Hysteresis and strain-dependent dynamic mechanical properties of epoxidized natural rubber filled with surface-oxidized carbon black

Author(s):  
Ajay K. Manna ◽  
P. P. De ◽  
D. K. Tripathy ◽  
S. K. De
1994 ◽  
Vol 67 (5) ◽  
pp. 845-853 ◽  
Author(s):  
A. Mallick ◽  
D. K. Tripathy ◽  
S. K. De

Abstract Increases in dynamic strain amplitude (DSA) causes changes in the dynamic mechanical properties of high abrasion furnace (HAF) carbon black filled polyacrylic acid (PAA) and epoxidised natural rubber (ENR) blends. But the changes are more prominent in comparison to conventional rubber vulcanizates. It is believed that crosslinking between PAA and ENR in the presence of carbon black results in the formation of a network-induced-agglomerate superstructure which, however, breaks down on the application of dynamic strain.


2013 ◽  
Vol 844 ◽  
pp. 109-112 ◽  
Author(s):  
Chesidi Hayichelaeh ◽  
Charoen Nakason ◽  
Anoma Thitithammawong

Epoxidized natural rubber (ENR)/Polypropylene (PP) thermoplastic vulcanizates were prepared by melt mixing method in an internal mixer. Influences of different mixing methods for incorporation of processing oil into the TPVs on tensile and dynamic mechanical properties of the TPVs and crystallinity of the PP were investigated. Results show that distribution of processing oil in the ENR/PP TPV is important due to the processing oil can promote and in the same time can interrupt an improvement in elastomeric properties of the TPV. Incorporation of processing oil into the ENR phase by preparation of oil extended ENR (the mixing method 1) before mixing with the PP was the better way to produce the TPV. It promoted the TPV with superior tensile and dynamic mechanical properties than the TPVs prepared from the mixing method 2 and 3 in which the processing oil was directly added into the PP phase. Furthermore, the TPV from the mixing method 1 had less effect of processing oil on the PP crystallization.


1992 ◽  
Vol 65 (5) ◽  
pp. 1016-1041 ◽  
Author(s):  
A. Y. Coran ◽  
J-B. Donnet

Abstract The Part I of this series described a rapid method for determining the quality of carbon-black dispersion. The second paper (Part II) was concerned with the kinetics of the dispersion of carbon black into natural rubber (dispersion quality as a function of mixing time) in an internal mixer. In this paper we consider the effects of changes in dispersion quality on the dynamic mechanical properties of both unvulcanized and vulcanized natural rubber. The effects of changes in the degree of carbon-black dispersion were measured by using a new prototype moving-die rheometer (which is presently being developed at Monsanto Instruments & Equipment Research Laboratory). By using this prototype rheometer, G′ and G″ were measured as functions of shear-strain amplitude, temperature, and frequency. Increases in the degree of carbon-black dispersion in uncured natural rubber (starting from very poor dispersion quality) give decreases in the values of both G′ and G″. The decrease in dynamic moduli with increases in the degree of carbon-black dispersion might be explained on the basis of a network of agglomerates which exists when the quality of dispersion is extremely poor. In the case of uncured samples, values of G′, measured at low strains (e.g. ±1%), become reduced after the imposition of a larger (±50%) sinusoidal shear strain for a short period of time (e.g. 3 s). Then, with the passage of time, the reduced value of G′ partially recovers. The extent of this recovery increases with increases in the dispersion rating DR. Similar results were obtained with respect to the loss modulus G″. In both cases, the extent of recovery is much less when the carbon black is very poorly dispersed. The unrecoverable proportion of G′ or G″ is also considered to be due to a network composed of mutually interactive agglomerates of carbon black.


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