“Aggregation in Block Copolymer Solutions”

1989 ◽  
Vol 177 ◽  
Author(s):  
M. Olvera de la Cruz

ABSTRACTThe ability to produce block copolymers has led to new materials with unique properties. The chemical connectivity of incompatible blocks forces segregation to occur at distances of the order of the block sizes. In block copolymer melts, the segregated domains form periodic ordered structures called microphases. Most block copolymers are strongly incompatible. In such cases, in order to ensure equilibrium microphase separated samples, the microphases are prepared from solution. Microphase separation in semidilute solutions of block copolymers in nonselective good solvent is analyzed. The solvent effects on the thermodynamics in the weak segregation limit are discussed. The concentration of block copolymer at the transition in good solvents, scales as φtN−.62and in ϑ solvents as N−.5. The transitions between microphase morphologies as a function of block copolymer concentration are studied.

Author(s):  
Lee M. Trask ◽  
Nacu Hernandez ◽  
Eric W. Cochran

This article explores the dynamics, thermodynamics, and small-angle scattering of block copolymers. The goal is to determine what drives the applications of block copolymers, i.e. how block copolymers behave and how they are characterized. The article begins with a summary of the experimental data and various theories that comprise our understanding of block copolymer thermodynamics, with particular emphasis on phase behavior and especially the theory of microphase separation. It then considers topics related to block copolymer dynamics, including diffusion, viscoelasticity and rheology, shear-processing, and the kinetics of self-assembly. It also discusses small-angle scattering techniques as applied to block copolymer characterization, including scattering from ordered block copolymer melts.


1989 ◽  
Vol 177 ◽  
Author(s):  
H. Henning Winter ◽  
Faith A. Morrison

Flow can transfer the microphase separated morphology of block copolymers into a state of global order. For tri-block copolymers with cylindrical domains, this has been demonstrated by Folkes et al. (1973) and Hadziioannou et al. (1979). who established the existence of ‘single crystals’ of hexagonally ordered cylinders with uniform director throughout a sheared sample. The director is aligned with the shear direction. In this study, we investigate the flow induced ordering of cylindrical domain structure at increasing levels of shear.


Soft Matter ◽  
2021 ◽  
Author(s):  
Mikhail K. Glagolev ◽  
Anna A Glagoleva ◽  
Valentina V Vasilevskaya

By means of molecular dynamics simulation, the process of the microphase separation in the melts of diblock helix-coil copolymers comprising a flexible and a helical block was studied. The resulting...


Polymers ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 794
Author(s):  
Volker Abetz

Block copolymers and block-copolymer-containing blends represent a fascinating class of soft matter and can self-assemble in a variety of ordered structures on the mesoscale [...]


Soft Matter ◽  
2020 ◽  
Vol 16 (17) ◽  
pp. 4311-4323
Author(s):  
Jingxue Zhang ◽  
Jiaping Wu ◽  
Run Jiang ◽  
Zheng Wang ◽  
Yuhua Yin ◽  
...  

The effects of chain architecture on the structural details and orientation of confined lamellae formed by symmetric AB-type block copolymer melts are studied.


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