+高级检索
网刊加载中。。。

使用Chrome浏览器效果最佳,继续浏览,你可能不会看到最佳的展示效果,

确定继续浏览么?

复制成功,请在其他浏览器进行阅读

Microstructure and Wear Resistance of Ni-Cr Alloy Laser Cladding Layer with High Cr Content  PDF

  • Pan Chaoyang
  • Liu Zongde
  • Shen Yue
  • Lu Xinjie
  • Mao Jie
  • Wang Xinyu
  • Li Jiaxuan
Key Laboratory of Power Station Energy Transfer Conversion and System, Ministry of Education, North China Electric Power University, Beijing 102206, China

Updated:2024-09-12

DOI:10.12442/j.issn.1002-185X.20230814

  • Full Text
  • Figs & Tabs
  • References
  • Authors
  • About
CN CITE
OUTLINE

Abstract

Four kinds of Ni-xCr alloy laser cladding layers (x=20, 40, 60 and 80, wt%) were prepared by high-speed laser cladding technique, and the relationship between microstructure and wear resistance of Ni-Cr alloy laser cladding layers with different Cr contents was investigated. The results show that the four Ni-Cr alloy laser cladding layers all have reticulated dendritic structures. Among them, Ni-20Cr and Ni-40Cr are single-phase γ-(Ni, Cr) solid solutions, and their wear mechanisms are adhesive wear and abrasive wear. With the increase in Cr content, Ni-60Cr and Ni-80Cr are γ-(Ni, Cr) phase and Cr phase, as well as Cr-rich precipitates, and their wear mechanisms are adhesive wear, abrasive wear and fatigue wear. A moderate increase in Cr content can enhance the hardness and wear resistance of Ni-Cr alloy laser cladding layer. However, excessive addition of Cr results in the precipitation of Cr-rich precipitates. The hardness of these precipitates is 2430.4 MPa, which is lower than the hardness of the Ni-60Cr matrix (4024.86 MPa) and Ni-80Cr matrix (7022.68 MPa). A hardness transition zone exists between the Cr-rich precipitates and the matrix. Cracks are likely to initiate and expand in this zone, leading to deep spalling, which is not conducive to the wear-resistant properties of the laser cladding layer. Ni-80Cr has the highest hardness, but its high Cr content leads to a large number of penetrating cracks and Cr-rich precipitates on the surface, ultimately resulting in the worst wear resistance. Ni-60Cr exhibits the best wear resistance due to its high hardness and dense microstructure.

Ni-Cr alloys are widely used in industries such as aerospace and energy due to their good resistance to oxidizing acids and salts, high-temperature oxidation and sulfidation corrosion[

1]. It is well known that the presence of Cr promotes the formation of a dense protective layer of Cr2O3 on the alloy surface, which reduces the oxidation rate of alloys[2–4]. Ni-Cr alloys are susceptible to wear and tear in corrosive environments. The addition of Cr significantly improves their mechanical properties, including strength, plastic toughness and hardness[5–6]. From an economic standpoint, Cr is more cost-effective than Ni. However, an excess of brittle primary α-Cr phases can negatively affect the mechanical properties of Ni-Cr-based alloys and lead to insufficient machinability[7]. Therefore, appropriately increasing the proportion of Cr in Ni-Cr alloys is of practical significance for improving alloy properties and reducing costs.

Usually, Ni-Cr alloys with high Cr content can only be molded by casting process[

8]. Hanke[9] et al used friction cladding process to prepare a Cr60Ni40 layer on nickel-based alloy, Nimonic 80A, and demonstrated that it is feasible to prepare Ni-Cr alloy coatings with high Cr content on a ductile substrate, expanding the application range. Bozzi[10] compared the microstructure and wear resistance properties of as-cast and laser-cladded Stellite alloys. They found that laser-cladded Stellite alloys have a finer microstructure and superior wear resistance. Song[11] et al examined the corrosion properties of Ni50Cr50 alloys prepared by four methods, including cold spray, HVOLF and HVOGF thermal spray and laser cladding. The study indicates that the Ni50Cr50 coating produced by laser cladding showcases superior performance owing to its dense microstructure. Laser cladding technique is characterized by a high solidification rate, low dilution and void ratio and strong metallurgical bonding strength compared with conventional methods, which endow laser cladding layer with fine crystal structures and new phases that are not available under equilibrium conditions. This ultimately leads to excellent properties and longevity, making it highly promising for industrial applications[12–15].

In the process of laser cladding, excessive heating and cooling rates can lead to precipitated phases in the laser cladding layer, which may have a certain influence on the performance of the laser cladding layer. Julian[

16] et al did not find precipitates in the microstructure of Cr60Ni40 alloy obtained through solid solution annealing, which only con-sisted of two phases: Ni-rich phase and Cr-rich phase. Chen[17] et al utilized laser cladding technique to produce Cr60Ni40 laser cladding layer with the same composition, and found that there are obvious Cr-rich precipitates in the Cr60Ni40 laser cladding layer. Although the oxidation rate of Cr-rich precipitates is slow, they can cause the formation of an uneven protective chromium oxide layer on the surface, resulting in the degradation of the corrosion resistance performance.

Currently, laser cladding technique is not widely used to prepare Ni-Cr alloys with high Cr content. Researchers primarily focus on the corrosion and high-temperature oxidation resistance of Ni-Cr alloys. The relationship between the microstructure of Ni-Cr alloy laser cladding layers with high Cr content and their wear-resistant properties is not yet fully understood. In this study, Ni-xCr alloy laser cladding layers with different Cr contents (x=20, 40, 60 and 80, wt%) were prepared on a Q235 steel substrate using laser cladding technique, the effects of Cr content on the microstructure and hardness of the Ni-Cr alloy laser cladding layers were an-alyzed, and the wear resistance of the laser cladding layers was evaluated by the wet-sand abrasive abrasion test, which provided theoretical references for the application of the Ni-Cr alloy laser cladding layer with high Cr content under wear conditions.

1 Experiment

1.1 Materials and laser cladding process

In this study, Q235 low carbon steel plate was selected as the substrate material and cleaned with acetone solution to eliminate rust and oil on surface. Four kinds of Ni-Cr alloy powders were prepared, named as Ni-20Cr, Ni-40Cr, Ni-60Cr and Ni-80Cr, with a particle size range of 38‒75 μm, and the chemical composition of the substrate material and the cladding material is shown in Table 1. A laser cladding system (RFL-C3000S, Wuhan Riggs Fiber Laser Technology Co., Ltd) was used to prepare the Ni-Cr alloy laser cladding layer under the following parameters: power of 1800 W, operating voltage of 220 V, spot diameter of 2 mm, scanning speed of 8.33 cm/s, overlap rate of 60%, powder flow rate of 20 g/min, laser focal length of 50±0.2 mm and laser cooler temperature of 24±0.5 °C, and the powder feeding system used argon protective gas with a flow rate of 15 L/min to prevent powder oxidation during the coating process. Fig.1 shows the sche-matic of high-speed laser cladding process. The Ni-Cr alloy with high Cr content is brittle and prone to cracking during the

Table 1  Chemical composition of materials (wt%)
MaterialNiCrFeSiC
Q235 - - Bal. 0.34 0.16
Ni-20Cr Bal. 20 - - -
Ni-40Cr Bal. 40 - - -
Ni-60Cr Bal. 60 - - -
Ni-80Cr Bal. 80 - - -

Fig.1  Schematic of the high-speed laser cladding process

preparation process, so liquid dye penetration was used to detect the cracking morphology of the laser cladding layer. The macroscopic surface of the laser cladding layer is shown in Fig.2, and the red penetrant penetrates the surface of Ni-80Cr, indicating that the laser cladding layer is full of cracks, while other three laser cladding layers are free of cracks. Laser cladding layers with a thickness greater than 4 mm was obtained through a multilayer cladding process, and wire cutting was used to process the laser cladding layers.

Fig.2  Macroscopic surfaces of Ni-20Cr (a1‒a2), Ni-40Cr (b1‒b2), Ni-60Cr (c1‒c2) and Ni-80Cr (d1‒d2)

1.2 Characterization method

X-ray diffractometer (XRD, Rigaku D/MAX-2400, Japan; Cu-Kα radiation, scanning range 10°‒90°, scanning rate 8°/min), scanning electron microscope (SEM, ZEISS EVO 18, Ger-many; accelerating voltage 20 kV) and energy dispersive X-ray spectroscope (EDS, Bruker Quantax, Germany) were used to analyze the phase composition, microstructure and elemental distribution of the laser cladding layer, respectively. The sample size was 10 mm×10 mm×10 mm (including substrate). Before observing the microstructure, the treated samples were subjected to surface erosion using aqua regia (HNO3-3HCl).

1.3 Vickers hardness test

The Vickers hardness of the surface and cross-section of the laser cladding layer was measured by an FM-300 microhard-ness tester, with a load of 0.98 N and a loading time of 15 s at 200 μm intervals.

1.4 Wear resistance test

According to ASTM G105-20 standard, 50 mm×25 mm×4 mm sample was subjected to wear performance testing by the MLS-225 wet sand wear tester. The abrasive consisted of deionized water and SiO2 of 212‒270 μm. The rubber wheel was 178 mm in diameter and rotated at 180 r/min under a load of 70 N. The reason for choosing wet sand as abrasive is that water can act as a lubricant, dissipate the heat generated by friction and prevent oxidation reactions[

18]. The samples were pre-ground at 2000 revolutions to eliminate experimental errors. Ten experimental cycles were set up, with each cycle consisting of 4000 revolutions. Weighing was repeated five times at the end of each cycle (accuracy 0.0001 g) and the volume loss was calculated using the following equation:

V=1000(W1-W0)ρ (1)

where V is the volume loss (mm3); W1 is the mass at the end of each cycle (g); W0 is the initial mass (g); ρ is the density (g/cm3). Finally, the wear morphology was analyzed.

2 Results and Discussion

2.1 Microstructure and composition

Fig.3 displays the XRD patterns of four laser cladding layers. The diffraction peaks of Ni-20Cr and Ni-40Cr correspond to the γ-(Ni,Cr) solid solution (fcc) with preferred crystal planes of (111), (200) and (220). Compared with the standard Ni peaks, the diffraction peaks of γ-(Ni,Cr) are shifted to the left at a small angle, which is due to the lattice distortion caused by the presence of Cr atoms in Ni lattices in the form of solutes, resulting in larger lattice constants and thus causing the shift of the diffraction peaks. The phenome-non of diffraction peak shift can be explained by Bragg's equa-tion: 2dsinθ=λ, where d represents the distance between crysta-lline planes, θ represents the angle between incident light and crystalline planes, and λ is the wavelength of the Cu target.

Fig.3  XRD patterns of different Ni-xCr alloys

With the increase in Cr content, the matrix element of Ni-Cr alloy starts to change from Ni to Cr. In addition to the pre-sence of γ-(Ni, Cr) peaks, Cr peaks can be detected in Ni-60Cr and Ni-80Cr alloys, whose preferred crystal planes are (110), (200) and (211). The shift of the γ-(Ni, Cr) peak is more signi-ficant due to the higher saturation of Cr atoms in the γ-(Ni, Cr) solid solution, leading to a higher degree of lattice distortion in γ-(Ni, Cr). During the cooling process, the solubility of Ni atoms in the Cr matrix decreases, resulting in no significant shift of the Cr peaks. Additionally, the relative intensity of the Cr peaks of Ni-80Cr is higher than that of Ni-60Cr.

Fig.4 shows the reticulated dendritic structures that are typical in laser cladding layers. The primary phase, which appears dark gray, is surrounded by the eutectic phase, which appears light gray. In Ni-20Cr and Ni-40Cr alloys, the dark gray primary phase is Ni-rich, while the light gray eutectic phase is Cr-rich. The Cr-rich phases account for 26.86% and 38.35% of the matrix in Ni-20Cr and Ni-40Cr alloys, respectively. The EDS results of different areas are listed in Table 2. The Cr content in the primary phases (area 1 and 4) is lower than that in the eutectic phases (area 2 and 3). Dendritic segregation causes compositional differences, resulting in different colors after etching. The solidification speed of laser cladding is fast, and some Cr atoms do not have enough time to diffuse and to solidify into the γ-Ni lattice[

19]. As a result, they are enriched in the intergranular region. Additionally, a few micropores are visible in the laser cladding layer due to the delayed escape of the protective gas.

Fig.4  Surface morphologies (a1‒d1 and a2‒d2) and cross-sectional (a3‒d3) morphologies of Ni-20Cr (a1‒a3), Ni-40Cr (b1‒b3), Ni-60Cr (c1‒c3) and Ni-80Cr (d1‒d3); Cr-rich precipitate (e1) and corresponding EDS mappings of element Ni (e2) and Cr (e3)

Table 2  EDS results of different areas in Fig.4 (wt%)
Area123456789
Ni 79.43 67.92 53.64 58.60 34.74 47.64 17.58 36.40 0
Cr 20.57 32.08 46.36 41.40 65.26 52.36 82.42 63.60 100

As the Cr content increases, the microstructure of Ni-Cr alloys with Cr as the matrix element changes. Black precipitates appear on the surface, with the size ranging from 15 μm to 30 μm. These precipitates are mainly composed of Cr atoms, and a few Ni atoms. The melting point of Cr is higher than that of Ni. During the laser cladding process, Cr undergoes solidification firstly, and the solubility of Ni in Cr is also relatively low. As a result, excess Cr cannot form a solid solution with Ni completely, leading to the formation of Cr-rich precipitates directly in the Ni-Cr alloy[

17]. The area fractions of each phase in Ni-60Cr and Ni-80Cr are analyzed: the Cr-rich precipitates in Ni-60Cr account for 15.03% and the matrix accounts for 84.97%; the fraction of Cr-rich precipitates in Ni-80Cr is 23.36% and that of the matrix is 76.64%. The results indicate that the higher the Cr content, the higher the amount of Cr-rich precipitate in the Ni-Cr alloy laser cladding layer. The matrix of both Ni-60Cr and Ni-80Cr exhibits a reticulated dendritic structure. Combined with the EDS results, it is evident that the primary phase in dark gray is rich in Cr, while the eutectic phase in light gray is rich in Ni. The Cr-rich phases in Ni-60Cr and Ni-80Cr account for 56.30% and 65.26% of the matrix, respectively.

Fig.4a3‒4d3 display the cross-sectional morphologies of four laser cladding layers. Ni-20Cr, Ni-40Cr and Ni-60Cr exhibit a dense microstructure with a few air holes. In contrast, the Ni-80Cr laser cladding layer has defects such as holes and cracks at the boundary of the substrate, as well as noticeable penetrating cracks on the surface. This is because the Cr-rich phase in the Ni-Cr alloy matrix usually exhibits high hardness and brittleness. Excessive Cr can also increase the proportion of Cr-rich phase in the Ni-Cr alloy matrix, leading to poor mechanical properties of the Ni-Cr alloy and easy initiation and propagation of cracks[

7,20].

2.2 Vickers hardness

Fig.5 displays the microhardness variation of each sample with respect to the distance from the laser cladding layer surface. The overall microhardness of Ni-80Cr is the highest, ranging within 6958‒7350 MPa, and that of Ni-60Cr is 3734‒4307 MPa. The microhardness of Ni-40Cr is approximately 2156 MPa, while that of Ni-20Cr is the lowest about 1960 MPa. The difference in microhardness between Ni-20Cr and Ni-40Cr is small, resulting in a relatively smooth overall mic-rohardness change. Through microstructure and micro-structure analysis, Ni-20Cr and Ni-40Cr are dominated by γ-(Ni,Cr) solid solution with low microhardness. In addition, the atomic radii of Cr and Ni are close to each other, the degree of lattice distortion in the formation of γ-Ni solid solution is small, and the solid solution strengthening effect is limited, so the hardness of Ni-40Cr is not obviously enhanced compared to that of Ni-20Cr.

Fig.5  Cross-section microhardness of Ni-xCr alloy laser cladding layers

As the Cr content continues to increase, the hardness begins to rise sharply. Compared with Ni-40Cr and Ni-20Cr, Ni-60Cr and Ni-80Cr with high Cr content possess more Cr-rich phases. The Cr-rich phase usually exhibits high hardness, which plays a crucial role in improving the hardness of Ni-Cr alloys. Ni-80Cr has more Cr-rich phases (65.26%), so it exhibits the highest microhardness.

The surface microhardness was analyzed separately, and the measurement results are shown in Fig.6. It is worth noting that the microhardness error values of Ni-60Cr and Ni-80Cr are relatively large compared with that of Ni-20Cr and Ni-40Cr. The microhardness fluctuation phenomenon may be related to the Cr-rich precipitates in Ni-60Cr and Ni-80Cr. The surface microhardness of four laser cladding layers is consistent with the cross-section microhardness. However, the microhardness of Cr-rich precipitates is only 2430.4 MPa, which is very lower than the matrix hardness of Ni-60Cr (4024.86 MPa) and Ni-80Cr (7022.68 MPa). The microhardness of Ni-20Cr and Ni-40Cr is lower, which is 2009 and 2333.38 MPa, respec-tively. Fig.7 presents the Vickers hardness indentation morpho-logy of Cr-rich precipitates and different matrixes, confirming the microhardness measurements. According to Conrath[

21], the addition of Cr does not completely and monotonically increase the hardness of Ni-Cr alloys. Instead, it results from the superposition of the hardness of the Cr-rich phase and the hardness of the Ni-rich phase. As the Cr content increases, the microhardness of Ni-Cr alloy will also increase. Therefore, the microhardness of Cr-rich precipitates with 100wt% Cr content is lower than that of Ni-60Cr matrix and Ni-80Cr matrix. However, when the Cr content reaches a critical value, the microhardness of Ni-Cr alloy will continue to decrease. For different preparation processes, this critical value may vary.

Fig.6  Surface microhardness of Ni-xCr alloy laser cladding layers and Cr-rich precipitate

Fig.7  Vickers hardness indentation morphologies of Ni-60Cr (a) and Ni-80Cr (b)

2.3 Wear resistance

Fig.8 shows the wear curves of four laser cladding layers. The wear process is not entirely a standard linear law, so a non-linear fitting is performed on the wear curve using the following formula:

V=aTn (2)

Fig.8  Wear volume loss curves of Ni-xCr alloy laser cladding layer

where a and n are constants; V represents the volume loss; T represents the number of turns. The results show that the volume loss increases gradually as the number of turns increases. According to the difference in wear rate, the wear curves can be divided into two stages, i.e., the running-in stage and the stable wear stage. In the running-in stage, the sample is just in contact with the abrasive grains and the wear rate is usually faster. As the abrasive grains continuously come into contact, the friction surface is gradually smoothed and the actual contact area is enlarged, leading to a decrease in the wear rate. At the same time, as the wear process continues, strain hardening effects occur on the surface, and the stable wear stage is reached[

22]. The volume loss in the stable wear stage increases almost linearly. The wear volume and the fitting results of wear curve are shown in Table 3. R2 values indicate the quality of the fitting results. According to the volume loss, the wear resistance is evaluated as follows: Ni-60Cr> Ni-40Cr >Ni-20Cr >Ni-80Cr.

Table 3  Wear volume and the fitting results of wear curve
SampleWear volume/mm3Fitting of wear curveR2
Ni-20Cr 4.1788 V=0.0168T 0.5238 0.968
Ni-40Cr 2.6575 V=0.0021T 0.6725 0.998
Ni-60Cr 2.4650 V=0.0087T 0.5362 0.993
Ni-80Cr 83.8460 V=0.6574T 0.4641 0.978

Fig.9a1‒9a2 display the surface morphologies of Ni-20Cr after wear. The wear volume loss of Ni-20Cr is 4.1788 mm3. Long and deep grooves are visible on the surface of Ni-20Cr, and the edges of the grooves produce a material buildup. This indicates that the abrasive grains have caused a severe ploughing effect on the surface of the material, which is a characteristic of abrasive wear[

23]. Microcracks and adhesive layer are visible on the surface, which indicates that adhesive wear also occurs on the sample. The EDS results of different areas are listed in Table 4. Area 1 of the adhesive layer exhibits a high concentration of O and Si, indicating the possibility of wear debris adhering to the wear surface[24]. The wear resistance of Ni-40Cr is marginally superior to that of Ni-20Cr, with the wear volume loss of 2.6575 mm3. Fig.9b1‒9b2 illustrate that the grooves on the surface of Ni-40Cr become shallower, and the microcracks and adhesive layer are significantly weakened. Small abrasive debris can also be observed during the wear process, which can cause more serious damage to the sample. However, the effect of the abrasive debris is essentially negligible compared with the effect of the initial abrasive grains size.

Fig.9  Surface morphologies of Ni-20Cr (a1‒a2), Ni-40Cr (b1‒b2), Ni-60Cr (c1‒c2), and Ni-80Cr (d1‒d2) after wear test

Table 4  EDS results of different areas in Fig.9 (wt%)
Area123456789101112
Ni 35.58 77.11 56.30 54.82 23.41 1.72 34.40 38.73 37.63 0 25.18 16.86
Cr 11.04 20.12 39.36 36.07 16.83 97.73 63.72 57.54 56.62 100 73.35 68.76
O 31.35 0.36 3.31 5.10 29.02 0.11 1.02 2.63 4.13 0 0 8.07
Si 22.03 2.41 1.03 4.01 30.74 0.44 0.86 1.10 1.62 0 1.47 6.31

When the Cr content is low (Ni-20Cr and Ni-40Cr), the Ni-Cr alloy laser cladding layer is dominated by the γ-(Ni,Cr) solid solution. This solid solution has good plasticity and low hardness. When subjected to the normal force exerted by the abrasive grain, the sample surface is prone to plastic deforma-tion. If the deformation exceeds its tensile limit, the surface will form cracks and collapse downward. Under repeated con-tact stress, the cracks will expand and cause shallow spalling. Meanwhile, the abrasive particles generate relative motion tangentially to the friction surface, resulting in the formation of grooves and adhesive layer[

22]. The wear mechanisms of Ni-20Cr and Ni-40Cr are abrasive and adhesive wear.

Ni-60Cr exhibits the best wear resistance, with the wear volume loss of 2.4650 mm3. Shallow and short grooves, as well as adhesion layers, are visible on the surface in Fig.9c1‒9c2. In contrast to Ni-20Cr and Ni-40Cr, deeper spalling pits with dimensions similar to Cr-rich precipitates are present on the surface of Ni-60Cr, indicating that spalling of Cr-rich pre-cipitates may have occurred. Additionally, expanding micro-cracks are observed around the spalling pits. EDS analysis of the pits reveals that area 6 has a high Cr content of 97.73wt%, suggesting the presence of Cr-rich precipitates in this area. Areas 7‒9 have Cr contents of 63.72%, 57.54% and 56.62%, respectively, suggesting that spalling of the craters occurs not only in the Cr-rich precipitates but also in the matrix. The Ni-80Cr sample exhibits the worst abrasion resistance, with the wear volume loss of 83.8460 mm3. As shown in Fig.9d1‒9d2, the surface of the Ni-80Cr sample is characterized by shallow, short grooves, adhesion layers and more pronounced deep pits. A transverse penetration crack is observed, which exists prior to the wear test. The area where the craters are located has a Cr content of 100wt%, without other elements present, indicating exfoliation of intact Cr-rich precipitate. As the Cr content increases (Ni-60Cr and Ni-80Cr), the Ni-Cr alloy laser cladding layer is dominated by Cr-rich phases, resulting in a significant increase in hardness and improved resistance to surface plastic deformation[

25]. Consequently, the extrusion and cutting effect of abrasive grains on the sample surface are weakened, leading to shorter and shallower grooves and a thinner adhesive layer. It should be noted that the Ni-60Cr and Ni-80Cr surfaces show deeper spalling pits, which are actually the spalling of Cr-rich precipitates.

The Cr-rich precipitates have a lower hardness (2430.4 MPa) than the matrix, which leads to a hardness transition zone between them. This transition zone is prone to generation and expanding of initial cracks under long-term contact stress, ultimately leading to fatigue damage and the formation of deeper spalling pits[

26]. The wear mechanisms of Ni-60Cr and Ni-80Cr include abrasive wear, adhesive wear and fatigue wear. The area fraction of Cr-rich precipitates in Ni-80Cr differs by 8.33% from that of Ni-60Cr. Although Ni-80Cr has the highest hardness, it exhibits the worst wear resistance, which may be attributed to the presence of numerous macro- cracks. The expansion rate of abrasive grains is much faster when they come into contact with these macro-cracks compared with in contact with micro-cracks, resulting in more significant volume loss.

3 Conclusions

1) The surface microstructures of the four kinds of Ni-Cr alloy laser cladding layers are all composed of primary and eutectic phases with a reticulated dendritic structure, and there is elemental segregation between the two phases. Ni-20Cr and Ni-40Cr are single-phase γ-(Ni,Cr) solid solutions, and Ni-60Cr and Ni-80Cr consist of γ-(Ni,Cr) phases and Cr phases. Cr-rich precipitates appear in the Ni-60Cr and Ni-80Cr and the amount increases with the increase in Cr content. Except for Ni-80Cr, the microstructure of other three laser cladding layers is uniform and dense, while Ni-80Cr has a large number of defects such as penetrating cracks and holes.

2) The microhardness of Ni-20Cr and Ni-40Cr is lower, 2009 and 2333.38 MPa, respectively. As the Cr content increases, more Cr-rich phases appear in the laser cladding layer, resulting in a significant increase in the microhardness of Ni-60Cr (4024.86 MPa) and Ni-80Cr (7022.68 MPa). However, this also causes the precipitation of low-microhardness Cr-rich precipitates (2430.4 MPa).

3) The wear resistance is evaluated by wear volume loss as follows: Ni-60Cr>Ni-40Cr>Ni-20Cr>Ni-80Cr. The wear me-chanisms of Ni-20Cr and Ni-40Cr are abrasive and adhesive wear, and the wear mechanisms of Ni-60Cr and Ni-80Cr include abrasive wear, adhesive wear and fatigue wear. There is a hardness transition zone between the Cr-rich precipitates and the cladding matrix. This zone is prone to initiation and expansion of cracks, which can result in deep spalling and reduce wear resistance. Ni-60Cr exhibits the best wear resistance due to its high hardness and dense microstructure.

References

1

Sequeira C A C, Cardoso D S P, Amaral L et al. Corrosion Reviews[J], 2016, 34: 187 [Baidu Scholar] 

2

Wang Xinyu, Liu Zongde, Cheng Kehan et al. Corrosion Sci-ence[J], 2023, 216: 111102 [Baidu Scholar] 

3

Sun Hua, Zhang Peng, Wang Jianqiang et al. Corrosion Sci- ence[J], 2018, 143:187 [Baidu Scholar] 

4

Gao Yuan, Liu Zongde, Wang Qi et al. Rare Metal Materials and Engineering[J], 2019, 48(12): 3846 [Baidu Scholar] 

5

Keskar N, Mani Krishna K V, Gupta C et al. Materials Today Communications[J], 2022, 33: 104831 [Baidu Scholar] 

6

Li Jiahong, Kong Dejun. Materials[J], 2018, 11: 137 [Baidu Scholar] 

7

Zheng Liang, Xiao Chengbo, Zhang Guoqing et al. Journal of Alloys and Compounds[J], 2012, 527: 176 [Baidu Scholar] 

8

Herda W, Swales G L, Tschentke et al. Materials and Corro- sion[J], 1968, 19: 679 [Baidu Scholar] 

9

Hanke S, Beyer M, Silvonen A et al. Wear[J], 2013, 301: 415 [Baidu Scholar] 

10

Bozzi A C, Ramos F D, Vargas D B O. Wear[J], 2023, 534‒525: 204857 [Baidu Scholar] 

11

Song B, Voisey K T, Hussain T. Surface and Coatings Technology[J], 2018, 337: 357 [Baidu Scholar] 

12

Siddiqui A A, Dubey A K. Optics & Laser Technology[J], 2021, 134: 106619 [Baidu Scholar] 

13

Liang Y, Liao Z Y, Zhang L L et al. Optics & Laser Techno- logy[J], 2023, 164: 109472 [Baidu Scholar] 

14

Arif Z U, Khalid M Y, Rehman E U et al. Journal of Manufacturing Processes[J], 2021, 68B: 225 [Baidu Scholar] 

15

Zhu Lida, Xue Pengsheng, Lan Qing et al. Journal of Manufacturing Processes[J], 2021, 138: 106915 [Baidu Scholar] 

16

Julian Krell, Arne Röttger, Werner Theisen. Wear[J], 2019, 432‒433: 102924 [Baidu Scholar] 

17

Chen Shanshan, Liu Zongde, Ning Huaqing et al. Materials Letters[J], 2023, 342: 134352 [Baidu Scholar] 

18

Bingley M S, Schnee S. Wear[J], 2005, 258: 50 [Baidu Scholar] 

19

Wang Qinying, Bai Shulin, Zhao Yunhong et al. Applied Surface Science[J], 2014, 303: 312 [Baidu Scholar] 

20

Shi Bowen, Li Tao, Guo Zhiwei et al. Optics & Laser Technology[J], 2022, 149: 107805 [Baidu Scholar] 

21

Conrath E, Berthod P. Materials at High Temperatures[J], 2016, 33: 189 [Baidu Scholar] 

22

Li Jiaxuan, Liu Zongde, Ning Huaqing et al. Surface and Coatings Technology[J], 2023, 474: 130068 [Baidu Scholar] 

23

Xia Yelin, Huang Zhaozhen, Chen Hanning et al. Rare Metal Materials and Engineering[J], 2021, 50(11): 2901 (in Chinese) [Baidu Scholar] 

24

Zhou Kai, Xie Faqin, Wu Xiangqing et al. Rare Metal Materials and Engineering[J], 2021, 50(8): 2831 (in Chinese) [Baidu Scholar] 

25

Li Gang, Zhang Jingbo, Wen Ying et al. Rare Metal Materials and Engineering[J], 2018, 47(6):1830 (in Chinese) [Baidu Scholar] 

26

Roy T, Lai Q, Abrahams R et al. Wear[J], 2018, 412‒413: 69 [Baidu Scholar]