Time-resolved crystallization study of absorbable polymers by synchrotron small-angle X-ray scattering

被引:0
|
作者
Andjelic, S
Jamiolkowski, D
McDivitt, J
Fischer, J
Zhou, J
Wang, ZG
Hsiao, BS
机构
[1] Ethicon Inc, Somerville, NJ 08876 USA
[2] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
关键词
poly(p-dioxanone); absorbable polymers; crystallization; synchrotron; small-angle X-ray scattering;
D O I
10.1002/1099-0488(20010101)39:1<153::AID-POLB140>3.0.CO;2-9
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Changes in the lamellar morphology that occurred during the quiescent isothermal crystallization of absorbable poly(p-dioxanone) (PDS) and PDS/poly(glycolide) block copolymer were studied by synchrotron small-angle X-ray scattering. Important morphological parameters such as the lamellar long period, the thicknesses of the crystal and amorphous phases, and the scattering invariant were estimated as a function of time, and trends observed over a nide range of experimental conditions are discussed. Thicker but more perfect lamellae were detected at higher crystallization temperatures. The breadth of the normalized semilog Lorentz-corrected intensity peak systematically decreased with increasing temperature. In addition, the values of the crystallization half-time and the Avrami exponent (n = 2.5), determined from the real-time changes in the lamellar development, showed superb agreement with the bulk crystallinity data generated from other experimental techniques, such as calorimetry and dielectric relaxation spectroscopy. (C) 2000 John Wiley & Sons, Inc.
引用
收藏
页码:153 / 167
页数:15
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