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MgH2
Journal of Cleaner Production · 2026 · IF 10.7

Synergistic water regulation and byproduct confinement in non-woven fabric-encapsulated Al@MgH2 for controlled hydrogen generation via parallel and sequential reactor designs

Yu Xiong,Lizhong Duan,Huihu Wang,Shenghao Jiang,Chenhuinan Wei,Xing Xiang,Yun Zhao,Qianyu Wang

Non-woven fabric-encapsulated Al@MgH 2 blocks achieve controlled hydrolysis. • Non-woven fabric regulates water mass transfer and restricts byproduct expansion. • The sequential reactor produces hydrogen at a rate of 0.84 mL s −1 for 5177 s. • This work provides a safe and scalable material-to-system solution for H 2 supply. Active Al-based composite hydrolysis for hydrogen production holds broad application prospects in proton exchange membrane fuel cells (PEMFCs). However, key challenges such as controllability of hydrogen production, byproduct recovery, and hydrogen purity still need to be addressed. This study tackles these issues by designing a non-woven fabric-encapsulated hydrogen production unit and two hydrolysis reactors. This unit consists of a non-woven fabric envelope and an internal Al@30 % MgH 2 block. The regular pore structure of the non-woven fabric regulates water mass transfer and confines byproducts. This leads to effective control of hydrogen production, enhanced solution utilization, and one-step byproduct recovery. The parallel and sequential hydrogen production reactors were designed according to the hydrolysis characteristics of the encapsulated unit. The flow paths of the reaction solution were controlled accordingly. Under low solution flow rate conditions, the parallel reactor achieved a stable hydrogen generation rate (sHGR) of 1.36 mL s −1 over 3573 s. The measured total hydrogen generation was 4579 mL. In contrast, the sequential reactor maintained a sHGR of 0.84 mL s −1 over 5177 s. The measured total hydrogen generation was 4448 mL. Purity tests confirmed that the hydrogen purity exceeded 99.2 %. This study combines physical encapsulation, solution injection strategy, and reactor design. This integrated approach overcomes the explosive reaction of active powders, achieves tunable hydrolysis kinetics, and provides a practical pathway from laboratory to application. Download: Download high-res image (509KB) Download: Download full-size image

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Journal of Materials Chemistry A · 2014 ·Vol. 2 ·期 9 ·3155-3162 · IF 0

In situ formation of lithium fast-ion conductors and improved hydrogen desorption properties of the LiNH2–MgH2 system with the addition of lithium halides

Bo Li,Yongfeng Liu,Chao Li,Mingxia Gao,Hongge Pan

Lithium halides were introduced into the LiNH2–MgH2 system by ball milling the corresponding chemicals under 50 bar of H2 to decrease the dehydrogenation temperature and enhance the dehydrogenation kinetics. The results show that the LiNH2–MgH2–0.05LiBr sample exhibited optimal hydrogen storage performance. The onset dehydrogenation temperature of the LiNH2–MgH2–0.05LiBr sample was only 120 °C, which represents a 55 °C reduction with respect to that of the pristine LiNH2–MgH2 sample. The dehydrogenation rate of the LiNH2–MgH2 sample at 210 °C was increased threefold upon addition of LiBr, which is attributed to the reduction in the dehydrogenation activation energy. Moreover, the addition of LiBr could significantly suppress ammonia emission during the dehydrogenation process of the LiNH2–MgH2 sample. Structural examinations reveal that the added LiBr could react with LiNH2 to form Li7(NH2)6Br during the dehydrogenation process. The in situ-formed Li7(NH2)6Br not only weakens the N–H bond but also promotes the migration of Li+, consequently improving the dehydrogenation kinetics of the LiNH2–MgH2 sample.

研究领域: 材料科学 · 能源存储与转换
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