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    Processing, rheology and structure of melt compounded PBT-clay nanocomposites having different chemical composition.

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    In this study the melt flow behavior of poly(butylene terephthalate)-clay nanocomposites produced by melt compounding was investigated. Four commercial organo-modified montmorillonites, differing mainly by the organic treatment used in the modification, were employed as nanometric fillers and blended with the poly(butylene terephthalate) (PBT) at two weight percentages each (6 and 9wt%). The process was carried out using a laboratory-scale twin-screw extruder at two different extrusion rates, in order to evaluate the effect of the shear rate during the process on microstructure and flow properties. In this regard, the nanocomposite samples were submitted to morphological analyses and rheological measurements in the dynamic regime. The effect of temperature on the flow behavior of the hybrids with respect to the neat PBT matrix was also investigated. The obtained data were related to the hybrid compositions and then to the chemical affinity between polymer and clay type. All the reported results have shown a gradual transition from a pseudo-Newtonian trend towards a pseudo-solid-like flow behavior with the increase of the clay loading and the dispersion/exfoliation level of the clay particles, due to the corresponding increase of the polymer-silicate interactions that slow the relaxation times of the PBT chains. Moreover, it was also evident that for the fillers having the higher affinity towards the PBT the nano-scale dispersion benefit from higher residence times, and therefore slower extrusion rates; on the contrary, for the fillers having poor interaction with the polymer, higher shear stress, and therefore higher extrusion rates, are needed to disrupt the clay tactoids in smaller particles. In the last part of the work, in order to verify if a relationship between flow properties and degree of exfoliation does actually exist, the rheological data were also processed using a simple semi-quantitative empirical method proposed in literature. The method failed for our systems, thus underlining the insufficiency of the rheological response alone in quantifying the exfoliation degree of an organoclay in the matrix

    Going Beyond Counting First Authors in Author Co-citation Analysis

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    The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed

    Rheological behavior of new melt compounded copolyamide nanocomposites

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    Abstract In this paper the rheological behavior of new polyamide-based nanocomposites produced by melt compounding using three different silicate loadings and screw speeds was investigated. The thermoplastic matrices selected were a polyamide 6 and its statistical copolymer having partially aromatic structure, whereas the clay was a commercial organo-modified montmorillonite. Hybrid systems were prepared by means of a laboratory-scale twin screw extruder and were submitted to rheological and structural investigations. The rheological experiments (dynamic frequency sweep, steady rate sweep and stress relaxation tests) were performed to evaluate the effect of both system composition (kind of matrix and clay content) and extrusion rate on the flow behavior of the nanocomposites. Rheology, that is highly sensitive to the nanoscale structure of the materials, put out a pseudo-solid like flow behavior at long times in the hybrids with silicate content higher than 6 wt% and produced with high extrusion rate; this response was related to the formation of an extended structural network across the polymer matrix due to strong polymer–silicate interactions that slow the relaxation times of the macromolecules. Corresponding to this behavior, TEM micrographs have shown a quite uniform dispersion of clay particles on micron-scale and a fair level of silicate exfoliation on nanoscale with a macroscopic preferential orientation of the layers in samples. The rheological measurements also reveal that this flow response is more marked for nanocomposites based on the copolyamide matrix, suggesting that this resin may have a higher silicate affinity respect to polyamide 6 homopolymer
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