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Article

Study of the Surface Integrity and High Cycle Fatigue Performance of AISI 4340 Steel after Composite Surface Modification

1
College of Materials and Metallurgy, Guizhou University, Guiyang 550025, China
2
Guizhou Key Laboratory of Materials Strength and Structure, Guiyang 550025, China
3
High Performance Metal Structure Material and Manufacture Technology National Local Joint Engineering Laboratory, Guiyang 550025, China
*
Author to whom correspondence should be addressed.
Metals 2019, 9(8), 856; https://doi.org/10.3390/met9080856
Submission received: 7 July 2019 / Revised: 2 August 2019 / Accepted: 3 August 2019 / Published: 6 August 2019
(This article belongs to the Special Issue Advanced Surface Enhancement)

Abstract

:
In the field of materials science, the fabrication of a material with severe surface plastic deformation and a good surface state is an issue encountered in the development of counterbalanced gradient materials. For this paper, AISI 4340 steel was first processed with abrasive water jet peening (AWJP) and then with ultrasonic surface rolling (USRE) to obtain a good surface state while maintaining large plastic deformation. The AISI 4340 steel composite surface was therefore modified, and the surface integrity and cycle fatigue performance were analyzed. The results show that the plastic deformation layer of the modified composite surface of the 4340 steel was 310 µm from the surface of the sample, the grain size 40 µm from the surface layer was refined to 70 nm, and the maximum surface roughness Ra is 0.06. The fatigue limit of the modified composite surfaces obtained by the tensile fatigue test was 595.7 MPa, which was 85.7 MPa higher than the 510 MPa fatigue limit of the unmodified matrix, indicating that the method of composite surface modification can produce a deep deformation layer while maintaining good surface conditions. The results show that work hardening caused by a composite surface treatment is the most important factor for improving the fatigue performance of materials.

1. Introduction

Under normal service conditions, the damage of mechanical or structural parts is primarily caused by fatigue, and the fatigue failure of materials often starts at the surface, where cracks often start to form and propagate [1,2,3]. So how to improve the surface quality of materials is an important consideration in material design and industrial application. Dixit et al. [4] put forward modeling requirements for material surface state and surface quality from the perspective of material design and modeling, reflecting the importance of material surface state and quality material modeling. However, Krahmer et al. [5] takes the surface integrity and surface state as the consideration point, and abrasive water jet, wire electrodischarge machining, laser to replace the traditional milling processing of tensile samples, shortening the processing time and having great industrial value in industrial applications, In practical application literature [6,7,8,9], ball-burnishing means can be adopted to significantly improve the surface quality of materials, so as to improve the corrosion resistance and wear resistance of materials and reduce the wear ratio of materials. In terms of material fatigue, Nie et al. [10] the surface state of titanium alloy after polishing can affect crack initiation in the fatigue process, thus affecting the fatigue performance of the material. Torres et al. [11] found that micro-cracks formed on the surface of AISI 4340 steel during shot peening would have an impact on the initiation location of cracks. Wu et al. [12] studied the influence of different polishing methods on the rotary bending fatigue life of nickel-based Alloy GH4169. Klein et al. [13] showed that the surface morphology had a significant impact on the cyclic deformation behavior of TWIP steel under high cycle fatigue. However, in literatures [14,15], special morphologies such as pits and pitting points are easy to form in the shot peening process, and local stress concentration is easy to cause, which will reduce the performance of materials. Therefore, it is a meaningful problem to design materials with good large deformation and good surface condition for the use of structural parts
The material used herein is an AISI 4340 steel; because of its high strength, toughness, good hardenability, and thermal stability, it is suitable for the manufacture of important parts that require a high strength and large cross section, such as large diameter turbine shafts and blades in heavy machinery. In metal structural parts such as transmission shafts, crankshafts and aircraft landing gears [16,17], various failures originate from the surface, so the treatment of the surface is particularly important.
In the design of this paper, AWJP is used to form a deep deformation layer on the surface. When a surface is rolled by an ultrasonic process to reduce the surface roughness, deformation is introduced that forms nanograins on the surface. The gradient structure is slowly extended, forming an ideal “nano–submicron–micron” gradient structure from the surface layer into the matrix that resists fatigue crack initiation and expansion. In the literature review done for this work, it was found that the combination of AWJP and ultrasonic surface rolling (USRE) was not reported in the literature when materials were subjected to surface strengthening treatments. In this paper, the surface modification treatment of the material is carried out by the method of USRE after AWJP, and the fatigue properties of the nano-gradient in of steel are also studied. The microstructure and fatigue limit of the 4340 steel after AWJP + USRE are determined to improve the theoretical basis for future industrial production and application.

2. Materials and Methods

The Principle of Abrasive Water Jet Peening and Ultrasonic Surface Rolling

The basic principle of AWJP is to spray a high-pressure, high-speed water jet that is carrying a large amount of abrasive energy in a specific way on the surface of the metal component so that it is plastically deformed at the recrystallization temperature (cold hardened layer). The goal is to produce an ideal grain structure (grain strengthening) and residual stress distribution (stress strengthening). The roughness of the surface is decreased to improve the performance of the material.
Ultrasonic surface rolling is a combination of ultrasonic energy and static load rolling to treat the surface of metal parts. The machining head applies an ultrasonic frequency that consists of a mechanical vibration at a certain amplitude along the normal direction of the workpiece surface. Under certain feeding conditions, the working head transmits a static pressure and ultrasonic shock vibration to the surface of the rotating mechanical component, causing a squeezing effect. Metallic materials undergo substantial elastoplastic deformation. After processing, the surface of the workpiece experiences a certain elastic recovery, and the plastic flow generated fills or partially fills the “valley” on the surface of the workpiece, thereby greatly reducing the surface roughness Ra to the nano level and improving the surface. The schematic diagram of composite surface modification is shown in Figure 1. In this paper, composite surface modification is defined as AWJP+USRE.
The experimental material used herein was 4340 steel, and its chemical composition is shown in Table 1. The tensile properties of the material measured at room temperature are shown in Table 2. The parameters of abrasive water shot peening and ultrasonic surface rolling are shown in Table 3 and Table 4. The heat treatment process involved heating at 850 °C for 90 min, oil quenching, and tempering at 540 °C for 240 min.
The heat-treated sample was finished into a funnel-type standard fatigue sample, and the smooth fatigue sample designed according to GB/T3075-2008 is shown in Figure 2. Then, the center portion of the sample was axially ground and polished to a mirror finish. The AISI 4340 steel was subjected to a 1 × 107 high-cycle fatigue test with axial r = −1 on a QBG-200 high-frequency fatigue tester (Qian Bang Company, Changchun, China). The resonance frequency of the sample was 140 Hz and the test was carried out at room temperature. The fatigue limit was determined by the lifting method and the single sample method when the specified cycle time is 107. The fatigue limit was calculated by the following formula [18]:
σ max = 1 m i = 1 n v i σ i
where m is the total number of effective fatigue tests (both failure and passage are included in the lifting process), n is the test stress level series, vi is the number of tests corresponding to the i-th stress level, and σi is the first level i stress level. Using the group test method, the stress level was measured to increase the corresponding fatigue life. Finally, the data obtained by the lifting method were taken as the horizontal point of the low stress of the S-N curve, and the fatigue life obtained by the high stress was taken as the high stress level point of the S-N curve, thereby resulting in a complete S-N curve. The first part of the test involves high-cycle fatigue testing of the polished substrate sample at room temperature. The second part involves performing AWJP on the curved surface in the middle of the sample. After the peening process, high-cycle fatigue testing was carried out, and the fatigue limit of the material was measured by the lifting method.
An OLS5000 laser confocal microscope (Oympus, Nishi-Shinjuku, Japan) was used to observe the surface of the intermediate curved section of the sample, and the roughness was measured. The microstructure of the surface and center of the composite surface modified samples was observed by laser confocal microscope (Oympus, Nishi-Shinjuku, Japan). The metallographic analysis was carried out on a cross section of the middle section. A SUPPA40 Zeiss field emission scanning electron microscope (Zeiss, Analytik Jena city, Thuringia, Germany) was used to observe the fatigue fracture. Energy dispersive spectroscopy (EDS) (Zeiss, Analytik Jena city, Thuringia, Germany) was used to analyze the chemical composition of the fatigued micro-region. Hardness testing was carried out on an HVS-1000 digital microhardness tester (Lunjie Motor Instrument Company, Shanghai, China) before and after AWJP and before and after USRE. The surface hardness of the sample after modification of the composite surface changes, Load 0.98 N, keep 10. With electrolytic peeling method on the GNR type X ray residual stress meter measuring residual stress with the change of deep layer and residual stress measurement by using fixed bits of heeling, relevant legal peak, test parameters for: alpha radiation Cr K bits Angle respectively 0° and 24.2° and 35.3° and 45°, 20 kV tube voltage, tube current is 5 mA, 147°~167° scan range, step distance of 0.1°. A disc was cut from the two samples by a wire electric discharge machine (G.N.R. s.r.l.- Analytical Instrument Group, Milan, Italy). After grinding, ion-thinning was performed to prepare a transmission electron microscopy (TEM) sample for microstructure observation.

3. Results

3.1. Specimen Surface Microstructure

The cross-sectional surface morphology of the sample before and after USRE was observed using a laser confocal microscope, as shown in Figure 3. In Figure 3a, a cross section of the AWJP + USRE specimen near the surface is shown, and it can be seen that the surface is severely plastically deformed. The subsurface layer forms a streamlined structure towards the rolling direction. Figure 3b shows the microstructure at the interior of the sample that comprises randomly distributed tempered martensite.
In the process of composite modification, two different applied loads act on the surface of the material to cause plastic deformation. During AWJP, the high-energy water flow bombards the surface of the sample to produce a highly strained and a deep deformation gradient layer. The surface of the material is then further processed by USRE, during which each working head and material contact generates a stress field on the surface of the material. Each small volume unit was plastically deformed. During processing, the load acted on different surfaces of the sample. The small volume unit in the new stress field was plastically deformed again so that the repeated process made the surface of the material nanosized. The deformation initially occurred on the surface of the sample. As the processing time increased, the amount of deformation gradually moves towards the core of the sample, so the texture of the material exhibits a gradient distribution along the thickness direction.

3.2. Fatigue Limit Curve and S-N Curve

Figure 4a,b show the fatigue limit diagrams of the experimental steel after composite surface modification and after the substrate is polished, respectively. It can be seen from the figure that the fatigue stress level of the polished base sample is calculated to be 3, and the fatigue stress level is 2 for the modified composite surface. The fatigue limit of the modified composite surface specimen is 595.7 MPa, which is 85.7 MPa higher than the fatigue limit of the polished matrix specimen (510 MPa). Figure 4c,d show the S-N curves of the modified composite surface and polished matrix samples. The corresponding stresses of the specimens with a modified composite surface are higher than those of the polished matrix and the composite surface. The S-N curve is flatter for the modified composite surface than that for the polished substrate, especially for the highly stressed part of the polished substrate. The data for the highly stressed part is relatively scattered, indicating that the fatigue life of the AISI 4340 steel after composite surface modification is not as sensitive to a change in the stress amplitude as the polished matrix.
In the fatigue experiment under stress control conditions, the relationship between stress amplitude and fatigue life can be expressed by the Basquin formula et al. [19]:
σ = σ f ( 2 N f ) b
where Nf is the fatigue life, σ is the stress amplitude, b is the fatigue strength index (also known as the Basquin index), and σ f is the fatigue strength coefficient or fatigue strength index (for a metal material, the σ f value is the true fracture strength of the material). In a double logarithmic coordinate system, the fatigue strength coefficient and the fatigue strength index can be obtained by linear fitting to σ-2Nf, and the Basquin equation for the polished matrix sample and modified composite surface can be expressed as shown in (3) and (4), respectively:
σ = 729 ( 2 N f ) 0.02322
σ = 720 ( 2 N f ) 0.01207
Compared with the polished base sample, the fatigue strength coefficient of the modified composite surface is not very different, and the fatigue strength index b of the sample is higher than that of the polished base sample. By studying the fatigue behaviour of coarse-grained (CG) Cu and ultra-fine-grained (UFG) Cu under both tension and compression modes, Li et al. [20], Höppel et al. [21] and Huang [22] revealed that b is affected by strain localization during crack initiation and the stress gradient during crack propagation. The value of b during UFG Cu tensile fatigue is decreased because the crack initiation mode changes from the CG persistent slip band (PSB) to an ultra-fine crystalline shear band (SB). SBs are more localized with respect to PSB strain, and in addition, grain refinement accelerates crack propagation. For the AWJP+USRE sample, the gradient structure improves the resistance to crack initiation during fatigue. In addition, because the gradient deformation layer is attached to a plastically good substrate and has a good work hardening ability, strain localization is suppressed. Moreover, the gradient structure from nanocrystals to coarse crystals provides good crack propagation resistance [23,24,25]. The AWJP + USRE sample has a high b value in both the crack initiation and expansion stages.

3.3. Fatigue Fracture

Through scanning electron microscopy (SEM) observation of the fatigue fracture of the polished substrate and the composite surface, Figure 5a–c show the fatigue fracture morphology of the polished samples. It can be seen from Figure 5a that the fatigue source of the polished samples is located on the surface of the samples and the sample is modified on the composite surface. The fatigue source of most of the sample is located in the subsurface or internal inclusion. When the fatigue life is greater than approximately 106 cycles, the fatigue fracture is mostly due to internal inclusion cracking. Figure 5d–f shows the typical high-cycle fatigue fracture morphology of the modified composite surface and polished substrate. The crack source region exhibits a typical “fish-eye” morphology at low magnification (Figure 5d). In the heart of the fish-eye structure, there is a sandwich structure (Figure 5e). The energy spectrum (Figure 5f) analysis shows that the fatigue fracture inclusion after modification mainly contains Mn, Al, O, Ca, S, Mg, and Al, so it is a composite oxide inclusion.
On the surface of the sample without the surface modification fatigue source, the source of the fatigue crack is on the surface. The dislocations move easier on the free surface than in the interior, and the free surface is preferred for dislocation nucleation [26,27,28]. In this paper, we discuss the influence of roughness on the effective stress concentration factor Kf. The greater the roughness, the larger the effective stress concentration factor Kf; the stress concentration of the surface is also an important reason for the dislocation-first nucleation, and the research findings are consistent. Generally, the surface is smooth. Cracks generally originate on the sample surface for unnotched specimens under high-cycle conditions. PSBs are a manifestation of strain localization. Generally, the strain in PSBs is tens to hundreds of times that of its surrounding area. Figure 5b shows the surface of the fatigue fracture, which is known as the surface-staying slip zone (PSB) and causes surface cracking.
In contrast, under the stress loading condition of σ = 600 MPa (Nf = 7.83 × 106), the formation of PSB or cracking is not observed in the fracture of the AWJP + USRE sample. However, fatigue fractures with the fish-eye shape have been observed. When the grain refines to submicron or nanoscale sizes, the plastic deformation mode of the alloy material during cyclic deformation changes from dislocation slip in the ultra-fine CSB to ultra-fine crystal shearing. The slip band [29,30] can be seen from the position of fatigue crack initiation in Figure 5d. The crack source is 0.8 mm from the surface, and the radius of the fish-eye region is 0.58 mm because the nano-gradient structure layer has a good uniform shape. The work hardening rate, work hardening ability and surface strain localization can be significantly suppressed [31] and prevent fatigue cracks from nucleating on the surface. Under the influence of the gradient structure, the fatigue source of the sample is fatigued by the gradient structure layer. The performance improvement is mainly reflected in the suppression of crack initiation.

4. Discussion

4.1. Effect of Roughness on Fatigue Life

Figure 6a,b is a polished sample’s surface topography and the height map, it can be seen from the Figure 6a surface has left scar left by the polishing process, from Figure 6c,d is the surface topography of samples after the abrasive water jet shot and a height map, from Figure 6c as you can see, the sample after AWJP surface has obvious pits left by abrasive particles, from Figure 7 shows the roughness of the surface of samples after the abrasive water jet shot Ra is 1.577 microns. From Figure 6e,f is abrasive water jet shot + ultrasonic surface rolling surface morphology of the samples after the figure and the height map, from Figure 6f can see sample results compound after surface modification, surface without abrasive water pit, which is formed by the shot peening, from Figure 7 shows the composite surface roughness on the surface of the modified for Ra = 0.06, shows that composite surface modification has greatly improve the surface quality of the material.
Surface modification methods are an important factor that affects the surface quality for certain part sizes and material properties. According to the principles of fracture mechanics, the larger the surface roughness value, the larger the notch effect; that is, the larger the stress concentration factor, the worse the fatigue performance. During AWJP, the entrainment of the abrasive high-pressure water flow is equivalent to a projectile with a very large energy bombarding the metal surface so that the surface of the metal forms a special surface topography, such as pits. The geometry of the phase is due to many small indentations, resulting in stress concentrations on the working surface of the part. It is known from the fracture mechanics that the surface after processing can be regarded as composed of numerous microscopic notches. The influence of these rough uneven notches on fatigue can be expressed by the theoretical stress concentration factor Kt [32]:
K t = 1 + 2 γ h ρ
where h is the height of the microscopic roughness, ρ is the radius of curvature of the valley, and γ is the correlation coefficient of the ratio of the unevenness to the height. From Equation (5), the deeper the valley, the smaller the radius of curvature, and the easier it is to form stress concentrations. The influence of the stress concentration factor on the fatigue properties of the material is also related to whether the material is sensitive to the notch. Therefore, the effective stress concentration factor Kf is introduced [33]:
K f = 1 + q ( K t 1 )
where q is the sensitivity of the material to stress concentration, which is a function of the material strength and shape of the micro-notch size. As the strength of the material increases, the value of ρ decreases and the value of q increases. Equation (6) shows that the larger the surface roughness is, the larger the stress concentration factor; that is, the larger the effective stress concentration factor is, the easier the fatigue crack initiation, and the lower the fatigue life. In contrast, crack initiation is difficult, so the fatigue life increases. Therefore, it is not easy to sprout a crack on a smooth surface, and cracks in samples after the composite treatment are initiated in the subsurface. This difference in the location of the crack initiation results in a higher initial life for the modified composite surface.

4.2. Residual Stress Impact on Fatigue Performance

It can be seen from Figure 8 that a residual stress of −472 MPa appears at a position of approximately 50 μm from the surface after AWJP. The residual stress after single rolling is −697 MPa, and the residual stress of the surface-modified composite is larger than those after single treatment methods and is −846 MPa. The residual stress introduced by the surface treatment has an important influence on the fatigue life of the sample. When the residual stress is superimposed on the fatigue load, the stress state of the sample changes, which affects the nucleation and expansion of a fatigue crack. In general, the residual stress affects the fatigue behaviour of a material in the same way as the load applied to the material. If the residual stress is compressive, the fatigue properties of the material can be improved; if it is a tensile stress, the fatigue properties of the material are decreased. The residual compressive stress generated by surface strengthening can not only suppress the initiation of fatigue cracks but also increase the crack closing effect and reduce the expansion rate of short cracks [34], which helps to improve the fatigue performance of the specimen.

4.3. Influence of Deformation Layer Structure on Fatigue Performance

Deformation-induced grain refinement is the main grain refinement mechanism in the composite modification process. AISI 4340 steel can be considered a high-level dislocation metal, so its plastic deformation is mainly carried out by dislocation slip. The dislocation gradually entangled with each other and formed cellular structure in the grain, as shown in Figure 9a. The dislocation density in the grains increases with increasing deformation, and the dislocations gradually become entangled with each other and form a cell structure inside the grain. As the amount of deformation continues to increase, the cell structure is turned into a subgrain (with an independent slip system). When the amount of deformation is further increased, a subcrystal is transformed into a grain with a small angle or a grain with a large angle [35]. On the surface of the metal, high strain rates are easily accommodated to create a rearrangement and annihilation in the vicinity of dislocation walls and dislocation entanglements. When the rate of dislocation generation and quenching reaches equilibrium, the grain size is correspondingly stable; Finally, a nanocrystalline structure with a randomly distributed orientation is formed. Eventually, the formation of new nanocrystalline grains is seen in Figure 9b the near surface region forms a nanocrystalline layer of approximately 100 µm.
Figure 10a–e is a composite surface modified AISI4340 steel and selected different depths of TEM bright field image and regional electron diffraction pattern from the sample surface. It can be seen from Figure 10 that as the depth of the surface layer increases, it is clear from the gradient diffraction ring in Figure 10 that the number of diffraction rings increases and the grain size decreases as it approaches the surface. As can be seen from Figure 11, after the surface nanocrystals pass through AWJP + USRE, the grain size is about 70–80 nm at a distance of 40 μm from the surface. At a depth of about 300 μm from the surface of the sample, the size of the crystal grains was about 1.6 μm in the vicinity of the substrate. It can be seen from Figure 10a that the evolution of the structure can be seen at a distance of 40 μm from the surface of the sample. The morphology is different from martensite and seems to be fragmentation. From Figure 10b at 80 μm from the surface of the sample, it can be seen in the TEM image that the black particles may be precipitated carbides due to the high tempering temperature. Martensite morphology is clearly seen in Figure 10d,e, including martensite mass and martensite bar. These results indicate that the deformation mechanism of the modified composite involves the transformation from martensite block in the transparent matrix to deformed and bent martensite to broken nanocrystals.
To reduce the energy of the system, the high-density dislocation grain size can significantly affect the crack initiation resistance during the fatigue process of the material. In general, grain refinement increases the strength of the material and improves its resistance to fatigue crack initiation. For smooth unnotched specimens, fatigue cracks generally develop on the surface of the material. Therefore, the introduction of nanocrystals on the surface of the sample increases the strength and hardness of the surface, inhibits crack initiation on the surface, and improves the fatigue properties of the material. The “nano-submicron” gradient structure from the surface layer to the matrix of the modified composite surface sample is an ideal structure to resist fatigue crack initiation and expansion.
The hardness is measured using a HVS-1000 microhardness tester (Lunjie Motor Instrument Company, Shanghai, China) on a sample treated with AWJP only and USRE only and a sample treated with AWJP + USRE. It can be seen from Figure 12 that the surface hardness after USRE can reach 471 HV, and the deformation is seen from the hardness curve. The layer is approximately 180 µm from the surface. The hardness of the surface after AWJP reaches 510 HV, the plastic rheology layer is approximately 200 µm from the surface. The composite surface modification combines the advantages between the two. The hardness reaches 586 HV and is 176 HV greater than that of the of the substrate (410 HV) and the plastic flow region. The layer changed at 280 µm from the surface of the substrate.
In the actual service of materials, the fatigue life of materials is a powerful guarantee for industrial safety production. Many scholars predict the fatigue life of materials [34,35]. To study the main factors affecting the fatigue performance of gradient structures, the paper by Bagherifard et al. [36] considered the effects of residual stress in this manner:
σ f = σ tf [ 1 + ( σ bf σ tf 1 ) ( x 2 / b ) K D ] ( F W H M P F W H M NP ) ( C SP C SNP )
where σf is the fatigue limit, σtf is the pull-fatigue limit, σbf is the bending fatigue limit, x’ is the relevant stress gradient (RSG), b is the size parameter of the sample, FWHMP is the half-width of the diffraction peak of the sample after surface treatment, FWHMNP is the half-width of the diffraction peak of the base material, CSP is the surface roughness of the sample after treatment, and CSNP is the surface roughness of the base material. It can be seen that the FWHM in the X-ray diffraction peak for the composite treatment is increased by 18.7% relative to the matrix FWHM. The fatigue properties of the materials before and after composite surface modification are improved by 16.8%. Therefore, the gradient structure after composite surface modification is the main reason for the fatigue properties of the materials. For the roughness coefficient CS, the roughness of the polished substrate has an Ra of 0.4, which meets the standard of finishing. The sample is sanded along the axial direction with sandpaper. Because the experiment involves tensile fatigue, the roughness does not fatigue the material. The effect of the residual stress on the fatigue performance in the nano-gradient structure has been investigated by scholars [37,38] who annealed the sample after peening, leaving the hardened layer and completely releasing the residual stress. The removal of the stress proves that the fatigue performance of the material is still greatly improved in the case of only the hard layer, and thus the residual stress does not appear to be the most important factor. In summary, the roughness and residual stress of the material play a positive role in the improvement of the fatigue properties of the material, and among the factors considered in this study, the gradient structure after the composite modification is the most important one for improving fatigue properties.

5. Conclusions

  • In the surface state, the modified composite plastic deformation layer reaches 310 µm from the surface. The composite modification at a depth of 90 µm is comparable to a single modified layer at a depth of 220 µm; the material Ra is reduced from 1.57 µm to 0.06 µm through after AWJP. A crystalline layer appears 40 µm away from the surface. The particle size reached 70 nm.
  • Composite modification can obtain a smooth gradient structure. the fatigue limit of the unmodified matrix is increased from 510 MPa to 595.9 MPa (an increase of 85.9 MPa), and the roughness, residual stress, and gradient are analysed herein. The effect of the structure on the fatigue properties of the material indicates that the gradient structure is the most important factor affecting the fatigue properties of the material. The surface and the fine grain on the surface can effectively prevent the initiation of fatigue crack in the fatigue process, and the large grain at the center can affect the propagation of fatigue crack in the fatigue process, so as to improve the fatigue performance of the material.

Author Contributions

Conceptualization, H.F. and L.Y.; methodology, H.F.; formal analysis, H.F.; writing—original draft preparation, H.F.; writing—review and editing H.F.; supervision, L.Y.

Funding

This research was funded by “National Natural Science Foundation of China, grant number 51671060” “The Science and Technology Project of Guizhou Province, grant number (2014) 6012” and “Guizhou Science and Technology Talent Cooperation Platform Project, grant number (2019) 5303”.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Schematic diagram of AWJP+USRE approach.
Figure 1. Schematic diagram of AWJP+USRE approach.
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Figure 2. Geometry of the fatigue test specimen (units: mm).
Figure 2. Geometry of the fatigue test specimen (units: mm).
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Figure 3. Metallographic structure of AISI 4340 steel: (a) Image of the outermost area and (b) image of the sample interior.
Figure 3. Metallographic structure of AISI 4340 steel: (a) Image of the outermost area and (b) image of the sample interior.
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Figure 4. The fatigue limit of 4340 steel processed with (a) 13% abrasive water jet peening (AWJP) + ultrasonic surface rolling (USRE) and (b) after polishing. The S-N curves of the 4340 steel processed with (c) AWJP + USRE and (d) after polishing.
Figure 4. The fatigue limit of 4340 steel processed with (a) 13% abrasive water jet peening (AWJP) + ultrasonic surface rolling (USRE) and (b) after polishing. The S-N curves of the 4340 steel processed with (c) AWJP + USRE and (d) after polishing.
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Figure 5. (a) the macroscopic diagram of fatigue fracture of Polishing, (b)local amplification of fatigue fracture of Polishing, (c) local amplification of fatigue fracture of Polishing, (d) macroscopic diagram of fatigue fracture of AWJP+USRE (e) local amplification of fatigue fracture of AWJP+USRE and (f)shows the energy spectrum of AWJP+USRE inclusions.
Figure 5. (a) the macroscopic diagram of fatigue fracture of Polishing, (b)local amplification of fatigue fracture of Polishing, (c) local amplification of fatigue fracture of Polishing, (d) macroscopic diagram of fatigue fracture of AWJP+USRE (e) local amplification of fatigue fracture of AWJP+USRE and (f)shows the energy spectrum of AWJP+USRE inclusions.
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Figure 6. (af) The surface topography and height of Polishing, AWJP, and AWJP + USRE.
Figure 6. (af) The surface topography and height of Polishing, AWJP, and AWJP + USRE.
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Figure 7. Surface roughness of materials under different processes.
Figure 7. Surface roughness of materials under different processes.
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Figure 8. Variation of the residual stress along the thickness direction.
Figure 8. Variation of the residual stress along the thickness direction.
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Figure 9. TEM image of the AWJP + USRP sample (a) at a depth of 200 µm and (b) a depth of 150 µm.
Figure 9. TEM image of the AWJP + USRP sample (a) at a depth of 200 µm and (b) a depth of 150 µm.
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Figure 10. AWJP + USRE AISI 4340 steel TEM bright-field images and selected area electron diffraction pattern for different depths from the sample surface. (a) 40 μm from the surface; (b) 80 μm from the surface; (c) 120 μm from the surface; (d) 200 μm from the surface; (e) 300 μm from the surface.
Figure 10. AWJP + USRE AISI 4340 steel TEM bright-field images and selected area electron diffraction pattern for different depths from the sample surface. (a) 40 μm from the surface; (b) 80 μm from the surface; (c) 120 μm from the surface; (d) 200 μm from the surface; (e) 300 μm from the surface.
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Figure 11. Comparison of grain size along the thickness direction.
Figure 11. Comparison of grain size along the thickness direction.
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Figure 12. Comparison of microhardness along the thickness direction.
Figure 12. Comparison of microhardness along the thickness direction.
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Table 1. Chemical compositions of 4340 steel.
Table 1. Chemical compositions of 4340 steel.
ElementCSiSPCrNiMoCuAl
Content0.420.300.00190.00210.901.650.250.140.009
Table 2. Mechanical properties of 4340 steel.
Table 2. Mechanical properties of 4340 steel.
Tensile Strength σb/MPaYield Strength σs/MPaElongation δ/%Reduction of Area ψ/%
1160109818.754.6
Table 3. Parameters of waterjet peening progress.
Table 3. Parameters of waterjet peening progress.
ParameterValues
Water flow pressure, MPa100
Forward speed, mm/min10
Speed, r/min30
Target distance, mm10
Nozzle angle90°
Table 4. Ultrasonic surface rolling processing parameters.
Table 4. Ultrasonic surface rolling processing parameters.
ParameterValues
Static pressure, N320
Amplitude, um6
Speed, r/min280
Forward speed, mm/r0.08
Rolling times3

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Fu, H.; Liang, Y. Study of the Surface Integrity and High Cycle Fatigue Performance of AISI 4340 Steel after Composite Surface Modification. Metals 2019, 9, 856. https://doi.org/10.3390/met9080856

AMA Style

Fu H, Liang Y. Study of the Surface Integrity and High Cycle Fatigue Performance of AISI 4340 Steel after Composite Surface Modification. Metals. 2019; 9(8):856. https://doi.org/10.3390/met9080856

Chicago/Turabian Style

Fu, Hai, and Yilong Liang. 2019. "Study of the Surface Integrity and High Cycle Fatigue Performance of AISI 4340 Steel after Composite Surface Modification" Metals 9, no. 8: 856. https://doi.org/10.3390/met9080856

APA Style

Fu, H., & Liang, Y. (2019). Study of the Surface Integrity and High Cycle Fatigue Performance of AISI 4340 Steel after Composite Surface Modification. Metals, 9(8), 856. https://doi.org/10.3390/met9080856

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