Shape-memory capability of binary multiblock copolymer blends with hard and switching domains provided by different components

被引:94
作者
Behl, Marc [1 ]
Ridder, Ute [2 ]
Feng, Yakai [3 ]
Kelch, Steffen [4 ]
Lendlein, Andreas [1 ]
机构
[1] GKSS Forschungszentrum Geesthacht GmbH, Polymer Res Inst, D-14513 Teltow, Germany
[2] Freudenberg Forsch Dienste KG, D-69465 Weinheim, Germany
[3] Tianjin Univ, Dept Polymer Sci & Technol, Tianjin 300072, Peoples R China
[4] Sika Technol AG, CH-8048 Zurich, Switzerland
关键词
BIOMEDICAL APPLICATIONS; POLYURETHANE BLENDS; POLYMERS; MISCIBILITY; DEGRADATION; IONOMERS;
D O I
10.1039/b810583a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The structural concept of shape-memory polymers (SMP) is based on two key components: covalent or physical crosslinks (hard domains) determining the permanent shape and switching domains fixing the temporary shape as well as determining the switching temperature T-sw. In conventional thermoplastic SMP hard and switching domains determining segments are combined in one macromolecule. In this paper we report on binary polymer blends from two different multiblock copolymers, whereby the first one provides the segments forming hard domains and the second one the segments forming the switching domains. A poly(alkylene adipate) mediator segment is incorporated in both multiblock copolymers to promote their miscibility as the hard segment poly(p-dioxanone) (PPDO) and the switching segment poly(epsilon-caprolactone) (PCL) are non-miscible. All polymer blends investigated showed excellent shape-memory properties. The melting point associated to the PCL switching domains T-m,T-PCL is almost independent of the weight ratio of the two blend components. At the same time the mechanical properties can be varied systematically. In this way complex synthesis of new materials can be avoided. Its biodegradability, the variability of mechanical properties and a Tsw around body temperature are making this binary blend system an economically efficient, suitable candidate for diverse biomedical applications.
引用
收藏
页码:676 / 684
页数:9
相关论文
共 32 条
[1]   Biodegradable, amorphous copolyester-urethane networks having shape-memory properties [J].
Alteheld, A ;
Feng, YK ;
Kelch, S ;
Lendlein, A .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (08) :1188-1192
[2]   Actively moving polymers [J].
Behl, Marc ;
Lendlein, Andreas .
SOFT MATTER, 2007, 3 (01) :58-67
[3]  
DEGOOT JH, 1997, BIOMATERIALS, V18, P613
[4]   Degradation of polycaprolactone/starch blends and composites with sisal fibre [J].
di Franco, CR ;
Cyras, VP ;
Busalmen, JP ;
Ruseckaite, RA ;
Vázquez, A .
POLYMER DEGRADATION AND STABILITY, 2004, 86 (01) :95-103
[5]  
El Feninat F, 2002, ADV ENG MATER, V4, P91, DOI 10.1002/1527-2648(200203)4:3<91::AID-ADEM91>3.0.CO
[6]  
2-B
[7]   Synthesis and characterization of α,ω-dihydroxy-telechelic oligo(p-dioxanone) [J].
Grablowitz, Hans ;
Lendlein, Andreas .
JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (38) :4050-4056
[8]   Synthesis of degradable, biocompatible, and tough block-copolyesterurethanes [J].
Hirt, TD ;
Neuenschwander, P ;
Suter, UW .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 1996, 197 (12) :4253-4268
[9]   Comparison of shape memory metals and polymers [J].
Hornbogen, E .
ADVANCED ENGINEERING MATERIALS, 2006, 8 (1-2) :101-106
[10]  
HU J, 2008, SHAPE MEMORY POLYM T