Morphological and kinetic analyses of regime transition for poly[(S)-lactide] crystal growth

被引:168
作者
Abe, H [1 ]
Kikkawa, Y
Inoue, Y
Doi, Y
机构
[1] Riken Inst Phys & Chem Res, Polymer Chem Lab, Wako, Saitama 3510198, Japan
[2] Tokyo Inst Technol, Midori Ku, Yokohama, Kanagawa 2268501, Japan
关键词
D O I
10.1021/bm015543v
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regime transitions of poly[(S)-lactide] (PLA) crystal growth from the melt were investigated by studying the morphological changes and carrying out kinetic analysis using microscopic techniques. PLA thin films with an average layer thickness of 100 nm were isothermally crystallized at a given crystallization temperature after melting at 220 degreesC. Following isothermal crystallization at a temperature below 145 degreesC, uniform two-dimensional spherulites having stacked flat-on lamellar texture were developed throughout the PLA thin films. On the basis of electron diffraction analysis for two-dimensional spherulites of PLA, it was found that the average growth direction of an individual lamellar crystal was parallel to the crystallographic b axis. At temperatures above 150 degreesC, hexagonal lamellar crystals were formed from the melt. Electron diffractograms of these lamellae showed that the crystal had orthogonal packing of PLA molecules and a truncated-lozenge-shaped growth behavior. The growth surfaces of the hexagonal crystal were parallel to either the crystallographic {110} or the {100} plane. The PLA crystal growth rate along the b axis direction was evaluated at various crystallization temperatures of the thin films. Kinetic analysis of crystal growth in the PLA thin film demonstrated that the regime transitions of PLA crystal growth, from regime III to regime II and from regime II to regime I, occur at around 120 and 147 degreesC, respectively. The transition from regime II to regime I induced morphological changes in the crystalline aggregates whereby spherulitic aggregates transformed into hexagonal lamellar stacking. As for the transition between regimes II and III, no obvious morphological change in the spherulitic crystal aggregates was observed.
引用
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页码:1007 / 1014
页数:8
相关论文
共 35 条
[1]   BASIC PROPERTIES OF POLYLACTIC ACID PRODUCED BY THE DIRECT CONDENSATION POLYMERIZATION OF LACTIC-ACID [J].
AJIOKA, M ;
ENOMOTO, K ;
SUZUKI, K ;
YAMAGUCHI, A .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1995, 68 (08) :2125-2131
[2]  
ALAMO R, 1985, J POLYM, V26, P1595
[3]   CRYSTALLIZATION KINETICS OF LONG-CHAIN N-ALKANES FROM THE MELT AND FROM SOLUTION [J].
ALAMO, RG ;
MANDELKERN, L ;
STACK, GM ;
KROHNKE, C ;
WEGNER, G .
MACROMOLECULES, 1994, 27 (01) :147-156
[4]   PREPARATION OF BIODEGRADABLE MICROSPHERES AND MICROCAPSULES .2. POLYACTIDES AND RELATED POLYESTERS [J].
ARSHADY, R .
JOURNAL OF CONTROLLED RELEASE, 1991, 17 (01) :1-21
[5]   CRYSTALLIZATION AND MORPHOLOGY OF A BACTERIAL THERMOPLASTIC - POLY-3-HYDROXYBUTYRATE [J].
BARHAM, PJ ;
KELLER, A ;
OTUN, EL ;
HOLMES, PA .
JOURNAL OF MATERIALS SCIENCE, 1984, 19 (09) :2781-2794
[6]   REGIME TRANSITIONS IN FRACTIONS OF ISOTACTIC POLYPROPYLENE [J].
CHENG, SZD ;
JANIMAK, JJ ;
ZHANG, A ;
CHENG, HN .
MACROMOLECULES, 1990, 23 (01) :298-303
[7]   MOLECULAR CONFORMATION OF POLY(S-LACTIC ACID) [J].
DESANTIS, P ;
KOVACS, AJ .
BIOPOLYMERS, 1968, 6 (03) :299-&
[8]   BIODEGRADABLE MATERIALS OF POLY(L-LACTIC ACID) .1. MELT-SPUN AND SOLUTION-SPUN FIBERS [J].
ELING, B ;
GOGOLEWSKI, S ;
PENNINGS, AJ .
POLYMER, 1982, 23 (11) :1587-1593
[9]   INVESTIGATION OF STRUCTURE OF SOLUTION GROWN CRYSTALS OF LACTIDE COPOLYMERS BY MEANS OF CHEMICAL-REACTIONS [J].
FISCHER, EW ;
STERZEL, HJ ;
WEGNER, G .
KOLLOID-ZEITSCHRIFT AND ZEITSCHRIFT FUR POLYMERE, 1973, 251 (11) :980-990
[10]   SYNTHESIS OF COPOLY(D,L-LACTIC ACID) WITH RELATIVELY LOW-MOLECULAR WEIGHT AND INVITRO DEGRADATION [J].
FUKUZAKI, H ;
YOSHIDA, M ;
ASANO, M ;
KUMAKURA, M .
EUROPEAN POLYMER JOURNAL, 1989, 25 (10) :1019-1026