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Home All issues Volume 8 (2021) Manufacturing Rev., 8 (2021) 22 Full HTML
Open Access
Issue
Manufacturing Rev.
Volume 8, 2021
Article Number 22
Number of page(s) 7
DOI https://doi.org/10.1051/mfreview/2021021
Published online 19 July 2021

© S.O. Akinwamide et al., Published by EDP Sciences 2021

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

1 Introduction

Aluminium matrix composites (AMCs) are vastly used in several engineering sectors for different applications. The commonly used matrix used for the fabrication of these classes of composites includes aluminium, magnesium, titanium, and copper [1]. Aluminium has been widely used due to its outstanding properties, which include improved ductility, exceptional thermal and electrical properties [2,3]. This class of materials also possesses the ability to sustain its properties at extremely low temperatures. However, these properties can be enhanced by incorporating another reinforcement particle(s) into the aluminium matrix, thereby resulting in the production of composites that are aluminium based [4,5].

The corrosion of aluminium and other metallic composites has been reported to be a significant challenge in manufacturing industries. Research has shown that the yearly loss and damage arising from corrosion in the United Kingdom, as an example, has been given to be approximately £ 5000 million [6]. However, this wasteful occurrence could be averted if factors such as proper material selection, correct design, and reinforcing of metallic matrixes with adequate reinforcement particles are carefully considered. Some specific corrosion problems associated with AMCs include but are not limited to porosity, micro-crevices, and galvanic coupling. Their significance depends on the choice of reinforcements and the processing route adopted during fabrication.

The selection of reinforcement used for enhancing the corrosion susceptibility of compacted AMCs has been a significant challenge, as different reinforcing particles will directly affect the corrosion properties of the resulting AMC [7]. Therefore, careful consideration must be put in place towards the selection of the suitable reinforcements. Commonly used particles include titanium nitride, titanium nitride, silicon carbide, titanium diboride, and alumina [8,9]. Further, the fabrication technique utilised for the fabrication of AMCs can affect the distribution of the TiFe and SiC in the matrix, thereby affecting the rate at which the composites resist corrosion.

Several methods, including casting, pressure infiltration, and additive manufacturing, exist for the fabrication of AMCs. However, the spark plasma sintering technique has become a common method of consolidation of admixed powders [10]. The powders are compacted after they are heated in a vacuum furnace below their melting points to allow diffusion of atoms present [11,12]. The corrosion behavior and microstructural properties of SiC reinforced AMCs produced using sintering technique were investigated in research conducted by Zakaria et al. [13]. The authors reported that the corrosion resistance of the compacted Al/SiC samples was improved with a respective increase in the volume fraction of SiC.

Another recent investigation by Akinwamide et al. [14] also reported on the corrosion susceptibility of Al/TiFe/SiC samples fabricated via casting route. The combination of SiC and TiFe recorded an improved corrosion property in comparison to other specimens. The enhanced corrosion resistance in these studies was attributed to the even distribution of the particles dispersed within the matrix. This present study presents the resistance of the Al/TiFe/SiC composites consolidated by spark plasma sintering technique to corrosion.

2 Materials and methods

The powders of pure aluminium (99% pure), silicon carbide, and ferrotitanium powders with respective average particle size and mesh size of 7 μm and 40, were used for this investigation. The composition of the TiFe and SiC reinforcement powders is presented in Table 1. Different volume fractions of the reinforcement particles were dispersed within the pure aluminum matrix using high-energy ball milling. The proportion of powder to ball ratio and milling speed of 1:10 and 150 revolutions per minute (rpm) were used to achieve this purpose. The sintering process of the alloyed powders was carried out in a nitrogen atmosphere at a pressure and temperature of 50 MPa and 550 °C, respectively. The milled powders were placed in 20 mm to ensure adequate densification of the sintered specimens. Electrochemical testing of the sintered specimens was analyzed using a VersaSTAT studio potentiostat which runs on a versa studio electrochemical software. Prior to the electrochemical test, the surface of the specimens was sectioned to a 10 mm × 10 mm dimension and ground from 200 to 1000 grits using silicon carbide emery papers. The polishing of the ground surface was carried out using 6 and 3 μ suspension on Aka Daran disc and diamond suspension on a polishing cloth. Potentiodynamic polarization and potentiostatic tests were used for assessing the susceptibility of the specimens to corrosion in 3.5 wt.% sodium chloride electrolyte. This electrolyte provided the corrosive environment due to the presence of aggressive chloride ions, which causes rapid deterioration of metallic materials. The scanning potentials and scan rate for potentiodynamic polarization were maintained within the range of −1.2 V and 0.9 V and 0.2 mV respectively. Potentiostatic tests were also carried out for 7200 s using the potential obtained from the passivation curve in the potentiodynamic polarization test. The corroded specimens were further analyzed for pits formation using scanning electron microscopes.

Table 1

Chemical composition of silicon carbide powder and ferrotitanium powders.

3 Results and discussion

3.1 Microstructural analysis

Shown in Figure 1 is the optical micrograph of the sintered specimens, with different volume percent of TiFe and SiC reinforcements. The inclusion of these reinforcements shows a significant effect on the microstructural evolution of the specimens [11]. Well-defined grains and little pores at intergranular regions are evident in the microstructure of the pure aluminium as shown in Figure 1a. In contrast, Figure 1b–d shows a uniform distribution of reinforcement between the aluminium grains. It is also observed that the presence of these reinforcement results in finer grains due to adequate compaction, which resulted from the sintering operation [15]. The pores seen in the sintered composites can be as attributed to different sizes of the particles contained in the composites. Further, an increased quantity of grain boundaries seen in the micrographs could result from decreased grain size due to high energy milling technique adopted for dispersion. The reinforcements which are evenly dispersed in the matrix could also be attributed to adequate milling time and speed employed during the milling/alloying of the powders. A detailed SEM image of the micrographs has been reported in a previous investigation by Akinwamide et al. [16].

thumbnail Fig. 1

Optical micrographs of (a) Pure aluminium (b) Al + 2% SiC (c) Al + 2% TiFe (d) Al + 2% TiFe + 2% SiC.

3.2 Potentiodynamic polarization

The initiation and growth of pits on the composites surface during exposure to aggressive ions, and the repassivation of disrupted oxide films present on the surface of aluminum-based composites is associated with metastable pitting. The formation of pits on aluminium composites is a vital reaction that helps assess the resistance of the specimens to corrosion. The potentiodynamic polarization plots for sintered specimens are presented in Figure 2. It is evident that the highest corrosion density of 7.10 μA is seen in pure aluminium, while the specimen incorporated with 2% TiFe reinforcement is seen to have the lowest current density of 2.57 μA and the highest corrosion potential of −0.660 V in comparison to other sintered composites. The current densities and corrosion potentials of the specimens were also seen to decrease and increase, respectively, with increased volume percent of SiC. A similar observation was reported in a study by Akinwamide et al. [14]. However, the samples incorporated with 2% SiC also exhibited a reduced thermodynamic tendency to corrode, from the sufficiently formed passive oxide layers on the sample's surface. The rapid formation of passive layers can be ascribed to the corrosion inhibiting effect of titanium, which is present in the ferrotitanium reinforcement. A related report was given in an investigation by Perez et al. [17]. The increased current density (7.10 μ) in addition to a decreased corrosion potential (–0.968 V) seen in the pure aluminium specimen could be as a result of chloride reactions, which resulted in formation of soluble aluminium hydroxide (according to Eqs. (1)–(3)) [18], which prevents the stability of oxide formed on the surface of pure aluminium specimen [14,19].

Furthermore, the fabricated composites are also observed to have been attacked by the aggressive chloride ions present in the electrolyte. This attack rapidly weakens the passive films formed on the specimen surface and also causes pitting corrosion due to the formation of intermetallic or secondary precipitates. However, the formed precipitates are susceptible to localized corrosion at grain boundaries [20,21]. An improved corrosion resistance exhibited by the binary alloys compared to the ternary alloy could be due to the cathodic reaction mechanism, which occurs during the pitting corrosion of aluminium composites in the chloride electrolyte. Al + 3 H 2 O → Al ( OH ) 3 + 3 H + + 3 e − (1) Al + 2 H 2 O → AlO ( OH ) + 3 H + + 3 e − (2) Al + 3 2 H 2 O → Al 2 O 3 + 3 H + + 3 e − .(3)

The rapid deterioration observed in pure aluminium, and the specimen with reinforcement addition of 2% SiC + 2% TiFe particles can be ascribed to an increase in the formation of pits, which delayed the rate at which the passive protective films are formed on the surface of the specimens. The improved corrosion resistance exhibited by the binary aluminium alloys could also result from the preferential corrosion at the interfaces of the Al/SiC/TiFe interfaces. This is a major reason why the choice of reinforcement particles remains essential during the fabrication of aluminium matrix composites. Reports have shown that aluminium composites become susceptible to galvanic corrosion due to the difference in the potentials of the aluminium matrix and the respective reinforcements [22–24]. The values seen from the Tafel fit of the potentiodynamic polarization curves of the samples are presented in Table 2.

thumbnail Fig. 2

Potentiodynamic polarization curves for sintered pure aluminium and composites.
Table 2

Tafel properties of pure aluminium and composites.

3.3 Potentiostatic polarization

Shown in Figure 3 are the potentiostaic plots for sintered specimens in the chloride electrolyte. The specimens exhibited different curves, indicating that the specimens react differently in the aggressive media. The binary alloys showed a continous stability in the test medium throughout the test, while the pure aluminium and composite reinforced with Al + 2% SiC + 2% TiFe attained stability after the first 1000 s. The initial fluctuations visible from the binary alloy can be attributed to the formation of passive films due to the presence of the single reinforcements of TiFe and SiC particles [25]. Further observation shows that the pure aluminium and the ternary alloy show an increased current density, indicating a reduced decrease to corrosion resistance. In contrast, the binary alloys exhibit a reduced current density. This also shows an improved corrosion resistance of the binary alloys [26]. The rapid deposition of the passive layer, which led to stability from the initiation till the end of the test, results from the balanced proportion of SiC and TiFe reinforcement particles in the aluminium matrix. Hence, it is not difficult to imagine that the growth of the deposited oxide film on the specimen's surface and its current density will proceed at a slower rate [27].

thumbnail Fig. 3

Potentiostatic plot of pure aluminium and sintered composites.

3.4 Micrographs of the corroded specimens

The SEM morphologies of the corroded specimens after potentiodynamic polarization tests are presented in Figure 4. From Figure 4a, even distribution and formation of corrosion deposits on preferential sites are evident. The dissolution of the oxide/metal interface, which produces a localized aggressive environment, can increase the rate at which blisters are formed on the aluminium matrix beneath the oxide passive layer [28]. Figure 4b also shows less attack on the specimen due to the dispersion of the silicon carbide particles in the matrix, thereby preventing the dissolution of the composite by the aggressive ions available in the test chloride medium [29]. In addition, the specimen with the incorporation of silicon carbide and ferrotitanium in Figure 4c reveals the presence of cracks and severe degradation of the specimen surface. This could be attributed to the higher volume percentage of the SiC particles present in the aluminum matrix [30]. The evidence of pits seen on the corroded surface of the reinforced specimens shows that the specimens are susceptible to intergranular attack [31].

The effect of mechanical attrition (milling) on grain refinement in aluminium matrix composites has been studied [32,33]. The grains of aluminium matrix composites are reportedly reduced to about 9 nm for body-centered cubic metals. In comparison, a reduction of about 13 nm is achievable in hexagonal close-packed and face-centered cubic metals. Therefore, the overall improvement in the corrosion resistance of the composites compared to the pure aluminium specimen can be ascribed to the grain refinement resulting from the high-energy ball milling technique adopted for dispersing the reinforcement particles within the aluminium matrix.

thumbnail Fig. 4

SEM images of sintered (a) pure aluminium (b) Al + 2% SiC (c) Al + 5% TiFe (d) Al + 5% SiC + 2% TiFe.

4 Conclusion

The corrosion behavior of sintered pure aluminium and composites incorporated with particles of TiFe and SiC was studied. The homogeneous dispersion of the particles within the matrix of aluminium was ascribed to factors that include sufficient milling speed, milling time, and fabrication technique. The potentiodynamic and potentiostaic polarization techniques showed that the binary alloys' corrosion resistance was improved compared to the ternary alloys. However, this improvement was attributed to the rapid repassivation of oxide films on the surface of the specimens, which resulted from the presence of incorporated particles. Post-corrosion observation of the surface of the specimen under SEM revealed pits and cracks, which resulted from the effect of aggressive chloride ions present in the test electrolyte. Overall, the incorporation of SiC and TiFe reinforcement particles was seen to improve the corrosion resistance of the sintered aluminium composites in comparison to the pure aluminium specimen.

Acknowledgments

The National Research Foundation, South Africa is appreciated for providing the funds used for this research.

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Cite this article as: Samuel Olukayode Akinwamide, Miltia Lesufi, Ojo Jeremiah Akinribide, Bukola Joseph Babalola, Peter Apata Olubambi, Studies on corrosion behaviour of sintered aluminium based composites in chloride environment, Manufacturing Rev. 8, 22 (2021)

All Tables

Table 1

Chemical composition of silicon carbide powder and ferrotitanium powders.

In the text
Table 2

Tafel properties of pure aluminium and composites.

In the text

All Figures

thumbnail Fig. 1

Optical micrographs of (a) Pure aluminium (b) Al + 2% SiC (c) Al + 2% TiFe (d) Al + 2% TiFe + 2% SiC.
In the text
thumbnail Fig. 2

Potentiodynamic polarization curves for sintered pure aluminium and composites.
In the text
thumbnail Fig. 3

Potentiostatic plot of pure aluminium and sintered composites.
In the text
thumbnail Fig. 4

SEM images of sintered (a) pure aluminium (b) Al + 2% SiC (c) Al + 5% TiFe (d) Al + 5% SiC + 2% TiFe.
In the text

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