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Morphology and properties of layered silicate‐polyethylene nanocomposite blown films
Author(s) -
Zhong Yang,
De Kee Daniel
Publication year - 2005
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.20306
Subject(s) - materials science , montmorillonite , nanocomposite , high density polyethylene , exfoliation joint , composite material , ethylene vinyl acetate , polyethylene , intercalation (chemistry) , low density polyethylene , ultimate tensile strength , polymer clay , silicate , polymer , chemical engineering , graphene , nanotechnology , inorganic chemistry , chemistry , engineering , copolymer
Film grade ethylene vinyl acetate (EVA), low density polyethylene (LDPE), and high density polyethylene (HDPE) were melt compounded with an organically modified montmorillonite, then blown into films. The morphology studies showed that all three types of film involve intercalated clay particles. The dependence of intercalation extent on the matrix as well as on the molecular weight of compatibilizers is discussed. The tensile testing data showed that the clay enhancing effects apply mainly to the modulus, instead of to the strength. The EVA‐based nanocomposite films exhibit the most significantly improved modulus while the HDPE‐based films have the least. Lower molecular weight compatibilizers could promote the clay enhancing effects while higher molecular weight compatibilizers could increase the matrix properties. Steady shear viscosities of an intercalated and an exfoliated system were also investigated. Comparing our data with that from the literature lead us to conclude that: 1) the zero‐shear viscosity of a nanocomposite is mainly determined by clay loading instead of by clay intercalation/exfoliation structures and the matrix viscosity; and 2) the clay orientation during a shear flow is highly dependent on the matrix flow behavior and to a lesser extent on the clay structural state. POLYM. ENG. SCI., 45:469–477, 2005. © 2005 Society of Plastics Engineers