Formation of superlattices in blends of 3-miktoarm star terpolymers with diblock copolymers

e-Polymers ◽  
2004 ◽  
Vol 4 (1) ◽  
Author(s):  
Volker Abetz ◽  
Shimei Jiang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Diblock Copolymers ◽  
Shell Structures ◽  
Core Shell ◽  
Transmission Electron ◽  
Miktoarm Star ◽  
Triblock Terpolymers ◽  
Cyclohexyl Methacrylate

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.

Novel pattern formation in blends of asymmetric ABC triblock terpolymers

e-Polymers ◽  
2004 ◽  
Vol 4 (1) ◽  
Author(s):  
Volker Abetz ◽  
Shimei Jiang ◽  
Astrid Göpfert
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Diblock Copolymers ◽  
Morphological Characterization ◽  
Core Shell ◽  
Specific Interactions ◽  
Transmission Electron ◽  
Triblock Terpolymers ◽  
Cyclohexyl Methacrylate ◽  
Macrophase Separation

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.

Formation of bismuth iron oxide based core–shell structures and their dielectric, ferroelectric and magnetic properties

2019 ◽  
Vol 7 (5) ◽  
pp. 1280-1291 ◽  
Author(s):  
Alaka Panda ◽  
R. Govindaraj ◽  
R. Mythili ◽  
G. Amarendra
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Magnetic Properties ◽  
Iron Oxide ◽  
Shell Structures ◽  
Core Shell ◽  
Bismuth Iron Oxide ◽  
The Core ◽  
Shell Nanostructures ◽  
Transmission Electron

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.

Structural Characterization of Nanoparticles Obtained by a Polyol Synthesis in the Bimetallic System Pt-Pd

2012 ◽  
Vol 1372 ◽  
Author(s):  
A. F. García-Ruiz ◽  
J. J. Velázquez Salazar ◽  
R. Esparza ◽  
N. Castillo
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Bimetallic Nanoparticles ◽  
Synthesis Method ◽  
Shell Structures ◽  
Polyol Synthesis ◽  
Core Shell ◽  
Thermal Methods ◽  
Transmission Electron ◽  
Bimetallic System

ABSTRACTA modified polyol synthesis has been utilized to study the different structures obtained in the bimetallic system of platinum (Pt) and palladium (Pd). Some results are shown in this work. Thermal methods under refluxing, carrying on the reaction up to 285 ºC, have been assayed to reduce metallic salts using ethylene glycol (EG) as reducer and polyvinylpyrrolidone (PVP) as protective reagent of the formed bimetallic nanoparticles. The special core-shell structure has been observed in these bimetallic nanoparticles, whose synthesis was assisted by Ag, showing polyhedral shapes. The average diameter size of the core has been estimated at 10 nm, and the diameter size of the shell in 13 nm, consequently the thickness of the shell is around 1.5 nm. Nanoparticles were structurally characterized with transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM) equipped with detector to generate high angle annular dark field (HAADF) images. This kind of structures have been studied and utilized to increase successfully the catalytic properties of monometallic nanoparticles of Pt or Pd according to other works. Here, the synthesis procedure is described; as the main results, several images are presented showing the obtained bimetallic core-shell structures and their fast Fourier transform (FFT), and also the size and the elemental analysis of the nanoparticles are reported, concluding that this synthesis method is very efficient for preparing bimetallic core shell structures.

Microheterogeneities of core-shell latexes probed by 1H spin diffusion and transmission electron microscopy

1995 ◽  
Vol 196 (4) ◽  
pp. 985-993 ◽  
Author(s):  
Stefan Spiegel ◽  
Katharina Landfester ◽  
Günter Lieser ◽  
Christine Boeffel ◽  
Hans Wolfgang Spiess ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Spin Diffusion ◽  
Core Shell ◽  
Transmission Electron

scholarly journals Polymeric Self-Assemblies Based on tetra-ortho-Substituted Azobenzene as Visible Light Responsive Nanocarriers

Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 2060
Author(s):  
Alejandro Roche ◽  
Luis Oriol ◽  
Rosa M. Tejedor ◽  
Milagros Piñol
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Diblock Copolymers ◽  
Uv Light ◽  
Morphological Changes ◽  
Nile Red ◽  
Green Light ◽  
Light Irradiation ◽  
Transmission Electron ◽  
Amphiphilic Diblock Copolymers

Most of reported polymeric light-responsive nanocarriers make use of UV light to trigger morphological changes and the subsequent release of encapsulated cargoes. Moving from UV- to visible-responsive units is interesting for the potential biomedical applications of these materials. Herein we report the synthesis by ring opening polymerization (ROP) of a series of amphiphilic diblock copolymers, into which either UV or visible responsive azobenzenes have been introduced via copper(I) catalyzed azide-alkyne cycloaddition (CuAAC). These copolymers are able to self-assemble into spherical micelles or vesicles when dispersed in water. The study of the response of the self-assemblies upon UV (365 nm) or visible (530 or 625 nm) light irradiation has been studied by Transmission Electron Microscopy (TEM), Cryogenic Transmission Electron Microscopy (Cryo-TEM), and Dynamic Light Scattering (DLS) studies. Encapsulation of Nile Red, in micelles and vesicles, and Rhodamine B, in vesicles, and its light-stimulated release has been studied by fluorescence spectroscopy and confocal microscopy. Appreciable morphological changes have been induced with green light, and the subsequent release of encapsulated cargoes upon green light irradiation has been confirmed.

Preparation of Carbon-Encapsulated Fe Core-Shell Nanostructures by Confined Arc Plasma

2011 ◽  
Vol 688 ◽  
pp. 245-249 ◽  
Author(s):  
Zhi Qiang Wei ◽  
Xiao Yun Wang ◽  
Hua Yang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Particle Size ◽  
Specific Surface ◽  
Surface Area ◽  
Core Shell ◽  
Arc Plasma ◽  
X Ray ◽  
The Core ◽  
Transmission Electron

Special carbon encapsulated Fe core-shell nanoparticles with a size range of 15–40 nm were successfully prepared via confined arc plasma method. The composition, morphology, microstructure, specific surface area, particle size of the product by this process were characterized via X-ray diffraction (XRD), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), X-ray energy dispersive spectrometry (XEDS) and BET N2adsorption. The experiment results shown that the carbon encapsulated Fe nanoparticles with clear core-shell structure, the core of the particles is body centered cubic (BCC) structure Fe, and the shell of the particles is disorder carbons. The particle size of the nanocapsules ranges from 15 to 40nm，with an averaged value about 30nm, the particles diameter of the core is about 16nm and the thickness of the shells is about 6-8 nm, and the specific surface area is 24 m2/g.

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