3.1 Analysis of corrosion morphology
The macro morphology and micro morphology of the surface corrosion of stress corrosion samples of high-strength bolts under different corrosion conditions are shown in Fig. 2 and Fig. 3 respectively.
It can be seen from Fig. 2-a that the surface of the high-strength bolt sample without corrosion shows bright metallic luster and no obvious corrosion phenomenon. While under the condition of the original simulated corrosion solution (Fig. 2-b), there are sepia and brownish red corrosion products partially covering the sample surface, and some areas of the surface still show obvious metallic luster, which indicates that only some areas of the sample surface have pitting corrosion, and the simulated corrosionsolution has little impact on the performance of the material. But under the condition of 20 times the concentration of the original simulated corrosion solution (Fig. 2-c), the surface of the high-strength bolt sample has been completely covered by a large number of sepia corrosion products and a small number of brownish red corrosion products, no obvious metal luster is found, and there is a few brownish black corrosion products near the substrate surface. And under the condition of 200 times the concentration of the original simulated corrosion solution (Fig. 2-d), the surface of the sample is completely covered by sepia corrosion products, and some areas appear brownishblack corrosion products.
With the decrease of pH value to 3.5 (Fig. 2-e), the sepia corrosion products on the surface of the sample are the most, and some corrosion products have peeled off.
Fig. 2-g shows that with the increase of temperature to 50 ℃, the content of brownish red corrosion products on the surface of the sample decreases sharply, while the bright sepia corrosion products cover the surface of the sample on a large scale. The corrosion products layers are relatively loose, and some brownish black products have peeled off.
As shown in Fig. 3, in different corrosion environments, the corrosion products on the surface of 20MnTiB high-strength bolt stress corrosion samples are obviously stratified, and the thickness of the corrosion layer increases with the concentration of simulated corrosionsolution. Under the condition of the original simulated corrosionsolution (Fig. 3-a), the corrosion products on the sample surface can be divided into two layers: the corrosion products on the outermost layer are evenly distributed, but a large number of turtle cracks appear; the inner layer is loose cluster corrosion products. Under thecondition of 20 times the concentration of the original simulated corrosion solution (Fig. 3-b), the corrosion layer on the sample surface can be divided into three layers: the outermost layer is mainly scattered cluster corrosion products, which are loose and porous and do not have good protection performance; the middle layer is a uniform corrosion product layer, but there are obvious cracks, so that the corrosive ions can pass through the cracks and erode the matrix; The inner layer is a dense corrosion product layer without obvious cracks, which has a good protective effect on the matrix. Under the condition of 200 times the concentration of the original simulated corrosion solution (Fig. 3-c), the corrosion layer on the sample surface can be divided into three layers: the outermost layer is a thin and uniform corrosion product layer; the middle layer is mainly petal shaped and sheet-like corrosion products; and the inner layer is a dense corrosion product layer without obvious cracks and holes, which has a good protective effect on the matrix.
It can be seen from Fig. 3-d that in the simulated corrosion environment of pH 3.5, there are a large number of flocculent or acicular corrosion products on the surface of 20MnTiB high-strength bolt samples. It is speculated that these corrosion products are mainly γ- FeOOH and a small amount of α- FeOOH staggered distribution [25], and there are obvious cracks in the corrosion layer.
It can be seen from Fig. 3-f that when the temperature increased to 50 ℃, no obvious dense inner rust layer is found in the structure of corrosion layer, indicating that there is a gap between the corrosion layers at 50 ℃, which makes the matrix not completely covered by corrosion products to supply protection, and the corrosion tendency of the matrix is deepened.
3.2 Loss analysis of mechanical properties
The mechanical properties of high-strength bolts under constant load stress corrosion in different corrosion environments are shown in Table 2:
Table 2
Mechanical properties of 20MnTiB high-strength bolt sample under constant load stress corrosion in different simulated corrosion environments(φ = 6.35mm)
Condition
|
Yield strength/MPa
|
Tensile strength/MPa
|
Elongation/%
|
Section
Shrinkage /%
|
Non-corrosion
|
1116
|
1228
|
17.48
|
44.88
|
1time concentration
|
1143
|
1215
|
17.78
|
43.78
|
20 times concentration
|
1126
|
1188
|
16.34
|
43.15
|
200 times concentration
|
1148
|
1191
|
16.31
|
43.62
|
pH3.5
|
1115
|
1176
|
16.05
|
45.35
|
pH7.5
|
1139
|
1193
|
15.27
|
43.15
|
50℃
|
1130
|
1186
|
15.77
|
42.05
|
Standard≥
|
940
|
1140
|
12
|
42
|
It can be seen from Table 2 that the mechanical properties of 20MnTiB high-strength bolt samples still meet the standard requirements after the dry and wet cycle accelerated corrosion test under different simulated corrosion environments, but there are some damages occur compared with the non-corroded sample. Under the concentration of the original simulated corrosion solution, the mechanical properties of the sample did not change significantly, but under the concentration of 20 times or 200 times of the simulated solution, the elongation of the sample decreased significantly. The mechanical properties were similar under 20 times and 200 times the concentration of the original simulated corrosion solution. When the pH of the simulated corrosion solution decreased to 3.5, the tensile strength and elongation of the sample decreased significantly. When the temperature rises to 50℃, the tensile strength and elongation decrease significantly, and the shrinkage of the section is very close to the standard value.
3.3 Macroscopic and microscopic analysis of fracture
The fracture morphology of 20MnTiB high-strength bolt stress corrosion samples under different corrosion environments is shown in Fig. 4, in turn is the macro morphology of the fracture, the central fiber area of the fracture, the micro morphology of the interface between the shear lip edge and the sample surface.
It can be seen from Fig. 4 that the fracture of stress corrosion samples of 20MnTiB high-strength bolts in different simulated corrosion environments presents a typical cup cone fracture, and compared with the samples without corrosion (Fig. 4-a), the area of fiber area in the center of fracture is relatively smaller, and the area of shear lip area is larger. This shows that after corrosion, the mechanical properties of the material are damaged obviously. With the increase of the concentration of the simulated corrosion solution, the dimple in the central fiber area of the fracture increased, and obvious tearing slitsappeared. When the concentration increases to 20 times of the original simulated corrosion solution concentration, there are obvious corrosion pits at the interface between the edge of the shear lip and the surface of the sample, and there are a lot of corrosion products on the surface of the sample.
In the simulated corrosion solution of pH3.5 (Fig. 4-e), the sample surface is serious corroded, the central fiber area is obviously small, and there are a lot of irregular tearing slits in the center of the fiber area. With the increase of the pH value of the simulated corrosion solution, the tearing band of the central fiber area of the fracture surface decreased, the dimple gradually decreased, and the dimple depth also gradually decreased.
When the temperature increased to 50 ℃ (Fig. 4-g), the shear lip aere of the fracture surface of the sample is the largest, the dimple in the central fiber area is significantly increased, and the dimple depth is also increased, and the corrosion products and pits at the interface between the edge of the shear lip and the sample surface are increased.