摘要
In this study, four chlorinated salts were incorporated as catalysts into aluminum composites through ball milling, resulting in the preparation of four activated aluminum composites (Al/Bi/M x Cl y ). The microstructure of these composites was thoroughly examined using Scanning Electron Microscopy (SEM), X-ray Photoelectron Spectroscopy (XPS), X-ray Diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy, and Thermogravimetric Analysis (TGA). Additionally, the hydrogen production characteristics of Al/Bi/M x Cl y during hydrolysis reactions were investigated. The findings indicate that various chloride salts (M x Cl y ) can be uniformly distributed on the surface of the activated aluminum composites. Among the four composites, Al/Bi/NH 4 Cl demonstrated the highest hydrogen production efficiency and volume at temperatures ranging from 10 to 40 °C. Specifically, at 40 °C, Al/Bi/NH 4 Cl achieved a maximum hydrogen generation rate of 82.2 mL‧g −1 ‧s −1 and a total hydrogen volume of 977 mL‧g −1 . Notably, even at 0 °C, Al/Bi/NH 4 Cl maintained a rapid hydrolysis reaction, with a hydrogen production rate of 19.8 mL‧g −1 ‧s −1 and a total hydrogen volume of 908 mL‧g −1 . To elucidate the hydrolysis reaction mechanism, the intermediate products, corrosion potentials, temperature variations, and pH changes within the reaction system were also analyzed in detail. The results confirmed that different M x Cl y catalysts exhibit distinct catalytic mechanisms for the reactive aluminum composites. Particularly, the addition of NH 4 Cl during the preparation process facilitated the formation of a multilayer structure in Al/Bi/NH 4 Cl, which effectively accelerated particle fragmentation during the hydrolysis. Furthermore, the acidic nature of NH 4 Cl efficiently suppressed the increase in solution pH, thereby reducing the deposition of aluminum hydroxide on the particle surfaces and enhancing the overall hydrolysis reaction of aluminum.
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