Corrosion Of Titanium Research Articles

The effect of dissolved oxygen and Shewanella algae on the corrosion mechanism of titanium in a simulated marine environment

The influence of dissolved oxygen (DO) and Shewanella algae on the corrosion behavior of pure titanium were systematically studied in this work. The formation of S. algae biofilms on titanium surface was facilitated by the anaerobic environment, which accelerated titanium corrosion. Upon the breakdown of passive film, S. algae acquired electrons from the titanium base substrate through extracellular electron transfer (EET) processes. Various EET-related genes were overexpressed by the low DO condition, leading to enhanced EET kinetics. High concentration DO increased TiO2 content and the thickness of passive film, which enhanced the protective effect and mitigated microbiologically influenced corrosion.

Comparative analysis of serum titanium level in patient with healthy dental implant and patients with peri-implantitis- A cross sectional prospective study

Objectives: Titanium dental implants can last for more than two decades in the oral environment. Corrosion of the implant surface can release metallic particles or ions into surrounding tissue. The metallic constituents like titanium in human blood serum have not been fully studied. The study compares titanium serum levels before and after dental implant placement and compares levels in patients with healthy implants and those with per-implantitis. Methods: The study comprised 2groups of Group 1 patient observing implant surgery and group 2 patients with diagnosed peri-implantitis. Each group comprised of 60 patients. Serum titanium level was measured from blood obtained from Group 1 at three different intervals (one month prior to implant surgery, 4th and 8th month after successful loading) and from Group 2 during the course of peri-implantitis by inductively coupled plasma–mass spectroscopy. The statistical analysis was done for the obtained data. Results: Analysis showed a raised level of serum titanium at 4th month of post implant placement (2.39 mg/dl) and in patient with peri-implantitis(2.94 mg/dl) and both levels are significantly differ (ANOVA test) from pre-surgical estimation of serum titanium level (1.79 mg/dl). Conclusions: Understanding the correlation between titanium corrosion and peri-implantitis is vital for enhancing the long-term success and safety of dental implants. Additional research is required to investigate these links and potential strategies to protect the well-being of implant patients.

A comparative study on the corrosion of pure titanium and titanium–12%zirconium alloy after different exposure periods of time in sodium chloride solution

In this work, the powder metallurgy technique was employed to manufacture pure titanium (Ti) and 88% titanium–12% zirconium (TiZr) alloy. The electrochemical corrosion investigations for pure Ti and the TiZr alloy were carried out after exposure for 30 min and 3 days in 3.5% NaCl solutions. The Nyquist and Bode plots obtained from the electrochemical impedance spectroscopy experiments revealed that the presence of Zr remarkably magnifies the corrosion resistance of Ti via increasing the impedance and degree of the phase angle, as well as the polarization and solution resistances. The potentiodynamic cyclic polarization measurements revealed that the presence of 12% Zr highly enhances the corrosion resistance of Ti. These polarization results showed that Zr addition reduces the corrosion of Ti via decreasing its corrosion rate. The intensity of the current when measured with increasing time of the experiment at −0.10 mV (Ag/AgCl) indicated that the addition of 12% Zr greatly decreases the absolute current, which indicates that alloying Zr within Ti reduces the severity of its corrosion in the chloride electrolyte. The morphology of the surfaces and the possible surface layer(s) for the corroded Ti and TiZr samples were analyzed using a scanning electron microscope and energy dispersive x rays. Results collectively depicted that the presence of Zr increases the corrosion resistance when alloyed with Ti.

Corrosion behaviors of TA2 and TA36 titanium alloys in a high-sulfur environment

The mixed medium of sulfur, H2S, CO2, and generated water in the developed sour gas fields in Sichuan-Chongqing Gasfield seriously corrodes pipelines. The carbon steel gathering system is not suitable for transporting such a medium and titanium alloy has become a hotspot due to its high specific strength and excellent resistance to H2S corrosion. The corrosion of titanium and titanium alloys in the mixed media of H2S, CO2, and water has been extensively explored, but their electrochemical corrosion behaviors in the presence of elemental sulfur are not clear. In this study, the effects of temperature and sulfur on the corrosion behaviors and electrochemical behaviors of TA2 and TA36 in the simulated solution were studied with hanging tests and high-temperature and high-pressure electrochemical corrosion method and the corrosion morphology was observed with a scanning electron microscope. When the temperature increased from 60 °C to 90 °C, the self-corrosion current of TA36 alloy was decreased by one order of magnitude and the corrosion rate of TA36 decreased, indicating the improved corrosion resistance. At the same temperature, the self-corrosion current of TA36 alloy was 28.8 % of that of TA2 and the corrosion resistance of TA36 alloy was better than that of TA2. Sulfur deposition accelerated the pitting corrosion of TA2 and TA36.

Antibiofilm peptides enhance the corrosion resistance of titanium in the presence of Streptococcus mutans.

Titanium alloys have gained popularity in implant dentistry for the restoration of missing teeth and related hard tissues because of their biocompatibility and enhanced strength. However, titanium corrosion and infection caused by microbial biofilms remains a significant clinical challenge leading to implant failure. This study aimed to evaluate the effectiveness of antibiofilm peptides 1018 and DJK-5 on the corrosion resistance of titanium in the presence of Streptococcus mutans. Commercially pure titanium disks were prepared and used to form biofilms. The disks were randomly assigned to different treatment groups (exposed to S. mutans supplied with sucrose) including a positive control with untreated biofilms, peptides 1018 or DJK-5 at concentrations of 5μg/mL or 10μg/mL, and a negative control with no S. mutans. Dynamic biofilm growth and pH variation of all disks were measured after one or two treatment periods of 48h. After incubation, the dead bacterial proportion, surface morphology, and electrochemical behaviors of the disks were determined. The results showed that peptides 1018 and DJK-5 exhibited significantly higher dead bacterial proportions than the positive control group in a concentration dependent manner (p < 0.01), as well as far less defects in microstructure. DJK-5 at 10μg/mL killed 84.82% of biofilms and inhibited biofilm growth, preventing acidification due to S. mutans and maintaining a neutral pH. Potential polarization and electrochemical impedance spectroscopy data revealed that both peptides significantly reduced the corrosion and passive currents on titanium compared to titanium surfaces with untreated biofilms, and increased the resistance of the passive film (p < 0.05), with 10μg/mL of DJK-5 achieving the greatest effect. These findings demonstrated that antibiofilm peptides are effective in promoting corrosion resistance of titanium against S. mutans, suggesting a promising strategy to enhance the stability of dental implants by endowing them with antibiofilm and anticorrosion properties.

Pitting Corrosion of Titanium Depending on the Properties of the Passive Film

Pitting corrosion behavior of Ti with passive film under breakdown was investigated from the points of film thickness and oxygen-related species in the film. A Ti specimen was passivated in a sulfuric acid solution at 5.0 VAg/AgCl at 323 and 353 K. A passivation current decreased, increased and then slightly decreased with increasing a passivation time, the periods were denoted as Region (i), (ii) and (iii), respectively. A pitting potential of the specimen passivated in Region (i) was almost independent of, and that in Regions (ii) and (iii) shifted higher with increasing the time. Change in an amount of water desorbed from the film with the time was similar to that in the pitting potential. It was found from XPS test that change in a film thickness with the passivation time was also similar to that in the pitting potential. Furthermore, the desorbed water was derived from hydroxide or both of hydroxide and bound water in the film. The findings indicate that the film passivated in Regions (ii) and (iii) was under breakdown, and suppression of the pitting corrosion is caused by increasing both of the film thickness and the amount of hydroxide and bound water in the film.

The effect of three dental cement types on the corrosion of dental implant surfaces

Statement of problemOne of the main challenges facing dental implant success is peri-implantitis. Recent evidence indicates that titanium (Ti) corrosion products and undetected-residual cement are potential risk factors for peri-implantitis. The literature on the impact of various types of dental cement on Ti corrosion is very limited. PurposeThis study aimed to determine the influence of dental cement on Ti corrosion as a function of cement amount and type. Materials and methodsThirty commercially pure Ti grade 4 discs (19 × 7mm) were polished to mirror-shine (Ra ≈ 40 nm). Samples were divided into 10 groups (n = 3) as a cement type and amount function. The groups were no-cement as control, TempBond NE (TB3mm, TB5mm, and TB8mm), FujiCEM-II (FC3mm, FC5mm, and FC8mm), and Panavia-F-2.0 (PC3mm, PC5mm, and PC8mm). Tafel’s method estimated corrosion rate (icorr) and corresponding potential (Ecorr) from potentiodynamic curves. Electrochemical Impedance Spectroscopy (EIS) data was utilized to obtain Nyquist and Bode plots. An equivalent electrical circuit estimated polarization resistance (Rp) and double-layer capacitance (Cdl). Inductively coupled plasma mass spectrometry (ICP-MS) analysis was conducted to analyze the electrolyte solution after corrosion. pH measurements of the electrolyte were recorded before and after corrosion tests. Finally, the corroded surface was characterized by a 3D white-light microscope and scanning electron microscope. Statistical analysis was conducted using either one-way ANOVA followed by Tukey’s Post Hoc test or Kruskal-Wallis followed by Dunn’s test based on data distribution. ResultsBased on cement amount, FC and PC significantly increased icorr in higher amounts (FC8mm-icorr = 8.22 × 10−8A/cm2, PC8mm-icorr = 5.61 × 10−8A/cm2) compared to control (3.35 × 10−8A/cm2). In contrast, TB3mm decreased icorr significantly compared to the control. As a function of cement type, FC increased icorr the most. EIS data agrees with these observations. Finally, corroded surfaces had higher surface roughness (Ra) compared to non-corroded surfaces. ConclusionThe study indicated that cement types FC and PC led to increased Ti-corrosion as a function of a higher amount. Hence, the implant stability could be impacted by the selection, excessive cement, and a potentially increased risk of peri-implantitis.

Molecular Insights into the Stability of Titanium in Electrolytes Containing Chlorine and Fluorine Ions.

Titanium and its alloys are protected by a compact and stable passive film, which confers resistance to corrosion by the primary halogen chloride (Cl-) while being less effective against fluoride (F-). Although researchers have recognized different macroscopic corrosion effects of these halide ions on titanium, the underlying mechanisms remain largely unexplored. In this work, the bonding of Cl-/F- with stable passive films was studied in neutral and acidic (pH = 2.3) conditions. The synergistic effect between the interfacial hydrogen bond (HB) structure and halogens on titanium corrosion was first revealed using first-principles calculation and Raman spectroscopy. F- forms more stable halogen-Ti bonds than Cl-, resulting in titanium degradation. The proton combined with F- exhibits a specific synergistic effect, causing corrosion of the passive film. The water hydrogen bond transformation index (HBTI) at the titanium/aqueous interface was 1.88 in an acidic solution containing F-, significantly higher than that in neutral/acid solutions containing Cl- (1.80/1.81) and a neutral solution containing F- (1.81). This work clarifies the structure-activity relationship between HBTI and the destruction of titanium passive films. We propose that the microstructure of the interfacial HB is an undeniable factor in the corrosion of titanium.

Radiation effect on the corrosion of disposal canister materials

The effects of radiation on the corrosion of canister materials were investigated for the reliable disposal of high-level radioactive waste. The test specimens were gamma-irradiated at a very low dose rate of approximately 0.1 Gy/h for six and twelve months. The copper and cast iron species were less corroded when irradiated. It is hypothesized that gamma rays suppress the formation of lower-enthalpy species like metal oxides and activate reductive reactions. In contrast, it was difficult to evaluate the effect of radiation on the corrosion of titanium and stainless steel.

Influence of Al2O3 reinforcements and Ti-Al intermetallics on corrosion and tribocorrosion behavior of titanium

Ti-Al2O3 composites have demonstrated favorable characteristics for use in load-bearing biomedical implant applications; however, the influence of Al2O3 reinforcement particles and Ti-Al intermetallics on the electrochemical and tribo-electrochemical responses of Ti are not well-understood. This study explored the corrosion and tribocorrosion characteristics of powder metallurgy-manufactured Ti-Al2O3 composites in a simple physiological saline solution at body temperature. Electrochemical analysis was performed by electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization and tribo-electrochemical mechanisms were explored under open circuit potential (OCP) against a 10 mm diameter alumina ball in a ball-on-plate tribometer with reciprocating configuration. Results revealed that the corrosion behavior of Ti was adversely affected by the development of a heterogeneous oxide film on the Ti matrix and the Ti-Al intermetallic phases formed by the interaction of Ti and Al2O3 particles. However, there was a drastic improvement in tribocorrosion behavior, evidenced by decreased corrosion tendency under sliding and a marked reduction in wear volume, primarily as a result of the decreased wear damage resulting from the load-bearing reinforcements.

Additively manufactured Ti-29Nb-21Zr shows improved oxide polarization resistance versus Ti-6Al-4V in inflammatory simulating solution.

Retrieval studies in the past two decades show severe corrosion of titanium and its alloys in orthopedic implants. This damage is promoted by mechanically assisted crevice corrosion (MACC), particularly within modular titanium-titanium junctions. During MACC, titanium interfaces may be subject to negative potentials and reactive oxygen species (ROS), generated from cathodic activation and/or inflammation. Additive manufacturing (AM) may be able to produce new, corrosion-resistant titanium alloys and admixtures that are less susceptible to these adverse electrochemical events. In this study, we characterize the impedance and corrosion properties of three new AM titanium materials, including Ti-6Al-4V with added 1% nano-yttria stabilized ZrO2 , admixed Ti-29Nb-21Zr, and pre-alloyed Ti-29Nb-21Zr. We aim to elucidate how these materials perform when subjected to high ROS solutions. We include conventionally and additively manufactured Ti-6Al-4V in our study as comparison groups. A 0.1 M H2 O2 phosphate-buffered saline (PBS) solution, simulating inflammatory conditions, significantly increased biomaterial OCP (-0.14 V vs. Ag/AgCl) compared to PBS only (-0.38 V, p = .000). During anodic polarization, Ti-6Al-4V passive current density more than doubled from 1.28 × 10-7 to 3.81 × 10-7 A/cm2 when exposed to 0.1 M H2 O2 . In contrast, Ti-29Nb-21Zr passive current density remained relatively unchanged, slightly increasing from 7.49 × 10-8 in PBS to 9.31 × 10-8 in 0.1 M H2 O2 . Ti-29Nb-21Zr oxide polarization resistance (Rp ) was not affected by 0.1 M H2 O2 , maintaining a high value (1.09 × 106 vs. 1.89 × 106 Ω cm2 ), while Ti-6Al-4V in 0.1 M H2 O2 solution had significantly diminished Rp (4.38 × 106 in PBS vs. 7.24 × 104 Ω cm2 in H2 O2 ). These results indicate that Ti-29Nb-21Zr has improved corrosion resistance in ROS containing solutions when compared with Ti-6Al-4V based biomaterials.

Biofilm formation by sulphate-reducing bacteria on different metals and their prospective role in titanium corrosion

ABSTRACT This study describes the biofilm formation by sulphate-reducing bacteria (SRB) on different materials, which has implications for the biomedical, pharmaceutical, food and chemical process industries. SRB was chosen as a model organism being an anaerobic bacterium. Biofilm formation on different materials and corrosion of titanium by SRB were monitored with time using confocal laser scanning microscopy and fluorescent FISH probes were used to authenticate the SRB strain. The thickness of the mono-culture SRB biofilm has ranged from 4 to 24 µm during thed 12–84 hr; however, the maximum biofilm thickness (24 µm) was recorded after 60 hr of growth. Planktonic growth of the SRB strain showed a log phase up to 48 hr and the sulphide production ranged from 2 to 14 mg l−1. For a comparative account, the SRB biofilm formation on copper was chosen as a positive control. Finally, the putative role of extracellular electron transfer by SRB in the biocorrosion process and the plausible mechanism of pitting corrosion of titanium is described in detail.

Influence of Fe3+ on titanium corrosion in H2SO4 solutions without and with F−

Abstract Influence of Fe3+ on the corrosion of titanium in H2SO4 solution without F− and with F− was investigated by electrochemical tests. The electrochemical test results showed that Fe3+ could significantly inhibit titanium corrosion in H2SO4 solution without F− and with F− by promoting the protective film formation on titanium. Titanium corrosion resistance (Rc) was positively related to the concentration of Fe3+ in H2SO4 without and with F−. A mechanism was proposed for Fe3+ inhibiting the corrosion of titanium in H2SO4 solution without and with F−.

Microbiologically influenced corrosion of titanium by Desulfovibrio vulgaris biofilm under organic carbon starvation

Desulfovibrio vulgaris biofilm was pre-grown on Ti coupons for 7 d and then the biofilm covered coupons were incubated again with fresh culture media with 10 % (reduced) and 100 % (normal) carbon source levels, respectively. After the pre-growth, sessile D. vulgaris cell count reached 107 cells/cm2. The sessile cell counts were 2 × 107 and 4.2 × 107 cells/cm2 for 10 % and 100 % carbon sources, respectively after the subsequent 7 d starvation test. The maximum pit depth after the 7 d pre-growth was 4.7 µm. After the additional 7 d of the starvation test, the maximum pit depth increased to 5.1 µm for 100 % carbon source vs 6.2 µm for 10 % carbon source. Corrosion current density (icorr) from potentiodynamic polarization data at the end of the 7 d starvation test for 10 % carbon source was more than 3 times of that for 100 % carbon source, despite a reduced sessile cell count with 10 % carbon source. The polarization resistance (Rp) started to decrease within minutes after 20 ppm (w/w) riboflavin (electron mediator) injection. The carbon starvation data and riboflavin corrosion acceleration data both suggested that D. vulgaris utilized elemental Ti as an electron source to replace carbon source as the electron donor during carbon source starvation.

Study on the galvanic corrosion of titanium and stainless steel couple with the synergistic effect of proton and fluoride ion

The galvanic corrosion of titanium/304 stainless steel (TA1/304SS) couple was investigated in neutral and acidic solution with and without fluorine ion (F-) using macro-electrochemical technique and scanning electrochemical microscope (SECM). The results show that the synergistic effect of H+ and F- affects the passive film on the surface of galvanic couple, resulting in a great change in heterogeneous reaction rate constant and surface electrochemical activity characterized by approach curve and surface mapping of SECM in feedback mode. In addition, a typical polarity reversal occurs in pH = 2.0 acidic solution with adding F- which the TA1 is anodic to 304SS.

The role of bacterial corrosion on recolonization of titanium implant surfaces: An in vitro study.

Inflammation triggered by bacterial biofilms in the surrounding tissue is a major etiological factor for peri-implantitis and subsequent implant failure. However, little is known about the direct effects of bacterial corrosion and recolonization on implant failure PURPOSE: To investigate the influence of oral commensals on bacterial corrosion and recolonization of titanium surfaces. Streptococcus sanguinis (S. sanguinis) and Porphyromonas gingivalis (P. gingivalis), which are key bacteria in oral biofilm formation, were cultured on commercially pure titanium and titanium-aluminum-vanadium (Ti6Al4V) plates in artificial saliva/brain heart infusion medium under aerobic or anaerobic conditions. Biofilm formation was examined after 7 and 21 days by crystal violet and live/dead staining. Titanium ions released into culture supernatants were analyzed over a period of 21 days by atomic absorption spectrometry. Visual changes in surface morphology were investigated using scanning electron microscopy. Biofilm formation on sterilized, biocorroded, and recolonized implant surfaces was determined by crystal violet staining. S. sanguinis and P. gingivalis formed stable biofilms on the titanium samples. Bacterial corrosion led to a significant increase in titanium ion release from these titanium plates (p < 0.01), which was significantly higher under aerobic conditions on pure titanium (p ≤ 0.001). No obvious morphological surface changes, such as pitting and discoloration, were detected in the titanium samples. During early biofilm formation, the addition of titanium ions significantly decreased the number of live cells. In contrast, a significant effect on biofilm mass was only detected with P. gingivalis. Bacterial corrosion had no influence on bacterial recolonization following sterilization of titanium and Ti6Al4V surfaces. Bacterial corrosion differs between oral commensal bacteria and leads to increased titanium ion release from titanium plates. The titanium ion release did not influence biofilm formation or bacterial recolonization under in vitro conditions.

Shear Bond Strength of Dental Cements on Titanium Alloy: Use of Different Restorative Materials

Different dental cements and restorative materials may have various impacts on the shear bond strength (SBS) to titanium alloy of dental implants, and some fluoride-containing cements may destroy the oxide layer of Ti alloys. The aim of this study was to evaluate the retention and SBS of different dental cements to titanium alloy using different restorative materials and also the corrosive effect of dental cements on titanium alloy. In this in-vitro study, a total of ninety titanium alloy discs (10×3 mm) and restorative material discs (7×3mm) consisting of Co-Cr soft metal, zirconia, and Ni-Cr were constructed. Three dental cement of 2 different compositional classes, glass ionomer (GI) and zinc phosphate (ZP), were used to cement the discs (n=10 in each paired disks). SBS was evaluated using a universal testing machine with a cross-head speed of 1mm/min. A stereomicroscope (×32) and a scanning electron microscope were used to determine the fracture pattern and titanium corrosion, respectively. Data were then analyzed statistically using one-way ANOVA and Tamhane comparison test (P&lt;0.05). The mean SBS of studied groups ranged from 0.12±0.07 to 6.2±0.97 Mpa, with the Ni-Cr and zirconia were demonstrated as the materials with the highest and lowest SBS to GI and ZP, respectively. The cements created a strong bond to the Co-Cr soft metal while the GI cement remained on restorative material disc surfaces in all samples, except in the zirconia sample. Mixed patterns were mostly seen in ZP cement groups. To conclude, applying fluoride-containing cements have no effect on titanium.

Electrochemical Corrosion of Titanium and Titanium Alloys Anodized in H2SO4 and H3PO4 Solutions

Titanium and its alloys have superior electrochemical properties compared to other alloy systems due to the formation of a protective TiO2 film on metal surfaces. The ability to generate the protective oxide layer will depend upon the type of alloy to be used. The aim of this work was to characterize the electrochemical corrosion behavior of titanium Ti-CP2 and alloys Ti-6Al-2Sn-4Zr-2Mo, Ti-6Al-4V, and Ti Beta-C. Samples were anodized in 1 M H2SO4 and H3PO4 solutions with a current density of 0.025 A/cm2. Electrochemical tests on anodized alloys were carried out using a three-electrode cell and exposed in two electrolytes, i.e., 3.5 wt % NaCl and 3.5 wt % H2SO4 solutions at room temperature. Scanning electron microscopy (SEM) was used to observe the morphology of anodized surfaces. The electrochemical techniques used were cyclic potentiodynamic polarization (CPP) and electrochemical noise (EN), based on the ASTM-G61 and G199 standards. Regarding EN, two methods of data analysis were used: the frequency domain (power spectral density, PSD) and time-frequency domain (discrete wavelet transform). For non-anodized alloys, the results by CCP and EN indicate icorr values of ×10−6 A/cm2. However, under anodizing conditions, the icorr values vary from ×10−7 to ×10−9 A/cm2. The PSD Ψ0 values are higher for non-anodized alloys, while in anodized conditions, the values range from −138/−122 dBi (A2·Hz−1)1/2 to −131/−180 dBi (A2·Hz−1)1/2. Furthermore, the results indicated that the alloys anodized in the H3PO4 bath showed an electrochemical behavior that can be associated with a more homogeneous passive layer when exposed to the 3.5 wt % NaCl electrolyte. Alloys containing more beta-phase stabilizers formed a less homogeneous anodized layer. These alloys are widely used in aeronautical applications; thus, it is essential that these alloys have excellent corrosion performance in chloride and acid rain environments.

Peri-Implantitis in Relation to Titanium Corrosion: Current Status and Future Perspectives

Peri-Implantitis in Relation to Titanium Corrosion: Current Status and Future Perspectives

Insight Into Corrosion of Dental Implants: From Biochemical Mechanisms to Designing Corrosion-Resistant Materials.

Purpose of ReviewDespite advanced technologies to avoid corrosion of dental implants, the mechanisms toward the release of metals and their role in the onset of peri-implant diseases are still under-investigated. Effective knowledge on the etiopathogenesis of corrosive products and preventive strategies mitigating the risks for surface degradation are thus in dire need. This review aimed to summarize evidence toward biocorrosion in the oral environment and discuss the current strategies targeting the improvement of dental implants and focusing on the methodological and electrochemical aspects of surface treatments and titanium-based alloys.Recent FindingsRecent studies suggest the existence of wear/corrosion products may correlate with peri-implantitis progress by triggering microbial dysbiosis, the release of pro-inflammatory cytokines, and animal bone resorption. Furthermore, current clinical evidence demonstrating the presence of metal-like particles in diseased tissues supports their possible role as a risk factor for peri-implantitis. For instance, to overcome the drawback of titanium corrosion, researchers are primarily focusing on developing corrosion-resistant alloys and coatings for dental implants by changing their physicochemical features.SummaryThe current state-of-art discussed in this review found corrosion products effective in affecting biofilm virulence and inflammatory factors in vitro. Controversial and unstandardized data are limitations, making the premise of corrosion products being essential for peri-implantitis onset. On the other hand, when it comes to the strategies toward reducing implant corrosion rate, it is evident that the chemical and physical properties are crucial for the in vitro electrochemical behavior of the implant material. For instance, it is foreseeable that the formation of films/coatings and the incorporation of some functional compounds into the substrate may enhance the material’s corrosion resistance and biological response. Nevertheless, the utmost challenge of research in this field is to achieve adequate stimulation of the biological tissues without weakening its protective behavior against corrosion. In addition, the translatability from in vitro findings to clinical studies is still in its infancy. Therefore, further accumulation of high-level evidence on the role of corrosion products on peri-implant tissues is expected to confirm the findings of the present review besides the development of better methods to improve the corrosion resistance of dental implants. Furthermore, such knowledge could further develop safe and long-term implant rehabilitation therapy.