Thermal, morphological and rheological characterization of poly(acrylic acid-g-styrene) amphiphilic graft copolymers

被引:39
|
作者
de la Fuente, JL
Wilhelm, M
Spiess, HW
Madruga, EL
Fernández-Garcia, M
Cerrada, ML
机构
[1] INTA, Inst Nacl Tecn Aeroespacial Esteban Terradas, Madrid 28850, Spain
[2] TU Barmstadt, Max Planck Res Grp, Barmstadt, Germany
[3] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[4] CSIC, Inst Ciencia & Tecnol Polimeros, E-28006 Madrid, Spain
关键词
poly(acrylic acid-g-styrene) arnphiphilic graft copolymers; DSC; TGA;
D O I
10.1016/j.polymer.2005.03.076
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 family of amphiphilic poly(acrylic acid-g-styrene), P(AA-g-S), graft copolymers has been prepared by quantitative hydrolysis from poly(tert-butyl acrylate-g-styrene), P(tBA-g-S), precursors and evaluated by H-1 NMR and FTIR. The thermal characterization of these copolymers as a function of the number of grafted repeat units has been performed by thermogravimetric analysis, TGA, differential scanning calorimetry, DSC, and dynamic mechanical experiments. A higher thermal stability of the PAA main chain was observed by TGA as incompatible PS is grafted onto it. Small-angle X-ray scattering, SAXS, measurements have confirmed the existence of phase separation in the graft copolymers and the morphological behavior was analyzed. An increase on microdomains size is observed when the number of grafts diminishes. Moreover, the presence of polar functional groups in the backbone chain leads to the formation of hydrogen bonds giving rise to a substantial modification of the linear viscoelastic response compared with that exhibited by the unhydrolyzed precursory copolymers, as observed by analysis of melt rheological measurements. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4544 / 4553
页数:10
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