Mechanical Properties of Shape-Memory Polymers, Polymer Blends, and Composites

Author(s):  
P. Poornima Vijayan
2009 ◽  
Vol 1190 ◽  
Author(s):  
Marc Behl ◽  
Ute Ridder ◽  
Wolfgang Wagermaier ◽  
Steffen Kelch ◽  
Andreas Lendlein

AbstractThe general design principle of shape-memory polymers (SMP) requires two key compo-nents: covalent or physical crosslinks (hard domains) determining the permanent shape and switching domains fixing the temporary shape as well as influencing the switching temperature Tsw. In conventional thermoplastic SMP hard and switching domains determining segments are combined in one macromolecule, e.g. block copolymers such as polyurethanes. Recently, binary polymer blends having shape-memory properties, from two different multiblock copolymers have been presented, whereby the first one is providing the segments forming hard domains and the second one the segments forming the switching domains. Besides the shape-memory proper-ties, the mechanical properties of such materials are application relevant. Here we investigate how the blend composition influences mechanical properties of this new class of shape-memory materials.


RSC Advances ◽  
2016 ◽  
Vol 6 (93) ◽  
pp. 90212-90219 ◽  
Author(s):  
Pengfei Yang ◽  
Guangming Zhu ◽  
Xuelin Shen ◽  
Xiaogang Yan ◽  
Jing Nie

A POSS–PCL shape memory network is synthesized. The cage-like POSS not only serves as a chemical netpoint, also causes improvement in mechanical properties. Optimized networks exhibit both excellent tensile strength and nearly complete recovery.


2005 ◽  
Author(s):  
Michelle M. Keihl ◽  
Robert S. Bortolin ◽  
Brian Sanders ◽  
Shiv Joshi ◽  
Zeb Tidwell

2014 ◽  
Vol 47 (19) ◽  
pp. 6791-6803 ◽  
Author(s):  
Cédric Samuel ◽  
Sophie Barrau ◽  
Jean-Marc Lefebvre ◽  
Jean-Marie Raquez ◽  
Philippe Dubois

2013 ◽  
Vol 2013 (0) ◽  
pp. _J044012-1-_J044012-5
Author(s):  
Kazuhiro SUGITANI ◽  
Kazuto TAKASHIMA ◽  
Toshiro NORITSUGU ◽  
Toshiharu MUKAI

Author(s):  
Matthew K. McBride ◽  
Brady T. Worrell ◽  
Tobin Brown ◽  
Lewis M. Cox ◽  
Nancy Sowan ◽  
...  

The ability to behave in a fluidlike manner fundamentally separates thermoset and thermoplastic polymers. Bridging this divide, covalent adaptable networks (CANs) structurally resemble thermosets with permanent covalent crosslinks but are able to flow in a manner that resembles thermoplastic behavior only when a dynamic chemical reaction is active. As a consequence, the rheological behavior of CANs becomes intrinsically tied to the dynamic reaction kinetics and the stimuli that are used to trigger those, including temperature, light, and chemical stimuli, providing unprecedented control over viscoelastic properties. CANs represent a highly capable material that serves as a powerful tool to improve mechanical properties and processing in a wide variety of polymer applications, including composites, hydrogels, and shape-memory polymers. This review aims to highlight the enabling material properties of CANs and the applied fields where the CAN concept has been embraced.


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