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Portugaliae Electrochimica Acta

Print version ISSN 0872-1904

Port. Electrochim. Acta vol.38 no.4 Coimbra June 2020

http://dx.doi.org/10.4152/pea.202004243 

ARTIGOS

Comparative Study of Pure Mg and AZ91D as Sacrificial Anodes for Reinforced Cement Concrete Structures in a Chloride Atmosphere

 

Yogesh Iyer Murthy*, Sumit Gandhia and Abhishek Kumarb

aDepartment of Civil Engineering, Jaypee University of Engineering and Technology, Guna, India

bDepartment of Applied Mechanics, Motilal Nehru National Institute of Technology, Allahabad, India

 

ABSTRACT

A comparative study of the corrosion behavior of pure magnesium and AZ91D anodes in reinforced cement concrete was undertaken in the present work. The steel reinforcements were electrochemically kept in contact with these anodes in a chloride atmosphere, and the half-cell potential drop was observed. Bare steel reinforcements were tied to the anodes and were also kept in a high chloride atmosphere to test the mechanical properties. The yield stress and ultimate tensile stress were found to decrease by approximately 50 MPa, while the reduction in percentage elongation was approximately 25% for reinforcements tied to AZ91D and pure Mg, at the end of 80 days, compared to the fresh steel reinforcement. The rate of corrosion of pure Mg was reportedly slightly higher compared to AZ91D, due to the presence of inter-metallics, as inferred through micro-graphs.

Keywords: cathodic protection, AZ91D, mechanical properties, half-cell potential, micro-characterization, inter-metallics.

 

Introduction

Cathodic protection (CP) of reinforced cement concrete (RCC) structures has been in practice since decades. This technique is widely used for structural integrity against corrosion in regions exposed to a chloride atmosphere or extreme marine environments [4,6]. The underlying principle of CP technique is based on an electro-chemical reaction involving the anodic dissolution of metal by providing electrons to the metal structure protection. The process of CP can be accomplished in two ways, viz. impressed current cathodic protection (ICCP) and galvanic coupling or sacrificial anoding of a suitable material. The most commonly used anode amongst the latter technique is pure magnesium (NMg) [3]. Its low efficiency (~50%) is surpassed by the very high negative potential, which in turn provides high current output. The corrosion rate of Mg is high, and hence, alloying is pursued. Amongst the alloys of Mg, AZ91D is a very commonly used alloy for CP. Although significant research could be found on the use of Mg and AZ91D for CP, there is very little work on the mechanical behavior of steel protected with these anodes and on the micro-structural characterization of such anodes [1-2,8]. Additionally, not much work is reported on the systematic experimental investigation of macro-cell corrosion of these anodes [1,4].

Thus, the primary focus of the current research is to compare the ability of pure Mg and AZ91D in the corrosion mitigation in RCC, study the mechanical behavior of bare steel reinforcements tied with the anodes in a high chloride atmosphere, and microscopically examining the corroded anodes. A systematic analysis of the corrosion behavior of the anodes is expected to aid in the selection of suitable anodes under different conditions.

 

Experimental set-up

The experiment was performed in two stages. Pure Mg and AZ91D anodes were first embedded in a reinforced concrete slab, and half-cell potential was measured for 270 days. Next, bare steel reinforcements were fastened with anodes and placed in a high chloride atmosphere for 80 days. The detailed experimental set-up is discussed below.

Reinforced concrete slab

Four reinforced cement concrete slabs of dimensions 1000 mm x 1000 mm x 100 mm were cast using 1:1.5:3 nominal mixes and a water to cement ratio of 0.45. All the slabs used 10 mm diameter steel reinforcements mats placed with a clear cover of 25 mm from all sides and with a center spacing of 190 mm, as shown in Fig. 1.

 

 

The surface area of the steel reinforcement mat was found to be 1.884 m2. The reinforcements were treated with a pickling solution, in order to remove corrosion sites. Anodes with 22 mm diameter and 250 mm long were centrally placed and tied intact to complete the electrochemical cell. Slab one and two were casted without NaCl and with 3.5% NaCl by weight of cement, respectively, using pure as cast Mg anodes. Similarly, slab three and four were cast without NaCl and with 3.5% NaCl by weight of cement using, as cast, AZ91D anode, respectively. The notations for all the slabs are shown in table 1. These slabs were constructed using tap water with specifications, as shown in table 2, on the same day, so as to maintain similar casting conditions.

 

 

 

The test for tap water was conducted strictly in accordance to IS: 10500:2012 [7]. Bureau of Indian Standards), and it was observed that the tap water consisted of 0.1 mg/L of free residual chlorine and 0.4 mg/L of fluoride ions. These free ions contribute to the conductivity of the electrolyte, viz. concrete, in this case. But, since all the slabs were cast with same free chloride and fluoride content, the effects of these ions are the same in all cases and, hence, innocuous.

Test set-up for bare steel in a chloride atmosphere

In order to further investigate the performance of pure Mg and AZ91D anodes on the corrosion prevention of bare steel reinforcements, three sets of six steel reinforcements were tied together intact, with a centrally placed anode to complete the electrochemical cell. All the samples were dipped in a high chloride atmosphere of 7.5% NaCl in tap water. Sample set one did not contain any anode; sample set two consisted of a AZ91D anode, while sample set three contained a pure Mg anode. These samples were tested for weight loss, tensile strength and microstructure. The set-up consisted of a container 1 m x 1 m x 1 m, as shown in Fig. 2.

 

 

The bare steel reinforcements were selected from the same lot of steel, so as to maintain a uniform chemical composition, and were treated with a pickling solution to remove initial corrosion sites. It was ensured that the samples were kept vertical and undisturbed in the container. All the readings were taken on the same days and at the same time, to nullify the effect of variations in relative humidity and temperature.

 

Results and discussion

Comparison of the potential of reinforcement embedded in concrete for a slab without anode, with a pure Mg anode and with AZ91D

Fig. 3 shows the variation of the negative potential of the concrete slab, with respect to Standard Calomel Electrode (SCE), at a distance of 10 cm from the anode, for different days.

 

 

In general, as expected, it could be found that, as the number of days increased, the negative potential w.r.t. SCE decreased. Another obvious result is that the slabs without NaCl had relatively less negative potentials. 

Further, among the two slabs without NaCl, it was found that the cathodic protection of the slab containing AZ91D (i.e. CP35AZ91D) without NaCl had the least negative potential. This could be attributed to the fact that the interaction of Al, Mg and Zn leads to the formation of various intermetallics, which have different electrochemical potentials, compared to pure Mg. Thus, the overall electrochemical potential of the alloy is lower, leading to a slower rate of corrosion.

Another interesting observation is the increasing trend of the negative potential during the 50th to 100th day. Since the slabs were exposed to atmosphere, the ingress of water during monsoon, led to an increased conductivity of the slab, leading to higher negative potential values.

The negative potential of the slab CP35M reduced drastically after nearly 175 days. This could be possible due to the rapid consumption of free chloride ions by pure Mg, according to the following reaction:

Mg + 2 Cl- ? MgCl2

This notion is further augmented by the fact that, as the number of days increased, several radial cracks along with white crystalline deposits could be observed around the pure Mg anode, which is due to the increased volume of MgCl2. The chemical composition of the crystalline white deposits was analyzed, and it was confirmed that the deposits typically consisted of MgCl2 and Cl2, the latter being in very low quantity, probably deposited due to condensation.

It is also observed that, by the 270th day, the negative potential of all slabs, except CP35AZ91D, were in the range of -200 to -300 mV w.r.t. SCE. Much higher negative potentials of the slab containing 3.5% NaCl and AZ91D anode further augment the proposition of the formation of intermettalics and, hence, reduced rates of interaction with Cl- ions.

Comparison of tensile strength in bare steel bars with AZ91D and pure Mg anode

Three sets of six bare steel reinforcements, 950 mm long and with 10 mm diameter, were closely tied with centrally placed anodes, with 22 mm diameter and 250 mm long. The cross section for the set-up is as shown in Fig. 4. The steel reinforcements were maintained at a height of 200 mm from the bottom, in order to ensure partial immersion, and were kept undisturbed. The temperature of the set-up was maintained at 27 °C. Steel rods were taken out on the 20th, 40th, 60th and 80th days and tested for tensile strength in a 100 ton Universal Testing Machine for yield stress, ultimate stress and % elongation. The results for the tensile test of AZ91D and pure Mg are presented in Fig. 5 (a and b), respectively.

 

 

 

From Fig. 5 it could be inferred that, compared to the fresh steel reinforcement, in both the cases, there was a drop in the yield stress and ultimate tensile stress by nearly 50 MPa, at the end of 80 days.

The drop in percentage elongation for these reinforcements is shown in Fig. 6. At the end of the test period, it was found that this reduction in percentage elongation was approximately 25% for reinforcements tied to AZ91D and pure Mg; however, the reduction in the case of AZ91D was observed to be slightly higher compared to pure Mg anodes.

 

 

Comparison of the rate of corrosion in bare steel bars with AZ91D and with pure Mg anode

The rate of corrosion in both the cases was evaluated and is presented in table 3, using the standard expression, as mentioned below:

where, W = weight loss in milligrams, D = density of steel (obtained as 7.89 g/cc), A= area of steel (cm2) and T= time of exposure to chloride atmosphere in hours.

 

 

One of the obvious results observed from table 3 is that the rate of corrosion is faster at the beginning, and slower as the time proceeds. Also, the rate of corrosion of pure Mg is slightly higher compared to AZ91D.

Microstructure of corroded anodes (Mg/ AZ91D) vs. un-corroded.

The anodes from the concrete were taken after 270 days of embedment, and observed microscopically using Hitachi S-3400N SEM equipped with Energy Dispersive Spectroscopy (EDS). The analysis of the samples was carried out with a 2 μm probe diameter, 10 kV accelerating voltage and 50 nA probe current. The error of the SEM measurements is estimated to be about ± 2 at. %.

Microstructure of pure Mg

Fig. 7 (a-d) reveals the backscattered electron images (BSEI) of corroded and un-corroded parts of pure Mg after 270 days of embedment in concrete, with gradually increased magnification of the area of interest, to systematically understand the features of the anode. Fig. 7 (a) shows the junction of the corroded and un-corroded regions of the anode. Three distinct features could be observed in the micrograph, namely, white, grey and spots of darker shade of grey. EDS spot analysis was carried out to deduce the composition of these features. The spectral composition of the white layer was found to be pure Mg, the grey layer consisted of MgO, while point analysis of the dark grey features confirmed the formation of MgCl2 in the corroded region. Fig. 7 (b) and 7(d) show the magnified images of the corroded regions, while Fig.7(c) shows the un-corroded region. It could be seen that there are grey regions in the pure Mg, due to the formation of MgO.

 

 

Further, Fig. 8 shows the area analysis of 400 μm of the corroded parts of pure Mg. The area analysis affirms the findings of EDS spot analysis, showing the presence of MgCl2 and MgO.

 

 

Microstructure of AZ91D

BSEI of the unpolished as-cast alloy revealed that the macroscopically smooth alloy anode actually consisted of ridges or protrusions (Fig.9(a)). The EDS spot analysis revealed that these ridges were composed of MgO, roughly 20 μm long.

 

 

The micro-structure of the polished un-corroded as-cast sample of AZ91D is shown in Fig. 9(b). The objective of analyzing the micro-structure of polished sample was to understand the internal structure of the alloy. It consists of a Mg matrix and inter-metallics, with well-developed primary dendrites distributed along the α-Mg grain boundaries. The inter-metallics consist of Mg17Al12 (dark grey) and Al2Mg5Zn2 (light grey).

Fig. 9(c) shows the BSEI of the corroded AZ91D alloy, after 270 days of embedment. It consists of irregular oxide nodules (primarily MgO) of varying sizes, ranging from 5 to 40 μm, formed due to the oxidation of the α-Mg matrix and craters of MgCl2, along with the matrix phase. The oxide nodules were formed preferentially at grain boundaries, while craters of MgCl2 were randomly distributed.

It could be observed that Mg17Al12 phase acts as a barrier, as well as a potential site for cathodic reaction. Similar observations were reported by Jonsson and Perrson [5]. Further, the area analysis of 400 μm (Fig. 9(d)) of the sample shows the findings pictographically above discussed.

From the 100 μm BSEI of the corroded AZ91D (Fig. 10), it is seen that crevices were formed along the grain boundaries which lead to the following conclusions:

 

 

  1. The Mg matrix gets oxidized to MgO or interacts with chloride forming MgCl2, both of which have higher volumes, leading to the expansion of the matrix and chipping off thereafter.
  2. The electro-chemical potential of the inter-metallics is lower compared to pure Mg, as the chloride ions have preferential interaction with Mg. Thus, the pure Mg matrix acts as “active-sites” for interaction, while inter-metallics are dormant sites. Consequently, the corrosion rate of AZ91D is lower compared to pure Mg.

Thus, it is seen that the process of corrosion of pure Mg and AZ91D is largely different on a microscopic scale. The reduced rate of corrosion is also mathematically compared in table 3.

 

Conclusion

In the current work, a systematic study was undertaken to investigate the mechanical properties of steel in an electro-chemical contact with pure Mg and AZ91D anodes, using concrete with 3.5% NaCl by weight of cement, and using bare steel in 7.5% NaCl dissolved in tap water. The potential of steel embedded in concrete with both the anodes showed a drop in the negative potential w.r.t. SCE, as the days increased. Relative humidity and temperature were found to influence the half-cell potential readings. The yield stress and ultimate tensile stress were found to decrease by approximately 50 MPa, while the reduction in percentage elongation was approximately 25% for reinforcements tied to AZ91D and pure Mg, at the end of 80 days, compared to the fresh steel reinforcement. The mechanical properties of steel coupled with both the anodes showed similar results, but the rate of corrosion of pure Mg was reportedly slightly higher compared to AZ91D, due to the presence of inter-metallics, as inferred through micro-graphs.

 

References

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  3. Fontana MG. Corrosion engineering. Tata McGraw-Hill Education., 2005.
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Received November 26, 2017; accepted June8, 2018

 

* Corresponding author. E-mail address: yogesh.murthy@juet.ac.in

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