SearcharxivSearch

arXiv · 2509.03363

Variation-matching sensitivity-based virtual fields for hyperelastic material model calibration

Abstract

Accurate identification of nonlinear material parameters from three-dimensional full-field deformation data remains a challenge in experimental mechanics. The virtual fields method (VFM) provides a powerful, computationally efficient approach for material model calibration, however, its success depends critically on the choice of virtual fields and the informativeness of available kinematic data. In this work, we advance the state-of-the-art discrete formulation of the sensitivity-based virtual fields (SBVF) method by systematically developing and comparing alternative variational and analytical SBVFs within a strain-invariant-based modeling framework. A central contribution of this work is the implementation and assessment of variation-based SBVFs (vSBVFs), formulated using directional G\^ateaux derivatives, as well as virtual fields derived from analytical differentiation (aSBVFs) which provide explicit, model-tailored virtual displacement fields for parameter identification. Using simulated noisy volumetric datasets, we demonstrate that vSBVFs and aSBVFs enable procedural, automated construction of optimal virtual fields for each material parameter, substantially enhancing the robustness and efficiency of calibration without the need for manual field selection or high temporal resolution in the data acquisition. We quantify data richness -- the effective diversity of sampled kinematic states -- showing that increased data richness via sample geometry and loading protocols leads to improved parameter identifiability. These findings establish a pathway for automated, noise-robust material model calibration suitable for future deployment with experimental full-field imaging of soft, complex materials, and provide a foundation for optimizing shape topology and extending to viscoelastic and anisotropic behaviors.

Explore related subjects

Keep this discovery

BibTeXRIS

Denislav P. Nikolov, Zhiren Zhu, Jonathan B. Estrada. 2025-09-03. Variation-matching sensitivity-based virtual fields for hyperelastic material model calibration. https://doi.org/10.1111/str.70031

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Slow Dynamics and the Geometry of Jammed Packings

Saddle points in the energy landscape of granular packings dominate the discrete steepest descent dynamics and ultimately determine the path that an out of mechanical equilibrium packing will follow and the resulting stable minimum that it will find. The saddle points that ultimately determine the resulting minima tend to be low-index saddle points. For models with an analytic energy landscape, such as the $p$-spin model, the steepest descent minimization path is affected by higher-index saddle points, which pull the system towards saddle points of decreasing index before arriving at the minima. Here, we examine the steepest descent minimization path of granular packings and compare them to the $p$-spin model. We show that the granular packing steepest descent minimization paths act like their smooth energy landscape counterparts and get attracted by saddle points. The index versus time curves for all models follow a shifted, stretched exponential. We further show that the shape parameter for the granular packings is unchanged when the energy landscape is modified to become analytic (Gaussian potential in a harmonic well) or non-local (Mari-Krzakala-Kurchan). The $p$-spin, on the other hand, has a significantly larger shape parameter. The reason is not due to the dimensionality, packing fraction, nonanalyticity, or the locality of the Hamiltonian of the models. The exact reason for the discrepancy in the shape parameter is \st{still} an unsolved mystery.

cond-mat.soft

A Phase-Field Study of Desiccation Crack Pattern Maturation under Drying-Wetting Cycles

The characteristic intersection angle of the desiccation crack relaxes from near \ang{90} toward \ang{120} under repeated drying--wetting cycles. However, the theoretical understanding of this relaxation is insufficient, especially the modeling of the drying--wetting cycles. Here we introduce a phase-field model of desiccation fracture, extending the model proposed in previous studies by adding crack healing and a scar effect left by past cracks. By repeating drying--wetting cycles in a finite element simulation, we find that the angle distribution develops a growing peak near \ang{120} as the cycle number increases, consistent with experiments. The standard deviation of the intersection angle from \ang{120} relaxes exponentially with a characteristic time of about 2.85 cycles. These results are consistent with experiments, except that the characteristic time is slightly smaller than the experimental value. Crack energy dominates the total energy and also relaxes exponentially with nearly the same characteristic cycle as the angle relaxation. This decay is driven mainly by a shortening of the effective crack length rather than a change in effective fracture toughness.

cond-mat.soft

Kinetics of ferritin crystal formation and melting in acoustically levitated droplets

Understanding protein crystallization pathways is essential for controlling crystallization in structural biology, materials science, and pharmaceutical applications. Classical nucleation theory does not fully capture crystallization processes for several proteins, including ferritin. Here, we combine acoustic levitation with small- and wide-angle X-ray scattering (SAXS and WAXS) to monitor ferritin crystallization in evaporating aqueous polyethylene glycol (PEG) solutions. Acoustic levitation rapidly drives the droplets through a broad range of protein and polymer concentrations, enabling time-resolved measurements of crystallization during evaporation. The scattering data show that ferritin crystals form during evaporation and subsequently lose their crystalline order upon further dehydration. Varying the PEG molecular weight switches between distinct crystallization pathways: one dominated by attractive protein-protein interactions and another dominated by repulsive interactions and excluded-volume effects. Furthermore, we find that lower molecular weight PEG (1000 g/mol) suppresses the dehydration-induced loss of crystalline order observed for higher molecular weight PEG (6000 g/mol), providing a simple strategy for improving protein crystal stability.

cond-mat.soft