The Effect of Carbon Black Surface Properties and Structure on Rheometer Cure Behavior

1972 ◽  
Vol 45 (1) ◽  
pp. 129-144 ◽  
Author(s):  
G. R. Cotten

Abstract The cure behavior of SBR and NR compounds was examined using the Monsanto Rheometer. The three cure parameters—induction period (td), rate of crosslinking reaction (k2) and maximum increase in torque (ΔL)—were derived from the Rheometer torque curves. The data so obtained were used to calculate Westlinning's αF-values. It was shown that (1) k2 decreases with increasing total acid concentration at the carbon black surface and (2) the value of αF is related to the filler structure and the crosslink density of the rubber matrix. It was also demonstrated that the crosslink density, as measured by ΔL, is influenced by the surface chemistry of carbon black. In SBR stocks the crosslink density increases with increasing total acid concentration, while in NR compounds the reverse is true. These findings were confirmed by examining the tensile properties of regular and oxidized HAF-LS black in SBR and NR compositions. Thus the effect of carbon black surface chemistry on crosslink density can be estimated, for a given recipe, from the value of k2. An empirical relationship between the cure parameters (αF and k2) and filler structure (as measured by extrusion shrinkage) was derived and tested on a wide range of carbon blacks. This relation gives a much better correlation coefficient than the simple relation between extrusion shrinkage and αF alone. Thus by full use of the Rheometer data, the extrusion shrinkage or other structure-related properties of carbon black filled stocks can be predicted.

Carbon ◽  
2005 ◽  
Vol 43 (10) ◽  
pp. 2218-2221 ◽  
Author(s):  
Khadija Nyazi ◽  
Abdelaziz Baçaoui ◽  
Abdelrrani Yaacoubi ◽  
Hans Darmstadt ◽  
Alain Adnot ◽  
...  

1997 ◽  
Vol 70 (5) ◽  
pp. 747-758 ◽  
Author(s):  
H. Lüchow ◽  
E. Breier ◽  
W. Gronski

Abstract The transversal 1H NMR relaxation of the bound rubber shell of carbon black loaded elastomers can be decomposed into three relaxation regimes corresponding to the loosely bound rubber, the rubber that is immobilized on the carbon black surface and a third component of intermediate mobility. The relaxation time T2 of the intermediate component is related to the end-to-end distance of polymer segments between adsorption sites on the carbon black surface, by converting the relaxation times to length scales on the basis of recent work on NMR relaxation of elastomeric networks. From measurements on SBR loaded with carbon black N 220, a distance of 2.3 nm was obtained in agreement with characteristic dimensions of crystallite sizes and surface roughness as determined by atomic force and scanning tunneling microscopy. The analysis was applied to novel inversion blacks which give lower tan δ/60°C, and rolling resistance without affecting tan δ/0°C and wet skid behavior. These blacks were found to possess a higher density of adsorption sites and a greater surface roughness as compared to standard carbon blacks. In addition to the surface characterization, the analysis of the mobile component of the compound allowed the estimation of the density of entanglement couplings between the rubber matrix and the bound rubber shell.


1968 ◽  
Vol 41 (2) ◽  
pp. 382-399 ◽  
Author(s):  
Marvin L. Deviney ◽  
Lawrence E. Whittington

Abstract Radiotracer techniques have been applied to the study of interactions of carbon black surface functional groups with two chosen organic systems. The basic reaction mechanisms demonstrated in this study may have implications in elastomer reinforcement. Direct radiochemical evidence supports the conclusions of Hallum and Drushel (based on less direct polarographic data) that surface quinonic groups exhibit hydrogen abstraction activity toward tertiary hydrogens in paraffinic hydrocarbons. Studies on the system carbon black and styrene using tritium radiotracer have provided direct evidence that phenolic hydrogens participate in the polymerization acceleration and graft polymer formation reaction and are transferred to the growing polystyrene chains as postulated by Donnet. Several methods have been developed for specifically labelling certain oxygenated functional groups on the carbon surface with tritium and for tritium labelling carbon black in aromatic hydrogen positions. The techniques developed in this work and the basic reaction mechanisms derived will permit this investigation to be extended into a radiochemical study of carbon black surface interactions with elastomer related systems of interest to the rubber industry.


Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 153
Author(s):  
Sang-Min Lee ◽  
Sang-Hye Lee ◽  
Jae-Seung Roh

In the present study, carbon black activated by CO2 gas was examined through XRD analysis, especially with regard to changes in its structural parameters. Based on the results, its activation process was thoroughly analyzed. The activation process was controlled by isothermally activating the carbon black inside a reaction tube through which CO2 gas flowed. With this approach, the degree of activation was varied as desired. At an early stage of the activation process, the amorphous fraction on the carbon black surface was preferentially activated, and later the less-developed crystalline carbon (LDCC) region inside the carbon black particles started to be activated. The latter process was attributable to the formation of pores inside the carbon black particles. As the activation process proceeded further, the more-developed crystalline carbon (MDCC) region started to be activated, thereby causing the pores inside the carbon black particles to grow larger. At the last stage of the activation process, La was found to be decreased to about 40 Å. This implied that the edges of the graphite crystals had been activated, thus causing the internal pores to grow and coalesce into larger pores. Activated conductive Super-P with enhanced pore properties is expected to have wide applications.


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