Effect of Elongation on the Electrical Anisotropy of Natural Rubber and SBR Vulcanizates Containing ISAF Carbon Black

1962 ◽  
Vol 35 (2) ◽  
pp. 317-325 ◽  
Author(s):  
R. Chasset ◽  
P. Thirion

Abstract The electrical resistivity of testpieces under different elongations, both parallel and at right-angles to the axis of elongation, was measured for two vulcanizates, i.e. one of natural rubber and the other of SBR, compounded with 20 volume per cent of ISAF black (Vulcan 6). Within the range of validity of Ohm's law, the main results of this study are as follows: a) the resistivities of both vulcanizates increase considerably with elongation, in both directions. b) on the whole, both vulcanizates are electrically anisotropic, since current flows more easily longitudinally than it does transversely. The anisotropy increases at the start with elongation, then becomes practically constant. However, the latter level is much higher with natural rubber, for which it corresponds to an anisotropy of about 1,000 and an elongation of around 150%. For SBR this level is only 20 to 30 and is reached at only 50% elongation. Owing to the complexity of the problem, no interpretation can yet be given for these differences. It will first be necessary to examine other elastomers and carbon blacks. For the time being, it may merely be stated that the electrical anisotropy of natural rubber and SBR reinforced vulcanizates differs as much as their mechanical properties, especially their tearing behavior.

Author(s):  
Yayoi Akahori ◽  
Misao Hiza ◽  
Soki Yamaguchi ◽  
Seiichi Kawahara

ABSTRACT Protein effect on vulcanization of NR, obtained from Hevea brasiliensis, was investigated by analyzing the crosslinking structure of the resulting vulcanizates prepared from untreated NR, deproteinized natural rubber (DPNR), and protein-free natural rubber (PFNR) by swelling methods and rubber-state NMR spectroscopy. The proteins present in NR were removed by three methods: deproteinization with enzyme, urea, or urea–acetone in the presence of sodium dodecyl sulfate. The amount of proteins present in NR, approximately 0.238 w/w%, was reduced to 0.000 w/w% by urea–acetone deproteinization, whereas it was reduced to approximately 0.003 and 0.019 w/w% by enzyme and urea deproteinizations, respectively. Hardness, swelling degree, and crosslinking structure depended on the amount of proteins. Changes in mechanical properties for the vulcanizates prepared from not only non-filler compounds but also carbon black–filled and silica-filled compounds were attributed to the amount of proteins.


2017 ◽  
Vol 744 ◽  
pp. 282-287
Author(s):  
Sarawut Prasertsri ◽  
Sansanee Srichan

This research aimed to develop the formulation of natural rubber filled with carbon black, silica and calcium carbonate for rubber calf nipple application. The reverse engineering was performed on the calf nipple product to analyze the rubber type and component by using Soxhlet extraction, thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR) techniques. Furthermore, mechanical properties were examined to act as benchmark for the rubber compound design. The results showed that rubber component in the nipple product was natural rubber, whereas two filler types revealed as carbon black and calcium carbonate with 10 and 35 of the total weight. In addition, rubber nipple showed the hardness of 46±1 Shore A and tensile strength of 5.3±0.60 MPa. From the investigation of the properties of developed rubber compounds in this work, it was found that the mechanical properties depended on type and content of filler. The required mechanical properties of vulcanizates were achieved at 20 phr of carbon black (N330), 20 phr of silica and 120 phr of calcium carbonate.


1962 ◽  
Vol 35 (3) ◽  
pp. 563-571 ◽  
Author(s):  
J. Janacek

Abstract The relation between the degree of crosslinking determined by means of swelling and the theoretical total contact surface of rubber to carbon black was investigated with vulcanizates of two elastomers which were cured by various vulcanization methods and using various concentrations—even extremely high ones—of carbon blacks with different specific surface, degrees of chain structure and chemical activities. A constant, α, the magnitude of which generally depends upon the degree of agglomeration of the carbon blacks and on the chemical nature of their surface as well as on the polymers used and the vulcanization method, but which is practically unrelated to the filler concentration, has been proposed to express the relative crosslinking activity of carbon blacks.


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