Role of strain rate in the strain-induced crystallization (SIC) of natural and synthetic isoprene rubber

2018 ◽  
Vol 51 (2) ◽  
pp. 221-226 ◽  
Author(s):  
Yuji Kitamura ◽  
Kiyoka Okada ◽  
Hiroyasu Masunaga ◽  
Masamichi Hikosaka
1983 ◽  
Vol 56 (2) ◽  
pp. 465-480
Author(s):  
J. L. Thiele ◽  
R. E. Cohen

Abstract The use of the creep T-jump experiment as a sensitive tool for elucidating the mechanistic behavior during the deformation of a complex material such as the carbon black filled elastomer has been illustrated. The activation energy for creep was determined as a function of stress for various vulcanizates. The effects of the choice of elastomer, and of variations in surface chemistry, structure, and loading of the filler, were studied. The T-jump results combined with electrical conductivity measurements confirmed the presence of a carbon black network which is considerably involved in the creep deformation process at low strain but not at high strain. In NR vulcanizates, there is a high-strain mechanism not observed in SBR vulcanizates; presumably strain-induced crystallization is responsible for the NR behavior. Oxidation of filler surfaces had essentially no effect on the creep deformation mechanisms, suggesting that, during creep, slippage of elastomers along the surface does not occur to any great extent for conventional or oxidized surfaces.


2006 ◽  
Vol 34 (2) ◽  
pp. 119-134 ◽  
Author(s):  
Syeda A. Hussain ◽  
Michelle S. Hoo Fatt

Abstract Tensile tests were conducted to obtain the deformation and failure characteristics of unfilled natural rubber (NR) and natural rubber with 25, 50, and 75 phr of N550 carbon black filler under quasistatic and dynamic loading conditions. The quasistatic tests were performed on an electromechanical INSTRON machine, while the dynamic test data were obtained from tensile impact experiments using a Charpy impact apparatus. In general, the modulus of the stress-extension ratio curves increases with increasing strain rate up to about 407, 367, 346, and 360 s−1 for unfilled, and 25, 50, and 75 phr for filled NR, respectively. Above these strain rates, the unfilled and filled natural rubber stress-extension ratio curves remained unchanged. The modulus increased with increasing strain rate because there was little time for stress relaxation. Above a critical strain rate, no change in modulus was observed because the time of the experiment was short compared to the lowest characteristic relaxation time of the material. Dynamic stress-extension ratio curves did not have the very sharp upturn at break, which is observed from strain-induced crystallization in natural rubber under quasistatic loading. Strain-induced crystallization appeared to be suppressed at high rates of loading. In fact, the highest dynamic tensile strength for the 25- and 50-phr carbon black-filled natural rubbers was smaller than those under quasistatic loading, while the highest dynamic tensile strength of the 75-phr carbon black-filled NR was greater than that in the static test. This indicated that high amounts of carbon black fillers will impede strain-induced crystallization in natural rubber.


2004 ◽  
Vol 77 (4) ◽  
pp. 711-723 ◽  
Author(s):  
Masatoshi Tosaka ◽  
Shinzo Kohjiya ◽  
Syozo Murakami ◽  
Sirilux Poompradub ◽  
Yuko Ikeda ◽  
...  

Abstract Strain-induced crystallization of natural rubber (NR) and synthetic isoprene rubber (IR) with various crosslinking densities was investigated by wide angle X-ray diffraction using a synchrotron radiation and simultaneous tensile measurements. The elongation ratio at the onset of crystallization (αc) was almost independent of crosslinking density. IR samples showed larger αc values than NR because of the lower stereoregularity of IR. These results suggest that the onset of crystallization is determined by increased melting temperature by strain due to an entropic reason. The amount of oriented amorphous component changed approximately linearly with strain, and was a little larger in IR than in NR when compared at the same elongation ratio. At small strain (and stress), crystallinity in IR was lower than in NR. These results indicate that, at small strain region, the more stress is assigned to oriented amorphous in IR than in NR.


2005 ◽  
Vol 128 (1) ◽  
pp. 28-33 ◽  
Author(s):  
Rebecca B. Dupaix ◽  
Dwarak Krishnan

Recently, a hyperelastic-viscoplastic constitutive model was developed for PET and the noncrystallizing copolymer PETG (R. B. Dupaix, Ph.D. thesis, MIT, 2003). The materials were found to behave very similarly under monotonic loading conditions and the single constitutive model was able to capture both materials’ behavior. However, differences were observed upon unloading, and it is expected that additional differences would be observed under more complex loading conditions. Here their behavior is investigated under nonmonotonic loading conditions, specifically under load-hold conditions. The model of Dupaix and Boyce (R. B. Dupaix, Ph.D. thesis, MIT, 2003) is modified to include Ahzi’s upper-bound model for strain-induced crystallization [Ahzi et al., Mech. Mater., 35(12), pp. 1139–1148 (2003)]. The crystallization model is adapted to include criteria for the onset of strain-induced crystallization which depend on strain rate and level of deformation. The strain-rate condition prevents crystallization from beginning prior to the deformation process slowing significantly. The level-of-deformation condition delays crystallization until the material has deformed beyond a critical level. The combined model demonstrates differences in behavior between PET and PETG during complex loading situations, indicating its ability to capture the fundamental criteria for the onset of strain-induced crystallization.


2015 ◽  
Vol 17 (23) ◽  
pp. 15331-15338 ◽  
Author(s):  
Nicolas Candau ◽  
Laurent Chazeau ◽  
Jean-Marc Chenal ◽  
Catherine Gauthier ◽  
José Ferreira ◽  
...  

The investigation on strain-induced crystallization, during complete cycles at high frequencies, highlighted for the first time the concomitant effects of the strain rate, memory of the chain alignment and self-heating.


Polymer ◽  
2014 ◽  
Vol 55 (10) ◽  
pp. 2535-2542 ◽  
Author(s):  
Pierre Yves Le Gac ◽  
Morgane Broudin ◽  
Gérard Roux ◽  
Jacques Verdu ◽  
Peter Davies ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (32) ◽  
pp. 25171-25182 ◽  
Author(s):  
Xuan Fu ◽  
Guangsu Huang ◽  
Zhengtian Xie ◽  
Wang Xing

The existence of a denser network domain formed by incorporation of filler and its vital role in determining the strain-induced crystallization behavior of nanocomposites is proved by in situ synchrotron X-ray diffraction characterization.


2015 ◽  
Vol 64 ◽  
pp. 244-252 ◽  
Author(s):  
Nicolas Candau ◽  
Rabia Laghmach ◽  
Laurent Chazeau ◽  
Jean-Marc Chenal ◽  
Catherine Gauthier ◽  
...  

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