Novel pattern formation in blends of asymmetric ABC triblock terpolymers

e-Polymers ◽  
2004 ◽  
Vol 4 (1) ◽  
Author(s):  
Volker Abetz ◽  
Shimei Jiang ◽  
Astrid Göpfert

Abstract A series of polystyrene-block-poly(1,2-butadiene)-block-poly(2-vinylpyridine) (SBV) triblock terpolymers were used to prepare blends with symmetric polystyrene-block-poly(2-vinylpyridine) (SV) and poly(2-vinylpyridine)-block-poly- (cyclohexyl methacrylate) (VC) diblock copolymers. Morphological characterization was carried out by transmission electron microscopy. These triblock terpolymers self-assemble into various core-shell type or lamellar morphologies. In the SBV/SV blends, macrophase separation between the two block copolymers, continuous centrosymmetric lamellae and stacks of non-centrosymmetric lamellae with antiparallel orientation were found. In the blends of SBV/VC, macrophase separation was never observed, what is due to the specific interactions between S and C domains. These systems showed among other morphologies also a cylindrical morphology in which rings surround the cylinders.

e-Polymers ◽  
2004 ◽  
Vol 4 (1) ◽  
Author(s):  
Volker Abetz ◽  
Shimei Jiang

Abstract In this contribution we report on the morphological structures formed in blends of microphase-separated 3-miktoarm star terpolymers of polystyrene-armpolybutadiene- arm-poly(2-vinylpyridine) (SBV*) and polystyrene-block-polybutadiene (SB), polystyrene-block-poly(2-vinylpyridine) (SV), poly(2-vinylpyridine)- block-poly(cyclohexyl methacrylate) (VC) diblock copolymers. The morphologies are characterized by transmission electron microscopy. Blends with similar morphologies as known from linear triblock terpolymers are found, like core-shell structures based on cylinders or gyroids. Other blends show very distorted morphologies, or morphologies similar to the ones found for pure 3-miktoarm star terpolymers. While attractive interactions between blocks of the two species enhance the formation of common superlattices, blends with too large diblock copolymers tend to macrophase-separate.


2003 ◽  
Vol 89 (3) ◽  
pp. 855-861 ◽  
Author(s):  
Zhengmin Li ◽  
Jinghe Yang ◽  
Yuanzhang Yu ◽  
Xingzhong Xu ◽  
Xiantan Meng ◽  
...  

2010 ◽  
Vol 09 (05) ◽  
pp. 399-406 ◽  
Author(s):  
A. A. EL-DALY

In this paper, we report a convenient and informative procedure for detecting the morphology and surface structure of individual gold nanocrystals using digital Crystal Image Software (CIS) processing of transmission electron microscopy (TEM) image, which comprises coalescence phenomena of these nanoparticles. The results show that the internal structure of Au nanoparticles has a core of gold atoms arranged as a Marks decahedron, surrounded by additional gold–organic compound layers forming a rigid surface layer, and its outer layer comprises four staple motif bridge molecules that resemble handles, formed an unusual pattern. The obtained results improved our understanding of the basics of the coalescence phenomena such as the driving mechanisms acting at different particle sizes. However, these discrete natures of the nanoparticles will assist in the understanding of principles of nanocore assembly and opens a new window for nanoparticles chemistry.


2019 ◽  
Vol 7 (5) ◽  
pp. 1280-1291 ◽  
Author(s):  
Alaka Panda ◽  
R. Govindaraj ◽  
R. Mythili ◽  
G. Amarendra

Bismuth and iron oxides subjected to ball milling followed by controlled annealing treatments showed the formation of core–shell nanostructures with Bi2Fe4O9 as the core and a shell of BiFeO3 and Bi25FeO40 phases as deduced based on the analysis of transmission electron microscopy results.


1995 ◽  
Vol 196 (4) ◽  
pp. 985-993 ◽  
Author(s):  
Stefan Spiegel ◽  
Katharina Landfester ◽  
Günter Lieser ◽  
Christine Boeffel ◽  
Hans Wolfgang Spiess ◽  
...  

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