EVA/PBT nanostructured blends synthesized by in situ polymerization of cyclic cBT (cyclic butylene terephthalate) in molten EVA

被引:28
作者
Bahloul, Walid [1 ,2 ,3 ]
Bounor-Legare, Veronique [1 ,2 ,3 ]
Fenouillot, Francoise [1 ,2 ,4 ]
Cassagnau, Philippe [1 ,2 ,3 ,4 ]
机构
[1] Univ Lyon, F-69000 Lyon, France
[2] Univ Lyon 1, F-69622 Villeurbanne, France
[3] CNRS, UMR5223, Lab Mat Polymeres & Biomat, F-69622 Villeurbanne, France
[4] CNRS, UMR5223, Mat Macromol Lab, F-69622 Villeurbanne, France
关键词
Copolymers; In situ polymerization; cBT; GRAFT-COPOLYMERS; BLOCK-COPOLYMERS; MORPHOLOGY; COMPATIBILIZATION; POLYMERS;
D O I
10.1016/j.polymer.2009.03.055
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(ethylene-co-vinyl acetate) (EVA)/poly(butylene terephthalate) copolymers were synthesized by the in situ polymerization of cyclic butylene terephthalate monomer (cBT) in the presence of molten EVA copolymer. Titanium phenoxide Ti(OPh)(4) which leads to the highest degree of grafting compared to the more classical titanium system was used as the initiator for the ring-opening polymerization of the cBT monomer. The corresponding copolymer was characterized fully by H-1 NMR after selective extraction from the blend. As a result, a maximum of 11.3 wt% of EVA-g-PBT copolymer was synthesized by this method. Examination of morphology by transmission electronic microscopy (TEM) showed a fine dispersion of PBT phase with size ranging from 100 to 500 nm in diameter. This gave evidence for a crown structure of the PBT phase that is coated by EVA-g-PBT copolymer. Finally, theological and mechanical studies highlighted a specific behaviour of this material with improved mechanical properties at room temperature. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2527 / 2534
页数:8
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