2017
DOI: 10.1016/j.jmmm.2016.12.135
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Characterization of SrCo 1.5 Ti 1.5 Fe 9 O 19 hexagonal ferrite synthesized by sol-gel combustion and solid state route

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Cited by 25 publications
(9 citation statements)
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“…The first weight-loss step occurred below approximately 350 • C and can be attributed to the combustion of residual organic acids and the pyrolysis of NO 3 − and organic phases to give an amorphous inorganic phase [5,32]. The second weight-loss step was due to the further transformation of amorphous inorganic phase into crystalline inorganic phase [33]. Additionally, in the DSC curves, the first weight-loss step was accompanied by a strong exothermic peak, which was centered at 262, 327, 277 and 297 • C, respectively.…”
Section: Tg-dsc Resultsmentioning
confidence: 99%
“…The first weight-loss step occurred below approximately 350 • C and can be attributed to the combustion of residual organic acids and the pyrolysis of NO 3 − and organic phases to give an amorphous inorganic phase [5,32]. The second weight-loss step was due to the further transformation of amorphous inorganic phase into crystalline inorganic phase [33]. Additionally, in the DSC curves, the first weight-loss step was accompanied by a strong exothermic peak, which was centered at 262, 327, 277 and 297 • C, respectively.…”
Section: Tg-dsc Resultsmentioning
confidence: 99%
“…The FTIR spectra show the characteristic peaks in the required region, which are 1413, 815.25, 542.71 and 432.48 cm −1 . From Figure 3a, it can be seen that the FTIR characteristics transmittance absorption peak at 1413 cm −1 was attributed to C–O stretching, CH 2 stretching, and C=O [51,52]. The absorption bands at 815.25 cm −1 and 728.12 cm −1 were assigned to the N–O bending vibration of NO 3 − , and to C–N stretching from the ammonium nitrate used in the reaction.…”
Section: Resultsmentioning
confidence: 99%
“…The absorption bands at 815.25 cm −1 and 728.12 cm −1 were assigned to the N–O bending vibration of NO 3 − , and to C–N stretching from the ammonium nitrate used in the reaction. [51,52,53].…”
Section: Resultsmentioning
confidence: 99%
“…The substitution of doping metal ions in the parent material can greatly enhance or tune the intrinsic magnetic properties of the material making them suitable for specific applications. In order to further enhance the magnetic and electric properties of M-type hexaferrites, several researches have been conducted by replacing the Fe 3+ ions by the various rare earth ions such as gadolinium (Gd) [6], neodymium (Nd) [7] as well as various divalent (Co 2+ , Mg 2+ ) and tetravalent (Ti 4+ , Sn 4+ , Zr 4+ ) cations [8]. Within the family of hexaferrites, the M-type hexaferrite has smaller Fe 3+ ions occupying the interstitial sites whereas the bigger ions Sr, Ba and oxides positioned inside the crystal lattice imparting a denser crystal structure [3].…”
Section: Introductionmentioning
confidence: 99%
“…Within the family of hexaferrites, the M-type hexaferrite has smaller Fe 3+ ions occupying the interstitial sites whereas the bigger ions Sr, Ba and oxides positioned inside the crystal lattice imparting a denser crystal structure [3]. Among the M-type hexaferrites, the strontium hexaferrites are found to have higher values of saturation magnetization (Ms = 74-92 emu/g) and large magnetocrystalline anisotropy [8]. The crystal structure of M-type hexaferrites is represented by the P63/mmc space group, 24 Fe 3+ ions occupying the five sites naming, three octahedral (12k, 4f2, and 2a), one tetrahedral (4f1) and one trigonal bipyramidal (2b) site [8].…”
Section: Introductionmentioning
confidence: 99%