Small strain mechanical properties of latex-based acrylic nanocomposite films

被引:6
作者
Plummer, Christopher J. G. [1 ]
Ruggerone, Riccardo [1 ]
Bourgeat-Lami, Elodie [2 ]
Manson, Jan-Anders E. [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Stn 12, Lab Technol Composites & Polymeres LTC, CH-1015 Lausanne, Switzerland
[2] Univ Lyon 1, CPE Lyon, Lab Chim Catalyse Polymeres & Procedes C2P2, LCPP Grp,CNRS,UMR 5265, F-69616 Villeurbanne, France
关键词
Emulsion polymerization; Nanocomposites; Differential scanning calorimetry (DSC); GLASS-TRANSITION; POLYMER; PARTICLES; BEHAVIOR; SEMICRYSTALLINE; REINFORCEMENT; COMPOSITES; MATRIX;
D O I
10.1016/j.polymer.2011.02.038
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A waterborne latex-based technique has been used to prepare acrylic films with laponite contents up to about 25 vol%. The laponite was attached to the surfaces of the latex particles, giving a cellular arrangement of laponite-rich regions at high laponite contents. Two regimes of reinforcement were observed, depending on whether T was above or below T-g, reinforcement at T > T-g being significantly greater than predicted by micromechanical models. Modulated differential scanning calorimetry and dynamic mechanical analysis showed part of the organic content of the films not to contribute to the glass transition. This "rigid amorphous fraction" (RAF) was argued to correspond to intercalated regions of the matrix. However, the RAF alone was insufficient to account for the observed increases in stiffness at T > T-g. The mechanical response is therefore discussed in terms of a four-phase model, in which intercalated laponite stacks are embedded in a matrix with reduced mobility, forming a foam-like structure, in turn embedded in a matrix with the properties of the bulk polymer. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2009 / 2015
页数:7
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