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Dynamic Rheological Studies of Poly(p-phenyleneterephthalamide) and Carbon Nanotube Blends in Sulfuric Acid
We have studied the dynamic scanning of liquid-crystalline (LC) poly(p-phenyleneterephthalamide) sulfuric acid (PPTA-H(2)SO(4)) solution, and its blend with single-walled carbon nanotubes (SWNTs), by using a flat plate rotational rheometer. The effects of weight concentration and molecular weight of...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871120/ https://www.ncbi.nlm.nih.gov/pubmed/20480024 http://dx.doi.org/10.3390/ijms11041352 |
Sumario: | We have studied the dynamic scanning of liquid-crystalline (LC) poly(p-phenyleneterephthalamide) sulfuric acid (PPTA-H(2)SO(4)) solution, and its blend with single-walled carbon nanotubes (SWNTs), by using a flat plate rotational rheometer. The effects of weight concentration and molecular weight of PPTA, as well as operating temperature, on dynamic viscoelasticity of the PPTA-H(2)SO(4) LC solution system are discussed. The transition from a biphasic system to a single-phase LC occurs in the weight concentration range of SWNTs from 0.1% to 0.2%, in which complex viscosity reaches the maximum at 0.2 wt% and the minimum at 0.1 wt%, respectively, of SWNTs. With increasing SWNT weight concentration, the endothermic peak temperature increases from 73.6 to 79.9 °C. The PPTA/SWNT/H(2)SO(4) solution is in its plateau zone and storage modulus (G′) is a dominant factor within the frequency (ω) range of 0.1–10 rad/s. As ω increases, the G′ rises slightly, in direct proportion to the ω. The loss modulus (G″) does not rise as a function of ω when ω < 1 s(−1), then when ω > 1 s(−1) G″ increases faster than G′, yet not in any proportion to the ω. |
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