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温度调控下极地菌在EH40钢表面的成膜特性与腐蚀机制研究OA

Film-forming Characteristics and Corrosion Mechanisms of Polar Bacteria on EH40 Steel Surfaces under Temperature Regulation

中文摘要英文摘要

目的 极地海洋工程材料在严酷环境下极易遭受微生物腐蚀(MIC)威胁.本研究旨在系统阐明环境温度对2株典型极地菌—Pseudoalteromonas elyakovii与 Halomonas axialensis 的附着成膜模式、胞外聚合物(EPS)组分演变及其介导的 EH40 钢腐蚀机制的调控规律.方法 模拟极地环境温度(4℃)与局部环境升温(18℃),开展 EH40钢腐蚀浸泡实验.利用失重法、电化学阻抗谱(EIS)与微区电化学(SVET)评价合金钢的腐蚀动力学与空间电偶效应;通过 SEM/EDS、XRD 与三维形貌分析界面产物膜层的演化;采用共聚焦激光扫描显微镜(CLSM)及多色荧光染色,解析生物膜架构、细胞活性及 EPS 组分的半定量分布.结果 升温至18℃时显著提升了2株菌的附着动力学与 EPS 丰度,但腐蚀路径发生特异性分化.P.elyakovii在 18℃下发生 EPS 优势组分由多糖向蛋白质的转换,富蛋白基质诱导了致密 CaCO3生物矿化层的原位沉积,实现对基体的显著屏蔽与腐蚀抑制(MICI 机制);相反,H.axialensis的 EPS始终以高渗透性多糖为主,18℃下其高度团聚的非均质生物膜放大了空间电偶效应,导致腐蚀形态由深窄点蚀向广浅片状演变,宏观腐蚀速率剧增.结论 环境温度通过重构极地菌生物膜的空间结构与 EPS 化学组分,驱动了腐蚀机理的本质切换.本研究不仅为极地极端环境下 MIC 风险评估提供了科学依据,也为基于微生物原位成膜的仿生表面抑腐策略提供了天然模板与新思路.

The work aims to present an original investigation into the temperature-driven bifurcation of microbiologically influenced corrosion(MIC)and microbiologically influenced corrosion inhibition(MICI)on EH40 marine alloy steel.Transcending conventional single-temperature MIC assessments,the distinct regulatory mechanisms are systematically elucidated by which ambient polar temperature(4℃)versus simulated seasonal warming(18℃)dictates biofilm architectural evolution,extracellular polymeric substances(EPS)compositional shifts,and subsequent electrochemical interfacial processes of two representative Arctic marine bacteria:Pseudoalteromonas elyakovii and Halomonas axialensis.To achieve this,a comprehensive micro-to-macro analytical methodology was established.The continuous evolution of the bio-interface was monitored via electrochemical impedance spectroscopy(EIS)to quantify charge transfer dynamics,while the scanning vibrating electrode technique(SVET)was innovatively employed for the in-situ spatial mapping of localized anodic and cathodic micro-galvanic currents across the bio-filmed surfaces.Macroscopic corrosion kinetics were validated through rigorous weight loss measurements over a 14-day exposure period.Furthermore,the spatial architecture of the polar biofilms and the semi-quantitative distribution of key EPS components were resolved with high spatial resolution through multi-color fluorescent staining combined with Confocal Laser Scanning Microscopy(CLSM).Interfacial biomineralization and corrosion product morphologies were systematically characterized through Scanning Electron Microscopy coupled with Energy Dispersive Spectroscopy(SEM/EDS),X-ray Diffraction(XRD),and Inductively Coupled Plasma Mass Spectrometry(ICP-MS).The experimental results revealed that elevating the temperature to 18℃significantly accelerated bacterial attachment kinetics and enhanced overall EPS abundance for both strains.However,CLSM and biochemical analyses uncovered a profound,strain-specific bifurcation in their subsequent mechanistic pathways.For P.elyakovii,the temperature shift triggered a fundamental functional reprogramming of its EPS,transitioning from a polysaccharide-dominated matrix at 4℃to a highly proteinaceous network at 18℃.This protein-rich EPS secreted a dense array of active functional groups(notably carboxyl and amino groups)that acted as highly efficient molecular nucleation templates.These templates captured ions from the seawater to induce the rapid,in-situ biomineralization of a compact calcium carbonate(calcite)layer.Rp data demonstrated that this hybrid bio-inorganic composite barrier dramatically elevated the interfacial polarization resistance by 3.2×105 Ω·cm2,effectively acting as a steric shield against the inward diffusion of corrosive species(O2 and Cl-).SVET mapping corroborated this by showing a near-complete suppression of localized anodic current peaks,confirming the onset of MICI.Conversely,the EPS of H.axialensis remained persistently dominated by highly permeable polysaccharides regardless of temperature.At 18℃,its biofilm evolved into a highly clumped,spatially heterogeneous architecture.This extreme non-uniformity established strong localized oxygen concentration cells.SVET analysis dynamically captured the intense micro-galvanic effects induced by this patchy biofilm,revealing highly localized anodic dissolution zones beneath thick biofilm clusters.Consequently,the corrosion morphology fundamentally shifted from the deep,narrow pitting observed at 4℃toward broad,shallow"sheet-like"localized attacks at 18℃,accompanied by a dramatic surge in the macroscopic corrosion rate to 0.22 mm/a.Ultimately,this work establishes a novel biofilm-corrosion mechanistic model,proposing for the first time that environmentally driven shifts in EPS chemistry(specifically the protein-to-polysaccharide ratio)and biofilm spatial heterogeneity are the primary fundamental regulators governing the transition between MIC and MICI.These discoveries provide critical scientific insights for the integrity assessment of structural steels in fluctuating extreme climates and suggest that harnessing specific protein-mediated biomineralizing biofilms could serve as a novel,nature-inspired corrosion control strategy.

郭娜;王玉浩;杨双龄;刘家兵;黄诗雨;郭章伟;刘涛

上海海事大学 海洋科学与工程学院,上海 201306上海海事大学 海洋科学与工程学院,上海 201306上海海事大学 海洋科学与工程学院,上海 201306上海海事大学 海洋科学与工程学院,上海 201306上海海事大学 海洋科学与工程学院,上海 201306上海海事大学 海洋科学与工程学院,上海 201306上海海事大学 海洋科学与工程学院,上海 201306

矿业与冶金

微生物腐蚀极地海洋细菌环境温度生物膜架构胞外聚合物生物矿化EH40钢表面防护

microbiologically influenced corrosion(MIC)polar marine bacteriaenvironmental temperaturebiofilm architectureextracellular polymeric substances(EPS)biomineralizationEH40 steelsurface protection

《表面技术》 2026 (18)

58-76,19

XX基础科研计划资助(JCKY2024413C003)上海市自然科学基金(24ZR1427800) XX Industrial Technology Development Program(JCKY2024413C003)the Natural Science Foundation of Shanghai(24ZR1427800)

10.16490/j.cnki.issn.1001-3660.2026.18.006

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