Tensile Strength of Polyurethane and other Elastomeric Block Copolymers

1976 ◽  
Vol 49 (1) ◽  
pp. 64-84 ◽  
Author(s):  
Thor L. Smith

Abstract The discussion in this paper has been focused on the strength of Polyurethane elastomers, data on other materials being presented for comparison and to illustrate factors that affect strength. Although the literature on Polyurethane elastomers is voluminous, only in recent years has it been widely recognized that plastic domains exist in most polyurethane formulations of technological importance. Evidence for domain formation and aspects of domain morphology are discussed in recent reviews. The morphology of domains in segmented polyurethane elastomers is more complex than of those in triblock elastomers and has not been studied extensively, although progress is being made, indicated by the discussions in recent publications and references cited therein. In view of the complexities of fracture and the limited information on the morphology and time-dependent mechanical properties of polyurethane elastomers, only general relations between strength and chemical structure have thus far been established. On the other hand, useful correlations can be established by considering the type, size, and concentration of the hard segments and whether strain-induced crystallization is a dominant factor.

1994 ◽  
Vol 27 (10) ◽  
pp. 2814-2819 ◽  
Author(s):  
Weiming Tang ◽  
Richard J. Farris ◽  
William J. MacKnight ◽  
Claus D. Eisenbach

2021 ◽  
Author(s):  
Yuhan Li ◽  
Wenjuan Li ◽  
Ailing Sun ◽  
Mengfan Jing ◽  
Xingjiang Liu ◽  
...  

A mechano-responsive strategy, known as strain-induced crystallization, is proposed to tailor room-temperature self-healing, highly mechanically-strong and unprecedentedly tough polyurethane elastomers.


Polymers ◽  
2021 ◽  
Vol 13 (13) ◽  
pp. 2060
Author(s):  
Shazia Naheed ◽  
Mohammad Zuber ◽  
Mahwish Salman ◽  
Nasir Rasool ◽  
Zumaira Siddique ◽  
...  

In this study, we evaluated the morphological behavior of polyurethane elastomers (PUEs) by modifying the soft segment chain length. This was achieved by increasing the soft segment molecular weight (Mn = 400–4000 gmol−1). In this regard, polycaprolactone diol (PCL) was selected as the soft segment, and 4,4′-cyclohexamethylene diisocyanate (H12MDI) and 1,6-hexanediol (HDO) were chosen as the hard segments. The films were prepared by curing polymer on Teflon surfaces. Fourier transform infrared spectroscopy (FTIR) was utilized for functional group identification in the prepared elastomers. FTIR peaks indicated the disappearance of −NCO and −OH groups and the formation of urethane (NHCOO) groups. The morphological behavior of the synthesized polymer samples was also elucidated using scanning electron microscopy (SEM) and atomic force microscopy (AFM) techniques. The AFM and SEM results indicated that the extent of microphase separation was enhanced by an increase in the molecular weight of PCL. The phase separation and degree of crystallinity of the soft and hard segments were described using X-ray diffraction (XRD). It was observed that the degree of crystallinity of the synthesized polymers increased with an increase in the soft segment’s chain length. To evaluate hydrophilicity/hydrophobicity, the contact angle was measured. A gradual increase in the contact angle with distilled water and diiodomethane (38.6°–54.9°) test liquids was observed. Moreover, the decrease in surface energy (46.95–24.45 mN/m) was also found to be inconsistent by increasing the molecular weight of polyols.


Soft Matter ◽  
2020 ◽  
Vol 16 (2) ◽  
pp. 447-455 ◽  
Author(s):  
Pinzhang Chen ◽  
Yuanfei Lin ◽  
Jingyun Zhao ◽  
Lingpu Meng ◽  
Daoliang Wang ◽  
...  

Micro-structural evolution of polybutadiene rubber in strain-temperature space, and the reconstruction of the macro-mechanical response.


RSC Advances ◽  
2016 ◽  
Vol 6 (98) ◽  
pp. 95601-95610 ◽  
Author(s):  
Yuko Ikeda ◽  
Preeyanuch Junkong ◽  
Takumi Ohashi ◽  
Treethip Phakkeeree ◽  
Yuta Sakaki ◽  
...  

Guayule and rubber dandelion natural rubbers are useful alternatives forHeveanatural rubber in terms of their strain-induced crystallization behaviours.


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