Polyurethane networks based on α,ω-dihydroxytelechelic and on random hydroxyl-functionalized side chain poly(2-chloroethyl vinyl ether)s: Synthesis and investigation of mechanical properties

1997 ◽  
Vol 198 (10) ◽  
pp. 3051-3064 ◽  
Author(s):  
Véronique Bennevault ◽  
Gilles Richard ◽  
Alain Deffieux
Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 773 ◽  
Author(s):  
Yuqing Qian ◽  
Xiaowei An ◽  
Xiaofei Huang ◽  
Xiangqiang Pan ◽  
Jian Zhu ◽  
...  

Dynamic structures containing polymers can behave as thermosets at room temperature while maintaining good mechanical properties, showing good reprocessability, repairability, and recyclability. In this work, alkyl diselenide is effectively used as a dynamic cross-linker for the design of self-healing poly(urea–urethane) elastomers, which show quantitative healing efficiency at room temperature, without the need for any catalysts or external interventions. Due to the combined action of the urea bond and amide bond, the material has better mechanical properties. We also compared the self-healing effect of alkyl diselenide-based polyurethanes and alkyl disulfide-based polyurethanes. The alkyl diselenide has been incorporated into polyurethane networks using a para-substituted amine diphenyl alkyl diselenide. The resulting materials not only exhibit faster self-healing properties than the corresponding disulfide-based materials, but also show the ability to be processed at temperatures as low as 60 °C.


1996 ◽  
Vol 20 (3) ◽  
pp. 277-282 ◽  
Author(s):  
Hongqin Shi ◽  
Shaw H. Chen ◽  
Mike E. De Rosa ◽  
Timothy J. Bunning ◽  
W. Wade Adams

1996 ◽  
Vol 33 (10) ◽  
pp. 1555-1563 ◽  
Author(s):  
U. W. Gedde ◽  
F. Liu ◽  
C. Hellermark ◽  
A. Hult ◽  
F. Sahlén ◽  
...  

2020 ◽  
Vol 11 (29) ◽  
pp. 4749-4759
Author(s):  
Dong Shi ◽  
Wen-Ying Chang ◽  
Xiang-Kui Ren ◽  
Shuang Yang ◽  
Er-Qiang Chen

Side-chain liquid crystalline polynorbornenes based on benzanilide mesogens exhibit rich self-organization behaviours and enhanced mechanical properties owing to the lateral hydrogen bond interaction that can be tuned by the spacer length.


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