We present the microdomain expansion and transition behavior of binary blends of polystyrene-b-poly(methyl methacrylate) (PS-b-PMMA)/PS homopolymers using small-angle X-ray scattering (SAXS) analysis, where the PS molecular weight (or chain length) was varied with chain length ratios (α) of 0.3, 1, and 2 with respect to the PS block length of the PS-b-PMMA. The d-spacing and order-to-disorder transition (ODT) by addition of PS homopolymers were significantly influenced by the PS molecular weight. In contrast to the typical decrease in d-spacing with increasing temperature in PS-b-PMMA, the d-spacing for PS-b-PMMA/PS homopolymers showed unusual behavior; specifically, it increased for shorter PS chains of α ≤ 1, but was independent of temperature for PS chains of α = 2. This variation can be attributed to a competing interaction between the thermal expansion effects of the microdomains with homopolymers and the decrease in the chain stretching between the two block components.
Bibliographical noteFunding Information:
This work was supported by the Nuclear R&D, NRF grants ( 2011-0022690 ), PAL and APCPI ERC program ( R11-2007-050-00000 ), which are funded by the Ministry of Education, Science & Technology (MEST), Korea.
All Science Journal Classification (ASJC) codes
- Organic Chemistry
- Polymers and Plastics
- Materials Chemistry