N80钢表面金属氮化物涂层的阻氢性能及机理

Research on hydrogen barrier performance and mechanism of metal nitride coatings on N80 steel surface

  • 摘要:
    目的 盐穴储氢场景下注采管面临严重的氢脆与腐蚀风险,亟需研发高效的阻氢防护涂层。系统性地评估并对比具有代表性的涂层,对于筛选与设计适用于盐穴储氢环境的涂层防护技术至关重要。
    方法 利用多弧离子镀法在N80钢上分别制备了TiN、AlCrN及(TiAlCrSiY)N涂层。采用Devanathan-Stachurski双电解池,在电化学监测的液相与气相两种充氢模式下,系统评价各涂层的阻氢渗透性能,并通过电化学极化曲线测试评估其耐腐蚀性。使用扫描电镜(Scanning Electron Microscope, SEM)、数码显微镜等对涂层的微观结构与性能进行表征。通过对比分析TiN、AlCrN及(TiAlCrSiY)N涂层的综合防护性能,探究其内在机理的差异,为盐穴储氢环境下的阻氢涂层选材与设计提供科学依据。
    结果 AlCrN涂层表现出最佳的综合性能,其表面最致密平整、缺陷最少,并具备最高硬度与最强结合力。(TiAlCrSiY)N涂层虽因多元素协同效应而耐腐蚀性最优,但存在较多表面团聚颗粒与微观缺陷,结合力在3种涂层中最差。氢渗透性能测试结果表明,AlCrN涂层阻氢效果最好,与N80基材相比,有效扩散系数降低了83.68%,在气相与液相条件下阻氢效率分别高达99.23%、84.76%。TiN、AlCrN及(TiAlCrSiY)N涂层均有较好的阻氢效果,同时可提高基材的表面强度,增强抗蚀性能。测试分析结果表明,涂层微观结构的致密性是决定其阻氢与力学性能的首要因素,而耐腐蚀性能主要受化学组分影响。
    结论 未来盐穴储氢库阻氢防护涂层开发应优先通过工艺优化来获得低缺陷的致密结构,其次进行成分优化增强化学稳定性,同步提升其耐腐蚀特性与机械性能,对于保障盐穴储氢库安全运行具有重要工程意义。

     

    Abstract:
    Objective Injection and production pipes in salt cavern hydrogen storage face severe risks of hydrogen embrittlement and corrosion. There is an urgent need to develop highly effective hydrogen barrier coatings. This study aims to systematically evaluate and compare representative coatings to guide the selection and design of protection technologies suited to the salt cavern hydrogen storage environment.
    Methods TiN, AlCrN, and (TiAlCrSiY)N coatings were prepared on N80 steel via multi-arc ion plating. Their hydrogen permeation resistance was systematically assessed using a Devanathan-Stachurski double-electrolytic cell under two hydrogen charging modes (electrochemical monitoring in liquid and gas phases). Corrosion resistance was evaluated through electrochemical polarization curve tests. The microstructures and properties of the coatings were characterized by scanning electron microscope (SEM) and digital microscopy. By comparing the comprehensive protective performance of TiN, AlCrN, and (TiAlCrSiY)N coatings, differences in underlying mechanisms were analyzed to provide a scientific basis for selecting and designing hydrogen barrier coatings for salt cavern hydrogen storage environments.
    Results The AlCrN coating demonstrated the best overall performance, featuring the densest, flattest surface, fewest defects, highest hardness, and strongest bonding. Although the (TiAlCrSiY)N coating exhibited superior corrosion resistance due to the synergistic effect of multiple elements, it had numerous surface agglomerates, micro-defects, and the weakest bonding among the three coatings. Hydrogen permeation tests showed that AlCrN provided the most effective barrier, reducing the effective diffusion coefficient by 83.68% compared to the N80 substrate, with hydrogen barrier efficiencies of 99.23% in the gas phase and 84.76% in the liquid phase. All three coatings—TiN, AlCrN, and (TiAlCrSiY)N—offered good hydrogen barrier properties and enhanced substrate strength and corrosion resistance. The test and analysis results indicated that coating microstructure compactness primarily determined hydrogen barrier and mechanical properties, while corrosion resistance depended mainly on chemical composition.
    Conclusion In developing hydrogen barrier coatings for salt cavern hydrogen storage, priority should be given to achieving a dense, low-defect structure through process optimization, followed by composition optimization to enhance chemical stability. Simultaneously improving corrosion resistance and mechanical properties is crucial for ensuring the safe operation of salt cavern hydrogen storage facilities.

     

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