Crystallization-driven migration of the low surface energy segment of a copolymer to the bulk

被引:16
作者
Cheung, Zhuo-Lin
Ng, Kai-Mo
Weng, Lu-Tao
Chan, Chi-Ming
Li, Lin
机构
[1] Hong Kong Univ Sci & Technol, Sch Engn, Dept Chem Engn, Hong Kong, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Adv Engn Mat Facil, Hong Kong, Hong Kong, Peoples R China
[3] Hong Kong Univ Sci & Technol, Mat Characterizat & Preparat Facil, Hong Kong, Hong Kong, Peoples R China
[4] Chinese Acad Sci, Inst Chem, State Key Lab Polymer Phys & Chem, Beijing 100080, Peoples R China
基金
中国国家自然科学基金;
关键词
crystallization; copolymer; surface segregation;
D O I
10.1016/j.polymer.2006.02.076
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
[(BA-C8)(18)-(6FBA)](n) was synthesized by condensation polymerization of poly(bisphenol A-co-octane) containing 18 repeat units with bromine end groups, (Br-(BA-C8)(18)-Br), and 4,4'- (hexafluoroisopropylidene)diphenol (6FBA). This copolymer was confirmed to be semicrystalline after a single melting temperature was detected by differential scanning calorimetry. The changes in the surface chemical composition were measured using time-of-flight secondary ion mass spectrometry and X-ray photoelectron spectroscopy, the changes in the surface energy were measured using contact angle measurements, and the changes in the surface morphology were detected using atomic force microscopy as the copolymer crystallized. A decrease in the surface fluorine concentration with time was detected because of the movement of the low surface energy units (6FBA) to the bulk during the development of the crystalline phase. This result shows that the decrease in the enthalpy as a result of crystallization overcomes the increase in the surface free energy due to the migration of the low surface energy units to the bulk and the decrease in entropy due to demixing. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3164 / 3170
页数:7
相关论文
共 35 条
[1]   Surface segregation in blends of polystyrene and perfluorohexane double end capped polystyrene studied by static SIMS, ISS, and XPS [J].
Affrossman, S ;
Bertrand, P ;
Hartshorne, M ;
Kiff, T ;
Leonard, D ;
Pethrick, RA ;
Richards, RW .
MACROMOLECULES, 1996, 29 (16) :5432-5437
[2]   PREFERENTIAL SURFACE-ADSORPTION IN MISCIBLE BLENDS OF POLYSTYRENE AND POLYVINYL METHYL-ETHER) [J].
BHATIA, QS ;
PAN, DH ;
KOBERSTEIN, JT .
MACROMOLECULES, 1988, 21 (07) :2166-2175
[3]  
Briggs D, 1997, SURF INTERFACE ANAL, V25, P725, DOI 10.1002/(SICI)1096-9918(199708)25:9<725::AID-SIA293>3.0.CO
[4]  
2-9
[5]   Direct observation of the growth of lamellae and spherulites by AFM [J].
Chan, CM ;
Li, L .
INTRINSIC MOLECULAR MOBILITY AND TOUGHNESS OF POLYMERS II, 2005, 188 :1-41
[6]   SURFACE-COMPOSITION OF A SERIES OF DIMETHYLSILOXANE UREA URETHANE SEGMENTED COPOLYMERS STUDIED BY ELECTRON-SPECTROSCOPY FOR CHEMICAL-ANALYSIS [J].
CHEN, X ;
GARDELLA, JA ;
HO, T ;
WYNNE, KJ .
MACROMOLECULES, 1995, 28 (05) :1635-1642
[7]   SURFACE SEGREGATION IN A POLYMER BLEND - COMPARISON BETWEEN MONTE-CARLO SIMULATION AND MEAN-FIELD THEORY [J].
CIFRA, P ;
BRUDER, F ;
BRENN, R .
JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (05) :4121-4127
[8]   DIFFERENT SURFACE PROFILES IN SURFACE DEMIXING OF POLYMER BLENDS [J].
CIFRA, P .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (12) :9157-9160
[9]   SURFACE STUDIES OF POLYMER BLENDS .3. AN ESCA, IR, AND DSC STUDY OF POLY(EPSILON-CAPROLACTONE) POLY(VINYL CHLORIDE) HOMOPOLYMER BLENDS [J].
CLARK, MB ;
BURKHARDT, CA ;
GARDELLA, JA .
MACROMOLECULES, 1989, 22 (12) :4495-4501
[10]  
GARDELLA JA, 1983, J AM CHEM SOC, V105, P4563