Dependence of the coercive force on the size of the core/shell nanoparticles magnetite/titanomagnetite

Author(s):  
M Shmykova ◽  
L Afremov ◽  
I Iliushin
Nanoscale ◽  
2019 ◽  
Vol 11 (37) ◽  
pp. 17471-17477 ◽  
Author(s):  
Jiaqi Chen ◽  
Dejing Meng ◽  
Hui Wang ◽  
Haiyun Li ◽  
Yinglu Ji ◽  
...  

Using DMAB as the Raman internal reference, the spatial trajectory of modulating 4-ATP molecules was tracked during the shell growth process.


2004 ◽  
Vol 818 ◽  
Author(s):  
U. Wiedwald ◽  
J. Lindner ◽  
M. Spasova ◽  
Z. Frait ◽  
M. Hilgendorff ◽  
...  

AbstractFerromagnetic Resonance experiments are used to investigate the magnetic properties of monodisperse Co/CoO core-shell nanoparticles with diameters of about 10nm. From frequency- dependent measurements at various frequencies of 9-80 GHz the g-value is determined to be 2.13 which suggests an fcc bulk-like environment of the Co atoms within the core of the particles. This result yields a direct measure of the ratio of orbital to spin magnetic moment νL/νS=0.065. Moreover, from temperature-dependent measurements of the resonance field the anisotropy energy is extracted and found much lower than the hcp bulk value.


NANO ◽  
2014 ◽  
Vol 09 (04) ◽  
pp. 1450042 ◽  
Author(s):  
CONG-WANG ZHANG ◽  
CHANG-CHUN ZENG ◽  
YING XU

Fe 3 O 4– SiO 2 core–shell structure nanoparticles containing magnetic properties were investigated for their potential use in drug delivery. The Fe 3 O 4– SiO 2 core–shell structure nanoparticles were successfully synthesized by a simple and convenient way. The Fe 3 O 4– SiO 2 nanoparticles showed superparamagnetic behavior, indicating a great application potential in separation technologies. From the application point of view, the prepared nanoparticles were found to act as an efficient drug carrier. Specifically, the surface of the core–shell nanoparticles was modified with amino groups by use of silane coupling agent 3-aminopropyltriethoxysilane (APTS). Doxorubicin (DOX) was successfully grafted to the surface of the core–shell nanoparticles after the decoration with the carboxyl acid groups on the surface of amino-modified core–shell structure nanoparticles. Moreover, the nanocomposite showed a good drug delivery performance in the DOX-loading efficiency and drug release experiments, confirming that the materials had a great application potential in drug delivery. It is envisioned that the prepared materials are the ideal agent for application in medical diagnosis and therapy.


2003 ◽  
Vol 774 ◽  
Author(s):  
Jiye Fang ◽  
Jibao He ◽  
Eun Young Shin ◽  
Deborah Grimm ◽  
Charles J. O'Connor ◽  
...  

Abstractγ-Fe2O3@Au core-shell nanoparticles were prepared through a combined route, in which high temperature organic solution synthesis and colloidal microemulsion techniques were successively applied. High magnification of TEM reveals the core-shell structure. The presence of Au on the surface of as-prepared particles is also confirmed by UV-Vis absorption. The magnetic core-shell nanoparticles offer a promising application in bio- and medical systems.


2007 ◽  
Vol 7 (12) ◽  
pp. 4311-4317 ◽  
Author(s):  
Koushik Dhara ◽  
Krishanu Sarkar ◽  
Partha Roy ◽  
Asim Bhaumik ◽  
Pradyot Banerjee

By one-step mixed-solvent mediated approach, we have prepared fluorescent organic core–shell nanoparticles with an oligomer (1) derived from the Schiff base condensation reaction of 2,6-diformyl-4-methylphenol and o-phenylenediamine at room temperature. The core and shell structures are generated by the same oligomer (1) featuring the aggregation structure in core different from that in shell. The radial packing factor distribution of oligomer cluster depending on the solvent interaction in the time of nucleation is mainly responsible for the single component core–shell formation. Different morphologies of the core–shell nanospheres (CSNS) and core–shell nanohemispheres (CSNHS) were generated simply by changing the concentration of 1 in chloroform-methanol mixed solvent (1:2). We observed that fluorescent emission from those core–shell nanoparticles is intense whereas as-synthesized oligomer (1) itself is non-fluorescent in dilute solution. The enhanced emission in the core–shell form with more than 50 times increase in fluorescent quantum yield vis-à-vis 1 is a remarkable feature of the study. As UV absorption spectra of nanoparticles are blue-shifted relative to their properties in solution, the observed strong emission in the solid state makes the oligomer an outstanding exception to a well-established rule based on the molecular exciton model. The core–shell nanoparticles have been characterized by FE-SEM, TEM, XRD, nanosecond (ns) time-resolved fluorescence dynamics, UV-Vis and fluorescence spectroscopy. The longer fluorescence lifetimes (τ) of core–shell nanoparticles (3.50 ns and 3.52 ns for CSNS and CSNHS respectively) than 1 as-synthesized (1.28 ns) implies that the formation of the nanoparticles restricts the rotation and vibration of the groups in the molecules. The factor that induces fluorescent enhancement of nanoparticles is mainly ascribed to the increase of radiative rate constant (kr) and simultaneous decrease of nonradiative rate constant (knr).


2017 ◽  
Vol 899 ◽  
pp. 221-226 ◽  
Author(s):  
M.M. Lima ◽  
J.P.Z. Gonçalves ◽  
C. Soares ◽  
Humberto Gracher Riella ◽  
S.C. Fernandes ◽  
...  

Core–shell Fe2O3@C nanoparticles are very studied due to its biocompatibility with plant and animals cells and due its special properties of chemical adsorption. Thus, the definition of an easy synthesis method of these nanoparticles is very important to the scientific studies and to future applications of these materials. For example, the properties of these nanoparticles depend of the combination between some processing parameters, as the temperature, time, chemical composition, atmosphere and others. The mass yield of the synthesis processes depend of these parameters and are important information. In this work the effect of temperature and of the concentration of the iron precursor were evaluated on the characteristics of the proposed nanoparticles. The nanostructures of Fe2O3 coated with carbon (Fe2O3@C) were synthetized by adapted co-precipitation hydrothermal rote. In 40.0 ml of distilled water was added 1.800 g of glucose, 6.006 g of urea, 0.500 g of polyethylene Glycol (PEG 1500) and different concentrations of iron nitrate Fe (NO2)3.9H2O and different temperature values were applied. The Fe2O3@C core-shell were characterized by scanning electron microscopy (SEM/FEG), Energy Dispersive Scanning (EDS) and X-ray Diffractions (XRD). Results showed that nanoparticles form clusters with different sizes that are dependent on the temperature values and Fe (NO3)3.9H2O concentration. The core-shell mass has a linear relation with the iron precursor mass and the reaction temperatures influences the microstructure of the core-shell nanoparticles.


2021 ◽  
Vol 8 (3) ◽  
Author(s):  
Sungho Lee ◽  
Tatsuya Miyajima ◽  
Ayae Sugawara-Narutaki ◽  
Katsuya Kato ◽  
Fukue Nagata

Biodegradable nanoparticles have been well studied as biocompatible delivery systems. Nanoparticles of less than 200 nm in size can facilitate the passive targeting of drugs to tumour tissues and their accumulation therein via the enhanced permeability and retention (EPR) effect. Recent studies have focused on stimuli-responsive drug delivery systems (DDS) for improving the effectiveness of chemotherapy; for example, pH-sensitive DDS depend on the weakly acidic and neutral extracellular pH of tumour and normal tissues, respectively. In our previous work, core–shell nanoparticles composed of the biodegradable polymer poly(lactic acid) (PLA) and the widely used inorganic biomaterial hydroxyapatite (HAp, which exhibits pH sensitivity) were prepared using a surfactant-free method. These PLA/HAp core–shell nanoparticles could load 750 wt% of a hydrophobic model drug. In this work, the properties of the PLA/HAp core–shell nanoparticles loaded with the anti-cancer drug paclitaxel (PTX) were thoroughly investigated in vitro . Because the PTX-containing nanoparticles were approximately 80 nm in size, they can be expected to facilitate efficient drug delivery via the EPR effect. The core–shell nanoparticles were cytotoxic towards cancer cells (4T1). This was due to the pH sensitivity of the HAp shell, which is stable in neutral conditions and dissolves in acidic conditions. The cytotoxic activity of the PTX-loaded nanoparticles was sustained for up to 48 h, which was suitable for tumour growth inhibition. These results suggest that the core–shell nanoparticles can be suitable drug carriers for various water-insoluble drugs.


2008 ◽  
Vol 8 (6) ◽  
pp. 2761-2780 ◽  
Author(s):  
Òscar Iglesias ◽  
Amílcar Labarta ◽  
Xavier Batlle

Some of the main experimental observations related to the occurrence of exchange bias in magnetic systems are reviewed, focusing the attention on the peculiar phenomenology associated to nanoparticles with core/shell structure as compared to thin film bilayers. The main open questions posed by the experimental observations are presented and contrasted to existing theories and models for exchange bias formulated up to date. We also present results of simulations based on a simple model of a core/shell nanoparticle in which the values of microscopic parameters such as anisotropy and exchange constants can be tuned in the core, shell and at the interfacial regions, offering new insight on the microscopic origin of the experimental phenomenology. Adetailed study of the magnetic order of the interfacial spins shows compelling evidence that most of the experimentally observed effects can be qualitatively accounted within the context of this model and allows also to quantify the magnitude of the loop shifts in striking agreement with the macroscopic observed values.


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