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Non-linear viscoelasticity of vapor grown carbon nanofiber/polystyrene composites

Identifieur interne : 000826 ( Hal/Curation ); précédent : 000825; suivant : 000827

Non-linear viscoelasticity of vapor grown carbon nanofiber/polystyrene composites

Auteurs : L. Zhao [République populaire de Chine] ; H. M. Yang [République populaire de Chine] ; Y. H. Song [République populaire de Chine] ; Y. J. Zhou [République populaire de Chine] ; G.-H. Hu [France] ; Q. A. Zheng [République populaire de Chine]

Source :

RBID : Hal:hal-00604140

Abstract

The strain (γ) dependences of viscoelasticity and electrical resistance (R) of vapor grown carbon nanofiber (VGCF)/polystyrene (PS) composites have been studied using simultaneous measurement technique. The composites containing at least 4 vol.% VGCF present two regions of strain softening at γ < 10% and γ > 30%, respectively. Using strain amplification factor introduced by hydrodynamic effects as vertical and horizontal shifting factors, the curves of dynamic storage modulus (G′) and loss modulus (G″) as a function of γ for the composites can be superposed, respectively, on those for the pure matrix at γ ≥ 30%. Significant deflection from the master curves can be observed at γ < 30%. R tested as a function of γ provides direct evidences for breakdown of filler-filler interactions even by a small strain perturbation. It is suggested that breakdown of filler-filler interactions plays a vital role in strain softening at small strains, whereas the matrix provides the main contribution to strain softening at large strains. Dynamic moduli $$ G_{{{text{f,}}(0.1% ,varphi )}}^{prime } $$ and $$ G_{{{text{f,}}(0.1% ,varphi )}}^{prime prime } $$ of the filler phase at volume fraction φ at 0.1% strain are used to account for the viscoelastic contribution of the initial filler structure. Ratios of dynamic moduli of the filler phase to the composite at 0.1% strain, $$ G_{{{text{f,}}0.1% }}^{prime } /G_{{{text{c,}}0.1% }}^{prime } $$ and $$ G_{{{text{f,}}0.1% }}^{prime prime } /G_{{{text{c,}}0.1% }}^{prime prime } $$ , exhibit percolation-like transition as a function of φ, which is in consistence with the electric percolation transition.

Url:
DOI: 10.1007/s10853-010-5098-8

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<div type="abstract" xml:lang="en">The strain (γ) dependences of viscoelasticity and electrical resistance (R) of vapor grown carbon nanofiber (VGCF)/polystyrene (PS) composites have been studied using simultaneous measurement technique. The composites containing at least 4 vol.% VGCF present two regions of strain softening at γ < 10% and γ > 30%, respectively. Using strain amplification factor introduced by hydrodynamic effects as vertical and horizontal shifting factors, the curves of dynamic storage modulus (G′) and loss modulus (G″) as a function of γ for the composites can be superposed, respectively, on those for the pure matrix at γ ≥ 30%. Significant deflection from the master curves can be observed at γ < 30%. R tested as a function of γ provides direct evidences for breakdown of filler-filler interactions even by a small strain perturbation. It is suggested that breakdown of filler-filler interactions plays a vital role in strain softening at small strains, whereas the matrix provides the main contribution to strain softening at large strains. Dynamic moduli $$ G_{{{text{f,}}(0.1% ,varphi )}}^{prime } $$ and $$ G_{{{text{f,}}(0.1% ,varphi )}}^{prime prime } $$ of the filler phase at volume fraction φ at 0.1% strain are used to account for the viscoelastic contribution of the initial filler structure. Ratios of dynamic moduli of the filler phase to the composite at 0.1% strain, $$ G_{{{text{f,}}0.1% }}^{prime } /G_{{{text{c,}}0.1% }}^{prime } $$ and $$ G_{{{text{f,}}0.1% }}^{prime prime } /G_{{{text{c,}}0.1% }}^{prime prime } $$ , exhibit percolation-like transition as a function of φ, which is in consistence with the electric percolation transition.</div>
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<title xml:lang="en">Non-linear viscoelasticity of vapor grown carbon nanofiber/polystyrene composites</title>
<author role="aut">
<persName>
<forename type="first">L.</forename>
<surname>Zhao</surname>
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<forename type="first">Y.H.</forename>
<surname>Song</surname>
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<forename type="first">Y.J.</forename>
<surname>Zhou</surname>
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<forename type="first">G.-H.</forename>
<surname>Hu</surname>
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<forename type="first">Q.A.</forename>
<surname>Zheng</surname>
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<idno type="eissn">1573-4803</idno>
<title level="j">Journal of Materials Science</title>
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<biblScope unit="issue">(8)</biblScope>
<biblScope unit="pp">pp. 2495-2502</biblScope>
<date type="datePub">2011</date>
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<abstract xml:lang="en">The strain (γ) dependences of viscoelasticity and electrical resistance (R) of vapor grown carbon nanofiber (VGCF)/polystyrene (PS) composites have been studied using simultaneous measurement technique. The composites containing at least 4 vol.% VGCF present two regions of strain softening at γ < 10% and γ > 30%, respectively. Using strain amplification factor introduced by hydrodynamic effects as vertical and horizontal shifting factors, the curves of dynamic storage modulus (G′) and loss modulus (G″) as a function of γ for the composites can be superposed, respectively, on those for the pure matrix at γ ≥ 30%. Significant deflection from the master curves can be observed at γ < 30%. R tested as a function of γ provides direct evidences for breakdown of filler-filler interactions even by a small strain perturbation. It is suggested that breakdown of filler-filler interactions plays a vital role in strain softening at small strains, whereas the matrix provides the main contribution to strain softening at large strains. Dynamic moduli $$ G_{{{text{f,}}(0.1% ,varphi )}}^{prime } $$ and $$ G_{{{text{f,}}(0.1% ,varphi )}}^{prime prime } $$ of the filler phase at volume fraction φ at 0.1% strain are used to account for the viscoelastic contribution of the initial filler structure. Ratios of dynamic moduli of the filler phase to the composite at 0.1% strain, $$ G_{{{text{f,}}0.1% }}^{prime } /G_{{{text{c,}}0.1% }}^{prime } $$ and $$ G_{{{text{f,}}0.1% }}^{prime prime } /G_{{{text{c,}}0.1% }}^{prime prime } $$ , exhibit percolation-like transition as a function of φ, which is in consistence with the electric percolation transition.</abstract>
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