17 research outputs found
Electromagnetic modelling of curved structures using a hybrid finite-volume finite-difference time-domain method
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN012962 / BLDSC - British Library Document Supply CentreGBUnited Kingdo
Preparation of Nickel Ferrite from thermolysis of Nickel Hexa(Formato)-Ferrate(III)Hexahydrate
Thermal decomposition of nickel hexa(formato) ferrate(III) decahydrate i.e. Ni3[Fe(HCOO)6]2.10H2O has been studied upto
973 K in static air atmosphere employing TG,DTG,DTA,DSC,XRD,ESR, Mössbauer and infrared spectroscopic techniques. Dehydration
occurs in two stages in the temperature range of 348-423 K. Immediately after the removal of the last water molecule, the anhydrous
complex undergoes decomposition till α-Fe2O3 and nickel carbonate are formed at 588 K. In the final stage of remixing of cations, a solid
state reaction between α-Fe2O3, and nickel carbonate leads to the formation of NiFe2O4, at a temperature (873 K) much lower than for
ceramic method. A high value of saturation magnetization i.e. 4440 gauss of the ferrite (NiFe2O4) shows its potential to function at high
frequencies
Mössbauer effect studies of alkali bis(citrato)ferrates(III)
Mössbauer spectra of alkali bis(citrato)ferrates(III) i.e. M3Fe(C 6H5O7)2. x H2O (M = Li, Na, Rb, Cs, NH4) at room temperature display a doublet, the isomer shift and quadrupole splitting values indicating these complexes to be high spin with octahedral symmetry. However, in case of K3Fe(C 6H5O7)2.4H2O a single broad absorption band has been observed. The isomer shift shows a decreasing trend with the increase in the electronegativity of the substituent cation. Isomer shift also increases with the increase in cationic size (Li+, Na+, K+, Rb+, Cs+, Na+4). A linear correlation between isomer shift and the separation C=O stretching frequencies (Δν) has also been observed.Les spectres Mössbauer de bis(citrato)ferrates alcalins, c'est-à-dire M 3Fe(C6H5O7)2. x H2 O (M = Li, Na, Rb, Cs, NH4) montrent un doublet à temperature ambiante ; le déplacement isomérique et la séparation quadrupolaire indiquent que ces complexes sont de spin élevé et de symétrie octaédrique. Dans le cas de K3Fe(C 6H5O7)2. 4 H2O nous observons cependant une seule ligne élargie. Le déplacement isomérique décroît quand l'électronégativité du cation en substitution croit ; il croit avec la taille du cation (Li+, Na+, K+, Rb+, Cs+, NH+4). Une corrélation linéaire entre le déplacement isomérique et l'intervalle (Δν) en modes de vibration C=O a également été observée
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