Triple Shape Memory Polymers: Constitutive Modeling and Numerical Simulation

2016 ◽  
Vol 83 (7) ◽  
Author(s):  
S. Moon ◽  
I. J. Rao ◽  
S. A. Chester

Recently, triple shape memory polymers (TSMPs) have been discovered; these materials can be programmed to switch between three distinct shapes. Previously, we introduced a model to describe the mechanical behavior of TSMPs; however, the earlier study was limited in scope to simple cases of uniaxial deformation. In this work, we build upon our prior work, and develop robust numerical methods and constitutive equations to model complex mechanical behavior of TSMPs in inhomogeneous deformations and loading conditions using a framework based on the theory of multiple natural configurations. The model has been calibrated to uniaxial experiments. In addition, the model has been implemented as a user material subroutine (UMAT) in the finite element package abaqus. To demonstrate the applicability of the developed constitutive model, we have numerically simulated two cases of three-dimensional bodies undergoing triple-shape cycles; triple-shape recovery response of a complex TSMP geometry and the triple-shape recovery response of a stent when it is inserted in an artery modeled as a compliant elastomeric tube.

2010 ◽  
Vol 123-125 ◽  
pp. 943-946 ◽  
Author(s):  
Zheng Fa Li ◽  
Zheng Dao Wang

Shape memory polymers own many advantages compared with traditional shape memory alloys or ceramics. In order to improve their shape recovery stress and realize a stable recovery response during the deployable process, the structure of SMP sandwich beam composed of two metallic skin and one SMP core is considered. The recovery behaviors of pure SMP and SMP beams reinforced by one-layer metallic skin are also discussed for comparison. The results confirm that the deployable properties of SMP matrix can be significantly improved by using sandwich structure.


Author(s):  
Tianjiao Wang ◽  
Jun Zhao ◽  
Chuanxin Weng ◽  
Tong Wang ◽  
Yayun Liu ◽  
...  

Shape memory polymers (SMPs) that change shapes as designed by external stimuli have become one of the most promising materials as actuators, sensors, and deployable devices. However, their practical applications...


Author(s):  
Mahesh Khanolkar ◽  
Jaskirat Sodhi ◽  
I. Joga Rao

The constitutive model for the mechanics of crystallizable shape memory polymers (CSMP) has been developed in the past [1, 2]. The model was developed using the theory of multiple natural configurations and has been successful in addressing a diverse class of problems. In this research work, the efficacy of the developed CSMP model is tested by applying it to the torsion of a cylinder, which is an inhomogeneous deformation. The crystallization of the cylinder is studied under two different conditions i.e. crystallization under constant shear and crystallization under constant moment.


2013 ◽  
Vol 3 (1) ◽  
pp. 49-50 ◽  
Author(s):  
Guoguang Niu

The term "shape memory effect" refers to the ability of a material to be deformed and fixed into a temporary shape, and to recover its original, permanent shape upon an external stimulus (1). Shape memory polymers have attracted much interest because of their unique properties, and applied tremendously in medical area, such as biodegradable sutures, actuators, catheters and smart stents (2, 3). Shape memory usually is a thermally induced process, although it can be activated by light illumination, electrical current, magnetic, or electromagnetic field (4-6). During the process, the materials are heated directly or indirectly above their glass transition temperature (Tg) or the melting temperature (Tm) in order to recover the original shape. Non-thermally induced shape memory polymers eliminate the temperature constrains and enable the manipulation of the shape recovered under ambient temperature (7, 8). Herein, we report a novel strategy of water induced shape memory, in which the formation and dissolution of poly(ethylene glycol) (PEG) crystal is utilized for the fixation and recovery of temporary deformation of hydrophilic polymer. This water-induced shape recovery is less sensitive to temperature, of which 95% deformation is fixed in circumstance and over 75% recovery is reached even at 0 oC.


Author(s):  
Shawn A. Chester ◽  
Vikas Srivastava ◽  
Claudio V. Di Leo ◽  
Lallit Anand

The most common shape-memory polymers are those in which the shape-recovery is thermally-induced. A body made from such a material may be subjected to large deformations at an elevated temperature above its glass transition temperature &Vthgr;g. Cooling the deformed body to a temperature below &Vthgr;g under active kinematical constraints fixes the deformed shape of the body. The original shape of the body may be recovered if the material is heated back to a temperature above &Vthgr;g without the kinematical constraints. This phenomenon is known as the shape-memory effect. If the shape recovery is partially constrained, the material exerts a recovery force and the phenomenon is known as constrained-recovery.


2021 ◽  
Vol 30 (3) ◽  
pp. 035030
Author(s):  
Jinsu Kim ◽  
Seung-Yeol Jeon ◽  
Seokbin Hong ◽  
Yongsan An ◽  
Haedong Park ◽  
...  

Polymers ◽  
2020 ◽  
Vol 12 (3) ◽  
pp. 542 ◽  
Author(s):  
David Santiago ◽  
Dailyn Guzmán ◽  
Francesc Ferrando ◽  
Àngels Serra ◽  
Silvia De la Flor

A series of bio-based epoxy shape-memory thermosetting polymers were synthesized starting from a triglycidyl phloroglucinol (3EPOPh) and trimethylolpropane triglycidyl ether (TPTE) as epoxy monomers and a polyetheramine (JEF) as crosslinking agent. The evolution of the curing process was studied by differential scanning calorimetry (DSC) and the materials obtained were characterized by means of DSC, thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA), stress-strain tests, and microindentation. Shape-memory properties were evaluated under free and totally constrained conditions. All results were compared with an industrial epoxy thermoset prepared from standard diglycidyl ether of Bisphenol A (DGEBA). Results revealed that materials prepared from 3EPOPh were more reactive and showed a tighter network with higher crosslinking density and glass transition temperatures than the prepared from DGEBA. The partial substitution of 3EPOPh by TPTE as epoxy comonomer caused an increase in the molecular mobility of the materials but without worsening the thermal stability. The shape-memory polymers (SMPs) prepared from 3EPOPh showed good mechanical properties as well as an excellent shape-memory performance. They showed almost complete shape-recovery and shape-fixation, fast shape-recovery rates, and recovery stress up to 7 MPa. The results obtained in this study allow us to conclude that the triglycidyl phloroglucinol derivative of eugenol is a safe and environmentally friendly alternative to DGEBA for preparing thermosetting shape-memory polymers.


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