Nanostructured polyolefins/clay composites: role of the molecular interaction at the interface

被引:25
作者
Passaglia, Elisa [1 ]
Bertoldo, Monica [2 ]
Coiai, Serena [3 ]
Augier, Sylvain
Savi, Stefania
Ciardelli, Francesco [2 ]
机构
[1] Univ Pisa, Dept Chem & Ind Chem, CNR, ICCOM Pisa Sect, I-56126 Pisa, Italy
[2] Univ Pisa, Dept Chem & Ind Chem, PolyLab INFM, I-56126 Pisa, Italy
[3] Italian Ctr Packaging CIP, I-30175 Venice, Italy
关键词
functionalized polyolefins; nanocomposites; polyolefin/clay interactions;
D O I
10.1002/pat.1107
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The extent of interphase interactions between polymer phase and inorganic particles is the driving force addressing the preparation/properties design in the field of the corresponding micro- and nanocomposites. In the case of preparation of nartocomposites based on polyolefins (POs) and inorganic compounds as potentially nanodispersed phase, the use of a PO with proper functional groups is necessary for the interface adhesion and stabilization of the nanostructured morphology. According to this approach, ethylene/propylene copolymers with a different propylene content were used for the preparation of nanocomposites through melt mixing with organophilic montmorillonites (OMMT). By taking into account the important role of functionalities grafted onto POs, two different synthetic approaches were compared here: (1) the dispersion of the inorganic filler was obtained by using previously functionalized POs bearing carboxylate groups as matrices; (2) the nanocomposites were prepared by performing contemporaneously the functionalization of POs (by using maleic anhydride (MAH) and/or diethyl maleate (DEM)) and the dispersion of the filler in a one-step process. The morphology of the nanocomposites as well as the variation of solubility and glass transition temperature (T-g) of the PO matrix were evaluated and tentatively discussed with reference to functionalization degrees, structure of PO, and preparation procedure. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:560 / 568
页数:9
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