This section outlines a theoretical background for the variational phase-field fracture model of solid deformable bodies. The model is considered isothermal and is derived under the assumptions of small-strain settings. The energy dissipation due to heat and sound release at the onset of fracture is neglected.
The general phase-field framework for monotonic fracture is derived first. The material behaviour is described by the elastoplastic material model based on the von Mises plasticity criterion with combined nonlinear isotropic and kinematic hardening. Lastly, the extension to cyclic fracture, i.e., fatigue is introduced.
Governing functional
An n-dimensional body \(\Omega \subset {\mathbb{R}}^{n}\), \(n \in \left[ {1,2,3} \right]\) with its surface \({\text{d}}\Omega \subset {\mathbb{R}}^{n - 1}\), evolving crack surface Γ(t) and displacement u is considered. Following the variational approach to fracture [19], the entire fracture process is governed by the minimization of the internal energy functional \(\Psi\) consisting of the body’s stored energy and the fracture induced dissipated energy, as follows
$$ \Psi = \int_{\Omega /\Gamma } {\psi \left( {{\varvec{\upvarepsilon}}} \right){\text{d}}\Omega } + \int_{\Gamma } {G_{c} {\text{d}}\Gamma } . $$
(1)
According to the Griffith’s theory of fracture, the materials fail upon reaching the critical value of fracture energy density Gc, which is a material property.
Fracture surface regularization
Explicit tracking of fracture surface Γ(t) can be numerically costly and complicated when the interactions between multiple cracks are considered, especially in 3D settings. Therefore, the basic idea of the phase-field models is to approximate this discrete surface Γ(t) by a crack density function \(\gamma \left( {\phi ,\nabla \phi } \right),\) using a phase-field order parameter \(\phi \in \left[ {0,1} \right]\) and length scale parameter l to control the width of the approximation zone. Parameter \(\phi\) describes the scalar damage field ranging smoothly between the broken \(\left( {\phi = 1} \right)\) and the intact \(\left( {\phi = 0} \right)\) material states, as proposed by Bourdin et al. [21]. That way the fracture surface energy \(\Psi^{{\text{f}}}\) can be calculated as a domain integral. Following the work of Miehe et al. [57] and model termed “Strain criterion with threshold model”, the crack density function is chosen as \(\gamma \left( {\phi ,\nabla \phi } \right) = \tfrac{3}{8\sqrt 2 }\left[ {\tfrac{1}{l}2\phi + l\left| {\nabla \phi } \right|^{2} } \right]\). Such model shows great resemblance to AT-1 model [58]. The local part of the crack density function γ is represented by a linear term responsible for recovering the linear elastic stage before the onset of fracture, which is not the case for the now-standard phase-field model with quadratic local term. The fracture induced dissipated energy can now be written as
$$ \Psi^{{\text{f}}} = \int_{\Omega } {\psi_{{\text{c}}} \left[ {2\phi + l^{2} \left| {\nabla \phi } \right|^{2} } \right]{\text{d}}\Omega } , $$
(2)
where \(\psi_{{\text{c}}} = \tfrac{3}{8\sqrt 2 }\tfrac{{G_{{\text{c}}} }}{l}\) is a constant specific fracture energy serving as an energetic threshold. Schematic representation of the sharp crack topology approximation by the phase-field parameter ϕ and the influence of length scale parameter l on the width of transition zone is clearly displayed in Fig. 3.
Bulk energy regularization
Correspondingly, the bulk energy term in (1) is regularized by the introduction of a monotonically decreasing degradation function \(g\left( \phi \right)\) to account for the subsequent loss of stiffness caused by the fracture initiation and propagation. The standard quadratic form \(g\left( \phi \right) = \left( {1 - \phi } \right)^{2}\) is chosen. For the detailed argumentation on the degradation function properties see Pham et al. [58] and Kuhn et al. [59]. The bulk energy term can now be written as
$$ \Psi^{{\text{b}}} = \int_{\Omega /\Gamma } {\psi \left( {{\varvec{\upvarepsilon}}} \right){\text{d}}\Omega } = \int_{\Omega }^{{}} {g\left( \phi \right) \cdot \psi \left( {{\varvec{\upvarepsilon}}} \right)} {\text{d}}\Omega . $$
(3)
Governing equations
The energy functional for the isotropic crack topology is written as
$$ \Pi = \Psi - W^{{{\text{ext}}}} $$
(4)
where \(W^{{{\text{ext}}}}\) is the external energy potential formulated as
$$ W^{{{\text{ext}}}} = \int_{\Omega } {{\overline{\mathbf{b}}}} \, \cdot {\mathbf{u}}\,{\text{d}}\Omega + \int_{\partial \Omega } {{\overline{\mathbf{t}}}} \cdot \,{\mathbf{u}}\,{\text{d}}\partial \Omega \,, $$
(5)
with \({\overline{\mathbf{b}}}\) and \({\overline{\mathbf{t}}}\) being the prescribed volume and surface force vectors, respectively. The regularized internal energy potential for monotonic fracture can now be written as follows
$$ \Psi \left( {{{\varvec{\upvarepsilon}}},\phi } \right) = \int_{\Omega } {g\left( \phi \right)\psi \left( {{\varvec{\upvarepsilon}}} \right){\text{d}}\Omega } + \psi_{{\text{c}}} \int_{\Omega } {\left[ {2\phi + l^{2} \left| {\nabla \phi } \right|^{2} } \right]{\text{d}}\Omega } . $$
(6)
The variation of the internal energy potential (6) yields
$$ {\updelta }\Psi = \tfrac{\partial \Psi }{{\partial {{\varvec{\upvarepsilon}}}}}\delta {{\varvec{\upvarepsilon}}} + \tfrac{\partial \Psi }{{\partial \phi }}\delta \phi = \int_{\Omega } {{{\varvec{\upsigma}}}\,{\updelta }{{\varvec{\upvarepsilon}}}\,} {\text{d}}\Omega + \int_{\Omega } {\left[ { - 2\left( {1 - \phi } \right)\psi \left( {{\varvec{\upvarepsilon}}} \right) + \tfrac{8\sqrt 2 }{3}\psi_{{\text{c}}} l\tfrac{{\partial \gamma \left( {\phi ,\nabla \phi } \right)}}{\partial \phi }} \right]} {\updelta }\phi \,{\text{d}}\Omega \,, $$
(7)
where the Cauchy stress σ is obtained as
$$ {{\varvec{\upsigma}}} = g\left( \phi \right)\frac{{\partial \psi \left( {{\varvec{\upvarepsilon}}} \right)}}{{\partial {{\varvec{\upvarepsilon}}}}} $$
(8)
Accordingly, the variation of the external energy potential is formulated as
$$ {\updelta }W^{{{\text{ext}}}} = \int_{\Omega } {{\overline{\mathbf{b}}}} \,{\updelta }{\mathbf{u}}\,{\text{d}}\Omega + \int_{\partial \Omega } {{\overline{\mathbf{t}}}} \,{\updelta }{\mathbf{u}}\,{\text{d}}\partial \Omega \,. $$
(9)
Implementing the small strain settings as \({{\varvec{\upvarepsilon}}} = \tfrac{1}{2}\left[ {\nabla {\mathbf{u}} + \nabla^{T} {\mathbf{u}}} \right]\) and the divergence theorem yields the variation of internal energy potential as
$$ \begin{aligned} \delta \Psi & = - \int_{\Omega } {\nabla \cdot {{\varvec{\upsigma}}}\delta {\mathbf{u}}} {\text{d}}\Omega + \int_{\Omega } {\left\{ {\tfrac{{{\text{d}}g\left( \phi \right)}}{{{\text{d}}\phi }}\psi \left( {{\varvec{\upvarepsilon}}} \right) + 2\psi_{{\text{c}}} \left[ {1 - l^{2} \Delta \phi } \right]} \right\}\delta \phi } {\text{d}}\Omega \\ & \quad + \,\int_{\partial \Omega } {{{\varvec{\upsigma}}} \cdot {\mathbf{n}}\delta {\mathbf{u}}} {\text{d}}\partial \Omega + 2\psi_{{\text{c}}} \int_{\partial \Omega } {l^{2} \nabla \phi \cdot {\mathbf{n}}\delta \phi } {\text{d}}\partial \Omega , \\ \end{aligned} $$
(10)
where n is the outward-pointing normal vector on the boundary ∂Ω. Corresponding strong form equations related to the minimization problem of the energy functional (4) can be now written as follows
$$ \nabla \cdot {{\varvec{\upsigma}}} + {\overline{\mathbf{b}}} = 0{\text{ in }}\Omega \,, $$
(11)
$$ {{\varvec{\upsigma}}} \cdot {\mathbf{n}} = {\overline{\mathbf{t}}}{\text{ on }}\partial \Omega_{{{\overline{\mathbf{t}}}}} \,, $$
(12)
$$ {\mathbf{u}} = {\overline{\mathbf{u}}}{\text{ on }}\partial \Omega_{{{\overline{\mathbf{u}}}}} \,, $$
(13)
$$ - l^{2} \Delta \phi + \left[ {1 + \tilde{D}} \right]\phi = \tilde{D}{\text{ in }}\Omega \,, $$
(14)
$$ \nabla \phi \cdot {\mathbf{n}} = 0{\text{ on }}\partial \Omega \,, $$
(15)
with \({\overline{\mathbf{u}}}\) as the prescribed displacement vector. The Helmholtz type equation (14) representing the evolution of the phase-field parameter ϕ is derived in terms of the crack driving state function D̃ [57], which takes the form
$$ \tilde{D} = \frac{{\psi \left( {{\varvec{\upvarepsilon}}} \right)}}{{\psi_{{\text{c}}} }} - 1. $$
(16)
It is then clear that the fracture evolution in the phase-field monotonic fracture model is governed by the deformation energy term \(\psi \left( {{\varvec{\upvarepsilon}}} \right)\). Note that \(\tilde{D}\) can be negative, leading to the unphysical solution \(\phi < 0\). Such behaviour is typical of models with linear local term in the crack density function \(\gamma\). A penalty function is introduced in [58]. On the other hand, the addition of Macaulay brackets also resolves the issue, as presented in [60, 61]
$$ \tilde{D} = \left\langle {\frac{{\psi \left( {{\varvec{\upvarepsilon}}} \right)}}{{\psi_{{\text{c}}} }} - 1} \right\rangle_{ + } . $$
(17)
Fracture irreversibility
The rate of dissipative fracture energy \(\dot{\Psi }^{{\text{f}}}\) has to be non-negative, \(\dot{\Psi }^{{\text{f}}} \ge 0\). Physically, it means preventing the crack healing after the load is removed. The basic idea is to somehow enforce the monotonicity of the phase-field parameter \(\phi\), i.e., \(\dot{\phi } \ge 0\). There are a few different approaches to irreversibility within the phase-field community, e.g., [32, 62]. In this work, the so-called implicit enforcement of the constraint is used. It is based on the previous observation of \(\tilde{D}\left( \psi \right)\) driving the fracture evolution (14). The irreversibility condition can be then imposed by introducing the history field parameter \({\mathcal{H}}\left( t \right)\) [22] as
$$ {\mathcal{H}}\left( t \right): = \max_{{\tau = \left[ {0,t} \right]}} \tilde{D}\left( {\psi \left( \tau \right)} \right){,} $$
(18)
thus rewriting the evolution equation (14) as
$$ - l^{2} \Delta \phi + \left[ {1 + {\mathcal{H}}} \right]\phi = {\mathcal{H}}{\text{ in }}\Omega \,. $$
(19)
As the crack driving force is now not allowed to decrease upon unloading, i.e., when \(\psi \left( {{\varvec{\upvarepsilon}}} \right)\) decreases, the constraint \(\dot{\phi } \ge 0\) is enforced. Furthermore, the introduction of history field parameter \({\mathcal{H}}\left( t \right)\) enables an elegant decoupling of the governing equation system characteristic to the staggered solution scheme.
Elastoplastic material model
The material behaviour is defined by the energy potential \(\psi \left( {{\varvec{\upvarepsilon}}} \right)\). In this work, the material is assumed to be elastoplastic to account for the ductile fracture phenomena characterized by an extensive plastic deformation prior to the onset of fracture. The energy potential \(\psi \left( {{\varvec{\upvarepsilon}}} \right)\) can then be written as
$$ \psi \left( {{\varvec{\upvarepsilon}}} \right) = \psi_{{\text{e}}} \left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} } \right) + \psi_{{\text{p}}} \left( {{{\varvec{\upvarepsilon}}}^{{\text{p}}} } \right), $$
(20)
where \({{\varvec{\upvarepsilon}}}^{{\text{e}}}\) and \({{\varvec{\upvarepsilon}}}^{{\text{p}}}\) represent elastic and plastic strain tensors additively contributing to the total strain \({{\varvec{\upvarepsilon}}} = {{\varvec{\upvarepsilon}}}^{{\text{e}}} + {{\varvec{\upvarepsilon}}}^{{\text{p}}}\). Such additive decomposition implies that the elastic response is not affected by plastic flow. Equation (3) now directly follows the phase-field ductile fracture model proposed in Miehe et al. [33], where the coupling between the accumulated plastic energy and fracture is achieved by the degradation of both elastic and plastic bulk energy.
Elastic energy density can be written as \(\psi_{{\text{e}}} \left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} } \right) = \tfrac{1}{2}\lambda {\text{tr}}^{2} \left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} } \right) + \mu {\text{tr}}\left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} } \right)^{2}\) with Lamé constants λ and μ. The plastic energy potential \(\psi_{{\text{p}}} \left( {{{\varvec{\upvarepsilon}}}^{{\text{p}}} } \right)\) can be represented by a large variety of plasticity models.Footnote 1 In this work, the von Mises yield criterion is used with the combined nonlinear isotropic and nonlinear kinematic hardening to account for cyclic plasticity. The plastic energy dissipation potential can then be written as
$$ \psi^{{\text{p}}} \left( {{{\varvec{\upvarepsilon}}}_{{}}^{{\text{p}}} } \right) = \int_{0}^{t} {\left( {{{\varvec{\upsigma}}}^{ * } - {{\varvec{\upalpha}}}} \right):{\dot{\mathbf{\varepsilon }}}_{{}}^{{\text{p}}} {\text{d}}t} , $$
(21)
where \({{\varvec{\upsigma}}}^{ * }\) is the effective (non-degraded) Cauchy stress tensor and \({{\varvec{\upalpha}}}\) is the backstress tensor accounting for the shift of the yield surface. Note that the equations are derived in the effective stress space, meaning that the plastic material behaviour is decoupled from the previously shown fracture part of the model. The effective plastic energy dissipation potential \(\psi^{{\text{p}}}\) is convex and positive satisfying \(\psi^{{\text{p}}} \left( 0 \right) = 0\). The von Mises pressure-independent yield function states
$$ F = \left\| {{\text{dev}}\left[ {{{\varvec{\upsigma}}}^{ * } } \right] - {{\varvec{\upalpha}}}} \right\| - \sqrt {\tfrac{2}{3}} \sigma_{{\text{y}}} \left( {\varepsilon_{{{\text{eqv}}}}^{{\text{p}}} } \right) \le 0, $$
(22)
where \(\left\| {\mathbf{x}} \right\| = \sqrt {{\mathbf{x}} \cdot {\mathbf{x}}}\) is an Euclidean norm. In the cyclic plasticity model with combined nonlinear kinematic hardening, the associated plastic flow is assumed as
$$ {\dot{\mathbf{\varepsilon }}}^{{\text{p}}} = \lambda \frac{\partial F}{{\partial {{\varvec{\upsigma}}}^{ * } }}, $$
(23)
where \(\lambda\) is the plastic multiplier. The assumption of associated plastic flow is acceptable for metals subjected to cyclic loading if microscopic details are not of interest. In Eq. (20), \(\dot{\varepsilon }_{{{\text{eqv}}}}^{{\text{p}}}\) is the equivalent plastic strain rate whose evolution is defined as
$$ \dot{\varepsilon }_{{{\text{eqv}}}}^{{\text{p}}} = \sqrt {\tfrac{2}{3}{\dot{\mathbf{\varepsilon }}}^{{\text{p}}} :{\dot{\mathbf{\varepsilon }}}^{{\text{p}}} } . $$
(24)
The saturation type isotropic hardening \(\sigma_{y} \left( {\varepsilon_{{{\text{eqv}}}}^{{\text{p}}} } \right) = \sigma_{y}^{0} + Q_{\infty } \left( {1 - \exp \left[ { - b\varepsilon_{{{\text{eqv}}}}^{{\text{p}}} } \right]} \right)\) controls the size of the yield surface, where \(\sigma_{y}^{0}\) is the elasticity limit, \(Q_{\infty }\) and \(b\) are material parameters defining the maximum increase in yield stress due to hardening at saturation (when \(\varepsilon_{{{\text{eqv}}}}^{{\text{p}}} \to \infty\)), and the rate of saturation, respectively.
Kinematic hardening evolution law is defined according to Chaboche [63] multicomponent model as
$$ {\dot{\mathbf{\alpha }}}_{k} = C_{k}^{{}} \frac{1}{{\sigma_{y} \left( {\varepsilon_{{{\text{eqv}}}}^{{\text{p}}} } \right)}}\left( {{{\varvec{\upsigma}}}^{ * } - {{\varvec{\upalpha}}}} \right)\dot{\varepsilon }_{{{\text{eqv}}}}^{{\text{p}}} - \gamma_{k}^{{}} {{\varvec{\upalpha}}}_{k} \dot{\varepsilon }_{{{\text{eqv}}}}^{{\text{p}}} . $$
(25)
Each backstress component \({{\varvec{\upalpha}}}_{k}\) is defined by the material parameters \(C_{k}\) and \(\gamma_{k}\) determining the initial kinematic hardening modulus and the rate of its decrease with increasing plastic deformation, respectively. The addition of the nonlinear term thus limits the translation of the yield surface in principal stress space. The total backstress tensor is then obtained as
$$ {{\varvec{\upalpha}}} = \sum\limits_{k} {{{\varvec{\upalpha}}}_{k} } . $$
(26)
When kinematic material parameters \(C_{k}\) and \(\gamma_{k}\) are set to zero, the model reduces to an isotropic hardening model. Moreover, when only \(\gamma_{k}\) is set to zero, the linear Ziegler hardening law is recovered, removing the limiting surface. The isotropic and kinematic hardening phenomena are schematically represented in Fig. 4 in the deviatoric stress space.
The combined isotropic-kinematic model features allow modelling of inelastic deformation in metals subjected to the cyclic loads and resulting in low-cycle fatigue failure. Such models are able to reproduce the characteristic cyclic phenomena as Bauschinger effect causing a reduced yield stress upon load reversal; plastic shakedown characteristic of symmetric stress- or strain-controlled experiments where soft or annealed metals tend to harden toward a stable limit, and initially hardened metals tend to soften; progressive “ratcheting” or “creep” in the direction of the mean stress related to the unsymmetrical stress cycles between prescribed limits; or the relaxation of the mean stress observed in an unsymmetrical strain-controlled experiment.
Modification for fracture in tension
To prevent the unphysical crack propagation in the compressive state, the bulk energy term can now be rewritten as
$$ \Psi^{b} = \int_{\Omega }^{{}} {\left\{ {g\left( \phi \right) \cdot \psi^{ + } \left( {{\varvec{\upvarepsilon}}} \right) + \psi^{ - } \left( {{\varvec{\upvarepsilon}}} \right)} \right\}} {\text{d}}\Omega , $$
(27)
by introducing an additive decomposition of the deformation energy where \(\psi^{ + } \left( {{\varvec{\upvarepsilon}}} \right) = \psi_{{\text{e}}}^{ + } \left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} } \right) + \psi_{{\text{p}}} \left( {{{\varvec{\upvarepsilon}}}^{{\text{p}}} } \right)\) and \(\psi^{ - } \left( {{\varvec{\upvarepsilon}}} \right) = \psi_{{\text{e}}}^{ - } \left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} } \right)\). The volumetric-deviatoric decomposition proposed by Amor [64] is used as
$$ \begin{gathered} \psi_{{\text{e}}}^{ + } : = \tfrac{1}{2}\left( {\lambda + \tfrac{2\mu }{n}} \right)\left\langle {{\text{tr}}\left( {{\varvec{\upvarepsilon}}} \right)} \right\rangle_{ + }^{2} + \mu \left( {{{\varvec{\upvarepsilon}}}_{{{\text{dev}}}} :{{\varvec{\upvarepsilon}}}_{{{\text{dev}}}} } \right), \hfill \\ \psi_{{\text{e}}}^{ - } : = \tfrac{1}{2}\left( {\lambda + \tfrac{2\mu }{n}} \right)\left\langle {{\text{tr}}\left( {{\varvec{\upvarepsilon}}} \right)} \right\rangle_{ - }^{2} , \hfill \\ \end{gathered} $$
(28)
in terms of Macaulay brackets \(\left\langle x \right\rangle_{ \pm } = \tfrac{x \pm \left| x \right|}{2}\). n represents the dimension number and \({{\varvec{\upvarepsilon}}}_{{{\text{dev}}}} : = \left( {{{\varvec{\upvarepsilon}}} - \tfrac{1}{3}{\text{tr}}\left( {{\varvec{\upvarepsilon}}} \right){\mathbf{I}}} \right)\) stands for the deviatoric part of the strain tensor. Since the plastic energy potential is derived in the deviatoric stress plane following the von Mises yield criterion, only the elastic deformation energy contributes to \(\psi^{ - } \left( {{\varvec{\upvarepsilon}}} \right)\). Correspondingly, Eq. (8) for stress \({{\varvec{\upsigma}}}\) is now rewritten as.
$${{\varvec{\upsigma}}} = g\left( \phi \right)\frac{{\partial \psi^{ + } \left( {{\varvec{\upvarepsilon}}} \right)}}{{\partial {{\varvec{\upvarepsilon}}}}} + \frac{{\partial \psi^{ - } \left( {{\varvec{\upvarepsilon}}} \right)}}{{\partial {{\varvec{\upvarepsilon}}}}}$$
(29)
while the crack driving state function now includes only the positive energy part as
$$ \tilde{D} = \left\langle {\frac{{\psi_{{\text{e}}}^{ + } }}{{\psi_{{\text{c}}} }} + \frac{{\psi_{{\text{p}}} }}{{\psi_{{\text{c}}} }} - 1} \right\rangle_{ + } . $$
(30)
Fatigue extension
The current model is actually capable of producing some features of the low-cyclic fatigue regime. The plastic potential (21) is monotonic and irreversible, by definition, causing the crack driving state function (30) to increase during the loading cycles, eventually leading to the onset of fracture. On the other hand, it is not able to reproduce the crack initiation, nor the crack growth, when the applied cyclic loads are below the plasticity limit in ductile materials, or the fracture limit in brittle materials, corresponding to the high-cyclic fatigue regime.
In this subsection, the phase-field model for brittle and ductile fracture is extended to account for the fatigue phenomena. The presented extension contains only one additional material parameter (\(\overline{\psi }_{\infty }\), explained later), enabling it to reproduce the main material fatigue features. The goal is then to produce a generalized phase-field framework which can, depending on the type of loading, recover brittle/ductile fracture in monotonic as well as low- and high-cycle fatigue regime, including the transition. The general idea is to introduce the fracture energy degradation due to the repeated externally applied loads. Physically, it would mean the degradation of material fracture properties during the cyclic loading, which eventually causes the crack initiation and propagation occurrence at lower loads. In a way, material “mileage” would be introduced. To that end, a local energy accumulation variable \(\overline{\psi }\left( t \right)\) is introduced accounting for the changes in deformation energy \(\psi \left( {{\varvec{\upvarepsilon}}} \right)\) during the loading cycles, thus taking the structural loading history into account. A fatigue degradation function \(\hat{F}\left( {\overline{\psi }} \right)\) is introduced only affecting the fracture energy term as discussed. The generalised internal energy potential can be now written as
$$ \begin{aligned} \Psi \left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} ,{{\varvec{\upvarepsilon}}}^{{\text{p}}} ,\phi ,\overline{\psi }} \right) &= \int_{\Omega } {\left\{ {g\left( \phi \right)\left[ {\psi_{{\text{e}}}^{ + } \left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} } \right) + \psi_{{\text{p}}} \left( {{{\varvec{\upvarepsilon}}}^{{\text{p}}} } \right)} \right] + \psi_{{\text{e}}}^{ - } \left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} } \right)} \right\}{\text{d}}\Omega } \\ &\quad +\, \int_{\Omega } {\hat{F}\left( {\overline{\psi }} \right)\psi_{{\text{c}}} \left[ {2\phi + l\left| {\nabla \phi } \right|^{2} } \right]{\text{d}}\Omega } \end{aligned} . $$
(31)
This model is in line with the phase-field fatigue fracture formulation for the brittle materials, proposed in Carrara et al. [51] and Alessi et al. [50]. In line with previous Sections, the modified crack driving state function D̃ is now defined as
$$ \tilde{D} = \left\langle {\frac{{\psi_{{\text{e}}}^{ + } }}{{\hat{F}\left( {\overline{\psi }} \right)\psi_{{\text{c}}} }} + \frac{{\psi_{{\text{p}}} }}{{\hat{F}\left( {\overline{\psi }} \right)\psi_{{\text{c}}} }} - 1} \right\rangle_{ + } . $$
(32)
Local energy accumulation variable \(\overline{\psi }\left( t \right)\)
This variable is conceived as a local measure of repeated deformation energy changes during the loading history. It is a major feature of the novel generalized phase-field fatigue formulation. To fully fit into this framework, it should not affect the proportional (monotonic) loading case. To satisfy this condition, in this work, the variable is introduced as the sum of negative differences of the total deformation energy during the cyclic loading. That way, the variable value increases only during the unloading part of the cycle, consequently degrading the fracture material properties. Note that the plastic deformation energy \(\psi_{{\text{p}}} \left( t \right)\) is dissipative, and therefore never decreasing. The degradation of fracture properties due to fatigue is then, in fact, only influenced by the repetitive changes in elastic deformation energy \(\psi_{{\text{e}}} \left( {{{\varvec{\upvarepsilon}}}^{{\text{e}}} } \right).\)
The basic idea is explained schematically on the example of 1D bar subjected to the sinusoidal displacement with load ratio \(R = 0\), defined as the ratio of the minimum and maximum loads during the cyclic loading, and three different amplitudes A1 < A2 < A3. Unlike the amplitudes A2 and A3, the loading amplitude A1 is below the material plastic limit, characteristic to the high-cycle fatigue regime. The evolution of total energy \(\left( {\psi_{{\text{e}}} + \psi_{{\text{p}}} } \right)\) and energy accumulation variable \(\overline{\psi }\left( t \right)\) is shown in Fig. 5.
The maximum deformation energy value of curve corresponding to the amplitude A1 does not increase through the course of cycles. On the other hand, the increase of the maximum total deformation energy due to the increase of plastic dissipation \(\psi_{{\text{p}}} \left( t \right)\) over the cycles can be clearly seen for curves corresponding to amplitudes A2 and A3. Furthermore, a clear peak shift to the left caused by the kinematic hardening plasticity is observed.
The only difference distinguishing between the high- and low-cycle fatigue regime is the influence of increasing plastic energy \(\psi_{{\text{p}}} \left( t \right)\) on the crack driving state function D̃ in the low-cycle fatigue regime. The competition is thus introduced between the total deformation energy \(\left( {\psi_{{\text{e}}} + \psi_{{\text{p}}} } \right)\) (whose maximal value is constant for the case of high-cyclic fatigue regime, and increasing in low-cyclic for the case of constant load amplitudes), and the fracture resistance decrease due to the repetitive change in elastic energy, i.e., fatigue.
The local energy accumulation function can be then formulated in the integral form as
$$ \overline{\psi }\left( t \right) = \int_{0}^{t} {\psi_{{\text{e}}} \left( t \right)H\left( { - \dot{\psi }_{{\text{e}}} } \right)} {\text{d}}t, $$
(33)
where \(H\left( { - \dot{\psi }_{{\text{e}}} } \right)\) is the Heaviside function taking the value of 1 when \(\dot{\psi }_{{\text{e}}} < 0\) and the value of 0 when \(\dot{\psi }_{{\text{e}}} \le 0\). The incremental form can be written as
$$ \overline{\psi }_{N} = \overline{\psi }_{N - 1} - \left\langle {\psi_{N} - \psi_{N - 1} } \right\rangle_{ - } , $$
(34)
where N is the cycle number.
The energy accumulation variable increases only during the unloading, thus not affecting the proportional loading cases, as clearly seen in Fig. 5b.
Mean load effect
The energy accumulation variable description implicitly includes the mean load effect often expressed by a load ratio \(R\). For the shown case of strain-control loaded bar, the load ratio can be expressed as \(R = \tfrac{{\varepsilon_{\min } }}{{\varepsilon_{\max } }},\) with \(\varepsilon_{{\text{M}}} = \tfrac{{\varepsilon_{\max } + \varepsilon_{\min } }}{2}\) being the mean strain imposed to the bar. The deformation energy amplitude can then be written as \(\Delta \psi_{{\text{e}}} = \tfrac{1}{2}E\left( {\varepsilon_{\max }^{2} - \varepsilon_{\min }^{2} } \right) = 2E\varepsilon_{{\text{M}}}^{2} \tfrac{{1 + R^{2} }}{{\left( {1 + R} \right)^{2} }},\) for the case where maximum load value does not reach the plastic yield limit, and \(R \ge 0\). This clearly proves the mean load, and the load ratio influence is implicitly considered in this energy accumulation variable description. It is further explained on the example of 1D bar loaded with sinusoidal displacements B1 and B2 of same amplitudes, but different mean values, as presented in Fig. 6.
Loads of the same displacement amplitudes, or strain therefore, with different mean values, produce much different deformation energy values. Consequently, the accumulated energy variable obtained by the higher mean load case (B2 in Fig. 6) increases much faster than in the lower mean load case (B1), as predicted.
Fatigue degradation function \(\hat{F}\left( {\overline{\psi }} \right)\)
Following the proper definition of the energy accumulation variable \(\overline{\psi }\left( t \right)\), the degradation of the fracture energy has to be defined. Herein, the fatigue degradation function \(\hat{F}\left( {\overline{\psi }} \right) \in \left[ {0,1} \right]\) is introduced. It should be continuous and piecewise differentiable with the following properties
$$ \begin{gathered} \hat{F}\left( {\overline{\psi } = 0} \right) = 1, \, \\ \hat{F}\left( {\overline{\psi } \to \infty } \right) = 0, \, \\ \frac{{{\text{d}}\hat{F}}}{{{\text{d}}t}}\left( {0 < \overline{\psi } < \infty } \right) \le 0. \\ \end{gathered} $$
(35)
Similar degradation function properties have been used in [50, 51]. In this work, three functions are presented fitting the description
$$ \begin{gathered} \hat{F}_{1} = \left( {1 - \frac{{\overline{\psi }}}{{\overline{\psi } + \overline{\psi }_{\infty } }}} \right)^{2} {\text{ for }}\overline{\psi } \in \left[ {0, + \infty } \right], \hfill \\ \hat{F}_{2} = \left( {1 - \frac{{\overline{\psi }}}{{\overline{\psi }_{\infty } }}} \right)^{2} {\text{ for }}\overline{\psi } \in \left[ {0,\overline{\psi }_{\infty } } \right], \hfill \\ \hat{F}_{3} = \left( {\xi \log \frac{{\overline{\psi }_{\infty } }}{{\overline{\psi }}}} \right)^{2} {\text{ for }}\overline{\psi } \in \left[ {\overline{\psi }_{\infty } ,10^{{\frac{1}{\xi }}} \cdot \overline{\psi }_{\infty } } \right]. \hfill \\ \end{gathered} $$
(36)
Their respective semi-logarithmic graphs are shown in Fig. 7. In Eq. (36), \(\overline{\psi }_{\infty }^{{}}\) is the newly introduced parameter used to bound the functions between 0 and 1, and is therefore included in every function. It can be seen as a fatigue material parameter whose physical interpretation will be provided through the next simple examples, as well as the numerical examples in Sect. 4. The parameter \(\xi\) embedded into \(\hat{F}_{3}\) is introduced to allow for better fine-tuning.
The following figures present the proposed fatigue degradation functions in terms of number of cycles N, for the cyclically loaded 1D bar. Pure elastic material behaviour is assumed leading to a constant change of the elastic deformation energy \(\Delta \psi\) between each cycle. A clear link between the number of cycles N, and energy accumulation variable \(\overline{\psi }\), can be then constructed as \(\overline{\psi } = \Delta \psi \cdot N.\) Figure 7 shows the influence of the parameter \(\overline{\psi }_{\infty }^{{}}\) in each function expressed as the multiples of elastic deformation energy increment at each cycle \(\Delta \psi\).
The parameter \(\overline{\psi }_{\infty }\) obviously affects the number of cycles at which the fatigue degradation takes off, with all other parameters being equal. The physical interpretation of this parameter will be explored through the parametric study conducted in Sect. 4. On the other hand, the increase in the loading amplitude would cause earlier onset of fatigue degradation. Lastly, the influence of the tuning parameter \(\xi\) is observed in Fig. 8.