The Role of Filler Networking in Dynamic Properties of Filled Rubber

1999 ◽  
Vol 72 (2) ◽  
pp. 430-448 ◽  
Author(s):  
Meng-Jiao Wang

Abstract Fillers, when added to polymer systems, are known to cause a considerable change in dynamic properties. For a given polymer and cure system, this paper discusses the impact of the filler network, both its strength and architecture, on the dynamic modulus and hysteresis during dynamic strain. It was found that the filler network can substantially increase the effective volume of the filler due to rubber trapped in the agglomerates, leading to high elastic modulus. The amount of trapped rubber was estimated according to Van der Poel theory. During cyclic strain, while the stable filler network can reduce the hysteresis of the filled rubber, the breakdown and reformation of the filler network would cause an additional energy dissipation resulting in higher hysteresis.

2002 ◽  
Vol 75 (4) ◽  
pp. 563-579 ◽  
Author(s):  
Hans-Detlef Luginsland ◽  
Joachim Fröhlich ◽  
André Wehmeier

Abstract The silane modification of precipitated silica for rubber applications is state-of-the-art. Usually, bifunctional silanes are used to provide a silica-to-rubber coupling. In this paper, the general effect of the silane modification on the Payne-effect of silica-filled compounds (S-SBR/BR) is investigated by applying the Rubber Process Analyzer (RPA). For this purpose, the amount as well as the type of silane have been varied. The alkyl chain length of monofunctional silanes determines their hydrophobation efficiency and therefore influences the degree of the silica network, whereas bifunctional silanes also contribute to the crosslinking and build up an in-rubber structure. The degree of the filler network is not only determined by the kind of silica modification, but also by the reinforcement behavior of the silica, mainly characterized by the CTAB surface area. The findings of this study give a better insight into the reinforcement of silica-filled rubber compounds and their dynamic properties.


1998 ◽  
Vol 71 (3) ◽  
pp. 520-589 ◽  
Author(s):  
Meng-Jiao Wang

Abstract In the past few years, an enormous amount of work has been reported on the progress in the application of conventional fillers and the development of new products to improve the reinforcement of rubber, dynamic properties in particular. While all agree that the filler as one of the main components of the filled-rubber composite, has a very important role in improving the dynamic performances of the rubber products; many new ideas, theories, practices, phenomena, and observations about how and especially why the filler alters the dynamic stress-strain response have been presented. This, of course, suggests that not only is the real world of the filled rubber complex and sophisticated but also multiple mechanisms may be involved. However, it must be admitted that the possibility exists for explaining the effect of all fillers on rubber properties ultimately in similar and relatively nonspecific terms, i.e., the phenomenon related to all filler parameters should follow a general rule or principle. It is the author's belief that, with regard to the effect of filler on the dynamic properties of a given polymer and cure system, filler networking, both its architecture and strength, is the main (although not only) parameter to govern the behavior of the filled rubber. From the thermodynamic and kinetic points of view, filler network formation is especially related to filler-filler, polymer-filler, as well as polymer-polymer interactions. As mentioned in the introduction, this paper is an attempt to review the effect of filler characteristics on dynamic properties in connection with processing conditions and additives. Since the polymer-filler interaction is not only affected by filler, what is also important are the characteristics of polymers such as chemical composition, chain microstructure including molecular weight and molecular weight distribution, configuration, stereoregularity, monomer unit distribution and sequence, and their functionality. All of these have a substantial influence on the physical and/or chemical interactions with other additives and filler surfaces, as well as on the interaction between polymer molecules themselves, which would impact not only the filler network formation but also the viscoelastic response of the polymer matrix. In addition, the polymer network structure which was formed during vulcanization and characterized by crosslink density, crosslink structure, and chain modification, is equally important in contributing to the overall dynamic properties of the filled rubber. In this paper, only some of these aspects have been discussed relative to their effect on filler network formation. Further discussion of these parameters is beyond the subject of the present paper. However, some guidance to these important topics is given in a handbook that was recently published.


1993 ◽  
Vol 66 (2) ◽  
pp. 178-195 ◽  
Author(s):  
Meng-Jiao Wang ◽  
Siegfried Wolff ◽  
Ewe-Hong Tan

Abstract Based on the concepts of the occlusion of rubber and random packing of spheres whose volume is equivalent to that permeated by individual aggregates, an equation was deduced to estimate the distance between carbon-black aggregates in filled rubber. It was found that when the interaggregate distance reaches a critical point which is approximately identical for all carbon blacks investigated (furnace blacks), the elastic modulus measured at very low strain deviates from the modified Guth-Gold equation. Tan δ and resilience are mainly determined by the distance between aggregates. These phenomena are related to filler networking which is determined by the attractive potential and the distance between individual aggregates. Since the factor Sf, used to characterize the strength of secondary filler networks in hydrocarbon rubbers and measured by means of inverse gas chromatography, is approximately the same for all furnace blacks, the interaggregate distance seems to determine filler networking. A comparison of fillers with different Sf (graphitized vs. nongraphitized carbon blacks, carbon black vs. silica) shows that at the same interaggregate distance, a lower Sf leads to higher tan δ of the filled vulcanizates.


2013 ◽  
Vol 44 (5) ◽  
pp. 311-319 ◽  
Author(s):  
Marco Brambilla ◽  
David A. Butz

Two studies examined the impact of macrolevel symbolic threat on intergroup attitudes. In Study 1 (N = 71), participants exposed to a macrosymbolic threat (vs. nonsymbolic threat and neutral topic) reported less support toward social policies concerning gay men, an outgroup whose stereotypes implies a threat to values, but not toward welfare recipients, a social group whose stereotypes do not imply a threat to values. Study 2 (N = 78) showed that, whereas macrolevel symbolic threat led to less favorable attitudes toward gay men, macroeconomic threat led to less favorable attitudes toward Asians, an outgroup whose stereotypes imply an economic threat. These findings are discussed in terms of their implications for understanding the role of a general climate of threat in shaping intergroup attitudes.


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