Autor: |
Hajduk, D. A., Takenouchi, H., Hillmyer, M. A., Bates, F. S., Vigild, M. E., Almdal, K. |
Zdroj: |
Macromolecules; June 30, 1997, Vol. 30 Issue: 13 p3788-3795, 8p |
Abstrakt: |
We reexamine the stability of hexagonally modulated layer (HML) and hexagonally perforated layer (HPL) morphologies in a number of block copolymer systems of low to moderate molecular weight. Using small-angle X-ray scattering and dynamic mechanical spectroscopy, we show that these structures are long-lived nonequilibrium states which convert to the bicontinuous gyroid (G) morphology upon isothermal annealing. Comparison of phase transition kinetics across chemically distinct systems spanning a wide range of molecular weights and monomeric friction coefficients reveals a composition dependence to these dynamics. This suggests effects associated with the mobility of individual chains are of lesser importance in explaining the apparent metastability of the HML and HPL structures; instead, the composition dependence of the transition mechanism appears to dominate the observed behavior. The revised phase behavior for these materials is in excellent agreement with mean-field predictions for diblock copolymer melts. |
Databáze: |
Supplemental Index |
Externí odkaz: |
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