Multifunctional coatings with simultaneous antibacterial and anticorrosive properties are essential for marine environments, oil and gas industry, medical settings, and domestic/public appliances to preserve integrity and functionality of pipes, instruments, and surfaces. In this work, we developed a simple and effective method to prepare graphene oxide (GO)-hybridized waterborne epoxy (GOWE) coating to simultaneously improve anticorrosive and antibacterial properties. The effects of different GO filler ratios (0.05, 0.1, and 0.5, 1 wt%) on the electrochemical and antibacterial behaviors of the waterborne epoxy coating were investigated over short- and long-term periods. The electrochemical behavior was analyzed with salt solution for 64 days. The antibacterial effect of GOWE coating was evaluated with Shewanella oneidensis (MR-1), which is a microorganism that can be involved in corrosion. Our results revealed that concentrations as low as 0.1 wt% of the GO was effective performance than the waterborne epoxy coating without graphene oxide. This result is due to the high hydrophilicity of the graphene oxide fillers, which allowed great dispersion in the waterborne epoxy coating matrix. Furthermore, this study used a corrosion relevant bacterium as a model organism, that is, Shewanella oneidensis (MR-1), which is more relevant for real-word applications. This as-prepared GO-hybridized waterborne polymeric hybrid film provides new insight into the application of 2D nanomaterial polymer composites for simultaneous anticorrosive and antibacterial applications.
Metals or alloys are widely used materials in industry and in our daily life; however, they are prone to electrochemical corrosion and biofilm formation, which can impact their performance (Fichman et al., 2014; Van Haute et al., 2018). The global economic loss of biofilm and corrosion is enormous, which is estimated to be 2.5 trillion (3.4% of the global GDP) (Lim, 2012; Koch et al., 2016; Nguyen et al., 2017a). Additionally, there is urgent health concerns involving increased chances of infection caused by various bacterial biofilms, especially in medical facilities (Mallakpour et al., 2021). To prevent such issues, special surface modifications involving antibacterial and anticorrosion properties are required for long-term applications of these metallic materials in industrial facilities (e.g., oil and gas equipment (Al Abbas et al., 2013) and marine industry (Lekbach et al., 2019)), biomedical implants (e.g., bone/tissue implants (Chopra et al., 2021; Zhang et al., 2021)), and domestic appliances (Nie et al., 2020). Hence, both anticorrosive and antibacterial coatings must be developed for these metallic surfaces. inorganic zinc coating
Epoxy is an efficient coating material and is commonly used to enhance the interfacial surface property due to its strong adhesion, excellent corrosion resistance, low curing shrinkage, good reservoir for additive corrosion inhibitors, and outstanding chemical properties (Li et al., 2018; Atta et al., 2020; Meng et al., 2020). However, the main drawback of epoxy coatings is their tendency to suffer from surface abrasion resulting in localized defects and corrosion, and the potential polymer degradation under UV radiation (Christopher et al., 2015). Therefore, recent studies have been conducted to incorporate inorganic fillers in the epoxy matrix to stimulate a synergic effect and overcome these challenges. For instance, inorganic particles, like montmorillonite, were shown to provide good barrier effect and enhance the bonding strength at the surface interface. However, there are still some issues with the incorporation of these inorganic fillers, such as complex manufacturing, high dosage, or easy cracking (Nematollahi et al., 2010; Meng et al., 2015).
More recently, nano-sized fillers (like SiO2, TiO2, and ZnO) have been studied to alleviate microscopic defects and enhance the cross-linking density of the coating due to their high specific surface area (Yadav et al., 2019). Among the nanofillers, graphene oxide (GO), as a relatively new class of materials for corrosion control (Georgakilas et al., 2015), has been considered as an ideal candidate for real potential large-scale applications due to its outstanding properties, including mechanical, electrical, low cost, aqueous/thermal stability, barrier effect, high specific surface area (∼2630 m2/g), and inherent antibacterial property (Geim and Novoselov, 2010; Compton et al., 2011; Georgakilas et al., 2015). Researchers have shown great interest in graphene oxide or graphene oxide-derivative composites for anticorrosive protection (Yu et al., 2014; Ding et al., 2019).
Furthermore, researchers have also found that graphene oxide composite polymeric coatings are promising antibacterial materials due to their ability to induce oxidative stress by reactive oxygen species (ROS) (Nguyen et al., 2017a). For instance, Liu et al. (2018) have reported that a solvent-borne epoxy with GO exhibited high antibacterial capability against E.coli. Graphene oxide has also shown to improve the antibacterial property of other polymers (e.g., poly DMA, poly (DMA-co-MEA)) in our previous studies (Fan et al., 2017; Peña-Bahamonde et al., 2018). Additionally, graphene oxide/GO and their derivatives have even exhibited a potential effect against COVID-19 (Hu et al., 2010).
Recently, modification of waterborne polymeric coatings with graphene oxide and its derivatives was exploited for specific functions and barrier performance enhancement, including antibacterial and anticorrosive properties (Mirmohseni et al., 2019; Ning et al., 2021). This interest arises from the increasing pressure for low carbon emission requirements, where waterborne polymers have been considered as a promising coating material with negligible VOC emission (Zhang et al., 2018; Chen et al., 2020). More recently, graphene oxide or its derivatives have been incorporated into waterborne polymeric matrix coatings, such as waterborne epoxy (WEP) and waterborne polyurethane (WPU) for simultaneous anticorrosive and antibacterial properties (Wang et al., 2018). However, most of the studies used Escherichia coli (E. coli) as their model organism, which is not involved in corrosive activity. Herein, in our study, to simulate the actual steel corrosion environment, an Fe (III) reduction bacterium (IRB) model, Shewanella oneidensis MR-1, which can contribute to steel corrosion (Glasauer et al., 2002), was applied to systematically investigate the antibacterial function for potential real applications.
Specifically, the objectives of this study are to systematically investigate the doping concentration of graphene oxide on the corrosion resistance of GOWE coating through a long-term electrochemical testing and to determine the antibacterial property of GOWE toward Shewanella oneidensis biofilm formation for both short-term and extended periods using confocal laser scanning microscopy (CLSM) analysis. The materials produced were fully characterized to determine the dispersion of graphene oxide nanofillers in the WEP matrix as well as the successful formation of GOWE films through optic spectra, Raman, and field emission scanning electron microscopy (FESEM) analysis. Our research presents an effective strategy to produce a GOWE coating with simultaneous anticorrosive property and antibacterial function, with the potential for further applications in industrial, medical, and domestic fields.
Waterborne epoxy resin (BECKOPOX EP 385W) and polyamine curing agent (BECKOPOX EH 613W) were obtained from Allnex Company (Langley, SC, United States). Luria–Bertani (LB) broth medium was purchased from Fisher-Scientific (Massachusetts, United States). Graphite (<20 μm), sulfuric acid (H2SO4, 98 wt%), sodium nitrate, potassium permanganate, and hydrogen peroxide (30 wt%) were purchased from Sigma Aldrich (Austin, TX, United States). Propidium iodide (PI) and SYTO9 dyes were obtained from Invitrogen Corporation (CA, United States). All reagents and solvents were used without further purification. All the chemicals were ACS grade.
Graphene oxide nanofiller was synthesized from natural graphite flakes using the modified Hummers’ method, which was reported in our previous study (Nguyen et al., 2017b). In brief, 2.5 g of graphite, 25 ml of concentrated H2SO4, and 2.0 g of KMnO4 were mixed in an ice bath and followed by stirring at 35°C for 10 h. Then the mixture was further heated at 90 ± 1°C for 1.5 h with a dropwise dosing of H2O2 solution. Finally, the graphene oxide suspension was centrifuged at 8000 rpm and washed four to five times with distilled water. The washed samples were further freeze-dried to achieve the final product.
Concentrations (wt%) of 0.05, 0.1, 0.5, and 1 graphene oxide were first dispersed in the waterborne epoxy resin by ultrasonic treatment for 1 h in an ice bath. Subsequently, a stoichiometric amount of the polyamine curing agent was added to the dispersion. The aforementioned mixture was magnetically stirred for 20 min, followed by sonication for 15 min to remove air bubbles. Then the coating mixture was applied onto a steel substrate (QD36, Q-Lab Corporation, Ohio, United States) to prepare GOWE coatings. The prepared coatings were left at room temperature for 24 h, followed by thermally curing at 120°C for 1 h. The film preparation procedure is shown in Figure 1. The dry film thickness of the control (without adding graphene oxide) and GOWE coatings were around 60 µm measured by a thickness gauge (byko-test 8500, BYK). The formulation of the waterborne epoxy coating with graphene oxide nanofillers is shown in Table 1.
FIGURE 1. Schematic illustration of the GOWE coating preparation.
TABLE 1. Formulation of graphene oxide-hybridized waterborne epoxy coating.
The corrosion resistance of coated samples was measured through electrochemical impedance spectroscopy (EIS) measurements by using the Reference 600+ Potentiostat (Gamry Instrument). The testing coatings were immersed in 3.5 wt% NaCl solution with an exposure area of 7.07 cm2. The steel panel, saturated calomel electrode (SCE), and platinum mesh with 6.25 cm2 surface area were used as working, reference, and counter electrodes, respectively. All EIS tests were run in a Faraday cage at room temperature using 10 mV AC perturbation with a frequency range of 105–10–2 Hz.
For the biofilm testing, the coating samples were cut into 2 × 2 cm small coupons. The backside and the edges of the coating coupons were applied with epoxy coating to avoid water penetration. The coating coupons after the biofilm testing were immersed in 3.5 wt% NaCl solution for corrosion resistance assay.
Antibacterial experiments were performed using a model metal reduction bacterium (S. oneidensis MR-1, Gram-negative). S. oneidensis MR-1 was cultured overnight in a freshly prepared Luria–Bertani broth medium (LB, 1.0 wt% tryptone, 0.5 wt% yeast extract, 1.0 wt% NaCl, and 1.5 wt% agar powder) with constant shaking (150 rpm, 30°C) by using a shaker (Thermo Fisher, United States). The pH of the medium was adjusted to 7.0. The initial concentration of bacteria in the LB media was in the range of ∼3.0 × 107 CFU/ml (OD600 = 0.60). The details of the microbial biofilm growth were described in our previous study (Nguyen et al., 2017a; Ansari et al., 2021). In brief, bacterial growth was batch cultivated in a sterile six-well plate (BioLite, United States) at 28°C in the LB medium. Before transferring to the plates, each coated steel plate was sterilized with UV light for 15 min in the biosafety hood. After that, 100 µl of the S. oneidensis culture was dosed to 10 ml of the LB growth media. Then 100 µl of the above diluted culture mixture plus 6 ml of the LB medium were transferred to six sterilized steel plates. The plates were further incubated at 30°C for short term (72 h) and long term (10 days) under static conditions. For the long-term test, the S. oneidensis culture medium was replaced with 2 ml fresh media each day. After the testing, the specimens were gently rinsed three times with phosphate-buffered saline (PBS) to remove nonadherent bacteria for further characterization (Nguyen et al., 2017a). All the testing were performed in triplicate and repeated at least three times for analysis.
All coupons coated with GOWE for corrosion and biofilm growth were characterized using Fourier transformed infrared spectroscopy, Raman spectroscopy, scanning electron microscopy (SEM), and confocal microscopy. The spectra were obtained with the Nicolet iS10 FT-IR spectrometer (resolution: 4 cm−1; scan number: 32) equipped with Nicolet smart attenuated total reflectance. The range of scanning wavenumber was from 4000 to 400 cm−1. The Raman measurements were conducted to analyze the elemental composition using a Czerny–Turner Raman microspectroscopy (IHR320, HORIBA Scientific). The analysis was done with an excitation wavelength of 532 nm. The field emission SEM (Tescan Lyra3) was used for capturing the structural morphology of the coated samples.
A confocal laser scanning microscope (CLSM, Leica Lasertechnik, Heidelberg, Germany) was used to investigate the distribution of living and dead cells on the coating interface. For the confocal imaging, the coating samples were removed from the liquid culture under a biosafety hood. The biofilms were stained with a live/dead backlight bacterial viability kit (Invitrogen) (Meng et al., 2020). This kit contains two nucleic acid dyes: SYTO 9 and propidium iodide (PI) (Fan et al., 2017). The detailed procedure of the biofilm formation quantification is described in our previous study (Nguyen et al., 2017a). All analyses were done in triplicate.
Before electrochemical impedance measurements, the open circuit potential (OCP) was measured to achieve a steady potential. In this study, the OCP value of graphene oxide hybrid coating (GOWE-0.1) was higher than that of the pure epoxy coating sample (data not shown), which indicated the barrier role of graphene oxide nanofiller in the epoxy matrix.
EIS measurements were performed to semi-quantitatively evaluate the overall anticorrosive properties of the developed GO-hybridized composite coatings with a different nano doping ratio at various immersion periods (0 to 64 days in 3.5 wt% NaCl solution). The Bode plots of log |Z| vs. log f for the prepared coatings are shown in Figure 2. The initial measurements showed that the impedance modulus at 0.01 Hz of all the coatings was larger than 1010 Ω·cm2, which indicated an excellent corrosion protection (Wang and Zhou, 2018). All the GOWE coatings maintained a much higher initial impedance modulus at 0.01 Hz (∼1011 Ω·cm2) (Figure 2B) than the pure epoxy coating (∼1010 Ω·cm2), which revealed that generally the graphene oxide nanofiller could significantly improve the inherent corrosion resistance of waterborne epoxy coatings. On the other hand, during the long-term immersion time in the saline solution, due to the diffusion of water and corrosion ions into the coating substrates (Zhou and Wang, 2013), both the GOWE and pure epoxy coatings showed a decreasing trend of impedance modulus at 0.01 Hz. This phenomenon was more evident for the pure waterborne epoxy coatings since the impedance modulus of GOWE-0 at a low frequency region reduced sharply with longer immersion time. The result shows a steep degradation of impedance modulus, which dropped about six orders of magnitude (1.90 × 1010 Ω·cm2 to 6.5 × 104 Ω·cm2) in 29 days of immersion and then remained stable for 64 days (Figure 2A).
FIGURE 2. (A) Bode plots of neat waterborne epoxy coating GOWE-0 (without graphene oxide) in the immersion of 3.5 wt% NaCl solution; and (B) Bode plots of GOWE coatings (GOWE-0.05, GOWE-0.1, GOWE-0.5, and GOWE-1) in the immersion of 3.5 wt% NaCl solution. The formulation of GOWE coatings is listed in Table 1.
In contrast, for GOWE-0.05 and GOWE-0.1 coatings, the impedance modulus at 0.01 Hz showed a much slower degradation trend than the other coatings, and maintained a value of up to 9.0 × 109 Ω·cm2 and 9.7 × 109 Ω·cm2 after 64 days of immersion, which corresponded to two and one orders of magnitude decline for GOWE-0.05 and GOWE-0.1, respectively. The results suggested that the graphene oxide nanofiller could effectively prevent corrosion. However, interestingly, with the increasing of the GO doping ratio, GOWE-0.5 and GOWE-1 coatings exhibited a higher initial low-frequency impedance modulus but they dropped three and four orders of magnitude, respectively, after 64 days of immersion. This drop could be the result of the aggregation of 2D graphene oxide nanosheets in the coating, and thus, some local “defects” were generated during the coating curing process, which deteriorated the barrier capability of the coatings (Pourhashem et al., 2020). This phenomenon was further confirmed via SEM imaging (Figure 2B). As a result, the concentrations of 0.1 wt% graphene oxide presented the best corrosion resistance than the other graphene oxide concentrations. These results illustrated that well-dispersed graphene oxide can effectively enhance the barrier properties of anticorrosion coatings.
Furthermore, from the SEM characterization of the coatings, the GOWE-0.1 coating film exhibited the best graphene oxide dispersion within the epoxy matrix, presenting a more homogeneous and smooth coating surface without significant defects or clusters (Figure 3B). The GOWE-0.5 (0.5 wt% GO) (Figure 3C), on the other hand, showed obvious defects on the coated surface, which came from the heterogenous dispersion of graphene oxide in the epoxy matrix when the graphene oxide content was high.
FIGURE 3. SEM images of the coatings: (A) WEP (control, without graphene oxide) with scale 1 µm, (B) WEP (control, without graphene oxide) with scale 500 nm, (C) GOWE-0.1 (0.1 wt% graphene oxide) with scale 1 µm, (D), GOWE-0.1 (0.1 wt% graphene oxide) with scale 500 nm, (E) GOWE-0.5 (0.5 wt% graphene oxide) with scale 1 µm, and (F) GOWE-0.5 (0.5 wt% graphene oxide) with scale 500 nm.
The growth of S. oneidensis on the coated surface was monitored to determine the antibacterial performance of the GOWE coatings. S. oneidensis growth mainly includes the process of initial attachment, cells’ rapid division on the surface, and isolated microcolonies formation. Eventually, biofilms will develop into an extensive three-dimensional structure with strong interactions with the surface due to electrostatic, Van der Waals, and hydrophobic forces (Thormann et al., 2004; Makabenta et al., 2021).
The analysis of the biofilm formed on the GOWE coatings was done via the live–dead staining and observation through confocal microscopy. In this work, the waterborne epoxy films (control) and GOWE films with different graphene oxide concentrations (0.05 wt%, 0.1 wt%, 0.5 wt%, and 1 wt%) were exposed to the culture of S. oneidensis MR-1 in the LB growth medium (containing 1 wt% NaCl) overnight to simulate a real environmental condition. As illustrated in Figure 4, the CLSM images for the surfaces of the control coating (without GO) and the bare steel coupon were almost completely green and had a thick biofilm after 72 h exposure, which demonstrated that a healthy biofilm was formed on these surfaces. In contrast, an overwhelming fraction of dead cells were observed on the surface of GOWE coating films, which demonstrated that graphene oxide had a high ability to inhibit bacterial growth (see Supporting Information). When the graphene oxide content increased from 0.05 wt% (Figure 4C) to 0.5 wt% (Figure 4E), less biofilm was observed on the coated surface. However, as the GO concentration increased to 1 wt% (Figure 4F), the antibacterial capacity reduced as seen from the increasing numbers of live cells (green) on the coated surface. The less uniform biofilm growth 1 wt% graphene oxide loading could be due to graphene oxide aggregation and subsequent random distribution in the coating. Considering the results of the salt corrosion above and the antimicrobial experiments, the 0.1 wt% graphene oxide concentration was considered the optimal dosage for the coating for simultaneous antibacterial and anticorrosion properties.
FIGURE 4. CLSM images of biofilm growth for 72 h on different coating surfaces. (A) bare steel; (B) WEP coating (control); (C) GOWE-0.05 (0.05 wt% GO); (D) GOWE-0.1 (0.1 wt% GO); (E) GOWE-0.5 (0.5 wt% GO); (F) GOWE-1(1 wt% GO). The green color corresponds to living bacterial cells growing on the surface. Experiments were run at 25°C under static batch condition. The units are in micron.
FIGURE 5. CLSM images of biofilms grown for (A) 24 h, (B) 96 h, and (C) 10 days for the WEP coating (control) and (D) 24 h, (E) 96 h, and (F) 10 days for GOWE-0.1 coating. The coating was stained with SYTO9 and PI prior to microscopic observation. The red color corresponds to dead bacterial cells and the green color corresponds to living bacterial cells. The scale is in microns.
After the antibacterial performance test, the coating samples were cleaned by sonication and DI water to be further analyzed to investigate the surface morphology through SEM. From the SEM images in Figure 6, there were no significant surface damages and accumulated corrosion products on the surface of the GOWE-0.1 coating during the 10 days testing, while rough surface and unremoved accumulated products were easily observed on the surface of the pure epoxy coating.
FIGURE 6. Surface morphology of the WEP coating (control) and GOWE-0.1 coating (0.1 wt% GO) after the exposure in S. oneidensis culture for (A) 24 h, control (B) 96 h, control, and (C) 10 days, control; (D) 24 h, GOWE-0.1 coating; (E) 96 h, GOWE-0.1 coating, and (F) 10 days, GOWE-0.1 coating.
In this study, Shewanella oneidensis MR-1, a facultative metallic-reducing bacterium with metabolic versatility including aerobic respiration and dissimilatory Fe (III) reduction, was employed as an Fe (III) reduction bacterium (IRB) model since it can be found under steel corrosion conditions (Wurzler et al., 2020). The influence of Fe reduction bacteria on the corrosion performance remains controversial. Recent literature reviews have demonstrated that the effects of Shewanella sp. biofilm on the corrosion behavior of a material can be negative or positive, and highly dependent on the specific environmental factors, such as aerobic or anoxic (anaerobic) conditions, the presence of different electron acceptors, associated metabolic activities, and metabolic versatility (Miller et al., 2016; Bertling et al., 2020; Jiang et al., 2020; Li et al., 2021). For example, Faisal et al. discovered that Shewanella oneidensis sp. could inhibit corrosion of X52 carbon steel through iron respiration (Al Abbas et al., 2013). Contrarily, more recently, Li et al. reported Shewanella sp. could accelerate uniform or pitting corrosions via bioanodic (biocathodic) EET (extracellular electron transfer) (Jiang et al., 2020; Li et al., 2021). Similarly, Miller et al. reported S. oneidensis MR-1 promoted corrosion under nitrate reducing conditions (Miller et al., 2016).
Therefore, understanding how Shewanella sp. contributes to the material corrosion is important since multiple environmental factors could synergistically promote or inhibit corrosion. Another aspect to be considered is the fact that most approaches for the protection of electrochemical corrosion and biofilm mediated corrosion have been developed by using nano patterning and surface treatment, which can resist bacterial attachment (Singhal et al., 2021), thus efficiently impeding short-range electron transfers between bacteria and substrates. However, from this angle, the actual effects of Shewanella oneidensis MR-1 on the composite polymeric coating, such as the epoxy coating, are still rarely reported. Hence, in this context, the real effects of Shewanella oneidensis MR-1 on corrosion were also investigated in this experiment.
Specifically, to study the influence of biofilm formation on the anticorrosive performance of GOWE coatings, GOWE-0.1 coating samples with and without biofilm were evaluated by the EIS measurement for 14 days. Figure 7 shows the impedance modulus at 0.01 Hz as a function of the immersion time for the control and GOWE-01 coating samples. Results show that the coating without bacteria exhibited better corrosion protection than the coating with bacteria. This fact clearly demonstrated that the biofilm formed on the coating surface would accelerate the corrosion. These results also supported the previous study that S. oneidensis could accelerate the corrosion progress of graphene oxide composite films under relative anaerobic conditions (Lou et al., 2021). Although our experiments were not done in strictly anaerobic conditions, the fact that we did not mix constantly the media with the cells to well aerate the growth media could have generated a microaerophilic and anoxic condition on the surface of the coupons that were at the bottom of the wells. This could have explained the corrosive effects with the S. oneidensis in the presence of salt in the growth medium.
FIGURE 7. Impedance modulus at 0.01 Hz as a function of the immersion time for GOWE-0.1 coatings with and without biofilm testing.
The morphological image of the as-prepared graphene oxide with the modified Hummers’ method is shown in Figure 8A. A sheet-like two-dimensional nanolayer structure was observed. The sharp edges and small few layers can be seen clearly. Figure 8B indicated the XRD patterns of the raw material graphite and the synthesized graphene oxide. A sharp diffraction peak of pure graphite was present at 2θ = 26° (002 plane), which corresponds to the graphite characteristic 002 plane (PDF No: 41-1487) and is consistent with the previous research (Li et al., 2014). For graphene oxide, the broader peak at 2θ = 10.7° was observed, which was assigned to (001) diffraction peak due to the chemical oxidation action. This result was very close to the reported value in the literature, and this suggested the successful synthesis of graphene oxide. Meanwhile, the disappearance of graphite (002) plane further proved that the complete oxidation of graphene oxide occurred after the chemical exfoliation (Paulchamy et al., 2015).
FIGURE 8. SEM image and XRD patterns of graphene oxide.
The coatings prior to the analyses were characterized. Here, we report the characterization results of the optimum graphene oxide concentration in the waterborne epoxy coating, which was determined to be 0.1 wt% from the abovementioned anticorrosive and antibacterial study. Therefore, the GOWE-0.1 coating film was characterized by Fourier transform infrared (FTIR) and Raman spectroscopy. The FTIR spectra of WEP (waterborne epoxy), GO (graphene oxide), and GOWE-0.1 (0.1 wt% GO) coatings are shown in Figure 9. The typical characteristic peaks of GO (blue curve in Figure 9) were observed at 1735 cm−1 (C = O stretching vibration of – COOH groups), 3600 cm−1 (O – H stretching vibrations), 1095 cm−1 (C – O – C stretching vibration), 1260 cm−1 (– COH stretching), 1408 cm−1 (tertiary C – OH stretching vibration), 1018 and 1636 cm−1 (C = C stretching), and 2968 cm−1 (– CH stretching), which are in good agreement with the previously reported graphene oxide spectrum (Paredes et al., 2008; Dreyer et al., 2010; Shen et al., 2010; Ma et al., 2016; Ensafi et al., 2017; Harfouche et al., 2017). Furthermore, the spectrum of waterborne epoxy (red curve in Figure 9) showed the typical characteristic IR band at 944 cm−1 (epoxide ring vibrations). Other representative groups of the epoxy resin include 1037, 1240, and 1110 cm−1 (symmetrical aromatic and aliphatic C – O stretch); 1183, 1296, and 1377 cm−1 (tertiary C – OH stretching vibration); 1458 cm−1 (deformation of C – H of CH2/CH3); 1503 and 1608 cm−1 (C = C of aromatic rings/C – C skeletal stretching); and 2878 and 2928 cm−1 (stretching C – H of CH2 and C – H aromatic and aliphatic), which confirm the characteristic bands of key functional groups in the epoxy matrix (Yu et al., 2016). For GOWE-0.1 coating (green curve in Figure 9), similar absorption bands were observed as the waterborne epoxy, especially in the region between 900 and 1600 cm−1 due to the relatively low content of graphene oxide in the epoxy matrix. A distinct new band was found in the GOWE-0.1 coating, which was not observed in the pure epoxy and assigned to the characteristic absorption peaks of graphene oxide at 1735 cm−1, which clearly showed a C = O bond for the carboxyl group due to the existence of graphene oxide. However, it is obvious that the intensity of the carboxyl groups (1735 cm −1) became weaker and hydroxyl groups (– OH, 3600 cm−1) disappeared when combining graphene oxide with the epoxy matrix. This indicates that some reactions might have occurred between the carboxyl and hydroxyl groups of graphene oxide with the curing agent during the curing process (Chauhana et al., 2018; Vryonis et al., 2019; Ding et al., 2021). As a result, a three-dimensional graphene oxide network structure was formed in the waterborne epoxy matrix (Her and Zhang, 2021).
FIGURE 9. Fourier transform infrared spectra of GO, waterborne epoxy (control), and GOWE-0.1.
The Raman spectrum of the GOWE-0.1 (0.1 wt% graphene oxide) film is shown in Figure 10. The peak of GO at 1590 cm−1 displayed the G-band, which corresponds to E2g phonon of sp2 carbon–carbon bond and isolated double bonds on graphene oxide sheets (Pan et al., 2017). D-band appeared at 1355 cm−1, which is the characteristic of the graphene tangential vibrational mode (the breathing modes of six-membered rings activated by defects) (Kudin et al., 2008). These Raman peaks for graphene oxide agree well with those reported previously by others (Díaz et al., 2017; Pan et al., 2017; Azizighannad and Mitra, 2018). The ratio of the intensity of the D and G bands (ID/IG) of the GOWE-0.1 coating was approximately 0.89 by integrating the areas of D and G peaks. This was aligned with the typical graphene oxide value obtained through oxidization and exfoliation of graphite as described in previous reports (Kudin et al., 2008; Jhajharia and Selvaraj, 2015), which demonstrated a good dispersion of the graphene oxide nanofillers in the waterborne epoxy matrix. Other Raman peaks located at 1012, 1156, 1709, 2639, and 2759 cm−1 are assigned to the vibrations of the epoxy (Kudin et al., 2008).
FIGURE 10. Raman spectra of the GOWE-0.1 coating.
The anticorrosive enhancement of graphene oxide-hybridized coating can be schematically illustrated in Figure 11. To understand the anticorrosive mechanism by graphene oxide nanofillers, the coating surface was cut 2 cm in length by a blade for both the WEP coating and GOWE-0.1 coating to simulate the accelerated local corrosion defects. The coated samples were first immersed in the salt solution (8 wt% NaCl) for 120 h. The images of the surfaces for waterborne epoxy coating with and without graphene oxide after immersion are shown in Figure 11. After 120 h testing, the WEP control (Figure 11A) clearly showed serious local corrosion that demonstrated the corrosion agents (e.g., Cl−, O2, and H2O) had penetrated through the interface of the epoxy/metal and hydrolytically destroyed the coating, which caused the pit corrosion (Chang et al., 2014). Furthermore, these pits near the crack regions on the coating could connect to each other first followed by the occurrence of spalling (Figure 11A).
FIGURE 11. Surface morphology of the WEP coating (control, without GO) and GOWE-0.1 (0.1 wt% GO) before and after the exposure in 8 wt% NaCl solution. (A) WEP coating 120 h; (C) GOWE-0.1 coating, 120 h; (B) schematic diagrams of the anticorrosive mechanism of the WEP coating and the GOWE coating.
On the other hand, there was no obvious corrosion defects on the surface of the GOWE-0.1 coating. In fact, the optimal GO content (0.1 wt%) was assumed to form a homogeneous three-dimensional network structure, according to the abovementioned analysis (sections 3.3, 3.4), which could prevent local corrosion and significantly retard the propagation of the defects within the network structure. Additionally, the better coating adhesion achieved by incorporating well-dispersed graphene oxide nanoplates in the epoxy allowed improved corrosive protection by the coating (Pourhashem et al., 2017). In addition, electrons from iron oxidation in the micro-anode region can migrate through conductive nanoparticles, such as graphene oxide, which can alleviate the oxidation–reduction reaction of corroded areas (Yu et al., 2017). As a result, the prepared composite coating exhibited better corrosion protection than the waterborne epoxy control (Figure 11), which was mainly attributed to the built three-dimensional network structure with well dispersed graphene oxide.
In this study, an effective graphene oxide-hybridized waterborne epoxy coating was successfully developed as a coating material. The best concentration of graphene oxide as a nanofiller was identified to be 0.1 wt% for simultaneous anticorrosive and antibacterial protection of steel. The protection of steel was observed for more than 60 days for both 3.5% NaCl and against S. oniedensis MR-1. The protection against S. oniedensis MR-1 against corrosion was probably due to the biofilm inhibition observed in the coated material, since the non-coated material and the materials lacking graphene oxide presented the establishment of a biofilm and corrosion. Therefore, the newly developed graphene oxide-hybridized waterborne epoxy coating can be potentially employed for applications that require simultaneous enhancement of anticorrosive and antibacterial functions.
Any data presented in this study is available upon request. Please contact the corresponding authors for any inquiries.
YZ was responsible for preparing the materials, characterizing and performing the antimicrobial investigation, and writing that aspect of the work. HW and CZ performed the corrosion investigation in the manuscript. DR and QZ were responsible for the conceptualization of the work, editing, and assisting with the data analysis.
The authors would like to acknowledge the following funding sources: Qatar National Research Foundation, award number: NPRP 9-318-1-064; the Robert A. Welch Foundation, award number: E-2011-20190330; and the National Science Foundation under Grant No. CHE-1904472.
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmats.2022.910152/full#supplementary-material
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Keywords: anticorrosive, antibacterial, graphene oxide, waterborne epoxy coating, antibiofilm
Citation: Zhou Y, Wang H, Zhang C, Zhou Q and Rodrigues DF (2022) Graphene Oxide-Hybridized Waterborne Epoxy Coating for Simultaneous Anticorrosive and Antibiofilm Functions. Front. Mater. 9:910152. doi: 10.3389/fmats.2022.910152
Received: 31 March 2022; Accepted: 07 June 2022; Published: 14 July 2022.
Copyright © 2022 Zhou, Wang, Zhang, Zhou and Rodrigues. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Qixin Zhou, cXpob3VAdWFrcm9uLmVkdQ==; Deborah F. Rodrigues, ZGZyaWdpcm9kcmlndWVzQHVoLmVkdQ==
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