102R2,1 = 1.17R2,2 = 1
B3NiBSi-13.2Cr0.29 × 102R3,3 = 1R3,1 = 1.21
4NiBSi-13.2Cr:PHS0.35 × 102R4,3 = 1.21R4,2 = 1.25
C5NiBSi-14Cr0.34 × 102R5,5 = 1R5,1 = 1.42
6NiBSi-14Cr:PHS0.47 × 102R6,5 = 1.38R6,2 = 1.68
D7NiBSi-16Cr1.10 × 102R7,7 = 1R7,1 = 4.58
8NiBSi-16Cr:PHS2.04 × 102R8,7 = 1.84R8,2 = 7.29
E9Ni80-20Cr0.35 × 102R9,9 = 1R9,1 = 1.46
10Ni80-20Cr:PHS0.40 × 102R10,9 = 1.14R10.2 = 1.67
Table 5. Wear rate at different chromium concentration, %.
Table 5. Wear rate at different chromium concentration, %.
w, Concentration of Cr, (%)9.911.813.214.015.216.0
i r , wear rate, mg/Nm, without heat treatment of the substrate4.243.823.422.912.10.91
i r , wear rate, mg/Nm, with heat treatment of the substrate3.513.352.892.111.350.49
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Kandeva, M.; Kalitchin, Z.; Stoyanova, Y. Influence of Chromium Concentration on the Abrasive Wear of Ni-Cr-B-Si Coatings Applied by Supersonic Flame Jet (HVOF). Metals 2021, 11, 915. https://doi.org/10.3390/met11060915

AMA Style

Kandeva M, Kalitchin Z, Stoyanova Y. Influence of Chromium Concentration on the Abrasive Wear of Ni-Cr-B-Si Coatings Applied by Supersonic Flame Jet (HVOF). Metals. 2021; 11(6):915. https://doi.org/10.3390/met11060915

Chicago/Turabian Style

Kandeva, Mara, Zhetcho Kalitchin, and Yana Stoyanova. 2021. "Influence of Chromium Concentration on the Abrasive Wear of Ni-Cr-B-Si Coatings Applied by Supersonic Flame Jet (HVOF)" Metals 11, no. 6: 915. https://doi.org/10.3390/met11060915

APA Style

Kandeva, M., Kalitchin, Z., & Stoyanova, Y. (2021). Influence of Chromium Concentration on the Abrasive Wear of Ni-Cr-B-Si Coatings Applied by Supersonic Flame Jet (HVOF). Metals, 11(6), 915. https://doi.org/10.3390/met11060915

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