Corrosion Of Steel Research Articles

Pitting corrosion of 4Cr13 steel in a chlorine tank

Abstract Pitting corrosion is harmful and often occurs in chloride solution. The pitting corrosion of 4Cr13 steel in a chlorine tank was investigated in this study. Cr-depleted rings were observed and the Cr-depleted ring coincided with the bumps consisting of corrosion product. Carbides distributed along the Cr-depleted ring were also observed. Many pitting with spherical or shallow shapes were observed by cross-section morphology exam. The depth of pitting for Sample A is smaller than that for Sample B which accorded with surface morphology. The corrosion product was composed of a Fe-rich outer layer and a Cr-rich inner layer. The Fe-rich outer layer will rapture and fall off with the increase of corrosion products, and then the Cr-rich inner layer was revealed. As a result, Cr-depleted rings were inspected with SEM-EDS. The pitting corrosion mechanism of 4Cr13 steel in the chlorine tank was also discussed.

Carbonation and corrosion of steel in fly ash concrete, concluding investigation of five-year-old laboratory specimens and preliminary field data

Carbonation development and reinforcement corrosion were investigated on concretes exposed for a five-year period at 90% RH, 20 ℃, and 5% CO2, and for a six-year period at natural carbonation. Portland cement-based binders with 0%, 18%, and 30% fly ash were investigated. The fly ash blends showed lower carbonation resistance compared to PC both at laboratory and field exposure, a large difference in carbonation performance was observed between the laboratory exposed specimens. The carbonation rate was fastest on the laboratory specimens and showed square-root time dependency the first 2.5 years, but reduced rate at later age. Deeper carbonation depths were in general observed in the vicinity of the reinforcement compared to the unreinforced laboratory exposed specimens. Not all specimens were fully carbonated at the steel-concrete interface. The correlation between degree of carbonation of the steel-mortar interface, the open circuit potential, and the observed corrosion of the steel bars varied between binders and bar position (top or bottom). The measured corrosion rate in the laboratory exposed (90% RH, 20 ℃, and 5% CO2) carbonated concrete was on average 0.2 μA/cm2, with an upper value of 0.6 μA/cm2. The highest corrosion rate was measured in the fly ash concrete. No corrosion rate data are yet available for the field exposed concretes.

Study on electrochemical corrosion dynamics of cathode dic shield in concrete crack

Abstract Corrosion of steel reinforcement is a primary factor that negatively impacts the service life and safety of bridges made of concrete. Cathodic protection techniques are widely used to protect reinforcing bars in concrete against corrosion. However, it is inevitable that corrosion cracks will develop in the concrete during long-term operation, which will significantly shorten the cathodic current protection distance and increase the degree of corrosion of the rebar within the cracks. Therefore, electrochemical experiments and characterization of corrosion forms were carried out based on the company’s design of a rectangular connection device, we studied HRB500 steel in 3 wt.% corrosion behavior in rectangular joints under different CP current densities in NaCl solution. The results showed that with increasing experimental time, the corrosion in the crevice transitioned from activation corrosion to oxygen concentration corrosion, with the open-pore potential of the HRB500 steel inside the crevice appearing as a positive shift and the open-pore potential outside the crevice shifting from positive to negative. When implementing cathodic protection, the corrosion of HRB500 steel within the crevice is activated, while the corrosion outside the crevice changes from anodic to mixed controlled corrosion and from full to pitting corrosion. With the increase of CP current density, the corrosion process of HRB500 steel outside the gap is mainly dominated by cathode control, then gradually weakens, and the corrosion form changes from pitting to comprehensive corrosion.

Corrosion Inhibition Properties of Corrosion Inhibitors to under-Deposit Corrosion of X65 Steel in CO2 Corrosion Conditions.

Under-deposit corrosion is widely present in the pipelines of oil and gas production, causing significant corrosion damage. In this paper, a novel electrochemical cathodic-polarization method was carried out to accelerate the formation of CaCO3 scale on a X65 steel surface in a simulated solution containing scaling ions. Subsequently, pre-scaled X65 steel was placed in a high temperature and pressure autoclave to conduct corrosion weight-loss experiments and in situ electrochemical measurements. The study mainly compared the corrosion inhibition behavior of four quaternary ammonium salt corrosion inhibitors, pyridinium quaternary salt (BPC), quinolinium quaternary salt (BQC), 8-hydroxyquinolinium quaternary salt (BHQ) and pyridinium (1-chloromethyl naphthalene) quaternary salt (1-CPN), in a simulated oilfield scale under corrosive conditions. The results of the weight-loss experiments demonstrated that the inhibition efficiencies of the corrosion inhibitors from high to low were as follows: 1-CPN < BHQ < BQC < BPC. The in situ electrochemical measurements showed that the immersion time and type of corrosion inhibitor had a pronounced influence on the corrosion and corrosion inhibition behavior of X65 steel with CaCO3 coating. It was also proved using both EIS and PC that 1-CPN shows the best inhibition performance in all. Lastly, the inhibition mechanism of corrosion inhibitors at under-deposit conditions was analyzed via a surface morphology observation of SEM.

Insights into the high and prolonged inhibition mechanism of pyridoxine hydrochloride as vitamin B6: a new green inhibitor slowing the acidic corrosion of mild steel

Insights into the high and prolonged inhibition mechanism of pyridoxine hydrochloride as vitamin B6: a new green inhibitor slowing the acidic corrosion of mild steel

Initial stage oxidation corrosion of commercial ferritic stainless steels with different Cr contents at 650 °C for solid oxide fuel cells

Selecting adequate ferritic stainless steel (FSS) with a high corrosion resistance and a low cost is critical for solid oxide fuel cells (SOFCs) operating at intermediate temperature. In this study, the corrosion behaviors of four commercial FSSs involving TS430, TY441, YG442, and TY445 with a Cr content ranging from 16.18 wt.% to 21.73 wt.% are investigated at 650 °C. The oxidation mass gains, microstructures of surface oxide scale, and electrical conductivities are measured. The effects of grain size as well as doped elements are estimated together with the Cr volatilization. Flaky Cr2O3 particles are formed on TS430 and TY441 dominated by the outward migration of Cr3+. In comparison, a thin and dense layer of chromia is observed on YG442 and TY445. A high Cr content and a uniformly distributed grain size are conducive to the formation of a thin and dense chromia scale on the FSS surface during the initial oxidation process. On the other hand, the addition of Nb, Ti, and Mo weakens the outward diffusion of Cr3+ and reduces the particle size of chromia. After oxidation at 650 °C for 120 h, scattered (Mn, Cr)3O4 spinel particles occur on TS430, YG442, and TY445. TY445 and YG442 exhibit a higher conductivity although all the results of area specific resistance (ASR) are less than 6 mΩ·cm2. Meanwhile, the effect of Cr volatilization is enlarged on the estimation of mass gain at 650 °C compared with even higher temperatures.

Experimental investigation on the high-temperature corrosion of 12Cr1MoVG boiler steel in waste-to-energy plants: Effects of superheater operating temperature and moisture

Waste-to-energy (WTE) technology via municipal solid waste incineration (MSWI) have developed very rapidly with the advantages of achievement on waste disposal and energy conversion. This technology is developing towards higher capacity and efficiency. Therefore, the operation parameters of WTE boilers must be improved. However, higher steam parameters means higher surface temperature of exchange tube in superheaters and reheaters in WTE boilers, resulting higher risk of engineering failure due to high-temperature corrosion. Additionally, the incineration of MSW releases flue gas with a high content of corrosive species and water vapor, which can cause severe high-temperature corrosion. This experimental investigation details the effect of surface temperature and water vapor concentration on the high-temperature corrosion behavior of 12Cr1MoVG boiler steel under an atmosphere mimicking MSWI. The corrosion test environment consists of high temperature, ash deposit and simulated flue gas of waste incineration according to a real WTE boiler. The experiment was conducted using a two-zone bench-scale tube furnace with a gas temperature of 600℃ and the sample temperatures of 380℃, 430℃, and 480℃. For the investigation of water vapor concentration effect, 18 % vol and 23 % vol were set up in this study. After 240 hours of exposure, the corrosion weight curves illustrated that the corrosion kinetics was highly dependent on the surface temperature of corrosion samples. Furthermore, an increase in water vapor concentration exacerbated the high-temperature corrosion. XRD analysis identified the corrosion products as metal chlorides and metal oxides. Cross-sectional SEM images and EDS analysis revealed that an increase in water vapor accelerated the corrosion rate of the steel samples due to chromium dilution behavior.

Effect of Cation Types on the Steel Corrosion Inhibition Behavior of Calcined Layered Double Hydroxides in Saturated Calcium Hydroxide Solution

Effect of Cation Types on the Steel Corrosion Inhibition Behavior of Calcined Layered Double Hydroxides in Saturated Calcium Hydroxide Solution

Effect of surface roughness on corrosion behavior of AISI 4340 high-strength steel in sodium chloride solutions

In this work, an AISI 4340 high-strength steel alloy was surface machined to have four different grades of roughness (Ra). The impact of changing Ra on the corrosion of the steel alloy in 3.5% NaCl solutions after 40 min and 24 h was performed using various electrochemical techniques. The cyclic polarization experiments showed that an increase in Ra increases the steel corrosion via enhancing the corrosion current of the alloy. The electrochemical impedance plots also indicated that an increase in Ra reduces the corrosion resistance of the alloy by decreasing the diameter of the semicircle obtained by the Nyquist spectra. The change in potentiostatic current vs time measurements, which were obtained at −350 mV (Ag/AgCl), confirmed that pitting attack occurs and its intensity further increases with increasing Ra for all steel samples. An increase in immersion time also reduces the resistance to corrosion due to the iron dissolution from the surface of the steel alloy. After corrosion, the surface was analyzed using a scanning electron microscope and energy dispersive spectroscopy investigations.

Development of anti-corrosive layer on steel alloy using novel synthesized 8-hydroxyquinoline-based inhibitors: Experimental and theoretical approach

New and generated from freshly synthesized 8-hydroxyquinoline derivatives, namely 6-chloro-3-((8-hydroxyquinolin-5-yl)methyl)benzo[d]oxazol-2(3H)-one (Q-Cl) and 3-((8-hydroxyquinolin-5-yl)methyl)-6-nitrobenzo[d]oxazol-2(3H)-one (Q-NO2), were identified and characterized by 13C and 1H NMR spectroscopy. After this, their ability to prevent mild steel corrosion in 1.0 M HCl were examined and evaluated by electrochemical testing and surface analyses coupled with density functional theory (DFT), and density functional based tight-binding (DFTB). It is found that these substances act as the efficient defending agents and their protection increase with their concentrations and depend on their molecular structures. The best inhibition efficiencies values are about 93.59 % and 90.92 % at 10−3 M Q-NO2 and Q-Cl, respectively. Furthermore, the effect of temperature solution indicated that the 8-hydroxyquinolin derivatives take their performance of 298–328 K. In addition, the calculated activation and thermodynamic parameters indicated that they interact with the metallic surface by the chemical adsorption supported by surface analysis result using SEM/EDX analysis. These findings were explained by the Langmuir adsorption isotherm approach, indicating the formation of a monolayer by the 8-hydroxyquinoline derivatives particle on the mild steel surface. Finally, the theoretical investigations DFT/DFTB demonstrate the interaction of the site of the 8-hydroxyquinoline derivatives particles with the mild steel surface to form a protective layer.

Development of Environmental Monitoring Sensor for Steel Corrosion in Concrete based on Micro-Electro-Mechanical Systems (MEMS)

Many bridges located near marine environments usually have high risk to lose their structural performance due to corrosion of reinforcing bars with chloride attack. While a huge amount of budget to maintain may be consumed for the structural maintenance methodologies, an efficient monitoring system for Reinforced Concrete (RC) structures in the corrosive environment is strongly demanded. Thus, structural health monitoring in real situations is significant for bridge asset management. The alternative way for preventing severe damage propagation is proactively monitoring the environmental condition containing chloride ion and its effect on the durability of concrete structures, for which numerous methods have been conventionally suggested such as dry gauze method to capture chlorides in air. In this study, Micro Energy Harvester (MEH) based on Micro-Electro-Mechanical Systems (MEMS) is technically applied to develop a sensor to identify the corrosion environment with chlorides in the exposure condition. MEMS is a rapidly evolving device, which enables to monitor the changes in natural frequency and amplitude at nodal locations of the targeting structure due to vibration-based electrostatic power generation induced by the corrosive environment. The purpose of this research is to develop a system for detecting the high corrosion-prone areas and finding the suitable metal sheet material for various chloride ion conditions, using the metal sheet as a cantilever structure for the MEMS device. 4 types of metal, aluminium, copper, iron and zinc are considered for the parametric experiments. Several scenarios are considered including chloride ion concentration, temperatures, and wet and dry conditions to compare the dominant frequency changes of each metal sheet and determine their sensitivity to corrosion environment. From the preliminary results, iron and zinc have a significant drop in frequency with the elapsed exposure period, which indicates that they are highly sensitive to the external chloride ion environment. These results offer an innovative and proactive approach to structural health monitoring for further developed applications. It enables prompt maintenance and early detection of potential issues for corrosion of steel bars in concrete, ensuring the longevity and safety of RC bridge structures.

Kopsia terengganensis’ alkaloids as potential green inhibitors for mild steel corrosion in CO2-saturated 3.5% NaCl medium

The corrosion inhibition potential of alkaloids from Kopsia terengganensis bark extract (KTBE) in mitigating the mild steel corrosion in a CO2-saturated 3.5% NaCl medium was evaluated. Standard corrosion evaluation methods, including weight loss test, electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization (PD) were employed, which revealing a concentration-dependent enhancement in KTBE's inhibition efficiency. At 500 ppm, the corrosion inhibition efficiency recorded the highest value of 90.63% based on the weight loss study and 87.38% based on electrochemical analysis. Tafel slopes in PD studies affirmed that KTBE functioned as an anodic-type inhibitor. The adsorption of the inhibitor is in accordance with the Langmuir adsorption isotherm with an adsorption free energy (ΔG°ads) of −26.47 kJ/mol, suggesting the binding of KTBE molecules by means of physisorption. Surface analysis conducted through scanning electron microscopy (SEM), energy dispersive X-ray (EDX) spectroscopy, and Fourier transform infrared spectroscopy (FTIR) confirmed the formation of a protective inhibitive layer on the surface of mild steel. The proposed corrosion inhibition mechanism involves electrostatic interactions between KTBE molecules and the mild steel surface. This comprehensive investigation underscores KTBE's potential as an effective corrosion inhibitor in corrosive environments.

Recent progress on the research of steel corrosion behavior and corrosion control in the context of CO2 geological utilization and storage: a review

Abstract CO2 geological utilization and storage (CGUS) is a key technology to achieve carbon neutrality goals. To apply CGUS on a larger scale, the issue of steel corrosion during the process must be addressed to mitigate technological risks. This paper provides an overview of CO2-induced steel corrosion mechanisms and identifies factors that influence corrosion. The impact of CO2 partial pressure, temperature, salinity, pH, impurities, and fluid flow on steel corrosion behavior are also discussed. With the presence of water, the corrosive effect of supercritical CO2 on steel is stronger than that of dissolved CO2 or gaseous CO2. As the temperature increases, the corrosion rate of steel first increases and then decreases. Increasing salinity and decreasing pH lead to an accelerated corrosion rate of steel. Corrosion inhibitors, coatings, and corrosion-resistant alloys are recommended protective measures against CO2-induced corrosion. Compared with coatings, corrosion inhibitors and corrosion-resistant alloys are more commonly used in CGUS projects. Future research directions include further exploration of the mechanisms underlying CO2-induced steel corrosion, clarifying the coupled effects of various environmental factors, and developing corrosion protection technologies under high-pressure and high-concentration CO2 conditions.

Adsorption studies of isoxazole derivatives as corrosion inhibitors for mild steel in 1M HCl solution: DFT studies and molecular dynamics simulation.

The corrosion of mild steel is a significant issue in various industries, prompting the need for effective corrosion inhibitors. This study focuses on understanding the corrosion inhibition properties of organic compounds derived from isoxazole, namely series Iso(a), Iso(b), Iso(c), Iso(d), Iso(e), Iso(f), Iso(g), and Iso(h), which could have implications for materials science and industrial applications. By investigating the influence of different substitutions on these compounds, valuable insights can be gained into designing better corrosion inhibitors for practical use. Theoretical studies were conducted using density functional theory (DFT) with the B3LYP functional and the 6-31G (d,p) basis set. These calculations enabled the evaluation of various parameters including frontier orbital energies (EHOMO, ELUMO), energy gap (∆E), electronegativity (χ), absolute hardness (η), softness (σ), fraction of transferred electrons (∆N), as well as local properties such as natural atomic populations and Fukui indices. Additionally, molecular dynamics simulations were performed to study the adsorption behavior of the inhibitors on the surface of Fe (110). The simulations were conducted using Materials Studio version 8.0 software package using COMPASS force field to understand the impact of different functional groups on the inhibitors before and after adsorption on the iron surface.

RECENT INNOVATIONS IN ORGANIC INHIBITORS FOR MILD STEEL IN CORROSIVE SOLUTIONS: A MINI REVIEW

Corrosion of mild steel in corrosive solutions is one of the major concerns in industries such as oil and gas, petrochemical and marine. The use of organic inhibitors has proven to be an effective method to protect mild steel from corrosion. This mini-review summarised recent innovations in organic inhibitors for mild steel in corrosive solutions. This article discusses the types of organic inhibitors, including adsorption, film-forming, mixed, synergistic and green inhibitors, their mechanism of action, and their application in various corrosive environments. The article then highlights recently published inhibitors such as quinoline derivatives, Schiff bases, amino acids, and polymers. These inhibitors have shown promising results in protecting mild steel from corrosion. The mini-review concludes by discussing the prospects of organic inhibitors for mild steel in corrosive solutions. Overall, this mini-review provides valuable insights into recent innovations in organic inhibitors for mild steel in corrosive solutions, which are useful for researchers and industries working on corrosion protection.

Synergistic mixture of Camellia Oleifera shell extract and KI as an eco-friendly and highly efficient composite inhibitor for steel corrosion in H2SO4 media

To address the severe corrosion problems faced by steel, a natural corrosion inhibitor derived from Camellia Oleifera shell extract (COSE) was developed. The effectiveness of COSE as well as its synergistic mixture of COSE/KI in inhibiting the corrosion of steel in H2SO4 was investigated using weightlessness and electrochemical techniques. The results show that the maximum inhibition efficiency of individual COSE is 77.28 % at 20 °C, and is increased to 93.08 % for the mixture of COSE/KI. The adsorption of COSE, KI and COSE/KI on steel surface conform to Langmuir adsorption isotherm. COSE/KI has a stronger adsorption than either COSE or KI. Electrochemical analysis indicates that COSE/KI is a hybrid inhibitor primarily focusing on the cathodic inhibition. Mixing COSE with KI shows considerably larger charge transfer resistance and smaller double-layer capacitance than individual COSE and KI. Characterization tests such as metallurgical microscopy, SEM, AFM and contact angle confirm that the addition of COSE/KI could reduce the roughness of steel surface, while increase the hydrophobicity, then effectively alleviate the corrosion on the steel surface. XPS analyses demonstrated that the corrosion inhibition layer on the steel surface was induced by the adsorption of the polar groups in COSE. The components responsible for COSE’s effectiveness were thoroughly examined using FTIR and liquid chromatography-mass spectrometry (LC-MS), which identified the presence of compounds such as flavonoids and phenylpropanoids. The synergistic effect of the active ingredients (rutin, quercetin, tea saponin, tea polyphenols, et al.) with KI was also confirmed. Finally, theoretical calculations were conducted to analyze properties of rutin, quercetin and tea polyphenols on the iron layer. The results show all these molecules exhibit efficient inhibition, with quercetin showing better inhibitive ability by parallel adsorption.

Evaluation of adsorption behaviour of benzylidene chitosan derivatives at mild steel/ 0.5 M H2SO4 solution interface

Four green benzylidene chitosan derivatives (BCs) were synthesized and evaluated as anti-corrosive substances for the first time against mild steel corrosion in 0.5 M H2SO4 solution. The synthesized BCs were laid to infrared spectroscopy and proton resonance spectroscopy for structural confirmation. Gravimetric and electrochemical experiments were accustomed to appraise the effectiveness of inhibitors, however, Scanning Electron Microscopy-Electron Dispersive Spectroscopy (SEM-EDS), Atomic Force Microscopy (AFM), and X-ray Photoelectron Spectroscopy (XPS) were exploited to evaluate the protective mechanism offered by benzylidene chitosan derivatives. Experimental results demarcate the synthesized inhibitors; Anisaldehyde modified Chitosan (CMB), 2-Hydroxy-4-methoxybenzaldehyde modified Chitosan (CHMB), 2,4-Dimethoxybenzaldehyde modified Chitosan (CDMB) and 2-Bromo-4-methoxybenzaldehyde modified Chitosan (CBMB) exhibiting praising inhibitory properties for mild steel corrosion and CDMB was seen possessed preferable inhibition potential at the finest concentration of 500 mgL-1 owing to the proximity of two electron-donating OCH3 groups. Furthermore, the inhibitors have been recorded to behave mixed type with pronounced impact on hydrogen evolution kinetics. The order of inhibition efficacy obtained was CDMB (98.8 %) > CHMB (95.4 %) > CMB (92.8 %) > CBMB (89.2 %) which was further validated by quantum chemical calculations which later opened up about the mechanistic approach involved in electron transfer from inhibitors to metallic vacant orbitals. Additionally, the effect of molecular structure possessed by synthesized inhibitors has been correlated with observed variation in their corrosion inhibition efficiency.

Prevention of severe pitting corrosion of 13Cr pipeline steel by a sulfate reducing bacterium using a green biocide cocktail

Prevention of severe pitting corrosion of 13Cr pipeline steel by a sulfate reducing bacterium using a green biocide cocktail

Polyethyleneglycol bisphenol A epichlorohydrin copolymer (PEG-BEC) as a highly efficient inhibitor for mild steel corrosion in 1M HCl solutions

In this work, the corrosion inhibition performance of polyethyleneglycol bisphenol A epichlorohydrin copolymer (PEG-BEC) against mild steel in 1 M HCl was studied by electrochemical and weight loss techniques. Scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDAX) were applied to characterize the surface morphology of the mild steel samples. The corrosion mitigation efficiency was observed to rise as the concentration of PEG-BEC rises in the corrosive medium while increasing the temperature (25 °C -65 °C) resulting in a drop in the inhibition ability. Furthermore, under hydrodynamic conditions, the corrosion of the mild steel was found to deteriorate both in the absence and presence of PEG-BEC. Just with 10 ppm, an inhibition efficiency (IE) of 97.6% was obtained at 25 °C by EIS. PEG-BEC acts as a mixed-type inhibitor as observed by potentiodynamic polarization (PDP) technique. The observed corrosion inhibition action of PEG-BEC could be ascribed to the adsorption of the molecules and the formation of a protective film on the steel surface as evidenced by static water contact angle (WCA). Langmuir isotherm best describes the PEC-BEG-metal adsorption with large Kads values indicating a thermodynamically stable nature inhibition process. The obtained ∆G°ads = -35.138 to -39.522 kJ/mol indicate that the PEG-BEC spontaneously adsorbed onto the steel with strong tendency to provide protection to the mild steel surface via combination of chemisorption and physisorption processes. The ΔHads -53.07 kJ/mol and ΔSads= +0.048 kJ/mol-k, respectively, suggests an exothermic reaction accompanied by relatively increase in entropy of the PEG-BEC adsorption on the mild steel surface.

Acceleration mechanism of riboflavin on Fe0-to-microbe electron transfer in corrosion of EH36 steel by Pseudomonas aeruginosa

Riboflavin (RF), as a common electron mediator that can accelerate extracellular electron transfer (EET), is usually used as a probe to confirm EET-microbiologically influenced corrosion (MIC). However, the acceleration mechanism of RF on EET-MIC is still unclear, especially the effect on gene expression in bacteria. In this study, a 13-mer antimicrobial peptide E6 and tetrakis hydroxymethyl phosphonium sulfate (THPS) were used as new tools to investigate the acceleration mechanism of RF on Fe0-to-microbe EET in corrosion of EH36 steel caused by Pseudomonas aeruginosa. 60 min after 20 ppm (v/v) THPS and 20 ppm THPS & 100 nM E6 were injected into P. aeruginosa 1 and P. aeruginosa 2 (two glass bottles containing P. aeruginosa with different treatments) at the 3-d incubation, respectively, P. aeruginosa 1 and P. aeruginosa 2 had a similar planktonic cell count, whereas the sessile cell count in P. aeruginosa 1 was 1.3 log higher than that in P. aeruginosa 2. After the 3-d pre-growth and subsequent 7-d incubation, the addition of 20 ppm (w/w) RF increased the weight loss and maximum pit depth of EH36 steel in P. aeruginosa 1 by 0.7 mg cm−2 and 4.1 μm, respectively, while only increasing those in P. aeruginosa 2 by 0.4 mg cm−2 and 1.7 μm, respectively. This suggests that RF can be utilized by P. aeruginosa biofilms since the corrosion rate should be elevated by the same value if it only acts on the planktonic cells. Furthermore, the EET capacity of P. aeruginosa biofilm was enhanced by RF because the protein expression of cytochrome c (Cyt c) gene in sessile cells was significantly increased in the presence of RF, which accelerated EET-MIC by P. aeruginosa against EH36 steel.