4.7 Article

Modeling Strategy for Enhanced Recovery Strength and a Tailorable Shape Transition Behavior in Shape Memory Copolymers

Journal

MACROMOLECULES
Volume 52, Issue 16, Pages 6045-6054

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.9b00992

Keywords

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Funding

  1. National Natural Science Foundation of China (NSFC) [11672342, 11725208]
  2. Newton Mobility Grant through Royal Society [1E161019]
  3. NSFC
  4. Royal academy of Engineering UK-Research Exchange with China and India

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By integrating the Fox-Flory equation and the rubber elasticity principle, a phenomenologically constitutive model was proposed in this study to describe high mechanical recovery strength and a tailorable shape transition behavior of shape memory polymer (SMP) copolymers. The thermodynamics of different monomers in the copolymers were formulated by considering their influences on glass-transition temperatures (T-g) and elastic moduli based on the Fox-Flory and Gordon-Taylor equations. Effects of the T-g, weight fraction, molecular weight, storage modulus, and rubbery modulus of various monomers on thermomechanical and shape recovery behaviors of the SMP copolymers were theoretically investigated and discussed. Working principles of enhanced mechanical strength and a tailorable shape transition behavior of the SMP copolymers have been well-described using this newly proposed model, which offers an effective strategy for designing SMPs with high mechanical strength and a desirable shape memory behavior. Furthermore, molecular dynamics simulations were used to predict the glass-transition temperature from a molecular scale and the experimental results fit well with our modeling results.

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