Self-Assembly and Graft Polymerization Route to Monodispersed Fe3O4@SiO2—Polyaniline Core–Shell Composite Nanoparticles: Physical Properties

2008 ◽  
Vol 8 (11) ◽  
pp. 5632-5639 ◽  
Author(s):  
Kakarla Raghava Reddy ◽  
Kwang-Pill Lee ◽  
Ju Young Kim ◽  
Youngil Lee

This study describes the synthesis of monodispersed core–shell composites of silica-modified magnetic nanoparticles and conducting polyaniline by self-assembly and graft polymerization. Magnetic ferrite nanoparticles (Fe3O4) were prepared by coprecipitation of Fe+2 and Fe+3 ions in alkaline solution, and then silananized. The silanation of magnetic particles (Fe3O4@SiO2) was carried out using 3-bromopropyltrichlorosilane (BPTS) as the coupling agent. FT-IR spectra indicated the presence of Fe—O—Si chemical bonds in Fe3O4@SiO2. Core–shell type nanocomposites (Fe3O4@SiO2/PANI) were prepared by grafting polyaniline (PANI) on the surface of silanized magnetic particles through surface initiated in-situ chemical oxidative graft polymerization. The nanocomposites were characterized by high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), Fourier transform infrared (FTIR) spectra, UV-visible spectroscopy, photoluminescence (PL) spectra, electrical conductivity and magnetic characteristics. HRTEM images of the nanocomposites revealed that the silica-modified magnetic particles made up the core while PANI made up the shell. The XPS spectrum revealed the presence of silica in the composites, and the XRD results showed that the composites were more crystalline than pure PANI. PL spectra show that composites exhibit photoluminescent property. Conductivity of the composites (6.2 to 9.4 × 10−2 S/cm) was higher than that of pristine PANI (3.7 × 10−3 S/cm). The nanocomposites exhibited superparamagnetism. Formation mechanism of the core–shell structured nanocomposites and the effect of modified magnetic nanoparticles on the electro-magnetic properties of the Fe3O4@SiO2/PANI nanocomposites are also investigated. This method provides a new strategy for the generation of multi-functional nanocomposites that composed of other conducting polymers and metal nanoparticles.

2017 ◽  
Vol 10 (05) ◽  
pp. 1750056 ◽  
Author(s):  
Huiping Shao ◽  
Jiangcong Qi ◽  
Tao Lin ◽  
Yuling Zhou ◽  
Fucheng Yu

The core–shell structure composite magnetic nanoparticles (NPs), Fe3O4@chitosan@nimodipine (Fe3O4@CS@NMDP), were successfully synthesized by a chemical cross-linking method in this paper. NMDP is widely used for cardiovascular and cerebrovascular disease prevention and treatment, while CS is of biocompatibility. The composite particles were characterized by an X-ray diffractometer (XRD), a Fourier transform infrared spectroscopy (FT-IR), a transmission electron microscopy (TEM), a vibrating sample magnetometers (VSM) and a high performance liquid chromatography (HPLC). The results show that the size of the core–shell structure composite particles is ranging from 12[Formula: see text]nm to 20[Formula: see text]nm and the coating thickness of NMDP is about 2[Formula: see text]nm. The saturation magnetization of core–shell composite NPs is 46.7[Formula: see text]emu/g, which indicates a good potential application for treating cancer by magnetic target delivery. The release percentage of the NMDP can reach 57.6% in a short time of 20[Formula: see text]min in the PBS, and to 100% in a time of 60[Formula: see text]min, which indicates the availability of Fe3O4@CS@NMDP composite NPs for targeting delivery treatment.


2017 ◽  
Vol 31 (33) ◽  
pp. 1750307 ◽  
Author(s):  
Ersin Kantar

In this study, we examine by comparing the dynamic magnetic and hysteretic properties of Ising-type endohedral fullerene (EF) with various dopant magnetic particles confined within a spherical cage. The model of EF X@C[Formula: see text] with X = spin-1/2, spin-1 and spin-3/2 is proposed to study the effect of the nature of core particle on the magnetic properties. The results were obtained by mean-field theory as well as Glauber-type stochastic dynamics, and focused on the response of thermal and hysteretic behaviors of systems. The system exhibits second- and first-order phase transitions. In three different core cases, the system also exhibits type-II superconductivity behavior with a dynamic hysteresis curves of the core. All results display magnetic properties of the EF which strongly depend on the nature of core particle. Moreover, core particle and core/shell (C–S) interaction are proposed as the basic factors affecting the magnetic properties of EF system.


2018 ◽  
Vol Volume 13 ◽  
pp. 3965-3973 ◽  
Author(s):  
Kamiar Zomorodian ◽  
Hamed Veisi ◽  
Mahmoud Mousavi ◽  
Mahmoud Ataabadi ◽  
Somayeh Yazdanpanah ◽  
...  

2013 ◽  
Vol 06 (06) ◽  
pp. 1350058 ◽  
Author(s):  
YUAN MING HUANG ◽  
QING-LAN MA ◽  
BAO-GAI ZHAI

A facile and green method was utilized to synthesize core-shelled Zn / ZnO microspheres by boiling Zn microparticles in water for improving the photocatalytic activity of ZnO . The synthesized Zn / ZnO core-shells were investigated by means of scanning electron microscope, X-ray diffractometer and photoluminescence spectrometer, respectively. The morphology analysis showed that the metallic Zn core was about 6 μm in diameter while the ZnO shell was about 600 nm in thickness. Compared to ZnO nanoparticles, the core-shelled Zn / ZnO microspheres exhibited improved photocatalytic activity in degrading methyl orange in water. Our results suggest that the metal–semiconductor junction formed at the Zn / ZnO interface is responsible for the enhanced photocatalytic activity of ZnO .


2001 ◽  
Vol 704 ◽  
Author(s):  
M. Toprak ◽  
D. K. Kim ◽  
M. Mikhailova ◽  
Y. Zhang ◽  
Y. K. Jeong ◽  
...  

AbstractNovel metallic capsules containing magnetite with given size in the sub-micron range have been produced. These nanocapsules are prepared in several steps through a colloidal templating approach. The first step is the synthesis of size-selected SiO2 nanospheres. The second step is coating the SiO2nanospheres by electroless deposition with gold, in order to form a porous gold shell around the silica. Electroless deposition is controlled by the concentration of gold in the coating solution. Subsequently, the core (SiO2) was removed to obtain gold capsules. The final step is the inclusion of magnetite nanoparticles inside these nanocapsules and recoating the capsules with gold in order to have continuous encapsulation. The nanocapsule and core-shell structure have been characterized by TEM and DSC


2015 ◽  
Vol 662 ◽  
pp. 217-220 ◽  
Author(s):  
Ondrej Milkovič ◽  
Jana Michaliková ◽  
Jozef Bednarčík ◽  
Štefan Michalik

This work deals with the strain at the core-shell interface of Fe nanoparticles. Series of Fe nanoparticles with various mean diameters were prepared by precipitation in solid state in binary Cu-Fe alloy. Further, nanoparticles were isolated by dissolution of Cu matrix. High-energy X-ray diffraction (XRD) was used to probe structure of nanoparticles. XRD measurements suggest presence of the core-shell structure, where core and shell of the nanoparticles are formed of α-Fe and CuFe2O4 phase, respectively. Strains in core and shell were estimated as a function of nanoparticles size by Williamson-Hall method.


2011 ◽  
Vol 688 ◽  
pp. 245-249 ◽  
Author(s):  
Zhi Qiang Wei ◽  
Xiao Yun Wang ◽  
Hua Yang

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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