Early stages of crystallization in isotactic polypropylene

被引:88
作者
Heeley, EL [1 ]
Maidens, AV
Olmsted, PD
Bras, W
Dolbnya, IP
Fairclough, JPA
Terrill, NJ
Ryan, AJ
机构
[1] Univ Sheffield, Dept Chem, Ctr Polymer, Sheffield S3 7HF, S Yorkshire, England
[2] SERC, Daresbury Lab, CLRC, Warrington WA4 4AD, Cheshire, England
[3] European Synchrotron Radiat Facil, CRG, DUBBLE, NWO,Netherlands Org Sci Res, F-38043 Grenoble, France
[4] Univ Leeds, Polymer IRC, Leeds LS2 9JT, W Yorkshire, England
[5] Univ Leeds, Dept Phys & Astron, Leeds LS2 9JT, W Yorkshire, England
关键词
D O I
10.1021/ma021373i
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
An experimental study of the early stages of crystallization in iPP has shown a qualitative difference between the behavior at low supercooling with that observed with a deep quench. To address previous misgivings in the limits of resolution of crystallites by wide-angle scattering, a new detector has been used that has many orders of magnitude improvements in count rate. At low degrees of undercooling there is a substantial gap between the appearance of a peak in the small-angle scattering, associated with electron density modulations, and the resolution of crystallites. This early growth in electron density has been analyzed in terms of a spinodal decomposition process and the stability limit of isotactic polypropylene determined for three different samples of varying molecular weight. The underlying physics of the early stages of crystallization are discussed and a number of scenarios eliminated; at high temperature Avrami kinetics are not observed whereas at low temperatures the structure in both the small-angle and wide-angle regimes grow contemporaneously following secondary nucleation.
引用
收藏
页码:3656 / 3665
页数:10
相关论文
共 55 条
[1]  
Avrami M., 1940, J CHEM PHYS, V8, P212, DOI [10.1063/1.1750631, DOI 10.1063/1.1750631]
[2]   KINETICS OF MICROSTRUCTURE REARRANGEMENT DURING ANNEALING OF COLD-DRAWN ISOTACTIC POLYPROPYLENE [J].
BABAJKO, S ;
SCHULTZ, JM .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1982, 20 (03) :497-508
[3]   Evolution of microstructure in the liquid and crystal directions in a quenched block copolymer melt [J].
Balsara, NP ;
Garetz, BA ;
Newstein, MC ;
Bauer, BJ ;
Prosa, TJ .
MACROMOLECULES, 1998, 31 (22) :7668-7675
[4]  
BALTACALLEJA FJ, 2002, P INT S POL CRYST JU
[5]   SPINODAL DECOMPOSITION OF A SYMMETRIC CRITICAL MIXTURE OF DEUTERATED AND PROTONATED POLYMER [J].
BATES, FS ;
WILTZIUS, P .
JOURNAL OF CHEMICAL PHYSICS, 1989, 91 (05) :3258-3274
[6]   Formation and decay of a smectic mesophase during orientation of a PET/PEN copolymer [J].
Blundell, DJ ;
Mahendrasingam, A ;
Martin, C ;
Fuller, W .
JOURNAL OF MATERIALS SCIENCE, 2000, 35 (20) :5057-5063
[7]   Characterization of strain-induced crystallization of poly(ethylene terephthalate) at fast draw rates using synchrotron radiation [J].
Blundell, DJ ;
MacKerron, DH ;
Fuller, W ;
Mahendrasingam, A ;
Martin, C ;
Oldman, RJ ;
Rule, RJ ;
Riekel, C .
POLYMER, 1996, 37 (15) :3303-3311
[8]   Orientation prior to crystallisation during drawing of poly(ethylene terephthalate) [J].
Blundell, DJ ;
Mahendrasingam, A ;
Martin, C ;
Fuller, W ;
MacKerron, DH ;
Harvie, JL ;
Oldman, RJ ;
Riekel, C .
POLYMER, 2000, 41 (21) :7793-7802
[9]   An SAXS/WAXS beamline at the ESRF and future experiments [J].
Bras, W .
JOURNAL OF MACROMOLECULAR SCIENCE-PHYSICS, 1998, B37 (04) :557-565
[10]   SIMULTANEOUS TIME RESOLVED SAXS AND WAXS EXPERIMENTS USING SYNCHROTRON RADIATION [J].
BRAS, W ;
DERBYSHIRE, GE ;
RYAN, AJ ;
MANT, GR ;
FELTON, A ;
LEWIS, RA ;
HALL, CJ ;
GREAVES, GN .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT, 1993, 326 (03) :587-591