Mechanism of a Solid-State Formation of La1-xSrxMnO3+δ (0 \u3c x \u3c 0.5) and Magnetic Characterization Thereof

Rich diversity of potential, substantially different micro-structural arrangements - reflecting on the wide potential set of interesting properties, ranging from high electrical conductivity to giant, collossal and/or low-field magnetoresistance to low Curie point - of LaSr-manganite materials opens possibilities for numerous scientific investigations oriented towards revealing correlations on the influence line: procedure of synthesis → inherent properties → measured properties → application of the material. The investigations of the influence of synthesis procedures and LaSr-manganite stoichiometries on the Curie point (and other magnetic characteristics) of the material, being the topic of this work, are attractive since they present a necessary primal step in the development of nano-magnetic drug carriers based on these materials. In the course of such an investigation, the mechanism of the formation of the desired manganite compounds by following a classical solid-state preparation method, was also studied

The Characterization of Nanosized Nickel-Zinc Ferrites Synthesized within Reverse Micelles of CTAB/1-Hexanol/Water Microemulsion

Stoichiometric nanocrystalline nickel–zinc ferrites were synthesized by a reverse micelle method following a multi-microemulsion approach. Different pH values were chosen for the alkali precipitating reaction during the synthesis of different powders. Synthesized, as-dried and subsequently calcined powders were characterized in terms of their magnetic properties. XRD analyses and specific-surface area measurements were used to determine the average particle sizes of the synthesized samples. DCS and TGA measurements were performed to reveal the phase transitions within the samples at elevated temperatures, whereas TEM was used to view and record the microstructure of the nanosized ferrite samples. A possible mechanism of the formation of the synthesized NiZn-ferrite was also discussed

Synthesis of Lanthanum-Strontium Magnanites by a Hydroxide-Precursor Co-Precipitation Method in Solution and in Reverse Micellar Microemulsion

Nanostructured lanthanum-strontium manganites have been synthesized using two different co-precipitation approaches, one in bulk solution, and the other in reverse micelles of CTAB/1-hexanol/1-butanol/water microemulsion. In both cases, precursor cations were precipitated by alkali precipitating agents. The properties of the material synthesized by using these two methods were compared in order to reveal potential advantages of microemulsion-assisted approach. The influence of the annealing conditions on the properties of synthesized manganites was investigated by using X-ray diffraction, transmission electron microscopy, differential thermal analysis, thermogravimetric analysis and magnetic measurements

Preparation of Silica-Coated Lanthanum-Strontium Manganite Particles with Designable Curie Point, for Application in Hyperthermia Treatments

Silica-coated lanthanum–strontium manganite particles with La0.76Sr0.24MnO3+δ stoichiometric formula, exhibiting Curie temperature at ∼40°C, were prepared by using a traditional solid-state method of synthesis of magnetic ceramic particles, followed by milling and a low-temperature coating procedure in an aqueous alcoholic alkali medium. The properties of the obtained material establish it as a potential candidate for self-regulated power-absorbing and temperature-controlling materials in hyperthermia treatments. Moreover, core-comprising LaSr–manganites with different stoichiometries, ranging from La0.5Sr0.5MnO3+δ to LaMnO3+δ, were synthesized, with magnetic and structural properties examined thereof. Herein reported findings can potentially be used in the preparation of silica-coated magnetic particles with designable Curie temperature, offering a wide range of possibilities of adapting the material to practical instrumental setups in drug delivery and hyperthermia treatments

Synthesis of Poly-Sodium-Acrylate (PSA)-Coated Magnetic Nanoparticles for Use in Forward Osmosis Draw Solutions

The synthesis of magnetic nanoparticles (MNPs) coated with hydrophilic poly-sodium-acrylate (PSA) ligands was studied to assess PSA-MNP complexes as draw solution (DS) solutes in forward osmosis (FO). For MNP-based DS, the surface modification and the size of the MNPs are two crucial factors to achieve a high osmolality. Superparamagnetic nanoparticles (NP) with functional groups attached may represent the ideal DS where chemical modifications of the NPs can be used in optimizing the DS osmolality and the magnetic properties allows for efficient recovery (DS re-concentration) using an external magnetic field. In this study MNPs with diameters of 4 nm have been prepared by controlled chemical co-precipitation of magnetite phase from aqueous solutions containing suitable salts of Fe2+ and Fe3+ under inert atmosphere and a pure magnetite phase could be verified by X-ray diffraction. Magnetic colloid suspensions containing PSA-coated MNPs with three different molar ratios of PSA:MNP = 1:1, 1:2 and 1:3 were prepared and assessed in terms of osmotic pressure, aggregation propensity and magnetization. Fourier Transform Infrared Spectroscopy (FTIR) confirmed the presence of PSA on coated MNPs and pristine PSA-MNPs with a molar ratio PSA:MNP = 1:1 exhibited an osmotic pressure of 30 bar. Molar ratios of PSA:MNP = 1:2 and 1:3 lead to the formation of less stabile magnetic colloid solutions, which led to the formation of aggregates with larger average hydrodynamic sizes and modest osmotic pressures (5.5 bar and 0.2 bar, respectively). After purification with ultrafiltration, the 1:1 nanoparticles exhibited an osmotic pressure of 9 bar with no aggregation and a sufficient magnetization of 25 emu/g to allow for DS regeneration using an external magnetic field. However, it was observed that the amount of PSA molecules attached to the MNPs decreased during DS recycling steps, leaving only strong chelate-bonded core-shell PSA as coating on the MNPs. This demonstrates the crucial role of MNP coating robustness in designing an efficient MNP-based DS for FO

Synthesis of Lanthanum-Strontium Manganites by Oxalate-Precursor Co-Precipitation Methods in Solution and in Reverse Micellar Microemulsion

Nanostructured lanthanum–strontium manganites were synthesized using two different co-precipitation approaches, one in bulk solution, and the other in reverse micelles of CTAB/1-hexanol/water microemulsion. In both cases, precursor cations were precipitated by using oxalic acid. The properties of the materials synthesized by using these two methods were compared in order to reveal potential advantages of the microemulsion-assisted approach. The influence of the annealing conditions on the properties of synthesized manganites was investigated by using X-ray diffraction, transmission electron microscopy, differential thermal analysis, thermogravimetric analysis and magnetic measurements

Four Novel Co-Precipitation Procedures for the Synthesis of Lanthanum-Strontium Manganites

Lanthanum-strontium manganites were synthesized using co-precipitation method with a reverse micellar microemulsion. Either oxalic acid, sodium hydroxide or tetramethylammonium hydroxide was used for the precipitation of precursor cations in a form that was subsequently calcined under various conditions in order to obtain perovskite manganite phase. Correlations between the properties of the synthesized powder and the calcination conditions have been put forth. The properties of the microemulsion-assisted synthesized material were compared with the samples prepared by following the supposedly similar chemical recombinations in bulk solutions, with an aim to challenge the fact that microemulsions in general have only templating effects on the morphology of co-precipitated powder. TEM measurements, X-ray diffraction analyses and magnetic measurements were used in order to gain an insight into the mentioned difference, which is an important one for the future understanding of the role that reverse micelles play in the processes of materials synthesis

A Mechanism for the Formation of Nanostructured NiZn Ferrites via a Microemulsion-Assisted Precipitation Method

Nanostructured NiZn ferrites were synthesized using two different techniques: first, a precipitation procedure in the reverse micelles of a CTAB/1-hexanol/H2O microemulsion, and second, precipitation in a bulk aqueous solution. XRD measurements, magnetic measurements, TEM imaging, analytical measurements and thermal analyses were used in an attempt to reveal the chemical pathway that leads to the formation of NiZn ferrite in the microemulsion and in the bulk aqueous solution. It was found that reverse micelles do not act as inert nano-sized reactors that influence only morphological properties of the synthesized powders, but have a decisive influence on the identity of the final product when compared to the non-microemulsion procedure, and therefore present the molecular structures which are actively engaged in the chemical pathway according to which the herein presented room temperature synthesis of NiZn ferrite nanoparticles takes place. The influence of the initial pH on the chemical pathway of reverse-micellar synthesis and the morphology of the synthesized particles was discussed after initially it was found that the pH of the precipitation ought to be higher than 8 in order to obtain the desired ferrite as a final product

Synthesis of Nanocrystalline Nickel-Zinc Ferrites within Reverse Micelles

Nanocrystalline nickel-zinc ferrites were synthesized via a reverse micelle microemulsion route. The precursor cations were precipitated in the microemulsion system CTAB/1-hexanol/water. A subsequent oxidizing reaction was used to synthesize the nickel-zinc ferrite. The obtained nanoparticles were less than 20 nm in size

Synthesis of Relatively Highly Magnetic Nano-Sized NiZn-Ferrite in Microemulsion at 45 oC

The procedure for the preparation of NiZn-ferrite powder with average particle size of 10 nm and saturation magnetization of 50 emu/g by using precipitation reaction between acidified sulphate precursor salts and NH4OH as the precipitating agent in the water-in-oil domain of the microemulsion CTAB/1-hexanol/water at 45 oC is presented herein. TEM measurements have revealed relatively uniform morphology of the particles, which are associated in coral-like agglomerates. EDS measurements have been used for qualitative analysis of the sample, whereby FAAS measurement has been performed in order to reveal the proportion of the cations in the sample - Ni : Zn : Fe = 0.17 : 0.18 : 2.64