Influence of Different Silanes on the Reinforcement of Silica-Filled Rubber Compounds

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.

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.


Polymers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1653
Author(s):  
Imran Hussain Syed ◽  
Jorge Lacayo-Pineda

A systematic study of several SBR compounds filled with carbon black of various grades were analysed with the high-frequency Dynamic Mechanical Analyzer (HF DMA) in order to quantify the degree of nonlinearity induced by fillers in rubber compounds. These filler grades indirectly reflect different degrees of microdispersion, which seems to be the main influence on the superharmonic resonance phenomenon observed in HF DMA. This statement arises from the comparison of the microdispersion observed in TEM images. In the second part of the paper, a model compound filled with carbon black is enhanced with a standard reinforcing resin, which leads to a more compact filler network. This induces a higher superharmonic resonance response as well as a higher transmissibility behaviour.


1994 ◽  
Vol 67 (2) ◽  
pp. 217-236 ◽  
Author(s):  
Timothy A. Okel ◽  
Walter H. Waddell

Abstract The effectiveness of predicting rubber performance based on measured silica physical properties in silica- and carbon black-filled compounds is presented for three rubber formulations: an off-the-road tire tread, a wire coat stock and a V-belt. Correlation and regression analyses were performed using SAS software for sixteen physical properties of thirteen precipitated silicas, and sixteen rubber compound performance characteristics of the three compounds. Silica physical properties studied include various measurements of surface area and structure, particle size, pH and impurities. Rubber performance characteristics studied include cure properties and physical properties such as stress/strain, tear strength, cut growth resistance, abrasion resistance and heat build-up. The present study confirms that silica surface area is the single best predictor of the effect that varying silica physical properties have on the physical performance of cured, carbon black-filled rubber compounds containing precipitated silica. Silica structure, as measured by DBP absorption and nitrogen or mercury pore volume, is a secondary predictor of certain rubber physical properties. The confidence limits of the predictions is dependent upon the concentration of precipitated silica used in the carbon black-filled rubber compound.


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.


2006 ◽  
Vol 73 ◽  
pp. 109-119 ◽  
Author(s):  
Chris Stockdale ◽  
Michael Bruno ◽  
Helder Ferreira ◽  
Elisa Garcia-Wilson ◽  
Nicola Wiechens ◽  
...  

In the 30 years since the discovery of the nucleosome, our picture of it has come into sharp focus. The recent high-resolution structures have provided a wealth of insight into the function of the nucleosome, but they are inherently static. Our current knowledge of how nucleosomes can be reconfigured dynamically is at a much earlier stage. Here, recent advances in the understanding of chromatin structure and dynamics are highlighted. The ways in which different modes of nucleosome reconfiguration are likely to influence each other are discussed, and some of the factors likely to regulate the dynamic properties of nucleosomes are considered.


1980 ◽  
Vol 53 (3) ◽  
pp. 437-511 ◽  
Author(s):  
D. W. Brazier

Abstract An attempt has been made to review the development of thermoanalytical procedures as they have been applied to elastomers and elastomer systems over the past 10 years. For all rubber industry products, temperature and its effects, either alone or in conjunction with the chemical environment, play an important role from the production stage through to the final failure of the product in the field. It is thus not surprising that thermal analysis, in which temperature is the prime variable, has found such diverse applications in elastomer studies. The identification and quantitative analysis of rubber formulations have received most attention. Such formulations produce characteristic “fingerprints” when studied in DTA, DSC, TG, or TMA. In DSC, the determination of the glass transition characteristics, the observation and determination of crystallinity, the detection of cyclization reactions, and the monitoring of thermal and oxidative degradation characteristics can all be observed in a single experiment covering the temperature range from −150 to +600°C. At normal heating rates, e.g., 20°C/min, such information is available in 40 min. TG/DTG analysis can yield the elastomer or elastomers content, oil and plasticizer, carbon black (level and often type), and inorganic ash in less than 60 min. Processing and curing can also be studied. Blend compatibility can be assessed on the basis of both Tg and crystallinity measurements and the data used to determine optimum mixing times. Sulfur vulcanization and peroxide curing of elastomers is readily monitored by DSC and can be used for confirmation analysis of the presence of curatives. Limitations in such analysis exist, but as understanding and ability to interpret cure exotherms increase, valuable information about the mechanism and the nature of the cured network will be obtained. The testing of rubber compounds involves many hours of labor by current procedures. The rapidity of thermal analysis promises to offer some relief. In addition to DSC and TG, TMA, a relatively new technique, offers a rapid approach to low-temperature testing. Dynamic mechanical analysis (DMA) offers a rapid route to determining dynamic properties, but as yet, relatively little has been published on the application of this new technique to elastomers. As environmental concern increases, techniques such as evolved gas analysis (EGA) and combined techniques such as TG/gas chromatography are predicted to play an important role. As for the future, it is readily apparent that the principles of the methods have been established and, in several cases, it now remains to reduce them to a practical level. In some areas, such as vulcanization studies, much remains to be undertaken to improve our interpretive skills. Although there is some indication that certain industries have produced “in-house” standards for the analysis of rubber compounds by DSC and TG/DTG, it will only be when national and international standards organizations study and produce standard procedures, that the techniques will be generally adopted. Maurer's prediction in 1969 of increased applications of DTA and TG in elastomer studies has undoubtedly proved correct, and with the proliferation of reliable commercial instrumentation, significant developments can be anticipated in the next decade.


2021 ◽  
Vol 0 (2) ◽  
pp. 36-43
Author(s):  
N.V. Shadrinov ◽  
◽  
A.A. Khristoforova ◽  

The results of the study of the complex of properties of an elastomeric composite material based on nitrile butadiene rubber BNKS-18 and ultrahigh molecular weight polyethylene are presented. The effect of UHMWPE on the vulcanization characteristics of rubber compounds, the physicomechanical properties of vulcanizates before and after thermal aging in a hydrocarbon environment and air, and also on the dynamic properties before and after curing are investigated.


2009 ◽  
Vol 81 (10) ◽  
pp. 1783-1798 ◽  
Author(s):  
Kazuya Saito

Extensive application of chemical thermodynamics to exotic aggregation formed in thermotropic liquid crystals is briefly described. Through thermodynamic analyses and considerations of experimental results on liquid crystals, the unexpected sharing of common properties by thermo- and lyotropic liquid crystals is demonstrated. In some thermotropic liquid crystals, the terminal alkyl chain attached to the molecular core is highly disordered, as indicated by the magnitude of configurational entropy. The molten chain serves as intramolecular solvent (self-solvent), as evidenced by the close similarity between phase diagrams against chain length and composition in the binary system with n-alkane. These facts lead to the quasi-binary picture of thermotropic liquid crystals. Consideration of the thermodynamic potential expanded in terms of density fluctuation gives a new insight into the multicontinuous phases formed in simple systems consisting of anisotropic, rodlike particles.


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