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We present a quantitative study of local segmental order in vulcanized natural and butadiene rubber far above the glass transition. Network chain order is dependent on the density of cross-links and is here derived from proton homonuclear residual dipolar couplings measured by static multiple-quantum NMR spectroscopy at low field. On the basis of a reasonable model of local chain structure and fast, uniaxially symmetric local motions, spin dynamics simulations are used to investigate the relationship between the experimentally determined residual coupling and the order parameter of the polymer backbone. The model is verified by site-resolved determinations of inter-and intraresonance residual couplings at high field. For both types of rubber, it is found that the distributions of the chain order parameter are rather narrow and in all cases well explained by the local coupling topology, thus excluding distributions of end-to-end separations or network chains lengths as important sources of broadening. This suggests that the NMR-detected order phenomenon cannot simply be captured with single-chain concepts. For natural rubber and poly(dimethylsiloxane), the relationship of the cross-link densities derived from the NMR-determined order parameter and from Flory-Rehner swelling experiments is linear as expected, yet the prefactors differ from the prediction by factors of 2 in different directions. We discuss the implications and the validity of the various models and approximations used for data analysis in light of recent results from computer simulations.

ABSTRACT:The effect of the incorporation of a bentonite on the vulcanization kinetics of natural rubber was investigated by means of both cure-meter testing and differential scanning calorimetry (DSC) under dynamic and isothermal conditions. The vulcanization curves showed that the modified clay behaved as an effective vulcanizing agent, accelerating the vulcanization reaction of the elastomer. A marked decrease in the induction time and optimum cure time of the elastomer were observed in the presence of the organoclay. Although the octadecylamine itself accelerated the vulcanization process, the octadecylamine-modified clay gave rise to a further noticeable increase in the vulcanization rate, which could be attributed to a synergetic effect between the filler and the amine. Moreover, in the presence of the organoclay, a dramatic increase in the torque value was obtained because of the formation of a higher number of crosslinks, which could be attributed to the confinement of the elastomer chains within the silicate galleries and, consequently, to better interactions between the filler and the rubber. However, no significant changes were observed in the unmodified clay composite. These results were in concordance with those obtained by DSC. In addition, the activation energy of the vulcanization process was also calculated by means of both techniques. A clear decrease in the activation energy was observed when the organoclay was added to the nanocomposite, which indicated that the layered silicate favored the processing of the elastomer.

Rubber compounds based on natural rubber (NR) reinforced with octadecylamine‐modified bentonite have been prepared via a vulcanization process and characterized by several techniques. The silicate nanolayers are exfoliated and uniformly dispersed in the polymer chains. Monsanto measurements have shown that the organoclay accelerates the vulcanization reaction and, furthermore, gives rise to a marked increase of the torque, indicating that the elastomer becomes more crosslinked in the presence of the organoclay. These results were corrobated by swelling measurements since a noticeable increase in the curing degree was observed when the organoclay was added to the rubber recipe. Moreover, thermodynamic parameters have shown an increase in the structural order of the nanocomposite. In addition, thermal analysis supports the assumption that the degree of curing of the elastomer increases when the organoclay is added to the elastomer. An appreciable increase of the involved heat during the curing reaction has been observed. Moreover, the Tg of the NR increases in the presence of the organoclay due to the confinement of the elastomer segment into the organoclay nanolayers, which restricts the mobility of the chains. Copyright © 2003 Society of Chemical Industry

This investigation describes two methods to obtain rubber composites based on natural rubber (NR) and organophilic layered silicates. In order to improve the exfoliation and compatibilization of the organoclays with the rubber matrix, a new approach which involves swelling of the organoclays with an elastomer solution prior to compounding has been used. The effect of the addition during swelling of a coupling agent, namely bis(trietoxysilylpropyl)tetrasulfan (TESPT), on the behaviour of the composites was also investigated. The results show that a low amount of organoclay (10 phr) significantly improves the properties of natural rubber. This suggests a strong rubber-organoclay interaction which is attributed to a high degree of rubber intercalation into the nanosilicate galleries, as was confirmed from X-ray diffraction. In addition, an ulterior improvement in the properties of the nanocomposites prepared by solution mixing is clearly observed, due to the better filler-rubber compatibility. An even further increase in the properties is observed by treating the silicate with a silane coupling agent. The silane functional groups modify the clay surface, thus reducing the surface energy, and consequently improving the compatibility with the rubber matrix.

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High performance polysulfone/γ-alumina biocom-patible nanocomposites are reported for the first time and the effects of γ-alumina surface modification are explored. We show that some fatty acids chemisorb over the surface of γ-alumina forming nanosized self-assembled structures. These structures present thermal transitions at high temperatures, 100 °C higher than the melting temperatures of the pure acids, and are further shifted about 50 °C in the presence of polysulfone. The chemistry involved in the chemisorption is mild and green meeting the stringent bio sanitary protocols for biocompatible devices. It has been found that the self-assembled structures increase mechanical strength by about 20% despite the foreseeable lack of strong particle−matrix interactions, which manifests as small variations in both the glass transition temperature and the Young's modulus. Electron microscopy observation of fractured surfaces has revealed that some acids induce an extended region of influence around the nanoparticles and this fact has been used to explain the enhancement of mechanical strength.

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