The phase behavior of a styrene-isoprene (SI) diblock copolymer, with block molecular weights of 1.1 ϫ 10 4 and 2.1 ϫ 10 4 g/mol, respectively, is examined in the neutral solvent bis(2-ethylhexyl) phthalate (DOP) and the styrene-selective solvent di-n-butyl phthalate (DBP). DBP is a good solvent for
Rheological studies on the phase dissolution in a block copolymer
✍ Scribed by Rui Xie; Bingxin Yang; Bingzheng Jiang; Qizhong Zhang; Yuanze Xu
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 253 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
✦ Synopsis
The microphase transition in a styrene-butadiene-styrene triblock copolymer was studied by rheometric mechanical spectroscopy. A high-temperature-melt rheological transition from the highly elastic, nonlinear viscous behavior typical of a multiphase structure to linear viscous behavior with insignificant elasticity typical of a single-phase structure was observed. The transition temperature is determined according to the discontinuity of the rheological properties across the transition region, which agrees well with the results obtained from the small angle X-ray scattering data and the expectation of the random phase approximation theory. Maybe for the first time, microphase dissolution was investigated rheologically. The storage modulus (G) and the loss modulus ( GЉ) increase with time during the process. An entanglement fluctuation model based on the segmental density fluctuations is presented to explain the rheological behavior in this dissolution process.
📜 SIMILAR VOLUMES
Unvulcanized and dynamically vulcanized blends of isotactic polypropylene (PP) and butadiene-styrene block copolymer (SBS), in the composition range of 10-40 wt % SBS content are prepared in an internal mixer and the vulcanization process is investigated through time-torque curves. Study of melt rhe
## Abstract We characterized metallocene‐catalyzed cyclo‐olefin copolymers (mCOCs) with similar heat distortion temperatures but dramatic differences in melt‐flow indices to understand how the molecular conformation affected their rheological and viscoelastic properties. The mCOC conformations were
**Several strategies are demonstrated** for the use of additive‐driven chemistries that take place in only one type of the nanosized domains of all‐organic and organic–inorganic hybrid block copolymer thin films. Such an approach is used to examine the convergence of “top–down” and “bottom–up” fabri