Chemical Stress Relaxation of Oil-Modified Phenolic Resin

1970 ◽  
Vol 27 (306) ◽  
pp. 705-712 ◽  
Author(s):  
Shunji Naganuma ◽  
Yuzo Takahashi
1986 ◽  
Vol 59 (4) ◽  
pp. 541-550 ◽  
Author(s):  
Kyung-Do Suh ◽  
Hidetoshi Oikawa ◽  
Kenkichi Murakami

Abstract From the experimental results of the present investigation, it is apparent that two kinds of networks which have a different three-dimensional network structure give quite different behavior of chemical stress relaxation, even if both networks have the same network chain density. The difference in three-dimensional network structure for the two kinds of rubber arises from the degree of entanglement, which changes with the concentration of the polymer chains prior to the crosslinking process. The direct cause of chemical relaxation is due to the scission of network chains by degradation, whereas the total relaxation is caused by the change of geometrical conformation of network chains. This then casts doubt on the basic concept of chemorheology which is represented by Equation 2.


1998 ◽  
Vol 71 (2) ◽  
pp. 157-167 ◽  
Author(s):  
G. R. Hamed ◽  
J. Zhao

Abstract Thin specimens of a black-filled, natural rubber vulcanizate have been held in uniaxial tension at 72°C and 200% elongation in a forced air oven. After substantial oxidative attack (inferred from stress relaxation), small edge cracks formed. Initially, these cracks grew perpendicular to the loading direction, but, upon reaching about 0.1 mm in depth, longitudinal crack growth commenced and fracture progressed by a kind of 0°-peel process with “splitting-off” of successive strands of rubber. This phenomenon is attributed to anisotropy in strength caused both by straining and by oxidative attack.


1962 ◽  
Vol 6 (24) ◽  
pp. S55-S56
Author(s):  
Arthur V. Tobolsky ◽  
Hyuk Yu

1973 ◽  
Vol 46 (2) ◽  
pp. 477-482
Author(s):  
Saburo Tamura ◽  
Kenkichi Murakami

Abstract Both initial network chain densities nM(0) and nS(0) of dicumyl peroxide- cured natural rubbers were determined from the tensile stress and swelling method, respectively. The difference between nM(0) and nS(0) was usually constant, independent of the magnitude of network chain density. That is, it was found that the number of entanglement network chains in the crosslinked natural rubber was usually constant, independent of network chain density. The entanglement network chain density nII(0) was 0.7×10−4 mole/cc. This led to the supposition that the molecular weight between entanglement points Me would be about 9000. Although this value is far from exact, it does not differ too greatly from the value found for noncrosslinked natural rubber. Next, in order to calculate the number of main-chain scissions of crosslinked polymers from their chemical stress relaxation, we proposed our modification of Tobolsky's equation. Using our equation, it was found that the scission of dicumyl peroxide-cured natural rubber occurred in the main chain only. Furthermore, this value agreed with the one obtained from the oxidation of toluene solution of noncrosslinked rubber under the same conditions.


1975 ◽  
Vol 19 (9) ◽  
pp. 2571-2581 ◽  
Author(s):  
John G. Curro ◽  
Edward A. Salazar

1967 ◽  
Vol 70 (2) ◽  
pp. 188-191
Author(s):  
Kenkichi MURAKAMI ◽  
Takae KUSANO ◽  
Shigeo NAKAMURA ◽  
Hideo KISE ◽  
Katsumichi ONO

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