Synthesis and thermal properties of poly(ethylene glycol)-poly(ε-caprolactone) copolymers

被引:190
作者
Bogdanov, B
Vidts, A
Van Den Bulcke, A
Verbeeck, R
Schacht, E
机构
[1] State Univ Ghent, Polymer Mat Res Grp, Dept Organ Chem, Inst Biomed Technol, B-9000 Ghent, Belgium
[2] State Univ Ghent, Sch Dent, Dept Dent Mat Sci, B-9000 Ghent, Belgium
关键词
poly(ethylene glycol)/poly(epsilon-caprolactone) copolymers; melting;
D O I
10.1016/S0032-3861(97)00444-8
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Three different types of polyester-polyether copolymers were synthesized by PEG initiated ring-opening polymerization of epsilon-caprolactone: an A-B and an A-B-A block copolymer and an (A)(2)-B star copolymer, where A is a poly(epsilon-caprolactone) (PCL) and B is a poly(ethylene glycol) (PEG) block. The monomer to initiator ratio was varied to obtain copolymers with different PCL block length and weight fraction ranging from 68-85 wt%. These PCL-PEG copolymers were characterized by means of g.p.c., n.m.r., d.s.c. and WAXD. In all types of copolymer the PCL constituent crystallizes first when cooling from the molten state. This leads to significant undercooling and imperfect crystallization of the PEG block. The mutual influence between PCL and PEG constituents is significantly stronger in the A-B-A block copolymers, having a central PEG block, and in the (A)(2)-B star copolymers. The effect of the PCL/PEG ratio on the melting and crystallization behaviour of the copolymers was investigated. The results obtained demonstrate that the thermal properties and morphology are affected significantly by the chain length of the PCL and PEG constituents in the copolymers and by the type of copolymers (sequence of the different blocks). (C) 1997 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1631 / 1636
页数:6
相关论文
共 18 条
  • [1] POLYETHER POLYESTER BLOCK COPOLYMERS BY NON-CATALYZED POLYMERIZATION OF EPSILON-CAPROLACTONE WITH POLY(ETHYLENE GLYCOL)
    CERRAI, P
    TRICOLI, M
    ANDRUZZI, F
    PACI, M
    PACI, M
    [J]. POLYMER, 1989, 30 (02) : 338 - 343
  • [2] POLY(ESTER-ETHER-ESTER) BLOCK-COPOLYMERS AS BIOMATERIALS
    CERRAI, P
    GUERRA, GD
    LELLI, L
    TRICOLI, M
    DELGUERRA, RS
    CASCONE, MG
    GIUSTI, P
    [J]. JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 1994, 5 (01) : 33 - 39
  • [3] PHYSICOMECHANICAL PROPERTIES OF DEGRADABLE POLYMERS USED IN MEDICAL APPLICATIONS - A COMPARATIVE-STUDY
    ENGELBERG, I
    KOHN, J
    [J]. BIOMATERIALS, 1991, 12 (03) : 292 - 304
  • [4] Gan ZH, 1996, J APPL POLYM SCI, V59, P961, DOI 10.1002/(SICI)1097-4628(19960207)59:6<961::AID-APP8>3.0.CO
  • [5] 2-N
  • [6] HOLLAND S J, 1986, Journal of Controlled Release, V4, P155, DOI 10.1016/0168-3659(86)90001-5
  • [7] JEDLINSKI Z, 1993, MAKROMOL CHEM, V194, P1681
  • [8] Kricheldorf HR, 1996, MACROMOL SYMP, V103, P85
  • [9] KRICHELDORF HR, 1993, MAKROMOL CHEM, V194, P715
  • [10] Lewis D.H., 1990, Biodegradable polymers as drug delivery systems, P1