Carbon Nanotube Elastomer Composites

2013 ◽  
Vol 844 ◽  
pp. 322-325
Author(s):  
Claudia Kummerlöwe ◽  
Norbert Vennemann ◽  
Achim Siebert

Composites of multi walled carbon nanotubes and several synthetic rubbers as well as natural rubber were investigated regarding their mechanical properties, electrical and thermal conductivity and vulcanization properties. The composites were prepared by a melt mixing process. Induction and cure times obtained from rheometer curves exhibited a considerable decrease with increasing filler loading and kinetic investigations using a first order model indicated a distinct reduction of the activation energy. An examination of the crosslink density by equilibrium swelling and hysteresis tensile testing showed a strong increase with carbon nanotube content. The analysis of the thermal conductivity revealed the presents of a considerable interfacial thermal resistance which restricts the contribution of carbon nanotubes to the composite thermal conductivity. The electrical percolation thresholds of the melt compounded composites depend on processing procedure as well as elastomer and CNT type. At least a partial exfoliation of the CNT aggregates was reached.

Author(s):  
Reza Moheimani ◽  
M Hasansade

This paper describes a closed-form unit cell micromechanical model for estimating the effective thermal conductivities of unidirectional carbon nanotube reinforced polymer nanocomposites. The model incorporates the typically observed misalignment and curvature of carbon nanotubes into the polymer nanocomposites. Also, the interfacial thermal resistance between the carbon nanotube and the polymer matrix is considered in the nanocomposite simulation. The micromechanics model is seen to produce reasonable agreement with available experimental data for the effective thermal conductivities of polymer nanocomposites reinforced with different carbon nanotube volume fractions. The results indicate that the thermal conductivities are strongly dependent on the waviness wherein, even a slight change in the carbon nanotube curvature can induce a prominent change in the polymer nanocomposite thermal conducting behavior. In general, the carbon nanotube curvature improves the nanocomposite thermal conductivity in the transverse direction. However, using the straight carbon nanotubes leads to maximum levels of axial thermal conductivities. With the increase in carbon nanotube diameter, an enhancement in nanocomposite transverse thermal conductivity is observed. Also, the results of micromechanical simulation show that it is necessary to form a perfectly bonded interface if the full potential of carbon nanotube reinforcement is to be realized.


2016 ◽  
Vol 53 (2) ◽  
pp. 215-230 ◽  
Author(s):  
JJ Espadas-Escalante ◽  
F Avilés ◽  
PI Gonzalez-Chi ◽  
AI Oliva

The thermal conductivity and fire response of multiwall carbon nanotube/polyurethane foam composites are investigated for ∼45 kg/m3 foams with multiwall carbon nanotube concentrations of 0.1, 1, and 2 wt.%. The thermal conductivity of such nanocomposites shows a modest increase with increased multiwall carbon nanotube content, which is explained by a high value of interfacial thermal resistance, as predicted by existent thermal models. A strong correlation between multiwall carbon nanotube content, foam’s cellular morphology, and fire behavior was observed. The flame propagation speed increases with the addition of 0.1 wt.% multiwall carbon nanotubes and then reduces as the multiwall carbon nanotube content increases. The mass lost after flame extinction reduces with the addition of multiwall carbon nanotubes, suggesting an increased resistance to flame attack due the multiwall carbon nanotube presence.


Energies ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1403
Author(s):  
Lingyu Zheng ◽  
Xuelai Zhang ◽  
Weisan Hua ◽  
Xinfeng Wu ◽  
Fa Mao

Calcium ions can react with polyethylene glycol (PEG) to form a form-stable phase change material, but the low thermal conductivity hinders its practical application. In this paper, hydroxylated multi-walled carbon nanotubes (MWCNTs) with different mass are introduced into PEG1500·CaCl2 form-stable phase change material to prepare a new type of energy storage material. Carbon nanotubes increased the mean free path (MFP) of phonons and effectively reduced the interfacial thermal resistance between pure PEG and PEG1500·CaCl2 3D skeleton structure. Thermal conductivity was significant improved after increasing MWCNTs mass, while the latent heat decreases. At 1.5 wt%, composite material shows the highest phase change temperature of 42 °C, and its thermal conductivity is 291.30% higher than pure PEG1500·CaCl2. This article can provide some suggestions for the preparation and application of high thermal conductivity form-stable phase change materials.


2013 ◽  
Vol 716 ◽  
pp. 373-378
Author(s):  
Qian Zhang ◽  
Xin Bao Gao ◽  
Tian Peng Li

Carbon nanotube/expanded graphite composite material was prepared by expanding the mixture of multi-walled carbon nanotubes and expansible graphite under the condition of high temperature. The microstructure and composition was studied by using SEM and XRD. The study shows that the tubular structure of carbon nanotubes in the composite material is changed by high temperature expanding process, and the microstructure is different with different expanding temperature. When the expanding temperature was 900°C, carbon nanotubes transformed, then attached to the surface of expanded graphite flake, so carbon nanotubes and expanding graphite combined strongly; globular carbon nanotubes attached to the surface of expanded graphite flake at the temperature of 700°C, both were combined much more strongly; carbon nanotubes retained the tube structure at the temperature of 500°C, combination was looser due to the simple physical adsorption. The result shows that the choice of expanding temperature has an important effect on microstructure of carbon nanotube/expanded graphite composite material.


2002 ◽  
Vol 739 ◽  
Author(s):  
Mark Hughes ◽  
George Z. Chen ◽  
Milo S. P. Shaffer ◽  
Derek J. Fray ◽  
Alan H. Windle

ABSTRACTNanoporous composite films of multi-walled carbon nanotubes (MWNTs) and either polypyrrole (PPy) or poly(3-methylthiophene) (P3MeT) were grown using an electrochemical polymerization technique in which the nanotubes and conducting polymer were deposited simultaneously. The concentration and dispersion of MWNTs in the polymerization electrolyte was found to have a significant effect on the thickness of polymer coated on each MWNT and hence the loading of MWNTs in the films produced. It has been shown that for an increasing concentration of MWNTs in the polymerization electrolyte, the thickness of polymer coated on each MWNT decreases. This relationship made it possible to minimize ionic diffusion distances within the nanoporous MWNT-PPy films produced, reducing their electrical and ionic resistance and increasing their capacitance relative to similarly prepared pure PPy films.


2017 ◽  
Vol 51 (12) ◽  
pp. 1693-1701 ◽  
Author(s):  
EA Zakharychev ◽  
EN Razov ◽  
Yu D Semchikov ◽  
NS Zakharycheva ◽  
MA Kabina

This paper investigates the structure, length, and percentage of functional groups of multi-walled carbon nanotubes (CNT) depending on the time taken for functionalization in HNO3 and H2SO4 mixture. The carbon nanotube content and influence of functionalization time on mechanical properties of polymer composite materials based on epoxy matrix are studied. The extreme dependencies of mechanical properties of carbon nanotube functionalization time of polymer composites were established. The rise in tensile strength of obtained composites reaches 102% and elastic modulus reaches 227% as compared to that of unfilled polymer. The composites exhibited best mechanical properties by including carbon nanotube with 0.5 h functionalization time.


RSC Advances ◽  
2016 ◽  
Vol 6 (83) ◽  
pp. 79563-79577 ◽  
Author(s):  
S. A. Habibiannejad ◽  
A. Aroujalian ◽  
A. Raisi

In this study different functional groups on the surface of carbon nanotube enhanced the performance of Pebax 1657/MWNTs.


Sign in / Sign up

Export Citation Format

Share Document