Changes in Crystalline Morphology, Thermal, and Mechanical Properties with Hydrolytic Degradation of Immiscible Biodegradable PPDX/PCL Blends

被引:12
作者
Brito, Y. [1 ]
Sabino, M. A. [2 ]
Ronca, G. [1 ]
Mueller, A. J. [1 ]
机构
[1] Univ Simon Bolivar, Dpto Cs Mat, Grp Polimeros, Caracas, Venezuela
[2] Univ Simon Bolivar, Grp B5IDA, Dpto Quim, Caracas, Venezuela
关键词
immiscible blends; hydrolytic degradation; polyesters; poly(epsilon-caprolactone); poly(p-dioxanone);
D O I
10.1002/app.28883
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Immiscible blends of high molecular weight commercial poly(p-dioxanone) (PPDX) and poly(epsilon-caprolactone) (PCL) were prepared by melt mixing in a wide composition range. The materials were exposed to a hydrolysis medium (phosphate buffer kept at a constant pH of 7.2) at 37 degrees C during 36 weeks. The change in weight of the samples as well as their thermal properties, morphology, spherulitic crystallization kinetics, and tensile properties were studied as a function of degradation time. As PCL does not experience weight loss during the entire degradation period explored here, weight loss was indicative of PPDX degradation only. The combined results Of calorimetry, spherulitic texture, and spherulite growth kinetics allowed Lis to establish that the PPDX component in the blends experiences a much faster degradation rate than in neat PPDX. Such increase in degradation rate Could be due to the larger surface area of PPDX component when it is dispersed in immiscible PCL. Nevertheless, the presence of PCL in the blends can extend the physical integrity of the samples in the degradation medium as well as their mechanical properties for longer periods of time as compared with neat PPDX. Therefore, the blends may be good candidates for replacing neat PPDX in specific applications requiring longer life time of the material. (C) 2008 Wiley Periodicals, Inc. J Appl Polym Sci 110: 3848-3858, 2008
引用
收藏
页码:3848 / 3858
页数:11
相关论文
共 30 条
[1]  
AKIRA I, 1994, POLYM DEGRAD STABIL, V45, P205
[2]   Nucleation and crystallization in double crystalline poly(p-dioxanone)-b-poly(ε-caprolactone) diblock copolymers [J].
Albuerne, J ;
Márquez, L ;
Müller, AJ ;
Raquez, JM ;
Degée, P ;
Dubois, P ;
Castelletto, V ;
Hamley, IW .
MACROMOLECULES, 2003, 36 (05) :1633-1644
[3]  
Anderson JM, 1998, POLYM INT, V46, P163, DOI 10.1002/(SICI)1097-0126(199807)46:3<163::AID-PI972>3.0.CO
[4]  
2-9
[5]   Interplay of fractionated crystallization and morphology in polypropylene/poly(ε-caprolactone) blends [J].
Balsamo, Vittoria ;
Gouveia, Laura M. .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2007, 45 (11) :1365-1379
[6]   LIFETIME PREDICTION IN THE HYDROLYTIC AGING OF POLYESTERS [J].
BELLENGER, V ;
GANEM, M ;
MORTAIGNE, B ;
VERDU, J .
POLYMER DEGRADATION AND STABILITY, 1995, 49 (01) :91-97
[7]  
Brito Yelitza, 2006, Rev. LatinAm. Metal. Mater., V26, P61
[8]   Comparative study of the effect of different nanoparticles on the mechanical properties and thermal degradation mechanism of in situ prepared poly(E-caprolactone) nanocomposites [J].
Chrissafis, K. ;
Antoniadis, G. ;
Paraskevopoulos, K. M. ;
Vassiliou, A. ;
Bikiaris, D. N. .
COMPOSITES SCIENCE AND TECHNOLOGY, 2007, 67 (10) :2165-2174
[10]  
Hyon SH, 1998, POLYM INT, V46, P196, DOI 10.1002/(SICI)1097-0126(199807)46:3<196::AID-PI914>3.0.CO