Study on kinetics of cathodic reduction of dissolved oxygen in 3.5% sodium chloride solution

Electrochemical reduction of dissolved oxygen in seawater on metals is of great importance for corrosion studies. The present paper studied cathodic reduction of dissolved oxygen on Q235 carbon steel in 3. 5% sodium chloride(NaCl)solutions by cyclic voltammetry(CV), electrochemical impedance spectroscopy(EIS), rotating disk electrode(RDE)and rotating ring-disk electrode(RRDE). The cyclic voltammetric results demonstrated the cathodic process on Q235 carbon steel in O2-saturated 3. 5% NaCl solution contains three reactions:dissolved oxygen reduction, iron oxides reduction and hydrogen evolution. The peak potential of oxygen reduction reaction(ORR)is-0. 85 V vs Ag/AgCl, 3 molL-1 KCl. The E1S results indicated that the ORR occurring on Q235 carbon steel is a 4-electron process and that no finite diffusion is caused by the intermediate of H2O2 produced by ORR. The RDE and RRDE voltammograms confirmed the EIS results and it was found that the number of transferred electrons for ORR was nearly 4, I. E. , dissolved oxygen reduced to water.     

Impedance characteristics of carbon steel under cathodic protection

INTRODUCTIONInpraCticalengineeringapplicati0ns,thecormsionofstalundercathodicprotalioncanbecontr0llediftheproodi0np0tenhalisset2O()t03(X)mVnegativewithaspeCttothenatamlcormsi0np0tenial(MasatSugi,l976,Takehiko,l972).Theprotalnp0tentia1edinpraedcalapplicationisbedonexperienceandtheory.Tooru(l985,l986)foundthattheopbocathodicproodionpotentialcoinddedwiththepotentialwhenpolarhati0nresistancemaxndnd,s0thiscoinedencecanbeedt00btainoptbore-sultforcarbonstalundercathodicpronaion.Inthiswork,the…     

Mitigation of hydrogen permeation into steel by bacteria:a new research proposal

A new research proposal was introduced aiming at solving the fundamental theory for reducing the risk of hydrogen embrittlement(HE) in high-strength steels by utilizing hydrogen-consuming microorganisms.The superior performance of high-strength steel can meet the material strength requirements for remote deep-sea marine engineering development.Due to the heavy corrosive marine environment,steel structures must be protected by cathodic protection.However,high-strength steel is sensitive to stress corrosion cracking and HE,and cathodic protection can promote hydrogen permeation into steel.Hydrogen-consuming microorganisms are widespread in the natural environment and they utilize the energy of hydrogen oxidation to survive.If we could make use of the hydrogen-consuming function of microorganisms to consume the hydrogen generated during the cathodic protection process,then the potential for cathodic protection can be reasonably lowered,ideally protecting the steel and simultaneously reducing the possibility of HE.     

Protection of steel piles in harbours by using DZ tape and cathodic polarization

An anticorrosion method using wet DZ¹ tape and electrochemical cathodic protection is suggested. The advantages of this method over internationally patented sealing techniques lie in its electrochemically open system, high adsorption of OH⁻ with resultant rise of pH, exchangeable electrolytes, simple pretreatment of the steel pipe, simplicity of application, lower cost, better protection even under ebb tide, and low transmission of oxygen and corrosion products. Contribution No. 1455 from the Institute of Oceanology, Academia Sinica     

Co-Production of Lipids,Eicosapentaenoic Acid,Fucoxanthin, and Chrysolaminarin by Phaeodactylum tricornutum Cultured in a Flat-Plate Photobioreactor Under Varying Nitrogen Conditions

The marine diatom Phaeodactylum tricornutum is a polymorphological, ecologically significant, and well-studied model of unicellular microalga. This diatom can accumulate diverse important metabolites. Herein, we cultured P. tricornutum in an internally installed tie-piece flat-plate photobioreactor under 14.5 m mol L~(-1)(high nitrogen, HN) and 2.9 m mol L~(-1)(low nitrogen, LN) of KNO_3 and assessed its time-resolved changes in biochemical compositions. The results showed that HN was inductive to accumulate high biomass(4.1 g L~(-1)). However, the LN condition could accelerate lipid accumulation in P. tricornutum. The maximum total lipid(TL) content under LN was up to 42.5% of biomass on day 12. Finally, neutral lipids(NLs) were 63.8% and 75.7% of TLs under HN and LN, respectively. The content of EPA ranged from 2.3% to 1.5% of dry weight during the growth period under the two culture conditions. Peak volumetric lipid productivity of 128.4 mg L~(-1)d~(-1) was achieved in the HN group(on day 9). The highest volumetric productivity values of EPA, chrysolaminarin, and fucoxanthin were obtained in the exponential phase(on day 6) under HN, which were 9.6, 93.6, and 4.7 mg L~(-1)d~(-1), respectively. In conclusion, extractable amounts of lipids, EPA, fucoxanthin, and chrysolaminarin could be obtained from P. tricornutum by regulating the culture conditions.     

Bioaccumulation and Biodegradation of Sulfamethazine in Chlorella pyrenoidosa

Intensive use of sulfamethazine(SM_2) in aquaculture has resulted in some detrimental effects to non-targeted organisms. In order to assess its potential ecological risk, it is crucial to have a good understanding on the bioaccumulation and biodegradation of SM_2 in Chlorella pyrenoidosa. The microalgae were treated with 2, 4, and 8 mg L~(-1) of sulfamethazine for 13 days, respectively, showing that the inhibition effects of sulfamethazine on the growth of Chlorella pyrenoidosa increased progressively as the concentrations of sulfamethazine increasing from 2 to 8 mg L~(-1). The peak concentrations of sulfamethazine accumulated in C. pyrenoidosa were 0.225, 0.325, and 0.596 ng per mg FW on day 13 for three treatment groups, respectively, showing a great ability to deplete sulfamethazine from the culture media. On day 13, the percentages of biotic degradation were 48.45%, 60.21% and 69.93%, respectively. The EC_(50) of 10.05 mg L~(-1) was derived which showed no significant risk for C. pyrenoidosa with a calculated risk quotient 1. The activities of superoxide dismutase and catalase increased progressively in response to sulfamethazine and showed a positive correlation to the treatment concentrations. The highest superoxide dismutase activity was achieved at the concentration of 8 mg L~(-1) after 2 d of exposure, which was 1.89 folds higher than that of the control. The activity of catalase has a similar pattern to that of superoxide dismutase with the maximum activity achieved at day 2, which was 3.11 folds higher compared to that of the control. In contrast to superoxide dismutase and catalase, the maximum glutathione S-transferase activity was observed at day 6, showing 2.2 folds higher than that of the control.     

IMPEDANCE CHARACTERISTICS OF CALCAREOUS DEPOSIT

The electrochemical impedance spectra for bare steel and sample covered with calcareous deposit in artificalseawater were determined; the dependence of the impedance on the potential was investigated, thesignificance of the impedance parameter R_f reflecting the effective protectiveness of the deposit is emphasized.Optimization of the cathodic polarization condition is discussed.     

Effect of Zinc Oxide Nanoparticles on Denitrification and Denitrifying Bacteria Communities in Typical Estuarine Sediments

For revealing the effects of increasing of zinc oxide nanoparticles(ZnO NPs) on denitrification and denitrifying bacteria communities in estuarine sediments, the surface sediments of two typical estuaries(the Yangtze River Estuary and the Yellow River Estuary) were added with medium concentration(170 mg L~(-1)) and high concentration(1700 mg L~(-1)) of ZnO NPs for anaerobic culture in laboratory. The concentration of NO_3~-and NO_2~-, the reductase activity and denitrification rate were measured by physicochemical analysis, nir S gene abundance and denitrifying bacteria communities by molecular biological methods. The results showed that ZnO NPs inhibited NO_3~-, NO_2~-reduction process and NO_3~-, NO_2~-reductase activity, and a stronger inhibition effect resulting from the higher ZnO NPs concentration. ZnO NPs decreased nirS gene abundance and community diversity of denitrifying bacteria. In addition, the inhibition degree of ZnO NPs on the denitrification process of sediments in different estuaries was different. These results were of great significance for evaluating the potential ecological toxicity and risks of nanomaterials in estuaries.     

Lead Induces Different Responses of Two Subpopulations of Phagocytes in the Holothurian Eupentacta fraudatrix

In view of increasing lead pollution(Pb~(2+)) of coastal waters, the compensatory abilities of holothurians need to be assessed. The goal of the work is to clarify the functional and phenotypical differences between two types of phagocytes(P1 and P2) in Eupentacta fraudatrix exposed to Pb(NO_3)_2. It has been shown that 2 mg L~(-1) lead exposure for 48 h increases the number of P2 phagocytes as compared to P1 cells, does not significantly affect cell viability in both P1 and P2 phagocyte fractions, and significantly enhances chromatin condensation in P2 but not in P1 phagocytes. A lead concentration of 4 mg L~(-1) increases the number of P1 phagocytes compared to that of P2 type, and does not change cell viability and chromatin condensation in P1 phagocytes. In the P2 type, it decreases cell viability and does not influence the level of apoptosis. The protection against lead-induced apoptosis is apparently mediated by the activities of antioxidant enzymes, especially glutathione S-transferase. The differences in labeling cell surface receptors of P1 and P2 phagocytes by plant lectins also indicate the specific phenotypic properties of these cells. The results clarify the potential and GSH-dependent mechanisms of immune adaptation in holothurians that have been shortly exposed to lead at concentrations close to the maximum environmentally relevant level in coastal waters. Additionally, P1 and P2 phagocytes are first shown to have different functions and phenotypes during the response to lead, which indicates the complexity of the phagocytic system in holothurians and contributes to understanding the immunity evolution.     

Salt-tolerant Microbiota Enhancing Contaminants Removal from Mariculture Wastewater Containing Sulfamethoxazole in an A/O-MBBR

The wide application of antibiotics in aquaculture requires an efficient treatment of the wastewater before discharging it into the environment. During the wastewater treatment, the influence of antibiotics on the performance of bioreactor should be well revealed due to their toxicity to the functional microbial community. In this study, the effect of feeding 10-30 mg L~(-1) sulfamethoxazole(SMX) in influent on the performance of an anoxic/oxic-moving bed biofilm reactor(A/O-MBBR) treating mariculture wastewater and the responding change of biofilm microbial communities was investigated. The COD average removal rate remained at 94.61%-97.34% with the dosage of SMX. Compared with that, the nitrifying removals of NH_4~+-N and NO_2~--N were violently inhibited by 30 mg L~(-1) SMX and denitrifying removal of the NO_3~--N decreased obviously with 20 mg L~(-1) or more SMX. The microbial community in the successful startup bioreactor was relatively abundant, while the diversity of microbial community decreased with the increase of feeding SMX. The salt-tolerant and SMX-resistant genera Arcobacter, Thiothrix, Desulfuromusa and Nitrosomonas were gradually enriched and finally played a vital role in converting COD and recycling nitrogen and sulfur. Hence, the present A/O-MBBR reactor with the salt-tolerant functional microbiota achieved efficient removal of pollutants in the presence of low concentration(e.g., 10 mg L~(-1)) SMX.     

Layer by Layer Assembly of Poly(Allylamine Hydrochloride)/Phosphate Ions and Poly(Sodium 4-Styrene Sulfonate) Membrane for Forward Osmosis Application

Based on the layer by layer(Lb L)assembly technology,the nano-scale composite membrane with excellent structure can be prepared by changing the polyelectrolyte and controlling the deposition conditions.Polyamines and phosphate ions(Pi)can be self-organized to form supramolecular systems which could be exploited to stabilize the interfacial architecture.The LbL membrane was made of the positively charged poly(allylamine hydrochloride)(PAH)self-organized with Pi and the negatively charged poly(sodium 4-styrene sulfonate)(PSS)alternatively on top of a poly(acrylonitrile)(PAN)substrate.Compared to the membrane without Pi,the membrane assembled by PAH/Pi improved forward of flux and reduced flux of salt.The concentration of PAH and PSS,deposition time,pH and number of layers showed significant influences on the performance of the membrane.In this experiment,we systematically investigated the preparation conditions and under the optimized conditions the prepared membrane exhibited high water fluxes of 13.5 L m^-2 h^-1 with corresponding salt to water flux,Js/Jv,ratio of 0.07 g L^-1 tested by forward osmosis when DI water as feed solution and 2 mol L^-1 MgCl2 as draw solution.     

Preparation of Clay/Biochar Composite Adsorption Particle and Performance for Ammonia Nitrogen Removal from Aqueous Solution

This study aimed to present a novel clay/biochar composite adsorption particle, which made from abandoned reed straw and clay to remove ammonia nitrogen(NH_4~+-N) from micro-contaminated water. The removal performance of NH_4~+-N by composite adsorption particle was monitored under different raw material proportions and initial NH_4~+-N concentration. Besides, adsorption kinetics and adsorption isotherms were investigated to reveal the adsorption mechanisms. The results showed that NH_4~+-N was effectively removed under optimal proportion of biochar, foaming agent and crosslinker with 20%, 3%, and 3%, respectively. The optimal contact time was 150 min and the best removal efficiency was 88.6% at initial NH_4~+-N concentration of 20 mg L~(-1). The adsorption performance was well described by the second order kinetic model and Freundlich model. The novel clay/biochar composite adsorption particle in this study demonstrated a high potential for NH_4~+-N removal from surface water.     

The bacterial diversity and community composition altered in the oxygen minimum zone of the Tropical Western Pacific Ocean

The oxygen minimum zones(OMZs) are globally expanding,yet the variation pattern of microbial communities related to dissolved oxygen levels remain unclear.Spatial variability of bacterial diversity and community composition(repre sented by 16 S rRNA) of six stations was investigated within the water column in the seamount area of Tropical Western Pacific Ocean(TWPO) in May 2019.The seawater has dissolved oxygen(DO) concentration of 3.01-6.68 mg/L and the core of the oxygen minimum zones was located between the depths of 650 m and 1 750 m.The bacterial alpha-diversity showed unimodal pattern with the decreasing DO with depths and peaked in the upper oxycline(UO) of OMZs.The bacterial community structure of the mixed layer(ML) and the bottom layer clustered and separated from each other,while those of UO and the OMZ core(OM) clustered and overlapped.Overall,bacterial community composition transitioned from being Alphaproteobacteria and Gammaproteobacteria-dominant in ML to being Gammaproteobacteria and Nitrososphaeria/Deltaproteobacteria-dominant in UO and OM,and then changed to being Clostridia and unidentified Actinobacteria-dominant in the bottom layer.Moreover,both bacterial alpha-diversity and the abundant classes fitted varying sectioned functions with DO.The DO solely explained 40.37% of the variation of bacterial community composition among layers(P0.001).The predicted function profiling showed that the water column was predominant by chemoheterotrophy,cyanobacteria,and photoautotrophy in ML,by chemoheterotrophy and nitrate/sulfide cycling in UO and OM,and by chemoheterotrophy and ferme ntation in the bottom layer.Our findings revealed the DO-associated variation in bacterial diversity and community composition,and help to clarify the potential responses of microbes and their involved biogeochemical processes to the expansion and intensification of OMZs.     

Study of the Corrosion Resistance of Electroless Ni-P Deposits in a Sodium Chloride Medium

The corrosion resistance of electroless Ni-P deposits with phosphorous contents from 12% to 14% in sodium chloride solutions was studied. The deposits were immersed in 3.5% NaCl solutions for 29 d to obtain the electrochemical parameters and were examined in a standard salt spray test for 15 d respectively. The corrosion resistance of the deposits was studied by poten- tio-dynamic scan, electrochemical impedance spectroscopy (EIS), X-ray diffraction (XRD) and cold-field emission scanning electron microscopy (FE-SEM) equipped with an energy dispersive X-ray detector (EDX). The patterns of XRD and the results of FE-SEM showed that the prepared deposits were amorphous. But after a 15 d standard salt spray test, a few pinholes appeared on the surface of the deposit and the weight content of phosphorus on the surface of the deposit was higher (which was beneficial to the formation of the passivation films) than that before the standard salt spray test when the nickel content was lower because the dissolved weight of nickel was greater than that of phosphorus. The results from potentio-dynamic scan and EIS showed that passivation films formed on the Ni-P deposit after immersion in the NaCl solutions, which decreased the corrosion rate of Ni-P samples. The results of this work show their potential applications in marine corrosion.     

A Laboratory Column Study on Particles Release in Remediation of Seawater Intrusion Region

In coastal areas, excessive exploitation of groundwater causes seawater intrusion. In artificial recharge of aquifer remediation process, the replacement of saltwater and freshwater with each other causes colloid release, and permeability also decreases. In this paper, the aquifer samples containing minimal clay mineral(mainly illite) in Dagu River aquifer were used. Adopting horizontal column experiments, we studied the influences of seepage velocity and ionic strength on particle release, as well as the relationship between them. In the column experiments, the Critical Salt Concentration(CSC) of the Dagu River aquifer was determined as 0.05 mol L~(-1) approximately. This result was basically consistent with the DLVO theoretical calculation. For the constant seepage velocity, the salinity descending rate and partical release were slower, and the peak of particle concentration was lower. However, the total amount of released particles was almost constant at different salinity descending rate. For constant salinity descending rates, the peak of particle concentration decreased as seepage velocity increased, but the total amount of released particles rose up. The experiments also indicated the existence of a critical seepage velocity, which dropped with the decrease of salt concentration. When the concentration of Na Cl solution decreased from 0.17 mol L~(-1) to 0.06 mol L~(-1), the critical seepage velocity decreased from 3 cm min~(-1)to 2.5 cm min~(-1), which is consistent to the results predicted by DLVO theory.     

ELECTROCHEMICAL STUDIES ON THE CATHODIC REACTION OF MARINE ATMOSPHERIC CORROSION

Electrochemical studies on the cathodic reaction of marine atmospheric corrosion using Kelvin probeas reference electrode showed that the rate of cathodic reaction-oxygen reduction first increases then de-creases, with the reaction maximizing at a certain thickness as the electrolyte film decreases duringevaporation. It was indicated that with decreasing electrolyte thickness by drying, the oxygen reduction ratewas accelerated by the faster oxygen diffusion due to the thinner electrolyte layer on the metal surface. Theresults also revealed that although the oxygen salting out effect has great influence on the rate of oxygenreduction, it is not the main causative factor for the decrease in cathodic limiting current in the case of avery thin electrolyte layer.     

近江牡蛎耗氧率和排氨率的研究

采用室内实验生态学方法研究近江牡蛎的耗氧率和排氨率。结果表明,在实验温度13~33℃范围内,近江牡蛎的耗氧率(RO)和排氨率(RN)与体重(W)均呈负相关,可用Y=aW-b表示。耗氧率和温度的关系可表示为RO=-c+b1t-b2 t2,耗氧率为0.626~2.354 mg.g-1.h-1;在温度13~28℃范围内,耗氧率随温度的升高而增加,28℃时,耗氧率达最大值,温度升高至33℃时,耗氧率反而下降。排氨率与温度的关系可表示为RN=c1e d1t,排氨率为0.075~0.318 mg.g-1.h-1,且随温度的升高,排氨率呈持续升高趋势。近江牡蛎呼吸和排泄Q10值范围分别为0.631~3.399和1.046~2.288。在28℃,不同规格近江牡蛎呼吸氧原子数与排出氨氮原子数的比值(nO/nN)均达到最大值。方差分析表明,体重、温度及二者的交互作用对近江牡蛎的耗氧率和排氨率均有极显著的影响(P<0.01)。近江牡蛎的日常代谢明显高于标准代谢,耗氧率和排氨率平均值分别提高46.8%和67.7%。     

Inhibitor-concentration-induced extreme behaviour in electrochemical parameters

ImODUcrIONIngeneral,fOrmosttypesofinhibitorstheperformancecanbecontinuouslyheight-enedbyincreasingtheconeentration.Thehighertheinhibitorconcentration,thestrongertheinhibitionbomes.However,nantobservationsshowedthatsometypesofinhibitorsexhibitedbotperformanceonlywithinashortediumrangeofinhibitorconcentrationinsulfuricaddso1ution,whichistheso-cailedphenornenonofinhibitorconcenhation-indutalextreminhibition.EpelbOin(l979)reportedthattheinhibitingeffidenCyrnaxdrindataroundlmml4ofpropargylalcoh…     

Spatial distribution and diurnal variation of chemical oxygen demand at the beginning of the rainy season in the Changjiang （Yangtze） River Estuary

A field observation was carried out in the Changjiang （Yangtze） River Estuary from May 19 to 26, 2003. A total of 29 stations, including 2 anchored stations, were occupied through almost the whole salinity gradient. Based on the observation data, biogeochemistry of chemical oxygen demand （COD） was examined. Spatial distribution pattern of COD shows that it decreased downstream. The COD concentration varied generally within a narrow range of 1.24-1.60 mg/L in the zone around the river mouth, beyond which it decreased rapidly to 0.20 mg/L. In the mixed water zone, the fluctuation in COD was smaller at 2 m above the bottom layer than at the surface layer in 48 h. In the seawater zone, the 48-h fluctuation at the surface was the largest, followed by that of 5 m below the surface and 2 m above the bottom layers in a range of from 2.50 to 0.55 mg/L. Freshwater discharge was the dominant source of COD in the estuary. The average COD beyond the river mouth was 2.7 mg/L, which accorded with the Chinese seawater quality Grade I. Relationships between dissolved oxygen and biogeochemical parameters such as suspended particulate matter, dissolved organic matter and chlorophyll-a were also discussed.