Study on Properties and Preparation of Thermoplastic Polyurethane Hot-Melt Adhesive

2011 ◽  
Vol 311-313 ◽  
pp. 1071-1076
Author(s):  
Jun Ling Tian ◽  
You Ming Cao ◽  
Xin Qi Zhou

The thermoplastic polyurethane elastomer (TPU) was firstly synthesized by using polybutylene adipate (PBA) as soft segments, methane-4-4’-diisocyanate(MDI) and 1,4–butanediol(BDO) as hard segments. The polyurethane hot-melt adhesive was then prepared by adding the tackifying resin, filler and other auxiliaries into the TPU matrix. The structure of the synthetic products was characterized by Infrared Spectrum and the thermal properties and microstructure of polyurethane hot-melt adhesive was tested by the thermogravimetric(TG) and the scanning electron microscopy(SEM), respectively. The results showed that the thermoplastic polyurethane elastomer had the expected structure, the shear strength of polyurethane hot-melt adhesive increased with the pentaerythritol abietate content increasing when the addition of the pentaerythritol abietate is less than 20 wt%, and decreased with the content of CaCO3 filler and petroleum resin increasing, respectively; the thermal stability was improved, and the char yields of the polyurethane blends increased with adding the filler CaCO3. When the molar ratio of PBA:MDI:BDO was 1:2:1, the addition of pentaerythritol abietate and filler CaCO3 was 20 wt% and 30 wt%, the comprehensive performance of PU hot-melt adhesive was better and the shear strength was 7.37 MPa.

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Youngho Eom ◽  
Seon-Mi Kim ◽  
Minkyung Lee ◽  
Hyeonyeol Jeon ◽  
Jaeduk Park ◽  
...  

AbstractSelf-repairable materials strive to emulate curable and resilient biological tissue; however, their performance is currently insufficient for commercialization purposes because mending and toughening are mutually exclusive. Herein, we report a carbonate-type thermoplastic polyurethane elastomer that self-heals at 35 °C and exhibits a tensile strength of 43 MPa; this elastomer is as strong as the soles used in footwear. Distinctively, it has abundant carbonyl groups in soft-segments and is fully amorphous with negligible phase separation due to poor hard-segment stacking. It operates in dual mechano-responsive mode through a reversible disorder-to-order transition of its hydrogen-bonding array; it heals when static and toughens when dynamic. In static mode, non-crystalline hard segments promote the dynamic exchange of disordered carbonyl hydrogen-bonds for self-healing. The amorphous phase forms stiff crystals when stretched through a transition that orders inter-chain hydrogen bonding. The phase and strain fully return to the pre-stressed state after release to repeat the healing process.


2020 ◽  
Author(s):  
Youngho Eom ◽  
Seon-Mi Kim ◽  
Minkyung Lee ◽  
Hyeonyeol Jeon ◽  
Sung Yeon Hwang ◽  
...  

Abstract Self-repairable materials strive to emulate curable and resilient biological tissue; however, their performance is currently insufficient for commercialization purposes because mending and toughening are mutually exclusive. Here, we report a carbonate-type thermoplastic polyurethane elastomer that self-heals at 35 °C and is as strong as footwear elastomers. This elastomer exhibits the highest tensile strength to date (43 MPa). Distinctively, it has abundant carbonyl groups in soft-segments and is fully amorphous with negligible phase separation due to poor hard-segment stacking. It operates in dual mechano-responsive mode through a reversible disorder-to-order transition of its hydrogen-bonding array; it heals when static and toughens when dynamic. In static mode, non-crystalline hard segments promote dynamic exchange of disordered carbonyl hydrogen-bonds for self-healing. The amorphous phase forms stiff crystals when stretched through a transition that orders inter-chain hydrogen bonding. The phase and strain fully return to the pre-stressed state after release to repeat healing process.


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