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Rubber system, filled

Comparative Mechanical Properties Data on Ordinary ZnO and Nano-ZnO-Filled Carboxylated Nitrile Rubber Systems... [Pg.94]

Equation 18.2 reveals the importance of energy dissipation in the fracmre of mbbery materials, that is, the strength of rubbers, whether filled or unfilled, is governed by the hysteresis energy dissipated in deforming the system. [Pg.537]

The average cross-sectional area of rubber in filled samples has been the subject of much discussion. In a filled system which swells to a foam-... [Pg.226]

The volume swelling ratios (Vr) are inversely proportional to the equilibrium volume fraction of the rubber in the corresponding swollen systems (filled and gum, represented by subscripts f and 0, respectively), such that ... [Pg.66]

In the early works by Soviet scientists (primarily the followers of P. A. Rebinder and G. V. Vinogradov) and Western investigators (H. C. Booij, R. I. Tanner, J. M. Simmons, T. Kataoka, R. Osaki, et al.) published between 1966 and 1968, the vibration was proven to produce a powerful effect on rheological properties of two-phase disperse systems, filled polymers, rubbers as wellas dissolved and molten polymers. [Pg.43]

Conductive adhesives are generally formulated from base polymers that are low-viscosity, thermosetting resins such as epoxies. Where elastomeric properties are required, silver-filled flexible epoxy and silver-filled silicone rubber systems are commercially available. [Pg.172]

B. (2S,3S)-2-Nitro-5-phenyl-1,3-pentanediol. A 500-mL, two-necked, round-bottomed flask equipped with a magnetic stirring bar, septum cap, and a rubber balloon filled with argon, is charged with 119 mL of THF and a 0.03 M THF solution of (R)-LLB catalyst (63.3 mL, 1.90 mmol) under an argon atmosphere. The system is... [Pg.153]

In rubber systems containing carbon black, flocculation may cause substantial changes in mechanical properties. Flocculation in these systems counteracts filler dispersion. Carbon black flocculation occurs in filled rubber stock during storage or during vulcanization in the absence of shear. " Temperature is the important kinetic factor which affects the flocculation rate (Figure 5.19). In addition to temperature and time, flocculation depends on the type of carbon black and its concentration. [Pg.262]

Yatsuyanagi F, Kaidou H, Ito M (1999) Relationship betwetai viscoelastic properties and characteristics of filler-gel in filled rubber system. Rubber Chem Technol 4 657-672... [Pg.15]

Chapter 4 investigates the rheological and the dynamic mechanical properties of rubber nanocomposites filled with spherical nanoparticles, like POSS, titanium dioxide, and nanosilica. Here also the crucial parameter of interfacial interaction in nanocomposite systems under dynamic-mechanical conditions is discussed. After discussing about filled mono-matrix medium in the first three chapters, the next chapter gives information about the nonlinear viscoelastic behavior of rubber-rubber blend composites and nanocomposites with fillers of different particle size. Here in Chap. 5 we can observe a wide discussion about the influence of filler geometry, distribution, size, and filler loading on the dynamic viscoelastic behavior. These specific surface area and the surface structural features of the fillers influence the Payne effect as well. The authors explain the addition of spherical or near-spherical filler particles always increase the level of both the linear and the nonlinear viscoelastic properties whereas the addition of high-aspect-ratio, fiberlike fillers increase the elasticity as well as the viscosity. [Pg.316]

Macaione et al [235] have used TG for the characterisation of SBR, BR and NR in mono-, di-, or triblend rubber systems and carbon-filled rubber composites and determined the percentage of highly volatile organics, elastomer(s), carbon-black, and inorganic residue for each sample. Lochmiiller et al [194] applied factor analytical methods to evaluate TG results of a series of rubber blends and mixtures composed of chloroprene rubber, NBR, and common rubber additives. TG and measurements of toluene extractable matter of cured siloxane rubbers thermally aged in inert gas atmosphere at 80° C showed a build-up of low-MW fragments in the rubber network with age [244]. [Pg.182]

F. Yatsuyagagi, H. Kaidou, N. Suzuki, and M. Ito, Relationship between secondary structure of fillers and the mechanical properties of silica filled rubber systems , ACS Rubber Division Meeting, Providence, RI, April (2001)... [Pg.72]

An interestii observation has been made in the work (96) to the effect that Kemet s equation is not sufficiently reliable for a complex stem a glass4ike polymer-rubber-like-filler-glass beads. In this case the best results can be obtained if the systems are conridered as a sin phase of a glass-like po mer with rubber in which glass beads are dispersed. Then the modulus of the me m is first calculated as a system filled with a polymeric filler, following which the calculated value is used for the evaluation of the composite material. [Pg.25]

Filled polymer systems of industrial importance, e.g., filled rubber compounds, filled thermoplastics are thus meso or microcomposites, possibly with a structuration (of the dispersed phase) at the nano or meso scale. Whilst no sizeable commercial application yet exist for nanocomposites rubbers or thermoplastics (to the author s knowledge), considerable research has been made since 1984 with so-called ex-foliated layered silicate "nano-clays." Exfoliation means that individual clay sheets, of around 1 nm thickness, have been separated and adequately dispersed in the matrix. Some reinforcement has indeed been demonstrated with such exfoliated nanoparticles but, generally with very specific rubber systems and/or at a cost of preparation that is hardly compatible with reasonable chances of commercialization. [Pg.7]

Having the interaction site well identified in a filled polymer system, in terms of chemical activity and surface, and a clear picture of the nature of the polymer-filler interaction allow quite convincing theoretical models to be developed. Such a favorable situation is however restricted to a few cases, namely silica/polysiloxane systems. With other systems, either the nature of the polymer-filler interaction is badly known or the size of the interaction site cannot be clearly quantified, or both. In such case however, the successful silica/PDMS case provides some interesting guidelines when assuming that, whatever are the respective chemical natures of the filler and the polymer, at least the physics is the same. As we have seen the author has successfully adapted this model to the case of carbon black/rubber systems, with however the additional difficulty that the surface area of the interaction site Aq cannot be known a priori (see Chapter 5, Section 5.1.5). [Pg.252]

Examples of Cure Systems in NR, SBR, and Nitrile Rubber. Table 6 offers examples of recipes for conventional, semi-EV, and EV cure systems ia a simple, carbon black-filled natural mbber compound cured to optimum (t90) cure. The distribution of cross-links obtained is found ia Figure 9 (24). [Pg.239]

Table 3. Properties of Carbon Black-Filled Natural Rubber Vulcanizates With Various Cure Systems ... Table 3. Properties of Carbon Black-Filled Natural Rubber Vulcanizates With Various Cure Systems ...
The early 1980s saw considerable interest in a new form of silicone materials, namely the liquid silicone mbbers. These may be considered as a development from the addition-cured RTV silicone rubbers but with a better pot life and improved physical properties, including heat stability similar to that of conventional peroxide-cured elastomers. The ability to process such liquid raw materials leads to a number of economic benefits such as lower production costs, increased ouput and reduced capital investment compared with more conventional rubbers. Liquid silicone rubbers are low-viscosity materials which range from a flow consistency to a paste consistency. They are usually supplied as a two-pack system which requires simple blending before use. The materials cure rapidly above 110°C and when injection moulded at high temperatures (200-250°C) cure times as low as a few seconds are possible for small parts. Because of the rapid mould filling, scorch is rarely a problem and, furthermore, post-curing is usually unnecessary. [Pg.839]


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See also in sourсe #XX -- [ Pg.269 , Pg.270 , Pg.271 , Pg.272 , Pg.273 , Pg.274 , Pg.275 , Pg.276 ]




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