scholarly journals Principles for Controlling the Shape Recovery and Degradation Behavior of Biodegradable Shape-Memory Polymers in Biomedical Applications

Micromachines ◽  
2021 ◽  
Vol 12 (7) ◽  
pp. 757
Author(s):  
Junsang Lee ◽  
Seung-Kyun Kang
Keyword(s):  
Shape Memory ◽  
Shape Recovery ◽  
Memory Performance ◽  
Shape Memory Polymers ◽  
Hydrolytic Activity ◽  
Thermomechanical Properties ◽  
Property A ◽  
High Tunability ◽  
Wide Range ◽  
Permanent Implant

Polymers with the shape memory effect possess tremendous potential for application in diverse fields, including aerospace, textiles, robotics, and biomedicine, because of their mechanical properties (softness and flexibility) and chemical tunability. Biodegradable shape memory polymers (BSMPs) have unique benefits of long-term biocompatibility and formation of zero-waste byproducts as the final degradable products are resorbed or absorbed via metabolism or enzyme digestion processes. In addition to their application toward the prevention of biofilm formation or internal tissue damage caused by permanent implant materials and the subsequent need for secondary surgery, which causes secondary infections and complications, BSMPs have been highlighted for minimally invasive medical applications. The properties of BSMPs, including high tunability, thermomechanical properties, shape memory performance, and degradation rate, can be achieved by controlling the combination and content of the comonomer and crystallinity. In addition, the biodegradable chemistry and kinetics of BSMPs, which can be controlled by combining several biodegradable polymers with different hydrolysis chemistry products, such as anhydrides, esters, and carbonates, strongly affect the hydrolytic activity and erosion property. A wide range of applications including self-expending stents, wound closure, drug release systems, and tissue repair, suggests that the BSMPs can be applied as actuators on the basis of their shape recovery and degradation ability.

scholarly journals Bio-Based Epoxy Shape-Memory Thermosets from Triglycidyl Phloroglucinol

Polymers ◽  
2020 ◽  
Vol 12 (3) ◽  
pp. 542 ◽  
Author(s):  
David Santiago ◽  
Dailyn Guzmán ◽  
Francesc Ferrando ◽  
Àngels Serra ◽  
Silvia De la Flor
Keyword(s):  
Shape Memory ◽  
Shape Recovery ◽  
Memory Performance ◽  
Crosslinking Agent ◽  
Shape Memory Polymers ◽  
Crosslinking Density ◽  
Mechanical Analysis ◽  
Diglycidyl Ether ◽  
Partial Substitution ◽  
Scanning Calorimetry

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.

Influence of Radialization Dosage on Shape Memory Effect of Polystyrene Copolymer

2008 ◽  
Vol 47-50 ◽  
pp. 690-693 ◽  
Author(s):  
Da Wei Zhang ◽  
Jin Song Leng ◽  
Yan Ju Liu
Keyword(s):  
Shape Memory ◽  
Shape Memory Effect ◽  
Memory Effect ◽  
Smart Materials ◽  
Shape Recovery ◽  
Memory Performance ◽  
Shape Memory Polymer ◽  
Shape Memory Polymers ◽  
Mechanical Analysis ◽  
Styrene Copolymer

This paper is concerned about the synthesis of shape memory styrene copolymer and the investigation of the influence of radialization dosage on its shape memory effect. As one of novel actuators in smart materials, shape memory polymers (SMPs) have been investigated intensively. Styrene copolymer with proper cross-linking degree can exhibit shape memory effect (SME). In this paper, the influence of radialization on shape memory effect of styrene copolymer was investigated through altering the dosage of radialization. The radialization dosage of styrene copolymer was determined by changed radicalization time. The glass transition temperature (Tg) of styrene copolymerwas measured by Dynamic Mechanical Analysis (DMA). The shape memory performance of styrene copolymer with different radiated dosage was also evaluated. Results indicated that the shape memory polymer (SMP) was synthesized successfully. The Tg increased from 60°C to 65°C followed by increasing the radialization dosage. Moreover, the SMP experienced good SME and the largest reversible strain of the SMP reached as high as 150%. When heating above Tg+30°C (different copolymers performed different Tg), the shape recovery speed of the copolymers increased with increasing the radialization dosage. However, the recovery speed decreased with increasing the radialization dosage at the same temperature of 95°C.

scholarly journals Analysis of Shape Memory Behavior and Mechanical Properties of Shape Memory Polymer Composites Using Thermal Conductive Fillers

Micromachines ◽  
2021 ◽  
Vol 12 (9) ◽  
pp. 1107
Author(s):  
Mijeong Kim ◽  
Seongeun Jang ◽  
Sungwoong Choi ◽  
Junghoon Yang ◽  
Jungpil Kim ◽  
...  
Keyword(s):  
Physical Properties ◽  
Shape Memory ◽  
Polymer Composites ◽  
Shape Recovery ◽  
Memory Performance ◽  
Shape Memory Polymer ◽  
Scanning Calorimetry ◽  
Wide Range ◽  
Nanocarbon Materials ◽  
Shape Memory Composite

Shape memory polymers (SMPs) are attracting attention for their use in wearable displays and biomedical materials due to their good biocompatibility and excellent moldability. SMPs also have the advantage of being lightweight with excellent shape recovery due to their low density. However, they have not yet been applied to a wide range of engineering fields because of their inferior physical properties as compared to those of shape memory alloys (SMAs). In this study, we attempt to find optimized shape memory polymer composites. We also investigate the shape memory performance and physical properties according to the filler type and amount of hardener. The shape memory composite was manufactured by adding nanocarbon materials of graphite and non-carbon additives of Cu. The shape-recovery mechanism was compared, according to the type and content of the filler. The shape fixation and recovery properties were analyzed, and the physical properties of the shape recovery composite were obtained through mechanical strength, thermal conductivity and differential scanning calorimetry analysis.

Novel Bismaleimide-Based Shape Memory Polymers: Comparison to Commercial Shape Memory Polymers

2011 ◽  
Author(s):  
Amber J. W. McClung ◽  
Joseph A. Shumaker ◽  
Jeffery W. Baur
Keyword(s):  
Shape Memory ◽  
Memory Performance ◽  
Shape Memory Polymers ◽  
Mechanical Analysis ◽  
Thermomechanical Properties ◽  
Transition Temperatures ◽  
Thermal And Mechanical Properties ◽  
Glass Transition Temperatures ◽  
Tan Δ ◽  
Heat Loads

A series of novel shape memory polymers, synthesized from 4-4-bismaleimidodiphenyl-methane, an extended chain aliphatic diamine, and a bis-isocyanate, have been created and characterized with the aim of providing a family of robust high temperature shape memory polymers with tailorable transition temperatures for use in reconfigurable aerospace structures. In the present study, three of the polymers are chosen for more detailed study of their thermomechanical properties. These materials are compared to commercial resins Veriflex® and Veriflex-E® which are styrene- and epoxy-based proprietary formulations, respectively. The thermal and mechanical properties are determined utilizing thermogravimetric analysis and dynamic mechanical analysis. The temperatures at which 2% weight loss is observed in dry air ranges from 272 to 305 °C for the synthesized polymers, and occurs at 242 and 317 °C for the commercial Veriflex® and Veriflex-E® respectively. The glass transition temperatures, as measured by the peak in the tan(δ) curve, for the synthesized polymers range from 110 to 144 °C which is a higher than the Veriflex® and Veriflex-E® achieve at 84.3 and 100 °C respectively. With operation temperatures of subsonic structural aircraft components often reaching 121 °C (250 °F), the transition temperatures of the bismaleimide-based shape memory polymers are clearly desirable to ensure that shape memory polymers used in aircraft structures will not be prematurely triggered by the existing heat loads. In addition, the shape memory performance of the bismaleimide-based shape memory polymers compares well with the Veriflex® and Veriflex-E® resins.

Investigate of Electrical Conductivity of Shape-Memory Polymer Filled with Carbon Black

2008 ◽  
Vol 47-50 ◽  
pp. 714-717 ◽  
Author(s):  
Xin Lan ◽  
Jin Song Leng ◽  
Yan Ju Liu ◽  
Shan Yi Du
Keyword(s):  
Electrical Conductivity ◽  
Carbon Black ◽  
Shape Memory ◽  
Shape Recovery ◽  
Volume Fraction ◽  
Shape Memory Polymer ◽  
Recovery Process ◽  
Thermomechanical Properties ◽  
Electrically Conductive ◽  
New System

A new system of thermoset styrene-based shape-memory polymer (SMP) filled with carbon black (CB) is investigated. To realize the electroactive stimuli of SMP, the electrical conductivity of SMP filled with various amounts of CB is characterized. The percolation threshold of electrically conductive SMP filled with CB is about 3% (volume fraction of CB), which is much lower than many other electrically conductive polymers. When applying a voltage of 30V, the shape recovery process of SMP/CB(10 vol%) can be realized in about 100s. In addition, the thermomechanical properties are also characterized by differential scanning calorimetery (DSC).

scholarly journals Water Triggered Shape Memory Materials

2013 ◽  
Vol 3 (1) ◽  
pp. 49-50 ◽  
Author(s):  
Guoguang Niu
Keyword(s):  
Shape Memory ◽  
Shape Recovery ◽  
Shape Memory Polymers ◽  
Electrical Current ◽  
Light Illumination ◽  
Poly Ethylene Glycol ◽  
Thermally Induced ◽  
Permanent Shape ◽  
Poly Ethylene ◽  
Novel Strategy

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.

scholarly journals A Large-Deformation Theory for Thermally-Actuated Shape-Memory Polymers and its Application

2010 ◽  
Author(s):  
Shawn A. Chester ◽  
Vikas Srivastava ◽  
Claudio V. Di Leo ◽  
Lallit Anand
Keyword(s):  
Glass Transition ◽  
Shape Memory ◽  
Deformation Theory ◽  
Shape Recovery ◽  
Large Deformations ◽  
Shape Memory Polymers ◽  
The Body ◽  
Thermally Induced ◽  
Thermally Actuated ◽  
Common Shape

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.

scholarly journals Shape-Memory Polymers for Biomedical Applications

2008 ◽  
Vol 54 ◽  
pp. 96-102 ◽  
Author(s):  
Andreas Lendlein ◽  
Marc Behl
Keyword(s):  
Shape Memory ◽  
Material Properties ◽  
Biomedical Applications ◽  
Traditional Approach ◽  
Shape Change ◽  
Shape Memory Polymers ◽  
Thermally Induced ◽  
Wide Range ◽  
Multifunctional Polymers ◽  
Suitable Process

Most polymers used in clinical applications today are materials that have been developed originally for application areas other than biomedicine. On the other side, different biomedical applications are demanding different combinations of material properties and functionalities. Compared to the intrinsic material properties, a functionality is not given by nature but result from the combination of the polymer architecture and a suitable process. Examples for functionalities that play a prominent role in the development of multifunctional polymers for medical applications are biofunctionality (e.g. cell or tissue specificity), degradability, or shape-memory functionality. In this sense, an important aim for developing multifunctional polymers is tailoring of biomaterials for specific biomedical applications. Here the traditional approach, which is designing a single new homo- or copolymer, reaches its limits. The strategy, that is applied here, is the development of polymer systems whose macroscopic properties can be tailored over a wide range by variation of molecular parameters. The Shape-memory capability of a material is its ability to trigger a predefined shape change by exposure to an external stimulus. A change in shape initiated by heat is called thermally-induced shape-memory effect. Thermally, light-, and magnetically induced shape-memory polymers will be presented, that were developed especially for minimally invasive surgery and other biomedical applications. Furthermore triple-shape polymers will be introduced, that have the capability to perform two subsequent shape changes. Thus enabling more complex movements of a polymeric material.

Characristics of Shape Memory Composites Combined with Shape Memory Alloy and Shape Memory Polymer

2013 ◽  
Vol 705 ◽  
pp. 169-172
Author(s):  
Xue Feng ◽  
Li Min Zhao ◽  
Xu Jun Mi
Keyword(s):  
Shape Memory ◽  
Room Temperature ◽  
Shape Recovery ◽  
Volume Fraction ◽  
Shape Memory Polymer ◽  
Young Modulus ◽  
Thermomechanical Properties ◽  
The Matrix ◽  
Shape Memory Composites ◽  
Shape Fixity

In order to develop high functionality of shape memory materials, the shape memory composites combined with TiNi wire and shape memory epoxy were prepared, and the mechanical and thermomechanical properties were studied. The results showed the addition of TiNi wire increased the Young modulus and breaking strength both at room temperature and at elevated temperature. The composites maintained the rates of shape fixity and shape recovery close to 100%. The maximum recovery stress increased with increasing TiNi wire volume fraction, and obtained almost 3 times of the matrix by adding 1vol% TiNi wire.

Deployable Process Analysis of Packaged SMP Sandwich Beam

2010 ◽  
Vol 123-125 ◽  
pp. 943-946 ◽  
Author(s):  
Zheng Fa Li ◽  
Zheng Dao Wang
Keyword(s):  
Shape Memory Alloys ◽  
Shape Memory ◽  
Sandwich Structure ◽  
Shape Recovery ◽  
Process Analysis ◽  
Sandwich Beam ◽  
Shape Memory Polymers ◽  
Recovery Stress ◽  
Recovery Response

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.

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