Abstract

The influence of metallurgical heterogeneities such as coring and intermetallic phases on the corrosion and stress corrosion cracking behaviours of AA7075 aluminium alloy forging was examined in 3.5 wt. % NaCl solution with and without plasma electrolytic oxidation coating. Electrochemical test results demonstrated significant improvement in the corrosion resistance of the alloy after PEO coating. Stress corrosion results show that the metallurgical heterogeneities resulted in a loss in elongation of the uncoated sample in NaCl (11.5%) when compared to the one tested in air (12.9%). The loss in elongation of the uncoated sample was shown to be due to localized corrosion-assisted mechanical cracking rather than true stress corrosion based on preexposure tensile tests followed by posttest metallographic observation of the stress corrosion tested samples. This was further confirmed by the fractographic examination of the failed samples, which exhibited a typical ductile cracking morphology for all the coated and uncoated specimens.

1. Introduction

High-strength, precipitation hardened aluminium alloys such as AA7075 are widely used in aerospace industries in view of the good stress corrosion cracking (SCC) resistance in T7 temper conditions [15]. Although this treatment offered good improvement in the SCC resistance, localized corrosion such as pitting remains a problem in commercial aluminum alloys containing intermetallic phases such as Al7Cu2Fe, (Al,Cu)6 (Fe,Cu), and Mg2Si. Hence several studies were directed towards understanding the influence of these phases on the galvanic corrosion of aluminum. Among these phases, Al7Cu2Fe was reported to be the most cathodic phase, which results in the development of pitting at the particle-matrix interface [6]. These pits were the initiation sites for fatigue crack resulting in premature failure of AA7075-T7351 alloy [7].

On this aspect, surface modification techniques such as laser surface melting (LSM) and plasma electrolytic oxidation (PEO) are widely employed for improving the corrosion resistance of light alloys such as aluminum and magnesium. Yue et al. [8] obtained significant improvement in the SCC resistance for 7075 aluminum alloy using excimer laser treatment. With respect to PEO, although this treatment was well proven towards enhancing the corrosion and wear resistance of aluminum alloys, the influence of such coating on the SCC resistance was not studied in detail. However, available results on the magnesium alloys indicated good improvement in the SCC resistance of AM50 magnesium alloy [9]. The same authors in another study reported only a marginal improvement for other alloys such as AZ61 [10] and AZ31HP alloys [11] by this coating. In spite of the above improvement, this coating could not completely prevent the SCC of those alloys.

Yet another problem is the cast structure resulting from inadequate homogenisation and improper working especially in the case of large forgings, which can also lead to localised corrosion similar to that of intermetallic phases. Hence,understanding the influence of these metallurgical heterogeneities on the localised corrosion as well as SCC resistance is of scientific importance. The interest behind the SCC investigation of this alloy was to understand the effect of cast structure on the mechanical behaviour although this alloy exhibits good SCC resistance in T7 temper condition. This was studied in the coated and uncoated condition using polarization and SSRT tests in 3.5 wt, % NaCl solution.

2. Experimental Procedures

2.1. Material

The substrate material used in the present investigation was AA7075-T7352 aluminium alloy forging, having the chemical composition (wt. %) 1.2–2.0 Cu, 5.1–6.1 Zn, 2.1–2.9 Mg, Si-0.15 max, Mn-0.1 max, and Fe-0.2 max. Mn-0.1 max. Cr-0.18–0.28 and Ti-0.1 max. Cast billet of 300 mm diameter and 400 mm height was used as an input material. The cast billet was further processed through series of forging operations involving number of preheatings for realization of components to the required dimension. The resulting forged material was solution treated at 470°C for 36 h and water quenched to room temperature. Subsequently the forging was stress-relieved by compression treatment (2–5%) followed by two-step aging at 107°C for 8 h and 177°C for 8 h, respectively. Standard flat rectangular specimens having effective gauge dimensions of 30 mm × 6 mm × 4 mm were used for tensile tests, which were tested at a crosshead speed of 2 mm/s. The mechanical properties of this alloy in the above heat-treated condition were 0.2% YS = 320 MPa, UTS = 425 MPa, and El. % = 11.2.

2.2. PEO Coating Formation

An alkali silicate solution (4 g/L KOH: 2 g/L Na2SiO3) was used as an electrolyte, and coating deposition was carried out at a constant current density of 0.2 A/cm2 using a specially designed 50 Hz frequency AC high-voltage power supply. The temperature of the electrolyte was maintained constant at 35°C using a heat exchanger throughout the coating process. The treatment time of the samples was 30 min. The samples were taken out of the electrolyte, thoroughly washed in cold running water, ultrasonically cleaned in the acetone medium, and dried.

2.3. Microstructure and Phase Analysis

For microstructural observations of the base metal, samples were sectioned and polished down to 5 μm alumina finish followed by etching in Keller’s reagent (5 mL HNO3, 3 mL HCl, 2 mL HF, and 190 mL distilled water) and examined under optical microscope. The thickness of the coating was measured under SEM using metallographic cross-section of the coated sample. X-ray diffraction analysis was performed using PANalytical model X-ray diffractometer with Cu-Kα radiation between 30° and 120° to identify the phases present in the coating. Similar measurements were performed on AA7075 alloy without coating for comparison purpose.

2.4. Electrochemical Corrosion Tests

Corrosion resistance of the PEO-coated and uncoated specimens was evaluated through potentiodynamic polarization tests using computer-controlled Zhaner IM6ex electrochemical workstation. The corrosion behaviour was examined in 3.5 wt. % NaCl solution using reagent grade NaCl salt and deionized water. Tests were carried out using a standard three-electrode setup with Pt as counterelectrode and saturated calomel electrode (SCE) as a reference. A scan rate of 0.5 mV/s was used for polarization tests starting from a value of 300 mV below the corrosion potential.

2.5. Slow Strain Rate Tensile (SSRT) Tests

Tests were carried out as per ASTM G129 at a strain rate of 5 × 10−7/s for both coated and uncoated samples in air and 3.5 wt. % NaCl as reference and corrosive environments, respectively. For uncoated specimens, tests were also carried out by preexposing the tensile specimens in the corrosive environment without any load for a period that corresponded to SSRT test duration, followed by testing in air after cleaning thoroughly in distilled water. This data along with the metallographic observations of the failed specimens gave information on whether pitting played any role in lowering the mechanical property of the specimens. A minimum of two samples was tested in all cases. SSRT was performed using CORTEST make CERT tensile testing machine using Perspex containers to hold the specimen in the environment. Similar specimens as used in tensile tests were used for SCC tests in which the PEO coating was provided within the gauge length. Before coating, the gauge length portion of the samples was polished up to 1000 grit SiC paper on all the sides to obtain a smooth surface and were degreased and ultrasonically cleaned in acetone. The average elongation of the specimen was measured by a pair of linear variable displacement transducers (LVDT) positioned on both sides of the specimen. Galvanic corrosion of the specimen and the grip material was avoided by using silicone rubber sealant by coating the interface between the specimen and grip portions. The elongation values measured in air and environment were used to assess the environmentally assisted cracking susceptibility of both coated and uncoated alloy forgings.

3. Results and Discussion

3.1. Microstructure and Coating Morphology

Figure 1 shows the microstructure of AA7075 alloy forging which evidently shows the dendritic structure due to inadequate working of the forging. Second phase particles seen as black in colour can be noted and are distributed randomly in the α-Al matrix. These particles were reported as Al7Cu2Fe, (Al,Cu) 6 (Fe,Cu), and so forth [6]. The surface morphology and cross-section of the ceramic alumina coating generated on this alloy were further observed under scanning electron microscope and are presented in Figure 2. Micropores of diameter less than 2 μm are evident on the coating and are characteristic of such PEO coatings [12]. Presence of numerous discharge channels and the rapidly solidified alumina can be seen on the surface of the coating (Figure 2(a)). The cross-sectional SEM image of the coated sample shows that the coating thickness is 20 μm (Figure 2(b)). Two distinct regions consisting of outer porous layer (10 μm) and inner compact layer (10 μm) can also be noted, which is in agreement with reported results of similar PEO coatings.

3.2. Phase Analysis

X-ray diffraction (XRD) pattern obtained for AA7075 alloy and the PEO coating generated on this alloy are presented in Figure 3. Analysis of the XRD spectra revealed that the component of the coating layer is mainly γ-Al2O3. The presence of aluminium peak could be due to the penetration of X-rays into the substrate. This may partly be due to the presence of pores in the coating as has been reported by other investigators [13]. With respect to the phase content of the coating, while the present study revealed only γ-Al2O3, reported results on other aluminium alloys showed the presence of both α and γ-Al2O3 phases together [14, 15]. Reported results indicate that γ-Al2O3 phase prevails in the early stage of coating process and gets transformed to α-Al2O3 depending on the cooling rate. It was also suggested that alloying elements such as Mg, Cu, and Zn ions diffused from the substrate increase the transformation temperature of γ to α-Al2O3 resulting in lower α-Al2O3 content. Among the three elements, Mg was shown to exhibit dominant effect towards increasing the transition temperature of γ to α-Al2O3 phase. This was shown to be due to the lower Mg–O bond energy of 166 KJ mol−1 for Mg–O when compared to 280 KJ mol−1 bond energy for Al–O. This in turn reduced the amount of alumina that transforms into the alpha phase during each plasma event. Hence, the absence of the α-Al2O3 in the present study can be attributed to the higher content of magnesium and Zn in the substrate as these elements suppress the transformation of γ to α Al2O3 phase.

3.3. Electrochemical Corrosion

The polarization curves obtained for the uncoated and PEO-coated AA7075 aluminium alloy in 3.5 wt. % NaCl solution are displayed in Figure 4. An examination of the polarization plots shows that the corrosion potential of the uncoated sample is more active (−0.6 V) and the resultant corrosion current density also was high (0.5 μA/cm2) compared to the PEO-coated samples (0.045 μA/cm2). This indicated a reduction in of the base metal by an order of magnitude as a result of 20 μm PEO alumina coating on this alloy.

Observation of the sample after polarization tests revealed severe localized corrosion of the case of uncoated sample (Figure 5(a)) and the same after light polishing and etching indicated irregular pitting as a result of the dislodgment of the dendritic core along with second phase particles (Figure 5(b)). The absence of localized corrosion on the PEO-coated specimen indicated the good barrier property of the PEO coating as it offered corrosion protection for the base alloy (Figure 5(c)). Such coating did not allow the environment to diffuse through the coating, which otherwise results in galvanic couple formation with the second phases present in the matrix resulting in severe localized corrosion promoted by dendritic coring and second phases as observed in the case of uncoated alloy. Xue et al. [16] through elemental analysis across the cross-section of the coating performed after corrosion tests detected the presence of chloride ions only on the porous layer and not on the compact inner layer. Hence, the corrosion resistance of the PEO coating is mainly derived from the inner compact layer although the outer layer had pores in it.

3.4. Slow Strain Rate Tests (SSRTs)

Figure 6 compares the stress-strain curves obtained for the uncoated (Figure 6(a)) as well as PEO-coated (Figure 6(b)) specimens that were tested in air and NaCl solution. The SSRT data such as UTS and % El. measured from the above plots, are summarized in Table 1. An examination of the stress-strain plots and the data in Table 1 shows that there was a reduction in elongation for the uncoated specimens in NaCl (11.5%) when compared to the one tested in air (12.9). With respect to the coated specimens, the values are comparable. However, no significant changes in UTS values were seen for both coated and uncoated specimens. The loss in tensile elongation (1.4%) observed for the uncoated specimens suggests that the alloy may be susceptible to environmental cracking.

Figure 6 also shows that the elongation of the sample that was preexposed to NaCl solution without any load followed by SSRT test in air was less when compared to the sample continuously strained in NaCl solution.

Posttest metallographic observation of the uncoated sample after SSRT indicated severe pitting corrosion throughout the gauge length (Figure 7(a)). Further examination after polishing and etching clearly reveals preferential attack of the coring and intermetallic phases promoting nucleation of cracks (Figure 7(b)). This observation along with the preexposure test results leads to the belief that the loss in tensile elongation observed for the uncoated sample may not be due to SCC. It can also be noted that the stereo macrograph of the coated sample after SSRT exhibited large number of microcracks as a result of SSRT test (Figure 7(c)). Fractographic examination of all the coated and uncoated tensile samples after SSRT revealed a typical ductile cracking morphology (Figures 8(a)8(d)). This again confirms that the reduction in elongation of the uncoated samples in NaCl was to be due to corrosion-assisted mechanical failure rather than true SCC.

The results obtained in the present work demonstrated that the metallurgical heterogeneities such as coring and intermetallic phases present in the alloy forging resulted in a loss in tensile elongation of 1.4% in the NaCl solution and the same could be improved by PEO coating although to a marginal extent (1.1%). However, the same coating was found to offer significant improvement in the general corrosion resistance. These results are in agreement with the reported results on magnesium alloys. The later results also reported that SCC was not completely eliminated by this PEO coating in spite of the marginal improvement. This was shown to be due to the numerous microcracks generated during straining of the sample in the corrosive environment. Hence, further work to be directed towards understanding the influence of various ions by modifying the bath composition and to render the coating more ductile in order to understand the real effect of such ceramic coating on the environmentally induced cracking behaviour of light alloys is needed.

4. Conclusions

Based on the results obtained by electrochemical corrosion and SSRT tests on alloy AA7075-T7351, the following conclusions were made.(1)The metallurgical heterogeneities such a dendritic coring and intermetallic phases resulted in severe localized corrosion of this alloy causing significant reduction in elongation of the alloy forging under slow strain rate conditions in 3.5 wt. % NaCl solution.(2)PEO coating was found to be effective towards improving such localized corrosion promoted by metallurgical heterogeneities by providing good barrier resistance. However, the same coating under SSRT conditions resulted in the generation of microcracks. Despite the numerous surface cracks and pores existing on the outer layer of the coating, the tensile properties of the alloy were not deteriorated even in the corrosive environment.(3)The deposited coating mainly consists of γ-Al2O3 phase. The absence of α-Al2O3 phase in the coating could be due to the increased concentrations of Mg and Zn in the alloy substrate(4) It is evident that the results obtained in the present work along with similar results published in the literature on magnesium alloys and PEO coating cannot be very useful especially for SCC resistance although it provided good general corrosion resistance. Hence, to understand the effectiveness of such coating, future work should be directed with modified bath composition so as to render crack tip passivation and to improve the ductility of the coating.

Acknowledgments

A. Venugopal, S. Manwatkar, and K. Sreekumar are grateful to Dr. P. P. Sinha, Deputy Director, MME, VSSC for the interest and encouragement shown in this work.