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Review of selected fundamental topics on the interaction between phase transformations, fracture, and other structural changes in inelastic materials is presented. It mostly focuses on the concepts developed in the author's group over last three decades and numerous papers that affected us. It includes a general thermodynamic and kinetic theories with sharp interfaces and within phase field approach. Numerous analytical (even at large strains) and numerical solutions illustrate the main features of the developed theories and their application to the real phenomena. Coherent, semicoherent, and noncoherent interfaces, as well as interfaces with decohesion and with intermediate liquid (disordered) phase are discussed. Importance of the surface- and scale-induced phenomena on interaction between phase transformation with fracture and dislocations as well as inheritance of dislocations and plastic strains is demonstrated. Some nontrivial phenomena, like solid-solid phase transformations via intermediate (virtual) melt, virtual melting as a new mechanism of plastic deformation and stress relaxation under high strain rate loading, and phase transformations and chemical reactions induced by plastic shear under high pressure are discussed and modeled.
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Scaling of relaxation and excess entropy in plastically deformed amorphous solids
When stressed sufficiently, solid materials yield and deform plastically via reorganization of microscopic constituents. Indeed, it is possible to alter the microstructure of materials by judicious application of stress, an empirical process utilized in practice to enhance the mechanical properties of metals. Understanding the interdependence of plastic flow and microscopic structure in these nonequilibrium states, however, remains a major challenge. Here, we experimentally investigate this relationship, between the relaxation dynamics and microscopic structure of disordered colloidal solids during plastic deformation. We apply oscillatory shear to solid colloidal monolayers and study their particle trajectories as a function of shear rate in the plastic regime. Under these circumstances, the strain rate, the relaxation rate associated with plastic flow, and the sample microscopic structure oscillate together, but with different phases. Interestingly, the experiments reveal that the relaxation rate associated with plastic flow at time t is correlated with the strain rate and sample microscopic structure measured at earlier and later times, respectively. The relaxation rate, in this nonstationary condition, exhibits power-law, shear-thinning behavior and scales exponentially with sample excess entropy. Thus, measurement of sample static structure (excess entropy) provides insight about both strain rate and constituent rearrangement dynamics in the sample at earlier times.
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- Award ID(s):
- 2003659
- PAR ID:
- 10230898
- Date Published:
- Journal Name:
- Proceedings of the National Academy of Sciences
- Volume:
- 117
- Issue:
- 22
- ISSN:
- 0027-8424
- Page Range / eLocation ID:
- 11887 to 11893
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript
- Journal Article:
- https://doi.org/10.1073/pnas.2000698117
