Crystallization in the thin and ultrathin films of poly(ethylene-vinyl acetate) and linear low-density polyethylene

被引:138
|
作者
Wang, Y
Ge, S
Rafailovich, M [1 ]
Sokolov, J
Zou, Y
Ade, H
Lüning, J
Lustiger, A
Maron, G
机构
[1] SUNY Stony Brook, Dept Mat Sci & Engn, Stony Brook, NY 11794 USA
[2] N Carolina State Univ, Dept Phys, Raleigh, NC 27695 USA
[3] Stanford Synchrotron Radiat Lab, Stanford, CA 94309 USA
[4] ExxonMobil Res & Engn Co, Annandale, NJ 08801 USA
[5] Hebrew Univ Jerusalem, Dept Appl Chem, IL-91904 Jerusalem, Israel
基金
美国国家科学基金会;
关键词
D O I
10.1021/ma030456b
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The crystallization of poly(ethylene-vinyl acetate) and linear low-density polyethylene (LLDPE) films spun-cast from the polymer/toluene solutions with as-cast thickness from 460 to 10 nm was studied. The lamellar thickness was measured using small-angle X-ray scattering (SAXS) and found to increase from 14 to 21 nm for films thinner than 100 nm. The morphology of LLDPE measured by scanning probe microscopy (SPM) showed an edge-on lamellae for the films thicker than 30 nm and flaton lamellae for the films thinner than 15 nm. A pseudo-"shish-kebab" tiny crystal structure was observed in between the larger lamellae. Crystallinity was confirmed using attenuated total reflectance-Fourier transformed infrared spectroscopy (ATR-FTIR) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. The shear modulation force microscopy technique (SMFM) was used to measure the melting point, T., which was found to decrease for films thinner than 100 nm. The rate of decrease was a function of the annealing protocol, but in all cases for films approximately 20 nm thick T-m was depressed by 35-40 degreesC. This large value cannot be predicted from the classical Gibbs-Thomson relation, unless a change in the effective heat of fusion is assumed due to surface interactions.
引用
收藏
页码:3319 / 3327
页数:9
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