Influence of block lengths and symmetries of block copolymers on phase behavior of polymer A/polymer B/block copolymer ternary blends

Polymer ◽  
2004 ◽  
Vol 45 (3) ◽  
pp. 1019-1026 ◽  
Author(s):  
Bing Dai ◽  
Mo Song ◽  
Douglas J. Hourston ◽  
Xuehao He ◽  
Haojun Liang ◽  
...  
2008 ◽  
pp. 391-417 ◽  
Author(s):  
Carlos Rodrguez ◽  
Arturo Lpez-Quintela ◽  
Md. Hemayet Uddin ◽  
Kenji Aramaki ◽  
Hironobu Kunieda

2009 ◽  
Vol 42 (8) ◽  
pp. 3063-3072 ◽  
Author(s):  
Guoliang Liu ◽  
Mark P. Stoykovich ◽  
Shengxiang Ji ◽  
Karl O. Stuen ◽  
Gordon S. W. Craig ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 178
Author(s):  
Jong Dae Jang ◽  
Young-Jin Yoon ◽  
Sang-Woo Jeon ◽  
Young Soo Han ◽  
Tae-Hwan Kim

Pluronic amphiphilic block copolymers, well known to have a phase behavior can be controlled by external conditions, have a wide range of potential for applications such as nanotemplates or nanobuilding blocks. However, the phase behaviors of Pluronic block copolymer/additive complexes with highly ordered phases have not been fully investigated. Here, we report the unusual molecular weight-dependent self-assembly of Pluronic block copolymer/additive complexes. Depending on the temperature and additive, Pluronic P65 block copolymer with a lower molecular weight showed the closed loop-like (CLL) phase behavior with the disorder-order-disorder-order phase transition in aqueous solution, whereas Pluronic P105 and P85 block copolymers with higher molecular weights underwent highly ordered continuous phase transitions with face centered cubic (FCC), hexagonal, and lamellar phases. It is expected that the specific phase behavior of the block copolymer/additive complex can be applied in optical devices such as nanotemplates or optical sensors for a highly ordered superlattice. Furthermore, this study provides a new route to control the phase behavior of the block copolymers without a complicated process.


2008 ◽  
Vol 64 (a1) ◽  
pp. C146-C146
Author(s):  
P. Thiyagarajan ◽  
V. Pol ◽  
D. Bohnsack ◽  
C.-T. Lo ◽  
B. Lee ◽  
...  

2010 ◽  
Vol 144 ◽  
pp. 143-157 ◽  
Author(s):  
Federica Lo Verso ◽  
Athanassios Z. Panagiotopoulos ◽  
Christos N. Likos

1995 ◽  
Vol 28 (10) ◽  
pp. 3597-3603 ◽  
Author(s):  
Maarten Svensson ◽  
Per Linse ◽  
Folke Tjerneld

1969 ◽  
Vol 22 (8) ◽  
pp. 1649 ◽  
Author(s):  
JR Urwin

Binary cluster integrals or excluded volumes for chemically different segment pairs in block copolymers of poly(isoprene : styrene) have been calculated from the equation derived by Froelich and Benoit for a two- sequence block copolymer. Expansion factors have been recalculated assuming a linear relation for [η]θ with respect to composition employing published values for polystyrene and polyisoprene. The results are discussed in relation to possible conformations of block copolymers.


2021 ◽  
Author(s):  
Isamu Akiba ◽  
Kazuo Sakurai

AbstractBlock copolymers are well recognized as excellent nanotools for delivering hydrophobic drugs. The formulation of such delivery nanoparticles requires robust characterization and clarification of the critical quality attributes correlating with the safety and efficacy of the drug before applying to regulatory authorities for approval. Static solution scattering from block copolymers is one such technique. This paper first outlines the theoretical background and current models for analyzing this scattering and then presents an overview of our recent studies on block copolymers.


Sign in / Sign up

Export Citation Format

Share Document