Electrical approach to monitor the thermal oxidation aging of carbon black filled ethylene propylene rubber

2004 ◽  
Vol 86 (2) ◽  
pp. 209-215 ◽  
Author(s):  
Yangyang Sun ◽  
Shijian Luo ◽  
Ken Watkins ◽  
C.P. Wong
1962 ◽  
Vol 35 (4) ◽  
pp. 1091-1100
Author(s):  
Peter E. Wei ◽  
John Rehner

Abstract In searching for new vulcanizing systems for ethylene-propylene elastomers, we have found several more classes of active agents, heretofore undisclosed. They are: (a) perhaloalkanes and some polyhaloalkanes; (b) polyhalocycloalkenes; and (c) poly-N-halobenzoguanamines. Specific examples are: hexachloroethane, octachloropropane, octachlorocyclopentene, perchlorofulvalene, and N,N,N′,N′-tetrachlorobenzoguanamine. These agents are all effective in ethylene-propylene rubber, and some are capable of vulcanizing polyethylene, polypropylene, polyisobutylene, butyl, and highly unsaturated rubbers and their blends. The agents are most effective in the presence of sulfur. All are active in carbon black stocks, and at least some are active in mineral-filled and oil-extended stocks. Some of the vulcanizing agents can be accelerated by certain oxides and salts of metals widely distributed over the periodic system. Among the most active accelerators are iron compounds, such as iron tallate, stearate, naphthenate, octoate, and oxalate, and corresponding combinations of iron oxide and the free acids. These accelerators are antagonized by the presence of zinc oxide. The chemical diversity of these classes of vulcanizing agents and the complex behavior of the accelerators mentioned preclude an explanation of the vulcanization chemistry at this time.


1997 ◽  
Vol 70 (1) ◽  
pp. 60-70 ◽  
Author(s):  
B. G. Soares ◽  
F. Gubbels ◽  
R. Jéro^me ◽  
E. Vanlathem ◽  
R. Deltour

Abstract Polystyrene/rubber blends have been loaded with carbon black (CB) and the filler localization in the two-phase polyblends has been studied in relation to the chemical structure of the rubber. The CB localization and the electrical conductivity are greatly influenced by the substitution of the rubber chains. In polystyrene/polybutadiene blends, the filler is localized within the polybutadiene phase. In contrast, in polystyrene/polyisoprene and polystyrene/ethylene—propylene rubber (EPM) blends, CB is mainly localized at the interface, so that the CB percolation threshold in cocontinuous two-phase polyblends is dramatically decreased.


1964 ◽  
Vol 37 (1) ◽  
pp. 229-245 ◽  
Author(s):  
L. P. Lenas

Abstract Ethylene-propylene rubber (EPR), a saturated elastomer, is usually vulcanized by a peroxide-sulfur curing system. However, several disadvantages associated with this system—undesirable odor for some applications, narrow curing range, and poor strength obtained with mineral fillers—emphasize the need for other reactive chemicals as crosslinking coagents for EPR. Certain polyfunctional monomers such as ethylene dimethacrylate, and polyfunctional polymers such as 1,2-polybutadiene were promising crosslinking coagents for EPR. When used in place of sulfur, they decrease peroxide requirements of moderately filled EPR compounds. They also impart higher states of cure, improve the cure cycle, and decrease odor. The coagents are much superior to sulfur in mineral-filled EPR compounds where, in addition to increasing the crosslinking efficiency, they also improve the wetting of the filler particles by the rubber. However, in highly loaded (carbon black and oil) EPR formulations, the superiority of the peroxide-coagent system is mainly due to the ability to replace sulfur and, consequently, to improve odor.


2017 ◽  
Vol 44 (5) ◽  
pp. 11-14 ◽  
Author(s):  
A.A. Ol'khov ◽  
L.S. Shibryaeva ◽  
Yu.V. Tertyshnaya ◽  
A.N. Kovaleva ◽  
E.L. Kucherenko ◽  
...  

The structure, properties, and kinetics of thermal oxidation of blends based on polyhydroxybutyrate (PHB) and ethylene propylene rubber (EPR) were studied. The physicomechanical properties were studied using a ZE-40 tensile testing machine (Germany), and the crystallisation temperature Tcr and melting temperature Tm of PHB in the blends were determined on a DSM-2M differential scanning calorimeter at a scanning rate of 16°C/min. The morphology of films was determined by scanning electron microscopy on a Hitachi S-570 microscope (Japan). The kinetics of thermal oxidation of the blends was assessed according to the amount of absorbed oxygen. With increase in the PHB content in the blend there is a reduction in the elongation at break and an increase in the tensile strength and modulus. Change in the PHB content and in the oxidation time leads to negligible changes in Tcr and Tm. It was established that the greatest reactivity of blends in relation to oxygen is observed in the range of PHB concentrations of 20–40%, where the greatest phase interface area is formed. It was shown that, by changing the ratios of EPR and PHB, it is possible to control the kinetics of thermal oxidation of the blends. It was shown that, in the range of concentrations of 50–70% PHB, phase inversion occurs in the blends.


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