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Globally, there is an increasing need for ceramic materials that have a variety of applications in the environment, for precision tools, and for the biomedical, electronics, and environmental industries. However, in order to obtain remarkable mechanical qualities, ceramics have to be manufactured at a high temperature of up to 1600 °C over a long heating period. Furthermore, the conventional approach presents issues with agglomeration, irregular grain growth, and furnace pollution. Many researchers have developed an interest in using geopolymer to produce ceramic materials, focusing on improving the performances of geopolymer ceramics. In addition to helping to lower the sintering temperature, it also improves the strength and other properties of the ceramics. Geopolymer is a product of polymerization involving aluminosilicate sources such as fly ash, metakaolin, kaolin, and slag through activation using an alkaline solution. The sources of the raw materials, the ratio of the alkaline solution, the sintering time, the calcining temperature, the mixing time, and the curing time may have significant impacts on the qualities. Therefore, this review aims to study the effects of sintering mechanisms on the crystallization of geopolymer ceramics, concerning the strength achieved. A future research opportunity is also presented in this review. [ABSTRACT FROM AUTHOR]

Highly crystalline single-domain magnetite Fe 3 O 4 nanoparticles (NPs) are important, not only for fundamental understanding of magnetic behaviour, but also for their considerable potential applications in biomedicine and industry. Fe 3 O 4 NPs with sizes of 10-300 nm were systematically investigated to reveal the fundamental relationship between the crystal domain structure and the magnetic properties. The examined Fe 3 O 4 NPs were prepared under well-controlled crystal growth conditions using a large-scale liquid precipitation method. The crystallite size of cube-like NPs estimated from X-ray diffraction pattern increased linearly as the particle size (estimated by transmission electron microscopy) increased from 10 to 64.7 nm, which indicates that the NPs have a single-domain structure. This was further confirmed by the uniform lattice fringes. The critical size of approximately 76 nm was obtained by correlating particle size with both crystallite size and magnetic coercivity; this was reported for the first time in this study. The coercivity of cube-like Fe 3 O 4 NPs increased to a maximum of 190 Oe at the critical size, which suggests strong exchange interactions during spin alignment. Compared with cube-like NPs, sphere-like NPs have lower magnetic coercivity and remanence values, which is caused by the different orientations of their polycrystalline structure.

Two kinds of ferromagnetic nanocomposite fiber comprising α″-Fe16N2 and α-Fe nanoparticles (NPs), which have the highest magnetic moments as hard and soft magnetic materials, respectively, embedded in polyvinylpyrrolidone (PVP) have been synthesized via the magneto-electrospinning method. Both α″-Fe16N2 and α-Fe were single-domain core-shell NPs with an average outer diameter of 50 nm and Al2O3 as the shell. Ferrofluid precursors used for the electrospinning were prepared by dispersing these NPs in a PVP-toluene-methanol solution. The results show that applying the magnetic field in the same direction as the electric field resulted in smaller and more uniform fiber diameters. Nanocomposite fibers containing α″-Fe16N2 had smaller diameters than those containing α-Fe NPs. These magnetic-field effects on the fiber formation were explained by referring to the kinetic energy of the moving jet in the electrospinning process. In addition, magnetic hysteresis curves showed an enhancement of the magnetic coercivity (H(c)) and remanence (M(r)) by 22.9% and 22.25%, respectively. These results imply a promising possibility of constructing bulk magnetic materials using α″-Fe16N2 NPs, which furthermore reveals attractive features for many other magnetic applications, such as magnetic sensors.