The tackifying effect of resins used in the tire industry highly depends on the compatibility and interaction strength with the rubber matrix. Here, uncured and cured styrene/butadiene rubber compounds, either in the presence or absence of a hydrocarbon aromatic tackifying resin, were studied by means of high-resolution and time-domain solid-state NMR (SSNMR) techniques to investigate resin/polymer interactions and the effect of the resin on the dynamics of polymer chains. C-13 direct excitation and cross-polarization spectra, combined with low-field measurements of H-1 T-1 and analysis of H-1 on-resonance free-induction decay, provided information on the dynamic heterogeneity of the samples and the degree of mixing between the resin and the rubber matrix. Moreover, H-1 T-1 and T-1 rho relaxation times at variable temperatures were used to investigate the effect of resin on both segmental dynamics activated at the glass transition and collective polymer dynamics. SSNMR findings were discussed in relation to crosslink density and T-g data. The obtained results show that the resin is intimately mixed with the polymer, while maintaining its rigid character. A slowdown of segmental dynamics, related to an increase in T-g, was found as a consequence of resin addition, while no effect was evidenced on fragility and collective polymer dynamics.

Influence of Resins on the Structure and Dynamics of SBR Compounds: A Solid-State NMR Study

Nerli, F;Nardelli, F
;
Geppi, M
;
Martini, F
Ultimo
2023-01-01

Abstract

The tackifying effect of resins used in the tire industry highly depends on the compatibility and interaction strength with the rubber matrix. Here, uncured and cured styrene/butadiene rubber compounds, either in the presence or absence of a hydrocarbon aromatic tackifying resin, were studied by means of high-resolution and time-domain solid-state NMR (SSNMR) techniques to investigate resin/polymer interactions and the effect of the resin on the dynamics of polymer chains. C-13 direct excitation and cross-polarization spectra, combined with low-field measurements of H-1 T-1 and analysis of H-1 on-resonance free-induction decay, provided information on the dynamic heterogeneity of the samples and the degree of mixing between the resin and the rubber matrix. Moreover, H-1 T-1 and T-1 rho relaxation times at variable temperatures were used to investigate the effect of resin on both segmental dynamics activated at the glass transition and collective polymer dynamics. SSNMR findings were discussed in relation to crosslink density and T-g data. The obtained results show that the resin is intimately mixed with the polymer, while maintaining its rigid character. A slowdown of segmental dynamics, related to an increase in T-g, was found as a consequence of resin addition, while no effect was evidenced on fragility and collective polymer dynamics.
2023
Pierigé, M; Nerli, F; Nardelli, F; Calucci, L; Cettolin, M; Giannini, L; Geppi, M; Martini, F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1180488
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