The effect of inhibiting molybdate used in anodizing-conversion treatment to improve corrosion protection of AA2030 aluminum alloy in different steps

In this article, different treatment baths for corrosion protection of 2030 aluminum alloy in addition to replacing the hexavalent chromium due to the European recommendation were employed. This work is divided into three steps of treatment: first, anodization using molybdate inhibitor without and with phosphoric acid and, then, pre-oxidation with sodium hydroxide. In the last step, we studied the influence of conversion coating with the combination of sodium molybdate and fluoride on the anodic layer formed on aluminum alloy 2030. In order to characterize the formed layers, we use microstructural characterization (SEM, AFM, and nano-indentation), which allows highlighting the surface condition as well as the morphological distribution, and electrochemical techniques such as potentiodynamic polarization and electrochemical impedance spectroscopy which shows that the anodization treatment of the aluminum alloy with phosphoric acid and sodium molybdate offered better corrosion resistance. This resistance increased with the use of pre-oxidation and then reached a maximum value of 99.8% efficiency with the addition of the molybdate conversion coating which causes an increase in the double layer and gave an alternative possibility of chromium VI.

conductivity, and good mechanical properties; and they offer great resistance to corrosion [5,6]. Aluminum of the 2030 series (Al-Cu-Mg-Pb) is an anodic alloy which has a very negative redox potential which causes the formation of an inert protective layer [7]. In order to improve the strength of the aluminum alloy and increase the protection against pitting corrosion (localized corrosion), several mechanical, chemical, and electrochemical methods have been carried out [8][9][10][11][12]. Anodizing, coatings, and inhibitors are used to develop a passive, conductive, and protective artificial layer which improves the physical and chemical properties of aluminum in inorganic electrolytes [13]. The electrochemical anodization process is more used in the surface treatment industry, it causes the formation of a thin film of alumina and improves its adhesion to aluminum alloy [14], and its thickness and structure are controlled by different parameters (time, temperature, flow rate, and composition of the bath) [15]. This treatment is an electrochemical conversion process which forms relatively dense barrier/poroustype oxide layers with a decorative appearance and higher resistance to corrosion and scratches [16][17][18], thus providing better adhesion of the alumina formed from the base material [8]. According to Yen et al., the surface structure of micro/nano-complex aluminum influences cell culture, which has been found to have a superhydrophilic surface in anodized aluminum [19]. In addition, the thermal performance test shows that the micro/nano-textured morphology of the anodized aluminum surface increases the heat transfer performance with the increase of the nanotube in the alumina layer (diameter and length of the pores) [20].
Anodic sulfuric oxidation (ASO) electrolytically forms a layer of alumina on the surface, effectively protecting alloys from corrosion [21], and this process results from the combination of aluminum and oxygen released [22].
Chromatic anodic oxidation (CAO) results in the formation of a thin film in the micrometer thickness and good rubbability [23]; therefore, it provides excellent corrosion protection. Due to the recommendation of environment and health (Reach 2016), several researches were carried out to replace and substitute it with molybdates, tungstates, permanganates, and vanadates, including chemical elements similar to chromium (groups VB, VIB, and VIIB of the periodic table) [24].
Molybdate anodic oxidation (MoAO) is widely used as a treatment meeting the environmental requirement for aluminum alloys with low toxicity under various conditions. Molybdate ions also show good inhibition in acidic solution and NaCl solution [25,26]. The layer formed is characterized by the presence of numerous fine pores [27]. These pores are the subject of a lot of works such as the research done by De Bonfils-Lahovary and Tao [28,29], from which it was concluded that the pores are not a form of surface cracking [30], but this surface porosity results from the loss of aluminum cations to the electrolyte [17].
An artificial layer of phosphate (PCC) and molybdate (MCC) conversion coating is commonly used to replace chromate conversion coating (CCC) [31]. The layer formed during MCC is considered as an insulating layer thanks to the oxidability of molybdate ions (MoO 4 2− ) and the reducibility of the Al substrate [32]. In this work, we study the effect of the combination of the two treatment processes. First, for the anodization as well as the conversion coating to have a durable and effective protection moreover to meet the requirement of REACH (Registration, Evaluation and Authorization of Chemicals), we choose a molybdate-based treatment. This study is therefore composed of two parts: the first is to study the treatments of anodization of A2030 alloy in the bath of molybdate (MoAO) without and with phosphoric acid in different concentrations and, secondly, the implementation of a treatment process including anodization, pre-oxidation, and conversion coating with molybdate. Optimal experimental conditions were determined to obtain films with good anti-corrosion performance.

Materials and pretreatment
The AA 2030 aluminum alloy with an exposed area of 0.5cm 2 sealed by epoxy resin was used in this work. Before the electrochemical study, the surface of Al was polished with 600, 800, 1000, and 1200 grit sic abrasive paper, rinsed with bidistilled water, then degreased with acetone ethanol, deionized water, and dried with air flow, in order to remove the impurities residual from surfaces.

Treatment solution
The treatment solution is prepared with three steps *First step (anodization): -S1 is an anodization with different concentrations of sodium molybdate and bidistilled water. -S2 is the combination of Na2MoO4 with the different concentrations of phosphoric acid and bidistilled water.
The treatment lasts 45 min at room temperature, under a potential of 14 Volt/cm 2 and stirring at a low speed. *Second step (pre-oxidation): --S3: before the anodization of the alloy in S2, the pre-oxidation with 4% NaOH and bidistilled water at 40°C was carried out with different immersion times (30s, 60s, and 90s).
Electrochemical characterization is done in a solution that contains (wt %) 3.5% NaCl. Every experience is repeated twice and the average value is reported to reach reproducibility of results.

Characterizations of the oxide layer and corrosion products
For the characterization of oxide layers formed after treatment, scanning electron microscopy (SEM), energy dispersive X-ray (EDS) spectrum analysis, AFM, and nanoindentation are required.

Electrochemical measurements
For the characterization of the oxide layer formed on the Al surface with an area of about 0.5 cm 2 , we used electrochemical studies, in an aggressive solution of 3.5% NaCl (% by weight) as an analyzer. The tests are carried out in a cell with three electrodes: aluminum as the working electrode (WE), Ag/AgCl as the reference electrode (RE), and platinum as the counter electrode (CE); the electrochemical workstation is Princeton Applied Research (VersaSTAT 3F, AMETEK). Before starting the electrochemical tests, the working electrodes (WE) should be immersed in the aggressive solution for a few minutes to have a more stable potential during the open circuit potential test (OCP). Electrochemical impedance spectroscopy (EIS) was performed over a frequency range from 100 kHz to 10 mHz with an excitation signal of 10 mV (RMS). The potentiostatic polarization (Tafel) measurements were measured from the cathodic to the anodic branch at ±250mV around OCP with a scan rate of 1 mV/s. Electrochemical parameters such as current density, anode, and cathode slope (ba and bc) were determined using Tafel plots.

Surface morphology
Scanning electron microscopy (SEM) images of the surface after treatment with S3 and S4 are shown in Fig. 1. In Fig. 1a, the surface of the alloy treated in S3 appears homogeneous with the presence of fine pores and the lines observed are due to mechanical polishing. This anodizing treatment is schematized in Fig. 2 and well explained by the following reactions: • Cathode: • Anode: Then: The layer of aluminum oxide formed above the metal corresponds to reactions 2 and 3, where the reduction of hydrogen at the cathode is presented in reaction 1, and the oxidation of aluminum at the level of anode by reaction 2, which causes the formation of the protective layer of alumina [33,34].
The surface morphology of the alloy after S4 treatment with a conversion in pH=4 is shown in Fig. 3; the latter shows that the increase in pH causes the formation of a cracked and less adherent oxide layer. Figure 4 explains this mechanism of corrosion by a series of reactions: Reactions 4 and 5 explain the dissolution of the alumina layer, where n shows the amount of water separated per mole of Al 2 O 3 [30]. Localized corrosion is the most common phenomenon for aluminum alloys, which is due to their heterogeneous microstructure [35,36].
After the treatment with S4 shown in Fig. 4b, a uniform non-porous layer is observed on the alloy, and its morphology is flake-like. According to Wang et al., the coating reacts with the high bath temperature to form boehmite products which penetrate into the pores and produce a flake-like cluster AlOOH as reaction 6 [37]. Figure 5 shows the nanopores formed in the oxide layer after anodization and conversion coating; these pores contain an inner layer containing pure alumina and an outer layer containing alumina contaminated with anions [38]. The absorption of molybdate at the aluminum surface causes the formation of conversion coatings  above the metal [33]; this mechanism is explained in reactions (7) and (8) and then in Fig. 5.
According to Bai et al. [38], we can explain the formation mechanism coating with two processes: treatment by the molybdate ions are absorbed on the surface then the absorbed ions react with the aluminum substrate to form conversion coatings.
Two different reactions are considered occurring on the surface: one is that molybdate ions react with H + existing on the interface of metal and solution to form molybdic acid and the latter hydrolyzes to form The addition of F − facilitates the surface reaction of aluminum alloy through the following reaction: (9). Due to the relatively weak oxidizability of molybdate ions, the chemical conversion coatings deposited directly on the aluminum alloy surface usually have weak adhesion force with the substrate but the use of a porous surface. Figure 5 helps to form more adhesive coatings [39]. Figure 6 shows the energy dispersive X-ray spectra (EDS) of the different treatments S3 and S4 respectively. The chemical composition of the oxide layer after S3 and S4 treatment is summarized in Tables 1 and 2 respectively. According to these results, the existence of molybdate (3.5%) was observed on the surface of the AA2030 alloy treated in S3, due to the composition of the anodizing bath. On the other hand, the appearance of an increase of molybdate (6.47%) after the S4 treatment confirms the formation of a molybdate conversion coating (MCC), and this indicates that the S4 treatment is beneficial for the formation of MoO 2 and Al 2 O 3 . The increase in copper illustrates the increase in the corrosion resistance of the layer formed during the treatment in S4.

Atomic force microscopy
Atomic force microscopy (AFM) is an effective and in situ method to acquire the surface morphology with high resolution. Figure 7 is the micrograph of the studied area of the signal line with dimensions of 20 × 20 μm 2 . It presents the 3D graph of the alloy after surface treatment in (a) S3 and (b) S4.
It can be deduced from Fig. 7a and b the layer morphology formed after treatment in S3 and S4 for 2030 aluminum alloy, which has a homogeneous distribution. Figure 7a shows needle-like small grain structures formed on the alloy treated in S3 with some scratches due to polishing and with an average surface roughness of 82.9 nm. The image   Table 2 The chemical composition of the oxide layer after three-step treatment in Fig. 7b appears relatively and evenly flat and smooth with an average surface roughness of 89.3 nm. The surface roughness of the alloy substrate is increased after the last processing step (S4) by the physical interactions, which improves the adhesion property of the coating to the material surface [40]; in addition, the electrical resistance decreases when the contact area increases [41,42]. Consequently, the Al treated in S4 could be considered as an efficient treatment to prevent corrosion.

Nano-indentation
Nano-indentation is a very important analysis technique to determine the elasticity modulus of the film formed on the aluminum alloy [43]. The contact with the penetrator and the material surface during nano-indentation results in the recording of the load depth and indentation with high electronic precision which leads to the deformation of elastics in the material [44]. This technique allows the characterization of oxide layers by determining the modulus of elasticity of the film [45,46]. Its value can also be determined using an Oliver and Pharr technique which is one of the most important techniques [47]. Figure 8 shows low displacement curves obtained by CSM mode in nano-indentation (a) and the depth of penetration as a function of time (b). After the same time and with the application of a constant load between 10 and 50 mN, the same phenomenon is observed for the two curves representing the S3 and S4 treatment, that is the increase of the penetration depth in parallel with the increase of the load and the time; on the other hand, in the curve of the sample treated in S3, the penetrator penetrates deeper compared to the one treated in S4; moreover, the displacement of the maximum fast load for the alloy treated in S4 is 900nm compared to that treated in S3 which is 1250nm, and the modulus of elasticity improves from 59 to 82 GPa during the treatment in S3 and S4 respectively. From this, it is concluded that the layer formed in S4 is more hard.

Electrochemical impedance spectroscopy (EIS)
The impedance spectra recorded for the AA2030 alloy according to the Nyquist representation after different treatments are shown in Figs. 9, 10, 11, and 12 (a). Figure 9a shows the different percentages of molybdate concentration, and the spectrum is characterized by a well-defined capacitive loop in the high-frequency range, which represents the interface reaction between the electrolyte solution and the substrate.  shows the impedance diagrams of the samples treated with 5% Mo and with a variation of the percentage of phosphoric acid. These show two capacitive loops in the high-frequency ranges for 6% and 1% phosphoric acid. The curve for 3% phosphoric acid shows a capacitive loop with the highest resistance part in the impedance diagram. Figure 11a is characterized by the value of the resistive part for the 60-s pre-oxidation time which has the largest capacitive loop. It is important to note that the inductive response was not observed for the treated samples. It is well known that the larger diameter of the semicircle, the corrosion resistance of the sample is better. In this way, the responses of the treated samples show larger semi-circles compared to the S1 samples, confirming that all treatments improve the corrosion resistance of the AA2030 alloy in 3.5% NaCl solution.
According to previous studies [48], the capacitive loops for the samples in the highfrequency range correspond to the charge transfer resistance on the substrate surface (R) and the capacitance (C). The low-frequency capacitive loop is attributed to the corrosion product layer, oxide film, and coating on the surface of the metal substrate but the absence of this phenomenon in Fig. 12a proves that the treatment has a compact layer. In summary, it is clear from Fig. 13 that the S4 treatment offers superior anti-corrosion performance for the AA2030 alloy.
Phosphate and molybdate ions can form heteropoly acid phosphorus-molybdate in the acid solution, which has strong oxidizing properties. Therefore, we assume that they will be bound together in a certain proportion, and phosphorus-molybdate can modulate the rate of oxide film formation and lead to improved resistance [49].
The Bode diagram shown in Figs. 9, 10, 11, and 12 (b) presents the variation of the impedance amplitude and phase angle. According to the literature, the impedance spectrum at high frequency reflects the characteristics of the porous layer of the film, while at low frequency reflects the characteristics of the barrier layer. Seen in the Bode diagram, the impedance modulus increases from S1 to S4, and the phase angles are positive so that their growth is parallel with the growth of the frequency which means that the treatment is improved with a compact layer. The inhibition efficiency (η) was calculated from the Nyquist diagram by the polarization resistance Rp, as in the following equation: The impedance parameters were derived from the EIS fitting curves for aluminum alloy 2030 in 3.5% NaCl for the different treatment baths and are listed in Table 3 where Rset and R0 were the solution resistance and the blank resistance respectively.
In accordance with Table 3, the inhibition efficiency was increased in parallel with the polarization resistance (Rp) to more than 99.8% at S4, confirming the excellent effect of the bath (S4) which combines between two corrosion treatment processes < anodizing and conversion coating > with the same inhibitor < sodium molybdate > for aluminum alloy 2030 in 3.5% NaCl.

Potentiodynamic polarization curve (Tafel)
The polarization curves of the aluminum alloy for the different treatment steps are shown in Fig. 14. Hence, the values of the corrosion potential (Ecorr) and the corrosion current density (Icorr) are key parameters for assessing the corrosion behavior of the films formed after the different treatments.
Rp × 100 Fig. 13 The real resistance part of EIS for different treatments  Table 4 reports the values related to the estimation of the corrosion parameters (Ecorr, cathodic (Bc), and anodic (Ba) tafel slopes and the corrosion current density (icorr)) for all the treatments studied. In Fig. 14, we observe dissolution of the anode for the aluminum alloy sample treated in baths S1 and S2, while for the sample treated in the other baths, the corrosion potential decreases and moves towards an anodic potential which causes the passivation of the anode. The anode slopes for the different treatments increase while the current density decreases which improves the anti-corrosion property of the aluminum alloy [50]. The polarization curve shows that oxygen diffusion controls the cathodic process of the S1 and S2 aluminum alloy in aggressive solution, while that of the S4-treated sample is controlled by an electrochemical process, during which the action of oxygen is effectively inhibited and thus the cathodic reaction and the corrosion rate have decreased, and these results confirm what has been obtained in electrochemical impedance spectroscopy studies, by estimating the positive effect of the S4 bath. To characterize the anti-corrosion properties of the oxide layer, the corrosion potential (Ecorr) increased from −0.57V for S3 to −0.69V for S4 and a significant improvement in corrosion performance is observed for the S4 treatment, which has the lowest Icorr of 3E−08 among all samples. In general, it has been reported that low Icorr leads to a low corrosion rate and good polarization resistance (Rp) of the coatings [51,52].