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Elastomere Friction - The Best Friend international

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10 L.Busse,A.LeGal,andM.Klüppel<br />

Fig. 5 T-sweeps for the loss modulus G ′′ .<br />

effect is minimal for weakly filled samples (S2K), moderate for medium filled<br />

ones (S4K, S6K) and dominant for highly filled sample S8K.<br />

Looking at the loss modulus G ′′ in Figure 5, the increase with filler content<br />

is obvious, too, but more proportional to the filler amount than in the T-sweep<br />

of G ′ . In both cases, the increase is smaller for low temperatures, as chain<br />

mobility is limited anyway under these circumstances.<br />

According to the time-temperature-superposition principle (TTS), temperature<br />

influence can be replaced by frequency influence, where cold rubber<br />

equals high frequency treatment and causes a glassy state with high stiffness,<br />

whereas a warm elastomer dominated by rubber matrix/ filler is connected<br />

to low frequencies. Indeed, by applying various frequencies at discrete temperatures<br />

on the sample, we get a bunch of branches for the moduli that can<br />

be constructed to a master curve for the whole frequency range over several<br />

decades by shifting the branches horizontally in order to form a continuous<br />

curve. Above the glass transition temperature, the shift factors obey the<br />

WLF relationship as shown in Figure 6, with WLF constants C1 = −3.85<br />

and C2 =91.2 ◦ CatTref =20 ◦ C to match the room temperature of friction<br />

measurements. Below about −45 ◦ C, the relative shift between the branches<br />

decreases.<br />

<strong>The</strong>se horizontal factors were extracted from the unfilled sample S0K<br />

(Figure 7), but are valid also for the filled samples. For high temperatures,<br />

the branches of filled samples are also vertically dispersed, so vertical shift<br />

factors need to be applied as well, independently for G ′ and G ′′ . <strong>The</strong> TTS is<br />

not valid anymore for filled elastomers in this temperature range, because the<br />

filler-filler bond instead of the polymer matrix then dominates the viscoelastic<br />

behaviour [19]. Shift factors for log G ′ and log G ′′ with linear slope in the

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