Ordering of Cylindrical Domains of Block Copolymers under Moving Temperature Gradient: Separation of ▽T-Induced Ordering from Surface-Induced Ordering

2008 ◽  
Vol 41 (18) ◽  
pp. 6787-6792 ◽  
Author(s):  
Kazuki Mita ◽  
Hirokazu Tanaka ◽  
Kenji Saijo ◽  
Mikihito Takenaka ◽  
Takeji Hashimoto
2008 ◽  
Vol 41 (22) ◽  
pp. 8789-8799 ◽  
Author(s):  
Kazuki Mita ◽  
Mikihito Takenaka ◽  
Hirokazu Hasegawa ◽  
Takeji Hashimoto

2007 ◽  
Vol 40 (16) ◽  
pp. 5923-5933 ◽  
Author(s):  
Kazuki Mita ◽  
Hirokazu Tanaka ◽  
Kenji Saijo ◽  
Mikihito Takenaka ◽  
Takeji Hashimoto

2017 ◽  
Vol 1 (3) ◽  
pp. 507-511 ◽  
Author(s):  
Jiangping Xu ◽  
Yi Yang ◽  
Ke Wang ◽  
Yuqing Wu ◽  
Jintao Zhu

With the addition of small molecules to emulsion droplets containing block copolymers, anisotropic convex lens-like particles with hexagonally stacked cylindrical domains can be readily achieved by using a single surfactant to create a neutral interface for both blocks.


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.


Nanoscale ◽  
2016 ◽  
Vol 8 (6) ◽  
pp. 3268-3273 ◽  
Author(s):  
Ting Qu ◽  
Yongbin Zhao ◽  
Zongbo Li ◽  
Pingping Wang ◽  
Shubo Cao ◽  
...  

2018 ◽  
Vol 9 (21) ◽  
pp. 2951-2963 ◽  
Author(s):  
Huda Nasser Al-Kharusi ◽  
Lipeng Wu ◽  
George Whittell ◽  
Robert Harniman ◽  
Ian Manners

The self-assembly of a ruthenium-containing polyferrocenylsilane in bulk and thin films yielded spherical or cylindrical domains in a PS matrix; pyrolysis provided a route to bimetallic Fe/Ru NPs for potential catalytic applications.


2008 ◽  
Vol 41 (18) ◽  
pp. 6780-6786 ◽  
Author(s):  
Kazuki Mita ◽  
Hirokazu Tanaka ◽  
Kenji Saijo ◽  
Mikihito Takenaka ◽  
Takeji Hashimoto

2002 ◽  
Vol 724 ◽  
Author(s):  
Elizabeth R. Wright ◽  
R. Andrew McMillan ◽  
Alan Cooper ◽  
Robert P. Apkarian ◽  
Vincent P. Conticello

AbstractTriblock copolymers have traditionally been synthesized with conventional organic components. However, triblock copolymers could be synthesized by the incorporation of two incompatible protein-based polymers. The polypeptides would differ in their hydrophobicity and confer unique physiochemical properties to the resultant materials. One protein-based polymer, based on a sequence of native elastin, that has been utilized in the synthesis of biomaterials is poly (Valine-Proline-Glycine-ValineGlycine) or poly(VPGVG) [1]. This polypeptide has been shown to have an inverse temperature transition that can be adjusted by non-conservative amino acid substitutions in the fourth position [2]. By combining polypeptide blocks with different inverse temperature transition values due to hydrophobicity differences, we expect to produce amphiphilic polypeptides capable of self-assembly into hydrogels. Our research examines the design, synthesis and characterization of elastin-mimetic block copolymers as functional biomaterials. The methods that are used for the characterization include variable temperature 1D and 2D High-Resolution-NMR, cryo-High Resolutions Scanning Electron Microscopy and Differential Scanning Calorimetry.


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