Electrochemical Tests to Evaluate the Stability of the Anodic Films on Dental Implants

Marino, C. E. B.; Mascaro, L. H.

doi:https://doi.org/10.4061/2011/574502

International Journal of Electrochemistry

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Abstract Introduction Experimental Results and Discussion Conclusions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2011 | Article ID 574502 | https://doi.org/10.4061/2011/574502

Electrochemical Tests to Evaluate the Stability of the Anodic Films on Dental Implants

C. E. B. Marino¹and L. H. Mascaro²

Academic Editor: Davood Nematollahi

Received12 Jan 2011

Revised12 Apr 2011

Accepted02 May 2011

Published26 Jun 2011

Abstract

The stability of anodic films potentiodynamically grown on titanium, titanium-grade 2, and Ti6Al4V alloy was studied in a simulated physiological electrolyte, up to 8.0 V, and at room temperature to determine the corrosion resistance levels of dental implants. In PBS (phosphate buffer saline) solution, thin titanium oxide films protect the surface of the Ti6%Al4%V alloy up to 6.0 V, pure Ti up to 8.0 V, and Ti-grade 2 up to 1.5 V. At more positive potentials, localized corrosion starts to occur possibly due to the alloy elements (Ti6Al4V-V and Al) and variable levels of interstitials (Ti-grade 2: C, N, and Fe, mainly). When the biomaterials were submitted to open-circuit conditions, in artificial saliva, the worst corrosion resistance was observed in dental implant (Ti-grade 2), according to the open-circuit potential values and reconstruction rate analysis of these oxide films. The XPS spectra revealed TiO₂ oxide as the main phase in the barrier oxide film coating the dental implant.

1. Introduction

The use of titanium as a material for surgical purposes began around the 1960s. For this purpose, this material must not cause any adverse biological reaction in the body, and it must also be stable and retain its functional properties. Due to its attractive mechanical and chemical characteristics and its property of “biofixation” with the periprosthetic tissue, titanium is established as one of the major materials used for manufacturing orthopedic implants [1]. The excellent corrosion resistance of titanium and its alloys results from the formation of very stable, continuous, highly adherent, and protective oxide films on metal surfaces. Because titanium itself is highly reactive and has extremely high affinity for oxygen, these beneficial surface oxide films form spontaneously and instantly when fresh metal surfaces are exposed to air. The nature, composition, and thickness of the protective surface oxides on titanium alloys depend on environment conditions. Titanium is normally covered with a thin oxide film, which largely determines the surface properties of an implant [1]. The high corrosion resistance of titanium is due to the formation of these protective oxide films (thickness 1 to 4 nm) [2], but body fluids contain chloride ions that can induce a breakdown of passive films on prostheses [3, 4]. Corrosion and surface film dissolution are two mechanisms for introducing additional ions in the human body. Extensive release of metal ions from prosthesis can result in adverse biological reactions and can lead to mechanical failure of the device [5].

The thin oxide film, naturally formed on a titanium substrate, is responsible for the excellent biocompatibility of titanium implants. This fact occurs because of the low level of electronic conductivity, a thermodynamically stable state in the physiological media, besides high corrosion resistance [6]. Previous studies have described a variety of properties of anodic oxide films, for example, surface morphology, crystal structures, and corrosion resistance [7]. One way to change the surface characteristics of implants is varying the properties of the oxide films always present on Ti surfaces. Oxidized implants change the properties of the titanium implant and play an important role during the dynamic buildup of the osteointegration process [1, 8]. Healy and Ducheyne [9] already investigated the superficial changes, stoichiometry, and absorbed surface species on titanium oxide during exposure to model physiological environments. As a result of these studies, it was observed that the oxide incorporates both Ca and P elements from the extra cellular fluid and that it increases in thickness as function of implantation time. Kuphasuk et al. [10] studied the electrochemical behavior of Ti, Ti6Al4V, NiTi, and three other titanium alloys at 37°C in Ringer’s solution. Electron diffraction patterns indicated that all titanium alloys were covered mainly with rutile-type oxide after corrosion tests, and the Ti and Ti5Al2.5Fe were the most resistant to corrosion. The study of the corrosion resistance in chloride media of Ti-based dental implants was investigated by Arslan et al. [11]. By the Tafel slopes and EIS Nyquist spectra, the galvanic corrosion was evaluated, and the Ti6Al4V/CoCr and Ti6Al4V/CrNi systems were to be similar corrosion behavior.

One of the problems associated with corrosion study of dental alloys is that the knowledge of the electrochemical environment of oral cavity is limited to simulating this media. The electrochemical properties of the oxide film and its long-term stability in biological environments play a decisive role for the biocompatibility of titanium implants [12–14].

A method of expanding the corrosion resistance of titanium into reducing environments is increasing the surface oxide film thickness by anodizing or thermal oxidation [1]. In the present work, the growth of the oxide and its stability in Ti, Ti-grade 2, and Ti6Al4V alloy were studied in physiological solutions at room temperature (~25°C) by electrochemical techniques. The titanium oxide characterization was made through X-ray photoelectron spectroscopy (XPS) and microstructural aspects by metallographic techniques.

2. Experimental

A conventional 250 mL three-electrode electrochemical cell was used. The working electrodes were Ti6%Al4% V (6% m/m and 4% m/m of Al and V, resp.) alloy rod (Titanium Industries-USA), pure Ti (Aldrich, 99.99%), and Ti-grade 2 (dental screw [15]) giving an area of ~1.26 cm², ~0.28 cm² and 0.062 cm², respectively, and were exposed to the electrolytes. Prior to the oxide growth, the electrodes were mechanically polished with silicon carbide paper of grade 600 and rinsed with distilled water. A platinum electrode was used as counterelectrode, and all potentials were measured against a saturated calomel electrode (SCE). The electrolytes were PBS solution (phosphate buffer saline-pH 7; 8.77 g·L⁻¹ NaCl, 3.58 g·L⁻¹ Na₂HPO₄, 1.36 g·L⁻¹ KH₂PO₄) [16] for the growth of the oxides and artificial saliva (pH 7; 0.4 g·L⁻¹ NaCl, 0.4 g·L⁻¹ KCl, 0.795 g·L⁻¹ CaCl₂·H₂O, 0.69 g·L⁻¹ NaH₂PO₄·H₂O, 0.005 g·L⁻¹ Na₂S·9H₂O, 1.0 g·L⁻¹ urea) [17] for the study of spontaneous dissolution process, at room temperature. All electrochemical measurements were carried out with a Microquimica-MQPG-01 electrochemical system. The initial and final potentials for the potentiodynamic growth at 50 mV·s⁻¹ of the oxides were V and V (versus SCE) range. The electrodes were polished and the oxides potentiodynamically grown up to , where the potential was held until a steady current was reached. Therefore, the circuit was open and the variation of potential with time (dissolution process) was analyzed for the Ti and its alloys covered with oxide electrodes, in artificial saliva solution. So, the stability of the anodic oxide in artificial saliva was studied. Finally, the anodic scan was repeated, in PBS solution, in order to obtain the potentiodynamic profile for the regrowth of any oxide that eventually had been dissolved [2]. The nature of the anodic oxides was investigated by X-ray photoelectron spectroscopy (XPS) using a Kratos Analytical XSAM HS Spectrometer having Mg Kα ( eV), X-ray source with power given by the emission of 15 mA at a voltage of 15 kV. The high-resolution spectra were obtained with analyzer energy of 20 eV. The binding energies were referred to the carbon 1s line, set at 284.8 eV. A least-square routine was used for the fitting of the peaks.

3. Results and Discussion

3.1. Anodic Growth and Stability of the Oxides

Cyclic voltammetry was used to characterize the pure Ti system, varying between 1.0 V and 8.0 V. This potential range was chosen because the corrosion process starts at potentials higher than 6.0 V, for Ti6Al4V alloy, in PBS solution [18, 19], and higher than 1.5 V, for Ti-grade 2, in the same solution, as will be discussed. The voltammogram shown in Figure 1 indicates that the Ti-grade 2 has a similar anodic transformation when compared with pure Ti [2]. This fact is possible due to the growth of a uniform oxide film, mainly TiO₂. However, the potential sweep in the positive direction shows an anodic current starting with –0.55 V for the titanium electrode [2] and –0.15 V for Ti-grade 2 electrode. The delay in starting potential oxide growth, in the case of dental implant (Ti-grade 2), could be explained by the presence of impurities and/or variable levels of interstitials into the biomaterial that causes differences in their stability. These hypotheses will be analyzed by microstructural and by chemical composition tests. With an increase in the potential, the current density remains almost constant indicating a process of thickening of the anodic surface film. After the growth and aging of the oxide films up to different potentials (), the circuit was open and the potential decaying was measured, to analyze the spontaneous dissolution of these different oxide films. From this, the immersion time in artificial saliva was varied. When the open-circuit potential (OCP) became stationary, a new potential sweep, from – 1.0 to 1.5 V, was carried out to regrow any film that might have been dissolved. In acid solutions, Blackwood et al. [20] proposed that the dissolution reaction of open-circuit breakdown of passive film on Ti might be written as

Following the OCP evolution, it is possible to understand the general interactions and the spontaneous dissolution of oxide grown up to 1.5 V that takes place at the biomaterials surface. The open-circuit potential of the pure Ti, Ti-grade 2, and Ti6Al4V alloy in artificial saliva is shown in Figure 2. In artificial saliva, the of all biomaterials, was stabilized after a week at values between –0.63 V and –0.24 V versus SCE. The worst corrosion resistance was observed in the dental implant (Ti-grade 2) according to lower and higher reconstruction rate (see below).

The anodic charges related to the formation () and reconstruction of the anodic oxide allowed for an evaluation of the magnitude of these processes, in PBS solution. These charges were obtained considering the areas under the anodic sweeps before and after OCP measurements in artificial saliva, which are integrated between –1.0 and 1.5 V. It means that the amount of current consumed while the electrochemical dissolution of the oxide film during was integrated. Figure 3 shows a typical valve metal behavior for the Ti-grade 2, and its anodic oxide grows according to the high-field model [2].

The oxide film reconstruction rate (RR, expressed as a percentage) is defined as being equal to the ratio between the and the [2], and these anodic charges were obtained by integration of the corresponding versus curves. Figure 4 shows the dependence of the reconstruction rate (RR%) on immersion time in artificial saliva. The RR values of oxides increase with immersion time and stabilize in 15% Ti-grade 2, 13% Ti6Al4V alloy, and 9% pure Ti, after around a week, in artificial saliva. So, the dissolution process of these oxide films is more effective in the dental implant (Ti-grade 2) in this physiological media as previously observed by potential sweep. Species from the electrolytic solution can be incorporated into the oxide matrix [20] leading to changes in its mechanical properties. The oxides have a natural level of internal stress, but the presence of incorporated foreign species affects directly the Pilling-Bedworth ratio (ratio between the oxide molar volume and the metal molar volume), inducing alterations in the internal stress that may cause the rupture of the protecting oxide film [21].

In agreement with what was previously stated, the impedance data previously described [11, 19, 22] show the influence of the Cl^- presence on the passive oxide stability. By completing this research, we already presented the characterization of these anodic films by electrochemical impedance [19]. The impedance response indicated the existence of a thin oxide film on dental implant that suffers a dissolution process during different immersion times. This fact was confirmed by resistive and capacitive behaviors, as the corrosion resistance of the Ti-grade 2 is less than pure Ti. The resistance of the passive film on Ti-grade 2 decreased when the exposure time is increased, due to the oxide breakdown followed by a dissolution process. The capacitive behavior indicated the presence of a uniform and thin oxide on the implant surface. The influence of chloride media on the stability of anodic films on titanium-based materials by voltammetric studies has been presented by our research members [18].

An average value of 2.5 nm V⁻¹ was obtained for the anodization rate in pure Ti oxides [2]. In the case of Ti-grade 2, the anodization rate is 2.1 nm V⁻¹ indicating a lower protect layer to a fixed final potential. This result is according to the magnitude of the reconstruction rate obtained to the dental implant in artificial saliva (see Figure 4). This worst corrosion resistance could be related to the presence of contaminants and impurities and/or to the microstructural variations that occur after thermal and conformational treatments. Therefore, the dental implant becomes more vulnerable to the corrosion processes [23].

In the corrosion-dissolution process, the presence of ions released from the implant could affect the tissue-bone material interactions that cause damage in the osteointegration process resulting from the looseness of implant. Marino and Mascaro [19] have found that the spontaneous dissolution rate of TiO₂ in sulfuric acid solutions, at various pHs, is first order with respect to proton concentration. Thus, we proposed that the oxide hydrolysis might be written as reaction (1). Therefore, a very slow chemical dissolution could be associated with the release of Ti(OH)₃ ⁺ ions and other unstable elements in oxide matrix.

4. Microstructural Analysis

The electrochemical results suggest that the corrosion resistance decreases with increasing levels of impurities. Therefore, the microstructural analysis could show the natural tendency of biomaterial corrosion resistance.

Information about the chemical composition and structural aspects of these biomaterials is essential to the knowledge of its behavior and stability in aggressive media, such as body fluids [24, 25]. The microstructures of the Ti, Ti-grade 2 and Ti6Al4V alloy were analyzed after mirror polishing and etching their surfaces with a Kroll solution (6 : 1 : 1000 v/v/v HNO₃ : HF : H₂O) for approximately 15 s. The adherent oxide film on the surface of Ti and Ti alloys requires strong etchings to minimize the staining problems that might obscure the microstructure.

Titanium has hexagonal close-packed atomic lattice structure (α titanium-phase) which is stable up to 882°C, and it transforms into a face-centered cubic structure (β titanium phase) above this temperature. Pure titanium is a soft and ductile metal, but the impurities or addition of alloying elements makes it harder and less ductile. In the Ti6Al4V alloy, the aluminum stabilizes the α phase and the vanadium stabilizes β phase. These alloying elements are known to increase the mechanical properties of titanium [1]. The addition of the elements aluminum and vanadium refined the grain size of the alloy [18]. The pure titanium microstructure shows a satisfactory homogeneity, indicating good corrosion resistance [20] (see Figure 5(a)).

(a)

(b)

Figure 5(b) shows the dental implant (Ti-grade 2) microstructure, in which the superficial deposition of the attack product is not uniform. This fact occurs because of the different expositions of the crystallographic planes, and each grain has its own crystalline orientation in relation to the attack plane. Comparing the pure Ti and Ti-grade 2 microstructures, it is possible to observe some important alterations. The Ti-grade 2 microstructure presents nonuniform grains. The elongated grains indicate that the material was deformed, without recrystallization, and sustain some strain hardening (tensioned regions) (see Figure 5). Also, notice that dark regions (more intensive attack) are in major proportions than clear regions, which confirms the partially strain-hardened material. These strain-hardened areas are anodic regions in corrosion process.

The difference in Ti purity levels and its fabrication characterizes the kinds of Ti grade 1, 2, 3, and 4 and their mechanical and corrosion resistance properties [1]. Thus, the microstructural analysis sustained that the lowest corrosion resistance of Ti-grade 2 is due to the levels of interstitials and other impurities, a fact that damages the osteointegration process [3].

5. Characterization of Oxide Film

The characterization of the passive oxide film coating Ti-grade 2 implant was done by X-ray photoelectron spectroscopy (XPS). The potential value was chosen in order to have passive films grown up to 1.5 V (~40 Å thick, according to previous results [2]), in PBS solution. Figure 6 presents the XPS spectrum for Ti 2p electron to the dental implant covered with titanium oxide film obtained in phosphate buffer solution. The spectrum shows the doublet referent to Ti 2p that consists at the peaks: Ti 2p_1/2 and Ti 2p_3/2. These subindices indicate the level of the element in spectroscopic analysis. The doublet was determined by the Ti 2p_3/2 peak with binding energy around 459.0 eV, which corresponds to the Ti⁴⁺ signal [26]. This indicates that TiO₂ is the main oxide present in the passive film, consistent with results reported previously using different approaches [18, 27].

When the surface analyzed was Ti6Al4V/oxide, the effects of alloying elements in passive films were examined by X-ray photoelectron spectroscopy (Figure 7). The peaks indicate that TiO₂ (Ti⁴⁺) is the major surface component for both Ti—grade 2 and Ti6Al4V alloy samples. The peak positions for TiO₂ were consistent with binding energy shifts expected for titanium in combination with oxygen in the form of TiO₂ [21, 27].

(a)

(b)

The high-resolution Al 2p spectrum results for the Ti6Al4V alloy sample are shown in Figure 7(b). The presence of elemental aluminum metal can be verified (Al⁰) at binding energy at 72.5 eV. Some authors [27, 28] reported the measured binding energies of surface Al and V to be consistent with oxides such as Al₂O₃ and V₂O₅ or even Al and V existing as ions at interstitial or substitutional sites in the Ti oxide matrix. In the present work, the thin oxide film on the Ti6Al4V alloy could be a “solid solution” of titanium oxide (TiO₂) that contains dissolved aluminum and vanadium. In addition, by the chemical environment analysis of Al, which indicated the absence of O atoms around it, and considering the values of ionic radius of these alloy elements, it was possible to suppose that both Al and V would be present as ions at interstitial sites in the Ti oxide matrix. The vanadium alloy element was not detected by XPS analysis but this element could be present in the oxide with concentrations lower than 0.1 at.% which represents the detection limit of the XPS technique.

Besides, the total XPS spectrum revealed Fe contaminant present in the Ti-grade 2 oxide matrix. The binding energy of Fe 2p peak is around 715.0 eV, and its atomic percentage is 1.8% which could affect its properties. For pure Ti and Ti6Al4V alloy, the absence of Fe was observed [28]. Finally, it was described that high levels of interstitials in dental implants affected the corrosion resistance and the osteointegration process [3, 5].

6. Conclusions

In this work, it was shown that thin titanium oxide films grown potentiodynamically protect the Ti-grade 2 surfaces up to 1.5 V in artificial saliva, at room temperature. At more positive potentials, corrosion processes start to occur. This can be explained due to the presence of variable levels of interstitials (impurities) in Ti-grade 2 screws that could decrease their corrosion resistance. The results were confirmed by metallographic and XPS data. The XPS spectra revealed the TiO₂ as the most important phase in the passive film, besides the presence of Fe traces that modify the dental implant properties. Therefore, Ti-grade 2 screws showed an increase of heterogeneity regarding its chemical composition and microstructural aspects when compared with pure Ti. These changes cause susceptibility to corrosion processes, in body fluids. So, the presence of oxide films coating the implant surface is a good pretreatment against corrosion processes, and it also increases the durability of these implants.

Acknowledgments

The authors are grateful to the Conselho Nacional para o Desenvolvimento Científico e Tecnológico (CNPq) for the scholarship and to the Fundação Araucária for the financial support.

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Copyright

Copyright © 2011 C. E. B. Marino and L. H. Mascaro. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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