Investigation of Crystallization Growth Characteristics of Mg[sub.2] Crystals under Unconstrained Conditions
Utilizing MgO as the precursor and deionized water as the solvent, this study synthesized nanoparticles of Mg(OH)[sub.2] via hydrothermal methods, aiming to control its purity, particle size, and morphology by understanding its growth under non-uniform nucleation. Characterization of crystal morphol...
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Veröffentlicht in: | Materials 2024-05, Vol.17 (9) |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Utilizing MgO as the precursor and deionized water as the solvent, this study synthesized nanoparticles of Mg(OH)[sub.2] via hydrothermal methods, aiming to control its purity, particle size, and morphology by understanding its growth under non-uniform nucleation. Characterization of crystal morphology and structure was conducted through scanning electron microscopy and X-ray diffraction, while laser particle size detection assessed the secondary particle size distribution. The study focused on how MgO’s hydrothermal process conditions influence Mg(OH)[sub.2] crystal growth, particularly through ion concentration and release rate adjustments to direct crystal growth facets. These adjustments shifted the dominant growth plane, enhancing the peak intensity ratio I001/I101 from 1.03 to 2.14, thereby reducing surface polarity and secondary aggregation of crystals. The study of the physicochemical properties of the same sample at different times revealed the pattern of crystal dissolution and recrystallization. A 2 h hydrothermal reaction notably altered the particle size distribution, with a decrease in particles sized 0.2~0.4 μm and an increase in those sized 0.4~0.6 μm, alongside new particles over 1 μm, indicating a shift toward uniformity through dissolution and recrystallization. Optimal conditions (6% magnesium oxide concentration, 160 °C, 2 h) led to the synthesis of highly dispersed, uniformly sized magnesium hydroxide, showcasing a simple, eco-friendly, and high-yield process. |
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ISSN: | 1996-1944 1996-1944 |
DOI: | 10.3390/ma17091956 |