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Energy Release Rate in Fracture Mechanics.

机译:断裂力学中的能量释放率。

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This dissertation aims at developing theories and methods to simulate dynamic crack propagation in large deformation. The analytical solution of linear elastic fracture mechanics is utilized to find the shape of the crack surface after deformation. It is discovered that the deformed shape of a line crack is an ellipse and the deformed shape of an elliptical void is also an ellipse under mode I tensile loading. A numerical example shows that the small strain formulation in linear elastic fracture mechanics overestimates the crack tip stress compared to large strain formulation. Therefore stress intensity factor, as a conclusion from linear elastic fracture mechanics, is not accurate in large deformation or at the close neighborhood of crack tip. Energy release rate fracture criterion is revisited by taking molecular dynamics point of view. It is proved by theory and numerical example that the critical energy release rate is not related to surface energy. The energy release rate is the decrease of potential energy per unit crack advance. The surface energy is the increase of potential energy per unit crack advance. The two quantities always have an opposite signs therefore they cannot be equal. It is suggested that the energy release rate is also the kinetic and/or thermal energy generation rate according to conservation of energy. It is noticed that the plasticity exists even in perfect brittle fracture due to the lattice reorientation occurring at the edge of the material. Fracture is a dynamic and irreversible process in nature. It is emphasized that proper region should be chosen to calculate the energy release rate. Such region should enclose the crack tip plastic zone and the part of the elastic zone that involves lattice relaxation, but exclude the plastic zone not related to crack. The same principle also applies to J-integral. Therefore such integral is path dependent. A general method is proposed to calculate energy release rate in molecular dynamics for dynamic or static, brittle or ductile fracture. The equivalency between interatomic potential energy and strain energy is established with new definitions for stress and strain in molecular dynamics. Here, in molecular dynamics, strain energy is defined as the area under the stress-strain curve. The stress and the strain are defined on each atom by taking the summation and the average, respectively, of the influence from all other atoms. Such stress and strain satisfy conjugacy in multi-atom cases with arbitrary configuration under zero temperature. Due to the equivalency of strain energy and interatomic potential energy, the potential energy release rate calculated in molecular dynamics is the same as the strain energy release rate in continuum mechanics. The node release method in finite element analysis is rigorously formulated and verified. The formula to calculate energy release rate in node release method is proposed and validated. The methods to control the crack speed, energy release rate, crack initiation, crack propagation and crack direction are proposed. With such methods, the following conclusions are made: (1) Node release method does not influence material behavior prior to crack extension. (2) Node release method is independent of the steps chosen to release the force. (3) The force-displacement relationship of the releasing nodes, often referred as the cohesive law, depends on the crack speed. The linear relationship is only valid with slow crack speed. (4) Node release method is able to calculate static energy release rate with great accuracy. The static energy release rate is dynamic energy release rate with a slow crack speed. (5) Node release method can be applied to specimen with no initial crack. Therefore the fracture toughness can be obtained from simple tension test. (6) Node release method can simulate dynamics crack propagation. The linear relationship between static and dynamics energy release rates, G=G0 (1--v/vR) , is in good agreement with simulation result. In the simulation, the crack speed asymptotically reaches Rayleigh wave speed in elastic material with fixed grip boundary condition. (7) It is discovered that plasticity is one of the mechanisms that reduces the crack speed. The crack in elasto-plastic material will asymmetrically reach 60% of Rayleigh wave speed. (8) The plasticity influences the crack path in mixed mode fracture. For convenience, all units are normalized Unless otherwise specified.
机译:本文旨在研究模拟大变形动态裂纹扩展的理论和方法。利用线性弹性断裂力学的解析解求出变形后裂纹表面的形状。发现在模式I拉伸载荷下,线裂纹的变形形状是椭圆形,并且椭圆形空隙的变形形状也是椭圆形。数值示例表明,与大应变公式相比,线性弹性断裂力学中的小应变公式高估了裂纹尖端应力。因此,根据线性弹性断裂力学得出的结论,应力强度因子在大变形或裂纹尖端附近不准确。从分子动力学的角度重新探讨了能量释放速率断裂准则。理论和数值算例表明,临界能量释放速率与表面能无关。能量释放速率是每单位裂纹前进的势能的减少。表面能是每单位裂纹前进的势能的增加。这两个量始终具有相反的符号,因此它们不能相等。建议能量释放速率也是根据能量守恒的动能和/或热能生成速率。注意到由于在材料边缘发生的晶格重新取向,甚至在完全脆性断裂中也存在可塑性。断裂本质上是一个动态且不可逆的过程。要强调的是,应该选择适当的区域来计算能量释放速率。该区域应包围裂纹尖端的塑性区和涉及晶格弛豫的弹性区部分,但不包括与裂纹无关的塑性区。相同的原理也适用于J积分。因此,这种积分取决于路径。提出了一种通用的方法来计算分子动力学中动态或静态,脆性或延性断裂的能量释放速率。原子间势能和应变能之间的等价关系是用分子动力学中应力和应变的新定义建立的。此处,在分子动力学中,应变能定义为应力-应变曲线下的面积。通过分别取所有其他原子的影响之和和平均值来定义每个原子的应力和应变。这样的应力和应变在零温度下以任意构型满足多原子情况下的共轭性。由于应变能和原子间势能的等价关系,分子动力学计算得出的势能释放率与连续力学中的应变能释放率相同。严格制定和验证了有限元分析中的节点释放方法。提出并验证了节点释放法中能量释放率的计算公式。提出了控制裂纹速度,能量释放速率,裂纹萌生,裂纹扩展和裂纹方向的方法。通过这种方法得出以下结论:(1)节点释放方法不影响裂纹扩展之前的材料性能。 (2)节点释放方法与选择释放力的步骤无关。 (3)释放节点的力-位移关系,通常称为内聚规律,取决于裂纹的速度。线性关系仅在裂纹速度较慢时有效。 (4)节点释放法能够高精度地计算出静态能量释放率。静态能量释放速率是具有缓慢裂纹速度的动态能量释放速率。 (5)节点释放方法可以应用于没有初始裂纹的试样。因此,可以通过简单的拉伸试验获得断裂韧性。 (6)节点释放方法可以模拟动力学裂纹的扩展。静态和动态能量释放速率之间的线性关系G = G0(1-v / vR)与仿真结果非常吻合。在模拟中,在具有固定抓地力边界条件的弹性材料中,裂纹速度渐近达到瑞利波速度。 (7)发现可塑性是降低裂纹速度的机制之一。弹塑性材料中的裂纹将不对称地达到瑞利波速的60%。 (8)塑性影响混合模式断裂的裂纹路径。为方便起见,所有单位均已标准化,除非另有说明。

著录项

  • 作者

    Wang, Leyu.;

  • 作者单位

    The George Washington University.;

  • 授予单位 The George Washington University.;
  • 学科 Engineering Mechanical.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 172 p.
  • 总页数 172
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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