Anticorrosive Properties of Green Silver Nanoparticles to Prevent Microbiologically Influenced Corrosion on Copper in the Marine Environment

Nalan Oya San Keskin·Esra Yaylaci·Selen Guclu Durgun,3·Furkan Deniz·Hasan Nazır

Abstract Microbiologically influenced corrosion is a global problem especially materials used in marine engineering.In that respect,inhibitors are widely used to control fouling and corrosion in marine systems.Most techniques used in inhibitor production are expensive and considered hazardous to the ecosystem.Therefore,scientists are motivated to explore natsural and green products as potent corrosion inhibitors especially in nano size.In this study,antibacterial and anticorrosive properties of green silver nanoparticles(AgNPs)were studied through weight loss,electrochemical characterization,and surface analysis techniques.The corrosion of copper(Cu)in artificial seawater(ASW),Halomonas variabilis(H.variabilis)NOSK,and H.variabilis+AgNPs was monitored using electrochemical measurements like open circuit potential(OCP),electrochemical impedance spectroscopy(EIS),and potentiodynamic polarization curves.AgNPs showed excellent antibacterial activity against pathogenic microorganisms.Electrochemical studies demonstrate a noticeable decrease in OCP and current density in ASW containing H.variabilis+AgNPs compared to both ASW and ASW inoculated with bacterium,which confirmed the decrease of corrosion rate of copper.Furthermore,the obtained voltammograms show that the silver nanoparticles were adsorbed on the copper electrode surface from the corrosion solution.Thus,the results prove that the novel idea of green silver nanoparticles acts as an anticorrosive film in the marine environment.

Keywords Antimicrobial.Copper.Electrochemical impedance spectroscopy.Transmission electron microscopy.Microbiologically influenced corrosion.Nanoparticle

1 Introduction

Copper(Cu)is extensively used in aqueous environment,heat exchangers,water cycling systems,and nuclear waste storage systems(Chen and Zhang 2018).Although Cu and its alloys are highly resistant to oxygen corrosion good corrosion resistance and antibacterial properties,still they are vulnerable to microbiologically influenced corrosion(MIC).Many Cu MIC problems and investigations have been reported in the literature(Abdolahi et al.2014;Chandra et al.2019;Jia et al.2019;Preethi et al.2019).

Due to corrosion and biofouling,materials’service life decrease,which is a serious technological and economic problem especially in the marine environment(Parthipan et al.2017;Starosvetsky et al.2007;Xu et al.2017).Because of the corrosion,around US$4 trillion was lost globally each year(Li et al.2015).

When metal surfaces submerged in the marine environments,various marine microorganisms such as bacteria,microalga,and their metabolic products attached on the surface of the metal within a few hours and begin to form biofilm(San et al.2012a;Wang et al.2004;Videla et al.1988).Especially,microbiologically influenced corrosion is involved in 50%of all pipeline failures(Wang et al.2014).

At the metal/biofilm interface,mature biofilm induces changes in the electrochemical conditions such as lowering pH due to secretion of acidic metabolites,reduction of dissolved oxygen due to microbial respiration underneath the biofilm,and localized high concentration of the electrolyte constituents(George et al.2003;Little and Lee 2007).The process is termed as microbiologically influenced corrosion(MIC).However,biofilm layers sometimes act as a diffusion barrier that decreased corrosion rates via preventing corrosive substance from degrading the metal surface termed microbiologically influenced corrosion inhibition(MICI)(Moradi et al.2019;San et al.2012b;Videla and Herrera 2009).

Microorganisms live almost everywhere.In different environments such as marine,oilfield,and soil environment,microbiologically influenced corrosion(MIC)occurs and often results in enormous economic loss and hazardous safety conditions in water environments(Liu and Cheng 2018)and many industries such as oil and gas,water utilities,and medical implant industry(Brauer et al.2017;Jia et al.2019).In order to protect metals/alloys from corrosion,coatings and inhibitors have been widely used in the industry(Ou et al.2018;Poulios et al.1999).Furthermore,they are rather inefficient.Therefore,there is an urgent need for environmentally friendly and sustainable corrosion control strategies(Kip and Van Veen 2015).

Recently,nanometallic particles have attracted much attention of the scientists due to the varied range of their application in many fields,including optics,electronics,magnetics,catalysis,biomedicine,and so forth(Firdhouse and Lalitha 2015;Huang et al.2019;Mittal et al.2014;Otari et al.2015).Especially,nanoparticles with antimicrobial activity fulfill the general needs of new anticorrosive materials(Baygar et al.2019).A number of nanoparticles with antimicrobial activities have been reported recently.For this reason,silver nanoparticles as antimicrobial agents have received much attention(Maharubin et al.2019;San Keskin et al.2016).

Physical and chemical methods are used for generation of metallic nanoparticles but these methods have low productivity and the chemical methods lead to contamination based on initiator chemicals,use of toxics solvents,and the formation of dangerous by-products(San Keskin et al.2016).The generation of safe and green chemistry bioprocesses for the synthesis of nanoparticles is an important matter of nanotechnology.Thus,there is an increasing need to improve high yield,confidential,clean,and environmentally friendly methods as the preparation of nanoparticles(Fayaz et al.2010;Nayak et al.2011;Thakur et al.2017).To this end,compared to physical and chemical methods,biosynthesis has appeared as an easy,clean,and applicable approach(Bhaumik et al.2016).Many reports on the synthesis of silver nanoparticles using bacteria drew the most interest in this area(Cao 2017).Using bacteria has one benefit for biosynthesis of nanoparticles due to ease of handling and their manipulation simply(Fayaz et al.2010;Hebbalalu et al.2013).There have been studies demonstrating that cell-free extracts of some bacterial species,like

Escherichia coli and Klebsiella pneumoniae(Shahverdi et al.2007),could encourage the synthesis of silver nanoparticles.

In the present work,green silver nanoparticles were synthesized from bacteria and used as biocorrosion inhibitors in order to improve the corrosion resistance of copper in marine environment influenced by halophilic bacterium,H.variabilis.

2 Material and Methods

2.1 Chemicals

The chemicals used in this experiment are silver nitrate(AgNO3),LB broth(Luria-Bertani),nutrient broth(NB),and nutrient agar(NA)obtained from Sigma-Aldrich.Other chemicals used were of analytical grade.

2.2 Preparation of Lysinibacillus sp.NOSK Cell-Free Extract for AgNPs Production

Strain was isolated from soil samples collected from the Ankara River at 6-in depth from surface on the NA plate supplemented with 5.0%methanol.The isolate was characterized as Lysinibacillus sp.with the molecular identification and later is named as Lysinibacillus sp.NOSK,which was stored in GenBank with KM241862 accession number(San Keskin et al.2015).To prepare Lysinibacillus sp.NOSK cell-free extract,a single clone of the isolate was transferred from the Luria-Bertani(LB)agar plate into 50 ml of sterile nutrient broth(NB)in a 100-ml Erlenmeyer flask.The flask was incubated at 30oC for 48 h on a rotary shaker(E 20/60,Biosan Latvia)at 100 rpm.After the incubation period,when the culture OD at 600 nm was between the ranges of 1 and 2,the cell-free extract recovered by centrifugation(4000 rpm,10 min at room temperature)and was used for further experiment.

2.3 Preparation of H.variabilis NOSK for MIC Analysis

Extremophiles are microorganisms that grow under conditions hostile to most organisms.Some of them,such as Halomonas bacterium which thrive in hypersaline environments,have been recognized for their potential use in biotechnological applications(Ye et al.2020).In hypersaline environments,ordinary bacteria can hardly survive but halophilic bacteria are frequently found in marine environment.For this reason,in this study,halophilic bacteria are isolated and identified genetically and investigated MIC in marine environments.

Brine,multicolor solar salt,saline soil,and saline mud samples were collected from Salt Lake,Turkey(39° 05′13.1″N,33° 23′37.8″E).Samples were collected in sterile plastic containers and were cultured not later than 18 h after collection.All samples were cultured in a saline nutrient broth with a final concentration of 3.5% sea salt.Cultures were incubated at 30 °C in an orbital shaker,at 150 rpm.After 7 days,resultant colonies were purified by repeated streaking on complete media agar.The isolates were stored at 4°C.Genetic characterization of the isolated bacterium was made on the basis of 16S rRNA.After phylogenetic analysis,sequence data are submitted to GenBank with the accession number of KX351792(https://www.ncbi.nlm.nih.gov/nuccore/KX351792.1).

For bacterium enrichment,LB medium(10 g/L tryptone,5 g/L yeast extract,10 g/L NaCl in 1 L of distilled water)with 3.5%NaCl was used.In addition,incubation conditions were at 30oC for 48 h on a rotary shaker at 100 rpm.The electrochemical experiments are performed in ASW inoculated with a 1% v/v 24 h bacterial culture(～109CFU/mL)(San et al.2012a).

2.4 Biosynthesis of AgNPs by Lysinibacillus sp.NOSK Cell-Free Extract

For the biosynthesis of AgNPs,10 ml of the cell-free extract was added to 90 ml of 1 mM AgNO3solution in a 100-ml Erlenmeyer flask(pH 8),which was incubated at 37oC on the orbital shaker set at 150 rpm in the dark.In our study,the change in the color of the mixture from pale yellow to brownish yellow after 6 h was observed and the color was darkened during the 72-h incubation period.

2.5 Characterization of Biogenic AgNPs

2.5.1 UV-Visible Spectroscopic Analysis

The absorption spectra of the samples taken at different time intervals of incubation were recorded by UV-Vis spectrophotometer(Shimadzu UV1200,Japan)at a resolution of 1 nm in a wavelength range between 300 and 750 nm using a 96-well plate.

2.5.2 Size Distribution and Zeta Potential Analysis

The average particle size distribution and zeta potential of AgNPs in colloidal solution were determined by using Zeta Sizer Nano Series(Malvern Instruments,ZEN 3600).The results were collected in ultrapure water at 25 °C and 173°backscatter angle.The electrophoretic mobility of the nanoparticle solution(1 mg mL-1)was analyzed.Data was altered to zeta(ζ-)potential and size values with the Helmholtz-Smoluchowski equation.

2.5.3 Nanoparticle Characterization

Biosynthesized AgNPs are analyzed to find out the presence of functional groups on the silver nanoparticles via ATRFTIR spectroscopy.The samples were completely freezedried by Christ Alpha Freeze Dryer(Germany)at-55 °C and the powders were subjected to FTIR measurement.The spectra were recorded by ATR-FTIR(Shimadzu,IRAffinity-1S model,with a DLATGS detector,diamond plate,Japan),in transmittance mode within the range of 400-4000 cm-1with 64 scans at a resolution of 4 cm-1.

2.5.4 Transmission Electron Microscopy

The shape of silver nanoparticles is determined using transmission electron microscopy(TEM).AgNPs’colloidal solution is dropped onto copper TEM grids and measurements are taken at an accelerating voltage(100-200 keV)(FEI HRTEM).

2.5.5 Antimicrobial Activity of AgNPs Against Pathogens

Four bacterial strains,namely,Bacillus subtilis(ATTC 6633),Staphylococcus aureus(ATTC 6338),Escherichia coli(ATTC 8739),and Klebsiella pneumoniae(ATTC 700603),are provided from American Type Culture Collection(ATCC),USA.All bacteria strains are commonly found in hospital-acquired infections.The cultures of B.subtilis,S.aureus,and E.coli were grown in LB at 37°C for overnight incubation on the orbital shaker at 100 rpm and the culture of K.pneumoniae was also grown in LB at 37°C for 48 h.These cultures were maintained in LB agar plate by continuous subculturing from time to time.

The antimicrobial activity of biosynthesized AgNPs is determined by colony forming unit(CFU)method and well diffusion method.In CFU method,the different concentrations of AgNPs(65 nM,130 nM,195 nM,and 260 nM)were added to sterile LB broth and inoculated separately with freshly grown Staphylococcus aureus(ATTC 6338),Bacillus subtilis(ATTC 6633),Klebsiella pneumoniae(ATTC 700603),and Escherichia coli(ATTC 8739).After incubation period,the inoculum was diluted and spread uniformly onto the individual plates.All the plates are incubated at 37oC and at the end of inoculation time,bacterium was counted.In well diffusion method,the cultures of organisms were inoculated to LB agar which are sterilized and cooled approximately 40-50 °C and were poured into petri dishes.After completely cooled,wells of 5-mm diameter were made on LB agar plate using gel puncture.The different concentrations of AgNPs(65 nM,130 nM,195 nM,and 260 nM)are filled into each well on all plates.After incubation at 37 °C,the variable levels of zone of inhibition are evaluated.

2.5.6 Growth Effect of AgNPs Against Corrosion Bacterium Halomonas variabilis NOSK

Bacterial growth after 5 h in the corrosion setup was measured by counting(CFU)method.The growth inhibition percentage was obtained with respect to the positive control.

2.5.7 In vitro Cytotoxicity of AgNPs

AgNPs have gained access into our daily life,and the inevitable human exposure to these nanoparticles has raised concerns about their potential hazards to the environment,health,and safety in recent years.For this reason,cytotoxic activities of biosynthesized AgNPs against HeLa cell lines were studied.HeLa cell line which is the cervical cancer cell line was grown in Dulbecco’s Modified Eagle Medium supplemented with 10% fetal bovine serum(FBS),100μg/mL penicillin,and 100μg/mL streptomycin at 37 °C in a humidified atmosphere of 95%air and 5%CO2.For reproduction,70%-80%of confluence and a density of 2×103cells per well in 96-well plate are incubated for 24 h in 95% air and 5% CO2incubator.3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-tetrazolium bromide(MTT)assay is used for the determination of the cytotoxic activity of biosynthesized AgNPs against HeLa cell lines.Different concentrations of the AgNPs in distilled water are added and incubated for 24 h at 5% CO2incubator.After incubation,10μL(5 mg/mL in PBS)of MTT was added to each well and incubated for 4 h at 37 °C.The resulting formazan was dissolved in 200μL of DMSO and the viable cells were determined by measuring the absorbance at 570 nm.The concentration of AgNPs showing 50% inhibition of viability(IC50values)was determined.The percentage of viability was calculated as the following formula:

2.6 Weight Loss Measurements

The corrosion rates of disks which have 0.5 cm2exposed area were monitored by weight loss technique.The weight loss was determined at 25 °C by weighing the cleaned samples before and after the copper disk in the ASW with the absence and presence of bacterium and AgNPs.The coupons were removed from the environments at the interval of 5 h;the cleaning procedure consisted of wiping the disks with a paper tissue and washing with distilled water and acetone,followed by oven drying at 80 °C.The rate of the corrosion was calculated based on the equation given below:

where K is a constant,T the time of exposure in hours,A the area in cm2,W is the mass loss in g,and D is the density of copper in g/cm2(Liu et al.2019).

2.7 Electrochemical Studies

Electrochemical analysis was conducted at room temperature in ASW which contained(g/L)26.29 NaCl,0.74 g KCl,0.99 g CaCl2,6.09 g MgCl26H2O,and 3.94 g MgSO4·7H2O and adjust the pH to 7.8 and store at 4°C.1 g/L concentration of glucose is added to the media as carbon and energy sources.In our three different corrosion analysis setup,the copper electrodes are placed in artificial seawater under sterile conditions,in the presence of H.variabilis NOSK and bacterium with AgNPs.In the setups,cell number in the bacterial solution was determined based on the standard calibration with the assumption that an OD600 nm value of 1.0 is equivalent to 109cells/mL.

EIS studies were conducted using CH Instruments Inc.,USA(Model CHI-608E),with a traditional three-electrode cell with a capacity of 90 mL,with platinum as the counter electrode,an Ag/AgCl(3 M KCl)as the reference electrode,and copper disk(0.5 cm2exposed area)as the working electrode.First,working electrode is polished with abrasive paper(400,600,800,and 1200 grade)and then cleaned with ethyl alcohol.At the end,in order to sterilize the samples,all the samples are exposed to ultraviolet(UV)light for 30 min.In addition,we confirmed the surface film formed by AgNPs after 5-h corrosion test with their electrochemical behavior in 50-mM phosphate buffer(pH 7.4)using cyclic voltammetry(scans originating at 100 mV/s(vs.Ag/AgCl)(Giovanni and Pumera 2012).

2.8 Statistical Analysis

ZSimpwin and EISSA data analysis software were used to fit the EIS data.All the measurements were recorded in triplicate and the results are expressed as means±the standard errors of the means.

3 Results and Discussion

3.1 Characterization of the Biogenic AgNPs

The reduction of aqueous AgNO3solution is a largely used method for biosynthesis of AgNPs(Mittal et al.2014).The first characterization analysis of the biosynthesized AgNPs is performed by using UV-Vis spectroscopy.Figure 1a shows the UV-Vis absorption spectra recorded from aqueous AgNO3—the cell-free extract of the Lysinibacillus sp.NOSK medium as a function of time of reaction.Inset shows the UV-Vis close look for the spectra of AgNPs at 1-to 8-h time intervals.After 6-h incubation,the color of the reaction mixture began to change that indicates more than 6 h required for the synthesis of detectable amount of AgNPs(Figure 1b).After 24 h,the light yellow color change to yellowish brown color;that is,the typical optical property of AgNPs’color shows the formation of nanoparticles.The density of the color of reaction mixture was directly proportional to the time of incubation.In addition,the characteristic surface plasmon resonance(SPR)peak of the mixture was between 420 and 430 nm,demonstrating the presence of AgNPs.The SPR spectra suggest that these AgNPs are spherical in shape(Gou et al.2015;Otari et al.2015).

In Figure 1,the inset shows the UV-Vis spectrum of AgNPs at 1-to 8-h time intervals.DLS data represent an average particle size and particle size distribution.The average particle size of the samples taken at different time intervals of incubation(30 min,1 h,2 h,3 h,4 h,5 h,6 h,8 h)is almost identical(Figure S1)and after 24 h of reaction,the size of the nanoparticles began to increase.From Figure 2a,it shows 42 nm was the average particle size distribution of AgNPs in colloidal solution for 24 h and 0.166 polydispersity index(PDI)was obtained.From Figure 2b and Figure 2c,it indicates that the average size values recorded for 48 h and 72 h are 61 nm and 76 nm,respectively.Thus,the particle size increase formed as time progressed can be associated with agglomeration.

The zeta potential measurement is an important demonstration of the stability of nanoparticles in colloidal solution.High absolute zeta potential(ξ＞±30 mV)attributes to a high electric surface charge on the AgNPs which can lead to strong repulsive power among the nanoparticles to prevent them from aggregation.The negative zeta potential of-23.1 mV is observed for 24 h that the capping molecules existing on the surface of AgNPs frequently contained negatively charged groups and are responsible for the stability(Table S1)(Arulmozhi et al.2013).

Figure 3 shows the vibrations of the amide I and amide II bands of the proteins of the sample for 24 h(Kardas et al.2014).The absorbance at 3619 cm-1and 3736 cm-1attributed to O-H stretching vibration modes of hydroxyl functional group and N-H stretching vibration modes of amino functional group in proteins(Gou et al.2015).The other bands such as 2923 cm-1,2851 cm-1,and 1741 cm-1can be related to CH2asymmetric stretching and CH2symmetric stretching of mainly lipids from proteins,nucleic acids and carbohydrates,and C=O stretching of triglycerides and cholesterol esters.All these functional groups may have an efficient role in the biosynthesis of AgNPs.It indicates that the release of extracellular biomolecules could probably perform the function of the formation and stabilization of AgNPs in colloidal solution(Fayaz et al.2010).

Figure 1(a)UV-Vis absorption spectra of silver nanoparticles.(b)The color change of the reaction mixture

Figure 2 Histogram of silver nanoparticle distributions.(a)24 h,(b)48 h,and(c)72 h

The TEM micrographs of the biosynthesized silver nanoparticles are shown in the Figure 4a,4b,and 4c with 50,5,and 2 nm scales,respectively.As seen in the TEM micrographs,synthesized AgNPs were spherical in shape.Furthermore,the selected area electron diffraction(SAED)patterns reveal that the particles are crystalline in nature(Figure 4d).

3.2 Antimicrobial Activity and In vitro Cytotoxicity of AgNPs

Figure 3 FTIR spectrum of the freeze-dried sample containing AgNPs

Silver has been utilized for many years in the field of medicine for bactericidal applications due to antimicrobial properties(Firdhouse and Lalitha 2015).Although the antimicrobial effects of the biosynthesized AgNPs are shown in several studies,the exact mechanism remains to be unexplained(Kim et al.2007).Most studies showed that the surface of the negatively charged bacterial cell membrane may attract positively charged AgNPs and interact with structural elements of the bacterial cell membrane,which may lead to structural changes disturbing permeability and respiration functions of the cells and finally cell death(Sondi and Salopek-Sondi 2004).Kim et al.(2007)reported that the free radical consisted of metal depletion from the surface of AgNPs may be responsible for antimicrobial activity which is known to destroy the cell membrane integrity.Moreover,particle dimension and shape may affect the bactericidal activities of AgNPs.The smaller AgNPs,which have large surface areas for interactions,would demonstrate more antibacterial efficacy than the larger AgNPs.This has been facilitated to interact with the cell wall of the bacterium and cause death of the cells(Kailasa et al.2019).

Figure 4 TEM micrograph of the biosynthesized silver nanoparticles.(a)50,(b)5,and(c)2 nm scales,and(d)the selected area electron diffraction(SAED)patterns

In the present study,the biosynthesized AgNPs showed antimicrobial activity against Gr(+)Staphylococcus aureus and Bacillus subtilis and Gr(-)Klebsiella pneumoniae and Escherichia coli dependent on the concentration of AgNPs(Peszke et al.2016).In CFU method,the number of bacterial colonies reduced with the increasing of the concentration of AgNPs.The growth inhibitory rates at different concentration of AgNPs with 65 nM,130 nM,195 nM,and 260 nM are calculated,respectively,as 75%,98%,100%,and %100 for S.aureus.The antimicrobial activity rates were 50%,100%,100%,and 100% for B.subtilis,in addition,100%,100%100%,and 100% in K.pneumoniae and 72.4%,97.52%,100%,and 100% in E.coli.In well diffusion method,the diameter of inhibition zones formed with the increase of the concentration of AgNPs(65 nM,130 nM,195 nM,and 260 nM)was recorded as,respectively,0,28.7±0.4,46.3±0.4,and 47.3±0.6 mm in S.aureus;0,24.2±0.1,25.0,and 32.8±0.4 mm in B.subtilis;0,13.0±0.8,25.7±0.2,and 29.7±0.3 mm in K.pneumoniae;and 0,0,27.7±0.2,and 26.3±0.3 mm in E.coli(Table S2).These results suggest that the inhibitory effect of AgNPs was more in gram-positive bacteria(S.aureus and B.subtilis)as compared with gram-negative bacteria(K.pneumoniae and E.coli).Gram-positive bacteria have an extra barrier of the outer membrane.Thus,gramnegative bacteria may be more resistant than gram-positive bacteria as is seen in our experiment results(Yeagle 2011).

In addition,growth effect of AgNPs in the corrosion setup showed that in the beginning(0 h),the number of the H.variabilis NOSK(ASW with no AgNPs)was 1010CFU/mL.After 5-h corrosion experiments,bacterium was decreased to 105CFU/mL(5 log)in the viable population of H.variabilis NOSK.

Coatings which contain antimicrobials were shown to inhibit microbial corrosion(Park et al.2004)especially silverbased coatings which were effective in the inhibition of biofilm formation(Shah et al.2019).However,it is really important to find the cytotoxic potential of the synthesized nanoparticles against cells.For this reason,biosynthesized AgNPs show dose-dependent cytotoxicity on HeLa cell lines.Cytotoxicity tests showed that 50%of the cells lose their viability at 120μg/mL of AgNPs that dosage has been considered as IC50 for HeLa cells(Figure 5).

Figure 5 Biosynthesized silver nanoparticles properties of the cytotoxicity on HeLa cell lines

3.3 Weight Loss

The outcomes of the weight loss experiments for copper disks in the presence and absence of bacterial strain and AgNPs after 5-h immersion were presented in Table S3.In the absence of bacterial strains(abiotic control),the corrosion rate of the Cu disk was 0.01134±0.001 mm y-1(0.0029 mg±0.002).In the presence of H.variabilis NOSK,the corrosion rate of the Cu disk was 001564±0.001 mm y-1which is slightly higher(0.004 mg±0.002)than abiotic environment due to bacterial activity.However,in the presence of AgNPs,corrosion rate reached the lowest value of 0.00782±0.002 mm y-1(0.002 mg±0.002);therefore,the addition of AgNPs protected the Cu disk in the ASW.Similar results were also made by Narenkumar et al.(2018).According to the authors,corrosion rate in the presence of AgNPs synthesis from plant extract material was drastically reduced.

3.4 OCP,TAFEL,and Electrochemical Impedance Analysis

The potentiodynamic polarization curves of the ASW,ASW incubated with H.variabilis NOSK,and ASW with incubated H.variabilis NOSK+AgNPs after 5-h immersion are presented in Figure 6.The electrochemical parameters such as corrosion potential(Ecorr),the corrosion current density(Icorr),anodic(βa)and cathodic(βc)Tafel values,and charge transfer values(Rct)and solution resistance(Rs)values are presented in Table 1.

Rsrepresents the resistance of solution,Rpthe resistance of passive film/biofilm pores,Rctthe resistance of charge transfer,QCPEthe CPE parameters,Qdlthe CPE parameters for double layer,andηthe dispersion parameters.The EIS measurements were carried out at 5-mV applied voltage at sinusoidal wave in the frequency range of 20 kHz-50 mHz in pH 8.0 Artificial seawater at room temperature.All values are means of triplicate tests

Figure 6 The potentiodynamic polarization curves of the ASW,ASW incubated with H.variabilis NOSK,and ASW with incubated H.variabilis NOSK+AgNPs after 5 h

Table 1 Electrochemical parameters of Cu corrosion inhibition in artificial seawater,artificial seawater inoculated with bacteria,and artificial seawater inoculated with bacteria+AgNPs

Figure 7 Electrochemical impedance spectrum.(a)Nyquist.(b)Bode phase plots of the copper in ASW.(c)Incubated with H.variabilis NOSK.(d)Incubated with H.variabilis NOSK+AgNPs

Open circuit potential analysis is a nondestructive method to monitor the potential change on the surface of the metal/alloy.Table 1 shows that the OCP value of ASW was-0.451 V vs Ag/AgCl,but after bacterium inoculation,OCP value slightly displaced toward more negative value(-0.525±0.01 V vs Ag/AgCl)which shows acceleration of corrosion.On the contrary,after addition of Ag nanoparticles,OCP value was modified to more positive value(-0.406±0.01 V vs Ag/AgCl).It has been evident from the polarization curve that there was a remarkable potential shift to more positive values for copper in H.variabilis NOSK+AgNPs(-0.52±0.02 V vs Ag/AgCl)as compared to copper in ASW(-0.60±0.02 V vs Ag/AgCl)and copper in ASW after H.variabilis NOSK inoculation(-0.62±0.02 V vs Ag/AgCl).Furthermore,after 5 h of incubation,the corrosion current density(Icorr)in the presence of H.variabilis NOSK was higher than the ASW(5.30±0.1μA cm-2),demonstrating that bacterium promoted Cu corrosion.As we expected,after adding AgNPs with bacterium,the corrosion current density began to decrease and reached the lowest value.Our results supported by earlier work of Preethi et al.(2019)investigated corrosion inhibition efficiency of zinc oxide nanoparticles(ZnONPs).In the presence of bacterium,Icorrwas increased and it leads to the dissolution of copper ions on the metal surface.On the other hand,in the presence of ZnONPs,Icorrwas reduced and the results reveal that nanoparticles form a protective film on the metal surface and thus inhibit the corrosion of Cu.

The interfacial phenomena of the biofilm formation and corrosion process development and characterization of the electrochemical reactions at the metal/biofilm interface are evaluated with EIS which is one of the most reliable methods(Yuan et al.2013).In our study,EIS results confirmed with Tafel results.Nyquist plots of copper immersed in ASW,inoculated with H.variabilis NOSK and H.variabilis NOSK+AgNPs,are plotted in Figure 7a.

The entire frequency region can be divided into two sub-regions,corresponding to two time constants as shown in Bode plots(log|Z|vs.log(f))in Figure 7b,c,and d(Bode phase plots of the copper in ASW(B),incubated with H.variabilis NOSK(C)and incubated with H.variabilis NOSK+AgNPs(D)).Rsis the solution resistance,Rfand Qfare the resistance and the capacitance of the biofilm,respectively.Rctand Qdlcorrespond to a charge transfer resistance and a double-layered capacitance,respectively.The higher Rpvalues correspond to lower corrosion rates(Liu et al.2017).The Rpvalue of copper in ASW was 681.43±0.1Ωcm2and after incubation,the Rpvalue decreases to 350.64±0.1Ωcm2,indicating severe MIC attack caused by the biofilm/bacterium.However,in the presence of AgNPs,the Rpvalue increased to 172670±3Ωcm2which was significantly diminished.The calculated Rctdata represents the ability to hinder electron transfer between the surface and the substrate.Thus,the lower Rctvalues in the ASW inoculated with H.variabilis NOSK mean the corrosion rate was higher(Zhou et al.2018).On the contrary,the highest Rctvalue was 172670±3Ωcm2in the ASW with H.variabilis NOSK+AgNPs.In addition,an electrical equivalent circuit comprised two time constants used to model the experimental values given in Figure 8.

Figure 8 Schematic illustration and an electrical equivalent circuit of the biocorrosion mechanism by H.variabilis NOSK+AgNPs

The AgNPs’surface film on copper electrode after 5 h was investigated upon their electrochemical behavior in 50-mM phosphate buffer(pH 7.4)with cyclic voltammetry in Figure 9.As can be seen from Figure 9,two characteristic peaks of Ag were observed after 5-h corrosion test.An oxidation peak corresponding to Ag to Ag+oxidation was observed with a peak potential of 0.178 V and a peak current of 13.8 mA,while on the reverse scan,a reduction peak appeared at-0.129 V with a peak current of 15.97 mA.These two peaks were not observed at the bare copper electrode as expected.In addition,the absence of copper peak after 5-h corrosion showed that the surface was completely covered with silver nanoparticles.Thus,it can be said from the obtained voltammograms that the silver nanoparticles were adsorbed on the copper electrode surface from the corrosion solution(Palisoc et al.2018).

4 Conclusions

Figure 9 Cyclic voltammograms.(a)Bare Cu electrode and(b)the copper electrode with AgNPs after 5-h corrosion at a scan rate of 100 mV/s in pH 7.4 phosphate buffer solution

In conclusion,due to adverse effects of the chemical and physical nanoparticles’synthesis methods,new and novel sustainable methods sought for the discovery.In this study,the biosynthesis of silver nanoparticles by the Lysinibacillus sp.NOSK bacteria is demonstrated.Biosynthesis of AgNPs is confirmed by using UV-Vis absorption,transmission electron microscopy(TEM),and Fourier transform infrared spectroscopy(FTIR).The average crystalline size and shape of the nanoparticles were 42 nm and spherical in shape,respectively.

In application,these nanoparticles exhibited efficient antimicrobial activity against gram-positive and gram-negative bacteria.In addition,the inhibition of halophilic bacterium’s biocorrosion on copper in marine environment was successfully evaluated in detail in this work.The EIS analysis showed increased Rpvalue for bacterium with AgNPs corresponding to lower corrosion rates.For this reason,biosynthesized AgNPs are used as an active antimicrobial corrosion inhibitor and these non-toxic nanoparticles have a potential to be used as antibacterial paints and coatings due to long-term protection property especially in marine industry.

FundingThis research is funded by the Scientific and Technological Research Council of Turkey(TÜBITAK,Project MAG#218 M508).

Supplementary InformationThe online version of this article(https://doi.org/10.1007/s11804-020-00188-6)contains supplementary material,which is available to authorized users.