The application of polymers as an essential class of material was greatly inhibited due to the aging failure of these versatile materials during normal use. Hence, it is generally recognized that stabilization against thermo-oxidative aging is indispensable to extend the service life of polymers for long-term applications. However, toxicity and pollution of the state-of-the-art antiaging technologies have long been puzzles in the polymer industry. Herein, sustainable carbon nanodots (CDs), synthesized by facile and cost-effective microwaveassisted pyrolysis, are used for first time as radical scavengers to resist the thermo-oxidative aging of elastomers. We have demonstrated that incorporation of the resultant CDs could be green and generic radical scavengers toward highly aging-resistant elastomers. Furthermore, by controlling the photoluminescent quantum yield of the CDs with various passivated agents, tunable radical scavenging activity was achieved. We established for the first time that the aging resistance originates from the prominent reactive radical scavenging activity of the CDs, which was rationally controlled by their photoluminescent quantum yield.
The use of silica to partially replace carbon black is a common practice in the fabrication of “green tires.” Although some degree of consensus has been approached concerning the improved performance conferred by silica substitution, such as the improved dispersion of carbon black, a quantitative understanding of the relationship between filler networking and the performance of rubber composites has not been established. Thus, an investigation focusing on filler network structure and the correlation between the network structure and the reinforcement of rubber composites was conducted. We prepared solution-polymerized styrene–butadiene rubber (SSBR) reinforced by carbon black and carbon black/silica in different ratios. To exclude as much of the effect from changed crosslinking, and figure out how filler blending influences filler dispersion and filler network structure, the silane generally used in the tire industry was not adopted. The quantitative predictor, the mass fractal dimension df, was derived from the Kraus model and the Huber–Vilgis model. We found that when the amount of substituted silica increases, the filler cluster branching decreases, accompanied by increased reinforcement efficiency. The depressed filler networking induced by silica substitution at an appropriate proportion leads to improved dynamic properties, including lower rolling resistance and better wet skid. When the silica proportion in the filler is too high, severe filler networking is observed, resulting in decreased reinforcing efficiency and impaired dynamic properties.
The
silane coupling agent has been used for ages to improve the
performance of silica-filled rubber composites. To improve the degree
of silanization of silica, ionic liquids (ILs) as a catalyst are incorporated
to the styrene–butadiene rubber/silica composites. The reaction
between bis[3-(triethoxysilyl)propyl]tetrasulfide and silica with
different basic ILs is investigated. The results show that the ILs
with stronger alkalinity exhibit higher catalytic efficiency. The
silanization occurs at lower temperature with the incorporation of
ILs. The parameters characterizing interfacial interactions show that
the interfacial adhesion is gradually improved with increasing alkalinity
of ILs. Consequently, the resulting composite with ILs possessing
strong alkalinity exhibits excellent whole performance compared with
the composites without ILs. Especially, the energy loss of the rubber
wheel in the rolling process is gradually decreased. The composites
exhibit excellent abrasion resistance and heat build-up.
The strategy of using hybrid fillers with different geometric shapes and aspect ratios has been established to be an efficient way to achieve high-performance polymer composites. While, in spite of the recently renowned advances in this field, the mechanism of synergistic behavior in the system is still unclear and equivocal. In this study, we systematically investigated the mechanism for the synergistic reinforcement in an elastomer reinforced by nanocarbon hybrids consisting of 2D reduced graphene oxide (rGO) and 1D carbon nanotubes (CNTs). The improved dispersion state of hybrid filler was attested by Raman, UV-Vis spectra and morphological observations. In addition to the phenomenological evidences, we substantiated a stronger confinement effect of hybrid network on chain dynamics, for the first time, with molecular concepts by dielectric relaxation analysis. The formation of a glassy interphase with orders of magnitude slower chain dynamics than that for bulk chains has been explicitly demonstrated in the hybrid system. Besides improved dispersion upon hybridization, it is believed the formation of a glassy interphase is another crucial factor in governing the synergistic reinforcement capability of hybrid composites. We envision this new finding provides significant insight into the mechanism of synergistic behavior in hybrid-filled polymer composites with molecular concepts.
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