ELECTROCHEMICAL SYNTHESIS OF DISPERSED BARIUM FERRITE USING ANODIC DISSOLUTION OF METAL

The process of anodic dissolution of iron (purity not less than 99%) in aqueous solutions of barium chloride, barium nitrate and binary electrolytes under galvanostatic conditions and by registration of potentiodynamic polarization curves was investigated. The influence of solution composition and concentration and the value of applied direct current on the intensity of anodic oxidation of iron was shown. It was revealed that the oxidation rate of metal in binary electrolytes containing barium chloride and barium nitrate is comparable with the intensity of anodic dissolution in a solution based on barium chloride. It was found that anodic polarization curve in solutions containing BaCl2 and Ba(NO3)2 has a complex form typical of passivated metals. There is a clear maximum of anodic oxidation current on this curve, as well as in barium nitrate solution, however the peak height is much higher (50-150 times). A method for the synthesis of dispersed barium ferrite, based on the anodic oxidation of iron in aqueous barium chloride and barium nitrate solutions with subsequent thermal treatment of the product of electrochemical dissolution was suggested. The phase and elemental composition and structural characteristics of obtained precursor and ferrite samples were examined using X-ray phase analysis. The influence of the heat treatment mode on the phase composition of the synthesized samples is shown. It is found that electrolysis with a soluble iron electrode using direct anode current in 0.05M BaCl2 + 0.5M Ba(NO3)2 solution and subsequent thermal treatment of the dissolution product at 1200 ° C provide the formation of dispersed system, whose phase composition is predominantly Ba0.87Fe11.08O17.15 (74%) and BaFe2O4 (17%).

Mechanical properties and water resistance of Vietnamese acacia and rubberwood after thermo-hygro-mechanical modification

Low density and poor mechanical performance often limit utilisation of sawn wood from fast-growing plantation forests. Thermo-hygro-mechanical modification (THM) of timber is one innovation for improving the properties of light-weight wood species. The objective of this study was to determine the effects of THM and subsequent thermal treatment on dry density, modulus of elasticity (MOE), compression strength, Brinell hardness, and swelling behaviour in immersion tests on two fast-growing Vietnamese species, acacia (Acacia mangium) and rubberwood (Hevea brasiliensis). Test boards were modified in an industrial kiln, in which a tangential thickness compression of 14% and 12% were aimed for acacia and rubberwood, respectively, either with or without subsequent thermal treatment at 210 °C. Dry density, MOE, Brinell hardness, compression strength, and dimensional changes in water immersion tests of specimens were measured from the modified and unmodified reference materials, the latter ones being kiln dried at 50 °C. The results showed that the responses of the mechanical properties were more evident for rubberwood than for acacia. In rubberwood, the MOE and compression strength of wood thermo-hygro-mechanically modified with or without thermal treatment were higher than those of kiln-dried reference specimens throughout the thickness profile. In case of acacia, similar differences between the modified and reference specimens were observed only in the surface layer. Density and Brinell hardness of thermo-hygro-mechanically modified rubberwood were higher than those of reference specimens, but after thermal treatment they did not differ from (acacia) or were lower (rubberwood) than those of THM specimens. Post-compression thermal treatment increased the hydrophobicity of THM specimens.

Modification of Lattice Structures and Mechanical Properties of Metallic Materials by Energetic Ion Irradiation and Subsequent Thermal Treatments

When materials are irradiated with high-energy ions, their energies are transferred to electrons and atoms in materials, and the lattice structures of the materials are largely changed to metastable or non-thermal equilibrium states, causing the modification of several physical properties. There are two processes for the material modification by ion irradiation; one is “the irradiation-enhanced process”, and the other is “the irradiation-induced process”. In this review, two kinds of recent results for the microstructural changes and the modifications of mechanical properties will be summarized: one is the hardness modification of dilute aluminum alloys, which is a result of the irradiation-enhanced process, and the other is the hardness modification of Ni-based intermetallic compounds as a result of the irradiation-induced process. The effect of the subsequent thermal treatment on the microstructures and the hardness for ion-irradiated dilute aluminum alloys is quite different from that for Ni-based intermetallic compounds. This result reflects the difference between the irradiation-enhanced process and the irradiation-induced process. Finally, possibilities of the ion irradiation and subsequent thermal treatment to industrial applications will also be discussed.

Thermal stability and miscibility of co-evaporated methyl ammonium lead halide (MAPbX3, X = I, Br, Cl) thin films analysed by in situ X-ray diffraction

We present the identification of crystalline phases by in situ X-ray diffraction during growth and monitor the phase evolution during subsequent thermal treatment of CH3NH3PbX3 (X = I, Br, Cl) perovskite thin films.

Direct synthesis of poly(benzoxazine imide) from an ortho-benzoxazine: its thermal conversion to highly cross-linked polybenzoxazole and blending with poly(4-vinylphenol)

A facile one-pot synthesis of a poly(benzoxazine imide), NDOPoda Bz, was prepared without the need for either the preparation of an amino-functionalized benzoxazine or subsequent thermal treatment.

Tailored fabrication of TiO2@carbon nanofibers composites via foaming agent migration

Based on the merits and demerits of conventional methods for fabricating TiO2@carbon nanofibers (TiO2@CNFs) composites, the composites were prepared via a foaming-assisted electrospinning strategy and subsequent thermal treatment.

Characterisation of Mn0.63Zn0.37Fe2O4 powders after intensive milling and subsequent thermal treatment

Commercial Mn-Zn powder (Mn0.63Zn0.37Fe2O4, 93 wt. % and Fe2O3 7 wt. %) was milled 0.5, 1, 2 and 4 hours in a planetary ball mill. The goal was to observe intensive milling influences on oxidation and reduction processes that will happen during subsequent heating. Powders were characterized with XRD, SEM and particle seizer. Subsequent heating was monitored on TGA/DTA in an air atmosphere. After compaction of the milled powders, sintering was also performed in a dilatometric device. Sintered specimens were characterized micro structurally with SEM on a fresh breakage. Obtained differential TGA diagrams suggest intensive changes during prolonged milling of the oxidation kinetics on heating. Ferrite powders changed with milling as well as with second run heating were characterized to enable determination of the potentially best ratio of milling and heating to be applied to obtain the desired microstructure.

Cobalt nanoparticles embedded in a porous carbon matrix as an efficient catalyst for ammonia decomposition

A metallic Co nanoparticle catalyst embedded in a carbon matrix catalyst was synthesized through a facile solvothermal method and subsequent thermal treatment.