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PREDICTING SUBSURFACE ENRICHMENT/DEPLETION PROCESSES DURING HIGH-TEMPERATURE OXIDATION OF ALLOY 625 THIN FOILS

机译:在高温氧化合金625薄箔期间预测地下富集/耗尽过程

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For its high creep resistance the commercial nickel-base alloy 625 (UNS N06625) relies on solid solution strengthening in combination with precipitation hardening by formation of δ-Ni_3Nb and (Ni,Mo,Si)_6C precipitates during high-temperature service. In oxidizing environments the alloy forms a slow growing, continuous, and well adherent chromia layer on the material surface which protects the alloy against rapid oxidation attack. The growth of the chromia base oxide scale results in oxidation-induced chromium depletion in the subsurface zone of the alloy. SEM analyses of the cross-sectioned specimens revealed that this process results in formation of a wide subsurface zone in which the mentioned strengthening phases are dissolved, in spite of the fact that both phases do not contain substantial amounts of chromium. The cross-sectional analyses revealed that, in parallel to the formation of a precipitate depleted zone, a thin, continuous layer of niobium-rich intermetallic precipitates formed in the immediate vicinity of the scale/alloy interface. Thermodynamic computer modeling (Thermo-Calc) along with diffusion simulation software (DICTRA) was used to predict the oxidation-induced subsurface phase enrichment and depletion during oxidation (acronym SPEDO) in alloy 625 as a function of time. The modeling results are compared with the experimental findings concerning oxide scale and subsurface depletion layer formation obtained by scanning electron microscopy (SEM/EDX/WDX). The subsurface phase enrichment/depletion effect during oxidation is found to be substantially less pronounced in thin foils than in thick specimens of alloy 625. It is illustrated that this effect is related to the smaller reservoirs of the scale-forming element chromium as well as that of the 5-Ni3Nb phase stabilizing element niobium. As the thinner specimens become more rapidly depleted in chromium resulting in flatter chromium depletion profiles, a much weaker driving force for uphill-diffusion of Nb towards the scale/alloy interface leads to a substantially less pronounced δ-phase enrichment/depletion.
机译:对于其高蠕变电阻,商业镍基合金625(Uns NO6625)依赖于通过在高温服务期间形成δ-Ni_3NB和(Ni,Mo,Si)_6C沉淀的沉淀硬化的固体溶液。在氧化环境中,合金在材料表面上形成缓慢的生长,连续和良好的粘附染色层,该层可以保护合金免受快速氧化攻击。染色氧化物氧化术的生长导致合金地下区中的氧化诱导的铬耗尽。横截面样本的SEM分析显示,该方法导致形成宽地下区域,其中提到的强化相是溶解的,尽管两个相没有含有大量的铬。横截面分析显示,平行于沉淀耗尽区的形成,薄,连续层的富含铌的金属间沉淀物,其在刻度/合金界面的立即形成。热力学计算机建模(Thermo-Calc)以及扩散模拟软件(DICTRA)用于预测合金625中的氧化(首字母缩略词)期间氧化诱导的地下相富集和耗尽作为时间的函数。将建模结果与通过扫描电子显微镜(SEM / EDX / WDX)获得的氧化尺度和地下耗尽层形成的实验结果进行比较。发现氧化过程中的地下相富集/耗竭效果在薄箔上基本上不如合金625的厚试样在薄箔上。说明该效果与尺度形成元素铬的较小储存器相关,以及该效果5-Ni3NB相稳定元素铌。随着较薄的试样在铬中变得更快地耗尽,导致漂白铬耗尽型材,用于朝向刻度/合金界面的Nb的上坡扩散的较弱驱动力导致基本上不那么明显的Δ相富集/耗尽。

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