2011
DOI: 10.5772/979
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Carbon Nanotubes - Polymer Nanocomposites

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Cited by 47 publications
(9 citation statements)
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“…In accordance with this approach, the percolation chain is formed as a result of a random distribution of nanotubes over polymer matrix bulk. Therewith the position of the percolation threshold is roughly inversely proportional to the aspect ratio of nanotubes comprising the percolation chain [1][2][3]. Such a dependence is derived from the percolation theory, and the comparison of results of model calculations with the relevant experimental data usually results in a good coincidence for the percolation threshold values of such materials.…”
Section: Model Of Charge Transportmentioning
confidence: 92%
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“…In accordance with this approach, the percolation chain is formed as a result of a random distribution of nanotubes over polymer matrix bulk. Therewith the position of the percolation threshold is roughly inversely proportional to the aspect ratio of nanotubes comprising the percolation chain [1][2][3]. Such a dependence is derived from the percolation theory, and the comparison of results of model calculations with the relevant experimental data usually results in a good coincidence for the percolation threshold values of such materials.…”
Section: Model Of Charge Transportmentioning
confidence: 92%
“…Nanocomposites on the basis of polymers doped with carbon nanotubes (CNT) present a typical example of such systems (see, for example Ref. [1][2][3][4] and the literature cited there). In such composites, at exceeding some critical value of CNT concentration, the percolation transition occurs which accompanies with the enhancement of the conductivity of the material by 10-12 orders of magnitude.…”
Section: Introductionmentioning
confidence: 99%
“…Covalent functionalization implies the formation of new chemical bonds, altering the original CNT structure. This reaction will change the carbon hybridization from sp 2 to sp 3 , causing the loss of the π-conjugation system of the graphene layer [42] responsible for most of the optical, electrical, and thermal properties of CNTs [43]. Despite this drawback, covalent functionalization presents many characteristics that make this approach highly attractive: it provides strong and very stable attachment of functional groups, entails higher selectivity, is more robust and better controlled than non-covalent functionalization, can be done in organic solvent or even without solvent, and offers a huge plethora of functional groups that can be used [44].…”
Section: Covalent Functionalizationmentioning
confidence: 99%
“…The use of OAS to modify starch is a recognized chemical approach to introduce the biopolymer of starch such as tapioca starch into industrial applications. With respect to the rheological properties of OSA modified starches in aqueous medium, evidence have been provided to suggest that OSA side chains can aggregate into hydrophobic domains in water at even quite low concentrations [44,45].…”
Section: Introductionmentioning
confidence: 99%
“…The OSA-modified tapioca starch is amphiphilic in nature, which can potentially functionalize CNTs via non-covalent wrapping [45]. The physical adsorption of these copolymers onto CNTs surfaces increases the hydrophobic feature of the OSA, which may effectively prevent the aggregation of CNTs.…”
Section: Introductionmentioning
confidence: 99%