The mechanisms of recrystallization after melting in syndiotactic polypropylene and isotactic polystyrene

被引:35
作者
Al-Hussein, M [1 ]
Strobl, G [1 ]
机构
[1] Univ Freiburg, Fak Phys, D-79104 Freiburg, Germany
关键词
D O I
10.1007/s10189-001-8045-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Several semicrystalline polymers show a recrystallization after melting during a heating scan. We have studied the mechanisms of such recrystallization processes for two different polymers, namely syndiotactic polypropylene (sPP) and isotactic polystyrene (iPS). This was done by monitoring the structure evolution during the recrystallization process and its changes during a subsequent heating scan via time-and temperature-dependent SAXS measurements, respectively. The results of this study showed that the sPP samples exhibited a recrystallization mechanism similar to the multi-stage route found upon initial crystallization of semicrystalline polymers from an entangled melt. Meanwhile, a different recrystallization mechanism was shown by the iPS samples. In this case, the recrystallization process proceeded as a direct growth into the melt in a one-step process. This is the first time we have observed such a mechanism which resembles the picture presented by the classical models for crystallization from an entangled polymer melt. The reason for such different mechanisms may be related to the initial melt state prior to crystallization. It seems as though, when crystallization sets in an entangled polymer melt, it follows the multi-stage route, whereas if the melt is locally disentangled, it proceeds by a direct growth mechanism.
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页码:305 / 314
页数:10
相关论文
共 22 条
[1]  
ALHUSSEIN M, UNPUB MACROMOLECULES
[2]   STRUCTURE TRANSFER FROM A POLYMERIC MELT TO THE SOLID-STATE .3. INFLUENCE OF KNOTS ON STRUCTURE AND MECHANICAL-PROPERTIES OF SEMICRYSTALLINE POLYMERS [J].
BAYER, RK .
COLLOID AND POLYMER SCIENCE, 1994, 272 (08) :910-932
[3]   THE MORPHOLOGY OF POLY(ARYL-ETHER-ETHER-KETONE) [J].
BLUNDELL, DJ ;
OSBORN, BN .
POLYMER, 1983, 24 (08) :953-958
[4]   CRYSTALLIZATION KINETICS OF ISOTACTIC POLYSTYRENE .I. SPHERULITIC GROWTH RATE [J].
BOON, J ;
CHALLA, G ;
VANKREVE.DW .
JOURNAL OF POLYMER SCIENCE PART A-2-POLYMER PHYSICS, 1968, 6 (10PA) :1791-&
[5]  
DOI M, 1986, THEORY POLYM DYNAMIC, P191
[6]  
FOUNGIES C, 1997, MACROMOLECULES, V30, P1392
[7]   A temperature- and molar mass-dependent change in the crystallization mechanism of poly(1-butene): Transition from chain-folded to chain-extended crystallization? [J].
Fu, Q ;
Heck, B ;
Strobl, G ;
Thomann, Y .
MACROMOLECULES, 2001, 34 (08) :2502-2511
[8]   The role of co-units in polymer crystallization and melting: New insights from studies on syndiotactic poly(propene-co-octene) [J].
Hauser, G ;
Schmidtke, J ;
Strobl, G .
MACROMOLECULES, 1998, 31 (18) :6250-6258
[9]   Steps in the transition of an entangled polymer melt to the partially crystalline state [J].
Heck, B. ;
Hugel, T. ;
Iijima, M. ;
Sadiku, E. ;
Strobl, G. .
NEW JOURNAL OF PHYSICS, 1999, 1
[10]  
Hoffman J.D., 1976, TREATISE SOLID STATE, DOI DOI 10.1007/978-1-4684-2664-9_7