Coupled chemo-electro-mechanical formulation for ionic polymer gels––numerical and experimental investigations
Introduction
Certain polyelectrolyte gels are distinguished by enormous swelling capabilities under the influence of external physical and chemical stimuli. No other kind of material attains comparable volume expansiveness. These unique properties make them most attractive candidates for a new promising generation of “pseudomuscular” actuators. The typical architecture of a polyelectrolyte gel consists of a network of crosslinked polymers to which electric charges are attached. Suitable polyelectrolyte gels can be synthesized by crosslinked copolymerisation of weakly ionisable comonomers often bonded chemically in a polymer network (see Fig. 1).
Variations in the surrounding chemical milieu or exposition to an external electric field may induce changes in the degree of ionisation of the polyelectrolyte gel and in the distribution of ions within the gel entailing a change in the swelling capacity of the gel. The characteristic deformations of polyelectrolyte gels under the influence of external fields lead to reversible bending. In the present study we want to model the mechanisms behind the effect of external electric fields on ionic polyelectrolyte gels leading to spatially different swelling and deswelling and thus to bending motions. In contrast to various studies in this field assuming a constant Donnan potential throughout the polyelectrolyte gels we investigate a coupled chemo-electro-mechanical formulation which is capable to describe the local swelling of a gel on the basis of concentration differences at the complete gel–solution interface.
Section snippets
Chemo-electro-mechanical multi-field formulation
The dynamic behavior of ionic polymer gels in electric fields has been investigated quasi-statically by Doi et al. (1992), Shiga and Kurauchi (1990), Shahinpoor (1995). Brock et al. (1994) have given a coupled formulation for the ion-dynamics and a theory for large displacements. Nemat-Nasser and Li (2000) have presented an electro-mechanical model for ionic polymer metal composites, while, Neubrand (1999), Grimshaw et al. (1990), de Gennes et al. (2000), Wallmersperger et al. (2001) have
Numerical simulation of electrical stimulation
In this section, electrical stimulation of an electrolyte polymer gel fiber is investigated.
The testcase is conducted for a fixed gel fiber (4 × 10 mm2) with a concentration of bound anionic groups cA−=5 mM, placed between two electrodes in a solution bath (50 × 50 mm2) having a concentration of cNa+(s)=cCl−(s)=1 mM (see Fig. 4). The boundary conditions for Na+ and Cl− in the solution near the electrodes are set to cNa+=cCl−=1 mM. Since the concentrations of H+ and OH− ions are very small, they can
Conclusion
In the present study, a coupled chemo-electro-mechanical multi-field formulation for polyelectrolyte gels has been presented. This formulation consists of convection–diffusion equations describing the chemical field, a Poisson equation for the electric field and a mechanical field equation. The model is capable to describe the local swelling and deswelling of ionic polymer gels as well as the ion concentrations and the electric potential in the gel and in the solution.
Numerical simulations of
References (10)
- et al.
A dynamic model of a linear actuator based on polymer hydrogel
J. Intell. Mater. Syst. Struct.
(1994) - et al.
Mechanoelectric effects in ionic gels
Europhys. Lett.
(2000) - et al.
Deformation of ionic polymer gels by electric fields
Macromolecules
(1992) - et al.
Kinetics of electrically and chemically induced swelling in polyelectrolyte gels
J. Chem. Phys.
(1990) - et al.
Polyelectrolyte gels in electric fields: A theoretical and experimental approach
Cited by (158)
Modeling coupled electrochemical and mechanical behavior of soft ionic materials and ionotronic devices
2022, Journal of the Mechanics and Physics of SolidsCitation Excerpt :The coupling between the electrochemical processes and large mechanical deformation in polyelectrolytes has been modeled previously in the context of environmentally responsive ionic gels and ionic electromechanical transducers. In current literature on electrochemically and mechanically coupled response of environmentally responsive polymers, there are various models accounting for the ionic-driven swelling of polymer gels (cf., e.g., Doi et al., 1992; De Gennes et al., 2000; Wallmersperger et al., 2004; Keller et al., 2011; Drozdov and deClaville Christiansen, 2015; Leichsenring and Wallmersperger, 2017; Zhang et al., 2020; Narayan and Anand, 2022). Recent years also saw notable efforts towards developing multiphysics framework for coupled electrochemistry and mechanics of soft ionic actuators, with most authors focusing on the mechanical response of ionic polymer-metal composites under external electric fields (cf., e.g., Nemat-Nasser, 2002; Toi and Kang, 2005; Nardinocchi et al., 2011; Rossi et al., 2018; Narayan et al., 2021).
Numerical modeling of contaminant advection impact on hydrodynamic diffusion in a deformable medium
2022, Journal of Rock Mechanics and Geotechnical EngineeringExperimental and numerical analysis of electroactive characteristics of scleral tissue
2022, Acta BiomaterialiaCitation Excerpt :A similar CEM model has been used to show promising microfluidic applications of stimuli-responsive hydrogels in high-speed valves and pumps [44]. The coupled CEM model explained the swelling of ionic polymer gels in terms of concentration differences at the gel–solution interface [45]. The differences in numerical predictions of a fully coupled CEM model and one-way chemo-electric to mechanical coupled models have also been presented [46].
A coupled electro-chemo-mechanical theory for polyelectrolyte gels with application to modeling their chemical stimuli-driven swelling response
2022, Journal of the Mechanics and Physics of SolidsModeling of stimuli-responsive hydrogels: a transient analysis
2022, The Mechanics of Hydrogels: Mechanical Properties, Testing, and ApplicationsThe status, barriers, challenges, and future in design for 4D printing
2021, Materials and Design
- 1
Tel.: +49-7071-29-73421; fax: +49-7071-29-5074.