2017
DOI: 10.1007/s10853-017-1113-7
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Should polymer nanocomposites be regarded as molecular composites?

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Cited by 32 publications
(12 citation statements)
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“…Thereby, asphaltenes act as reinforcing particles at the room temperature, and as plasticizers at elevated ones. Wherein, the mixture containing 10 wt% of asphaltenes can be considered as an example of a molecular nanocomposite, [ 77‐79 ] since the size of both asphaltene molecules and their nanoaggregates is of the order of a few nanometers and the asphaltenes are dissolved in the medium of block copolymer (ie, deagglomerated to a nanoscale level). At higher asphaltene content, the strength decreases to its initial value, probably due to the agglomeration of asphaltenes.…”
Section: Resultsmentioning
confidence: 99%
“…Thereby, asphaltenes act as reinforcing particles at the room temperature, and as plasticizers at elevated ones. Wherein, the mixture containing 10 wt% of asphaltenes can be considered as an example of a molecular nanocomposite, [ 77‐79 ] since the size of both asphaltene molecules and their nanoaggregates is of the order of a few nanometers and the asphaltenes are dissolved in the medium of block copolymer (ie, deagglomerated to a nanoscale level). At higher asphaltene content, the strength decreases to its initial value, probably due to the agglomeration of asphaltenes.…”
Section: Resultsmentioning
confidence: 99%
“…An obvious way forward is to adapt the continuum mechanics theories developed for macroscopic composites, such as those reinforced by carbon or glass fibers, to composites at the nanoscale. Some researchers have taken an opposing viewpoint and have suggested that polymer nanocomposites are actually quasi-homogeneous molecular blends that should be regarded as molecular composites or self-reinforced compo-sites (12,13) and that the properties are controlled by interactions on the molecular scale between the nanoparticles and the polymer matrix.…”
Section: (A)mentioning
confidence: 99%
“…The iPP/0.5%-VGCF nanocomposite in itself exhibited higher values than the neat iPP, showing the best dispersion of fully exfoliated single nanofibers with no aggregates. These well dispersed individual nanofibers of high aspect ratio could increase the energy by the classical debonding/fiber breakage/pull-out mechanism of fiber reinforced composites [10,20]. Conversely, the iPP/0.5%-GNP nanocomposite contained GNP aggregates of micro dimension, which contributed to the improvement of the fracture energy by the classical mechanism of crack-front pinning at adjacent particles and bowing away from them to increase the crack front surface area [21].…”
Section: Discussionmentioning
confidence: 99%
“…This finding reflects mainly the tensile strength and Young's modulus, where nanosystems suffer from aggregation, which impairs load transfer. This state may be different for the fracture toughness, which increases through mechanisms other than load transfer, e.g., crack front bowing and pull out [10,11]. Based on these findings, we examined the effect of geometry and chemical structure of the nanofillers on the fracture energy, and possible hybrid effects of hybrid systems comprised of isotactic polypropylene with different nanofillers.…”
mentioning
confidence: 99%