The hydration of different active MgO under an unforced and ultrasonic condition was conducted in this paper to investigate the chemical kinetics model of the apparent reaction and discuss the mechanism combined with the product morphology. The dynamics fitting result shows that both the first-order and multi-rate model describe the hydration process under ultrasound well, while only the multi-rate model was right for the hydration process under an unforced condition. It indicated that the rate order of hydration was different in the hydration process under an unforced condition. The XRD and SEM show that the MgO hydration was a process of dissolution and crystallization. Part of the magnesium ions produced by dissolution of MgO did not diffuse into the solution in time, and adhered to the magnesium oxide surface and grew in situ instead. As a result, the difference in the hydration rate of the remaining MgO particles becomes wider and not in the same order (order of magnitude). The ultrasonic cavitation could prevent the in-situ growth of Mg(OH)₂ crystal nuclei on the surface of MgO. It not only greatly improved the hydration rate of MgO and produced monodisperse Mg(OH)₂ particles, but also made the first-order kinetics model fit the hydration process of MgO well.

This paper investigated the effects of using or not using potassium butyl xanthate (PBX) as a collector on the flotation kinetics of talc and chalcopyrite. By means of atomic force microscopy (AFM), Fourier-transform infrared spectroscopy (FTIR), a contact angle measuring instrument and particle size analyzer, the underlying causes behind the flotation rate changes of talc and chalcopyrite are analyzed. Experimental results showed that in collectorless flotation, the law of change in the flotation rate constant (k) of the two minerals over time is independent of pH, and k values of chalcopyrite are much smaller than those of talc. In the presence of PBX, the flotation speed of chalcopyrite greatly increases, and the k values of chalcopyrite are far larger than those of talc. This is mainly because the amount of xanthate adsorbed on the surface of chalcopyrite is large and the adsorption is in the form of chemisorption, while the adsorption of xanthate on the talcum surface is in very small amounts and in the form of physical adsorption. Simulation results indicated that the collectorless flotation of chalcopyrite conform to the classical first-order kinetics model and the Kelsall model, whereas that of talc only conform to the latter, which is due to the layered structure of talc. In the presence of the collector, talc flotation conforms to the two model, because talc has a higher floatability and particle morphology has less influence on the flotation rate.

Utilizing MgO as the precursor and deionized water as the solvent, this study synthesized nanoparticles of Mg(OH)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)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.

Carbon Capture, Utilization, and Storage (CCUS) technology plays a crucial role in China’s journey toward achieving “carbon neutrality”. To ensure the optimal efficiency and risk mitigation of CO₂-EOR projects, it is imperative to enhance the safety system. This study develops a comprehensive safety evaluation system for the CO₂-EOR project at Dagang Oilfield, employing a combination of the Analytic Hierarchy Process (AHP) and expert scoring. The AHP method is used to analyze the relative importance of various safety factors, while expert scoring is employed to determine the weight of each factor. The system establishes four primary evaluation indexes and 17 secondary evaluation indexes. This score indicates the relative safety of the blocks, with a lower score reflecting higher safety. A safety assessment is conducted on the Ye 21 and Ye 22 blocks using this system, which results in an assessment score of 1.2721 (less risky), indicating a relatively low overall risk. The study aims to provide a practical framework for the safety evaluation of CO₂-EOR projects, and the proposed method can be applied to other CCUS projects globally to enhance safety and risk management.

With the rapid development of the polymer materials industry and the improvement of people's environmental awareness, magnesium hydroxide has been widely used in polymer materials due to its high decomposition temperature, non-toxic smoke suppression, and the advantages of neutralizing harmful gases produced by polymer combustion. However, the conventional preparation methods of magnesium hydroxide exhibit several issues, including high hydrophilicity, elevated polarity, and limited compatibility with polymers. This research proposes an improved method by adding sodium stearate and KH560 modifier, controlling the rate of magnesium oxide and preparing magnesium hydroxide flame retardants using a modifier-directed hydration method. Various characterizations confirmed its morphology, particle size and structure. The magnesium hydroxide exhibits low polarity, small particle size, stable structure and excellent hydrophobicity (with a contact angle of 120.32°, and a free energy of 1.34mN/m). In parallel, the magnesium hydroxide/polypropylene composites demonstrate excellent flame retardancy (LOI of 25%, V-1 grade) and simultaneously enhance the dispersion of magnesium hydroxide within the polypropylene matrix, improving the material's toughness and strength.