scholarly journals Role of Strain Crystallization in the Fatigue Resistance of Double Network Elastomers

2003 ◽  
Vol 76 (4) ◽  
pp. 892-898 ◽  
Author(s):  
P. G. Santangelo ◽  
C. M. Roland

Abstract Double networks were prepared from guayule rubber (GR), deproteinized natural rubber (DPNR), and styrene-butadiene rubber (SBR), and their properties compared to conventional “single networks” having the same crosslink density. Substantial residual strains (> 150%) were obtained in all double networks, whereby the modulus parallel to the residual strain was enhanced. For the two strain-crystallizing elastomers, the fatigue resistance of the double networks (for extensions parallel to the residual strain) was higher than for their single network counterparts. Moreover, the guayule rubber, which is more strain-crystallizable than DPNR, exhibited the greater enhancement. For the amorphous SBR, on the other hand, the network structure had an insignificant effect on the fatigue life. These results demonstrate that longer mechanical fatigue lifetimes in double network rubbers are a consequence of their intrinsic orientation. This provides the capacity to retain crystallinity at the front of growing cracks, even in the absence of stress. The origin of the improved fatigue resistance is similar to the mechanism responsible for the better performance of strain-crystallizing rubbers subjected to non-relaxing cyclic deformations.

Nanomaterials ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 486 ◽  
Author(s):  
Elkid Cobani ◽  
Irene Tagliaro ◽  
Marco Geppi ◽  
Luca Giannini ◽  
Philippe Leclère ◽  
...  

Sepiolite (Sep)–styrene butadiene rubber (SBR) nanocomposites were prepared by using nano-sized sepiolite (NS-SepS9) fibers, obtained by applying a controlled surface acid treatment, also in the presence of a silane coupling agent (NS-SilSepS9). Sep/SBR nanocomposites were used as a model to study the influence of the modified sepiolite filler on the formation of immobilized rubber at the clay-rubber interface and the role of a self-assembled nanostructure in tuning the mechanical properties. A detailed investigation at the macro and nanoscale of such self-assembled structures was performed in terms of the organization and networking of Sep fibers in the rubber matrix, the nature of both the filler–filler and filler–rubber interactions, and the impact of these features on the reduced dissipative phenomena. An integrated multi-technique approach, based on dynamic measurements, nuclear magnetic resonance analysis, and morphological investigation, assessed that the macroscopic mechanical properties of clay nanocomposites can be remarkably enhanced by self-assembled filler structures, whose formation can be favored by manipulating the chemistry at the hybrid interfaces between the clay particles and the polymers.


2017 ◽  
Vol 58 (1) ◽  
pp. 74-85 ◽  
Author(s):  
Joyeeta Ghosh ◽  
Soumyajit Ghorai ◽  
Satyaban Bhunia ◽  
Madhusudan Roy ◽  
Debapriya De

2015 ◽  
Vol 17 (17) ◽  
pp. 11217-11228 ◽  
Author(s):  
Jiji Abraham ◽  
Hanna J. Maria ◽  
Soney C. George ◽  
Nandakumar Kalarikkal ◽  
Sabu Thomas

The aim of the present work is to investigate the role of the sorption technique in analysing the compatibility and the reinforcing effect of MWCNTs as a filler in the SBR matrix.


2007 ◽  
Vol 119 ◽  
pp. 115-118
Author(s):  
Kyoung Sub Lee ◽  
Mi Jeong Han

Styrene-butadiene rubber (SBR) nanocomposites were prepared from organically modified montmorillonite (OMMT). To enhace the dispersion properties of OMMT in SBR matrix, polybutadiene was modified with tetramethyl siloxane substituted with benzylamine, and the master batches of those were prepared by a solution process using tetrahydrofuran. SBR/master batch nanocomposites could be obtained by melt-compounding followed by hot-press vulcanization. Xray diffraction (XRD) studies revealed that the interlayer distances of OMMT were increased and the nanocomposites had the intercalated and exfoliated structures of OMMT by the nanocomposition of SBR with the master batch. Mechanical and dispersion properties of the nanocomposites from the master batch are superior to those of nanocomposites without master batch.


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