Influence of spinodal decomposition on magnetic properties of Fe28Cr16Co

1996 ◽  
Vol 152 (1-2) ◽  
pp. 213-218 ◽  
Author(s):  
F. Vodopivec ◽  
B. Breskvar
2020 ◽  
pp. 2007668
Author(s):  
Ziyuan Rao ◽  
Biswanath Dutta ◽  
Fritz Körmann ◽  
Wenjun Lu ◽  
Xuyang Zhou ◽  
...  

2019 ◽  
Vol 806 ◽  
pp. 1188-1199 ◽  
Author(s):  
Xu-Hao Han ◽  
Ji-Bing Sun ◽  
Hong-Wei Wang ◽  
Zhi-Xin Dong ◽  
Ying Zhang ◽  
...  

1983 ◽  
Vol 54 (8) ◽  
pp. 4502-4511 ◽  
Author(s):  
Tsung‐Shune Chin ◽  
Tien‐Shou Wu ◽  
C. Y. Chang

2015 ◽  
Vol 152 ◽  
pp. 68-71 ◽  
Author(s):  
V.P. Menushenkov ◽  
M.V. Gorshenkov ◽  
D.G. Zhukov ◽  
E.S. Savchenko ◽  
M.V. Zheleznyi

2012 ◽  
Vol 510-511 ◽  
pp. 315-320 ◽  
Author(s):  
S. Akbar ◽  
Z. Ahmad ◽  
M.S. Awan ◽  
M.N. Sarwar ◽  
M. Farooque

This study is focused on the development of isotropic Fe-Cr-Co based permanent magnets. Two compositions Fe-25Co-30Cr-3.5Mo-0.8Ti-0.8 and Fe-24 Co-32Cr-0.5Si-0.8V-0.8Ti were tried to optimize by adjusting heat treatment cycle. A modified single step heat treatment cycle was established which made processing easy and quick. Alloys were prepared in tri-arc melting furnace under inert atmosphere of Argon. Samples were solution treated at 1250 °C for 5 hours followed by water quenching. Then a spinodal decomposition heat treatment cycle in the temperature range 620 645 °C was applied in order to produce magnetism in this material. Samples were characterized for metallographic, chemical, structural and magnetic properties using Optical microscope, Scanning electron microscope equipped with Energy dispersive spectrometer, X-ray diffractometer and DC magnetometer. This study reveals that magnetic properties are sensitive to the spinodal decomposition temperature. Only + 5 °C change in temperature from optimum temperature can cause remarkable attenuation in magnetic properties. Magnetic properties of the alloys were achieved by controlling the spinodal decomposition temperature and subsequent cooling rate. The best magnetic properties in Mo and V containing alloys were obtained as 880 Oe (Hc), 7960 G (Br), 2.3 MGOe (BHmax) and 700 Oe (Hc), 7750 G (Br), 1.8 MGOe (BHmax), respectively.


Author(s):  
A.R. Pelton ◽  
A.F. Marshall ◽  
Y.S. Lee

Amorphous materials are of current interest due to their desirable mechanical, electrical and magnetic properties. Furthermore, crystallizing amorphous alloys provides an avenue for discerning sequential and competitive phases thus allowing access to otherwise inaccessible crystalline structures. Previous studies have shown the benefits of using AEM to determine crystal structures and compositions of partially crystallized alloys. The present paper will discuss the AEM characterization of crystallized Cu-Ti and Ni-Ti amorphous films.Cu60Ti40: The amorphous alloy Cu60Ti40, when continuously heated, forms a simple intermediate, macrocrystalline phase which then transforms to the ordered, equilibrium Cu3Ti2 phase. However, contrary to what one would expect from kinetic considerations, isothermal annealing below the isochronal crystallization temperature results in direct nucleation and growth of Cu3Ti2 from the amorphous matrix.


Author(s):  
June D. Kim

Iron-base alloys containing 8-11 wt.% Si, 4-8 wt.% Al, known as “Sendust” alloys, show excellent soft magnetic properties. These magnetic properties are strongly dependent on heat treatment conditions, especially on the quenching temperature following annealing. But little has been known about the microstructure and the Fe-Si-Al ternary phase diagram has not been established. In the present investigation, transmission electron microscopy (TEM) has been used to study the microstructure in a Sendust alloy as a function of temperature.An Fe-9.34 wt.% Si-5.34 wt.% Al (approximately Fe3Si0.6Al0.4) alloy was prepared by vacuum induction melting, and homogenized at 1,200°C for 5 hrs. Specimens were heat-treated in a vertical tube furnace in air, and the temperature was controlled to an accuracy of ±2°C. Thin foils for TEM observation were prepared by jet polishing using a mixture of perchloric acid 15% and acetic acid 85% at 10V and ∼13°C. Electron microscopy was performed using a Philips EM 301 microscope.


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