Abstract
Light activated polymers (LAPs) are a class of contemporary materials that when irradiated with light respond with mechanical deformation. Among the different molecular mechanisms of photoactuation, here we study radical induced bond exchange reactions (BERs) that alter macromolecular chains through an addition-fragmentation process where a free chain whose active end group attaches then breaks a network chain. Thus the BER yields a polymer with a covalently adaptable network. When a LAP sample is loaded, the macroscopic consequence of BERs is stress relaxation and plastic deformation. Furthermore, if light penetration through the sample is nonuniform, resulting in nonuniform stress relaxation, the sample will deform after unloading in order to achieve equilibrium. In the past, this light activation mechanism was modeled as a phase evolution process where chain addition-fragmentation process was considered as a phase transformation between stressed phases and newly-born phases that are undeformed and stress free at birth. Such a modeling scheme describes the underlying physics with reasonable fidelity but is computationally expensive. In this paper, we propose a new approach where the BER induced macromolecular network alteration is modeled as a viscoplastic deformation process, based on the observation that stress relaxation due to light irradiation is a time-dependent process similar to that in viscoelastic solids with an irrecoverable deformation after light irradiation. This modeling concept is further translated into a finite deformation photomechanical constitutive model. The rheological representation of this model is a photoviscoplastic element placed in series with a standard linear solid model in viscoelasticity. A two-step iterative implicit scheme is developed for time integration of the two time-dependent elements. We carry out a series of experiments to determine material parameters in our model as well as to validate the performance of the model in complex geometrical and loading configurations. The comparison between the finite element simulations and experiments shows that the model can accurately capture the response of the LAP under a wide range of coupled photo-mechanical loading conditions, such as light induced stress relaxation, creep in tension, and bending. Furthermore, we demonstrate the versatility of the model by simulating a series of examples that exhibit complex three-dimensional, time-dependent photodeformation, including photoorigami, photoforming, and photobulge tests.
Original language | English |
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Pages (from-to) | 84-103 |
Number of pages | 20 |
Journal | Journal of the Mechanics and Physics of Solids |
Volume | 70 |
Issue number | 1 |
DOIs | |
Publication status | Published - Oct 2014 |
Externally published | Yes |
Keywords
- Covalent adaptive network
- Finite deformation constitutive model
- Light activated polymers
- Photo-induced viscoplasticity
- Photoforming