论文标题
溶解驱动的应力腐蚀和氢的一般多相理论
A generalised, multi-phase-field theory for dissolution-driven stress corrosion cracking and hydrogen embrittlement
论文作者
论文摘要
我们提出了一种基于磁场的电化学机械制剂,用于建模力学增强腐蚀和弹性塑料固体中的氢辅助破裂。多阶段的方法是首次使用应力腐蚀破裂的一般框架,既结合了阳极溶解和氢化机制。我们使用有限元法实现了我们的理论,并将其定义为主要运动学变量,位移成分,相位场腐蚀阶参数,金属离子浓度,相位场断裂阶参数和氢浓度。介绍了代表性的案例研究,以展示该模型在各种材料和环境中的预测能力,从而与基准测试和实验观察达成了有希望的一致性。我们表明,提出的广义配方可以作为环境的函数捕获阳极溶解和氢驱动的破坏机制之间的相互作用。包括从一个到另一个到另一个的过渡,它们的协同行动和个人发生。这样的广义框架可以为环境材料相互作用带来新的见解以及对应激腐蚀破裂的理解,如此处通过为Gruhl的开创性实验提供的第一个仿真结果所证明的那样。
We present a phase field-based electro-chemo-mechanical formulation for modelling mechanics-enhanced corrosion and hydrogen-assisted cracking in elastic-plastic solids. A multi-phase-field approach is used to present, for the first time, a general framework for stress corrosion cracking, incorporating both anodic dissolution and hydrogen embrittlement mechanisms. We numerically implement our theory using the finite element method and defining as primary kinematic variables the displacement components, the phase field corrosion order parameter, the metal ion concentration, the phase field fracture order parameter and the hydrogen concentration. Representative case studies are addressed to showcase the predictive capabilities of the model in various materials and environments, attaining a promising agreement with benchmark tests and experimental observations. We show that the generalised formulation presented can capture, as a function of the environment, the interplay between anodic dissolution- and hydrogen-driven failure mechanisms; including the transition from one to the other, their synergistic action and their individual occurrence. Such a generalised framework can bring new insight into environment-material interactions and the understanding of stress corrosion cracking, as demonstrated here by providing the first simulation results for Gruhl's seminal experiments.