Crystal structure and magnetic properties of perovskite YFe1-xMnxO3 nanopowders synthesized BY CO-PRECIPITATION method

2019 ◽  
Vol 96 ◽  
pp. 105922 ◽  
Author(s):  
A.T. Nguyen ◽  
Vinh N.T. Pham ◽  
T. Tr L. Nguyen ◽  
V.O. Mittova ◽  
Q.M. Vo ◽  
...  
2019 ◽  
Vol 546 (1) ◽  
pp. 48-56
Author(s):  
Ze Wu ◽  
Yang Song ◽  
Ruonan Zhang ◽  
Lianwei Shan ◽  
Limin Dong ◽  
...  

2019 ◽  
Vol 45 (17) ◽  
pp. 21768-21772 ◽  
Author(s):  
Tien A. Nguyen ◽  
Vinh N.T. Pham ◽  
Hanh T. Le ◽  
Diem H. Chau ◽  
V.O. Mittova ◽  
...  

2015 ◽  
Vol 1112 ◽  
pp. 19-22
Author(s):  
Umi Nuraini ◽  
Lita Amalia ◽  
Kurniawati C. Rosyidah ◽  
M. Zainuri

Synthesis of Zn doped Barium M-Hexaferrite (BaFe12-xZnxO19) has been performed by co-precipitation method. The purified iron sand from Tulungagung is used as a precursor of Fe3O4. Synthesis of Zn doped Barium M-Hexaferrite (BaFe12-xZnxO19) with variations of x = 0.3, 0.5, and 0.7 wt % has been calcined at temperatures of 1000°C for 5 hours. Ion Zn2+ (with 0 ≤ x ≤ 0.7 wt %) does not change the crystal structure of Barium M-Hexaferrite (BaM), but give a slight displacement of the peak position of the diffraction pattern. SEM figures showed that Zn doped Barium M-Hexaferrite (BaFe12-xZnxO19) have a hexagonal structure, similar to BaM structure. Doping of Zn has changed the magnetic properties of Barium M-Hexaferrit (BaM), from hard magnetic become soft magnetic. Barium M-Hexaferrit (BaM) has a value of Coercivity Field (Hc) and Remanence Magnetization (Mr) is 0.03734 T and 8.334 emu/g. At variation x = 0.3, the Remanence Magnetization (Mr) reaches the highest value. At this point, a value of Coercivity Field (Hc) and Remanence Magnetization (Mr) is 0.0506 T and 14.782 emu/gram respectively.


2021 ◽  
Vol 3 (1) ◽  
pp. 21-28
Author(s):  
Nining S Asri

The synthesis of soft magnetic NixZn1-xFe2O4 with variations in composition (x = 0,2 – 0,8) by the co-precipitation method has been carried out. The research objective was to determine the effect of x variation on the crystal structure, microstructure, magnetic properties, and density. The samples were characterized by their crystal structure using XRD, microstructure using FE-SEM, magnetic properties using VSM, and physical properties (True Density). The XRD analysis results obtained two phases, the major phase is nickel-zinc ferrite, and Fe2O3 shows as the minor phase. The crystal size increased and the lattice parameters decreased with the increase in nickel content. The results of FE-SEM analysis at x = 0.2 are spherical in shape with an average particle size found about 47.07 nm. The results of VSM analysis showed that the increase in nickel content, the higher the magnetization saturation value, and the super-paramagnetic properties of all samples obtained. The results of the analysis of physical properties show that true density decreases with an increase of nickel content in each sample.


Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 341
Author(s):  
Tien Hiep Nguyen ◽  
Gopalu Karunakaran ◽  
Yu.V. Konyukhov ◽  
Nguyen Van Minh ◽  
D.Yu. Karpenkov ◽  
...  

This paper presents the synthesis of Fe–Co–Ni nanocomposites by chemical precipitation, followed by a reduction process. It was found that the influence of the chemical composition and reduction temperature greatly alters the phase formation, its structures, particle size distribution, and magnetic properties of Fe–Co–Ni nanocomposites. The initial hydroxides of Fe–Co–Ni combinations were prepared by the co-precipitation method from nitrate precursors and precipitated using alkali. The reduction process was carried out by hydrogen in the temperature range of 300–500 °C under isothermal conditions. The nanocomposites had metallic and intermetallic phases with different lattice parameter values due to the increase in Fe content. In this paper, we showed that the values of the magnetic parameters of nanocomposites can be controlled in the ranges of MS = 7.6–192.5 Am2/kg, Mr = 0.4–39.7 Am2/kg, Mr/Ms = 0.02–0.32, and HcM = 4.72–60.68 kA/m by regulating the composition and reduction temperature of the Fe–Co–Ni composites. Due to the reduction process, drastic variations in the magnetic features result from the intermetallic and metallic face formation. The variation in magnetic characteristics is guided by the reduction degree, particle size growth, and crystallinity enhancement. Moreover, the reduction of the surface spins fraction of the nanocomposites under their growth induced an increase in the saturation magnetization. This is the first report where the influence of Fe content on the Fe–Co–Ni ternary system phase content and magnetic properties was evaluated. The Fe–Co–Ni ternary nanocomposites obtained by co-precipitation, followed by the hydrogen reduction led to the formation of better magnetic materials for various magnetically coupled device applications.


2018 ◽  
Vol 44 (17) ◽  
pp. 20782-20789 ◽  
Author(s):  
Rohit R. Powar ◽  
Varsha D. Phadtare ◽  
Vinayak G. Parale ◽  
Hyung-Ho Park ◽  
Sachin Pathak ◽  
...  

2010 ◽  
Vol 322 (21) ◽  
pp. 3470-3475 ◽  
Author(s):  
Yue Zhang ◽  
Zhi Yang ◽  
Di Yin ◽  
Yong Liu ◽  
ChunLong Fei ◽  
...  

2015 ◽  
Vol 1101 ◽  
pp. 286-289 ◽  
Author(s):  
Maya Rahmayanti ◽  
Sri Juari Santosa ◽  
Sutarno

Gallic acid-modified magnetites were synthesized by one and two-step reactions via the newly developed sonochemical co-precipitation method. The two-step reaction included the formation of magnetite powder and mixing the magnetite powder with gallic acid solution, while the one-step reaction did not go through the formation magnetite powder. The obtained gallic acid-modified magnetites were characterized by the Fourier Transform Infrared (FTIR) spectroscopy, the X-Ray Diffraction (XRD) and the Scanning Electron Microscopy (SEM). More over, the magnetic properties were studied by using a Vibrating Sample Magnetometer (VSM). The characterization results showed that there were differences in crystalinity, surface morphology and magnetic properties of products that were formed by one and two-step reactions.


Sign in / Sign up

Export Citation Format

Share Document