TY - JOUR
T1 - Effect of scale and surface chemistry on the mechanical properties of carbon nanotubes-based composites
AU - Lachman, Noa
AU - Green, Adam
AU - Iuster, Noa
AU - Lellouche, Jean Paul
AU - Wagner, H. Daniel
N1 - NES MAGNET of the Israel Ministry of Trade and IndustryThis research was conducted with the assistance of Plasan Sasa LTD., and with the financial support of the NES MAGNET program of the Israel Ministry of Trade and Industry. The generosity of the Harold Perlman family and of the G.M.J. Schmidt Minerva Centre of Supramolecular Architectures is also greatly acknowledged. H. D. Wagner is the recipient of the Livio Norzi Professorial Chair in Materials Science.
PY - 2012/7/15
Y1 - 2012/7/15
N2 - In this article, Multi-Walled Carbon Nanotubes (MWCNTs) of varying diameters, both untreated and polycarboxylated, were dispersed at constant weight percentage in an epoxy matrix, and resulting fracture toughnesses (K Ic) were measured in each case. We show that changing the MWCNT diameter has two effects on the composite fracture toughness: (i) a small MWCNT diameter enables larger interfacial surface for adhesion maximization, which increases toughness; (ii) at the same time, it limits the available pull-out energy and reduces the MWCNT ability to homogeneously disperse in the matrix due to this same large active surface: this decreases toughness. Most commercially available MWCNTs have a length range of several μm, thus an optimal diameter exists which depends on MWCNT wall thickness and surface treatment. Such optimal diameter maximizes pull-out energy and thus composite fracture toughness. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2012 Carbon nanotubes (CNTs), when sufficiently dispersed in a polymer matrix, offer exceptional mechanical properties as reinforcement fillers in nanocomposite materials. In addition to homogeneous dispersion, optimization of the interfacial bonding between both contacting phases is essential for CNT incorporation to reach full potential. In this study, multiwalled CNTs of various diameters, both untreated pristine and polycarboxylated, were dispersed at equal weight percentage in an epoxy matrix, and resulting fracture toughnesses have been measured. An optimal diameter exists depending on CNT thickness and surface treatment.
AB - In this article, Multi-Walled Carbon Nanotubes (MWCNTs) of varying diameters, both untreated and polycarboxylated, were dispersed at constant weight percentage in an epoxy matrix, and resulting fracture toughnesses (K Ic) were measured in each case. We show that changing the MWCNT diameter has two effects on the composite fracture toughness: (i) a small MWCNT diameter enables larger interfacial surface for adhesion maximization, which increases toughness; (ii) at the same time, it limits the available pull-out energy and reduces the MWCNT ability to homogeneously disperse in the matrix due to this same large active surface: this decreases toughness. Most commercially available MWCNTs have a length range of several μm, thus an optimal diameter exists which depends on MWCNT wall thickness and surface treatment. Such optimal diameter maximizes pull-out energy and thus composite fracture toughness. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2012 Carbon nanotubes (CNTs), when sufficiently dispersed in a polymer matrix, offer exceptional mechanical properties as reinforcement fillers in nanocomposite materials. In addition to homogeneous dispersion, optimization of the interfacial bonding between both contacting phases is essential for CNT incorporation to reach full potential. In this study, multiwalled CNTs of various diameters, both untreated pristine and polycarboxylated, were dispersed at equal weight percentage in an epoxy matrix, and resulting fracture toughnesses have been measured. An optimal diameter exists depending on CNT thickness and surface treatment.
KW - Structure-property relation
KW - nanocomposites
KW - toughness
UR - http://www.scopus.com/inward/record.url?scp=84861812999&partnerID=8YFLogxK
U2 - https://doi.org/10.1002/polb.23085
DO - https://doi.org/10.1002/polb.23085
M3 - مقالة
SN - 0887-6266
VL - 50
SP - 957
EP - 962
JO - Journal of Polymer Science, Part B: Polymer Physics
JF - Journal of Polymer Science, Part B: Polymer Physics
IS - 14
ER -