Issues

 / 

2019

 / 

vol. 17 / 

Issue 3

 



Download the full version of the article (in PDF format)

B. K. Ostafiychuk, V. S. Bushkova, N. I. Riznychuk, R. S. Solovei, I. P. Yaremiy
«Nickel–Yttrium Ferrite Nanopowders for Solving Environmental Problems»
425–438 (2019)

PACS numbers: 68.37.Hk, 68.43.Mn, 68.43.Nr, 75.50.Tt, 78.67.Rb, 81.07.Wx, 81.16.Be

Among the family of spinel ferrites, nickel ferrite NiFe2O4 obtained by ceramic technology was widely studied due to its tremendous properties such as high electromagnetic performance, excellent chemical stability and mechanical hardness, and moderate saturation magnetization, making it as a good contender for the application as soft magnets and low-loss materials at high frequencies. The structure, mechanical, magnetic, electrical, and dielectric properties of nickel ferrite are dependent on several factors including the method of fabrication, sintering time and temperature, chemical composition, type and amount of dopant, grain structure. The sol–gel processing with autocombustion (SGA) technique was used for the synthesis of NiYxFe2?xO4 (x???0.0, 0.1, 0.2, 0.3, 0.4, 0.5) ferrite nanoparticles. The mixed solution was dried at temperature around 403 K. During evaporation, the solution becomes viscous and finally formed as a xerogel. At further elevation of temperature, the organic constituents are decomposed with the generation of gases such as CO2, N2 and H2O; therefore, the xerogel automatically ignited. The autocombustion was completed within a few seconds, yielding the nanopowders of nickel–yttrium ferrites. The XRD results confirm single-phase formation of the as-prepared NiFe2O4 sample. The powders substituted with Y3? ions, except the spinel-type phase, contain additional ?-Fe2O3 and Y2O3 phases too. The powder sizes decrease from 43 nm to 17 nm with increase in amount of Y3? ions. The EDX results confirm the presence of Ni, Fe, Y, and O elements in Ni–Y-ferrite powders. The infrared (IR) spectra were recorded at the room temperature in the range from 400 cm?1 to 4000 cm?1; they confirm the spinel structure. As found, the adsorption capacity of Ni–Y ferrite increases, while the substitutions with Y3+ ions increase. The adsorption process increases with increasing pH, has a maximum at pH???7, and depends on the dye type.

Keywords: ferrite, nanopowder, EDX analysis, IR spectroscopy, adsorption capacity

https://doi.org/10.15407/nnn.17.03.425

References
1. G. Kochetov, D. Zorya, and J. Grinenko, Civil and Environmental Engineering, 1, No. 4: 301 (2010). https://doi.org/10.15587/2312-8372.2018.152615
2. B. J. Kahdum, A. J. Lafta, and A. M. Johdh, Polish Journal of Chemical Technology, 19, No. 3: 61 (2017). https://doi.org/10.1515/pjct-2017-0050
3. K. H. Gonawala and M. J. Mehta, Int. Journal of Engineering Research and Applications, 4, No. 5: 102 (2014).
4. V. S. Bushkova and I. P. Yaremiy, J. Magn. Magn. Mater., 461: 37 (2018). https://doi.org/10.1016/j.jmmm.2018.04.025
5. E. J. Mohammad, S. H. Kathim, and A. J. Lafta, Int. J. Chem. Sci., 14, No. 2: 993 (2016).
6. V. S. Bushkova, J. Nano- and Electron. Phys., 7: 03021 (2015).
7. A. Rais, A. Addou, M. Ameri, N. Bouhadouza, and A. Merine, Appl. Phys. A, 111: 665 (2013). https://doi.org/10.1007/s00339-012-7304-9
8. V. S. Bushkova, Low Temperature Phys., 43: 1724 (2017). https://doi.org/10.1063/1.5012788
9. M. Patange, S. E. Shirsath, S. S. Jadhav, K. S. Lohar, D. R. Mane, K. M. Jadhav, Mater. Lett., 64: 722 (2010). https://doi.org/10.1016/j.matlet.2009.12.049
10. O. P. Perez, H. Sasaki, A. Kasuya, B. Jeyadevan, K. Tohji, T. Hihara, K. Sumiyama, J. Appl. Phys., 91: 6958 (2002). https://doi.org/10.1063/1.1452193
11. K. K. Bharathi, G. Markandeyulu, and J. A. Chelvane, J. Magn. Magn. Mater., 321: 3677 (2009). https://doi.org/10.1016/j.jmmm.2009.07.011
12. M. Jacintha, P. Neeraja, M. Sivakumar, and K. Chinnaraj, J. Supercond. Nov. Magn., 30: 237 (2017). https://doi.org/10.1007/s40097-017-0248-z
13. V. S. Bushkova and B. K. Ostafiychuk, Powder Metall. and Metal Ceram., 54: 509 (2016). https://doi.org/10.1007/s11106-016-9743-x
14. A. Shaikh, S. Jadhav, S. Watawe, and B. Chongnle, Mat. Sci. Lett., 44: 192 (2000). https://doi.org/10.1016/S0167-577X(00)00025-2
15. W. N. Martens, J. T. Kloprogge, R. L. Frost, and L. Rintoul, J. of Raman Spectroscopy, 35, No. 3: 208 (2004). https://doi.org/10.1002/jrs.1136
16. J. Kri an, J. Mo ina, I. Bajsi , and M. Mazaj, Acta. Chim. Slov., 59, No. 1: 163 (2012).
Creative Commons License
This article is licensed under the Creative Commons Attribution-NoDerivatives 4.0 International License
© NANOSISTEMI, NANOMATERIALI, NANOTEHNOLOGII G. V. Kurdyumov Institute for Metal Physics of the National Academy of Sciences of Ukraine, 2019
© B. K. Ostafiychuk, V. S. Bushkova, N. I. Riznychuk, R. S. Solovei, I. P. Yaremiy, 2019

E-mail: tatar@imp.kiev.ua Phones and address of the editorial office About the collection User agreement