Nanoconfinement as a tool to study early stages of polymer crystallization

被引:40
作者
Beiner, Mario [1 ]
机构
[1] Univ Halle Wittenberg, Inst Phys, D-06099 Halle, Germany
关键词
confinement; crystallization; nucleation; polyethylene; polymorphism; thermodynamics;
D O I
10.1002/polb.21491
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This article promotes the idea that crystallization experiments under confinement can be an interesting tool to learn more about the early stages of polymer crystallization in bulk systems. Based on various results from the recent literature, it is demonstrated that crystalline forms that are metastable, transient, or inaccessible in bulk samples can be easily obtained and studied in nanoscopic compartments. This is interesting in the light of the recent discussion about thermodynamic reasons for the temporary occurrence of a mesophase at the growth front of crystals in bulk polymers, in particular, about a hexagonally packed mesophase in polyethylene. The experimental findings for nanoconfined methylene sequences seem to support indirectly thermodynamic approaches explaining the occurrence of a mesophase based on the small thickness of the crystal at the growth front. A first estimate for the critical crystal thickness d(mc) defining the transition from hexagonal to orthorhombic packing in case of confined methylene sequences is provided based on results for side chain polymers. Further perspectives of crystallization experiments on confined systems are discussed. (C) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:1556 / 1561
页数:6
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