Studies on dynamic creep of carbon black-filled rubber vulcanizates.

1989 ◽  
Vol 62 (7) ◽  
pp. 448-458
Author(s):  
Kunihiko FUJIMOTO ◽  
Tatsuhiko HATAKEYAMA
2015 ◽  
Vol 6 (2) ◽  
pp. 159-172 ◽  
Author(s):  
Junping Song ◽  
Lianxiang Ma ◽  
Yan He ◽  
Wei Li ◽  
Shi-Chune Yao

2012 ◽  
Vol 19 (01) ◽  
pp. 1250003
Author(s):  
JIAN CHEN ◽  
YONGZHONG JIN ◽  
JINGYU ZHANG ◽  
YAFENG WU ◽  
CHUNCAI MENG

Bound rubber in carbon black (CB) filled rubber (natural rubber (NR) and styrene–butadiene rubber (SBS)) was prepared by the solvent method. The nanomorphology of CB and rubber/CB soluble rubber was observed by atomic force microscope. The results show that high-structure CB DZ13 has a "grape cluster" structure which consists of many original particles with the grain size of about 30–50 nm. Graphitizing process of CB decreases the amount of bound rubber. The NR/DZ13 soluble rubber with island–rim structure has been obtained, where the islands are DZ13 particles and the rims around the islands are occupied by NR film. But when the graphitized DZ13 particles were used as fillers of rubber, we have only observed that some graphitized DZ13 particles were deposited on the surface of the globular-like NR molecular chains, instead of the spreading of NR molecular chains along the surface of DZ13 particles, indicating that graphitized DZ13 has lower chemical activity than ungraphitized DZ13. Especially, we have already observed an interesting unusual bound rubber phenomenon, the blocked "bracelet" structure with the diameter of about 600 nm in which CB particles were blocked in ring-shaped SBS monomer.


1993 ◽  
Vol 66 (2) ◽  
pp. 317-328 ◽  
Author(s):  
Asahiro Ahagon

Abstract Analysis is made for the origin of the mixing-induced tensile property variation of a filled rubber. Attention is paid to the hydrodynamic effect f(ϕe) of the filler, defined here as the factor to adjust the deviation of 100% modulus from the theory of rubber elasticity. For the rubbers mixed under variety of conditions, the f(ϕe)'s are calculated from the observed values of the modulus, at 25°C and 100°C, and the crosslink density. The variation of the f(ϕe) is considered to be governed by the mobility of the polymer confined in agglomerates of the filler. The mobility variation due to mixing seems to be mainly influenced by agglomerate size at 25°C, and by agglomerate size and chemical constraints at 100°C. Therefore, the f(ϕe)'s at the two temperatures are suggested to be useful measures of the state of carbon-black micro-dispersion. The extensibility of the rubbers is closely related f(ϕe). This indicates that the failure property is also governed by the mobility of the confined polymer.


2003 ◽  
Vol 91 (1) ◽  
pp. 577-588 ◽  
Author(s):  
J. Léopoldès ◽  
C. Barrès ◽  
J. L. Leblanc ◽  
P. Georget

2009 ◽  
Vol 87-88 ◽  
pp. 86-91 ◽  
Author(s):  
Yan He ◽  
Hai Tao Li ◽  
Lian Xiang Ma

The thermal conductivities of two rubbers filled with different carbon black (N330 and N375) are measured by experiments, and compared with five theoretical models calculated results. It is shown that thermal conductivity of carbon-filled rubber is obviously enhanced with increase of the volume filler fraction of carbon black and the thermal conductivity of carbon-filled rubber is related to the microstructure and morphology of carbon black. The estimated thermal conductivities by using the model proposed in our previous paper are of the same variation as the experimental ones of N330 carbon/rubber and N375 carbon/rubber during the range of volume fraction from 2% to 20%.


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