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Morphological features and melting behavior of nanocomposites based on isotactic polypropylene and multiwalled carbon nanotubes
Author(s) -
AvilaOrta Carlos A.,
MedellínRodríguez Francisco J.,
DávilaRodríguez Mario V.,
AguirreFigueroa Yrayda A.,
Yoon Kyunghwan,
Hsiao Benjamin S.
Publication year - 2007
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.26823
Subject(s) - tacticity , materials science , nucleation , lamellar structure , crystallization , nanocomposite , carbon nanotube , composite material , chemical engineering , morphology (biology) , polypropylene , polymer chemistry , polymer , polymerization , chemistry , organic chemistry , biology , engineering , genetics
Nanocomposites based on low molar mass isotactic polypropylene (iPP) and a low concentrations (1–2 wt %) of multiwalled carbon nanotubes (MWCNTs) were studied using thermal analysis, optical and electronic microscopy, and X‐ray diffraction/scattering techniques. It was first determined that MWCNT decrease induction time and act as nucleating agents of the iPP crystals during nonisothermal crystallization. One of the consequences of the nucleation effect was that the original spherulitic morphology of iPP was transformed into a fibrillar‐like. The corresponding long period of the original well‐defined lamellar structure slightly increased suggesting the formation of thicker crystals in samples containing MWCNT. The nature of the α‐iPP crystalline structure was not affected by MWCNT. After nonisothermal crystallization, two melting endotherms were present during thermal scanning of the iPP/MWCNT nanocomposites their proportion changing with the heating rate. After resolving the total DSC signal in its components using MDSC, the overall evolution of such behavior could be explained in terms of the melting/recrystallization mechanism. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007

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