Effect of new crosslinkages on continuous chemical stress relaxation of polymers

1972 ◽  
Vol 10 (12) ◽  
pp. 941-943 ◽  
Author(s):  
Kenkichi Murakami ◽  
Saburo Tamura
1972 ◽  
Vol 3 (1) ◽  
pp. 60-66 ◽  
Author(s):  
Arthur V. Tobolsky ◽  
Yuzo Takahashi ◽  
Shunji Naganuma

1966 ◽  
Vol 39 (5) ◽  
pp. 1640-1655 ◽  
Author(s):  
Walter Scheele ◽  
Karl-Heinz Hillmer

Abstract Temperature dependence of the chemical stress relaxation in oxygen of a series of natural rubber vulcanizates, extracted and unextracted, with the same pretreatment was investigated. Decrease of tension to about 50 per cent of the original was followed, using the half lives as a measure of velocity. The following observations were made: 1) Relaxation velocity of unextracted thiuram vulcanizates increases with increasing sulfur content; the activation energy decreases. 2) The relaxation velocities of extracted thiuram vulcanizates are independent of sulfur content of the mixtures and significantly greater than those of unextracted samples. This is caused by the loss of dithiocarbamate on extraction. 3) Other natural rubber vulcanizates (dithiocarbamate, MBT and peroxide vulcanizates) give the same relaxation half lives after extraction. 4) The relative importance of random scission and crosslink scission was discussed.


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.


1970 ◽  
Vol 27 (306) ◽  
pp. 705-712 ◽  
Author(s):  
Shunji Naganuma ◽  
Yuzo Takahashi

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.


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