Effect of Controlled Chain-Scission Damage on Viscoelasticity in Double Network Elastomers

Abstract Background The relationship between molecular-scale chain scission and bulk viscoelasticity in soft polymer networks remains incompletely understood, particularly in multiple network elastomers, where energy dissipation arises from the interaction between irreversible chain-scission damage and reversible time-dependent mechanics. Objective This study aims to elucidate how cumulative, progressive chain-scission damage influences bulk viscoelasticity in double network elastomers through both experiments and constitutive modeling. Methods A non-swelling, platinum-cured silicone double network elastomer was synthesized and served as a model system to investigate damage-induced effects on viscoelasticity. Cyclic tensile loading was applied to introduce systematically controlled chain-scission damage. The changes in viscoelastic properties were characterized via stress relaxation tests and dynamic mechanical analysis. A constitutive model coupling hyperelasticity with damage-induced viscosity through stretch-mediated chain-scission kinetics and chain-length-dependent disentanglement kinetics was established to describe the observed damage-viscosity coupling. Results Experiments revealed that cumulative bond breaking in the double network elastomer contributes not only to Mullins-type softening but also to measurable increases in apparent relaxation time and viscoelastic dissipation rate. The proposed model successfully reproduced damage-related effects, including both irreversible primary hysteresis caused by network damage and narrower, persistent secondary hysteresis due to damage-induced viscoelastic dissipation. Conclusion Although the damage-induced viscoelastic dissipation was small compared to the energy directly dissipated by bond breaking, our results provide direct experimental evidence and quantification that internal molecular damage can modulate bulk time-dependent constitutive behavior. These findings lay the foundation for predictive modeling of dissipative mechanics mediated by damage–viscoelasticity coupling in complex multiple network elastomers.

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Publication Details

Journal
Experimental Mechanics
Published
2026-06-30
DOI
https://doi.org/10.1007/s11340-026-01344-9
Primary Topic
Elasticity and Material Modeling
Type
article
Field-Weighted Citation Impact
0.00

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article

Effect of Controlled Chain-Scission Damage on Viscoelasticity in Double Network Elastomers

Bingyang Zhang, C.-Y. Hui, B. Zhu, A. T. Zehnder
Experimental Mechanics
Elasticity and Material Modeling
article

Effect of Controlled Chain-Scission Damage on Viscoelasticity in Double Network Elastomers

Bingyang Zhang, C.-Y. Hui, B. Zhu, A. T. Zehnder
article en

Abstract

Abstract Background The relationship between molecular-scale chain scission and bulk viscoelasticity in soft polymer networks remains incompletely understood, particularly in multiple network elastomers, where energy dissipation arises from the interaction between irreversible chain-scission damage and reversible time-dependent mechanics. Objective This study aims to elucidate how cumulative, progressive chain-scission damage influences bulk viscoelasticity in double network elastomers through both experiments and constitutive modeling. Methods A non-swelling, platinum-cured silicone double network elastomer was synthesized and served as a model system to investigate damage-induced effects on viscoelasticity. Cyclic tensile loading was applied to introduce systematically controlled chain-scission damage. The changes in viscoelastic properties were characterized via stress relaxation tests and dynamic mechanical analysis. A constitutive model coupling hyperelasticity with damage-induced viscosity through stretch-mediated chain-scission kinetics and chain-length-dependent disentanglement kinetics was established to describe the observed damage-viscosity coupling. Results Experiments revealed that cumulative bond breaking in the double network elastomer contributes not only to Mullins-type softening but also to measurable increases in apparent relaxation time and viscoelastic dissipation rate. The proposed model successfully reproduced damage-related effects, including both irreversible primary hysteresis caused by network damage and narrower, persistent secondary hysteresis due to damage-induced viscoelastic dissipation. Conclusion Although the damage-induced viscoelastic dissipation was small compared to the energy directly dissipated by bond breaking, our results provide direct experimental evidence and quantification that internal molecular damage can modulate bulk time-dependent constitutive behavior. These findings lay the foundation for predictive modeling of dissipative mechanics mediated by damage–viscoelasticity coupling in complex multiple network elastomers.

Experimental Mechanics
Texas State University (US), Cornell University (US)
National Science Foundation, Cornell Center for Materials Research, Division of Materials Research, Division of Civil, Mechanical and Manufacturing Innovation
Openalex Percentile: Top 13%
Elasticity and Material Modeling
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