Experimental investigation on ferrofluid properties of Cd doped Co-Zn ferrites

被引:0
作者
Manimegalai, R. [1 ]
Sendhilnathan, S. [2 ]
Chithambaram, V. [3 ]
Kumar, M. [4 ]
机构
[1] K Ramakrishnan Coll Engn, Dept Phys, Trichy 621112, Tamilnadu, India
[2] Univ Coll Engn, Dept Phys, Pattukkottai Campus, Rajamadam 614701, Tamilnadu, India
[3] Karpaga Vinayaga Coll Engn & Technol, Dept Phys, Chengalpattu 603308, Tamilnadu, India
[4] Kings Engn Coll, Dept Chem, Chennai, India
关键词
Cobalt ferrite; cadmium doping; Crystalline size; Williamson-Hall method; Tetrahedral; Octahedral; MAGNETIC-PROPERTIES; NANOPARTICLES; FLUID;
D O I
10.15251/DJNB.2023.182.547
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The Co-Zn ferrites Coo.SZno.SCdxFe(2_x)04 (x-0.0, 0.1, 0.2, 0.3, 0.4, and 0.5) were synthesized by CO-precipitation method. The dielectric and structural properties has been investigated by effect of Cd doping in Co-Zn spinel ferrites. Dielectric constants were studied dependence of the frequency and temperature thus revealed that the dielectric dispersion based on the Maxwell -Wagner method polarizations are agreed with Koop's conceptualization theory. Further, dielectric properties were studies over a frequency range from 10 kHZ to 30 MHZ. The dielectric constant is varied from 2.4 to 8.4 for real parts and 0.008 to 0.42 for imaginary parts, respectively. The tangent loss also recorded as 0.003 to 0.052 at 1 MHZ due to Co ions concentrations. In high and low frequencies of grain and grain boundary contribution is an important evident for obtained dielectric constant. The obtained values of coercivity (Hc) for these ferrites range between 280.4 Oe to 1380.3 Oe, based on VSM data. By converting Zn2+ and Cd2+ to cobalt magnetic ions it is possible to convert the magnetic properties of cobalt ferrite into a potential individual for numerous technical uses. The dielectric loss at room temperature and at high frequencies is found to be quite negligible. It is also discovered that when Cd is substituted, the dielectric loss tangent reduces.
引用
收藏
页码:547 / 555
页数:9
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